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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Description of key information

Key value for chemical safety assessment

Acute toxicity: via oral route

Link to relevant study records
Reference
Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1981-01-28
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Acceptable for reliability but not in detail documented. Study report meets basic scientific principles. Study was conducted prior to GLP and OECD guideline implementation.
Reason / purpose for cross-reference:
reference to same study
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Principles of method if other than guideline:
No further information available.
GLP compliance:
no
Test type:
standard acute method
Limit test:
no
Species:
rat
Strain:
Wistar
Sex:
male/female
Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Doses:
3.1 mg/kg
5.0 mg/kg
5.5 mg/kg
6.2 mg/kg
7.2 mg/kg
No. of animals per sex per dose:
5 male and 5 female were used for each dose level.
Control animals:
no
Sex:
male/female
Dose descriptor:
LD50
Effect level:
4.97 mL/kg bw
Based on:
test mat.
95% CL:
3.68 - 5.36

At Single dose of 5.0 - 7.2 mL/kg/bw all male and female rats had the following symptoms: Unsteady locomotion, hemiplegia of the hind limbs, unkempt coats, loss of weights and a general loss of activity. Animals dosed from level 5.5 up to dose level 7.2 mL/kg/bw additional symptoms were observed such as lateral and ventral position of the animals. The symptoms occured one hour after administration and were evident until end of the study. Mortality was noted from 2. until 12. study day. All findings are applicable for male and female rats. No significant differences between both sexes.

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The calculated LD50 value of Butyl cyanoacetate is 4.97 mL/kg/bw (confidence interval for p < 0.05 = 3.68 - 5.36 mL/kg/bw). Therefore, the test item will be not classified as acute toxic according to GHS/CLP classification criteria..
Executive summary:

The study was performed 1981, before GLP- and OECD-testing guidelines were available and in force.

The calculated LD50 value of Butyl cyanoacetate is 4.97 mL/kg/bw (confidence interval for p < 0.05 = 3.68 - 5.36 mL/kg/bw). Therefore, the test item will be not classified as acute toxic according to GHS/CLP classification criteria..

Endpoint conclusion
Endpoint conclusion:
no adverse effect observed

Additional information

Justification for classification or non-classification