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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
no adverse effect observed (not sensitising)
Additional information:

The Key study was performed on an analog substance according to Magnusson-Kligman Maximization Assay,

Induction phase

The assays are run by applying a minimally irritating dose of the test compound (5% propylene glycol and freund's adjuvant) the to the shaved flanks of Dunkin-Hartley guinea pigs for approximately 3 weeks.

Challenge phase

About 1x week after the last application, the undiluted chemical or 50% in petrolatum is re-applied to the animals.

Scoring of erythema and edema (24 and 48 hours) is accomplished by adding up all the animals that responded in a group of ten and expressing it as a percentage (incidence) and determined the intensity of teach response on a scale of 0-4.

Result

Scores of zero in all test animals were obtained at all time points examined. The test material does not appear to be a sensitizer in the guinea pig.


Migrated from Short description of key information:
The Key study was performed on an analog substance according to Magnusson-Kligman Maximization Assay. Scores of zero in all test animals were obtained at all time points examined. The test material does not appear to be a sensitizer in the guinea pig.

Respiratory sensitisation

Endpoint conclusion
Endpoint conclusion:
no study available

Justification for classification or non-classification

In accordance with EU CLP Regulation (EC) No. 1272/2008, classification of this substance is not required for skin sensitisation.

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