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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data
Justification for type of information:
Data from secondary source

Data source

Reference
Reference Type:
other: authoritative database
Title:
Acute oral toxicity study of test chemical was performed in rats.
Author:
U.S. National Library of Medicine
Year:
2017
Bibliographic source:
ChemIDplusA TOXNET Database

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
other: As mentioned below
Principles of method if other than guideline:
Acute oral toxicity study of test chemical was performed in rats
GLP compliance:
not specified
Test type:
other: not specified
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
(Z)-9-Octadecen-1-ol ethoxylated
EC Number:
500-016-2
EC Name:
(Z)-9-Octadecen-1-ol ethoxylated
Cas Number:
9004-98-2
Molecular formula:
C58H116O21
IUPAC Name:
9-Octadecen-1-ol, monoether with polyethylene glycol, (Z)-
Details on test material:
- Name of test material (IUPAC name): 9-Octadecen-1-ol, monoether with polyethylene glycol, (Z)-
- Common name: Polyoxyl 10 oleyl ether
- Molecular formula: C58H116O21
- Molecular weight: 312.534 g/mol
- Smiles notation: C(CCCCCCCOCCO)\C=C/CCCCCCCC
- Substance type: Organic

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
No data available

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
not specified
Details on oral exposure:
No data available
Doses:
2700 mg/kg bw
No. of animals per sex per dose:
No data available
Control animals:
not specified
Details on study design:
No data available
Statistics:
No data available

Results and discussion

Preliminary study:
No data available
Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
2 700 mg/kg bw
Based on:
test mat.
Remarks on result:
other: 50% mortality was observed
Mortality:
50% mortality was observed at dose 2700 mg/kg bw
Clinical signs:
other: No data available
Gross pathology:
No data available
Other findings:
No data available

Applicant's summary and conclusion

Interpretation of results:
other: Not classified
Conclusions:
the LD50 value was considered to be 2700mg/kg bw,When rats were treated with test chemical orally.
Executive summary:

In acute oral toxicity study, rats were treated with test chemical orally.50% mortality was observed in treated rats at 2700mg/kg bw.Therefore, LD50 was considered to be 2700mg/kg bw,when rats were treated with test chemical orally.