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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

Currently viewing:

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 B.1 tris.
GLP compliance:
yes
Test type:
standard acute method
Limit test:
yes

Test animals

Species:
other: Rat,(Wistar)

Administration / exposure

Vehicle:
propylene glycol

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 200 mg/kg bw
Mortality:
Male: 200 mg/kg bw; Number of animals: 3; Number of deaths: 0
Female: 200 mg/kg bw; Number of animals: 3; Number of deaths: 0
Female: 2000 mg/kg bw; Number of animals: 3; Number of deaths: 3
Clinical signs:
Signs of toxicity related to dose levels:
No mortality occurred among males and females treated 200
mg/kg body weight. All females dosed at 2000 mg/kg were
found dead within 40 minutes post-treatment.


Lethargy was noted in all males dosed at 200 mg/kg on day 1
only. No clinical signs were noted among the females.
Gross pathology:
Effects on organs:
Macroscopic examination of the animals treated at 200 mg/kg
body weight at termination did not reveal any abnormalities.
Gray-white discolouration of the glandular mucosa in the
stomach was found in all females dosed at 2000 mg/kg at
macroscopic post mortem examination.

Applicant's summary and conclusion

Interpretation of results:
harmful
Remarks:
Migrated information Criteria used for interpretation of results: EU