Inventario CE
Inventario CE
Applicazioni nidificate
Inventario CE
The EC inventory published below is a copy as received from the JRC in 2008 on the founding of ECHA. It is comprised of the following lists:
- EINECS (European INventory of Existing Commercial chemical Substances) as published in O.J. C 146A, 15.6.1990. EINECS is an inventory of substances that were deemed to be on the European Community market between 1 January 1971 and 18 September 1981. EINECS was drawn up by the European Commission in the application of Article 13 of Directive 67/548/EEC, as amended by Directive 79/831/EEC, and in accordance with the detailed provisions of Commission Decision 81/437/EEC. Substances listed in EINECS are considered phase-in substances under the REACH Regulation.
- ELINCS (European LIst of Notified Chemical Substances) in support of Directive 92/32/EEC, the 7th amendment to Directive 67/548/EEC. ELINCS lists those substances which were notified under Directive 67/548/EEC, the Dangerous Substances Directive Notification of New Substances (NONS) that became commercially available after 18 September 1981.
- NLP (No-Longer Polymers). The definition of polymers was changed in April 1992 by Council Directive 92/32/EEC amending Directive 67/548/EEC, with the result that substances previously considered to be polymers were no longer excluded from regulation. Thus the No-longer Polymers (NLP) list was drawn up, consisting of such substances that were commercially available between 18 September 1981 and 31 October 1993.
Database contains 106212 unique substances/entries.
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The distillate obtained during the heat treatment of low temperature coal tar pitch having an approximate distillation range of 100°C to 400°C (212°F to 752°F). Composed primarily of a complex mixture of aromatic compounds.
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310-276-7
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140413-63-4
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The distillate obtained during the heat treatment of low temperature coal tar pitch having an approximate distillation range of 100°C to 400°C (212°F to 752°F). Composed primarily of a complex mixture of aromatic compounds.
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The distillate from the vacuum distillation of the residue of the atmospheric distillate from the product of coal treated with a solvent in the presence of hydrogen at high temperatures (over 427°C (800°F)). Composed primarily of hydrocarbons boiling in a range of approximately 288°C to 454°C (550°F to 850°F). May contain minor amounts of organic oxygen compounds, nitrogen compounds, and sulfur compounds.
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270-078-0
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68410-07-1
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The distillate from the vacuum distillation of the residue of the atmospheric distillate from the product of coal treated with a solvent in the presence of hydrogen at high temperatures (over 427°C (800°F)). Composed primarily of hydrocarbons boiling in a range of approximately 288°C to 454°C (550°F to 850°F). May contain minor amounts of organic oxygen compounds, nitrogen compounds, and sulfur compounds.
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The distillate from the reaction products of the aqueous distillate from the destructive distillation of wood and ethyl alcohol.
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232-449-5
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8030-89-5
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The distillate from the reaction products of the aqueous distillate from the destructive distillation of wood and ethyl alcohol.
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The distillate from the fractionation of the liquid product from the treatment of coal with a solvent in the presence of hydrogen at high temperatures (above 427°C (800°F)) having a boiling range of approximately 193°C to 288°C (380°F to 550°F). Composed primarily of hydrocarbons. May contain minor amounts of organic oxygen compounds, nitrogen compounds, and sulfur compounds.
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272-773-4
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68911-57-9
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The distillate from the fractionation of the liquid product from the treatment of coal with a solvent in the presence of hydrogen at high temperatures (above 427°C (800°F)) having a boiling range of approximately 193°C to 288°C (380°F to 550°F). Composed primarily of hydrocarbons. May contain minor amounts of organic oxygen compounds, nitrogen compounds, and sulfur compounds.
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The distillate from the fractionation of the liquid obtained by treating coal with a solvent in the presence of hydrogen at high temperatures (over 427°C (800°F)). It boils in the range of approximately 193°C to 249°C (380°F to 480°F).
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270-080-1
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68410-09-3
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The distillate from the fractionation of the liquid obtained by treating coal with a solvent in the presence of hydrogen at high temperatures (over 427°C (800°F)). It boils in the range of approximately 193°C to 249°C (380°F to 480°F).
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The distillate from the fractional distillation of low-temperature coal tar having an approximate distillation range of 240°C to 360°C (464°F to 680°F). Composed primarily of hydrocarbons and phenolic compounds.
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310-234-8
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140203-24-3
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The distillate from the fractional distillation of low-temperature coal tar having an approximate distillation range of 240°C to 360°C (464°F to 680°F). Composed primarily of hydrocarbons and phenolic compounds.
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The distillate from the fractional distillation of low-temperature coal tar having an approximate distillation range of 235°C to 450°C (455°F to 842°F). Composed primarily of hydrocarbons.
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310-236-9
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140203-26-5
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The distillate from the fractional distillation of low-temperature coal tar having an approximate distillation range of 235°C to 450°C (455°F to 842°F). Composed primarily of hydrocarbons.
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The distillate from the fractional distillation of high-temperature coal tar having an approximate distillation range of 280°C to 450°C (536°F to 842°F). Composed primarily of tri- and polynuclear aromatic hydrocarbons.
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310-231-1
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140203-21-0
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The distillate from the fractional distillation of high-temperature coal tar having an approximate distillation range of 280°C to 450°C (536°F to 842°F). Composed primarily of tri- and polynuclear aromatic hydrocarbons.
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The distillate from the fractional distillation of high-temperature coal tar having an approximate distillation range of 260°C to 310°C (500°F to 590°F). It consists primarily of di- and trinuclear aromatic and heterocyclic hydrocarbons.
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310-284-0
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141321-67-7
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The distillate from the fractional distillation of high-temperature coal tar having an approximate distillation range of 260°C to 310°C (500°F to 590°F). It consists primarily of di- and trinuclear aromatic and heterocyclic hydrocarbons.
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The distillate from the fractional distillation of high-temperature coal tar having an approximate distillation range of 220°C to 450°C (428°F to 842°F). Composed primarily of three to four membered condensed ring aromatic hydrocarbons and other hydrocarbons
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310-233-2
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140203-23-2
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The distillate from the fractional distillation of high-temperature coal tar having an approximate distillation range of 220°C to 450°C (428°F to 842°F). Composed primarily of three to four membered condensed ring aromatic hydrocarbons and other hydrocarbons
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The distillate from the fractional distillation of high-temperature coal having an approximate distillation range of 30°C to180°C (86°F to 356°F). Composed primarily of C4 to C6 alifatic and aromatic hydrocarbons with carbon disulfide, cyclopentadiene and some hydrogen sulfide.
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310-300-6
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185323-42-6
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The distillate from the fractional distillation of high-temperature coal having an approximate distillation range of 30°C to180°C (86°F to 356°F). Composed primarily of C4 to C6 alifatic and aromatic hydrocarbons with carbon disulfide, cyclopentadiene and some hydrogen sulfide.
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The distillate from the fractional distillation of high temperature coal tar boiling in a range of approximately 235°C to 255°C (455°F to 491°F). Composed primarily of indole and isomeric monoethylnaphthalenes.
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310-302-7
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185323-43-7
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The distillate from the fractional distillation of high temperature coal tar boiling in a range of approximately 235°C to 255°C (455°F to 491°F). Composed primarily of indole and isomeric monoethylnaphthalenes.
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The distillate from the fractional distillation of gasification coal tar having an approximate distillation range of 280°C to 400°C (536°F to 752°F). Composed primarily of aromatic and other hydrocarbons, phenolic compounds, and organic nitrogen compounds.
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310-228-5
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140203-18-5
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The distillate from the fractional distillation of gasification coal tar having an approximate distillation range of 280°C to 400°C (536°F to 752°F). Composed primarily of aromatic and other hydrocarbons, phenolic compounds, and organic nitrogen compounds.
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The distillate from the fractional distillation of gasification coal tar having an approximate distillation range of 225°C to 330°C (437°F to 636°F). Composed primarily of naphthalene homologs, trinuclear aromatic hydrocarbons that may also contain heteroatoms, alifatic and naphthenic hydrocarbons, phenol homologs, and dinuclear phenols.
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310-224-3
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140203-15-2
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The distillate from the fractional distillation of gasification coal tar having an approximate distillation range of 225°C to 330°C (437°F to 636°F). Composed primarily of naphthalene homologs, trinuclear aromatic hydrocarbons that may also contain heteroatoms, alifatic and naphthenic hydrocarbons, phenol homologs, and dinuclear phenols.
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The distillate from the fractional distillation of coal gasification tar having an approximate boiling range of 350°C to 450°C (662°F to 842°F). Composed primarily of phenanthrene and anthracene homologs, tetranuclear aromatic hydrocarbons that may also contain heteroatoms, high-boiling alifatic and naphthenic hydrocarbons, and polynuclear phenols.
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310-229-0
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140203-19-6
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The distillate from the fractional distillation of coal gasification tar having an approximate boiling range of 350°C to 450°C (662°F to 842°F). Composed primarily of phenanthrene and anthracene homologs, tetranuclear aromatic hydrocarbons that may also contain heteroatoms, high-boiling alifatic and naphthenic hydrocarbons, and polynuclear phenols.
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The distillate from the distillation of the pitch obtained from bituminous high temperature tar. Composed primarily of tri- and polynuclear aromatic hydrocarbons and boiling in the range of approximately 300°C to 470°C (572°F to 878°F). The product may also contain heteroatoms.
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295-312-9
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91995-51-6
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The distillate from the distillation of the pitch obtained from bituminous high temperature tar. Composed primarily of tri- and polynuclear aromatic hydrocarbons and boiling in the range of approximately 300°C to 470°C (572°F to 878°F). The product may also contain heteroatoms.
