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Potassium arsenite

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Potassium arsenite
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.033.332 Edit this at Wikidata
EC Number
  • ortho: 236-680-2
UNII
  • InChI=1S/AsHO2.K/c2-1-3;/h(H,2,3);/q;+1/p-1
    Key: HEQWEGCSZXMIJQ-UHFFFAOYSA-M
  • ortho: InChI=1S/AsO3.3K/c2-1(3)4;;;/q-3;3*+1
    Key: OZYUYLWHROWIFJ-UHFFFAOYSA-N
  • meta: [O-][As]=O.[K+]
  • ortho: [K+].[K+].[K+].[O-][As]([O-])[O-]
Properties
AsKO2
Molar mass 146.019 g/mol
Appearance white hygroscopic powder
Density 8.76 g/cm3[dubious – discuss]
Melting point ~ 300 °C (572 °F; 573 K) (decomposes)
slightly soluble
Hazards
Lethal dose or concentration (LD, LC):
14 mg/kg (oral, rat)[2]
NIOSH (US health exposure limits):
PEL (Permissible)
 [1910.1018] TWA 0.010 mg/m3[1]
REL (Recommended)
 Ca C 0.002 mg/m3 [15-minute][1]
IDLH (Immediate danger)
 Ca [5 mg/m3 (as As)][1]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Potassium arsenite (KAsO2) is an inorganic compound that exists in two forms, potassium meta-arsenite (KAsO2) and potassium ortho-arsenite (K3AsO3). It is composed of arsenite ions (AsO33− or AsO2−) with arsenic always existing in the +3 oxidation state.[3] Like many other arsenic containing compounds, potassium arsenite is highly toxic and carcinogenic to humans. Potassium arsenite forms the basis of Fowler’s solution, which was historically used as a medicinal tonic, but was removed from market due to serious adverse effects.[4][5] Potassium arsenite is still, however, used as a rodenticide.[6]

Properties

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Potassium arsenite is an inorganic salt that exists as an odorless white solid. It is largely soluble in water and only slightly soluble in alcohol. Solutions of potassium arsenite contain moderate concentrations of hydroxide, and are thus slightly basic.[7] While potassium arsenite is noncombustible, heating it results in its decomposition and the formation of toxic fumes that include arsine, arsenic oxides, and potassium oxides. Potassium arsenite also reacts with acids to yield toxic arsine gas.[6]

The structure was determined by X-ray crystallography. As found for related As(III) compounds, the arsenic is pyramidal. The [AsO3]− subunits are connected by two bridging oxides.[8]

Preparation

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Aqueous potassium arsenite, more commonly known as Fowler’s solution, can be prepared by heating arsenic trioxide (As2O3) with potassium hydroxide (KOH) in the presence of water.[9][10] The reaction is shown below

As2O3 (aq) + 2 KOH (aq) → 2 KAsO2 (aq) + H2O

Uses

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In the eighteenth century English physician Thomas Fowler (1736–1801)[11] utilized potassium arsenite to remedy a number of conditions including anemia, rheumatism, psoriasis, eczema, dermatitis, asthma, cholera, and syphilis. Furthermore, in 1865 the potential uses of potassium arsenite expanded as Fowler’s solution was used as the first chemotherapeutic agent to treat leukemia, however the effects were only temporary. Surprisingly enough, this specific use was inspired by potassium arsenite’s role in improving digestion and producing a smoother coat in horses.[4] Potassium arsenite is also a key inorganic component of certain wood preservatives, rodenticides, insecticides, and herbicides.[7]

Health effects

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The toxicity of potassium arsenite arises from arsenic’s high affinity for sulfhydryl groups. The formation of these arsenite-sulfur bonds impairs the functionality of certain enzymes such as glutathione reductase, glutathione peroxidases, thioredoxin reductase, and thioredoxin peroxidase. These enzymes are all closely affiliated with the defense of free radicals and the metabolism of pyruvate. Thus, exposure to potassium arsenite and other arsenite containing compounds results in the production of damaging oxygen free radicals and the arrest of cellular metabolism.[12]

