Registration Dossier

Data platform availability banner - registered substances factsheets

Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The study preceeds current OECD guidelines, however is equivalent to OECD Guideline 404 (Acute Dermal Irritation / Corrosion). No GLP, however the study is sufficiently reported and the results unambiguous.

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1987
Report date:
1987

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
not specified
GLP compliance:
no
Test type:
standard acute method

Test material

Constituent 1
Chemical structure
Reference substance name:
N-[3-(dimethylamino)propyl]-N,N',N'-trimethylpropane-1,3-diamine
EC Number:
223-362-3
EC Name:
N-[3-(dimethylamino)propyl]-N,N',N'-trimethylpropane-1,3-diamine
Cas Number:
3855-32-1
Molecular formula:
C11H27N3
IUPAC Name:
(3-{[3-(dimethylamino)propyl](methyl)amino}propyl)dimethylamine
Test material form:
gas under pressure: refrigerated liquefied gas

Test animals

Species:
other: Rat and Mouse

Administration / exposure

Route of administration:
oral: drinking water
Vehicle:
water
Control animals:
no

Results and discussion

Effect levelsopen allclose all
Sex:
male
Dose descriptor:
LD50
Effect level:
2.37 mL/kg bw
Based on:
test mat.
Remarks on result:
other: Male Rat
Sex:
female
Dose descriptor:
LD50
Effect level:
ca. 2.3 mL/kg bw
Based on:
test mat.
95% CL:
>= 2.09 - <= 2.51
Remarks on result:
other: Female rat
Sex:
male
Dose descriptor:
LD50
Effect level:
ca. 2.19 mL/kg bw
Based on:
test mat.
95% CL:
>= 1.97 - <= 2.46
Remarks on result:
other: Male Mouse
Sex:
female
Dose descriptor:
LD50
Effect level:
ca. 1.68 mL/kg bw
Based on:
test mat.
95% CL:
>= 1.49 - <= 1.87
Remarks on result:
other: Female Mouse
Mortality:
Obsrved in all treated groups.
Clinical signs:
other: Decreased activity, ataxia, dyspnea and writhing
Other findings:
Signs of toxicity were observed immediately after treatment and jpersisted les than 24 hours post-treatment (corrosive)

Applicant's summary and conclusion

Interpretation of results:
moderately toxic
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
Rat - Acute Oral Toxicity LD50 1598 mg/kg
The substance is severely irritating and corrosive to the skin and eyes. This material is irritating and corrosive to the nasal and respiratory tract