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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
short-term repeated dose toxicity: dermal
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: secondary citation

Data source

Referenceopen allclose all

Reference Type:
review article or handbook
Title:
IUCLID Dataset: 4-Isopropylanilin
Author:
ECB
Year:
2000
Bibliographic source:
European Chemical Bureau (ECB) European Commission 19.02.2000
Reference Type:
secondary source
Title:
Unnamed
Year:
1974

Materials and methods

Test guideline
Guideline:
other: Internal Guideline Hoechst AG
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
4-isopropylaniline
EC Number:
202-797-2
EC Name:
4-isopropylaniline
Cas Number:
99-88-7
Molecular formula:
C9H13N
IUPAC Name:
4-(propan-2-yl)aniline
Test material form:
other: liquid
Details on test material:
as prescribed in IUCLID Dataset

Test animals

Species:
rabbit
Strain:
not specified
Sex:
not specified
Details on test animals or test system and environmental conditions:
no data

Administration / exposure

Type of coverage:
not specified
Vehicle:
not specified
Details on exposure:
application of 1 ml once per day on 5 days
as undiluted testsubstance and
as 10 % solution (solvent not given)
Analytical verification of doses or concentrations:
not specified
Duration of treatment / exposure:
5 days
Frequency of treatment:
once per day
Doses / concentrations
Remarks:
Doses / Concentrations:
1 ml undiluted testsubstance or 1 ml of a 10 % solution
Basis:

No. of animals per sex per dose:
no data
Control animals:
not specified
Details on study design:
application of 1 ml once per day on 5 days
as undiluted testsubstance and
as 10 % solution (solvent not given)
Positive control:
no data

Examinations

Observations and examinations performed and frequency:
details not reported
Sacrifice and pathology:
no data
Statistics:
no data

Results and discussion

Results of examinations

Details on results:
undiluted the tesubstance was strong irritating; as 10 % solution it is evaluated as irritating

Effect levels

Dose descriptor:
NOAEL
Sex:
not specified
Basis for effect level:
other: undiluted the tesubstance was strong irritating; as 10 % solution it is evaluated as irritating
Remarks on result:
not determinable
Remarks:
no NOAEL identified

Target system / organ toxicity

Critical effects observed:
not specified

Applicant's summary and conclusion

Executive summary:

Application of 1 ml once per day on 5 days as undiluted testsubstance or as 10 % solution (solvent not given).

Undiluted the tesubstance was strong irritating; as 10 % solution it is evaluated as irritating