Brief Profile

The Brief Profile summarizes the non-confidential data on substances as it is held in the databases of the European Chemicals Agency (ECHA), including data provided by third parties. The Brief Profile is automatically generated; note that it does not currently distinguish between harmonised classification and minimum classification; information requirements under different legislative frameworks may therefore not be fully up to date or complete. For accuracy reasons, substance manufacturers and imports have the responsibility to consult official sources, e.g. the electronic edition of the Official Journal of the European Union.
This Brief Profile is covered by the ECHA Legal Notice.

Substance Description

Substance identity

  • EC / List name: Creosote oil, acenaphthene fraction
  • IUPAC name: 1,2-dihydroacenaphthylene; 1-methylnaphthalene; 2-methylnaphthalene; 9H-fluorene; anthracene; naphthalene; pentacyclo[10.6.2.0²,⁷.0⁹,¹⁹.0¹⁶,²⁰]icosa-1(18),2,4,6,8,10,12,14,16,19-decaene; phenylbenzene; quinoline
  • Other names
EC / List no.:
292-605-3
CAS no.:
90640-84-9
Index number:
648-098-00-X
Molecular formula:
C112H87N
SMILES:
C1=CC2=CC=CC=C2C=C1.C1=CC=C2N=CC=CC2=C1.CC1=CC2=CC=CC=C2C=C1.CC1=CC=CC2=CC=CC=C12.C1CC2=C3C1=CC=CC3=CC=C2.C1=CC=C(C=C1)C1=CC=CC=C1.C1C2=CC=CC=C2C2=C1C=CC=C2.C1=CC2=CC3=CC=CC=C3C=C2C=C1.C1=CC=C2C(=C1)C=C1C=CC3=CC=CC4=CC=C2C1=C34
InChI:
InChI=1S/C20H12.C14H10.C13H10.2C12H10.2C11H10.C10H8.C9H7N/c1-2-7-17-15(4-1)12-16-9-8-13-5-3-6-14-10-11-18(17)20(16)19(13)14;1-2-6-12-10-14-8-4-3-7-13(14)9-11(12)5-1;1-3-7-12-10(5-1)9-11-6-2-4-8-13(11)12;1-3-9-4-2-6-11-8-7-10(5-1)12(9)11;1-3-7-11(8-4-1)12-9-5-2-6-10-12;1-9-5-4-7-10-6-2-3-8-11(9)10;1-9-6-7-10-4-2-3-5-11(10)8-9;1-2-6-10-8-4-3-7-9(10)5-1;1-2-6-9-8(4-1)5-3-7-10-9/h1-12H;1-10H;1-8H,9H2;1-6H,7-8H2;1-10H;2*2-8H,1H3;1-8H;1-7H AuxInfo=1/0/N:33,34,45,38,44,46,35,42,41,48,49,39,43,47,37,40,36,50,52,51;76,77,84,83,89,78,85,82,87,80,88,79,86,81;66,73,67,72,65,74,68,71,63,64,75,69,70;104,109,105,108,103,110,113,112,106,102,111,107;90,99,91,95,98,100,92,94,97,101,93,96;21,16,11,18,19,15,17,12,20,14,13;32,27,22,26,23,29,28,31,30,25,24;1,6,9,8,2,5,10,7,3,4;58,53,60,57,59,54,61,56,55,62/E:;(1,2,3,4)(5,6,7,8)(9,10)(11,12,13,14);(1,2)(3,4)(5,6)(7,8)(10,11)(12,13);(1,2)(3,4)(5,6)(7,8)(10,11);(1,2)(3,4,5,6)(7,8,9,10)(11,12);;;(1,2,3,4)(5,6,7,8)(9,10);/rA:113CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCNCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC/rB:s1;d-2;s3;d-4;d-1s5;s4;d-7;s8;s3d-9;;s11;d-12;s13;d-14;d-11s15;s14;d-17;s18;s13d-19;s20;;s22;d-23;s24;d-25;d-22s26;s25;d-28;s29;s24d-30;s30;;d-33;s34;d-35;s36;s33d-37;s37;d+39;s40;d-41;s42;d+43;s44;d-45;s46;d+47;s48;s36d+49;s40s50;s43s47d-51;;s53;d-54;s55;d-56;d-53s57;s56;d-59;s60;s55d-61;;s63;s64;d-65;s66;d-67;d+64s68;s69;d+70;s71;d-72;s73;s63s70d+74;;d-76;s77;d+78;s79;d+80;s81;d-82;s83;d-84;s81s