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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
1976
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Short report, limited documentation, non-GLP, females only

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1976
Report date:
1976

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
yes
Remarks:
females only, limit dose = 5000 mg/kg
GLP compliance:
no
Remarks:
pre-dates GLP
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
3-hydroxy-2'-methyl-2-naphthanilide
EC Number:
205-205-0
EC Name:
3-hydroxy-2'-methyl-2-naphthanilide
Cas Number:
135-61-5
Molecular formula:
C18H15NO2
IUPAC Name:
3-hydroxy-N-(2-methylphenyl)naphthalene-2-carboxamide
Constituent 2
Reference substance name:
Naphtol AS-D
IUPAC Name:
Naphtol AS-D

Test animals

Species:
rat
Strain:
Wistar
Sex:
female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
other: sesame oil
Doses:
5000 mg/kg bw
No. of animals per sex per dose:
10
Control animals:
no
Details on study design:
- Duration of observation period following administration: 14 days
- Frequency of weighing: 1/week
- Necropsy of survivors performed: yes
- Other examinations performed: clinical signs, body weight, necropsy

Results and discussion

Effect levels
Sex:
female
Dose descriptor:
LD0
Effect level:
> 5 000 mg/kg bw
Remarks on result:
other: Limit test
Mortality:
none detected
Clinical signs:
other: none detected
Gross pathology:
no effects
Other findings:
none

Applicant's summary and conclusion

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