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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
acute toxicity: other routes
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Non-GLP non-guideline, available as unpublished report, restrictions in design and/or reporting.

Data source

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

Materials and methods

Principles of method if other than guideline:
Five Kisslegg mice per sex per dose were exposed to 33.25, 66.5, 133, 266 and 2128 mg/kg bw of the test substance by intraperitoneal injection followed by a 14 day observation period . Besides mortality, clinical sings and bodyweights were recorded. In addition necropsy was performed on all animals.
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
3-chloropropionyl chloride
EC Number:
210-890-4
EC Name:
3-chloropropionyl chloride
Cas Number:
625-36-5
Molecular formula:
C3H4Cl2O
IUPAC Name:
3-chloropropanoyl chloride
Details on test material:
- Name of test material (as cited in study report): beta-Chlorpropionylchlorid

Test animals

Species:
mouse
Strain:
other: Kisslegg
Sex:
male/female

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
other: water and Traganth
Details on exposure:
- Test concentrations used were 0.5, 1, 2 and 20 % (G/V).
- Application volume: 5 mL/kg
Doses:
25, 50, 100, 200, 1600 cmm/kg (33.25, 66.5, 133, 266 and 2128 mg/kg bw with a relative density of 1.33)
No. of animals per sex per dose:
5
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
ca. 42.56 mg/kg bw
Based on:
test mat.
Remarks on result:
other: Original value is 32 ccm/kg
Mortality:
- 33.25 mg/kg bw: 1/10 animals died within 48 hour. 3/10 animals after 7 days and 4/10 at the end of the observation period.
- 66.5 mg/kg bw: 8/10 animals were dead after 7 days. No additional mortality occurred.
- 133 mg/kg bw: 2/10 animals died within 48 hour. 8/10 animals after 7 days and 9/10 at the end of the observation period.
- 266 mg/kg bw: 8/10 animals were dead within 24 hours. Within 7 days all animals were dead
- 2128 mg/kg bw : Within 1 hour 3/10 were dead. After 24 hours after exposure all animals were dead.
Clinical signs:
- 2128 mg/kg bw : Immediately lying in the prone position, forced breathing, slight apathy, closed eyes.
- 266 mg/kg bw: Immediately trembling, twitching and staggering, forced breathing, long legged gait. The next days intermittent breathing, apathy and lying in the prone position.
- 133 mg/kg bw: Immediately accelerated breathing, trembling, stretching, and long legged gait. In the next days lying in the prone position, intermittent breathing, ruffled fur, sticky eyes. The one surviving animals showed no clinical signs after 9 days.
- 66.5 mg/kg bw: Immediately long legged gait, forced breathing, closed eyes. The next days ruffled fur was observed. Lying in the prone position after 7 days. After 8 days no clinical signs observed.
- 33.25 mg/kg bw: Immediately forced breathing, delayed movement of the hind limbs, eyes semi-closed. The next three days accelerated breathing and ruffled fur. After 6 days no clinical signs observed.
Body weight:
No data
Gross pathology:
Adhesions in the abdominal cavity.

Applicant's summary and conclusion