Registration Dossier

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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data

Data source

Reference
Reference Type:
review article or handbook
Title:
Unnamed
Year:
2013

Materials and methods

Test guideline
Qualifier:
equivalent or similar to guideline
Guideline:
OECD Guideline 402 (Acute Dermal Toxicity)
Version / remarks:
Details of the exact method are not given in the CIR text
GLP compliance:
not specified
Remarks:
results given in the CIR review do not give details of the GLP status of the work carried out
Test type:
fixed dose procedure

Test material

Constituent 1
Chemical structure
Reference substance name:
D-Glucopyranose, oligomeric, C10-16-alkyl glycosides
Cas Number:
110615-47-9
Molecular formula:
C18H36O6
IUPAC Name:
D-Glucopyranose, oligomeric, C10-16-alkyl glycosides
Specific details on test material used for the study:
50% ai (as C10-16 APG; n: 1.6)

Test animals

Species:
rabbit
Strain:
New Zealand White
Sex:
male/female

Administration / exposure

Type of coverage:
not specified
Vehicle:
unchanged (no vehicle)
No. of animals per sex per dose:
5

Results and discussion

Effect levels
Key result
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Based on:
test mat.
Mortality:
None of the animals died during the study
Clinical signs:
other: Slight depression, hunched posture, mild to marked erythema, and marked desquamation were observed.

Applicant's summary and conclusion

Interpretation of results:
GHS criteria not met