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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2020

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
GLP compliance:
yes (incl. QA statement)
Test type:
fixed dose procedure

Test material

Constituent 1
Chemical structure
Reference substance name:
9-oxo-9H-thioxanthene-4-carboxylic acid
EC Number:
849-175-2
Cas Number:
51762-56-2
Molecular formula:
C14H8O3S
IUPAC Name:
9-oxo-9H-thioxanthene-4-carboxylic acid

Test animals

Species:
rat
Strain:
Wistar
Sex:
female

Administration / exposure

Route of administration:
oral: drinking water
Vehicle:
olive oil
Details on oral exposure:
14-days observation period.
Doses:
The starting dose was selected from the fixed dose levels of 5, 50, 300, and 2000 mg/kg body weight.
No. of animals per sex per dose:
6 females

Results and discussion

Effect levels
Key result
Sex:
female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Clinical signs:
other: No signs of intoxication, change of health, nor any other adverse reactions during 24 hours and 14-days observation period at limit dose of 2000 mg/kg body weight was observed. Animals No 1-3 exhibit slight piloerection after 2 hours from administration a
Gross pathology:
All animals were necropsied. No visible pathological findings were observed in animals dosed with 2000 mg/kg body weight.

Applicant's summary and conclusion