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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

Oral: LD50 > 5000 mg/kg bw, male/female, rat, OECD401, Gardner 1988

Key value for chemical safety assessment

Acute toxicity: via oral route

Endpoint conclusion
Dose descriptor:
LD50
Value:
5 000 mg/kg bw

Additional information

Oral:

A single oral toxicity study conducted under GLP according to guideline OECD 401 is available (Gardner 1988). The study is considered to be relevant, reliable (Klimisch 1) and adequate for the purposes of risk assessment, classification and labeling.

Since none of the three doses elicited mortalities above 40% in either sex, the LD50 of the test material in rats was estimated to be >5000 mg/kg bw.

Justification for classification or non-classification

The available value for the acute oral toxicity (rat), LD50>5000 mg/kg bw does not lead to a corresponding classification of the substance, according to the criteria given in Directive 67/548/EEC, as amended for the 28th time in Directive 2001/59/EC, Annex VI, 3.2.1-3.2.3.

 

The available value for the acute oral toxicity (rat), LD50>5000 mg/kg bw does not lead to a corresponding classification of the substance, according to the criteria in Regulation (EC) No. 1272/2008, Annex I, Part 3, 3.1.2.