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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Comparable to guideline study, predates GLP, available as unpublished report, minor limitations in reporting but otherwise adequate for assessment.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1968

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Methyloxirane
EC Number:
200-879-2
EC Name:
Methyloxirane
Cas Number:
75-56-9
Molecular formula:
C3H6O
IUPAC Name:
2-methyloxirane
Details on test material:
No data

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Carworth Farm E , Manor Farm
- Age at study initiation: 12 weeks
- Weight at study initiation: 150-250 gram
- Fasting period before study: 4 pm- 10am
- Housing: 5 per cage
- Diet : ad libitum after dosing
- Water : ad libitum
- Acclimation period:14 days


ENVIRONMENTAL CONDITIONS
recorded but reported


Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Details on oral exposure:
all liquids were given undiluted by intubation in single doses on a ml/kg basis.
Doses:
in ml/kg not specified; only reported as LD50
No. of animals per sex per dose:
5
Control animals:
not specified
Statistics:
By probit analysis. and by use of Weil's tables of moving averages.

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
382 - 587 mg/kg bw
Mortality:
no data
Clinical signs:
other: no data
Gross pathology:
no data

Any other information on results incl. tables

No details on findings were reported, except the LD 50 values.

Applicant's summary and conclusion