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Details

Stereochemistry ACHIRAL
Molecular Formula O3S
Molecular Weight 80.063
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge -2

SHOW SMILES / InChI
Structure of SULFITE ION

SMILES

[O-]S([O-])=O

InChI

InChIKey=LSNNMFCWUKXFEE-UHFFFAOYSA-L
InChI=1S/H2O3S/c1-4(2)3/h(H2,1,2,3)/p-2

HIDE SMILES / InChI

Molecular Formula H2O3S
Molecular Weight 82.079
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Sulfites are compounds that contain the sulfite ion. The sulfite ion is the conjugate base of bisulfite. Although its acid is elusive, its salts are widely used. Sulfite is used in the photography industry to protect developing solutions from oxidation, in the pulp and paper industry, in water treatment as an oxygen scavenger agent, as a desulfurizing and dechlorinating agent in the leather industry and as a bleaching agent in textile industry. Sodium sulfite is a component in many pharmaceuticals, which is effective to maintain the potency and stability of drugs. It is added to a number of drug preparations as an antioxidant and antimicrobial agent. Sulfite is used as a food preservative. Topical, oral or parenteral exposure to sulphites has been reported to induce a range of adverse clinical effects in sensitive individuals, ranging from dermatitis, urticaria, flushing, hypotension, abdominal pain and diarrhoea to life-threatening anaphylactic and asthmatic reactions. Exposure to the sulphites arises mainly from the consumption of foods and drinks that contain these additives; however, exposure may also occur through the use of pharmaceutical products, as well as in occupational settings. Sulfite is accepted for use as a food additive in Europe. Sodium sulfite is generally recognized as safe by FDA. It is included in FDA Inactive Ingredients Database (epidural, IM, IV, and SC injections; inhalation solution; ophthalmic solutions; oral syrups and suspensions; otic solutions; topical creams and emulsions). Included in nonparenteral medicines licensed in the UK.

Approval Year

PubMed

PubMed

TitleDatePubMed
High performance liquid chromatographic determination of bound sulfide and sulfite and thiosulfate at their low levels in human serum by pre-column fluorescence derivatization with monobromobimane.
1992 Nov
Comparison of a new, bismuth-iron-sulfite-cycloserine agar for isolation of Clostridium perfringens with the tryptose-sulfite-cycloserine and blood agars.
1997 Feb
Nutritional aspects of dissimilatory sulfate reduction in the human large intestine.
1997 Nov
Sulfite is released by human neutrophils in response to stimulation with lipopolysaccharide.
1998 Nov
Ahomocysteinemia in molybdenum cofactor deficiency.
1998 Sep
Probing the interaction of dengue virus envelope protein with heparin: assessment of glycosaminoglycan-derived inhibitors.
2001 Jun 21
The effect of a denture adhesive on the colonization of Candida species in vivo.
2003 Sep
A mechanism of sulfite neurotoxicity: direct inhibition of glutamate dehydrogenase.
2004 Oct 8
Patents

Sample Use Guides

The acceptable daily intake for sodium sulfite has been set at up to 350 mg/kg body-weight daily.
Route of Administration: Oral
Sulfite was rapidly converted to sulfate by isolated rat hepatocytes at concentrations ranging from 200 umol/L to 2 mmol/L. Incubation of isolated rat hepatocytes with 0.5, 1, or 2 mmol/L sulfite resulted in a time-dependent increase in the amount of free glutathione, but not cysteine, associated with the cells.
Substance Class Chemical
Created
by admin
on Sat Dec 16 01:41:23 GMT 2023
Edited
by admin
on Sat Dec 16 01:41:23 GMT 2023
Record UNII
15744271E9
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SULFITE ION
Common Name English
SULFUROUS ACID, ION(2-)
Common Name English
SULFITE(2-)
Common Name English
SULFITE DIANION
Common Name English
SULFITE
Systematic Name English
SULFITE (SO32-)
Common Name English
Code System Code Type Description
EPA CompTox
DTXSID4049791
Created by admin on Sat Dec 16 01:41:23 GMT 2023 , Edited by admin on Sat Dec 16 01:41:23 GMT 2023
PRIMARY
FDA UNII
15744271E9
Created by admin on Sat Dec 16 01:41:23 GMT 2023 , Edited by admin on Sat Dec 16 01:41:23 GMT 2023
PRIMARY
CHEBI
17359
Created by admin on Sat Dec 16 01:41:23 GMT 2023 , Edited by admin on Sat Dec 16 01:41:23 GMT 2023
PRIMARY
PUBCHEM
1099
Created by admin on Sat Dec 16 01:41:23 GMT 2023 , Edited by admin on Sat Dec 16 01:41:23 GMT 2023
PRIMARY
CHEBI
26823
Created by admin on Sat Dec 16 01:41:23 GMT 2023 , Edited by admin on Sat Dec 16 01:41:23 GMT 2023
PRIMARY
CHEBI
48854
Created by admin on Sat Dec 16 01:41:23 GMT 2023 , Edited by admin on Sat Dec 16 01:41:23 GMT 2023
PRIMARY
CAS
14265-45-3
Created by admin on Sat Dec 16 01:41:23 GMT 2023 , Edited by admin on Sat Dec 16 01:41:23 GMT 2023
PRIMARY
Related Record Type Details
ACTIVE MOIETY