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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
1977
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
secondary literature

Data source

Referenceopen allclose all

Reference Type:
publication
Title:
Fragrance raw materials monographs Ethyl Undecylenate
Author:
Opdyke and Letizia
Year:
1982
Bibliographic source:
(1982) Food chem Toxicol. 20, p. 687
Reference Type:
secondary source
Title:
Unnamed
Year:
1977
Report date:
1977

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
The study was conducted in 1977 according to a protocol similar to OECD Guideline 401 (Acute Oral Toxicity), which was adopted in 1981.
GLP compliance:
not specified
Test type:
other: not specified
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Ethyl undec-10-enoate
EC Number:
211-734-8
EC Name:
Ethyl undec-10-enoate
Cas Number:
692-86-4
Molecular formula:
C13H24O2
IUPAC Name:
ethyl undec-10-enoate

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
not specified
Details on oral exposure:
not specified
Doses:
5000 mg/kg bw
No. of animals per sex per dose:
not specified
Control animals:
not specified
Details on study design:
not specified

Results and discussion

Effect levels
Key result
Sex:
not specified
Dose descriptor:
LD50
Remarks:
rat
Effect level:
> 5 000 mg/kg bw
Based on:
not specified

Applicant's summary and conclusion

Interpretation of results:
other: Data cannot be used for assignment due to limited documentation, but can be used as part of a weight of evidence approach.
Conclusions:
No indication for acute oral toxicity was reported.