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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Study period:
1981
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: well documented study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1981
Report date:
1981

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
5 mice per sex and dose are injected i.p. with different doses of the test substance. Clinical signs and lethality are evaluated during a 14 day observation period and the LD50 is determined. Surviving animals are necropsied and gross changes recorded.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2,4,6-trimethylbenzoyl chloride
EC Number:
213-339-6
EC Name:
2,4,6-trimethylbenzoyl chloride
Cas Number:
938-18-1
Molecular formula:
C10H11ClO
IUPAC Name:
2,4,6-trimethylbenzoyl chloride
Details on test material:
- Name of test material (as cited in study report): 2.4.6-trimethylbenzoylchlorid
- Physical state: liquid
- Analytical purity: no data

Test animals

Species:
mouse
Strain:
NMRI
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Herilan, H.Eggersmann KG
- Age at study initiation: no data
- Weight at study initiation: 22-28g
- Fasting period before study: 15-20h
- Acclimation period: no data

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
olive oil
Doses:
200mg/kg
700mg/kg
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: 15min, 30min, 1h, 2h, 5h after injection, daily thereafter. Weighing performed on days 2-4, 7, 13
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 200 - < 700 mg/kg bw
Based on:
test mat.
Mortality:
all animals in the high dose died within7days, all animals in the low dose survived
Clinical signs:
Dypnoe, apathy, bad general state in both groups
tremor, jerks, spastic gait, stretching, piloerection in the high dose
Body weight:
high dose: decrease in males, slight gain in females (until death on days 2-4)
low dose: decrease until day four, recovery to initial weight until day 14
Gross pathology:
dead animals: substance deposits in the peritoneum
necropsied survivors: no findings

Applicant's summary and conclusion

Conclusions:
The LD50 in mice after i.p. injection of the test substance was found to be greater than 200mg/kg, but lower than 700mg/kg.