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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: inhalation
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
other: The study was not performd to GLP and reporting of methods is sparse. However, the study outcomes are unambiguous and predictable. Therefore the study is deeemd sufficiently reliable.

Data source

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

Materials and methods

Test guideline
Qualifier:
no guideline followed
Principles of method if other than guideline:
Whole-body exposure.
GLP compliance:
not specified
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:
solid - liquid: suspension
Remarks:
migrated information: dispersion

Test animals

Species:
rat
Strain:
other: Charles River rats
Sex:
male/female
Details on test animals or test system and environmental conditions:
Young adult albino rats were employed as test animals. The rats were selected after having been under observation for at least 5 days to insure their general health and suitability for testing. The animals were housed in stainless steel cages and permitted a standard laboratory diet plus .water
ad libitum, except during inhalation exposure.

Administration / exposure

Route of administration:
inhalation: vapour
Type of inhalation exposure:
whole body
Vehicle:
clean air
Details on inhalation exposure:
Vapour was generated by passing a stream of clen, dry air through the diluted test material in a gas washing bottle. The resulting air/vapour mixture ws then introduced to the exposure chamber.
Analytical verification of test atmosphere concentrations:
no
Duration of exposure:
ca. 14 d
Remarks on duration:
Whole-body exposure.
No. of animals per sex per dose:
5 males, 5 females
Control animals:
no

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LC50
Remarks on result:
other: No effects attributable to the test material were observed
Mortality:
None observed
Clinical signs:
other: None observed
Body weight:
No changes observerd outside of normal ranges
Gross pathology:
No gross effect reported

Applicant's summary and conclusion

Interpretation of results:
sligthly toxic
Remarks:
Migrated information Criteria used for interpretation of results: EU
Conclusions:
There were no adverse reactions noted during exposure or the 14-day observaticn period which followed. The average 2- week body weight gains were within the normal limits.

The LC50 was calculated as >1.48 mg/L (rat) 1-hr. (no deaths)