Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: oral
Type of information:
experimental study
Adequacy of study:
other information
Study period:
30th December 1998 - 25th January 1999
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study without detailed documentation

Data source

Materials and methods

GLP compliance:
not specified
Test type:
standard acute method
Limit test:
no

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Doses:
50, 150, 500 and 2,000 mg/kg
No. of animals per sex per dose:
5
Control animals:
not specified

Results and discussion

Mortality:
LD50 183 mg/kg body weight

Applicant's summary and conclusion