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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Endpoint conclusion:
no study available
Effect on fertility: via inhalation route
Endpoint conclusion:
no study available
Effect on fertility: via dermal route
Endpoint conclusion:
no study available
Additional information

Dangerous Substance Directive (67/548/EEC)

The substance does not need to be classified and labelled for reproductive toxicity under Directive 67/548/EEC, as amended for the 31st time in Directive 2009/2/EC.

 

Classification, Labelling, and Packaging Regulation (EC) No 1272/2008

The substance does not need to be classified and labelled for reproductive toxicity under Regulation (EC) No 1272/2008, as amended for the sixth time in Regulation EC No 605/2014.


Short description of key information:
No experimental study is available. The test substance is intended for use in an industrial setting only, and thus oral uptake is not an anticipated route of exposure. Upon hydrolysis of the test substance, boron trifluoride and acetonitrile are formed among other dissociation products. The test substance itself and its direct hydrolysis products are highly corrosive and would lead to severe parental toxicity well before internal doses of the hydrolysis products are reached that could potentially cause effects on fertility or development. This would also result in unwarranted distress for the animals. Therefore, any reproductive study with the test substance is scientifically unjustified. Due to the corrosive properties of the substance, suitable risk management measures for dermal and inhalative exposure need to be taken (gloves, respiratory protection). Relevant human exposure via oral, dermal and inhalative uptake can be excluded, which justifies waiving of developmental toxicity and teratogenicity testing according to annex XI, section 3 of Regulation (EC) 1907/2006 (REACH).

Justification for classification or non-classification

Dangerous Substance Directive (67/548/EEC)

The substance does not need to be classified and labelled for reproductive toxicity under Directive 67/548/EEC, as amended for the 31st time in Directive 2009/2/EC.

 

Classification, Labelling, and Packaging Regulation (EC) No 1272/2008

The substance does not need to be classified and labelled for reproductive toxicity under Regulation (EC) No 1272/2008, as amended for the sixth time in Regulation EC No 605/2014.

Additional information