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EC number: 202-987-5 | CAS number: 101-90-6
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Acute Toxicity: inhalation
Administrative data
- Endpoint:
- acute toxicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- weight of evidence
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- data from handbook or collection of data
Data source
Referenceopen allclose all
- Reference Type:
- publication
- Title:
- The Toxicology of Epoxy Resins
- Author:
- Hine CH, Kodama JK, Anderson HH, Simonson DW, Wellington JS.
- Year:
- 1 958
- Bibliographic source:
- AMA Archives of Industrial Health
- Reference Type:
- publication
- Title:
- The Toxicology of Glycidol and Some Glycidyl Ethers
- Author:
- Hine CH, Kodama JK, Wellington JS, Dunlap MK, Anderson HH
- Year:
- 1 956
- Bibliographic source:
- AMA Arch Indust Health 14:250-264
- Reference Type:
- publication
- Title:
- Toxicology and safe handling of CBP-55 (Technical 1-chloro-3-romopropene-1)
- Author:
- Hine CH, Anderson HH, Moon HD, Kodama JK, Morse M, Jacobsen NW
- Year:
- 1 953
- Bibliographic source:
- AMA Arch Indust Hyg, 7: 118-136
Materials and methods
Test guideline
- Qualifier:
- no guideline available
- Principles of method if other than guideline:
- Groups of six rats were exposed to saturated vapors of diclycidyl resorcinol at 30±1 °C within 8 hours, by passage through the liquids in two fritted glass bubblers connected in series in a glass chamber of 19.5 L capacity. The motor-driven syringe assembly delivered measured amounts of the test compound from a 10 mL. Luer-Lok syringe into an evaporator through which metered air moved at a uniform rate. The air flow was set at approximately 3 to 11 L per minute, depending on the concentration desired. Nominal concentrations were calculated by the standard gas-concentration formula of Jacobs and were checked by determining the total quantity of material vaporized.
- GLP compliance:
- no
- Remarks:
- pre-GLP
- Test type:
- other: 8-hour exposure to saturated vapors (the maximum attainable concentration)
- Limit test:
- yes
Test material
- Reference substance name:
- m-bis(2,3-epoxypropoxy)benzene
- EC Number:
- 202-987-5
- EC Name:
- m-bis(2,3-epoxypropoxy)benzene
- Cas Number:
- 101-90-6
- Molecular formula:
- C12H14O4
- IUPAC Name:
- 2-({3-[(oxiran-2-yl)methoxy]phenoxy}methyl)oxirane
- Test material form:
- liquid: viscous
Constituent 1
Test animals
- Species:
- rat
- Strain:
- Long-Evans
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- TEST ANIMALS
- Source: commercial laboratory in Gilroy, California
- Weight at study initiation: 110-150 g
- Housing: six to a cage
- Diet: standard laboratory pellets
- Water: tap water
- Acclimation period: for about two weeks
ENVIRONMENTAL CONDITIONS
- Temperature (°C): 14 and 18
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure:
- whole body
- Vehicle:
- air
- Details on inhalation exposure:
- GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Exposure apparatus: Motor-driven syringe assembly: Luer-Lok syringe into an evaporator through which metered air moved at a uniform rate
- Exposure chamber volume: 19.5 L
- Method of holding animals in test chamber: 6 animals/chamber
- Method of conditioning air: high concentration was obtained by bubling air through a fritted glass disc immersed in the compound, which was held in a glass container
- Source and rate of air: air flow was set at 3 to 11 L/min, depending on the concentration desired
- Temperature, humidity, pressure in air chamber: 30±1 °C - Analytical verification of test atmosphere concentrations:
- no
- Remarks:
- the concentration was too low to permit accuracy of determination
- Duration of exposure:
- 8 h
- Concentrations:
- saturated vapour of diglycidyl resorcinol
- No. of animals per sex per dose:
- 6 males
- Control animals:
- no
- Details on study design:
- - Duration of observation period following administration: 10 days
- Frequency of observations and weighing: noted weighing changes
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, gross pathology - Statistics:
- one level tested
Results and discussion
Effect levels
- Key result
- Sex:
- male
- Dose descriptor:
- other:
- Remarks:
- the maximum attainable concentration
- Effect level:
- other: the maximum attainable concentration
- Based on:
- test mat.
- Exp. duration:
- 8 h
- Remarks on result:
- not determinable due to absence of adverse toxic effects
- Mortality:
- Not reported
- Clinical signs:
- other: Not reported
- Body weight:
- Not reported
- Gross pathology:
- Not reported
- Other findings:
- No systemic toxicity has resulted from inhalation of the saturated vapours
Applicant's summary and conclusion
- Interpretation of results:
- other: no toxicity hazard could be associated at the maximum attainable concentration
- Conclusions:
- The test item diglycidyl resorcinol does not need to be classified as no toxicity hazard could be associated at the maximum attainable concentration.
- Executive summary:
The six rat males of the Long-Evans strain (bw 110 -150 g) were exposed with the saturated vapor of diglycidyl resorcinol for eight hours.
The authors concluded that no practical toxicity hazard could be associated.
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