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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
migrated information: read-across based on grouping of substances (category approach)
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Basic data given

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Range-finding toxicity data: List IV
Author:
Smyth, H.F., Jr. et al.
Year:
1951
Bibliographic source:
Arch Ind Hyg Occup Med 4 (2): 119-122
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:
as cited in: Journal of industrial hygiene and toxicology 26 (8): 269-273

Materials and methods

Principles of method if other than guideline:
Rabbits are epidermally treated with the undiluted test substance for 4 days.
GLP compliance:
no
Test type:
standard acute method

Test material

Constituent 1
Reference substance name:
Dibutyl adipate
EC Number:
203-350-4
EC Name:
Dibutyl adipate
Cas Number:
105-99-7
IUPAC Name:
dibutyl adipate
Details on test material:
- Name of test material (as cited in study report): Dibutyl adipate
- Analytical purity: no data

Test animals

Species:
rabbit
Strain:
not specified
Sex:
not specified

Administration / exposure

Type of coverage:
occlusive
Vehicle:
unchanged (no vehicle)
Details on dermal exposure:
Undiluted test material was applied to the clipped skin of the rabbits trunk. The dose is retained under a flexible film of rubber, vinyl plastic or the like, selected to be impervious to the chemical.
Duration of exposure:
4 days
Doses:
no data
(several dosages differing by a multiple of 10)
No. of animals per sex per dose:
6 animals (overall)
Control animals:
not specified
Details on study design:
- Duration of observation period following administration: 14 days
no further information available

Results and discussion

Effect levelsopen allclose all
Sex:
not specified
Dose descriptor:
LD50
Effect level:
20 mL/kg bw
Based on:
test mat.
Remarks on result:
other: LD50 was determined graphically.
Sex:
not specified
Dose descriptor:
LD50
Effect level:
19 220 mg/kg bw
Based on:
test mat.
Remarks on result:
other: calculated based on a density of 0.96 g/mL

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
CLP: not classified
DSD: not classified