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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

No acute toxicity studies are available for N-Formylaminosorbose. However, there are acute toxicity studies for the structural analogue N-Formylaminosorbit (CAS 89182-60-5):
Oral (Rat-Wistar, GLP, OECD TG 401): LD50 > 2000 mg/kg
[Bayer AG, Report No. PH-18819, 1990-02-20]
Inhalation (Rat-Wistar, GLP, OECD TG 403, EU Method B.2, OPPTS 870.1300): LC50 > 4575 mg/m³
[Bayer AG, Report No. PH-34479, 2006-06-01]

Key value for chemical safety assessment

Additional information

No acute toxicity studies are available for N-Formylaminosorbose. However, there are acute toxicity studies for the structural analogue N-Formylaminosorbit (CAS 89182-60-5):

The acute oral toxicity of N-Formylaminosorbit was studied in male and female rats.

The acute oral LD50 was determined to be > 2000 mg/kg.

The acute inhalation toxicity of N-Formylaminosorbit was studied in male and female rats.

The LC50 inhalation (aerosol, 4 h) was determined to be > 4575 mg/m³ (the maximum attainable mean solid aerosol concentration).

Justification for classification or non-classification

Based on the study results a classification according to Directive 67/548/EEC and Regulation (EC) No. 1272/2008 (CLP) is not required.