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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Acute oral toxicity: LD50 = 8530 mg/kg bw

Acute dermal toxicity: LD50 >= 5000 mg/kg bw

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records
Reference
Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data
Qualifier:
no guideline available
Principles of method if other than guideline:
No more details available, database match.
GLP compliance:
not specified
Species:
rat
Route of administration:
oral: unspecified
Sex:
not specified
Dose descriptor:
LD50
Effect level:
8 530 mg/kg bw
Interpretation of results:
GHS criteria not met
Conclusions:
The oral median lethal dose (LD50) in the rat is reported as being 8530 mg/kg bw.
Executive summary:

The oral median lethal dose (LD50) in the rat is reported as being 8530 mg/kg bw.

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
LD50
Value:
8 530 mg/kg bw

Acute toxicity: via inhalation route

Endpoint conclusion
Endpoint conclusion:
no study available

Acute toxicity: via dermal route

Link to relevant study records
Reference
Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data
Qualifier:
no guideline available
Principles of method if other than guideline:
No more details available, database match.
GLP compliance:
not specified
Species:
rabbit
Sex:
not specified
Dose descriptor:
discriminating dose
Effect level:
>= 5 000 mg/kg bw
Interpretation of results:
GHS criteria not met
Conclusions:
Median lethal dose (LD50) in the rabbit following demal administration is reported to be in excess of 5000 mg/kg bw.
Executive summary:

Median lethal dose (LD50) in the rabbit following demal administration is reported to be in excess of 5000 mg/kg bw.

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed
Dose descriptor:
discriminating dose
Value:
5 000 mg/kg bw

Additional information

Justification for classification or non-classification

Based on the results of the available data the substance does not require to be classified and labelled according to Regulation 1272/2008/EC (CLP) or Directive 67/548/EEC (DSD).