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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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: oral
Type of information:
experimental study
Adequacy of study:
key study
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP complianced.

Data source

Reference
Reference Type:
other: Inquiry result from ECHA
Title:
Unnamed
Year:
2013

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
other: Directive 92/69/CEE, B.1
GLP compliance:
yes
Test type:
standard acute method
Limit test:
no

Test material

Constituent 1
Chemical structure
Reference substance name:
-
EC Number:
425-980-0
EC Name:
-
Cas Number:
129499-78-1
Molecular formula:
C12H18O11
IUPAC Name:
L-Ascorbic acid 2-glucoside

Test animals

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

Administration / exposure

Vehicle:
water
Remarks:
distilled

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 2 000 mg/kg bw
Mortality:
Male: 1000mg/kg bw; Number of animals: 5; Number of deaths: 0
Male: 2000mg/kg bw; Number of animals: 5; Number of deaths: 0
Female: 1000mg/kg bw; Number of animals: 5; Number of deaths: 0
Female: 2000mg/kg bw; Number of animals: 5; Number of deaths: 0
Clinical signs:
Signs of toxicity related ot dose levels:
MORTALITE:
Aucune mortalite pendant l'essai.
SIGNS CLINIQUES:
Des selles molles ont etes observees pendant l'essai.
POIDS CORPORELS:
Aucun changement n'a ete note.
Gross pathology:
Effects on organs:
Aucun effet sur les organes.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU