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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: dermal
Type of information:
experimental study
Adequacy of study:
key study
Study period:
1989
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1989

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
EU Method B.3 (Acute Toxicity (Dermal))
GLP compliance:
yes
Test type:
standard acute method
Limit test:
yes

Test material

Constituent 1
Chemical structure
Reference substance name:
N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine
EC Number:
219-145-8
EC Name:
N-(3-aminopropyl)-N-dodecylpropane-1,3-diamine
Cas Number:
2372-82-9
Molecular formula:
C18H41N3
IUPAC Name:
bis(3-aminopropyl)(dodecyl)amine

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female

Administration / exposure

Type of coverage:
semiocclusive
Vehicle:
unchanged (no vehicle)
Duration of exposure:
24 h
Doses:
2000 mg/kg bw corresponding to 600 mg a.i./kg bw (undiluted test substance)
No. of animals per sex per dose:
5 per sex per dose.
Control animals:
no

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 600 mg/kg bw
Based on:
act. ingr.
Remarks on result:
other: based on 30% purity

Applicant's summary and conclusion

Interpretation of results:
Category 3 based on GHS criteria
Conclusions:
Under the study conditions, the LD50 of the test substance in Sprague-Dawley rats was established at >600.0 mg a.i./kg bw. It must however be noted that the animals were sacrificed due to severe suffering linked to skin corrosion and that toxicity was not of systemic nature.
Executive summary:

A study was conducted to determine the acute dermal toxicity of the test substance according to EU Method B.3, in compliance with GLP. Five rats per sex per dose were exposed to the test substance at a concentration of 2000 mg/kg bw (corresponding to 600 mg a.i./kg bw based on a purity of 30%). Under the study conditions, the LD50 of the test substance in Sprague Dawley rats was established at >600.0 mg a.i./kg bw. It must however be noted that the animals were sacrificed due to severe suffering linked to skin corrosion and that toxicity was not of systemic nature (Jones, 1989).