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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: inhalation

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Administrative data

Endpoint:
acute toxicity: inhalation
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
other: study report does not give sufficient experimental details

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1967
Report date:
1967

Materials and methods

Principles of method if other than guideline:
other: acute inhalation toxicity study
GLP compliance:
no
Test type:
other: acute inhalation toxicity study

Test material

Constituent 1
Chemical structure
Reference substance name:
N-(1,4-dimethylpentyl)-N'-phenylbenzene-1,4-diamine
EC Number:
221-374-3
EC Name:
N-(1,4-dimethylpentyl)-N'-phenylbenzene-1,4-diamine
Cas Number:
3081-01-4
Molecular formula:
C19H26N2
IUPAC Name:
N1-(5-methylhexan-2-yl)-N4-phenylbenzene-1,4-diamine
Details on test material:
Santoflex 14

Test animals

Species:
rat
Strain:
not specified
Sex:
male

Administration / exposure

Route of administration:
inhalation
Type of inhalation exposure:
whole body
Vehicle:
other: unchanged (no vehicle)
Duration of exposure:
6 h
No. of animals per sex per dose:
4
Control animals:
not specified

Results and discussion

Any other information on results incl. tables

Average temoerature inside chamber: 76.5 °F

Average relative humidity inside chamber: 60.0 %

Amount of sample to start: 100 g

revovered: 99.8 g

vaporized or left: 0.2 g( 0.2 %)

Mortality: none

All animals survived the six hour exposure as well as the following ten day observation period.

Clinical signs: Some discomfort developed during exposure but there was no weakness of consequence. Nasal and ocular mucosae remained free of inflammation. Occasional irregular breathing was noted. Behavior appeared normal in 24 -hours. The ten day observation period was uneventful.

Applicant's summary and conclusion