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EC number: 202-853-6 | CAS number: 100-44-7
- 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
Repeated dose toxicity: oral
Administrative data
- Endpoint:
- sub-chronic toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- other information
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Klimisch 2e as the study is well documented, meets generally accepted scientific principles and acceptable for assessment
Data source
Reference
- Reference Type:
- publication
- Title:
- Chronic bioassay of benzyl chloride in F344 rats and (C57BL/6J x BALB/c)F1 mice
- Author:
- Lijinsky W.
- Year:
- 1 986
- Bibliographic source:
- J. Natl.Cancer Inst., 76: 1231-1236
Materials and methods
- Principles of method if other than guideline:
- Female and male rats were repeatedly exposed to the test substance by oral gavage in a subchronic test. During the experiment they were weekly weighed and at the end of the experiment they were sacrificed and examined histopathologically.
- GLP compliance:
- not specified
- Limit test:
- no
Test material
- Reference substance name:
- α-chlorotoluene
- EC Number:
- 202-853-6
- EC Name:
- α-chlorotoluene
- Cas Number:
- 100-44-7
- Molecular formula:
- C7H7Cl
- IUPAC Name:
- (chloromethyl)benzene
- Reference substance name:
- chloromethylbenzene
- IUPAC Name:
- chloromethylbenzene
- Details on test material:
- - Name of test material (as cited in study report): benzyl chloride
- Physical state: colorless liquid
- Analytical purity: 97.5–98 %
- Composition of test material, percentage of components: Besides 97.5 - 98% benzylchloride, six or seven minor components (e.g. benzene and toluene) each constituting 0.1% or more
- Other:
Supplier: Fisher Scientific Co., Fairlawn, NJ
No more data available
Constituent 1
Constituent 2
Test animals
- Species:
- rat
- Strain:
- Fischer 344
- Sex:
- male/female
Administration / exposure
- Route of administration:
- oral: gavage
- Vehicle:
- corn oil
- Analytical verification of doses or concentrations:
- no
- Duration of treatment / exposure:
- 26 weeks
- Frequency of treatment:
- once daily, 3 times/week
Doses / concentrations
- Remarks:
- Doses / Concentrations:
15, 30, 62, 125 or 250 mg/kg
Basis:
actual ingested
- No. of animals per sex per dose:
- 10 male and 10 female rats/group
- Control animals:
- yes, concurrent vehicle
Results and discussion
Effect levels
open allclose all
- Dose descriptor:
- NOEL
- Effect level:
- 6.4 mg/kg bw/day (nominal)
- Sex:
- female
- Basis for effect level:
- other: corresponds to 15 mg/kg
- Dose descriptor:
- NOEL
- Effect level:
- 12.9 mg/kg bw/day (nominal)
- Sex:
- male
- Basis for effect level:
- other: corresponds to 30 mg/kg
- Dose descriptor:
- LOEL
- Effect level:
- 12.9 mg/kg bw/day (nominal)
- Sex:
- female
- Basis for effect level:
- other: corresponds to 30 mg/kg
- Dose descriptor:
- LOEL
- Effect level:
- 26.6 mg/kg bw/day (nominal)
- Sex:
- male
- Basis for effect level:
- other: corresponds to 62 mg/kg
Target system / organ toxicity
- Critical effects observed:
- not specified
Any other information on results incl. tables
Dose of 30 mg/kg (12.9 mg/kg bw/day)
- a few females had hyperkeratosis of the forestomach.
Dose of 62 mg/kg (26.6 mg/kg bw/day)
- females: only 4 survived to 26 weeks; acute myocardial necrosis in 4 and hyperplasia of the forestomachwas observed
- statistically significant depression of weight gain in males, in females the weight gain depression was smaller
Dose of 125 mg/kg (53.6 mg/kg bw/day)
- all females died within 2 weeks
- all males died within 3 weeks
- cause of death was mainly severe acute and chronic gastritis of the forestomach (often with ulcers). In many cases there was also acute myocardial necrosis and edema of the heart
Dose of 250 mg/kg (107.1 mg/kg bw/day)
- all rats died within 2 weeks
- common cause of death was acute myocardial necrosis and edema of the heart
Applicant's summary and conclusion
- Conclusions:
- The authors tested the oral toxicity of benzyl chloride by repeatedly exposing female and male rats to the test substance by oral gavage in a subchronic test. In these test conditions the NOEL was 6.4 and 12.9 mg/kg bw/day and the LOEL was 12.9 and 26.6 mg/kg bw/day for females and males respectively.
- Executive summary:
The authors tested the oral toxicity of benzyl chloride (CAS n° 100-44-7) by repeatedly exposing female and male F344 rats to the test substance by oral gavage in a subchronic test. The test substance was mixed with corn oil and administered once a day, three times a week for 26 weeks.Ten rats/sex were exposed to 15, 30, 62, 125 or 250 mg/kg and a control group was included. During the experiment the rats were weighed and at the end of the experiment tha animals were sacrificed and examined histopathologically.
In these test conditions, a few females exposed to 30 mg/kg (12.9 mg/kg bw/day) had hyperkeratosis of the forestomach. At a dose of 62 mg/kg (26.6 mg/kg bw/day) only four females survived till the end of the experiment (26 weeks). Furthermore acute myocardial necrosis was observed in 4 female rats and hyperplasia of the forestomach was also noted. Also at 62 mg/kg depression of weight gain was seen in females and males, but only for males this decrease in weight gain was statistically significant. Exposure to 125 mg/kg (53.6 mg/kg bw/day) led to death within 2 weeks for all females and 3 weeks for all males. The cause of death was mainly severe acute and chronic gastritis of the forestomach (often with ulcers) and in many cases there was also acute myocardial necrosis and edema of the heart. Finally after exposure to 250 mg/kg (107.1 mg/kg bw/day) all rats died within 2 weeks and the most common cause of death was acute myocardial necrosis and edema of the heart.
Finally, in the test conditions , the aurhors established the NOEL was 6.4 and 12.9 mg/kg bw/day and the LOEL was 12.9 and 26.6 mg/kg bw/day for female and male rats respectively.
No data is available on the GLP status of the study. Although some details of the study are lacking, the study itself is well conducted, well documented, meets generally accepted scientific principles and acceptable for assessment. Therefore we consider it reliable with restrictions, Klimisch 2e.
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