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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
read-across from supporting substance (structural analogue or surrogate)
Adequacy of study:
supporting study
Study period:
1973
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Comparable to guideline study with acceptable restrictions (no GLP)
Justification for type of information:
Ethyl 2-cyanoacrylate (ECA) is a structural homologue that contains additional CH2-group (see attached justification).

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1973
Report date:
1973

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
GLP compliance:
no
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
Ethyl 2-cyanoacrylate
EC Number:
230-391-5
EC Name:
Ethyl 2-cyanoacrylate
Cas Number:
7085-85-0
Molecular formula:
C6H7NO2
IUPAC Name:
ethyl 2-cyanoacrylate
Test material form:
liquid
Details on test material:
- Name of test material: Depend, IS 04E
- Description of test material: transparent, viscous liquid

Test animals

Species:
rat
Strain:
not specified
Sex:
male
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: the body weight ranged from 206 to 246 g
- Fasting period before study: 18 hours

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
No. of animals per sex per dose:
6 male albino rats
Control animals:
no
Details on study design:
The test compound was administered by oral intubation to 1 group of 6 male albino rats fasted for 18 hours prior to dosing. The animals were observed during the day of dosing and daily thereafter for 14 days. Decents during the study were examined for gross lession.

Results and discussion

Effect levels
Key result
Sex:
male
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Based on:
test mat.
Mortality:
One rat died on the fourth day.
Gross pathology:
Hemorrhagic lungs. Solid mass in stomach, not adhered to stomach wall but too large to pass through pyloric valve. Cardic portion of stomach distended. Food in intestines as in a normal rat. One rat had dilated intestinal blood vessels.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The oral LD50 of ethyl-2-cyanoacrylate is estimated to be higher than 5000 mg/kg body weight in rats for a single dose. Therefore the test substance ethyl-2-cyanoacrylate is practically nontoxic according to the EC-guideline 93/21.
Therefore, the test substance ethyl-2-cyanoacrylate can be considered as practically nontoxic. Based on structural analogy and a comparable reaction mechanism (polymerization in contact with moisture), it is concluded that the acute toxicity potential of 2-methoxyethyl 2-cyanoacrylate will also be low.