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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1983
Report date:
1983

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
not specified
GLP compliance:
not specified
Test type:
standard acute method

Test material

Constituent 1
Chemical structure
Reference substance name:
(3-chloro-2-hydroxypropyl)dimethyloctadecylammonium chloride
EC Number:
221-083-1
EC Name:
(3-chloro-2-hydroxypropyl)dimethyloctadecylammonium chloride
Cas Number:
3001-63-6
Molecular formula:
C23H49ClNO.Cl
IUPAC Name:
(3-chloro-2-hydroxypropyl)dimethyloctadecylazanium chloride
Constituent 2
Chemical structure
Reference substance name:
Propane-1,2-diol
EC Number:
200-338-0
EC Name:
Propane-1,2-diol
Cas Number:
57-55-6
Molecular formula:
C3H8O2
IUPAC Name:
propylene glycol
Test material form:
liquid
Details on test material:
Aqueous solution

Test animals

Species:
rat
Strain:
Wistar
Sex:
male/female
Details on test animals or test system and environmental conditions:
Mass: 127-168 g (male); 130-156 g (female), Age: 48-56 Days (male) .; 59-70 Days (female)
Acclimatization time before start of test: 5 days
Feeding: Standardized Laboratory Animal Feed ALTROMIN®, Hydration:Water ad libitum. room temperature: 21 ° C +/- 2 ° C, Relative humidity: 50 - 60%, Room lighting: 12 hrs. Illuminated tube lighting /12 hours Darkness,
room hygiene: Laboratory and cage cleaning by means of Commercial antiseptic, instrument disinfection and sterilization with autoclave and hot air sterilizer

Administration / exposure

Route of administration:
oral: gavage
Vehicle:
unchanged (no vehicle)
Details on oral exposure:
The test product was in the form of a liquid of yellowish color and was applied undiluted. pH 5.85, Density 0.99g/ml. Application volume 2.15 ml/kg - 5.62 ml/kg. These volumes corresponded to a dosage range between 2129 and 5207 mg / kg
Doses:
2.15-5.62 ml / kg
No. of animals per sex per dose:
5
Control animals:
not specified

Results and discussion

Effect levelsopen allclose all
Sex:
female
Dose descriptor:
LD50
Effect level:
3 784 mg/kg bw
Sex:
male
Dose descriptor:
LD50
Effect level:
5 137 mg/kg bw
Mortality:
The deaths took place mostly between the 4th and 6th day following application. Later death cases also occurred after 9 to 13 days.
Clinical signs:
other: A substance-specific poisoning picture could not be raised in either male or female animals. Irrespective of the dose in the test, their well-being was negatively impacted 1 to 3 days after the application of the test product, during which diarrhea and ru

Any other information on results incl. tables

 Dose (ml/kg)  Sex  Mortality (x/n)  Mortality (%)
 2.15  0/5  0
 3.16  M  0/5  0
 3.83  M  1/5  20
 4.64  M  4/5  80
 5.62  M  3/5  60
 2.15  F  0/5  0
 3.16  F  1/5  20
 3.83  F  3/5  60
 4.64  F  4/5  80
 5.62  F  4/5  80

Applicant's summary and conclusion

Interpretation of results:
Category 4 based on GHS criteria
Conclusions:
Based on LD50 of 3784 mg/kg of the test solution (40% solution of the active ingredient), the LD50 of (3-Chloro-2-hydroxypropyl)dimethyloctadecylammonium chloride would be 1514 mg/kg.