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N hydroxyphthalimide nhpi

Manufactured by Merck Group
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Sourced in Poland, Germany

N-hydroxyphthalimide (NHPI) is a chemical compound used as a laboratory reagent. It serves as an oxidizing agent in various chemical reactions. NHPI is primarily utilized in organic synthesis and catalysis applications.

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Lab products found in correlation

Ethylbenzene, by Thermo Fisher Scientific (1 mentions) P chloranil, by Merck Group (1 mentions) Hydrogen peroxide, by Thermo Fisher Scientific (1 mentions) Co acac 2, by Merck Group (1 mentions)

Close spelling variants of this product

N-hydroxyphthalimide

3 protocols using n hydroxyphthalimide nhpi

1

Functionalized Carbon Nanotubes for Catalysts

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The following compounds were used as-received: multiwalled carbon nanotubes with carboxylic functional groups (MWCNT-COOH, 95% Cheaptubes, Grafton, VT, USA), ethylbenzene (99% Acros Organics), CoCl2 (POCH, Gliwice, Poland), CuCl2 (POCH, Gliwice, Poland), MnCl2 (POCH, Gliwice, Poland), N-hydroxyphthalimide (NHPI, Sigma-Aldrich, Steinheim, DE, USA), NH3 25 % solution (Chempur, Piekary Śląskie, Poland).
Peckh K, & Orlińska B. (2021). Transition Metal Salts of Carboxylated Multiwalled Carbon Nanotubes in Combination with N-hydroxyphthalimide as Catalytic Systems for Hydrocarbon Oxidation. Materials, 14(9), 2314.
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2

Tetrachloro-p-benzoquinone Oxidation

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Tetrachloro-1,4-benzoquinone (TCBQ; tetrachloro-p-benzoquinone or p-chloranil), N-hydroxyphthalimide (NHPI), and all other chemicals were purchased from Sigma. The oxygen-18-enriched H2O (90%, [18O]-H2O) was purchased from J&K. The chemicals were used as received without further purification. All stock solutions (20 mM) were prepared by dissolving the chemicals in CH3CN.
Li F., Huang C.H., Xie L.N., Qu N., Shao J., Shao B, & Zhu B.Z. (2016). An Exceptionally Facile Two-Step Structural Isomerization and Detoxication via a Water-Assisted Double Lossen Rearrangement. Scientific Reports, 6, 39207.
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3

Olefin Oxidation Using Hydrogen Peroxide

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Alpha Plus C30+ olefins (Chevron-Phillips, Diegem, Belgium), hydrogen peroxide (30 or 50 wt.% in water, Acros Organics), tungstic acid (Fluka), cetyldimethyl(2-hydroxyethyl)ammonium dihydrogen phosphate (Luviquat, 30% in water, Aldrich, Steinheim, Germany), N-hydroxyphthalimide (NHPI, Sigma-Aldrich, Steinheim, Germany), Co(acac)2 (Sigma-Aldrich), and methylcyclohexane (MCH, Alfa Aesar, Karlsruhe, Germany) were commercially available and used without purification.
Peckh K., Lisicki D., Talik G, & Orlińska B. (2020). Oxidation of Long-Chain α-Olefins Using Environmentally-Friendly Oxidants. Materials, 13(20), 4545.
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