Molecular structure of Magnesium monoperoxyphthalate hexahydrate, CAS Number: 84665-66-7
Magnesium monoperoxyphthalate hexahydrate (CAS 84665-66-7)
Application:
Magnesium monoperoxyphthalate hexahydrate is a mild, general oxidizing agent
CAS Number:
84665-66-7
Purity:
~80%
Molecular Weight:
494.64
Molecular Formula:
C16H10MgO10•6H2O
Supplemental Information:
This is as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.
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SDS & Certificate of Analysis
Magnesium monoperoxyphthalate hexahydrate is a mild, general oxidizing agent that is a suitable replacement for peroxycarboxylic acids and is capable of effecting many types of general oxidation reactions. It serves as a catalyst in various organic reactions and plays a role in the synthesis of numerous organic compounds, including dyes and polymers. Additionally, it is employed in the synthesis of various biomolecules and is utilized to investigate enzyme-catalyzed reactions.
Magnesium monoperoxyphthalate hexahydrate (CAS 84665-66-7) References
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- 1,1-dioxonaphtho[1,2-b]thiophene-2-methyloxycarbonyl (alpha-Nsmoc) and 3,3-dioxonaphtho[2,1-b]thiophene-2-methyloxycarbonyl (beta-Nsmoc) amino-protecting groups. | Carpino, LA., et al. 2007. J Org Chem. 72: 1729-36. PMID: 17286441
- Mutagenicity of aromatic amines and amides with chemical models for cytochrome P450 in Ames assay. | Inami, K., et al. 2009. Toxicol In Vitro. 23: 986-91. PMID: 19563884
- Efficacy of three surface disinfectants against spores of Clostridium difficile ribotype 027. | Horejsh, D. and Kampf, G. 2011. Int J Hyg Environ Health. 214: 172-4. PMID: 21134785
- Epidemiology and acquisition of extended-spectrum beta-lactamase-producing Enterobacteriaceae in a septic orthopedic ward. | Agostinho, A., et al. 2013. Springerplus. 2: 91. PMID: 23539506
- Enantiopure Trisubstituted Tetrahydrofurans with Appendage Diversity: Vinyl Sulfone- and Vinyl Sulfoxide-Modified Furans Derived from Carbohydrates as Synthons for Diversity Oriented Synthesis. | Dey, D. and Pathak, T. 2016. Molecules. 21: PMID: 27240328
- Catalytic Oxygenative Allylic Transposition of Alkenes into Enones with an Azaadamantane-Type Oxoammonium Salt Catalyst. | Nagasawa, S., et al. 2017. Chemistry. 23: 10276-10279. PMID: 28577334
- Unusual Oxidative Dimerization in the 3-Aminothieno[2,3-b]pyridine-2-carboxamide Series. | Stroganova, TA., et al. 2021. ACS Omega. 6: 14030-14048. PMID: 34124427
- Exhaustive Baeyer-Villiger oxidation: a tailor-made post-polymerization modification to access challenging poly(vinyl acetate) copolymers. | Ma, P., et al. 2022. Chem Sci. 13: 11746-11754. PMID: 36320906
- Semi-Synthesis and Biological Evaluation of 25(R)-26-Acetoxy-3β,5α-Dihydroxycholest-6-One. | Maimaitiming, M., et al. 2023. Mar Drugs. 21: PMID: 36976240
- The antimicrobial properties of magnesium monoperoxyphthalate hexahydrate. | Baldry, MG. 1984. J Appl Bacteriol. 57: 499-503. PMID: 6397460
Ordering Information
| Product Name | Catalog # | UNIT | Price | Qty | FAVORITES | |
Magnesium monoperoxyphthalate hexahydrate, 50 g | sc-252981 | 50 g | $47.00 | |||
Magnesium monoperoxyphthalate hexahydrate, 250 g | sc-252981A | 250 g | $129.00 |