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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

The similar substance 1 was tested in a local lymphnode assay in 5 mice per dose (at 100, 50 and 25%). Following 3 days of treatment, on day 6 mice received 125I-iododeoxyuridine and 10-5M fluorodeoxyuridine and were terminated 5 hours later. The lymphnodes were excised, pooled and prepared cells suspensions were assessed for 125I incorporation. Simulation indices were calculated to be 2.72, 3.56 and 4.44 at 25, 50 and 100%. The EC3 was calculated to be 33.25%. Based on this finding the substance is considered a skin sensitizer (category 1B).

A prediction with the QSAR dyes RC 2.0 Developed by Milano Chemometrics and QASR research group Dept. Earth and Environmental Science, University Milano was performed on Reactive Blue 171, and the substance resulted not classified.

Read across is discussed in section 13

Key value for chemical safety assessment

Skin sensitisation

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (sensitising)

Respiratory sensitisation

Endpoint conclusion
Endpoint conclusion:
no study available

Justification for classification or non-classification

The test substance needs to be classified as a skin sensitizer: category 1B H317 according to Regulation (EC) No 1272/2008 (CLP)