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EC number: 204-331-3 | CAS number: 119-53-9
- 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
1. SUMMARY FROM HSDB for CAS 119 -53 -9 (benzoin)
Benzoin was found to be negative when tested for mutagenicity using the
Salmonella/microsome preincubation assay, using the standard protocol
approved by the National Toxicology Program (NTP). Benzoin was tested in
as many as 6 Salmonella typhimurium strains (TA1535, TA1537, TA1538, TA97, TA98,
and TA100) in the presence and absence of rat and hamster liver S-9, at
doses of 0.033, 0.0333, 0.100, 0.333, 0.3333, 0.667, 1.000, and 3.3333
mg/plate. The highest ineffective dose tested in any S. typhimurium strain
was 3.3333 mg/plate. Precipitate was observed in most cultures at the high
dose and also some clearing of the background bacterial lawn was also
seen. [Mortelmans K et al; Environ Mutagen 8:1-119 (1986)]
... Levels of Evidence of Carcinogenicity: Male Rats: Negative; Female
Rats: Negative; Male Mice: Negative; Female Mice: Negative. [Bioassay of
Benzoin for Possible Carcinogenicity (1980) Technical Rpt Series No. 204
DHEW Pub No. (NIH) 80-1760, U.S. Department of Health Education and
Welfare, National Cancer Institute, Bethesda, MD 20014]
A bioassay of benzoin for possible carcinogenicity was conducted by
incorporating the test chemical in diets of F344 rats and B6C3F1 mice. ...
Groups of 50 male rats were fed diets containing 125 or 250 ppm benzoin
for 104 wk, and similar groups of female rats received feed containing 250
or 500 ppm. Groups of 50 mice if each sex were fed diets containing 2,500
or 5,000 ppm benzoin for 104 wk. Groups of 50 untreated rats and mice of
each sex were used as matched controls. ... Under the conditions of this
bioassay, benzoin was not carcinogenic in F344 rats or B6C3F1 mice. Levels
of Evidence of Carcinogenicity: Male Rats: Negative; Female Rats:
Negative; Male Mice: Negative; Female Mice: Negative. [Bioassay of Benzoin
for Possible Carcinogenicity (1980) Technical Rpt Series No. 204 DHEW Pub
No. (NIH) 80-1760, U.S. Department of Health Education and Welfare,
National Cancer Institute, Bethesda, MD 20014]
2. OECD Toolbox experimental data
Benzoin was found positive in an in vitro mammalian chromosome aberration test (Chinese hamster lung cells)
without metabolic activation, negative in the in vivo mouse micronucleus test and negative in a mammalian
in vitro cell gene mutation assay (mouse lymphoma cells).
Endpoint Conclusion: No adverse effect observed (negative)
Justification for classification or non-classification
At the found effect levels there is no requirement for classification
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