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Diss Factsheets
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EC number: 203-214-4 | CAS number: 104-57-4
- 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
Acute Toxicity: dermal
Administrative data
- Endpoint:
- acute toxicity: dermal
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- other: Only basic information given.
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 1 960
Materials and methods
Test guideline
- Qualifier:
- no guideline followed
- Principles of method if other than guideline:
- In an acute dermal toxicity study, the shaved skin of 6 male mice were exposed to the test item with 0.25 % esterine over a period of 2 hours. The detection of the esterine resorption was used as a indirect proof of the inclusion of the solvent.
- GLP compliance:
- no
Test material
- Reference substance name:
- Benzyl formate
- EC Number:
- 203-214-4
- EC Name:
- Benzyl formate
- Cas Number:
- 104-57-4
- Molecular formula:
- C8H8O2
- IUPAC Name:
- benzyl formate
Constituent 1
Test animals
- Species:
- mouse
- Strain:
- not specified
- Sex:
- male
- Details on test animals or test system and environmental conditions:
- no data
Administration / exposure
- Type of coverage:
- occlusive
- Details on dermal exposure:
- TEST SITE
- Area of exposure: The contact area was limited by small cylindrical glass containers (diameter 17, height 10 mm) which were closed at the top with waterproof adhesive tape and fixed with commercially available glue on the abdominal skin. Thus, the area of exposure was 2.2 cm². - Duration of exposure:
- 2 hours
- Doses:
- Test substance was tested as solution agent together with 0.25 % eserine.
- No. of animals per sex per dose:
- 6
- Control animals:
- no
- Details on study design:
- No data
- Statistics:
- No data
Results and discussion
- Mortality:
- No mortality occurred.
- Clinical signs:
- No data
- Body weight:
- No data
- Gross pathology:
- No data
Any other information on results incl. tables
Results of the resorption test of the test item with 0.25 % eserine
Solution agent for eserine (0.25 % solution) |
Minutes to increase the lifting height (mean) |
More minutes until reaching the maximum lift height (mean) |
Number of analyzed trials |
Test item |
- (10) |
- |
6 |
- An application of the test item alone also did not lead to an intoxication.
Applicant's summary and conclusion
- Interpretation of results:
- study cannot be used for classification
- Conclusions:
- In the present study, the test item showed no dermal absorption after an exposure period of 2 hours in mice. Thus, a toxic effect at this dose can be excluded under the experimental conditions chosen.
- Executive summary:
In this study the percutane resorption of the test item with 0.25 % eserine was observed. The shaved skin of 6 male mice were exposed to the test item with 0.25 % eserine over a period of 2 hours. The detection of the eserine resorption was used as an indirect proof of the inclusion of the solvent. Eserine was not absorbed under the said experimental conditions. It can be concluded that the test item was also not absorbed. Thus, a toxic effect of the test item at this dose can be excluded under the experimental conditions chosen. An exposure to the test item alone also did not lead to an intoxication.
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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