85;d-86;s79s87;s76d-88;;d-90;s91;d-92;s93;s90d-94;s93;d+96;s97;d-98;s99;s96d-100;;s102;d-103;s104;d-105;d-102s106;s106;d-108;s109;s107d-110;s111;s102s112;/rC:-2.6673,-.77,0;-1.3337,-1.54,0;0,-.77,0;0,.77,0;-1.3337,1.54,0;-2.6673,.77,0;1.3338,1.54,0;2.6673,.77,0;2.6673,-.77,0;1.3338,-1.54,0;6.6273,-.49,0;7.9609,-1.26,0;9.2946,-.49,0;9.2946,1.05,0;7.9609,1.82,0;6.6273,1.05,0;10.6284,1.82,0;11.9621,1.05,0;11.9621,-.49,0;10.6284,-1.26,0;10.6284,-2.8,0;15.9221,-.63,0;17.2558,-1.4,0;18.5893,-.63,0;18.5893,.91,0;17.2558,1.68,0;15.9221,.91,0;19.9231,1.68,0;21.2568,.91,0;21.2568,-.63,0;19.9231,-1.4,0;22.5905,-1.4,0;5.2173,-8.4993,0;4.7133,-7.0443,0;3.2009,-6.7531,0;2.1927,-7.9173,0;2.6969,-9.3724,0;4.2091,-9.6634,0;1.6887,-10.5366,0;.1765,-10.2456,0;-.8316,-11.4097,0;-2.344,-11.1186,0;-2.848,-9.6634,0;-4.3602,-9.3724,0;-4.8644,-7.9173,0;-3.8562,-6.7531,0;-2.344,-7.0443,0;-1.3358,-5.88,0;.1765,-6.171,0;.6805,-7.6263,0;-.3276,-8.7903,0;-1.8398,-8.4993,0;9.1773,-9.2839,0;10.511,-10.0539,0;11.8447,-9.2839,0;11.8447,-7.7439,0;10.511,-6.9739,0;9.1773,-7.7439,0;13.1783,-6.9739,0;14.512,-7.7439,0;14.512,-9.2839,0;13.1783,-10.0539,0;22.2547,-6.6219,0;23.5005,-7.5271,0;25.0069,-7.2069,0;26.0373,-8.3514,0;25.5615,-9.816,0;24.0551,-10.1363,0;23.0247,-8.9919,0;21.4847,-8.9919,0;20.4543,-10.1363,0;18.9479,-9.816,0;18.472,-8.3514,0;19.5024,-7.2069,0;21.0088,-7.5271,0;-4.001,-17.3139,0;-4.001,-15.7739,0;-2.6674,-15.0039,0;-1.3337,-15.7739,0;0,-15.0039,0;1.3338,-15.7739,0;2.6673,-15.0039,0;4.001,-15.7739,0;4.001,-17.3139,0;2.6673,-18.0839,0;1.3338,-17.3139,0;0,-18.0839,0;-1.3337,-17.3139,0;-2.6674,-18.0839,0;7.961,-16.5438,0;8.731,-15.2103,0;10.271,-15.2103,0;11.041,-16.5438,0;10.271,-17.8775,0;8.731,-17.8775,0;12.581,-16.5438,0;13.351,-15.2103,0;14.891,-15.2103,0;15.661,-16.5438,0;14.891,-17.8775,0;13.351,-17.8775,0;21.1888,-17.5529,0;19.7819,-16.9264,0;19.621,-15.3948,0;20.8668,-14.4897,0;22.2737,-15.1162,0;22.4346,-16.6478,0;24.0024,-14.4897,0;25.2484,-15.3948,0;25.0873,-16.9264,0;23.6806,-17.5529,0;23.2046,-19.0175,0;21.6646,-19.0175,0;
Type of substance:
UVCB
Origin:
Organic
Registered compositions:
11
Of which contain:
0 impurities relevant for classification
0 additives relevant for classification
Substance Listed:
EINECS (European INventory of Existing Commercial chemical Substances) List

Hazard classification & labelling

Danger! According to the harmonised classification and labelling (ATP01) approved by the European Union, this substance may cause cancer.

Additionally, the classification provided by companies to ECHA in REACH registrations identifies that this substance may be fatal if swallowed and enters airways, is toxic to aquatic life with long lasting effects, is suspected of causing genetic defects, may cause damage to organs through prolonged or repeated exposure, causes skin irritation and may cause an allergic skin reaction.

