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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Type of information:
other: Expert Statement
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: Expert Statement, no study available
Principles of method if other than guideline:
Expert statement
GLP compliance:
no

Description of key information

Based on physico-chemical properties, oral absorption and distribution through-out the body is expected. Dermal absorption is low due to hydrophilic properties of the substance.These assumptions are further supported by the results of the oral acute toxicity study was well as the skin sensitisation study, revealing some effects.Absorption via the inhalation route is, due to physico-chemical properties of the test item, not expected. Bioaccumulation of the substance is not expected after continuous exposure. The test substance is expected to be excreted unchanged via urine and to a lower extent via faeces.

For further inforamtion see toxicokinetik statement attachted.

Key value for chemical safety assessment

Bioaccumulation potential:
no bioaccumulation potential

Additional information