Magnesium Monoperoxyphthalate

Magnesium monoperoxyphthalate
Names
	Preferred IUPAC name Magnesium bis(2-carbonoperoxoylbenzoate)
	Other names H48; MMPP
Identifiers
CAS Number	78948-87-5;
3D model (JSmol)	Interactive image;
ChemSpider	2006682;
EC Number	279-013-0;
PubChem CID	3081588;
UNII	YN884S965H;
	SMILES [Mg++].OOC(=O)C1=CC=CC=C1C([O-])=O.OOC(=O)C1=CC=CC=C1C([O-])=O;
Properties
Chemical formula	C16H10MgO10
Molar mass	386.551 g·mol−1
Hazards
Flash point	173.4 °C (344.1 °F; 446.5 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Magnesium monoperoxyphthalate (MMPP) is a water-soluble peroxy acid used as an oxidant in organic synthesis. Its main areas of use are the conversion of ketones to esters (Baeyer-Villiger oxidation), epoxidation of alkenes (Prilezhaev reaction), oxidation of sulfides to sulfoxides and sulfones, oxidation of amines to produce amine oxides, and in the oxidative cleavage of hydrazones.^[1]

Due to its insolubility in non-polar solvents MMPP has seen less use than the more widely used meta-chloroperoxybenzoic acid (mCPBA). Although work up procedures are more simply handled in polar solvents, usage of MMPP to oxidize nonpolar substrates in biphasic media combined with a phase transfer catalyst have been inefficient.^[1] Despite this MMPP has certain advantages over mCPBA including a lower cost of production and increased stability.^[1]

MMPP is also used as the active ingredient in certain surface disinfectants such as Dismozon Pur.^[2] As a surface disinfectant MMPP exhibits a broad spectrum biocidal effect including inactivation of endospores.^[3] Its wide surface compatibility enables its use on sensitive materials, such as plastic and rubber equipment used in hospitals. Additionally MMPP has been investigated as a potential antibacterial agent for mouthwashes and toothpaste.^[4]

References

↑ ^1.0 ^1.1 ^1.2 Carvalho, João F.S.; Silva, M. Manuel Cruz; Sá e Melo, M. Luisa (2009). "Highly efficient epoxidation of unsaturated steroids using magnesium bis(monoperoxyphthalate) hexahydrate". Tetrahedron 65 (14): 2773–81. doi:10.1016/j.tet.2009.01.100.
↑ "Magnesium Monoperoxyphthalate". ndrugs. http://www.ndrugs.com/?s=Magnesium Monoperoxyphthalate. Retrieved 19 December 2013.
↑ Baldry, M.G.C. (1984). "The antimicrobial properties of magnesium monoperoxyphthalate hexahydrate". Journal of Applied Bacteriology 57 (3): 499–503. doi:10.1111/j.1365-2672.1984.tb01416.x. PMID 6397460.
↑ Scully, Crispian; El-Kabir, Mohamed; Greenman, John; Porter, Stephen R.; Mutlu, Serdar; Barton, Ian; Adair, Richard (1999). "The effects of mouth rinses and dentifrice-containing magnesium monoperoxyphthalate (mmpp) on oral microflora, plaque reduction, and mucosa". Journal of Clinical Periodontology 26 (4): 234–8. doi:10.1034/j.1600-051X.1999.260406.x. PMID 10223394.

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[Carvalho-1] 1.0 ^1.1 ^1.2 Carvalho, João F.S.; Silva, M. Manuel Cruz; Sá e Melo, M. Luisa (2009). "Highly efficient epoxidation of unsaturated steroids using magnesium bis(monoperoxyphthalate) hexahydrate". Tetrahedron 65 (14): 2773–81. doi:10.1016/j.tet.2009.01.100.

[ndrugs-2] "Magnesium Monoperoxyphthalate". ndrugs. http://www.ndrugs.com/?s=Magnesium Monoperoxyphthalate. Retrieved 19 December 2013.

[Baldry-3] Baldry, M.G.C. (1984). "The antimicrobial properties of magnesium monoperoxyphthalate hexahydrate". Journal of Applied Bacteriology 57 (3): 499–503. doi:10.1111/j.1365-2672.1984.tb01416.x. PMID 6397460.

[Scully-4] Scully, Crispian; El-Kabir, Mohamed; Greenman, John; Porter, Stephen R.; Mutlu, Serdar; Barton, Ian; Adair, Richard (1999). "The effects of mouth rinses and dentifrice-containing magnesium monoperoxyphthalate (mmpp) on oral microflora, plaque reduction, and mucosa". Journal of Clinical Periodontology 26 (4): 234–8. doi:10.1034/j.1600-051X.1999.260406.x. PMID 10223394.