Breakdown of all 147 C&L notifications submitted to ECHA

Carc. 1B H350 Harmonised Classification
Asp. Tox. 1 H304
Aquatic Chronic 2 H411
Muta. 2 H341
STOT RE 2 H373
Skin Irrit. 2 H315
Skin Sens. 1A H317
0% 10% 20% 30% 40% 50% 60% 70% 80% 90% 100%

https://echa.europa.eu/diss-blank-theme/images/cnl/graph/tick.png Harmonised Classification

https://echa.europa.eu/diss-blank-theme/images/cnl/graph/Reach.png REACH registration dossiers notifications

https://echa.europa.eu/diss-blank-theme/images/cnl/graph/CLP.png CLP notifications

Properties of concern

  • C
  • Ss

Regulatory activities

Registration, Evaluation, Authorisation & Restriction of Chemicals (REACH)

Registration
Pre-registration:
Substance pre-registered under REACH.
Registration:
This substance has 8 active registrations under REACH, 1 Joint Submission(s) and 0 Individual Submission(s).
Please see Registrants/Suppliers details.
Evaluation
Dossier Evaluation:
Registration dossiers submitted to ECHA for this substance have been evaluated under REACH.
Substance Evaluation:
Authorisation
Candidate List:
Annex XIV (Authorisation List):
Restriction
Annex XVII (Restriction List):
Some uses of this substance are restricted under Annex XVII of REACH.

Classification Labelling & Packaging (CLP)

Harmonised C&L:
A European Union Harmonised Classification & Labelling has been assigned to this substance.
Notification:
Classification & Labelling has been notified by industry to ECHA for this substance.

Biocidal Products Regulation (BPR)

Active Substance:
Biocidal Products:

Prior Informed Consent (PIC)

Annex I:
This substance is subject to the Prior Informed Consent regulation and to export notification procedure from 06-Jan-2003
Annex V:

European Union Observatory for Nanomaterials (EUON)

EUON:

About this substance

This substance is manufactured and/or imported in the European Economic Area in 100 000 - 1 000 000 tonnes per year.

This substance is used in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.

ECHA has no public registered data indicating whether or in which chemical products the substance might be used.

ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

This substance is used in the following activities or processes at workplace: the low energy manipulation of substances bound in materials or articles, potentially closed industrial processing with minerals/metals at elevated temperature (e.g. smelters, furnaces, refineries, coke ovens) and production of mixtures or articles by tabletting, compression, extrusion or pelletisation.

Release to the environment of this substance can occur from industrial use: in the production of articles, formulation of mixtures, formulation in materials and manufacturing of the substance. Other release to the environment of this substance is likely to occur from: outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).

ECHA has no public registered data indicating whether or into which articles the substance might have been processed.

This substance is used in the following products: coating products, adhesives and sealants and inks and toners.

This substance is used in the following areas: formulation of mixtures and/or re-packaging. This substance is used for the manufacture of: textile, leather or fur and machinery and vehicles.

This substance is used in the following activities or processes at workplace: transfer of chemicals, roller or brushing applications, treatment of articles by dipping and pouring, closed batch processing in synthesis or formulation, mixing in open batch processes and batch processing in synthesis or formulation with opportunity for exposure.

Release to the environment of this substance can occur from industrial use: in the production of articles. Other release to the environment of this substance is likely to occur from: outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives), outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials) and indoor use.

This substance is used in the following products: coating products and adhesives and sealants. This substance has an industrial use resulting in manufacture of another substance (use of intermediates).

This substance is used in the following activities or processes at workplace: transfer of chemicals, closed batch processing in synthesis or formulation, laboratory work, transfer of substance into small containers, mixing in open batch processes, batch processing in synthesis or formulation with opportunity for exposure and closed, continuous processes with occasional controlled exposure.

Release to the environment of this substance can occur from industrial use: formulation of mixtures, in the production of articles and formulation in materials.

This substance is used in the following products: coating products and fuels. This substance has an industrial use resulting in manufacture of another substance (use of intermediates).

This substance is used in the following areas: formulation of mixtures and/or re-packaging. This substance is used for the manufacture of: mineral products (e.g. plasters, cement), metals and chemicals.

