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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
basic toxicokinetics, other
Remarks:
Assessment of the toxicokinetic behaviour to the extent that can be derived from the relevant available information
Type of information:
other: summary of available information
Adequacy of study:
key study
Study period:
Feb. 2020
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
test procedure in accordance with generally accepted scientific standards and described in sufficient detail
Objective of study:
absorption
distribution
excretion
metabolism
Qualifier:
no guideline available
Principles of method if other than guideline:
Assessment of the toxicokinetic behaviour of the substance to the extent that can be derived from the relevant available information - according to REACH, Annex VIII, 8.8.1 column 1
GLP compliance:
no
Specific details on test material used for the study:
structural information for the substance used for this assessment
Metabolites identified:
no

see section overall remarks, attachments

Description of key information

toxicokinetic of the substance is assessed based on physicochemical information.

No other information available

Key value for chemical safety assessment

Bioaccumulation potential:
low bioaccumulation potential
Absorption rate - oral (%):
100
Absorption rate - dermal (%):
10
Absorption rate - inhalation (%):
10

Additional information