Sodium bisulfite

For research use only. Not for therapeutic Use.

  • CAT Number: R071132
  • CAS Number: 7631-90-5
  • Molecular Formula: NaHSO3in aqueous solution
  • Molecular Weight: 104.06
  • Purity: ≥95%
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Sodium bisulfite(Cat No.:R071132), is a chemical compound commonly used as a food preservative and a reducing agent in various industrial applications. In the food industry, it serves as a preservative and antioxidant, preventing the oxidation and discoloration of fruits and vegetables, and is used in the production of various processed foods, such as dried fruits and wines. In industrial processes, sodium bisulfite is employed for water treatment, particularly in the removal of chlorine and chloramine from water supplies. It also has applications in the photographic industry, as a bleach, and in pharmaceuticals for certain chemical reactions and as a preservative.


Catalog Number R071132
CAS Number 7631-90-5
Synonyms

NaHSO3.nH2O

Molecular Formula NaHSO3in aqueous solution
Purity ≥95%
Storage RT
IUPAC Name sodium;hydrogen sulfite
InChI InChI=1S/Na.H2O3S/c;1-4(2)3/h;(H2,1,2,3)/q+1;/p-1
InChIKey DWAQJAXMDSEUJJ-UHFFFAOYSA-M
SMILES OS(=O)[O-].[Na+]
Reference

<span style=”font-family:arial,helvetica,sans-serif;”><span style=”font-size:12px;”>1.<span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Hayatsu, Hikoya, et al. &quot;Reaction of sodium bisulfite with uracil, cytosine, and their derivatives.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Biochemistry</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;9.14 (1970): 2858-2865.<br />
2.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Abdolmaleky, Hamid Mostafavi, et al. &quot;Epigenetic alterations of the dopaminergic system in major psychiatric disorders.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Pharmacogenomics in drug discovery and development</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>. Humana Press, 2008. 187-212.<br />
3.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Arroyo‐Abad, Uriel, et al. &quot;Synthesis of two new arsenolipids and their identification in fish.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>European Journal of Lipid Science and Technology</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;118.3 (2016): 445-452.</span></span></span>

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