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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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

Toxicological information

Acute Toxicity: oral

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Administrative data

Endpoint:
acute toxicity: oral
Type of information:
other: summary of experimental results
Adequacy of study:
supporting study
Reliability:
4 (not assignable)
Rationale for reliability incl. deficiencies:
abstract
Remarks:
summary of experimental results, citing i.a. the available OECD 404 and 405 study, but original study report of the present information is not available

Data source

Reference
Reference Type:
other company data
Title:
Unnamed
Year:
1983
Report date:
1983

Materials and methods

Principles of method if other than guideline:
The acute oral LD50 was determined in rats.
GLP compliance:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
Betaines, coco alkyldimethyl(3-sulfopropyl)
EC Number:
269-225-1
EC Name:
Betaines, coco alkyldimethyl(3-sulfopropyl)
Cas Number:
68201-55-8
Molecular formula:
C7H17NO3S·[CH2]6-16
IUPAC Name:
[3-(dodecyldimethylazaniumyl)propyl]trioxo-λ⁶-sulfanuide
Constituent 2
Chemical structure
Reference substance name:
Water
EC Number:
231-791-2
EC Name:
Water
Cas Number:
7732-18-5
Molecular formula:
H2O
IUPAC Name:
Water

Test animals

Species:
rat

Administration / exposure

Route of administration:
oral: unspecified

Results and discussion

Effect levelsopen allclose all
Dose descriptor:
LD50
Effect level:
6.4 mL/kg bw
Based on:
test mat.
Dose descriptor:
LD50
Effect level:
ca. 3 200 mg/kg bw
Based on:
act. ingr.
Remarks:
recalculated from the 50% aqueous solution

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met
Conclusions:
The acute LD50 oral was determined to be 6.4 ml/kg in rats for a 50% solution of the registered substance, which corresponds to a LD50 oral of ca. 3.2 g/kg. So the substance does not need to be classified as acutely toxic via the oral route.
Executive summary:

The acute LD50 oral was determined to be 6.4 ml/kg in rats for a 50% solution of the registered substance, i.e. LD50 = ca. 3.2 g/kg, no classification as acutely toxic is triggered.