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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
1978
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non standard test design, with little reporting detail

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1978
Report date:
1978

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Inhalation-Risk-Test was performed in principle as described in OECD Guideline 403. It demonstrates the toxicity of an atomosphere saturated with vapors of the volatile components of a test substance at the temperature chosen for vapor generation (20°C and 60°C).
GLP compliance:
no
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Methyl benzoylformate
EC Number:
239-263-3
EC Name:
Methyl benzoylformate
Cas Number:
15206-55-0
Molecular formula:
C9H8O3
IUPAC Name:
methyl oxo(phenyl)acetate
Details on test material:
- Physical state: liquid (tested were vapours at 20 and 60°C)

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: mean: male: 171 g; female: 158 g

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
not specified
Vehicle:
air
Details on inhalation exposure:
GENERATION OF TEST ATMOSPHERE / CHAMBER DESCRIPTION
- Source and rate of air: 200L air/h
- System of generating test atmospere: Vapor is generated by bubbling 200 L/h air at 20°C and 100 L/h air at 60°C through a substance column of about 5 cm above a fritted glass disc in a glass cylinder for 7 hours.
- Pressure in air chamber: 760 mm/Hg
Analytical verification of test atmosphere concentrations:
no
Duration of exposure:
7 h
Concentrations:
not determined
No. of animals per sex per dose:
3
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: daily, weighing at beginning and at the end of the study
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC0
Effect level:
other: vapours formed at 20°C and 60°C
Based on:
test mat.
Exp. duration:
7 h
Mortality:
none
Clinical signs:
other: none
Gross pathology:
no abnormalities detected

Applicant's summary and conclusion

Interpretation of results:
other: vapours at 20°C and 60°C are not acutely toxic