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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Additional information

Three fully reliable studies (Covance Laboratories 1998/ KS K1/ Ames test; Bioservice Scientific Laboratories 2010/ K1 KS/ In vitro Mammalian Cell Gene Mutation Assay; Bioservice Scientific Laboratories 2010/ K1 KS/ In vitro Mammalian Chromosome Aberration Test) are available for 2-Propanol, 1,1'-[[3-[(3-aminopropyl)amino]propyl]imino]bis-, N-tallow alkyl derivs. in vitro covering all mandatory endpoints of genetic toxicity in vivo.

All tests are negative therefore there is no indication of a mutagenic potential of the test item.


Short description of key information:
- genetic toxicity in vitro: negative, 3 studies (Covance Laboratories 1998/ KS K1/ Ames test; Bioservice Scientific Laboratories 2010/ K1 KS/ In vitro Mammalian Cell Gene Mutation Assay; Bioservice Scientific Laboratories 2010/ K1 KS/ In vitro Mammalian Chromosome Aberration Test)

Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

Based on the above stated results a classification of 2-Propanol, 1,1'-[[3-[(3-aminopropyl)amino]propyl]imino]bis-, N-tallow alkyl derivs. for genetic toxicity is not necessary according to CLP as implementation of UN GHS in the EU (REGULATION (EC) No 1272/2008 OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL).