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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1982
Report date:
1982

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Animals tested were all females ca. 14 weeks old and had an average weight at the beginning of the test of 161 g. The rats tested were kept in groups of 5 under following conditions: 22 +/- 1.5 °C; 12 h light/dark cycle; humidity 60 +/- 5%
Food (Altromin R 1324) and tap water were provided at libitum during the entire test period.
Duration of observation: 14 days.
GLP compliance:
no
Test type:
acute toxic class method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
α,4-dichlorotoluene
EC Number:
203-242-7
EC Name:
α,4-dichlorotoluene
Cas Number:
104-83-6
Molecular formula:
C7H6Cl2
IUPAC Name:
1-chloro-4-(chloromethyl)benzene
Details on test material:
p-Chlorobenzyl chloride, solid.

Test animals

Species:
rat
Strain:
Wistar
Sex:
female
Details on test animals or test system and environmental conditions:
Test animals:
Wistar rats, females, ca. 14 weeks old. Average weight at the beginning of the test: 161 g.
Tested in groups of 5 animals. Conditions: 22 +/- 1.5°C; 12h light/dark cycle; humidity 60 +/- 5%
Source: Winkelmann, Borchen

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
polyethylene glycol
Details on oral exposure:
The test substance was composited with Lutrol (polyethylene glycol) and administered by gavage.
The mixture was given once.
Doses:
100, 500, 800, 900, 1000, 1500 mg/kg bw
No. of animals per sex per dose:
10

Results and discussion

Effect levels
Sex:
female
Dose descriptor:
LD50
Effect level:
786 mg/kg bw
Based on:
test mat.

Applicant's summary and conclusion

Conclusions:
The LD50 value for acute oral toxicity is 786 mg/kg bw in female Wistar rats.