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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

Key value for chemical safety assessment

Repeated dose toxicity: via oral route - systemic effects

Endpoint conclusion
Dose descriptor:
NOAEL
500 mg/kg bw/day
Study duration:
subchronic
Species:
rat

Repeated dose toxicity: inhalation - systemic effects

Endpoint conclusion
Endpoint conclusion:
no study available

Repeated dose toxicity: inhalation - local effects

Endpoint conclusion
Endpoint conclusion:
no study available

Repeated dose toxicity: dermal - systemic effects

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
NOAEL
5 000 mg/kg bw/day
Study duration:
subchronic
Species:
rat

Repeated dose toxicity: dermal - local effects

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Additional information

No repeat dose toxicity information by the inhalation route is available. Because of the very low volatility of this substance and the low toxicity demonstrated by other routes, it can be concluded that toxicity by the inhalation route is not of concern.

Based on observations from other members of this category, it can be concluded that the data from TEGME is a good conservative surrogate to predict the properties of this substance and that it will have low repeat dose toxicity by all routes of exposure.  NOAELs can be predicted from TEGME after taking into account molecular weight differences.

Justification for classification or non-classification

No adverse effects are seen below the thresholds for classification. The data available is sufficiently robust to meet this classification purpose and to derive a reliable NOAEL.