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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1971
Report date:
1971

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 402 (Acute Dermal Toxicity)
GLP compliance:
no
Remarks:
; GLP was not compulsory at the time the study was conducted.
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
4-methylanisole
EC Number:
203-253-7
EC Name:
4-methylanisole
Cas Number:
104-93-8
Molecular formula:
C8H10O
IUPAC Name:
1-methoxy-4-methylbenzene
Details on test material:
- Name of test material (as cited in study report): p-Methylanisole
- Analytical purity: no data given

Test animals

Species:
rabbit
Strain:
New Zealand White
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 2.5 - 3 kg

Administration / exposure

Type of coverage:
occlusive
Vehicle:
not specified
Details on dermal exposure:
TEST SITE
- Area of exposure: approx. 240 cm2
- Type of wrap if used: Cover was a sleeve and Webril padding
- Test site was clipped and left intact in half of the animals, while lightly abraded in the remaining animals
- Amount(s) applied: 5 ml/kg bw
Duration of exposure:
14 days
Doses:
5 ml/kg bw => 4850 mg/kg bw (calculated using density : 970 g/l)
No. of animals per sex per dose:
6 animals per dose (no further data)
Control animals:
not specified
Details on study design:
Toxic effects and mortality were recorded daily for 14 days
Pathology: gross necropsy

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 4 850 mg/kg bw
Remarks on result:
other: >5 ml/kg bw (calculation based on a density of 970 g/l)
Mortality:
No deaths occured, all animals survived.
Clinical signs:
Erythema score: 2-3 in 6/6 animals
Edema score: 1-3 in 5/6 animals
Scaling in 5/6 animals
Eschar in 3/6 animals

According to the authors, no other effects were seen.
Gross pathology:
According to the authors, no effects were seen.

Applicant's summary and conclusion