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Diss Factsheets
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EC number: 201-152-2 | CAS number: 78-87-5
- 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
An excellent package of GLP experimental studies have been performed to cover the mutagenicity potential in bacteria and mammalian cells “in vitro” as well as “in vivo” approach. All studies were performed both with metabolic activation and without metabolic activation in order to check if any metabolic process can activate or enhance the mutagenic effects, if any.
Results from in vitro genotoxicity tests (bacterial, fungal, mammalian systems; with and without
metabolic activation) are mixed, with both positive and negative studies, indicating that 1,2-dichloropropane may have in vitro mutagenic potential. However, results from two last in vivo studies demonstrate that 1,2-dichloropropane was not active in an mouse micronucleus test or a rat dominant lethal assay. These findings indicate that 1,2-dichloropropane is not an in vivo somatic or germ cell genotoxicant, despite widespread distribution throughout the body. In addition, results from adequate carcinogenicity assays (see discussion on section 5.8) in rats and mice provide supplementary information on the mutagenic potential of 1,2-dichloropropane in vivo. The findings (limited to liver tumors in mice and no convincing evidence of carcinogenicity in the rat) indicate that the compound is not a genotoxic carcinogen.
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
Based on the results of the reported studies and taking into account the literature, 1,2-dichloropropane does not meet the classification criteria as genotoxic.
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