Additionally, arsenite containing compounds have also been labeled carcinogens. The carcinogenicity of potassium arsenite arises from its ability to inhibit DNA repair and methylation. This impairment of the cellular machinery can lead to cancer because the cells can no longer repair or arrest mutations and a tumor results.[13] All of these conditions exhibit the hazardous nature of potassium arsenite and other arsenite containing compounds. This is evidenced by a LD50 of 14 mg/kg for rats and a TDL of 74 mg/kg for humans.[14]

Notes

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  1. ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0038". National Institute for Occupational Safety and Health (NIOSH).
  2. ^ nih.gov
  3. ^ Lide, D. R. (1993). CRC Handbook Chemistry & Physics 74th Edition. CRC-Press. ISBN 0-8493-0474-1.
  4. ^ a b Jolliffe, D. M. (1993). "The history of the use of arsenicals in man". Journal of the Royal Society of Medicine. 86 (5): 287–289. doi:10.1177/014107689308600515. PMC 1294007. PMID 8505753.
  5. ^ Lander J.J.; Stanley R.J.; Sumner H.W.; Boswell D.C.; Aach R.D. (1975). "Angiosarcoma of the Liver associated with Fowler's Solution (Potassium Arsenite)". Gastroenterology. 68 (6): 1582–1586. doi:10.1016/S0016-5085(75)80148-X. PMID 1169181.
  6. ^ a b Potassium Arsenite. http://nj.gov/health/eoh/rtkweb/documents/fs/1557.pdf
  7. ^ a b U.S. Dept. of Health and Human Services, Public Health Service (October 2, 2014). "Arsenic and Inorganic Arsenic Compounds" (PDF). Report on Carcinogens, Thirteenth Edition.
  8. ^ Emmerling, Franziska; Röhr, Caroline (2003). "Die neuen Oxoarsenate(III) AAsO2 (A = Na, K, Rb) und Cs3As5O9. Darstellung, Kristallstrukturen und Raman-Spektren / The New Oxoarsenates(III) AAsO2 (A = Na, K, Rb) and Cs3As5O9. Synthesis, Crystal Structures and Raman Spectra". Zeitschrift für Naturforschung B. 58 (7): 620–626. doi:10.1515/znb-2003-0704.
  9. ^ Caspari, Charles (1901). A Treatise on Pharmacy for Students and Pharmacists (2nd ed.). Philadelphia: Lea Brothers and Co.
  10. ^ Tinwell, H.; Stephens, S. C.; Ashby, J. (1991). "Arsenite as the probable active species in the human carcinogenicity of arsenic: mouse micronucleus assays on Na and K arsenite, orpiment, and Fowler's solution". Environmental Health Perspectives. 95: 205–210. doi:10.2307/3431125. JSTOR 3431125. PMC 1568403. PMID 1821373.
  11. ^ Doyle, Derek (2009). "Notoriety to respectability: a short history of arsenic prior to its present day use in haematology". British Journal of Haematology. 145 (3): 309–317. doi:10.1111/j.1365-2141.2009.07623.x. PMID 19298591. S2CID 6676910.
  12. ^ Chen, Sai-Juan; Zhou, Guang-Biao; Zhang, Xiao-Wei; Mao, Jian-Hua; The ́, Hugues de; Chen, Zhu (16 June 2011). "From an old remedy to a magic bullet: molecular mechanisms underlying the therapeutic effects of arsenic in fighting leukemia". Blood. 117 (24): 6425–37. doi:10.1182/blood-2010-11-283598. PMC 3123014. PMID 21422471.
  13. ^ Xiong, Lei; Wang, Yinsheng (5 February 2010). "Quantitative Proteomic Analysis Reveals the Perturbation of Multiple Cellular Pathways in HL-60 Cells Induced by Arsenite Treatment". Journal of Proteome Research. 9 (2): 1129–1137. doi:10.1021/pr9011359. PMC 2819029. PMID 20050688.
  14. ^ "Potassium arsenite". TOXNET: Toxicology Data Network. Retrieved 6 December 2014.
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