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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: other routes
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
1979 - 1980
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable, well documented report which meets basic scientific principles.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1980
Report date:
1980

Materials and methods

Principles of method if other than guideline:
other: BASF-Test
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2,2-dimethyloxirane
EC Number:
209-193-8
EC Name:
2,2-dimethyloxirane
Cas Number:
558-30-5
Molecular formula:
C4H8O
IUPAC Name:
2,2-dimethyloxirane
Details on test material:
- Name of test material: iso Butylenoxid
- Lot/batch No.: 78/874 (Substance-No.)
- Other: Test substance: as prescribed by 1.1 - 1.4

Test animals

Species:
mouse
Strain:
NMRI
Sex:
male/female

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
CMC (carboxymethyl cellulose)
Details on exposure:
2-20% emulsion in aqueous 0.5 % carboxymethyl cellulose
Doses:
200, 700, 2000 mg/kg bw
No. of animals per sex per dose:
5 animals
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of observations: several times on the day of application and daily thereafter
- Necropsy of survivors performed: yes

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 700 - < 2 000 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

After application of 200 and 700 mg/kg bw 0/5 animals died.

After application of 2000 mg/kg bw 5/5 animals died after 1 hour.

Applicant's summary and conclusion

Executive summary:

In an acute intraperitoneal toxicity study according to an internal BASF method (BASF AG, 1980), animals were given a single dose of 2,2-dimethyloxirane i.p. (2, 7 and 20 % emulsion in aqueous 0.5 % carboxymethyl cellulose) at 200, 700 and 2000 mg/kg bw. Mice were then observed for mortality and for clinical symptoms of toxicity for 14 days. All animals were subjected to necropsy. The LD50 was estimated as >700 and < 2000 mg/kg bw. This acute intraperitoneal study is classified as acceptable.