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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Link to relevant study record(s)

Reference
Endpoint:
hydrolysis
Type of information:
(Q)SAR
Adequacy of study:
key study
Study period:
2017
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
results derived from a valid (Q)SAR model and falling into its applicability domain, with adequate and reliable documentation / justification
Justification for type of information:
The substance falls within the applicability domain of the selected (Q)SAR method.
Qualifier:
according to guideline
Guideline:
other: OECD Toolbox v 3.4
GLP compliance:
no
Preliminary study:
Not applicable
Transformation products:
no
Key result
Remarks on result:
other: Hydrolytically stable based on OECD Toolbox modeling
Details on results:
Under the study conditions, no hydrolysis was predicted in basic, neutral and acidic conditions
Validity criteria fulfilled:
not applicable
Conclusions:
Under the study conditions, no hydrolysis was predicted in basic, neutral and acidic conditions.
Executive summary:

A study was conducted to determine the hydrolysis of the test substance by modelling using the OECD Toolbox (v 3.4). Under the study conditions, no hydrolysis was predicted in basic, neutral and acidic conditions (OECD Toolbox, 2017).

Description of key information

Key value for chemical safety assessment

Additional information

A study was conducted to determine the hydrolysis of the test substance by modelling using the OECD Toolbox (v 3.4). Under the study conditions, no hydrolysis was predicted in basic, neutral and acidic conditions (OECD Toolbox, 2017).