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Toxicological information

Acute Toxicity: oral

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
supporting study
Study period:
1956
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: Original study cited not available for review. Included for completion only using information from a secondary source.

Data source

Referenceopen allclose all

Reference Type:
secondary source
Title:
Ethyl acetate SIDS initial assessment profile.
Year:
2004
Bibliographic source:
OECD SIAM 14, Paris, 2002
Report Date:
2002
Reference Type:
review article or handbook
Title:
Unnamed
Year:
1956

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Acute Oral Toxicity method, no further details available
GLP compliance:
no
Test type:
standard acute method
Limit test:
no

Test material

Reference
Name:
Unnamed
Type:
Constituent
Details on test material:
- Name of test material (as cited in study report): No data

Test animals

Species:
rat
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
not specified
Doses:
no data
No. of animals per sex per dose:
no data
Control animals:
not specified

Results and discussion

Effect levels
Sex:
not specified
Dose descriptor:
LD50
Effect level:
5 620 mg/kg bw

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Executive summary:

In a study for which only the results are available, an acute oral LD50 value of 5620 mg/kg for ethyl acetate in the rat was reported.