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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
September to October 1996
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1996
Report date:
1996

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
Version / remarks:
1981
GLP compliance:
yes
Test type:
acute toxic class method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
17-Hydroxy-1,4,6-pregnatriene-3,20-dione
EC Number:
613-906-1
Cas Number:
66212-25-7
Molecular formula:
C21 H26 O3
IUPAC Name:
17-Hydroxy-1,4,6-pregnatriene-3,20-dione

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Doses:
2000 mg/kg (application volume 10 mL/kg)
No. of animals per sex per dose:
3
Control animals:
no

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

No animal died in the course of the study. Moreover, no clinical signs, no effects on body weight and body weight gain and no abnormalities at necropsy were observed.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The test item is of low oral toxicity.
Executive summary:

The single oral administration of the test substance (ZK 5668) to male and female rats at a dose of 2000 mg/kg was tolerated without any mortality. No compound-related clinical signs and effects on body weight were observed and there were no macroscopic pathological signs.

The acute oral toxicity of 1,4,6 -Trienol in rats is therefore above 2000 mg/kg body weight.