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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1977
Report date:
1977

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
Testing was performed before OECD guideline published.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
12-oxahexadecan-16-olide
EC Number:
229-755-6
EC Name:
12-oxahexadecan-16-olide
Cas Number:
6707-60-4
Molecular formula:
C15H28O3
IUPAC Name:
1,6-dioxacycloheptadecan-7-one
Test material form:
liquid
Specific details on test material used for the study:
name of testing material: 77-227 Hibiscolide

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
oral: unspecified

Results and discussion

Preliminary study:
Acute oral toxicity in rates
Effect levels
Key result
Sex:
not specified
Dose descriptor:
LD50
Effect level:
5 000 mg/kg bw
Based on:
test mat.
Mortality:
0

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
10 rats were used in the study. The animals were observed over a 14 day period for mortality and/or systemic effects. A gross necropsy was conducted on all animals.
The oral LD50 of 12-oxahexadecanolide in rats exceeded 5000 mg/kg with 0/10 deaths at that dose
Executive summary:

The oral LD50 of 12-oxahexadecanolide in rats exceeded 5000 mg/kg with 0/10 deaths at that dose.

Cevolide does not met the criteria for classication according the CLP Regulation (EC) No. 1272/2008.