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The distillate from the benzole recovery from coking plants. The benzole is from low-temperature coal tar. The distillate has an approximate boiling range of 45°C to 75°C (113°F to 167°F). Composed primarily of cyclopentadiene and may contain dimeric dicyclopentadiene.
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310-312-1
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186554-25-6
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The distillate from the benzole recovery from coking plants. The benzole is from low-temperature coal tar. The distillate has an approximate boiling range of 45°C to 75°C (113°F to 167°F). Composed primarily of cyclopentadiene and may contain dimeric dicyclopentadiene.
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The distillate from the acidification of alkaline washed lignite tar distillate boiling in the range of approximately 200°C to 230°C (392°F to 446°F). Composed primarily of m- and p-ethylphenol as well as cresols and xylenols.
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302-662-9
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94114-29-1
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The distillate from the acidification of alkaline washed lignite tar distillate boiling in the range of approximately 200°C to 230°C (392°F to 446°F). Composed primarily of m- and p-ethylphenol as well as cresols and xylenols.
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The distillate from low temperature coal tar having an approximate distillation range of 100°C to 450°C (212°F to 842°F). Composed primarily of aromatic and other hydrocarbons, phenolic compounds, and aromatic nitrogen compounds.
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310-275-1
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140413-62-3
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The distillate from low temperature coal tar having an approximate distillation range of 100°C to 450°C (212°F to 842°F). Composed primarily of aromatic and other hydrocarbons, phenolic compounds, and aromatic nitrogen compounds.
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The distillate from lignite tar boiling in the range of approximately 80°C to 250°C (176°F to 482°F). Composed primarily of aliphatic and aromatic hydrocarbons and monobasic phenols.
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302-674-4
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94114-40-6
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The distillate from lignite tar boiling in the range of approximately 80°C to 250°C (176°F to 482°F). Composed primarily of aliphatic and aromatic hydrocarbons and monobasic phenols.
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The distillate from high temperature coal tar having an approximate distillation range of 130°C to 250°C (266°F to 410°F). Composed primarily of naphthalene, alkylnaphthalenes, phenolic compounds, and aromatic nitrogen bases.
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266-016-7
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65996-82-9
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The distillate from high temperature coal tar having an approximate distillation range of 130°C to 250°C (266°F to 410°F). Composed primarily of naphthalene, alkylnaphthalenes, phenolic compounds, and aromatic nitrogen bases.
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The distillate from high temperature coal tar having an approximate distillation range of 130°C to 210°C (266°F to 410°F). Composed primarily of indene and other polycyclic ring systems containing a single aromatic ring. May contain phenolic compounds and aromatic nitrogen bases.
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310-254-7
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140362-63-6
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The distillate from high temperature coal tar having an approximate distillation range of 130°C to 210°C (266°F to 410°F). Composed primarily of indene and other polycyclic ring systems containing a single aromatic ring. May contain phenolic compounds and aromatic nitrogen bases.
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The distillate from either high temperature coal tar, coke oven light oil, or coal tar oil alkaline extract residue having an approximate distillation range of 130°C to 210°C (266°F to 410°F) Composed primarily of indene and other polycyclic ring systems containing a single aromatic ring. May contain phenolic compounds and aromatic nitrogen bases.
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266-013-0
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65996-79-4
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The distillate from either high temperature coal tar, coke oven light oil, or coal tar oil alkaline extract residue having an approximate distillation range of 130°C to 210°C (266°F to 410°F) Composed primarily of indene and other polycyclic ring systems containing a single aromatic ring. May contain phenolic compounds and aromatic nitrogen bases.
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The distillate from either high temperature coal tar or coke oven light oil having an approximate distillation range of 130°C to 210°C (266°F to 410°F). Composed primarily of indene and other polycyclic ring systems containing a single aromatic ring. May contain phenolic compounds and aromatic nitrogen bases.
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310-253-1
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140362-62-5
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The distillate from either high temperature coal tar or coke oven light oil having an approximate distillation range of 130°C to 210°C (266°F to 410°F). Composed primarily of indene and other polycyclic ring systems containing a single aromatic ring. May contain phenolic compounds and aromatic nitrogen bases.
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The distillate from coke oven light oil having an approximate distillation range below 100°C (212°F). Composed primarily of C4 to C6 aliphatic hydrocarbons.
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266-023-5
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65996-88-5
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The distillate from coke oven light oil having an approximate distillation range below 100°C (212°F). Composed primarily of C4 to C6 aliphatic hydrocarbons.
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The distillate from coal tar having an approximate distillation range of 220°C to 450°C (428°F to 842°F). Composed primarily of three to four membered condensed ring aromatic hydrocarbons and other hydrocarbons.
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266-026-1
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65996-91-0
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The distillate from coal tar having an approximate distillation range of 220°C to 450°C (428°F to 842°F). Composed primarily of three to four membered condensed ring aromatic hydrocarbons and other hydrocarbons.
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The distillate from coal tar having an approximate distillation range of 100°C to 450°C (212°F to 842°F). Composed primarily of two to four membered condensed ring aromatic hydrocarbons, phenolic compounds, and aromatic nitrogen bases.
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266-027-7
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65996-92-1
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The distillate from coal tar having an approximate distillation range of 100°C to 450°C (212°F to 842°F). Composed primarily of two to four membered condensed ring aromatic hydrocarbons, phenolic compounds, and aromatic nitrogen bases.
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The distillate from coal gasification tar having an approximate distillation range of 80°C to 420°C (176°F to 788°F). Composed primarily of aromatic and other hydrocarbons, phenolic compounds, and aromatic nitrogen compounds.
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310-226-4
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140203-17-4
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The distillate from coal gasification tar having an approximate distillation range of 80°C to 420°C (176°F to 788°F). Composed primarily of aromatic and other hydrocarbons, phenolic compounds, and aromatic nitrogen compounds.
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The distillate from aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oils, having an approximate boiling range of 155°C to 180°C (311°F to 356°F). Composed primarily of indene, indan, and trimethylbenzenes.
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310-252-6
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140362-61-4
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The distillate from aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oils, having an approximate boiling range of 155°C to 180°C (311°F to 356°F). Composed primarily of indene, indan, and trimethylbenzenes.
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The distillate from aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oils, having an approximate boiling range of 155°C to 180°C (311°F to 356°F). Composed primarily of indene, indan and trimethylbenzenes.
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292-626-8
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90641-03-5
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The distillate from aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oils, having an approximate boiling range of 155°C to 180°C (311°F to 356°F). Composed primarily of indene, indan and trimethylbenzenes.
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The distillate from alkali-washed naphthalene oil having an approximate distillation range of 180°C to 220°C (356°F to 428°F). Composed primarily of naphthalene, alkylbenzenes, indene and indan.
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292-627-3
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90641-04-6
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The distillate from alkali-washed naphthalene oil having an approximate distillation range of 180°C to 220°C (356°F to 428°F). Composed primarily of naphthalene, alkylbenzenes, indene and indan.
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The distillate from alkali-washed naphthalene oil from high temperature coal tar having an approximate distillation range of 180°C to 220°C (356°F to 428°F). Composed primarily of naphthalene, alkylbenzenes, indene, and indan.
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310-256-8
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140362-65-8
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The distillate from alkali-washed naphthalene oil from high temperature coal tar having an approximate distillation range of 180°C to 220°C (356°F to 428°F). Composed primarily of naphthalene, alkylbenzenes, indene, and indan.
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The distillate from a mixture of coal tar and aromatic petroleum streams having an approximate distillation range of 220°C to 450°C (428°F to 842°F). Composed primarily of 3- to 4-membered condensed ring aromatic hydrocarbons.
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269-159-3
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68188-48-7
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The distillate from a mixture of coal tar and aromatic petroleum streams having an approximate distillation range of 220°C to 450°C (428°F to 842°F). Composed primarily of 3- to 4-membered condensed ring aromatic hydrocarbons.
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The dilute aqueous solution extracted from the gas evolved in the high temperature (greater than 700°C (1292°F)) destructive distillation of coal. Composed primarily of ammonium carbonate and other ammonium salts. May contain other water-soluble substances including phenol.
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266-014-6
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65996-80-7
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The dilute aqueous solution extracted from the gas evolved in the high temperature (greater than 700°C (1292°F)) destructive distillation of coal. Composed primarily of ammonium carbonate and other ammonium salts. May contain other water-soluble substances including phenol.
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The dilute aqueous solution condensed from the gas evolved in the low-temperature destructive distillation of coal. Composed primarily of ammonium carbonate and other ammonium salts.
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309-970-2
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101794-87-0
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The dilute aqueous solution condensed from the gas evolved in the low-temperature destructive distillation of coal. Composed primarily of ammonium carbonate and other ammonium salts.
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The deposit removed from crude coal tar storages. Composed primarily of coal tar and carbonaceous particulate matter.
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293-764-1
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91082-50-7
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The deposit removed from crude coal tar storages. Composed primarily of coal tar and carbonaceous particulate matter.
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The cooking aqueous solution formed by the absorption of sulfur dioxide gas in an aqueous solution of sodium hydroxide or sodium carbonate. It is used to produce the pulp from wood chips.
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270-710-5
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68477-10-1
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The cooking aqueous solution formed by the absorption of sulfur dioxide gas in an aqueous solution of sodium hydroxide or sodium carbonate. It is used to produce the pulp from wood chips.
