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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: other routes

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Administrative data

Endpoint:
acute toxicity: other routes
Type of information:
migrated information: read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
supporting study
Study period:
1979-01-17 to 1979-02-13
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
test procedure in accordance with generally accepted scientific standards and described in sufficient detail

Data source

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

Materials and methods

Test guideline
Qualifier:
no guideline followed
GLP compliance:
no
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
3-chloro-4-fluoroaniline
EC Number:
206-682-8
EC Name:
3-chloro-4-fluoroaniline
Cas Number:
367-21-5
Molecular formula:
C6H5ClFN
IUPAC Name:
3-chloro-4-fluoroaniline

Test animals

Species:
mouse
Strain:
NMRI
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation (mean): Male: 20-22 g; Female: 20-28 g
- Fasting period before study: 15-20 hours before application
- Diet: From Herilan MRH-Haltung; H. Eggersmann KG


Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
CMC (carboxymethyl cellulose)
Remarks:
0.5 % aqu. solution
Details on exposure:
Applied volume: 10 mL/kg bw
Doses:
700, 200 mg/kg bw
No. of animals per sex per dose:
5
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of observations and weighing: Daily
- Necropsy of survivors performed: Yes
- Examinations performed: Clinical signs, body weight

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
ca. 700 mg/kg bw
Based on:
test mat.
Mortality:
Male:
700 mg/kg bw: 3 animals
200 mg/kg bw: 0 animals


Female:
700 mg/kg bw: 1 animal
200 mg/kg bw: 0 animals

Clinical signs:
At 700 mg/kg bw:
Dyspnoea, apathy, stagger, tremble, spastic gait, balance disturbance, clonic cramp, cyanosis etc.

At 200 mg/kg bw
Dyspnoea, agitation, stagger, cyanosis

Body weight:
No effects reported
Gross pathology:
No intra-abdominal substance precipitation or adhesion.

Applicant's summary and conclusion