Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1975
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: non-GLP Study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1975
Report date:
1975

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Principles of method if other than guideline:
Study performed before 1987.
GLP compliance:
not specified
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
3-chlorobutan-2-one
EC Number:
223-834-9
EC Name:
3-chlorobutan-2-one
Cas Number:
4091-39-8
Molecular formula:
C4H7ClO
IUPAC Name:
3-chlorobutan-2-one
Constituent 2
Reference substance name:
3-Chloro-2-butanone
IUPAC Name:
3-Chloro-2-butanone
Test material form:
other: coluorless liquid
Details on test material:
no info about substance purity in study report

Test animals

Species:
rat
Strain:
Wistar
Sex:
male
Details on test animals or test system and environmental conditions:
60 male Wistar rats bred at the institute were used for testing.
Bodyweight 205 +/- 14 g.
Animals were kept 16 hours before substance administration
without feed (drinking water ad libitum).

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Remarks:
3% (v/v)
Details on oral exposure:
3-Chloro-2-butanone was applicated in a 3% (volume/volume) aqueous solution.
1 drop of Tween 40 was added per 100 mL solution. Oral (gavage) administration.

Doses:
Six dose groups: 0.900; 0.818; 0.744; 0.676; 0.615; 0.554 mL/kg
No. of animals per sex per dose:
10 animals (male) per dose (six dose groups)
Control animals:
not specified
Details on study design:
Mortality was monitored 24 hours and 14 days after substance application.
Statistics:
no data

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
ca. 0.615 mL/kg bw
Based on:
test mat.
Mortality:
9/10; 6/10; 6/10; 6/10; 5/10; 1/10 (after 1 day)
9/10; 6/10; 6/10; 6/10; 5/10; 1/10 (after 14 day)
Clinical signs:
Clinical symptoms were observed - at all dose groups - 1-2 minutes after substance administration..
Symptoms were a lateral position, paralysis of skeletal muscles.
Laboured breathing occured dose depended; combined with pronounced abdominal breathing.

Body weight:
no data
Gross pathology:
no data
Other findings:
Mortality occured during the first day; the first animals died 4 hours after substance administration.
The animals surviving 14 days showed a reduced food and water consumption, course and
untended fur, curved back and reduced mobility.

Applicant's summary and conclusion

Interpretation of results:
Category 4 based on GHS criteria
Remarks:
Migrated information
Conclusions:
Classification as Toxicity Category IV.
Executive summary:

The LD50 dose after a single oral administration of 3-chloro-2-butanone

in male Wistar rats was found to be 0.615 mL/kg bw (14 days).