This substance is used in the following activities or processes at workplace: transfer of chemicals, closed batch processing in synthesis or formulation, closed, continuous processes with occasional controlled exposure, potentially closed industrial processing with minerals/metals at elevated temperature (e.g. smelters, furnaces, refineries, coke ovens) and laboratory work.

Release to the environment of this substance can occur from industrial use: in the production of articles, formulation of mixtures, as an intermediate step in further manufacturing of another substance (use of intermediates), formulation in materials and in processing aids at industrial sites. Other release to the environment of this substance is likely to occur from: outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives) and outdoor use in long-life materials with low release rate (e.g. metal, wooden and plastic construction and building materials).

This substance is used in the following activities or processes at workplace: transfer of chemicals, closed, continuous processes with occasional controlled exposure, laboratory work, closed batch processing in synthesis or formulation, transfer of substance into small containers and closed processes with no likelihood of exposure.

Release to the environment of this substance can occur from industrial use: manufacturing of the substance, as an intermediate step in further manufacturing of another substance (use of intermediates) and formulation of mixtures.

Precautions for using this substance have been recommended by its registrants under REACH, as follows:

Prevention statements

When handling this substance: do not handle until all safety precautions have been read and understood; do not breathe the dust, fume, gas, mist, vapours or spray; avoid release to the environment; wear protective gloves and/or clothing, and eye and/or face protection as specified by manufacturer/supplier.

Response statements

In case of incident: If exposed or concerned: get medical advice/attention. Do not induce vomiting.

Guidance on the safe use of the substance provided by manufacturers and importers of this substance.

Registrants/suppliers

  • Arsol Aromatics GmbH & Co. KG, Uferstr. 105 45881 Gelsenkirchen Germany
  • BILBAINA DE ALQUITRANES, S.A., OBISPO OLAECHEA, 49 48903 LUCHANA-BARACALDO VIZCAYA Spain
  • DEZA a.s., Masarykova 753 75701 Valasske Mezirici Czech Republic
  • ExponentOR30, The Lenz Hornbeam Park Road HG28RE Harrogate North Yorkshire United Kingdom
  • Industrial Quimica del Nalon, S.A., Avda. Galicia 31 33005 Oviedo Asturias Spain
  • Koppers Denmark ApS, Avernakke 5800 Nyborg Denmark
  • RAIN CARBON BVBA, Vredekaai 18 9060 Zelzate Belgium
  • RÜTGERS Germany GmbH, Kekulestr. 30 44579 Castrop-Rauxel Germany
  • Koppers Netherlands B.V., Molenlaan 55 1422 XN Uithoorn Netherlands
  • Koppers UK Limited, Huntsman Drive Port Clarence Works TS2 1SD Middlesborough United Kingdom

Other names

  • 1,2-dihydroacenaphthylene; 1-methylnaphthalene; 2-methylnaphthalene; 9H-fluorene; anthracene; naphthalene; pentacyclo[10.6.2.0²,⁷.0⁹,¹⁹.0¹⁶,²⁰]icosa-1(18),2,4,6,8,10,12,14,16,19-decaene; phenylbenzene; quinoline
  • Creosote Oil, Acenaphthene Fraction
  • Creosote oil, acenaphthene fraction; Wash Oil
  • Wash oil
  • Creosote oil, acenaphthene fraction
  • Creosote oil, acenaphthene fraction (A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240°C to 280°C (464°F to 536°F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.)
  • Creosote oil, acenaphthene fraction; wash oil (A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240°C to 280°C (464°F to 536°F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.)
  • Wash Oil (A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240°C to 280°C (464°F to 536°F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.)
  • [A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240°C to 280°C (464°F to 536°F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.] (A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240°C to 280°C (464°F to 536°F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.)
  • Acenaphthene
  • Creosote Oil
  • Methylnaphthalene
  • Methylnaphthalene oil
  • PO I
  • Prací Olej I
  • Tar Fraction
  • Teer Fraktion
  • Wash Oil

Scientific properties

Physical and chemical properties

This section provides physicochemical information compiled from all automatically processable data from REACH registration dossiers that is available to ECHA at the time of generation. The quality and correctness of the information remains the responsibility of the data submitter. The Agency thus cannot guarantee the correctness of the information displayed.