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The constituent amino acids produced by the hydrolysis of caseins.
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265-363-1
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65072-00-6
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The constituent amino acids produced by the hydrolysis of caseins.
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The constituent amino acids derived by hydrolysis of proteins.
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310-296-6
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9015-54-7
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The constituent amino acids derived by hydrolysis of proteins.
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The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700°C (1292°F)) destructive distillation of coal. Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons with a high solid content of coal- and coke-type materials.
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273-615-7
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68990-61-4
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The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700°C (1292°F)) destructive distillation of coal. Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons with a high solid content of coal- and coke-type materials.
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The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700°C (1292°F)) destructive distillation of coal. A black viscous liquid denser than water. Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons. May contain minor amounts of phenolic compounds and aromatic nitrogen bases.
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266-024-0
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65996-89-6
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The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in the high temperature (greater than 700°C (1292°F)) destructive distillation of coal. A black viscous liquid denser than water. Composed primarily of a complex mixture of condensed ring aromatic hydrocarbons. May contain minor amounts of phenolic compounds and aromatic nitrogen bases.
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The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in low temperature (less than 700°C (1292°F)) destructive distillation of coal. A black viscous liquid denser than water. Composed primarily of condensed ring aromatic hydrocarbons, phenolic compounds, aromatic nitrogen bases, and their alkyl derivatives.
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266-025-6
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65996-90-9
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The condensation product obtained by cooling, to approximately ambient temperature, the gas evolved in low temperature (less than 700°C (1292°F)) destructive distillation of coal. A black viscous liquid denser than water. Composed primarily of condensed ring aromatic hydrocarbons, phenolic compounds, aromatic nitrogen bases, and their alkyl derivatives.
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The complex residuum produced by the distillation of tallow fatty acids. It contains primarily glycerides, C16-20 saturated fatty acids, C36 dimer acid, C54 trimer acid and heavier polymeric acids.
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274-307-5
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70084-85-4
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The complex residuum produced by the distillation of tallow fatty acids. It contains primarily glycerides, C16-20 saturated fatty acids, C36 dimer acid, C54 trimer acid and heavier polymeric acids.
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The complex residuum obtained by chilling cottonseed oil and separating off the liquid oil. Contains primarily triglycerides having a high proportion of saturated fatty acids.
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274-332-1
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70131-59-8
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The complex residuum obtained by chilling cottonseed oil and separating off the liquid oil. Contains primarily triglycerides having a high proportion of saturated fatty acids.
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The complex residuum from the regeneration of solvents used to recover butadiene from other C4 hydrocarbons. It consists primarily of furfural polymers and furfural butadiene polymers. Calcium carboxylates, furfural and methoxypropionitrile may also be present.
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269-776-8
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68333-21-1
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The complex residuum from the regeneration of solvents used to recover butadiene from other C4 hydrocarbons. It consists primarily of furfural polymers and furfural butadiene polymers. Calcium carboxylates, furfural and methoxypropionitrile may also be present.
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The complex residuum from the lime-treatment of ammonia liquor. Contains calcium carbonate, calcium sulfate, calcium hydroxide residual ammonia with trace amounts of other chemicals.
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273-648-7
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68991-61-7
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The complex residuum from the lime-treatment of ammonia liquor. Contains calcium carbonate, calcium sulfate, calcium hydroxide residual ammonia with trace amounts of other chemicals.
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The complex residuum from the distillation of the products from the hydrolysis of C16-18 and C18-unsaturated fatty acid glycerides. It contains predominantly trialkylglycerides and undistilled carboxylic acids.
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274-561-7
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70321-71-0
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The complex residuum from the distillation of the products from the hydrolysis of C16-18 and C18-unsaturated fatty acid glycerides. It contains predominantly trialkylglycerides and undistilled carboxylic acids.
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The complex residuum from the distillation of the methyl esters of coconut oil fatty acids. It consists predominantly on mono-, di-, and triglycerides of coconut oil fatty acids, unsaponifiable material, polymerized unsaturated fatty acids, phosphatides.
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273-192-9
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68953-21-9
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The complex residuum from the distillation of the methyl esters of coconut oil fatty acids. It consists predominantly on mono-, di-, and triglycerides of coconut oil fatty acids, unsaponifiable material, polymerized unsaturated fatty acids, phosphatides.
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The complex residuum from the distillation of the methyl esters of C8-18 and C18-unsatd. fatty acids. It consists primarily of trialkyl glycerides and undistilled methyl esters of the fatty acids.
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271-690-0
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68604-39-7
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The complex residuum from the distillation of the methyl esters of C8-18 and C18-unsatd. fatty acids. It consists primarily of trialkyl glycerides and undistilled methyl esters of the fatty acids.
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The complex residuum from the distillation of the methyl esters of C14-18 and C16-18-unsatd. fatty acids. It consists primarily of trialkyl glycerides and undistilled methyl esters of the fatty acids.
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271-691-6
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68604-40-0
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The complex residuum from the distillation of the methyl esters of C14-18 and C16-18-unsatd. fatty acids. It consists primarily of trialkyl glycerides and undistilled methyl esters of the fatty acids.
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The complex residuum from the distillation of the methyl ester of C16-18 and C18-unsatd. fatty acids. It consists primarily of trialkyl glycerides and undistilled methyl ester of the fatty acids.
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271-692-1
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68604-41-1
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The complex residuum from the distillation of the methyl ester of C16-18 and C18-unsatd. fatty acids. It consists primarily of trialkyl glycerides and undistilled methyl ester of the fatty acids.
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The complex residuum from the distillation of the 80% or greater limonene terpene fraction from oil of turpentine. It consists predominantly of hydrocarbons, alcohols, ethers, aldehydes and ketones.
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269-829-5
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68334-40-7
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The complex residuum from the distillation of the 80% or greater limonene terpene fraction from oil of turpentine. It consists predominantly of hydrocarbons, alcohols, ethers, aldehydes and ketones.
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The complex residuum from the distillation of sulfate turpentine. It consists predominantly of diterpenes, sesquiterpenes, and polyterpenes with some high boiling oxygenated terpenes.
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273-108-0
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68938-00-1
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The complex residuum from the distillation of sulfate turpentine. It consists predominantly of diterpenes, sesquiterpenes, and polyterpenes with some high boiling oxygenated terpenes.
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The complex residuum from the distillation of products from the thermal hydrodealkylation of alkylnaphthalene and toluene. It consists predominantly of bi- and polynuclear aromatic hydrocarbons such as naphthalenes, biphenyl, fluorene and phenanthrene.
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269-799-3
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68333-90-4
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The complex residuum from the distillation of products from the thermal hydrodealkylation of alkylnaphthalene and toluene. It consists predominantly of bi- and polynuclear aromatic hydrocarbons such as naphthalenes, biphenyl, fluorene and phenanthrene.
|
Details | |
|
The complex residuum from the distillation of products from the caustic oxidation of castor oil. It consists primarily of C16-18 fatty acids monomers, C36 dimers, C54 trimers and higher polymeric acids.
|
273-298-5
|
68956-05-8
|
The complex residuum from the distillation of products from the caustic oxidation of castor oil. It consists primarily of C16-18 fatty acids monomers, C36 dimers, C54 trimers and higher polymeric acids.
|
Details | |
|
The complex residuum from the distillation of geraniol. It consists predominantly of C20 diterpenes and diterpene ethers, and C10 branched glycols.
|
274-325-3
|
70131-51-0
|
The complex residuum from the distillation of geraniol. It consists predominantly of C20 diterpenes and diterpene ethers, and C10 branched glycols.
|
Details | |
|
The complex residuum from the distillation of ethylbenzene. It consists primarily of polyethylbenzenes and ethyldiphenyl ethanes with various small amounts of diethylbenzenes and butylbenzenes.
|
273-494-0
|
68987-42-8
|
The complex residuum from the distillation of ethylbenzene. It consists primarily of polyethylbenzenes and ethyldiphenyl ethanes with various small amounts of diethylbenzenes and butylbenzenes.
|
Details | |
|
The complex residuum from the distillation of C8-18 alkylamines. It may contain C8-18 alkylamines, di-C8-18-alkylamines, tri-C8-18-alkylamines, and C8-18 amides.
|
272-783-9
|
68911-69-3
|
The complex residuum from the distillation of C8-18 alkylamines. It may contain C8-18 alkylamines, di-C8-18-alkylamines, tri-C8-18-alkylamines, and C8-18 amides.
|
Details | |
|
The complex residuum from the distillation of C10-16-alkyldimethylamines. It may contain alkyl bromides and undistilled alkylamines.
|
271-665-4
|
68603-57-6
|
The complex residuum from the distillation of C10-16-alkyldimethylamines. It may contain alkyl bromides and undistilled alkylamines.
|
Details | |
|
The complex residuum from the amine system for removal of hydrogen sulfide. It consists primarily of hydrogen, methane and ethane with various small amounts of nitrogen, carbon dioxide and hydrocarbons having carbon numbers predominantly in the range of C3 through C5.
|
270-668-8
|
68476-27-7
|
The complex residuum from the amine system for removal of hydrogen sulfide. It consists primarily of hydrogen, methane and ethane with various small amounts of nitrogen, carbon dioxide and hydrocarbons having carbon numbers predominantly in the range of C3 through C5.
|
Details | |
|
The complex residuum from the alkylation of aniline with ethylene. It consists primarily of polymeric materials, ethylated anilines such as 2,4,6-triethylaniline, 2-sec-butyl-6-ethylaniline, ar-sec-butyldiethylaniline and diethylaniline dimer, diphenylamine and ar-ethyldiphenylamine.
