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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP study according EU/OECD guideline.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2001

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EU Method B.1 tris (Acute Oral Toxicity - Acute Toxic Class Method)
GLP compliance:
yes
Test type:
acute toxic class method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
3-methoxy-4-methyl-4,5-dihydro-1H-1,2,4-triazol-5-one
EC Number:
619-590-1
Cas Number:
135302-13-5
Molecular formula:
C4H7N3O2
IUPAC Name:
3-methoxy-4-methyl-4,5-dihydro-1H-1,2,4-triazol-5-one

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
other: Cremophor EL 2% (v/v)
Doses:
2000 mg/kg body weight (bw)
No. of animals per sex per dose:
three male rats, three female rats
Control animals:
no

Results and discussion

Effect levelsopen allclose all
Sex:
female
Dose descriptor:
LD50
Effect level:
> 2 500 mg/kg bw
Sex:
male
Dose descriptor:
LD50
Effect level:
> 2 500 mg/kg bw

Any other information on results incl. tables

A dose of 2,000 mg/kg body weight was tolerated by male and female rats without mortalities, clinical signs, effects on weight development and gross pathological findings.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Based on the present investigations, the test substance is therefore to be regarded as relatively non-toxic and not to be classified according to Guideline 79/831/EEC.