239321

Solfito di sodio

ACS reagent, ≥98.0%

• Formula condensata: Na₂SO₃
• Numero CAS: 7757-83-7
• Peso molecolare: 126.04
• Numero CE: 231-821-4
• Numero MDL: MFCD00003503
• Codice UNSPSC: 12352302
• ID PubChem: 329752528
• NACRES: NA.21

Proprietà

• Grado: ACS reagent
• agenzia: suitable for SM 5210
• Saggio: ≥98.0%
• Stato: powder or crystals
• Impurezze: Free acid, passes test; ≤0.005% insolubles; ≤0.03 meq/g Titr. free base
• pH: 9.0-10.5 (25 °C, 126 g/L)
• Solubilità: water: soluble 126 g/L at 20 °C
• Anioni in tracce: chloride (Cl^-): ≤0.02%
• Cationi in tracce: Fe: ≤0.001%; heavy metals (as Pb): ≤0.001%
• Stringa SMILE: [Na+].[Na+].[O-]S([O-])=O
• InChI: 1S/2Na.H2O3S/c;;1-4(2)3/h;;(H2,1,2,3)/q2*+1;/p-2; GEHJYWRUCIMESM-UHFFFAOYSA-L

Descrizione

Descrizione generale

Sodium sulfite is a water-soluble inorganic salt that is commonly used as a reducing agent. It is also used for sulfonation and sulfomethylation reactions. Additionally, it is used in the textile industry as a bleaching, de-sulfurizing, and dechlorinating agent. As an oxygen and free chlorine scavenger, Na₂SO₃ is employed in the water treatment process. Sodium sulfite participates in the purification and isolation of aldehydes and ketones by forming adducts with them. Other uses include the production of sodium thiosulfate, detergents, and dyes.

Applicazioni

Sodium sulfite can be used:

• As a reducing agent in the hydroxylation of arylboronic acids and arylboronic esters into corresponding phenols.
• In the transformation of α-amino alcohol methanesulfonate hydrochlorides to sodium α-amino alkanesulfonates.
• As a SO₂ precursor in the multigram synthesis of DABCO·(SO₂)₂ abbreviated as DABSO.

Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 13 - Non Combustible Solids
• Classe di pericolosità dell'acqua (WGK): WGK 1
• Punto d’infiammabilità (°F): Not applicable
• Punto d’infiammabilità (°C): Not applicable