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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Principles of method if other than guideline:
Organisation for Economic Co-operation and Development
(OECD), OECD Guidelines for Testing of Chemicals, Section 4,
Health Effects. No.423, "Acute Oral Toxicity - Acute Toxic
Class Method", 2001


European Community (EC), Council Directive 67/548/EEC, Annex
V, Part B, Methods for the Determination of Toxicity, as
last amended by Commission Directive 2004/73/EC, B.1 tris:
"Acute Toxicity (Oral) - Acute Toxic Class Method", 2004.


United States Environmental Protection Agency (EPA). Health
Effects Test Guidelines, OPPTS 870.1100, Acute Oral
Toxicity. Office of Prevention, Pesticides and Toxic
Substances (7101), EPA 712-C-98-190, 2002.


Japanese Ministry of Agriculture, Forestry and Fisheries
(JMAFF), 12 Nousan, Notification No 8147, November 2000,
including the most recent partial revisions.
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test animals

Species:
other: Rat, Wistar strain Crl:WI

Administration / exposure

Vehicle:
other: None (The test substance was heated up to maximum of 40°C prior to dosing)

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 429 mg/kg bw
Mortality:
Female: 2860 mg/kg bw; Number of animals: 3; Number of deaths: 3
Female: 429 mg/kg bw; Number of animals: 3; Number of deaths: 0
Clinical signs:
other: Signs of toxicity related to dose levels: One female was found dead on Day 1 and two animals were sacrificed for ethical reasons on Day 2. No further mortality occurred. 2860 mg/kg bw: Lethargy, flat or hunched posture, uncoordinated movements, l
Gross pathology:
Effects on organs:
No abnormalities were found at macroscopic post mortem
examination of the animals.

Applicant's summary and conclusion

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