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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.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:
experimental study
Adequacy of study:
key study
Study period:
Study completion date - 01 January 1988.
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
data from handbook or collection of data

Data source

Reference
Reference Type:
publication
Title:
Experimental studies of the biological action of fluosilicic acid salts.
Author:
Rumyantsev, G.I.; Nóvikov, S.M.; Mélnikova, N.N.; Lévchenko, N.I.; Kóseva, E.E. and Kochetkova, T.A.
Year:
1988
Bibliographic source:
Gigiena i Sanitariya, (V/O Mezhdunarodnaya Kniga, 113095 Moscow, USSR) V.1- 1936- 53(11), 80,1988
Report date:
1988

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:
disodium;hexafluorosilicon(2-)
Cas Number:
16893-85-9
Molecular formula:
Na2SiF6
IUPAC Name:
disodium;hexafluorosilicon(2-)

Test animals

Species:
mouse
Strain:
not specified
Sex:
not specified

Administration / exposure

Route of administration:
oral: drinking water
Vehicle:
water
Control animals:
not specified

Results and discussion

Effect levels
Key result
Sex:
not specified
Dose descriptor:
LD50
Effect level:
70 mg/kg bw
Based on:
test mat.
Mortality:
Details not available
Clinical signs:
other: - PERIPHERAL NERVE AND SENSATION: Flaccid paralysis without anesthesia (usually neuromuscular blockage); - BEHAVIORAL: Ataxia; - BEHAVIORAL: Muscle contraction or spasticity

Applicant's summary and conclusion

Interpretation of results:
Category 3 based on GHS criteria
Conclusions:
LD50 for sodium hexafluorosilicate was found to be 70 mg/kg bw.
Executive summary:

The acute oral toxicity of sodium hexafluorosilicate was evaluated in this study conducted with mice. The test substance was administered via drinking water. Flaccid paralysis resulting from neuromuscular blockage, ataxia and muscle contraction or spasticity were the clinical signs observed in this study. The study concluded that the LD50 for sodium hexafluorosilicate was 70 mg/kg bw.