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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
comparable to guideline study
Remarks:
Follows standard guidelines, under GLP

Data source

Reference
Reference Type:
other company data
Title:
Unnamed
Year:
1992

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: Annex V
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
A mixture of: 2-ethylhexyl mono-D-glucopyranoside; 2-ethylhexyl di-D-glucopyranoside
EC Number:
414-420-0
EC Name:
A mixture of: 2-ethylhexyl mono-D-glucopyranoside; 2-ethylhexyl di-D-glucopyranoside
Cas Number:
125590-73-0
Molecular formula:
(C6H10O5)n, C8H18O n = 1,2
IUPAC Name:
Reaction mass of 2-ethylhexyl mono-D-glucopyranoside and 2-ethylhexyl di-D-glucopyranoside

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female

Administration / exposure

Vehicle:
water

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Mortality:
Male 2000 mg/kg bw, number of animals: 5, number of death: 0
Male 5000 mg/kg bw, number of animals: 5, number of death: 2
Female 2000 mg/kg bw, number of animals: 5, number of death: 0
Female 5000 mg/kg bw, number of animals: 5, number of death: 2
Clinical signs:
other: Signs of toxicity related to dose levels: Death were observed between 5 hours and 2 days after dosing. Pilo-erection, hunched posture, abnormal gait, lethargy, decreased respiratory rate and pallor of the extremities were observed in both sexes at both d
Gross pathology:
Effects on organs: no macroscopic findings were observed in any animals surviving treatment. Congestion of blood vessels of the small and large intestines was observed in one female which died following 5000 mg/kg.

Applicant's summary and conclusion

Interpretation of results:
not classified