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Diss Factsheets

Administrative data

Key value for chemical safety assessment

Effects on fertility

Link to relevant study records
Reference
Endpoint:
toxicity to reproduction
Remarks:
other: fertility
Type of information:
migrated information: read-across based on grouping of substances (category approach)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Guideline:
other: read across (grouping according to proteinbinding by OASIS)
GLP compliance:
not specified
Species:
rat
Sex:
male/female
Route of administration:
oral: unspecified
Duration of treatment / exposure:
45d
Dose descriptor:
LOEL
Effect level:
5.26 mg/kg bw/day (nominal)
Based on:
test mat.
Sex:
male/female
Reproductive effects observed:
not specified
Effect on fertility: via oral route
Endpoint conclusion:
adverse effect observed
Dose descriptor:
LOAEL
5.26 mg/kg bw/day
Study duration:
subchronic
Species:
rat
Effect on fertility: via inhalation route
Endpoint conclusion:
no study available
Effect on fertility: via dermal route
Endpoint conclusion:
no study available
Additional information

The results for fertility toxicity in an OECD Toolbox study was LOEL (rat,oral, 45d) 5.26 mg/kg bw/day

The results for developmental tox/teratogenecity in an OECD Toolbox study was LOEL (rat,oral, 45d) 21.9 mg/kg bw/day

Effects on developmental toxicity

Link to relevant study records
Reference
Endpoint:
developmental toxicity
Type of information:
migrated information: read-across based on grouping of substances (category approach)
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Guideline:
other: read across (grouping according to proteinbinding by OASIS)
GLP compliance:
not specified
Species:
rat
Route of administration:
oral: unspecified
Duration of test:
45d
Dose descriptor:
LOEL
Effect level:
21.9 mg/kg bw/day (nominal)
Based on:
test mat.
Basis for effect level:
other: developmental toxicity
Abnormalities:
not specified
Developmental effects observed:
not specified
Effect on developmental toxicity: via oral route
Endpoint conclusion:
adverse effect observed
Dose descriptor:
LOAEL
21.9 mg/kg bw/day
Study duration:
subchronic
Species:
rat
Effect on developmental toxicity: via inhalation route
Endpoint conclusion:
no study available
Effect on developmental toxicity: via dermal route
Endpoint conclusion:
no study available

Justification for classification or non-classification

Data lacking

Additional information