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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
dermal absorption in vivo
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
year of publication: 2002
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Only secondary source
Cross-reference
Reason / purpose for cross-reference:
reference to other study

Data source

Reference
Reference Type:
review article or handbook
Title:
European Union Risk Assessment Report - o-Anisidin
Author:
European Chemicals Bureau
Year:
2002
Bibliographic source:
European Commission, Joint Research Center, EUR 19834 EN, 2nd Priority list, Volume 15

Materials and methods

Test material

Constituent 1
Chemical structure
Reference substance name:
o-anisidine
EC Number:
201-963-1
EC Name:
o-anisidine
Cas Number:
90-04-0
Molecular formula:
C7H9NO
IUPAC Name:
2-methoxyaniline

Results and discussion

Signs and symptoms of toxicity:
yes
Remarks:
ataxia, lacrimation, eyelid constriction, ruffeled fur, at day 1 post application urine was orange
Dermal irritation:
yes
Remarks:
very slight to moderate irritative effects 30 min post application which were all reversible within 72 h

Any other information on results incl. tables

Dermal resorption can be assumed from other studies on toxicity of o-anisidine.

Applicant's summary and conclusion

Conclusions:
There were no in vivo studies specifically dealing with the metabolism of o-anisidine. However, from effects observed in toxicological studies it can be assumed that o-anisidine is resorbed after dermal application.