Appearance/physical state / colour

Study results
  • 1 study submitted
  • 1 study processed
C Physical state at 20°C and 1013 hPa
Liquid (100%) [1]
C Form
Other (100%) [1]
C Odour
Other (100%) [1]
C Substance type
Organic (100%) [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
C Summaries
  • 2 summaries submitted
  • 2 summaries processed
Physical state at 20°C and 1013 hPa
Liquid (100%)

Melting/freezing point

Study results
  • 1 study submitted
  • 1 study processed
R Melting / freezing point
-12 °C @ 101 kPa [2]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Melting / freezing point at 101 325 Pa
-14.85 - -12.15 °C

Boiling point

Study results
  • 2 studies submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study 1
Weight of evidence
Other
Data waiving
Not feasible 1
Sci. unjustified
Exposure cons.
Other
R Summaries
  • 2 summaries submitted
  • 1 summary processed
Boiling point at 101 325 Pa
237.63 °C

Density

Study results
  • 1 study submitted
  • 1 study processed
R Density
0.99 - 1.09 g/cm³ @ 20 °C [3]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Relative density at 20°C
1.05 - 1.088

Vapour pressure

Study results
  • 1 study submitted
  • 1 study processed
R Vapour pressure
38.5 - 1 300 Pa @ 20 - 103 °C [4]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Vapour pressure
11.17 - 38.5 Pa @ 20 - 25.16 °C

Partition coefficient

Study results
  • 2 studies submitted
  • 1 study processed
R Log Pow
3.4 - 4.2 @ 25 °C and pH 7 - 7.5 [1]

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence 1
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Log Kow (Log Pow)
1.98 - 3.8 @ 25 °C

Water solubility

Study results
  • 4 studies submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study 1
Supporting study 3
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Water solubility
25 - 6 110 mg/L @ 20 °C

Solubility in organic solvents / fat solubility

Data not provided by the registrant

Surface tension

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
R Summaries
  • 1 summary submitted
  • 1 summary processed
Surface tension at 20 °C
45.62 mN/m

Flash point

Study results
  • 1 study submitted
  • 1 study processed
R Flash point
61 - 108 °C @ 101 kPa [2]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Flash point at 101 325 Pa
101 - 108 °C

Auto flammability

Study results
  • 1 study submitted
  • 1 study processed
R Autoflammability / self-ignition
525 °C @ 101.3 kPa [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Autoflammability / self-ignition at 101 325 Pa
480 - 525 °C

Flammability

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Explosiveness

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Oxidising

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Oxidation reduction potential

Data not provided by the registrant

pH

Data not provided by the registrant

Dissociation constant

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
R Summaries
  • 1 summary submitted
  • 1 summary processed
pKa at 20 °C
4.95

Viscosity

Study results
  • 1 study submitted
  • 1 study processed
R kinematic viscosity (in mm²/s)
4.88 [1]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Static viscosity at 20 °C
4.88 mm²/s
Dynamic viscosity at 20 °C
3.375 mPa.s

Environmental fate and pathways

This section provides environmental fate and pathways information compiled from all automatically processable data from REACH registration dossiers that is available to ECHA at the time of generation. The quality and correctness of the information remains the responsibility of the data submitter. The Agency thus cannot guarantee the correctness of the information displayed.

Phototransformation in air

Study results
  • 0 studies submitted
  • 0 studies processed

No data available

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Half life in air
11.065 h
Degradation rate constant with OH radicals
0 cm³ molecule-1 d-1

Hydrolysis

Study results
  • 1 study submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
Summaries
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Phototransformation in water

Study results
  • 0 studies submitted
  • 0 studies processed

No data available

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
Half-life in water
3.333 months

Phototransformation in soil

Data not provided by the registrant

Biodegradation in water - screening tests

Study results
  • 6 studies submitted
  • 3 studies processed
C Interpretation of results
Inherently biodegradable (67%), Readily biodegradable (33%) [3]

Type of Study provided
Studies with data
Key study 3
Supporting study 2
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
C Summaries
  • 2 summaries submitted
  • 2 summaries processed
Biodegradation in water
Under test conditions no biodegradation observed (100%)

Biodegradation in water & sediment - simulation tests

Data not provided by the registrant

Biodegradation in soil

Study results
  • 2 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence 1
Other
Data waiving
Not feasible
Sci. unjustified 1
Exposure cons.
Other
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Half-life in soil
20 - 109 days @ 20 - 22 °C

Bioaccumulation: aquatic / sediment

Study results
  • 4 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Studies with data
Key study 1
Supporting study 3
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Bioaccumulation Factor (BCF) - L/kg ww
3.8 - 1 000 L/kg ww

