3D model (JSmol)
|UN number||UN 3264|
|Molar mass||66.00 g/mol|
|Appearance||colorless, deliquescent crystals or oily liquid|
1.22 g/cm3 (50 wt% aq. solution)
|Melting point||26.5 °C (79.7 °F; 299.6 K)|
|Boiling point||130 °C (266 °F; 403 K) decomposes|
|Solubility||very soluble in alcohol, ether|
|Safety data sheet||JT Baker|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|what is ?)(|
Hypophosphorous acid (HPA), or phosphinic acid, is a phosphorus oxyacid and a powerful reducing agent with molecular formula H3PO2. It is a colorless high-melting compound, which is soluble in water, dioxane, and alcohols. The formula for this acid is generally written H3PO2, but a more descriptive presentation is HOP(O)H2, which highlights its monoprotic character. Salts derived from this acid are called hypophosphites.
Preparation and availability
The acid is prepared industrially via a two step process: Firstly, hypophosphite salts of the alkali and alkaline earth metals result from the reaction of white phosphorus with hot aqueous solution of the appropriate hydroxide, e.g. Ca(OH)2.
- P4 + 4 OH− + 4 H2O → 4 H
2 + 2 H2
The salt is then treated with a strong, non-oxidizing acid to give the free hypophosphorous acid:
2 + H+ → H3PO2
HPA is usually supplied as a 50% aqueous solution. Anhydrous acid cannot be obtained by simple evaporation of the water, as the acid ready oxidises to phosphorous acid and phosphoric acid and also disproportionates to phosphorous acid and phosphine. Pure anhydrous hypophosphorous acid can be formed by the continuous extraction of aqueous solutions with diethyl ether.
Reactions and uses
In organic chemistry, H3PO2 can be used for the reduction of arenediazonium salts, converting ArN+
2 to Ar–H. When diazotized in a concentrated solution of hypophosphorous acid, an amine substituent can be removed from arenes.
Owing to its ability to function as a mild reducing agent and oxygen scavenger it is sometimes used as an additive in Fischer esterification reactions, where it prevents the formation of colored impurities.
It is used to prepare phosphinic acid derivatives.
DEA List I chemical status
Because hypophosphorous acid can reduce elemental iodine to form hydroiodic acid, which is a reagent effective for reducing ephedrine or pseudoephedrine to methamphetamine, the United States Drug Enforcement Administration designated hypophosphorous acid (and its salts) as a List I precursor chemical effective November 16, 2001. Accordingly, handlers of hypophosphorous acid or its salts in the United States are subject to stringent regulatory controls including registration, recordkeeping, reporting, and import/export requirements pursuant to the Controlled Substances Act and 21 CFR §§ 1309 and 1310.
Organophosphinic acids (Phosphinates)
Organophosphinic acids have the formula R2PO2H. The two hydrogen atoms directly bound to phosphorus in phosphinic acid are replaced by organic groups. For example, formaldehyde and H3PO2 react to give (HOCH2)2PO2H. Similarly, phosphinic acid adds to Michael acceptors, for example with acrylamide it gives H(HO)P(O)CH2CH2C(O)NH2. The Cyanex family of dialkylphosphinic acids are used in hydrometallurgy to extract metals from ores.
Few metal complexes have been prepared from H3PO2, one example is Ni(O2PH2)2.
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- ChemicalLand21 Listing
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- Dulong prepared acide hypo-phosphoreux by adding barium phosphide (Ba3P2) to water, which yielded phosphine gas (PH3), barium phosphate, and barium hypophosphite. Since the phosphine gas left the solution and the barium phosphate precipitated, only the barium hypophosphite remained in solution. Hypophosphorous acid could then be obtained from the filtrate by adding sulfuric acid, which precipitated barium sulfate, leaving hypophosphorous acid in solution. See:
- Dulong (1816) "Extrait d'un mémoire sur les combinaisons du phosphore avec l'oxigène" (Extract from a memoir on the compounds of phosphorus with oxygen), Annales de Chimie et de Physique, 2 : 141–150. [in French]
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- Robison, M. M.; Robison, B. L. "2,4,6-Tribromobenzoic acid". Organic Syntheses. 36: 94.; Collective Volume, 4
- Kornblum, N. (1941). "3,3′-Dimethoxybiphenyl and 3,3′-Dimethylbiphenyl". Organic Syntheses. 21: 30. doi:10.15227/orgsyn.021.0030.
- Karla Bravo-Altamirano, Jean-Luc Montchamp (2008). "Palladium-Catalyzed Dehydrative Allylation of Hypophosphorous Acid with Allylic Alcohols". Org. Synth. 85: 96. doi:10.15227/orgsyn.085.0096.CS1 maint: Uses authors parameter (link)
- Gordon, P. E.; Fry, A. J.; Hicks, L. D. (23 August 2005). "Further studies on the reduction of benzylic alcohols by hypophosphorous acid/iodine" (PDF). ARKIVOC. 2005 (vi): 393–400. ISSN 1424-6376.
- 66 FR 52670—52675. 17 October 2001.
- 21 CFR 1309
- 21 USC, Chapter 13 (Controlled Substances Act)