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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

By oral route the key study is the study conducted by Société Française Hoechst (1987) according to OECD guideline 407 on rats. A no effect level of 100 mg/kg bw/d was established for glyoxal 40% (i.e. 40 mg/kg bw/d related to the active ingredient). This value is supported by the studies by Ueno (1991a, b) on rats which obtained a LOEL of 107 mg/kg bw/d related to pure glyoxal, as well as by the study from Union Carbide (1966) on dogs which derived a NOEL of 115 mg/kg bw/d related to pure glyoxal. In a subacute inhalation study on rats for 29 days, a NOEL of 0.4 mg/m3 was derived for local effects and of > 10 mg/m3 for the systemic toxicity (40%glyoxal). No dermal repeated toxicity studies have been performed.

Key value for chemical safety assessment

Additional information

Justification for classification or non-classification