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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1969
Report date:
1969

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:
Isobutyryl chloride
EC Number:
201-194-1
EC Name:
Isobutyryl chloride
Cas Number:
79-30-1
Molecular formula:
C4H7ClO
IUPAC Name:
2-methylpropanoyl chloride
Details on test material:
- Name of test material (as cited in study report): Isobuttersäurechlorid

Test animals

Species:
mouse
Sex:
male/female

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
water
Doses:
0.25, 0.64, 0.80, 1, 1.25, 1.6, 4, 32 mg/kg bw
No. of animals per sex per dose:
10
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of observations: 1 hour, 1 day, 2 days, 7 days and 14 days after injection.
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, gross pathology

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Effect level:
0.8 - 1 mg/kg bw
Based on:
test mat.
Mortality:
After 14 days:
0/20 deaths at 0.25 mg/kg bw
6/20 deaths at 0.64 mg/kg bw
4/20 deaths at 0.8 mg/kg bw
12/20 deaths at 1 mg/kg bw
16/20 deaths at 1.25 mg/kg bw
19/20 deaths at 1.67 mg/kg bw
20/20 deaths at 4 and 32 mg/kg bw
At the highest dose first deaths were observed 1 hour after administration. Over the entire dose range first deaths occurred after about 48 hours.
Clinical signs:
0.25-1.6 mg/kg bw:
directly after injection: tremble, convulsions and uncoordinated movements, extension and retardation of extremities during movement, heavy breathing, avoidance of abdominal position and fallen-in flanks. The following days: abdominal posture, apathy, closed eyes with stuck together eyelids, apnea and bristly fur. Surviving animals showed no symptoms after 3-11 days.

4 and 32 mg/kg bw:
directly after injection: jumping and stagger, heavily accelarated breathing. After about 10 minutes: abdominal position, bushy fur, closed eyes and apathy. Continuation of symptoms untill death in the following days.
Gross pathology:
Animals dying during the test: dark-blooded abdominal cavity, corosive lesions of gastrointestinal tract, slight abdominal adhesions, fatty liver (1 naimal) vessel-injected winding of small intestine.
Animals sacrificed after the observation period: adhesions in the liver area

Applicant's summary and conclusion