|
276-460-3
|
72207-55-7
|
The complex residuum from the alkylation of aniline with ethylene. It consists primarily of polymeric materials, ethylated anilines such as 2,4,6-triethylaniline, 2-sec-butyl-6-ethylaniline, ar-sec-butyldiethylaniline and diethylaniline dimer, diphenylamine and ar-ethyldiphenylamine.
|
Details | |
|
The complex residue resulting from the vacuum distillation of C6-24 fatty alcohols which is derived from hydrogenation of C6-24 fatty acids methyl esters. It consists predominantly of satd. fatty alcohols having carbon numbers greater than C18, dimerization products, and long chain esters having carbon numbers greater than C32 and boils at > 250°C (482°F) at 10 torr.
|
310-080-1
|
102242-49-9
|
The complex residue resulting from the vacuum distillation of C6-24 fatty alcohols which is derived from hydrogenation of C6-24 fatty acids methyl esters. It consists predominantly of satd. fatty alcohols having carbon numbers greater than C18, dimerization products, and long chain esters having carbon numbers greater than C32 and boils at > 250°C (482°F) at 10 torr.
|
Details | |
|
The complex residue resulting from the vacuum distillation of C6-24 and C6-24 unsatd. fatty alcohols which is derived from hydrogenation of C6-24 and C6-24 unsatd. fatty acids methyl esters. It consists predominantly of satd. and unsatd. fatty alcohols having carbon numbers greater than C18, dimerization products, and long chain esters having carbon numbers greater than C32 and boils at > 250°C (482°F) at 10 torr.
|
310-079-6
|
102242-48-8
|
The complex residue resulting from the vacuum distillation of C6-24 and C6-24 unsatd. fatty alcohols which is derived from hydrogenation of C6-24 and C6-24 unsatd. fatty acids methyl esters. It consists predominantly of satd. and unsatd. fatty alcohols having carbon numbers greater than C18, dimerization products, and long chain esters having carbon numbers greater than C32 and boils at > 250°C (482°F) at 10 torr.
|
Details | |
|
The complex residue resulting from the vacuum distillation of C12-24 unsatd. fatty alcohols which is derived from hydrogenation of C12-24 unsatd. fatty acids methyl esters. It consists predominantly of unsatd. fatty alcohols having carbon numbers greater than C18, dimerization products, and long chain esters having carbon numbers greater than C32 and boils at > 250°C (482°F) at 10 torr.
|
310-081-7
|
102242-50-2
|
The complex residue resulting from the vacuum distillation of C12-24 unsatd. fatty alcohols which is derived from hydrogenation of C12-24 unsatd. fatty acids methyl esters. It consists predominantly of unsatd. fatty alcohols having carbon numbers greater than C18, dimerization products, and long chain esters having carbon numbers greater than C32 and boils at > 250°C (482°F) at 10 torr.
|
Details | |
|
The complex residue resulting from the distillation of C6-24 glycerides which is derived from saponification of natural fats having a carbon range of C6-24. It consists predominantly of glycerides of C6-24 unsatd. fatty acids and other oligomers.
|
310-088-5
|
102242-56-8
|
The complex residue resulting from the distillation of C6-24 glycerides which is derived from saponification of natural fats having a carbon range of C6-24. It consists predominantly of glycerides of C6-24 unsatd. fatty acids and other oligomers.
|
Details | |
|
The complex residue resulting from the distillation of C6-24 fatty acids which is derived from hydrogenation of saponified natural fats having carbon numbers in the range of C6-24. It consists predominantly of glycerides of C6-24 fatty acids, sterols, and wax esters and boils at > 150°C (302°F) at 10 torr.
|
310-084-3
|
102242-53-5
|
The complex residue resulting from the distillation of C6-24 fatty acids which is derived from hydrogenation of saponified natural fats having carbon numbers in the range of C6-24. It consists predominantly of glycerides of C6-24 fatty acids, sterols, and wax esters and boils at > 150°C (302°F) at 10 torr.
|
Details | |
|
The complex residue resulting from the distillation of C6-24 and C6-24 unsatd. fatty acids which is derived from saponification of natural fats having a carbon range of C6-24. It consists predominantly of glycerides of C6-24 and C6-24 unsatd. fatty acids, sterols, and wax esters and boils at > 150°C (302°F) at 10 torr.
|
310-082-2
|
102242-51-3
|
The complex residue resulting from the distillation of C6-24 and C6-24 unsatd. fatty acids which is derived from saponification of natural fats having a carbon range of C6-24. It consists predominantly of glycerides of C6-24 and C6-24 unsatd. fatty acids, sterols, and wax esters and boils at > 150°C (302°F) at 10 torr.
|
Details | |
|
The complex residue resulting from the distillation of C6-24 and C6-24 unsatd. fatty acids methyl esters which is derived from natural fats having a carbon range of C6-24. It consists predominantly of satd. and unsatd. fatty acids methyl esters having carbon numbers greater than C20, dimerization products, and wax esters and boils at > 200°C (392°F) at 10 torr.
|
310-083-8
|
102242-52-4
|
The complex residue resulting from the distillation of C6-24 and C6-24 unsatd. fatty acids methyl esters which is derived from natural fats having a carbon range of C6-24. It consists predominantly of satd. and unsatd. fatty acids methyl esters having carbon numbers greater than C20, dimerization products, and wax esters and boils at > 200°C (392°F) at 10 torr.
|
Details | |
|
The complex residue resulting from the distillation of C12-24 unsatd. fatty acids which is derived from saponification of natural fats having a carbon range of C12-24. It consists predominantly of glycerides of C12-24 unsatd. fatty acids, sterols, and wax esters and boils at > 150°C (302°F) at 10 torr.
|
310-085-9
|
102242-54-6
|
The complex residue resulting from the distillation of C12-24 unsatd. fatty acids which is derived from saponification of natural fats having a carbon range of C12-24. It consists predominantly of glycerides of C12-24 unsatd. fatty acids, sterols, and wax esters and boils at > 150°C (302°F) at 10 torr.
|
Details | |
|
The complex reaction product of blended acids and blended alcohols which simulates the composition of natural beeswax. It consists primarily of C18-30-alkyl ester of C16-32 fatty acids, C16-32 fatty acids and C22-34 alkanes.
|
275-286-5
|
71243-51-1
|
The complex reaction product of blended acids and blended alcohols which simulates the composition of natural beeswax. It consists primarily of C18-30-alkyl ester of C16-32 fatty acids, C16-32 fatty acids and C22-34 alkanes.
|
Details | |
|
The complex organic residue from the distillation of pyroligneous acids obtained from the destructive distillation of wood.
|
295-468-8
|
92061-56-8
|
The complex organic residue from the distillation of pyroligneous acids obtained from the destructive distillation of wood.
|
Details | |
|
The complex of antimony and tannins with the substance identified in the Colour Index by Colour Index Constitution Number, C.I.42535.
|
273-548-3
|
68989-19-5
|
The complex of antimony and tannins with the substance identified in the Colour Index by Colour Index Constitution Number, C.I.42535.
|
Details | |
|
The complex liquid combination obtained by chilling soybean oil or hydrogenated soybean oil and separating off the liquid oil. Contains primarily triglycerides.
|
272-848-1
|
68918-03-6
|
The complex liquid combination obtained by chilling soybean oil or hydrogenated soybean oil and separating off the liquid oil. Contains primarily triglycerides.
|
Details | |
|
The complex liquid combination obtained by chilling mixed vegetable oil and separating off the liquid oil. Contains primarily triglycerides.
|
269-821-1
|
68334-29-2
|
The complex liquid combination obtained by chilling mixed vegetable oil and separating off the liquid oil. Contains primarily triglycerides.
|
Details | |
|
The complex combination produced by the high temperature (816°C (1500°F)) calcination of bastnaesite. It consists primarily of rare earth oxides, fluorides, and oxyfluorides.
|
272-694-5
|
68909-13-7
|
The complex combination produced by the high temperature (816°C (1500°F)) calcination of bastnaesite. It consists primarily of rare earth oxides, fluorides, and oxyfluorides.
|
Details | |
|
The complex combination of products produced by the distillation of products from a 2-ethyl-1-hexanol manufacturing process. It consists predominantly of organic compounds such as alcohols, aldehydes, esters, carboxylic acids and acetals having carbon numbers predominantly in the range of C4 through C16 and boiling in the range of 150°C to 308°C (302°F to 586°F).
|
271-832-1
|
68609-68-7
|
The complex combination of products produced by the distillation of products from a 2-ethyl-1-hexanol manufacturing process. It consists predominantly of organic compounds such as alcohols, aldehydes, esters, carboxylic acids and acetals having carbon numbers predominantly in the range of C4 through C16 and boiling in the range of 150°C to 308°C (302°F to 586°F).
|
Details | |
|
The complex combination of polyalkylated pyridines derived from coal tar distillation or as high-boiling distillates approximately above 150°C (302°F) from the reaction of ammonia with acetaldehyde, formaldehyde or paraformaldehyde.
|
269-929-9
|
68391-11-7
|
The complex combination of polyalkylated pyridines derived from coal tar distillation or as high-boiling distillates approximately above 150°C (302°F) from the reaction of ammonia with acetaldehyde, formaldehyde or paraformaldehyde.
|
Details | |
|
The complex combination of organic compounds remaining after the aqueous alkali extraction of oxidized light petroleum distillate.