Bioaccumulation: terrestrial

Data not provided by the registrant

Adsorption/desorption

Study results
  • 2 studies submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study 2
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Koc at 20°C
320 - 4 280

Henrys law constant (H)

Study results
  • 0 studies submitted
  • 0 studies processed

No data available

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 2 summaries submitted
  • 2 summaries processed
Henry's law constant
0.233 - 240 Pa.m³.mol-1 @ 20 - 25 °C

Distribution modelling

Data not provided by the registrant

Ecotoxicological information

This section provides ecotoxicological information compiled from all automatically processable data from REACH registration dossiers that is available to ECHA at the time of generation. The quality and correctness of the information remains the responsibility of the data submitter. The Agency thus cannot guarantee the correctness of the information displayed.

Predicted No-Effect Concentration (PNEC)

R Summaries
  • 2 summaries submitted
  • 2 summaries processed

The Predicted No-Effect Concentration (PNEC) value is the concentration of a substance below which adverse effects in the environment are not expected to occur. Please note that when more than one summary is provided, PNEC values may refer to constituents of the substance and not to the substance as a whole. More detailed information is available in the dossiers.

Hazard for Aquatic Organisms
Freshwater 1.7 µg/L (1)
Intermittent releases (freshwater) 110 µg/L (1)
Marine water 170 ng/L (1)
Intermittent releases (marine water) No hazard identified (1)
Sewage treatment plant (STP) 1.6 mg/L (1)
Sediment (freshwater) 720 µg/kg sediment dw (1)
Sediment (marine water) 72 µg/kg sediment dw (1)
Hazard for Air
Air No hazard identified (2)
Hazard for Terrestrial Organism
Soil 150 µg/kg soil dw (1)
Hazard for Predators
Secondary poisoning 7.2 mg/kg food (1)

Short–term toxicity to fish

Study results
  • 6 studies submitted
  • 3 studies processed
P/RResults
LC50 (4 days) 580 - 3 100 µg/L [2]
LC50 (72 h) 600 µg/L [1]
LC50 (48 h) 650 µg/L [1]
LC50 (24 h) 840 µg/L [1]
LL50 (4 days) 79 mg/L [1]

Type of Study provided
Studies with data
Key study 1 2
Supporting study 3
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
LC50 for freshwater fish
79 mg/L

Long–term toxicity to fish

Study results
  • 3 studies submitted
  • 2 studies processed
P/RResults
NOEC (34 days) 332 µg/L [1]
NOEC (32 days) 345 - 509 µg/L [2]
NOEC (28 days) 520 µg/L [2]
LOEC (34 days) 495 µg/L [1]
LOEC (32 days) 509 - 682 µg/L [2]

Type of Study provided
Studies with data
Key study 2
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
EC10 / LC10 or NOEC for freshwater fish
320 µg/L
EC10 / LC10 or NOEC for marine water fish
520 µg/L

Short–term toxicity to aquatic invertebrates

Study results
  • 2 studies submitted
  • 1 study processed
P/RResults
EL50 (48 h) 2.7 mg/L [1]
EL100 (48 h) 5 mg/L [1]
EL10 (48 h) 2.2 mg/L [1]
NOELR (48 h) 1 mg/L [1]
LOELR (48 h) 2.5 mg/L [1]

Type of Study provided
Studies with data
Key study 1
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
EC50 / LC50 for freshwater invertebrates
2.7 mg/L

Long–term toxicity to aquatic invertebrates

Study results
  • 2 studies submitted
  • 1 study processed
P/RResults
EC10 (7 days) 42 - 64 µg/L [2]

Type of Study provided
Studies with data
Key study 1
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
EC10 / LC10 or NOEC for freshwater invertebrates
42 µg/L

Toxicity to aquatic algae and cyanobacteria

Study results
  • 3 studies submitted
  • 2 studies processed
P/RResults
EC10 (72 h) 38 - 308 µg/L [2]
EL50 (72 h) 20 - 25 mg/L [2]
NOELR (72 h) 10 mg/L [1]
LOELR (72 h) 25 mg/L [1]

Type of Study provided
Studies with data
Key study 1 1
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
EC50 for freshwater algae
25 mg/L
EC10 or NOEC for freshwater algae
38 µg/L

Toxicity to aquatic plants other than algae

Data not provided by the registrant

Toxicity to microorganisms

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
EC50 for microorganisms
670 mg/L
EC10 or NOEC for microorganisms
36 mg/L

