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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Link to relevant study record(s)

Description of key information

As reported in Chemical Information Profile for Alkylaniline NTP 2009 with reference to Liu et all., Chem Res Toxicol, 20:1300-1308,2007 2-ethylaniline is N-Acetylated by N-acetyltransferase 2 but not by N-acetyltransferase 1.

In Chemical Information Profile for Alkylaniline NTP 2009 is reported also a general methabolism mechanism in rats for Arylamines: Arylamines are metabolized by ring oxidation,N-glucuronidation,N-acetylation, and N-oxidation; in the liver (of mammals) they are metabolized toN-hydroxyarylamines by monooxygenases (usually cytochrome P450) before binding to hemoglobin. Moreover the hemoglobin binding index in female rats is lower for 2-ethylaniline (5.1) if compared with aniline (22) or 3- and 4-ethylniline (12.7 and 5.8 respectively) (4) (Sabbioni,Environ Health Perspect, 102(Suppl. 6):61-67,1994).

Key value for chemical safety assessment

Additional information