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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
weight of evidence
Study period:
No data
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Abstract only.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1971
Report date:
1971

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
The acute toxicity of the test substance was investigated in Wistar rats with an average weight of 150 g. The test substance was administered by oral gavage with 0.5 mL/100 g body weight, to a group of 10 rats (5 male and 5 female) followed by a 10 day observation period.
GLP compliance:
not specified
Test type:
other: No data
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
1,2,3,4,4a,7,8,8a-octahydro-2,4a,5,8a-tetramethyl-1-naphthyl formate
EC Number:
265-742-1
EC Name:
1,2,3,4,4a,7,8,8a-octahydro-2,4a,5,8a-tetramethyl-1-naphthyl formate
Cas Number:
65405-72-3
Molecular formula:
C15H24O2
IUPAC Name:
1,2,3,4,4a,7,8,8a-octahydro-2,4a,5,8a-tetramethyl-1-naphthyl formate
Test material form:
liquid

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: Average weight of 150 g

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
not specified
Doses:
0.5 mL/ 100 g body weight
No. of animals per sex per dose:
Five/sex/dose
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 10 days

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 5 other: g/kg body weight
Based on:
test mat.
Mortality:
There was no mortality during the study.
Clinical signs:
other: Relatively minor symptoms such as drowsiness, slight diarrhoea and slight piloerection. All toxic effects were resolved 24 hours after administration.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The LD50 of the test substance was > 5 g/kg body weight.
Executive summary:

Method

The acute toxicity of the test substance was investigated on Wistar rats with an average weight of 150g. The product was administered by stomach tube at 0.5mL/100g body weight, to a group of 10 rats (5 male and 5 female).

 

Results

Administration of a single dose of 0.5mL/100 g of bodyweight of the product produced no mortality during the10 days following the application of the substance.

Relatively minor symptoms such as drowsiness, accompanied with a slight diarrhea and low piloerection was demonstrated. Any toxic effects disappeared within 24 hours of applying the test substance.

The LD50 of the product is > 5 g/kg body weight (rat) and is therefore regarded as very low toxicity.