Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: dermal
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: acceptable data, report with limited documentation

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1977
Report date:
1977

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Determination of dermal LD50 of test substance in rabbits
GLP compliance:
no
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
3-methyl-2-butenyl acetate
EC Number:
214-730-4
EC Name:
3-methyl-2-butenyl acetate
Cas Number:
1191-16-8
Molecular formula:
C7H12O2
IUPAC Name:
3-methylbut-2-en-1-yl acetate
Test material form:
other: liquid
Details on test material:
- Name of test material (as cited in study report): Prenyl Acetate
- Sample marking: 77-400
No additional details provided

Test animals

Species:
rabbit
Strain:
not specified
Sex:
not specified

Administration / exposure

Type of coverage:
not specified
Vehicle:
not specified
Duration of exposure:
not specified
Doses:
5000 mg/kg bw
No. of animals per sex per dose:
10
Control animals:
not specified
Details on study design:
- Frequency of observations and weighing: not specified; the animals were observed for mortality and/or toxic signs.
- Necropsy of survivors performed: yes
No further details provided
Statistics:
No data

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Based on:
test mat.
Remarks on result:
other: no mortality observed
Mortality:
No mortality occurred.
Clinical signs:
other: Toxic signs included diarrhea.
Gross pathology:
Necropsy findings included a brown exudate in the anogenital area, and changes in intestines (red areas), liver (dark), lungs (dark areas), kidneys (dark, mottled), and spleen (dark) in single animals.

Applicant's summary and conclusion