Sediment toxicity

Study results
  • 1 study submitted
  • 1 study processed
P/RResults
LC10 (10 days) 46.8 - 156 mg/kg sediment dw [2]
LC50 (10 days) 63.3 - 211 mg/kg sediment dw [2]

Type of Study provided
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
R Summaries
  • 1 summary submitted
  • 1 summary processed
EC50 / LC50 for marine water sediment
211 mg/kg sediment dw
EC10 / LC10 or NOEC for marine water sediment
156 mg/kg sediment dw

Endocrine disrupter testing in aquatic vertebrates – in vivo

Data not provided by the registrant

Toxicity to terrestrial macroorganisms except arthropods

Study results
  • 2 studies submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study 2
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Toxicity to terrestrial arthropods

Study results
  • 3 studies submitted
  • 1 study processed
P/RResults
NOEC (28 days) 25 - 50 mg/kg soil dw [2]
LOEC (28 days) 25 - 100 mg/kg soil dw [2]
LC10 (28 days) 3.4 - 10 mg/kg soil dw [2]
EC50 (28 days) 111 mg/kg soil dw [1]
LC50 (28 days) 15.9 - 46.8 mg/kg soil dw [2]

Type of Study provided
Studies with data
Key study 1
Supporting study 2
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Toxicity to terrestrial plants

Study results
  • 1 study submitted
  • 1 study processed
P/RResults
EC50 (14 days) 25 mg/kg soil dw [1]

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence 1
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Toxicity to soil microorganisms

Study results
  • 3 studies submitted
  • 2 studies processed
P/RResults
NOEC (28 days) 1 g/kg soil dw [2]
NOEC (14 days) 316 mg/kg soil dw [1]
EC50 (28 days) 1 g/kg soil dw [2]
EC50 (14 days) 798 mg/kg soil dw [1]

Type of Study provided
Studies with data
Key study 2
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Toxicity to birds

Study results
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Type of Study provided
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Toxicity to mammals

Data not provided by the registrant

Toxicological information

This section provides toxicological information compiled from all automatically processable data from REACH registration dossiers that is available to ECHA at the time of generation. The quality and correctness of the information remains the responsibility of the data submitter. The Agency thus cannot guarantee the correctness of the information displayed.

Derived No- or Minimal Effect Level (DN(M)EL)

M/C Summaries
  • 2 summaries submitted
  • 2 summaries processed

The derived no- or minimum effect level (DN(M)EL) is the level of exposure above which a human should not be exposed to a substance. Please note that when more than one summary is provided, DN(M)EL values may refer to constituents of the substance and not to the substance as a whole. More detailed information is available in the dossiers.

Data for WORKERS
INHALATION Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DMEL) 240 µg/m³ carcinogenicity
Acute /short term: No hazard identified
Local Effects
Long-term: No hazard identified
Acute /short term: No hazard identified
DERMAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DMEL) 68 µg/kg bw/day carcinogenicity
Acute /short term: No hazard identified
Local Effects
Long-term: High hazard (no threshold derived)
Acute /short term: Low hazard (no threshold derived)
EYE Exposure
No hazard identified
Data for the GENERAL POPULATION
INHALATION Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DMEL) 100 ng/m³ carcinogenicity
Acute /short term: No hazard identified
Local Effects
Long-term: No hazard identified
Acute /short term: No hazard identified
DERMAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: No hazard identified
Acute /short term: No hazard identified
Local Effects
Long-term: No hazard identified
Acute /short term: No hazard identified
ORAL Exposure Threshold Most sensitive study
Systemic Effects
Long-term: (DMEL) 60 ng/kg bw/day carcinogenicity
Acute /short term: No hazard identified
EYE Exposure
No hazard identified

Toxicokinetics, metabolism, and distribution

Study results
Study data: basic toxicokinetics
  • 7 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Study data: basic toxicokinetics
Studies with data
Key study 1
Supporting study 1 5
Weight of evidence
Other
Data waiving
no waivers
Study data: dermal absorption
  • 4 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: dermal absorption
Studies with data
Key study 3
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Bioaccumulation potential:
No bioaccumulation potential
Absorption values
Dermal: 2 %

Acute toxicity

Study results
oral
  • 3 studies submitted
  • 1 study processed
P/RResults
LD50 2 000 mg/kg bw (rat) [1]
LD0 2 000 mg/kg bw (rat) [1]

