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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

GLP guideline study (OECD TG 401, adopted 1987): LD50, oral, rat >2000 mg/kg bw.
GLP guideline study (OECD TG 402, adopted 1987): LD50, dermal, rat>2000 mg/kg bw.

Key value for chemical safety assessment

Additional information

Acute toxicity, oral route:

A GLP guideline study (OECD TG 401, adopted 1987) for assessment of oral toxicity of Dimethylmalonate is available. Five animals per sex (Bor: WISW (SPF Cpb) rats) were treated by gavage with a limit dose of 2000 mg/kg bw test substance. During observation period no mortality or clinical signs at all were observed. Thus an LD50 >2000 mg/kg bw was deduced.

Acute toxicity, inhalation route:

No data available.

Acute toxicity, dermal route:

A GLP guideline study (OECD TG 402, adopted 1987) for assessment of dermal toxicity of Dimethylmalonate is available. Five animals per sex (Bor: WISW (SPF Cpb) rats) were treated for 24 hours with a semiocclusive dressing with a limit dose of 2000 mg/kg bw test substance. During observation period no mortality, clinical signs or local irritancy were observed. Thus an LD50 >2000 mg/kg bw was deduced.

Justification for classification or non-classification

Dangerous Substance Directive (67/548/EEC)

-No classification required for acute toxicity

Classification, Labeling, and Packaging Regulation (EC) No. 1272/2008 (last amended by EC/286/2008 (2011-03-10)):

-Oral and dermal route: no classification required