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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: No OECD Guideline or GLP defined

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1992
Report date:
1992

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: 84/449/EWG; L 251.
Principles of method if other than guideline:
In an acute dermal toxicity study in male and female Wistar rats the animals were treated with the test substance for 24 h on the shaved back and flank. The dose tested was 2000 mg/kg bw.
GLP compliance:
yes
Test type:
other: acute dermal toxicology study in rats
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Dichloromethylbenzene
EC Number:
249-854-8
EC Name:
Dichloromethylbenzene
Cas Number:
29797-40-8
Molecular formula:
C7H6Cl2
IUPAC Name:
(dichloromethyl)benzene
Details on test material:
99.02 % Dichlortoluol-Isomer-Mixture:
<0.05 % o-Chlortoluol,
<0.05 % m+p-Chlortoluol,
6.6 % 2.6-Dichlortoluol,
25.9 % 2.4-Dichlortoluol,
44.9 % 2.5-Dichlortoluol,
9.2 % 2.3-Dichlortoluol,
12.6 % 3.4-Dichlortoluol

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Type of coverage:
occlusive
Vehicle:
not specified
Duration of exposure:
24 h
Doses:
2000 mg/kg bw.
No. of animals per sex per dose:
5
Control animals:
not specified

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The LD 50 was >2000 mg/kg bw.
Executive summary:

In an acute dermal toxicity study in male and female Wistar rats the animals were treated with the test substance for 24 h on the shaved back and flank. The dose tested was 2000 mg/kg bw. After 24 h the occlusive coverage was removed and the leftovers of test substance were washed with lukewarm water. Up to 30 minutes after application the female and male animals made sounds. After one hour all animals were symptom-free. No local skin changes were observed. During the 14 day observation-period no animal died. The LD 50 therefore was >2000 mg/kg bw.