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Sodium hydrosulfite, tech._Molecular_structure_CAS_7775-14-6)
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Sodium hydrosulfite, tech.

Catalog No. 33381 Name Alfa Aesar
CAS Number 7775-14-6 Website
M. F. Na2O4S2 Telephone
M. W. 174.10714 Fax
Purity 85+% Email
Storage Chembase ID: 129519

SYNONYMS

Title
连二亚硫酸钠 , tech.
IUPAC name
disodium sulfinatosulfinate
IUPAC Traditional name
disodium dithionite
Synonyms
Sodium dithionite
Sodium hypodisulfite

DATABASE IDS

MDL Number MFCD00011640
EC Number 231-890-0
Merck Index 148626
CAS Number 7775-14-6

PROPERTIES

Purity 85+%
Apperance Powder
Melting Point 52°C dec.
GHS Pictograms GHS02
GHS Pictograms GHS07
GHS Hazard statements H251-H302
European Hazard Symbols X
European Hazard Symbols Oxidising Oxidising (O)
GHS Precautionary statements P280-P235+P410-P301+P312-P420-P407-P501A
Risk Statements 7-22-31
Safety Statements 7/8-26-28-43
Storage Warning Moisture Sensitive
TSCA Listed
Hazard Class 4.2
UN Number UN1384
Packing Group II

DETAILS

REFERENCES

  • Useful reducing agent for a variety of functional groups. Often used in aqueous mixtures in combination with a base such as bicarbonate to prevent decomposition of the reagent by acid.
  • Examples of reductions with the reagent:
  • Nitroso compounds to amines: Org. Synth. Coll., 2, 33 (1943); 4, 247, (1963). Azo compounds to amines: Org. Synth. Coll., 1, 49 (1941); 2, 35, 39 (1943). Quinones to hydroquinones: Org. Synth. Coll., 4, 16 (1963). Aldehydes and ketones to alcohols: Synthesis, 246 (1977); for a phase-transfer method giving improved yields, see: J. Chem. Soc., Chem. Commun., 1080 (1979). For selective 1,4-reduction of conjugated aldehydes and ketones in the presence of unconjugated, see: Tetrahedron Lett., 36, 1107 (1995). Dehalogenation of ɑ-halo ketones: Synth. Commun., 12, 261 (1982).
  • For a review of reductions with dithionite, including nitrogen functions, carbonyl compounds and 1,4-reductions of enones, see: Bull. Soc. Chim. Fr., 565 (1986).
  • Also useful in small amounts as a decolorizing agent in the purification of organic compounds; see, e.g.: Org. Synth. Coll., 3, 86, 637 (1955); 4, 45 (1963).