Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study with acceptable restrictions

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2015
Report date:
2015

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 423 (Acute Oral toxicity - Acute Toxic Class Method)
GLP compliance:
no
Remarks:
(study performed according to SOP in a laboratory that conforms to GLP but report not audited by the QAU)
Test type:
acute toxic class method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
1-chloro-3-iodo-5-(trifluoromethyl)benzene
EC Number:
812-243-7
Cas Number:
1189352-83-7
Molecular formula:
C7 H3 Cl F3 I
IUPAC Name:
1-chloro-3-iodo-5-(trifluoromethyl)benzene

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
female

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
methylcellulose
Doses:
300 and 2000 mg/kg
No. of animals per sex per dose:
3 females/group
Control animals:
not specified

Results and discussion

Effect levels
Key result
Sex:
female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Mortality:
No mortality observed at both doses.
Clinical signs:
No information
Body weight:
No information
Gross pathology:
No information

Applicant's summary and conclusion

Interpretation of results:
Category 5 based on GHS criteria
Conclusions:
In this study conducted with MR-008-2 (Q6F62), an intermediate product of ML925 synthesis, the maximal dose tested was non-lethal (2000 mg/kg) and LD50 was higher than 2000 mg/kg. Therefore, MR-008-2 (Q6F62) can be classified in Category 5 of the Globally Harmonized Classification System (GHS).