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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

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Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: limited but acceptable documented study report which meets basic scientific principles

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1973
Report date:
1973

Materials and methods

Principles of method if other than guideline:
other: acute dermal toxicity study
GLP compliance:
no
Test type:
other: acute dermal 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:
rabbit
Strain:
New Zealand White
Sex:
male/female

Administration / exposure

Type of coverage:
semiocclusive
Vehicle:
unchanged (no vehicle)
Duration of exposure:
24 h
Doses:
5010, 7940 mg/kg
No. of animals per sex per dose:
1 to 2 per dose
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 5 010
Remarks on result:
other: Clinical signs: reduced appetite and activity (survivors), increasing weakness, collapse and death (decents); gross autopsy:hemorrhagic areas of the lung, liver, spleen, and kidney discoloration, gastrointestinal inflammation (decents)

Any other information on results incl. tables

Mortality:

time of mortality: 8 days

5010 mg/kg: 0/1 male

7940 mg/kg: 1/1 male, 0/1 female, combinded: 1/2

Signs of intoxication: reduced appetite and activity (four to seven days in survivors), increasing weakness, collapse and death (decent)

Gross autopsy:

Decent: hemorrhagic areas of the lung, liver, spleen, and kidney discoloration, gastrointestinal inflammation

Survivors (14 days): Viscera appeared normal

Applicant's summary and conclusion

Executive summary:

LD50 rabbit: >5010 mg/kg