|
271-630-3
|
68602-99-3
|
The complex combination of organic compounds remaining after the aqueous alkali extraction of oxidized light petroleum distillate.
|
Details | |
|
The complex combination of hydrocarbons produced from the distillation of thermally cracked styrene residues. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C10 and boiling in the range of approximately 153°C to 199°C (307°F to 391°F).
|
272-920-2
|
68920-43-4
|
The complex combination of hydrocarbons produced from the distillation of thermally cracked styrene residues. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C10 and boiling in the range of approximately 153°C to 199°C (307°F to 391°F).
|
Details | |
|
The complex combination of hydrocarbons produced by the vacuum distillation of products from the production of 1,6-hexanediol. It consists predominantly of dimers and trimers of ethers of hydrocarbons having carbon numbers predominantly in the range of C4 through C6 with various small amounts of glycols and ethers of the same carbon numbers and boiling in the range of approximately 250°C to 400°C (482°F to 752°F).
|
273-061-6
|
68937-29-1
|
The complex combination of hydrocarbons produced by the vacuum distillation of products from the production of 1,6-hexanediol. It consists predominantly of dimers and trimers of ethers of hydrocarbons having carbon numbers predominantly in the range of C4 through C6 with various small amounts of glycols and ethers of the same carbon numbers and boiling in the range of approximately 250°C to 400°C (482°F to 752°F).
|
Details | |
|
The complex combination of hydrocarbons produced by the hydroformylation of nonene. It consists predominantly of C9 olefins and paraffins, C10 alcohols and aldehydes, and C30 acetals and boils in the range of approximately 135°C to 415°C (275°F to 779°F).
|
273-111-7
|
68938-04-5
|
The complex combination of hydrocarbons produced by the hydroformylation of nonene. It consists predominantly of C9 olefins and paraffins, C10 alcohols and aldehydes, and C30 acetals and boils in the range of approximately 135°C to 415°C (275°F to 779°F).
|
Details | |
|
The complex combination of hydrocarbons produced by the hydroformylation of dodecene. It consists predominantly of C12 olefins and paraffins, C13 alcohols and aldehydes, and C39 acetals and boils in the range of approximately 160°C to 450°C (320°F to 842°F).
|
271-251-3
|
68527-06-0
|
The complex combination of hydrocarbons produced by the hydroformylation of dodecene. It consists predominantly of C12 olefins and paraffins, C13 alcohols and aldehydes, and C39 acetals and boils in the range of approximately 160°C to 450°C (320°F to 842°F).
|
Details | |
|
The complex combination of hydrocarbons produced by the distillation of the products from the hydrogenation of isohexanal from the hydroformylation of pentene. It consists predominantly of C5 olefins and paraffins and C6 alcohols and aldehydes and boils in the range of approximately 45°C to 151°C (113°F to 304°F).
|
273-109-6
|
68938-02-3
|
The complex combination of hydrocarbons produced by the distillation of the products from the hydrogenation of isohexanal from the hydroformylation of pentene. It consists predominantly of C5 olefins and paraffins and C6 alcohols and aldehydes and boils in the range of approximately 45°C to 151°C (113°F to 304°F).
|
Details | |
|
The complex combination of hydrocarbons produced by the distillation of the products from the acetylation of 4-tert-butylcyclohexanol. It may contain such compounds as 4-tert-butylcyclohexanol acetate, tert-butylcyclohexane and tert-butylbenzene.
|
272-772-9
|
68911-56-8
|
The complex combination of hydrocarbons produced by the distillation of the products from the acetylation of 4-tert-butylcyclohexanol. It may contain such compounds as 4-tert-butylcyclohexanol acetate, tert-butylcyclohexane and tert-butylbenzene.
|
Details | |
|
The complex combination of hydrocarbons produced by the distillation of products from the hydrogenation of isooctanal from the hydroformylation of heptene. It consists predominantly of C8-9 primary aliphatic alcohols, C14-18 dimer alcohols, C>16 acetals and esters and C>10 acid sodium salts and boils in the range of approximately 185°C to 385°C (365°F to 725°F).
|
271-236-1
|
68526-88-5
|
The complex combination of hydrocarbons produced by the distillation of products from the hydrogenation of isooctanal from the hydroformylation of heptene. It consists predominantly of C8-9 primary aliphatic alcohols, C14-18 dimer alcohols, C>16 acetals and esters and C>10 acid sodium salts and boils in the range of approximately 185°C to 385°C (365°F to 725°F).
|
Details | |
|
The complex combination of hydrocarbons produced by the distillation of products from the hydrogenation of isooctanal from the hydroformylation of heptene. It consists predominantly of C7 olefins and paraffins and C8 alcohols and aldehydes and boils in the range of approximately 85°C to 183°C (185°F to 361°F).
|
271-242-4
|
68526-96-5
|
The complex combination of hydrocarbons produced by the distillation of products from the hydrogenation of isooctanal from the hydroformylation of heptene. It consists predominantly of C7 olefins and paraffins and C8 alcohols and aldehydes and boils in the range of approximately 85°C to 183°C (185°F to 361°F).
|
Details | |
|
The complex combination of hydrocarbons produced by the distillation of products from the hydrogenation of isononanal. It consists predominantly of C6 olefins and paraffins and C9 alcohols and aldehydes and boiling in the range of approximately 110°C to 202°C (230°F to 396°F).
|
273-110-1
|
68938-03-4
|
The complex combination of hydrocarbons produced by the distillation of products from the hydrogenation of isononanal. It consists predominantly of C6 olefins and paraffins and C9 alcohols and aldehydes and boiling in the range of approximately 110°C to 202°C (230°F to 396°F).
|
Details | |
|
The complex combination of hydrocarbons produced by the distillation of products from the hydrogenation of isodecanal from the hydroformylation of nonene. It consists predominantly of C9 olefins and paraffins and C10 alcohols and aldehydes and boils in the range of 135°C to 205°C (275°F to 401°F).
|
271-241-9
|
68526-93-2
|
The complex combination of hydrocarbons produced by the distillation of products from the hydrogenation of isodecanal from the hydroformylation of nonene. It consists predominantly of C9 olefins and paraffins and C10 alcohols and aldehydes and boils in the range of 135°C to 205°C (275°F to 401°F).
|
Details | |
|
270-153-8
|
68411-90-5
|
The complex combination of hydrocarbons produced by the distillation of products from the hydrogenation of adiponitrile. It contains such compounds as 6-aminohexanamide, 6-aminohexanenitrile, bishexamethylenetriamine, 1,2-cyclohexanediamine, and decanediamines.
|
Details | ||
|
The complex combination of hydrocarbons produced by the distillation of products from the air oxidation of cyclohexane after removal of acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 172°C to 324°C (342°F to 615°F).
|
271-816-4
|
68609-04-1
|
The complex combination of hydrocarbons produced by the distillation of products from the air oxidation of cyclohexane after removal of acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 172°C to 324°C (342°F to 615°F).
|
Details | |
|
The complex combination of hydrocarbons produced by the distillation of products from the air oxidation of cyclohexane after removal of acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C6.
|
271-818-5
|
68609-05-2
|
The complex combination of hydrocarbons produced by the distillation of products from the air oxidation of cyclohexane after removal of acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C6.
|
Details | |
|
The complex combination of hydrocarbons produced by the distillation of products from cumene manufacturing process. It consists primarily of diisopropylbenzene with various small amounts of C4 substituted benzenes and heavier non-aromatic hydrocarbons.
|
273-050-6
|
68936-98-1
|
The complex combination of hydrocarbons produced by the distillation of products from cumene manufacturing process. It consists primarily of diisopropylbenzene with various small amounts of C4 substituted benzenes and heavier non-aromatic hydrocarbons.
|
Details | |
|
The complex combination of hydrocarbons produced by the distillation of products from an ethylene manufacturing process. It consists predominantly of aromatic hydrocqdarbons having carbon numbers predominantly in the range of C5 through C11.
|
272-951-1
|
68921-67-5
|
The complex combination of hydrocarbons produced by the distillation of products from an ethylene manufacturing process. It consists predominantly of aromatic hydrocqdarbons having carbon numbers predominantly in the range of C5 through C11.
|
Details | |
|
The complex combination of hydrocarbons produced by the distillation of products from 1,6-hexanediol manufacturing process. It consists primarily of alcohols and glycols having carbon numbers predominantly in the range of C4 through C6 and boiling at approximately 127°C (260°F).
|
271-831-6
|
68609-64-3
|
The complex combination of hydrocarbons produced by the distillation of products from 1,6-hexanediol manufacturing process. It consists primarily of alcohols and glycols having carbon numbers predominantly in the range of C4 through C6 and boiling at approximately 127°C (260°F).
|
Details | |
|
The complex combination of hydrocarbons obtained in the production of 1,6-hexanediol. It consists predominantly of alcohols, glycols, and oxides of hydrocarbons having carbon numbers predominantly in the range of C1 through C6 and boiling in the range of approximately 60°C to 195°C (140°F to 383°F).
|
273-060-0
|
68937-28-0
|
The complex combination of hydrocarbons obtained in the production of 1,6-hexanediol. It consists predominantly of alcohols, glycols, and oxides of hydrocarbons having carbon numbers predominantly in the range of C1 through C6 and boiling in the range of approximately 60°C to 195°C (140°F to 383°F).
|
Details | |
|
The complex combination of hydrocarbons obtained in a hydrofiner-powerformer process and boiling in a range of approximately 27°C to 210°C (80°F to 410°F).
