Selenous acid

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Selenous acid[1]
Structural formula
Ball-and-stick model
Names
IUPAC names
Selenous acid
Selenic(IV) acid
Other names
Selenious acid
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
KEGG
UNII
  • InChI=1S/H2O3Se/c1-4(2)3/h(H2,1,2,3) checkY
    Key: MCAHWIHFGHIESP-UHFFFAOYSA-N checkY
  • InChI=1/H2O3Se/c1-4(2)3/h(H2,1,2,3)
    Key: MCAHWIHFGHIESP-UHFFFAOYAW
  • O[Se+]([O-])O
Properties
H2SeO3
Molar mass 128.97 g/mol
Appearance white hygroscopic crystals
Density 3.0 g/cm3
Melting point decomposes at 70 °C
very soluble
Solubility soluble in ethanol
Acidity (pKa) 2.46, 7.3[2]
Conjugate base Hydrogenselenite
−45.4·10−6 cm3/mol
Pharmacology
Intravenous infusion
Legal status
Related compounds
Other anions
selenic acid
hydrogen selenide
Other cations
sodium selenite
Related compounds
sulfurous acid
tellurous acid
polonous acid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references
Selenious Acid
External links
AHFS/Drugs.comMonograph
Legal
License data
Identifiers
DrugBank


Selenous acid (or selenious acid) is the chemical compound with the formula H2SeO3. Structurally, it is more accurately described by (HO)2SeO. It is the principal oxoacid of selenium; the other being selenic acid.

Uses

Industry

The major use is in protecting and changing the color of steel, especially steel parts on firearms.[3] The so-called cold-bluing process uses selenous acid, copper(II) nitrate, and nitric acid to change the color of the steel from silver-grey to blue-grey or black. Alternative procedures use copper sulfate and phosphoric acid instead. This process deposits a coating of copper selenide and is fundamentally different from other bluing processes which generate black iron oxide. Some older razor blades were also made of blued steel.[3]

Another use for selenious acid is the chemical darkening and patination of copper, brass and bronze, producing a rich dark brown color that can be further enhanced with mechanical abrasion.[citation needed]

It is used in organic synthesis as an oxidizing agent for the synthesis of 1,2-dicarbonyl compounds, e.g. in laboratory preparation of glyoxal (ethane-1,2-dione) from acetaldehyde.[4]

Selenious acid is a key component of the Mecke reagent used for drug checking.[5]

Medical

Selenious acid is a trace element indicated in people as a source of selenium.[6][7]

Side effects

Like many selenium compounds, selenous acid is highly toxic in excessive quantities, and ingestion of any significant quantity of selenous acid is usually fatal, however it is an approved dietary source in proper amounts. Symptoms of selenium poisoning can occur several hours after exposure, and may include stupor, nausea, severe hypotension and death.[8]

Formation and properties

Selenous acid is analogous to sulfurous acid, but it is more readily isolated. Selenous acid is easily formed upon the addition of selenium dioxide to water. As a crystalline solid, the compound can be seen as pyramidal molecules that are interconnected with hydrogen bonds. In solution it is a diprotic acid:[9]

H
2
SeO
3
H+
+ HSeO
3
 (pKa = 2.62)
HSeO
3
H+
+ SeO2−
3
 (pKa = 8.32)

It is moderately oxidizing in nature, but kinetically slow. In 1 M H+
:

H
2
SeO
3
+ 4 H+
+ 4 e ⇌ Se + 3 H
2
O
 (Eo = +0.74 V)

In 1 M OH
:

SeO2−
3
+ 4 e + 3 H
2
O
⇌ Se + 6 OH
 (Eo = −0.37 V)

Selenous acid is hygroscopic.[10][11]

References

  1. Lide DR (1998). Handbook of Chemistry and Physics (87 ed.). Boca Raton, Florida: CRC Press. pp. 4–81. ISBN 0-8493-0594-2.
  2. Ka and pKa for Polyprotic Acids. ucdsb.on.ca
  3. 3.0 3.1 Scarlato EA, Higa J (28 June 1990). "SELENIUM (PIM483)". Archived from the original on 29 September 2010. Retrieved 29 December 2010.
  4. "Glyoxal Bisulfite" Archived 2020-09-24 at the Wayback Machine, Organic Syntheses, Collected Volume 3, p.438 (1955).
  5. "Colour Test Reagents-Kits for Preliminary Identification of Drugs of Abuse" (PDF). National Institute of Justice. 2000-07-01. Archived (PDF) from the original on 2010-04-01. Retrieved 2012-01-26.
  6. "Selenious acid injection, solution". DailyMed. 1 May 2020. Archived from the original on 29 August 2021. Retrieved 22 October 2020.
  7. "Drug Approval Package: Selenious Acid Injection". U.S. Food and Drug Administration (FDA). Archived from the original on 3 December 2020. Retrieved 22 October 2020.
  8. "Material Safety Data Sheet - Product Name: Reagent for Special Opiates" (PDF). Sirchie Finger Print Laboratories, Inc. May 12, 2006. Archived from the original (PDF) on October 18, 2006.
  9. Holleman AF, Wiberg E (2001). Inorganic Chemistry. San Diego: Academic Press. ISBN 0-12-352651-5.
  10. Lide DR, ed. (1995). CRC Handbook of Chemistry and Physics (76th ed.). Boca Raton, FL: CRC Press Inc. pp. 4–82.
  11. "Selenious acid". PubChem. Archived from the original on 2020-09-24. Retrieved 2020-01-17.

External links

  • "Selenious acid". Drug Information Portal. U.S. National Library of Medicine. Archived from the original on 2021-08-29. Retrieved 2021-03-16.