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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
skin irritation: in vivo
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: Study meets generally accepted scientific standards, acceptable for assessment.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1970
Report date:
1970

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 404 (Acute Dermal Irritation / Corrosion)
Deviations:
yes
Remarks:
observation period: 8 days
Principles of method if other than guideline:
The skin irritation test was conducted according to a BASF-internal standard protocol. White Vienna rabbits were treated with the substance for 1 min, 5 min, 15 min, or 20 h, respectively, under occlusive conditions.
There were two experiments performed.
During the first experiment two rabbits were exposed to the test substance for 1 min, 5 min, or 15 min on their backs.
During the second experiment two rabbits were exposed to the test substance for 20 h on their backs and their ears.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
N,N'-bis(3-aminopropyl)propane-1,3-diamine
EC Number:
225-007-8
EC Name:
N,N'-bis(3-aminopropyl)propane-1,3-diamine
Cas Number:
4605-14-5
Molecular formula:
C9H24N4
IUPAC Name:
N,N'-bis(3-aminopropyl)propane-1,3-diamine

Test animals

Species:
rabbit
Strain:
Vienna White
Details on test animals or test system and environmental conditions:
TEST ANIMALS
- Weight at study initiation: 2.45, 2,77, 3.7 and 2.95 kg

Test system

Type of coverage:
not specified
Preparation of test site:
not specified
Vehicle:
unchanged (no vehicle)
Controls:
no
Duration of treatment / exposure:
The first experiment :1 min, 5 min, 15 min
The second experiment: 20 h
Observation period:
8 d
Number of animals:
4
Details on study design:
REMOVAL OF TEST SUBSTANCE
- Washing: yes (exposure 1, 5, 15 min) first with undiluted Lutrol, then with an aqueous Lutrol solution (50 %); not specified in the second experiment (exposure 20 h)

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
erythema score
Basis:
mean
Time point:
24 h
Score:
>= 2
Reversibility:
not reversible
Remarks on result:
other: full thickness necrosis observed after 15 min exposure.
Irritation parameter:
edema score
Basis:
mean
Time point:
24 h
Score:
>= 2
Reversibility:
not reversible
Remarks on result:
other:
Remarks:
full thickness necrosis obsered after 15 min of exposure.

Applicant's summary and conclusion

Interpretation of results:
Category 1B (corrosive) based on GHS criteria
Conclusions:
The application of the test substance to rabbit skin caused full thickness necrosis. Exposure duration: 15 min. Reading: 24 h post application.