Registration Dossier

Administrative data

Endpoint:
basic toxicokinetics, other
Type of information:
other: expert judgement
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Data derived from expert Judgement
Justification for type of information:
There is no specific requirement to generate toxicokinetic information in the REACH Regulation (EC 1907/2006). As reported in the Annex VIII, it is required to perform an assessment of the toxicokinetic behaviour of the substance to the extent that can be derived from the relevant available information.

Data source

Reference
Reference Type:
other: Assessment
Title:
Unnamed
Year:
2017

Materials and methods

Objective of study:
other: Assessment
Principles of method if other than guideline:
Assessment
GLP compliance:
no

Test material

Reference
Name:
Unnamed
Type:
Constituent
Test material form:
solid: particulate/powder

Results and discussion

Metabolite characterisation studies

Metabolites identified:
not measured
Remarks:
evaluation based on assessment

Applicant's summary and conclusion

Conclusions:
No bioaccumulation potential.