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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
acute toxicity: oral
Adequacy of study:
other information

Data source

Reference
Reference Type:
other: Body responsible for the test
Title:
Unnamed

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: Annex V (B1 bis)
GLP compliance:
yes
Test type:
fixed dose procedure

Test animals

Species:
other: Rat (Wistar)

Administration / exposure

Vehicle:
other: Distilled water
No. of animals per sex per dose:
Preliminary sighting study: 2 (male)
Preliminary sighting study: 2 (female)
Main study: 5 (male)
Main study: 5 (female)

Results and discussion

Preliminary study:
Species/strain: Rat (Wistar)
mg/kg bw: Evident toxicity: ; Mortality:
Effect levelsopen allclose all
Sex:
male/female
Dose descriptor:
discriminating dose
Effect level:
50 mg/kg bw
Dose descriptor:
other: 50 mg/kg bw (fixed dose initial)
Remarks on result:
other: No. with evident toxicity: ; No. of deaths: ; No. of animals used:
Dose descriptor:
other: 50 mg/kg bw (fixed dose initial)
Remarks on result:
other: No. with evident toxicity: ; No. of deaths: 0; No. of animals used: 5
Clinical signs:
other: Signs of toxicity: In a preliminary study one male animal died 6 hours after dosing with 500 mg/kg. Clinical signs of toxicity observed in one male and one female were hunched posture, lethargy, pilo-erection, decreased respiratory rate ataxia and in
Gross pathology:
Effects on organs:
There were no pathological abnormalitites noted at necropsy
in the main study.

Applicant's summary and conclusion

Interpretation of results:
harmful
Remarks:
Migrated information