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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: GLP screening study
Cross-referenceopen allclose all
Reason / purpose for cross-reference:
reference to same study
Reason / purpose for cross-reference:
reference to other study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1998
Report date:
1998

Materials and methods

Principles of method if other than guideline:
3 single oral doses of test material were administered to three groups of rats.
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
2,4-dichloro-5-isopropoxyaniline
EC Number:
255-258-9
EC Name:
2,4-dichloro-5-isopropoxyaniline
Cas Number:
41200-96-8
Molecular formula:
C9H11Cl2NO
IUPAC Name:
2,4-dichloro-5-(propan-2-yloxy)aniline
Details on test material:
- Name of test material (as cited in study report): 2,4-dichloro 5-isopropoxy aniline (DIA)
- Storage condition of test material: stored in the dark at room temperature in air-tight containers

Test animals

Species:
rat

Administration / exposure

Route of administration:
oral: unspecified
Doses:
25; 200 and 2000 mg/kg bw

Results and discussion

Effect levels
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Under the test conditions, 2,4-Dichloro-5-isopropoxyaniline is not classified for acute oral toxicity in the rat according to the criteria of the Regulation (EC) 1272/2008 and the Directive 67/548/EEC as the LD 50 is higher than 2000 mg/kg bw.
Executive summary:

In an acute oral toxicity screening study, performed in compliance with the GLP, three groups of rats were given a single oral dose of undiluted 2,4-Dichloro-5-isopropoxyaniline (named as 2,4-dichloro 5-isopropoxy aniline (DIA) in the study report) at doses of 25; 200 or 2000 mg/kg bw.

 

Oral LD50rat > 2000 mg/kg bw

Under the test conditions, 2,4-Dichloro-5-isopropoxyaniline is not classified for acute oral toxicity in the rat according to the criteria of the Regulation (EC) 1272/2008 and the Directive 67/548/EEC as the LD 50 is higher than 2000 mg/kg bw.