Registration Dossier

Administrative data

Link to relevant study record(s)

Reference
Endpoint:
basic toxicokinetics, other
Type of information:
other: expert statement
Adequacy of study:
key study
Study period:
2021
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment
Objective of study:
toxicokinetics
Qualifier:
according to guideline
Guideline:
other: according to ECHA Guidance R.7c, June 2017, v.3
Type:
absorption
Results:
estimated for risk assessement purposes: oral 50%; dermal 50%; inhalation 50%
Conclusions:
Based on the available data and according to a qualitative assessment according to ECHA Guidance R.7c, June 2017, v.3, the substance has not a bioaccumulation potential.

Description of key information

The toxicokinetics of the substance CAS 68877 / EC 272-559-0 has been assessed based on the physicochemical properties and available toxicological data and following the ECHA Guidance R.7c from June 2017 (version 3.0).

Key value for chemical safety assessment

Bioaccumulation potential:
no bioaccumulation potential
Absorption rate - oral (%):
50
Absorption rate - dermal (%):
50
Absorption rate - inhalation (%):
50

Additional information