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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Effects on fertility

Effect on fertility: via oral route
Dose descriptor:
NOAEL
1 000 mg/kg bw/day
Additional information

This is the only reproductive toxicity study available for this substance.


Short description of key information:
In a rat oral one-generation reproductive toxicity study conducted to OECD 415 and to GLP (Safepharm Laboratories Ltd., 1992) the NOAEL for parental general toxicity and for reproductive toxicity for triethoxyisobutylsilane was at least 1000 mg/kg bw/day, as no adverse effects were observed at any dose.

Effects on developmental toxicity

Description of key information
In an oral developmental toxicity study conducted to OECD 414 and to GLP (Safepharm Laboratories Ltd., 1991) there were no effects on rat foetal development and the NOAEL was therefore at least 1000 mg/kg bw/day (the highest dose tested). 
Effect on developmental toxicity: via oral route
Dose descriptor:
NOAEL
1 000 mg/kg bw/day
Additional information

In addition to the key developmental study, no adverse effects on the landmarks of offspring development or on the offspring response to simple reflexological tests were observed in a one-generation reproductive toxicity study (Safepharm Laboratories Ltd., 1992).

Justification for classification or non-classification

Based on the available oral reproductive and developmental toxicity studies, triethoxyisobutylsilane is not classified for effects on fertility or development according to Regulation 1272/2008/EC.

Additional information