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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1989-10-11 to 1989-11-06
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study was performed according to EG Guideline B.1. 84/449/EWG, OECD 401 and GLP.
Cross-reference
Reason / purpose for cross-reference:
reference to same study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1989
Report date:
1989

Materials and methods

Test guidelineopen allclose all
Qualifier:
according to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
no
Qualifier:
according to guideline
Guideline:
EU Method B.1 (Acute Toxicity (Oral))
Deviations:
no
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
5'-chloro-2'-methoxyacetoacetanilide
EC Number:
258-189-2
EC Name:
5'-chloro-2'-methoxyacetoacetanilide
Cas Number:
52793-11-0
Molecular formula:
C11H12ClNO3
IUPAC Name:
N-[5-chloro-2-(methoxyacetyl)phenyl]acetamide
Constituent 2
Reference substance name:
Acetessig-4-chlor-o-anisidid
IUPAC Name:
Acetessig-4-chlor-o-anisidid
Test material form:
solid: particulate/powder
Remarks:
migrated information: powder
Details on test material:
Appearance: white solid powder
Purity: > 99%
Lot: T021
Storage: in the dark at 20°C, under a hood

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
other: Starch slime 2%
Doses:
3 dose concentrations:
Male: 1600 mg/kg, 2000 mg/kg, 2500 mg/kg bw
Female: 2000 mg/kg bw

4'000 mg/kg
5'000 mg/kg
6'300 mg/kg
8'000 mg/kg
No. of animals per sex per dose:
5 animals per dose
Male and female rats used.
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.

Any other information on results incl. tables

Results:

Dose Level in mg/kg bw

Male animals

mortality

Female animals

mortality

 

absolute

relative (%)

absolute

relative (%)

1600

0 / 5

0

-

-

2000

2 / 5

40

0 / 5

0

2500

2 / 5

40

-

-

 

 

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
The LD50 to male and female rats of the test item was determined to be greather than 2000 mg/kg body weight.
Executive summary:

The study was performed according to EG Guideline B.1. 84/449/EWG, OECD 401 and GLP.

The LD50 to male and female rats of the test item was determined to be greather than 2000 mg/kg body weight.