Skip to Content
MilliporeSigma
All Photos(2)

Documents

283207

Sigma-Aldrich

Magnesium bis(monoperoxyphthalate) hexahydrate

greener alternative

80%, technical grade

Synonym(s):

MMPP

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
(HO2CC6H4CO3)2Mg·6H2O
Molecular Weight:
494.64
EC Number:
279-013-0
MDL number:
MFCD00149614
UNSPSC Code:
12352002
PubChem Substance ID:
24857092
NACRES:
NA.22

grade

technical grade

Quality Level

200

assay

80%

reaction suitability

reagent type: oxidant

greener alternative product characteristics

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

mp

93 °C (dec.) (lit.)

greener alternative category

Aligned,

SMILES string

O.O.O.O.O.O.OOC(=O)c1ccccc1C(=O)O[Mg]OC(=O)c2ccccc2C(=O)OO

InChI

1S/2C8H6O5.Mg.6H2O/c2*9-7(10)5-3-1-2-4-6(5)8(11)13-12;;;;;;;/h2*1-4,12H,(H,9,10);;6*1H2/q;;+2;;;;;;/p-2

InChI key

WWOYCMCZTZTIGU-UHFFFAOYSA-L

Looking for similar products? Visit Product Comparison Guide

Related Categories

General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product MMPP is an alternative to widely used oxidant MCPBA as it is cheap, stable in the solid state, safer in handling and easier to use and thus aligns with the principle "Designing Safer Chemicals". For more information see the below articles.
Magnesium bis(monoperoxyphthalate) hexahydrate as mild and efficient oxidant for the synthesis of selenones.
Magnesium Bis(monoperoxyphthalate) Hexahydrate (MMPP).
Highly efficient epoxidation of unsaturated steroids using magnesium bis(monoperoxyphthalate) hexahydrate.

Application

A safer, greener oxidizing reagent that is a suitable replacement for peroxycarboxylic acids and is capable of effecting many types of oxidation reactions.

Oxidation Reactions Using Magnesium Monoperphthalate: A Comparison with m-Chloroperoxybenzoic Acid
Reagent for:
  • Trans-diaxial hydroxylation under bismuth(III) triflate catalyst
  • Oxidation rections under mild conditions
  • Epoxidation of unsaturated steroids
  • Synthesis of ring-B oxygenated steroids as anticancer agents

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Eye Dam. 1 - Org. Perox. E - Skin Corr. 1C

Storage Class

5.2 - Organic peroxides and self-reacting hazardous materials

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Slide 1 of 1

1 of 1

Dichloromethane anhydrous, ≥99.8%, contains 40-150 ppm amylene as stabilizer

Sigma-Aldrich

270997

Dichloromethane

Ming-Yi Chen et al.
The Journal of organic chemistry, 69(8), 2884-2887 (2004-04-13)
A protocol that uses moist magnesium monoperoxyphthalate (MMPP) as an oxidant under microwave irradiation rapidly yields a variety of glycosyl sulfoxides from corresponding sulfides in high yields with high selectivity.
Chan-Woo Park et al.
Journal of microbiology and biotechnology, 27(7), 1359-1366 (2017-05-18)
(
Heaney, H.; Newbold, A. J.
Tetrahedron Letters, 42, 6607-6607 (2001)
Wasserman, H. H. et al
Tetrahedron Letters, 43, 3351-3351 (2002)
Broughan, P. et al
Synthesis, 1015-1015 (1987)
View All Related Papers

Articles

Oxidizing and Reducing Agents

Oxidation and reduction reactions are some of the most common transformations encountered in organic synthesis

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service