Type of Study provided
oral
Studies with data
Key study 1
Supporting study 2
Weight of evidence
Other
Data waiving
no waivers
inhalation
  • 2 studies submitted
  • 1 study processed
P/RResults
LC0 (4 h) 404 - 522 mg/m³ air (rat) [2]
M/CInterpretations of results
Other [1]

inhalation
Studies with data
Key study 2
Supporting study
Weight of evidence
Other
Data waiving
no waivers
dermal
  • 1 study submitted
  • 1 study processed
P/RResults
LD50 2 000 mg/kg bw (rat) [1]
LD0 2 000 mg/kg bw (rat) [1]

dermal
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
other routes
  • 0 studies submitted
  • 0 studies processed

No data available

other routes
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Oral route:
No adverse effect observed Discriminating dose 2 000 mg/kg bw
Dermal route:
No adverse effect observed Discriminating dose 2 000 mg/kg bw

Irritation / corrosion

Study results
Study data: skin
  • 4 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Study data: skin
Studies with data
Key study 1
Supporting study
Weight of evidence 3
Other
Data waiving
no waivers
Study data: eye
  • 4 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: eye
Studies with data
Key study 1
Supporting study 3
Weight of evidence
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Skin
Adverse effect observed (irritating)
Eye
No adverse effect observed (not irritating)

Sensitisation

Study results
Study data: skin
  • 1 study submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Study data: skin
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Study data: respiratory
  • 0 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: respiratory
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Skin sensitisation
Adverse effect observed (sensitising)

Repeated dose toxicity

Study results
Study data: oral
  • 3 studies submitted
  • 1 study processed
P/RResults
NOAEL (mouse): 175 mg/kg bw/day [1]
LOAEL (mouse): 350 mg/kg bw/day [1]

Type of Study provided
Study data: oral
Studies with data
Key study 1
Supporting study 2
Weight of evidence
Other
Data waiving
no waivers
Study data: inhalation
  • 1 study submitted
  • 1 study processed
P/RResults
NOAEC (rat): 5.4 - 22 000 mg/m³ air [4]
LOAEC (rat): 49 - 128 000 mg/m³ air [4]

Study data: inhalation
Studies with data
Key study 1
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Study data: dermal
  • 1 study submitted
  • 0 studies processed

No automatically processable data submitted

Study data: dermal
Studies with data
Key study
Supporting study 1
Weight of evidence
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Oral route - systemic effects:
Adverse effect observed BMD05 4.7 mg/kg bw/day (chronic, mouse)
Dermal route - systemic effects:
Adverse effect observed LOAEL 34 mg/kg bw/day (chronic, mouse)
Inhalation route - systemic effects:
Adverse effect observed NOAEC 22 mg/m³ (subchronic, rat)
Inhalation route - local effects:
Adverse effect observed NOAEC 22 mg/m³ (subchronic, rat)

Genetic toxicity

Study results
Study data: in vitro
  • 5 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Study data: in vitro
Studies with data
Key study 1
Supporting study 2
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 2
Study data: in vivo
  • 1 study submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: in vivo
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
Summaries
  • 1 summary submitted
  • 0 summaries processed

No automatically processable data submitted

Carcinogenicity

Study results
  • 5 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Studies with data
Key study 2
Supporting study 3
Weight of evidence
Other
Data waiving
no waivers
M/C Summaries
  • 1 summary submitted
  • 1 summary processed
Oral route:
Adverse effect observed T25 6 mg/kg bw/day (chronic, rat)
Inhalation route:
Adverse effect observed LOAEC 52 mg/m³ (chronic, rat)

Toxicity to reproduction

Study results
Study data: reproduction
  • 2 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Type of Study provided
Study data: reproduction
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 2
Study data: developmental
  • 1 study submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: developmental
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
Not feasible
Sci. unjustified
Exposure cons.
Other 1
Study data: other studies
  • 0 studies submitted
  • 0 studies processed

Study data not processed for brief profile

Study data: other studies
Studies with data
Key study
Supporting study
Weight of evidence
Other
Data waiving
no waivers
Summaries
  • 0 summaries submitted
  • 0 summaries processed

No data available

Neurotoxicity

Data not provided by the registrant

Immunotoxicity

Data not provided by the registrant

Endocrine disrupter mammalian screening - in vivo

Data not provided by the registrant