|
271-058-4
|
68514-79-4
|
The complex combination of hydrocarbons obtained in a hydrofiner-powerformer process and boiling in a range of approximately 27°C to 210°C (80°F to 410°F).
|
Details | |
|
The complex combination of hydrocarbons obtained from the initial water quenching of the effluent gases from a thermal cracking of ethane, propane or light naphtha. This stream is likely to contain 5 wt. % or more of 4- to 6- membered condensed ring aromatic hydrocarbons.
|
273-782-6
|
69013-21-4
|
The complex combination of hydrocarbons obtained from the initial water quenching of the effluent gases from a thermal cracking of ethane, propane or light naphtha. This stream is likely to contain 5 wt. % or more of 4- to 6- membered condensed ring aromatic hydrocarbons.
|
Details | |
|
The complex combination of hydrocarbons obtained from recycling of an extract from a reforming process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8, primarily benzene.
|
270-744-0
|
68477-63-4
|
The complex combination of hydrocarbons obtained from recycling of an extract from a reforming process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8, primarily benzene.
|
Details | |
|
The complex combination of hydrocarbons obtained from prefractionation (continuous distillation) of coke oven light oil. It consists predominantly of naphthalene, coumarone and indene and boils above 148°C (298°F).
|
285-076-5
|
85029-51-2
|
The complex combination of hydrocarbons obtained from prefractionation (continuous distillation) of coke oven light oil. It consists predominantly of naphthalene, coumarone and indene and boils above 148°C (298°F).
|
Details | |
|
The complex combination of hydrocarbons obtained from a thermal hydrodealkylation process. It consists predominantly of aromatic hydrocarbons, primarily biphenyl, and boiling approximately above 110°C (230°F).
|
273-556-7
|
68989-41-3
|
The complex combination of hydrocarbons obtained from a thermal hydrodealkylation process. It consists predominantly of aromatic hydrocarbons, primarily biphenyl, and boiling approximately above 110°C (230°F).
|
Details | |
|
The complex combination of hydrocarbons obtained from a benzene recovery unit. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65°C to 230°C (149°F to 446°F). This stream may contain 3 vol. % or more benzene.
|
272-889-5
|
68919-15-3
|
The complex combination of hydrocarbons obtained from a benzene recovery unit. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65°C to 230°C (149°F to 446°F). This stream may contain 3 vol. % or more benzene.
|
Details | |
|
The complex combination of hydrocarbons obtained by the thermal decomposition (at 399°C (750°F) or higher) of kerogen. It consists of hydrocarbons and heterocyclic compounds containing nitrogen, sulfur or oxygen.
|
269-646-0
|
68308-34-9
|
The complex combination of hydrocarbons obtained by the thermal decomposition (at 399°C (750°F) or higher) of kerogen. It consists of hydrocarbons and heterocyclic compounds containing nitrogen, sulfur or oxygen.
|
Details | |
|
The complex combination of hydrocarbons obtained by the pyrolysis fractionation at 816°C (1500°F) of naphtha and raffinate. It consists predominantly of hydrocarbons having a carbon number of C9 and boiling at approximately 204°C (400°F).
|
270-344-6
|
68425-29-6
|
The complex combination of hydrocarbons obtained by the pyrolysis fractionation at 816°C (1500°F) of naphtha and raffinate. It consists predominantly of hydrocarbons having a carbon number of C9 and boiling at approximately 204°C (400°F).
|
Details | |
|
The complex combination of hydrocarbons obtained by the hydroformylation of ethylene and propylene. Contains alcohols, esters, ethers, acetals, ketones, aldehydes and hydrocarbons.
|
273-553-0
|
68989-33-3
|
The complex combination of hydrocarbons obtained by the hydroformylation of ethylene and propylene. Contains alcohols, esters, ethers, acetals, ketones, aldehydes and hydrocarbons.
|
Details | |
|
The complex combination of hydrocarbons obtained by the hydration of ethylene. It contains primarily alcohols, aldehydes and ethers.
|
273-502-2
|
68987-66-6
|
The complex combination of hydrocarbons obtained by the hydration of ethylene. It contains primarily alcohols, aldehydes and ethers.
|
Details | |
|
The complex combination of hydrocarbons obtained by the fractionation of reaction products of diethylene glycol and ammonia. It may contain such compounds as bis(2-aminoethyl) ether, (methoxyethyl)morpholine, 2-(2-aminoethoxy)ethanol, and (aminoethyl)morpholine.
|
272-711-6
|
68909-76-2
|
The complex combination of hydrocarbons obtained by the fractionation of reaction products of diethylene glycol and ammonia. It may contain such compounds as bis(2-aminoethyl) ether, (methoxyethyl)morpholine, 2-(2-aminoethoxy)ethanol, and (aminoethyl)morpholine.
|
Details | |
|
The complex combination of hydrocarbons obtained by the dehydrogenation and extractive distillation of an isoamylene feed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8.
|
273-303-0
|
68956-47-8
|
The complex combination of hydrocarbons obtained by the dehydrogenation and extractive distillation of an isoamylene feed. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8.
|
Details | |
|
The complex combination of hydrocarbons obtained by the dealkylation of toluene. It consists primarily of benzene and toluene with various small amounts of aromatic hydrocarbons having carbon numbers predominantly greater than C8.
|
273-225-7
|
68953-80-0
|
The complex combination of hydrocarbons obtained by the dealkylation of toluene. It consists primarily of benzene and toluene with various small amounts of aromatic hydrocarbons having carbon numbers predominantly greater than C8.
|
Details | |
|
The complex combination of hydrocarbons obtained by the catalytic alkylation of benzene with propylene. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately -40°C to 70°C (-40°F to 158°F). This stream may contain 1 to 20 vol. % of benzene.
|
272-890-0
|
68919-16-4
|
The complex combination of hydrocarbons obtained by the catalytic alkylation of benzene with propylene. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately -40°C to 70°C (-40°F to 158°F). This stream may contain 1 to 20 vol. % of benzene.
|
Details | |
|
The complex combination of hydrocarbons obtained by the catalytic alkylation of benzene with propylene. It consists of hydrocarbons having carbon numbers predominantly in the range of C12 through C20 and boiling in the range of approximately 250°C to 350°C (482°F to 662°F).
|
272-891-6
|
68919-17-5
|
The complex combination of hydrocarbons obtained by the catalytic alkylation of benzene with propylene. It consists of hydrocarbons having carbon numbers predominantly in the range of C12 through C20 and boiling in the range of approximately 250°C to 350°C (482°F to 662°F).
|
Details | |
|
The complex combination of hydrocarbons obtained by the aldol condensation of C4 aldehydes. It consists primarily of alcohols, esters, ethers, ketones, aldehydes and hydrocarbons.
|
273-585-5
|
68990-21-6
|
The complex combination of hydrocarbons obtained by the aldol condensation of C4 aldehydes. It consists primarily of alcohols, esters, ethers, ketones, aldehydes and hydrocarbons.
|
Details | |
|
The complex combination of hydrocarbons obtained by the acid isomerization of linalool. It consists primarily of monoterpenes, terpene alcohols and oxygenated cyclic compounds.
|
277-225-8
|
73018-51-6
|
The complex combination of hydrocarbons obtained by the acid isomerization of linalool. It consists primarily of monoterpenes, terpene alcohols and oxygenated cyclic compounds.
|
Details | |
|
The complex combination of hydrocarbons obtained as a raffinate from a Lurgi separation unit. It consists predominantly of non-aromatic hydrocarbons with various small amounts of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8.
|
270-349-3
|
68425-35-4
|
The complex combination of hydrocarbons obtained as a raffinate from a Lurgi separation unit. It consists predominantly of non-aromatic hydrocarbons with various small amounts of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8.
|
Details | |
|
The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This lower boiling fraction consists predominantly of C5-C7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having a carbon number predominantly of C5. This stream may contain benzene.
|
267-565-5
|
67891-80-9
|
The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This lower boiling fraction consists predominantly of C5-C7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having a carbon number predominantly of C5. This stream may contain benzene.
|
Details | |
|
The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This higher boiling fraction consists predominantly of C5-C7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having carbon number predominantly of C5. This stream may contain benzene.
|
267-563-4
|
67891-79-6
|
The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This higher boiling fraction consists predominantly of C5-C7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having carbon number predominantly of C5. This stream may contain benzene.
|
Details | |
|
The complex combination of hydrocarbons from the distillation of the products from catalytic cracked distillates and catalytic cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C1 through C4.
|
269-617-2
|
68307-98-2
|
The complex combination of hydrocarbons from the distillation of the products from catalytic cracked distillates and catalytic cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C1 through C4.
|
Details | |
|
The complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils approximately below 288°C (550°F).
|
270-722-0
|
68477-31-6
|
The complex combination of hydrocarbons from the distillation of catalytic reformer fractionator residue. It boils approximately below 288°C (550°F).
|
Details | |
|
The complex combination of dry gases from a gas concentration unit. It consists of hydrogen, hydrogen sulfide and hydrocarbons having carbon numbers predominantly in the range of C1 through C3.
|
270-774-4
|
68477-92-9
|
The complex combination of dry gases from a gas concentration unit. It consists of hydrogen, hydrogen sulfide and hydrocarbons having carbon numbers predominantly in the range of C1 through C3.
|
Details | |
|
The complex combination of diglycerides of fatty acids linked to the choline ester of phosphoric acid.
|
232-307-2
|
8002-43-5
|
The complex combination of diglycerides of fatty acids linked to the choline ester of phosphoric acid.
