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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
1969
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: experimental details lacking; however, followed accepted methodology at time of testing

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1969
Report date:
1969

Materials and methods

Test guideline
Qualifier:
no guideline available
Principles of method if other than guideline:
The test has been conducted prior to the current OECD guideline however, the LD50 calculation was based on an accepted method (Miller and Tainter).
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
(E)-4-decenal
EC Number:
265-741-6
EC Name:
(E)-4-decenal
Cas Number:
65405-70-1
Molecular formula:
C10H18O
IUPAC Name:
(E)-4-decenal
Test material form:
other: liquid
Details on test material:
Material: GIV 3-1094 (Decenal trans)

Test animals

Species:
rat
Strain:
not specified
Sex:
male
Details on test animals or test system and environmental conditions:
The animals were fasted 12 hours prior to dosing.

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Details on oral exposure:
Oral intubation
Doses:
100, 316, 1000, 3160, 5000 and 10000 mg/Kg
No. of animals per sex per dose:
6 groups of 6 animals (1 dose/animal)
Control animals:
no

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
> 7 000
Based on:
test mat.
Remarks on result:
other: as calculated by method of Miller and Tainter
Other findings:
principle toxic effect: Sedation

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Based on this test the LD50 was determined to be 7000 mg/kg bw.