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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
experimental study
Adequacy of study:
other information
Reliability:
3 (not reliable)
Rationale for reliability incl. deficiencies:
other: No enough details. Documentation is insufficient for assessment.

Data source

Reference
Reference Type:
publication
Title:
Short-term toxicity tests on the mono and di methyl ethers of hydroquinone
Author:
Hodge HC, Sterner JH, Maynard EA, Thomas J.
Year:
1949
Bibliographic source:
J. Ind. Hyg. Toxicol. 31, 79-92.

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
acute toxicity by i.p. route
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
1,4-dimethoxybenzene
EC Number:
205-771-9
EC Name:
1,4-dimethoxybenzene
Cas Number:
150-78-7
Molecular formula:
C8H10O2
IUPAC Name:
1,4-dimethoxybenzene
Details on test material:
no data

Test animals

Species:
mouse
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Route of administration:
intraperitoneal
Vehicle:
not specified
Details on exposure:
- Doses / concentrations:
Groups of 10 to 22 mice were given doses of paradimethoxybenzene ranging from 30 to 80 mg per animal, as follow:
- 10 animals in group treated with 30 mg (average body weight was 29 gm). Dose: 1034 mg/kg
- 10 animals in group treated with 35 mg (average body weight was 29 gm). Dose: 1207 mg/kg
- 22 animals in group treated with 40 mg (average body weight was 27 gm). Dose: 1481 mg/kg
- 20 animals in group treated with 50 mg (average body weight was 27 gm). Dose: 1852 mg/kg
- 10 animals in group treated with 60 mg (average body weight was 25 gm). Dose: 2400 mg/kg
- 10 animals in group treated with 70 mg (average body weight was 27 gm). Dose: 2592 mg/kg
- 12 animals in group treated with 80 mg (average body weight was 25 gm). Dose: 3200 mg/kg
Doses:
30; 35; 40; 50; 60; 70; 80 mg/animal corresponding to 1034; 1207; 1481; 1852; 2400; 2592; 3200 mg/kg bw.
No. of animals per sex per dose:
10 to 22 animals per dose group, sex unspecified
Control animals:
not specified
Details on study design:
no data
Statistics:
no data

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
1 100 mg/kg bw
Mortality:
The 30 mg dose killed 30%,
the 35 mg dose killed 70%,
the 40 mg dose killed 73%,
the 50 and 60 mg dose killed 80%,
the 70 and 80 mg dose killed 100% of the treated animals.
Clinical signs:
Mice given paradimethoxybenzene intraperitoneally developed a wobbly gait immediately following injection. This was followed in a few minutes by paralysis of the hind quarters, accompanied by spasms perhaps of anoxial origin. At the higher doses, mice appeared to be in a narcosis about 15 minutes after injection. Some mice still exhibited degrees of anesthesia as long as 18 hours after injection.
Body weight:
no data
Gross pathology:
no data
Other findings:
no data

Applicant's summary and conclusion