|
Details | |
|
The complex combination of alkanolamines from the distillation of reaction products of ammonia and oxirane. It consists predominantly of triethanolamine, diethanolamine and higher amines from the reaction of triethanolamine and oxirane.
|
273-224-1
|
68953-70-8
|
The complex combination of alkanolamines from the distillation of reaction products of ammonia and oxirane. It consists predominantly of triethanolamine, diethanolamine and higher amines from the reaction of triethanolamine and oxirane.
|
Details | |
|
The complex combination obtained from the depentanizer stabilization of hydrotreated kerosine. It consists primarily of hydrogen, methane, ethane, and propane with various small amounts of nitrogen, hydrogen sulfide, carbon monoxide and hydrocarbons having carbon numbers predominantly in the range of C4 through C5.
|
272-775-5
|
68911-58-0
|
The complex combination obtained from the depentanizer stabilization of hydrotreated kerosine. It consists primarily of hydrogen, methane, ethane, and propane with various small amounts of nitrogen, hydrogen sulfide, carbon monoxide and hydrocarbons having carbon numbers predominantly in the range of C4 through C5.
|
Details | |
|
The complex combination obtained by the reaction of acetaldehyde with formaldehyde. Contains pentaerythritol oligomers and their acetals, formals, hemiacetals and hemiformals.
|
270-480-6
|
68442-60-4
|
The complex combination obtained by the reaction of acetaldehyde with formaldehyde. Contains pentaerythritol oligomers and their acetals, formals, hemiacetals and hemiformals.
|
Details | |
|
The complex combination obtained by boiling the vegetable oil deodorizer distillate with mineral acid and optionally, further separating the oil phase from the aqueous phase.
|
273-216-8
|
68953-54-8
|
The complex combination obtained by boiling the vegetable oil deodorizer distillate with mineral acid and optionally, further separating the oil phase from the aqueous phase.
|
Details | |
|
The complex combination consisting primarily of phosphatides, neutral oil and water obtained by hydration of soybean oil with water, salt solutions, or dilute acids followed by recovery of precipitated gum.
|
272-212-3
|
68783-89-1
|
The complex combination consisting primarily of phosphatides, neutral oil and water obtained by hydration of soybean oil with water, salt solutions, or dilute acids followed by recovery of precipitated gum.
|
Details | |
|
The combination primarily 1,6-hexanediol and 1,5-pentanediol obtained by hydrogenolysis of mixed esters in the production of 1,6-hexanediol and boiling in the range of 200°C to 245°C (392°F to 473°F).
|
273-164-6
|
68952-17-0
|
The combination primarily 1,6-hexanediol and 1,5-pentanediol obtained by hydrogenolysis of mixed esters in the production of 1,6-hexanediol and boiling in the range of 200°C to 245°C (392°F to 473°F).
|
Details | |
|
The combination of wastes formed by the coking of bituminous coal tar pitch. It consists predominantly of carbon.
|
295-549-8
|
92062-34-5
|
The combination of wastes formed by the coking of bituminous coal tar pitch. It consists predominantly of carbon.
|
Details | |
|
The combination of phenols extracted, using isobutyl acetate, from the ammonia liquor condensed from the gas evolved in low-temperature (less than 700°C (1292°F)) destructive distillation of coal. It consists predominantly of a mixture of monohydric and dihydric phenols.
|
284-881-9
|
84988-93-2
|
The combination of phenols extracted, using isobutyl acetate, from the ammonia liquor condensed from the gas evolved in low-temperature (less than 700°C (1292°F)) destructive distillation of coal. It consists predominantly of a mixture of monohydric and dihydric phenols.
|
Details | |
|
The char resulting from processing coal in a closed reactor using an exothermic reaction and controlling the feed and air supply. Composed primarily of carbon. May contain varying amounts of ash, sulfur, volatile material and moisture.
|
270-070-7
|
68409-95-0
|
The char resulting from processing coal in a closed reactor using an exothermic reaction and controlling the feed and air supply. Composed primarily of carbon. May contain varying amounts of ash, sulfur, volatile material and moisture.
|
Details | |
|
The cellular carbonaceous mass resulting from the high temperature (greater than 700°C (1292°F)) destructive distillation of coal. Composed primarily of carbon. May contain varying amounts of sulfur and ash.
|
266-010-4
|
65996-77-2
|
The cellular carbonaceous mass resulting from the high temperature (greater than 700°C (1292°F)) destructive distillation of coal. Composed primarily of carbon. May contain varying amounts of sulfur and ash.
|
Details | |
|
The carbon-containing residue from the low-temperature carbonization coking of pitch from high-temperature coal tar. Consists primarily of carbon. Also contains small amounts of sulfur and ash.
|
310-274-6
|
140413-61-2
|
The carbon-containing residue from the low-temperature carbonization coking of pitch from high-temperature coal tar. Consists primarily of carbon. Also contains small amounts of sulfur and ash.
|
Details | |
|
The carbon containing residue from the mutual coking of coal and pitch at high temperature (above 700°C or 1272°F). Consists chiefly of carbon, can also contain heteroatoms and ash.
|
310-222-2
|
140203-13-0
|
The carbon containing residue from the mutual coking of coal and pitch at high temperature (above 700°C or 1272°F). Consists chiefly of carbon, can also contain heteroatoms and ash.
|
Details | |
|
The carbon containing residue from the carbonization coking of pitch from high temperature (>700°C or >1272°F) coal tar. Consists primarily of carbon. Also contains small amounts of sulfur and ash.
|
310-221-7
|
140203-12-9
|
The carbon containing residue from the carbonization coking of pitch from high temperature (>700°C or >1272°F) coal tar. Consists primarily of carbon. Also contains small amounts of sulfur and ash.
|
Details | |
|
The by-product from the destructive distillation of coal. Almost black semisolid. A complex combination of aromatic hydrocarbons, phenolic compounds, nitrogen bases and thiophene.
|
232-361-7
|
8007-45-2
|
The by-product from the destructive distillation of coal. Almost black semisolid. A complex combination of aromatic hydrocarbons, phenolic compounds, nitrogen bases and thiophene.
|
Details | |
|
The brown polymeric product from the decomposition of organic matter, particularly dead plants. This combination of polymers may contain aromatic and heterocyclic structures, carboxy groups, and nitrogen.
|
215-809-6
|
1415-93-6
|
The brown polymeric product from the decomposition of organic matter, particularly dead plants. This combination of polymers may contain aromatic and heterocyclic structures, carboxy groups, and nitrogen.
|
Details | |
|
The bottoms from fractionation boiling approximately above 360°C (680°F).
|
271-073-6
|
68515-32-2
|
The bottoms from fractionation boiling approximately above 360°C (680°F).
|
Details | |
|
The barium salt of the substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 50420.
|
270-933-8
|
68510-98-5
|
The barium salt of the substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 50420.
|
Details | |
|
The aqueous solution resulting from the reaction of lignocellulosic substances (wood or other agricultural fiber sources) with one or more pulping chemicals including those used in the kraft, sulfite, semichemical or other pulping processes. Composition is highly variable and includes excess pulping chemicals, dissolved and degraded cellulose, hemicellulose and lignin.
|
266-111-3
|
66071-92-9
|
The aqueous solution resulting from the reaction of lignocellulosic substances (wood or other agricultural fiber sources) with one or more pulping chemicals including those used in the kraft, sulfite, semichemical or other pulping processes. Composition is highly variable and includes excess pulping chemicals, dissolved and degraded cellulose, hemicellulose and lignin.
|
Details | |
|
The aqueous solution obtained by the distillation and extraction of oxidized alkaline lignin liquor.
|
271-021-2
|
68514-06-7
|
The aqueous solution obtained by the distillation and extraction of oxidized alkaline lignin liquor.
|
Details | |
|
The aqueous slurry produced when anthracene is contacted with water in a cooling tower. It consists primarily of anthracene.
|
270-058-1
|
68409-72-3
|
The aqueous slurry produced when anthracene is contacted with water in a cooling tower. It consists primarily of anthracene.
|
Details | |
|
The aqueous liquor produced during the desulfurization of coke-oven gas by the Stretford process (high temperature destructive distillation). Consists primarily of an alkaline solution of sodium thiocyanate and sodium thiosulfate with traces of vanadium and suspended sulfur.
|
293-802-7
|
91082-87-0
|
The aqueous liquor produced during the desulfurization of coke-oven gas by the Stretford process (high temperature destructive distillation). Consists primarily of an alkaline solution of sodium thiocyanate and sodium thiosulfate with traces of vanadium and suspended sulfur.
|
Details | |
|
The aqueous layer formed by the acidulation of vegetable-oil soap during the production of vegetable-oil. Composed primarily of sodium sulfate with minor amounts of vegetable-oil and neutral materials of vegetable origins.
|
272-793-3
|
68911-90-0
|
The aqueous layer formed by the acidulation of vegetable-oil soap during the production of vegetable-oil. Composed primarily of sodium sulfate with minor amounts of vegetable-oil and neutral materials of vegetable origins.
|
Details | |
|
The aqueous layer formed by acidulation of tall-oil soap with sulfuric acid during the production of tall oil. Composed primarily of a solution of sodium sulfate, the remaining being lignin and tall oil.
|
266-038-7
|
65997-02-6
|
The aqueous layer formed by acidulation of tall-oil soap with sulfuric acid during the production of tall oil. Composed primarily of a solution of sodium sulfate, the remaining being lignin and tall oil.
