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EC number: 413-370-7 | CAS number: 17351-75-6 RAPICURE CHVE
- 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
Endpoint summary
Administrative data
Key value for chemical safety assessment
Additional information
Mutagenicity of 1,4 -cyclohexane dimethanol divinyl ether was tested in a bacterial reverse mutation GLP study according to japanese guidelines for Screening Mutagenicity Testing Of Chemicals. The Strains TA 98, TA100, TA1535, TA1537 and Ecoli WP2uvr were used. Due to cytotoxicity the test was performed in concentration range from 0.6 to 78 µg/plate witout S9 -Mix and 2.4 to 625 µg/plate with metabolic activation. Positive and solvent controls gave the expected results. No mutagenic activity of the test compound was found under the conditions of the test.
Mammalian gene mutation (HGPRT locus) of dimethylol-1,4-cyclohexane divinylether was tested with and without metabolic activation in Chinese hamster ovary cells (CHO). The concentration rang tested was 5-50 µg/ml (without metabolic activation) and 60-400 µg/ml (with metabolic activation by S9-Mix). Higher concentrations appeared to be cytotoxic in a dose range finding study. No induction of forward mutations was observe in any of the experiments. Positive and negative controls gave the expected results.
Beyond this, mutagenicity of dimethanol-1,4 -cyclohexane divinylether was investigated in a in-vivo micronucleus test in mice according to OECD no. 474. 5 male and female mice per dose and time point received a single oral doses of 0, 300, 600 and 1200 mg/kg 1,4 dimethanol cyclohexane divinylether in corn oil. Erythrocytes from bone marrow were harvested 24, 48 and 72 h post application. There was no induction of micronucleus formation. From a dose dependent decrease of the PCE/NCE ration it can be concluded that test substance has reached bone marrow cells. Mortality and lethargy of animal receiving 1200 mg/kg demonstrate that the maximal tolerable oral dose was tested. Negative and positive controls gave expected results. Dimethanol-1,4 -cyclohexane divinylether is considered non-klastogenic in-vivo.
Short description of key information:
No mutagenic activity of dimethanol 1,4 cyclohexane divinylether was observed in tests with bacteria, mamalian cell culture and in vivo in mammals.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
Classification for genetic toxicity is not warranted according to the criteria of EU Classification, Labelling and Packaging of Substances and Mixtures (CLP) Regulation (EC) No. 1272/2008.
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