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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Currently viewing:

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
study well documented, meets generally accepted scientific principles, acceptable for assessment

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1971
Report date:
1971

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Animals were treated with a single dose and observed during 14 days.
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Isodecyl acrylate
EC Number:
215-542-5
EC Name:
Isodecyl acrylate
Cas Number:
1330-61-6
Molecular formula:
C13H24O2
IUPAC Name:
2-methyloctyl prop-2-enoate
Test material form:
other: liquid

Test animals

Species:
rat
Strain:
Wistar
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Source: Mellon Institute
- Age at study initiation: 3 - 4 weeks
- Weight at study initiation: 90 - 120 g
- Diet (e.g. ad libitum): Rockland diets
- Water (e.g. ad libitum): ad libitum

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Details on oral exposure:
undiluted substance
Doses:
20, 10 and 5 ml/kg
No. of animals per sex per dose:
5
Control animals:
no
Details on study design:
no
Statistics:
no

Results and discussion

Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
9 486 mg/kg bw
Remarks on result:
other: original data: 10.7 ml/kg
Remarks:
LD50 (mg/kg) = LD50 (ml/kg) x density x 1000 = 10.7 x 0.8866 x 1000 = 9486 mg/kg
Mortality:
20.0 ml/kg: 5/5 animals died on day 0, 1 ,1 ,3 and 5
10.0 ml/kg: 2/5 animals died on day 2 and 3
5.0 ml/kg: 0/5; all animals survived
Clinical signs:
other: Prostrate and heavy breathing within one hour; sluggish at 24 hours, slightly sluggish 5 min after dose.
Gross pathology:
Congestion throught thee lungs and the abdominal viscera in the victims; livers mottled.
Other findings:
no

Any other information on results incl. tables

Dosage; ml/kg

Dead / Dosed

Days to Death

Weight Change

Signs and/or Sympthoms

20.0

5/5

0,1,1,3,5

-

Prostrate and heavy breathing within one hour; sluggish at 24 hours, slightly sluggish 5 min after dose.

10.0

2/5

2,3

67 to 73

5.0

0/5

-

68 to 91

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
Based on the results on this acute study, an oral LD50 of 9486 mg/kg was calculated in rats.
Executive summary:

In this study, rats were treated orally with isodecyl acrylate a single dose of 5, 10 or 20 ml/kg.

This study was conducted as a range-finding test according to the method described by Smyth HF Jr. and Carpenter CP (1948).

All animals treated with 20 ml/kg died in the 5 days after administration. Two animals died at the dose of 10 ml/kg on day 2 and 3.

A LD50 value of approx. 9486 mg/kg bw (10,7 ml/kg) was determined.