|
Details | |
|
The aqueous extract produced by an acidic wash of alkali-washed napthalene oil. Composed primarily of acid salts of various aromatic nitrogen bases including pyridine, quinoline and their alkyl derivatives.
|
292-623-1
|
90641-00-2
|
The aqueous extract produced by an acidic wash of alkali-washed napthalene oil. Composed primarily of acid salts of various aromatic nitrogen bases including pyridine, quinoline and their alkyl derivatives.
|
Details | |
|
The aqueous extract produced by an acidic wash of alkali-washed carbolic oil. Composed primarily of acid salts of various aromatic nitrogen bases including pyridine, quinoline and their alkyl derivatives.
|
292-622-6
|
90640-99-6
|
The aqueous extract produced by an acidic wash of alkali-washed carbolic oil. Composed primarily of acid salts of various aromatic nitrogen bases including pyridine, quinoline and their alkyl derivatives.
|
Details | |
|
The aqueous extract from naphthalene oil produced by an alkaline wash such as aqueous sodium hydroxide. Composed primarily of the alkali salts of various phenolic compounds.
|
292-611-6
|
90640-89-4
|
The aqueous extract from naphthalene oil produced by an alkaline wash such as aqueous sodium hydroxide. Composed primarily of the alkali salts of various phenolic compounds.
|
Details | |
|
The aqueous extract from carbolic oil produced by an alkaline wash such as aqueous sodium hydroxide. Composed primarily of the alkali salts of various phenolic compounds.
|
292-610-0
|
90640-88-3
|
The aqueous extract from carbolic oil produced by an alkaline wash such as aqueous sodium hydroxide. Composed primarily of the alkali salts of various phenolic compounds.
|
Details | |
|
The aqueous extract from alkali-washed low-temperature coal tar middle oil produced by an acidic wash, such as aqueous sulfuric acid. An aqueous solution containing primarily the acid salts of various aromatic nitrogen bases.
|
310-295-0
|
141785-67-3
|
The aqueous extract from alkali-washed low-temperature coal tar middle oil produced by an acidic wash, such as aqueous sulfuric acid. An aqueous solution containing primarily the acid salts of various aromatic nitrogen bases.
|
Details | |
|
The anthracene-rich solid obtained by the crystallization and centrifuging of anthracene oil. It is composed primarily of anthracene, carbazole and phenanthrene.
|
292-603-2
|
90640-81-6
|
The anthracene-rich solid obtained by the crystallization and centrifuging of anthracene oil. It is composed primarily of anthracene, carbazole and phenanthrene.
|
Details | |
|
The anthracene oil fraction obtained from the fractional distillation of high temperature coal tar is debased using sulfuric acid, and subsequently neutralized with aqueous ammonia to obtain free bases. Contains chiefly acridine, carbazole, and higher boiling bases. It distills in the range 325°C to 365°C (619°F to 689°F).
|
310-242-1
|
140203-31-2
|
The anthracene oil fraction obtained from the fractional distillation of high temperature coal tar is debased using sulfuric acid, and subsequently neutralized with aqueous ammonia to obtain free bases. Contains chiefly acridine, carbazole, and higher boiling bases. It distills in the range 325°C to 365°C (619°F to 689°F).
|
Details | |
|
The alcoholic solution of macerated Vanilla planifolia.
|
232-463-1
|
8047-24-3
|
The alcoholic solution of macerated Vanilla planifolia.
|
Details | |
|
The acqueous extract from creosote oil produced by an acidic wash such as aqueous sulfuric acid. Composed primarily of acid salts of quinoline and isoquinoline.
|
310-212-8
|
91995-30-1
|
The acqueous extract from creosote oil produced by an acidic wash such as aqueous sulfuric acid. Composed primarily of acid salts of quinoline and isoquinoline.
|
Details | |
|
447-000-0
|
-
|
THBP
|
Details | ||
|
THANCAT AN 20
|
407-360-1
|
116230-20-7
|
THANCAT AN 20
|
Details | |
|
THANCAT AN 10
|
404-810-9
|
4524-95-2
|
THANCAT AN 10
|
Details | |
|
431-120-5
|
-
|
TGBMA MONOMER
|
Details | ||
|
TG-SA
|
411-570-9
|
41481-66-7
|
TG-SA
|
Details | |
|
453-520-9
|
-
|
TFXOH
|
Details | ||
|
458-390-7
|
6226-25-1
|
TFOL-TF
|
Details | ||
|
435-890-3
|
652-18-6
|
TFBA
|
Details | ||
|
TFA-4713
|
418-960-8
|
-
|
TFA-4713
|
Details | |
|
TFA LYS-PRO TOSYLATE; TFA LYSYL PROLINE PARA-TOLUENE SULPHONATE
|
402-160-0
|
-
|
TFA LYS-PRO TOSYLATE; TFA LYSYL PROLINE PARA-TOLUENE SULPHONATE
|
Details | |
|
453-420-5
|
-
|
TETT
|
Details | ||
|
TETRAMYL
|
421-930-7
|
-
|
TETRAMYL
|
Details | |
|
TETRAMMINE PALLADIUM SULFATE
|
426-980-3
|
13601-06-4
|
TETRAMMINE PALLADIUM SULFATE
|
Details | |
|
TETRAFLUOROQUINOLONE
|
406-710-0
|
-
|
TETRAFLUOROQUINOLONE
|
Details | |
|
TETRACONAZOLE
|
407-760-6
|
112281-77-3
|
TETRACONAZOLE
|
Details | |
|
TETRACHLOROTEREPHTHALONITRILE
|
401-550-8
|
1897-41-2
|
TETRACHLOROTEREPHTHALONITRILE
|
Details | |
|
449-410-5
|
-
|
TETRABENZYLCYCLEN
|
Details | ||
|
426-730-3
|
123439-82-7
|
TETRAAMMIN-PLATIN(II)-DIHYDROGENCARBONAT; TETRAMMINE PLATINUM HYDROGEN CARBONATE; TETRAAMMINE PLATINUM (II) HYDROGEN CARBONATE
|
Details | ||
|
425-270-0
|
134620-00-1
|
TETRAAMMIN-PALLADIUM-DIHYDROGENCARBONAT; TETRAMMINE PALLADIUM HYDROGEN CARBONATE; TETRAAMMINE PALLADIUM (II) HYDROGEN CARBONATE
|
Details | ||
|
458-640-5
|
-
|
TETRAALLYLSILAN
|
Details | ||
|
TERTIARYBUTYLPHOSPHINE; TERTIÄRBUTYLPHOSPHIN
|
423-330-0
|
-
|
TERTIARYBUTYLPHOSPHINE; TERTIÄRBUTYLPHOSPHIN
|
Details | |
|
TERTIARYBUTYLARSINE; TERTIÄRBUTYLARSIN
|
423-320-6
|
4262-43-5
|
TERTIARYBUTYLARSINE; TERTIÄRBUTYLARSIN
|
Details | |
|
437-440-1
|
-
|
TERT-AMYL OXALATE
|
Details | ||
|
429-810-6
|
-
|
TERRESTRAL
|
Details | ||
|
436-900-9
|
39290-90-9
|
TERRACESS P
|
Details | ||
|
445-620-6
|
39318-30-4
|
TERRACESS L
|
Details | ||
|
427-830-1
|
-
|
TERON N-718K
|
Details | ||
|
TEPIC-H
|
423-400-0
|
59653-74-6
|
TEPIC-H
|
Details | |
|
423-030-1
|
-
|
TELEPHOTO 1
|
Details | ||
|
447-860-7
|
144177-62-8
|
TELAM
|
Details | ||
|
427-760-1
|
-
|
TEGUDORPHINE
|
Details | ||
|
460-100-9
|
342573-75-5
|
TEGO IL IMES
|
Details | ||
|
TEGO ANTIFOAM C2600
|
400-960-4
|
-
|
TEGO ANTIFOAM C2600
|
Details | |
|
459-280-1
|
388603-24-5
|
TED-15L
|
Details | ||
|
429-390-4
|
-
|
TECHMORE VG 3101L
|
Details | ||
|
TEBUCONAZOLE RESP. HWG 1608
|
403-640-2
|
107534-96-3
|
TEBUCONAZOLE RESP. HWG 1608
|
Details | |
|
TDEAT
|
437-500-7
|
4419-47-0
|
TDEAT
|
Details | |
|
432-830-8
|
-
|
TCPY
|
Details | ||
|
434-220-7
|
-
|
TCPM
|
Details | ||
|
434-390-2
|
-
|
TCPC
|
Details | ||
|
446-820-6
|
-
|
TCO; TRICYCLIC DIHYDROQUINOLINE; TRICYCLIC OLEFIN; TRICYCLIQUE DIHYDRO QUINOLEINE; TRICYCLONE
|
Details | ||
|
427-360-5
|
-
|
TCO 197
|
Details | ||
|
421-300-1
|
138564-59-7
|
TCN INTERMEDIATE
|
Details | ||
|
420-970-2
|
-
|
TCDO; TETRACHLORODEKAOXID-KOMPLEX IN WÄSSRIGER LÖSUNG
|
Details | ||
|
418-030-1
|
-
|
TCD-DI-HEA
|
Details | ||
|
TCD EMULGATOR
|
407-410-2
|
-
|
TCD EMULGATOR
|
Details | |
|
423-440-9
|
-
|
TBYT
|
Details | ||
|
TBUAP
|
450-360-1
|
82560-12-1
|
TBUAP
|
Details | |
|
TBTU
|
423-040-4
|
125700-67-6
|
TBTU
|
Details | |