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EC number: 202-710-8 | CAS number: 98-88-4
- 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
Carcinogenicity
Administrative data
- Endpoint:
- carcinogenicity: inhalation
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- comparable to guideline study
Data source
Reference
- Reference Type:
- publication
- Title:
- Über das Auftreten von Krebs bei Mäusen nach Inhalation von Benzotrichlorid und Benzoylchlorid
- Author:
- Yoshimura H., Takemoto K.; Fukuda K. and Matsushita H.
- Year:
- 1 986
- Bibliographic source:
Japanese Journal of Industrial health, 28: 352-359
Materials and methods
- Principles of method if other than guideline:
- Carcinogenicity induced by repeated inhalation
(For details on methodology see section examinations) - GLP compliance:
- not specified
Test material
- Reference substance name:
- Benzoyl chloride
- EC Number:
- 202-710-8
- EC Name:
- Benzoyl chloride
- Cas Number:
- 98-88-4
- Molecular formula:
- C7H5ClO
- IUPAC Name:
- benzoyl chloride
- Test material form:
- liquid
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- ICR
- Sex:
- male
Administration / exposure
- Route of administration:
- inhalation: vapour
- Type of inhalation exposure (if applicable):
- not specified
- Vehicle:
- unchanged (no vehicle)
- Analytical verification of doses or concentrations:
- no
- Duration of treatment / exposure:
- 5 months
- Frequency of treatment:
- twice weekly for 30 minutes
- Post exposure period:
- 9 months
- No. of animals per sex per dose:
- 30 (28 were evaluated)
- Control animals:
- yes
Results and discussion
Results of examinations
- Relevance of carcinogenic effects / potential:
- No significant increase in incidence of pulmonary tumors or skin tumors was observed in mice exposed to vapourized benzoyl chloride compared to controls
Any other information on results incl. tables
Table: Tumor incidence in mice by inhalation of benzoyl chloride vaporized at 50°C
Period (month) | Number of mice | Number of lung tumor (%) | Number of skin tumor (%) |
2-6 | 8 | 0 | 0 |
-10 | 13 | 0 | 2 (15.4) |
-14 | 7 | 3 (42.9) | 0 |
Total | 28 | 3 (10.7) | 2 (7.1) |
- Results in detail:
All 8 treated mice that died during the exposure period did not have tumors. Between the end of exposure (5 months) and month 10, 2/13 mice had developed skin papillomas. From month 10 till the end of the experiment 1/7 mice had lung adenomas, 2/7 had lung adenocarcinoma. Thus the overall tumour incidence was 3/28 (10.7%) for the lung and 2/28 (7.1%) for the skin.
In the control 3/30 (10%) mice developed lung adenomas during the 12 months observation period and no other tumors were observed.
No significant increase in the incidence of pulmonary tumors and skin tumors was observed in the treated animals in comparison to the control.
- Pathological changes in the skin:
At the end of exposure hair-loss and inflammation was observed.
Applicant's summary and conclusion
- Conclusions:
The authors tested the carcinogenicity of benzoyl chloride through inhalation of vapourized test substance. The authors observed no significant increase in the incidence of pulmonary tumors and skin tumors in comparison to the controls. Hence, benzoyl chloride is non carcinogenic.- Executive summary:
The authors tested the carcinogenicity of benzoyl chloride (CAS n° 98-88-4) through inhalation by exposing ICR male mice to benzoyl chloride vapour. A total of 30 mice were exposed to benzoyl chloride vapourized at 50°C twice weekly for 30 minutes during 5 months. Afterwards they were observed for another 9 months. Furthermore pathological changes in the respiratory system and skin were noted.
Eight treated mice died during the exposure period and none of them had tumors. Between the end of exposure (5 months) and month 10, 2/13 mice had developed skin papillomas. From month 10 till the end of the experiment 1/7 mice had lung adenomas and 2/7 had lung adenocarcinoma. Thus the overall tumour incidence was 3/28 (10.7%) for the lung and 2/28 (7.1%) for the skin for the treated mice. Furthermore, at the end of exposure hair-loss and inflammation was observed in the treated mice.
In the control 3/30 (10%) mice developed lung adenomas during the 12 months observation period and no other tumors were observed. Comparing the results of the test aniamls with the control shows no significant increase in the incidence of pulmonary tumors and skin tumors. Hence, benzoyl chloride may be considered as non-carcinogenic after repeated dose inhalation of vapourized benzoyl chloride.
The GLP status of the study is unknown. Although the study would benefit from a more elaborate description of clinical signs, gross pathology and weight development, it is nevertheless sufficiently documented, meets generally accepted scientific principles and is acceptable for assessment. Thus the study is reliable with restrictions, Klimisch 2e.
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