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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Additional information

1,1,3,3-tetrabutylurea was tested in vitro and in vivo:

Bacterial Reverse Mutation Assays according to OECD Guideline 471 and EC directive 92/69/EEC, L 383 A: part B: Methods for the Determination of Toxicity - Mutagenicity (Escherichia coli WP2 uvr A - reverse mutation assay) with the strains S. typhimurium TA 1535, TA 1537, TA 1538, TA 98 and TA 100 and with E. coli WP2 uvr A

Mammalian Erythrocyte Micronucleus Test with rats according to OECD Guideline 474.

In all tests negative results have been obtained.


Endpoint Conclusion: No adverse effect observed (negative)

Justification for classification or non-classification

As 1,1,3,3-tetrabutylurea was tested negative in vitro and also in vivo, there is no need for classification and labelling.