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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Skin sensitisation

Endpoint conclusion
Endpoint conclusion:
adverse effect observed (sensitising)
Additional information:

Testing for sensitizing properties of 3 -chloro-o-toluidine was performed in female Pirbright white guinea pigs according to the method of Buehler as described in the OECD 406. Dermal induction was performed using 100% test substance. The control group was exposed to semi-liquid paraffin only. First challenge treatment was carried out with 100% test substance, second challenge treatment was performed with 50% test substance in petrolatum. After first challenge treatment two of 20 animals of the treatment group showed well defined erythema 24 hours after removal of the patches. Second challenge treatment resulted in very slight to well-defined erythema, dry rough skin and fine scales in three of 20 animals of the treatment group 24 and 48 hours after removal of the patches. The animals of the control group showed no signs of irritation after the first and second challenge treatment. Based on the results of this study 3-chloro-o-toluidine showed evidence for sensitizing properties.


Migrated from Short description of key information:
Sensitising (GLP Guideline Study, Hoechst, 94.0006, 1994)

Respiratory sensitisation

Endpoint conclusion
Additional information:
Migrated from Short description of key information:
no data available

Justification for classification or non-classification

Dangerous Substance Directive (67/548/EEC)

The available study is considered reliable and suitable for classification purposes under 67/548/EEC. As a result the substance is considered to be classified for skin sensitsation (R43) under Directive 67/548/EEC, as amended for the 28th time in Directive 2001/59/EC.

 

Classification, Labelling, and Packaging Regulation (EC) No. 1272/2008

The available experimental test data is reliable and suitable for classification purposes under Regulation 1272/2008. As a result the substance is considered to be classified for skin sensitisation (Category 1B) under Regulation (EC) No. 1272/2008.