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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

QSAR modelling of the components of the substance, monoethyl, diethyl and triethyl citrate do not indicate strtuctural elements leading to protein binding and potential sensitisation.

Data are available on one constituent of the substance, triethyl citrate. A guinea pig maximisation test found strong evidence of the potential for sensitisation but a human repeat insult patch test found no evidence of sensitisation occurring in humans. The substance was judged to be a non-sensitiser based on the criteria established by the FDA for sensitisation of human subjects

Justification for classification or non-classification

Based on the available data the substance does not require to be classified and labelled according to Regulation 1272/2008/EC (CLP) or Directive 67/548/EEC (DSD).