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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Only short abstract available. In the publication less than basic data is given.
Cross-reference
Reason / purpose for cross-reference:
reference to same study

Data source

Reference
Reference Type:
publication
Title:
THE PLACE OF THE RANGE FINDING TEST IN THE INDUSTRIAL TOXICOLOGY LABORATORY
Author:
Smyth, H. F. Jr. and Carpenter, C. P.
Year:
1944
Bibliographic source:
Journal of Industrial Hygiene and Toxicology 26:269 - 273

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Rats were given a single dose by gavage of different concentrations of hexanoic acid until two dosages differing by a multiple of ten are identified with one concentration killing some or all animals and the other one killing no or some animals. Then the LD50 value was estimated graphically.
GLP compliance:
no
Test type:
other: "range-finding" oral toxicity study
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Hexanoic acid
EC Number:
205-550-7
EC Name:
Hexanoic acid
Cas Number:
142-62-1
Molecular formula:
C6H12O2
IUPAC Name:
hexanoic acid

Test animals

Species:
rat
Strain:
other: albino Wistar
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight rats: 90 - 120 g

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
water
Doses:
The applied doses differed by a multiple of ten; not further specified.
No. of animals per sex per dose:
6 males per dose
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 14 days

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
3 000 mg/kg bw
Based on:
test mat.
Remarks on result:
other: estimated value

Applicant's summary and conclusion