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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Key value for chemical safety assessment

Effects on fertility

Description of key information

In the key combined repeated dose with the reproduction/developmental toxicity screening test in rats (OECD 422), there were no effects of the test item on fertility; therefore, a No Observed Adverse Effect Level (NOAEL) for the test item was 1000 mg/kg bw/day (top dose).

Effect on fertility: via oral route
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
NOAEL
1 000 mg/kg bw/day
Study duration:
subacute
Species:
rat
Quality of whole database:
The key study was a good quality study, conducted using OECD Guideline 422 and complies with GLP and was therefore assigned 1 (reliable without restrictions).
Effect on fertility: via inhalation route
Endpoint conclusion:
no study available
Effect on fertility: via dermal route
Endpoint conclusion:
no study available
Additional information

In a key combined repeated dose with the reproduction/developmental toxicity screening test in rats with the test item, no toxicologically-relevant parental reproductive effects were observed. All findings recorded were within the range of normal background alterations.

Effects on developmental toxicity

Description of key information

In the key combined repeated dose with the reproduction/developmental toxicity screening test in rats (OECD 422), there were no effects of the test item on pup development; therefore, a No Observed Adverse Effect Level (NOAEL) for the test item was 1000 mg/kg bw/day (top dose).

Effect on developmental toxicity: via oral route
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
NOAEL
1 000 mg/kg bw/day
Study duration:
subacute
Species:
rat
Quality of whole database:
The key study was a good quality study, conducted using OECD Guideline 422 and complies with GLP and was therefore assigned 1 (reliable without restrictions).
Effect on developmental toxicity: via inhalation route
Endpoint conclusion:
no study available
Effect on developmental toxicity: via dermal route
Endpoint conclusion:
no study available
Additional information

In a key combined repeated dose with the reproduction/developmental toxicity screening test in rats with the test item, no toxicologically-relevant developmental effects were observed. All findings recorded were within the range of normal background alterations.

Justification for classification or non-classification

Based on the results of a Combined Repeated Dose Toxicity Study with the Reproduction/Developmental Toxicity Screening Test in rats, the test substance does not requite classification for reproductive toxicity according to CLP (Regulation EC No 1272/2008).

Additional information