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104548-30-3

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104548-30-3 Usage

Description

OXONE TETRABUTYLAMMONIUM SALT is a versatile and efficient oxidizing agent that is widely used in various chemical reactions and industries due to its unique properties and ability to catalyze a range of oxidation processes.

Uses

Used in Chemical Synthesis:
OXONE TETRABUTYLAMMONIUM SALT is used as a reagent for the oxidation of Hantzsch 1,4-Dihydropyridines catalyzed by manganese(III) Schiff Base complexes. This application is crucial in the synthesis of various organic compounds and pharmaceuticals.
Used in Pharmaceutical Industry:
OXONE TETRABUTYLAMMONIUM SALT is used as a reagent for the epoxidation of alkenes, which is an essential step in the synthesis of various pharmaceutical compounds, including antibiotics and other therapeutic agents.
Used in Petrochemical Industry:
OXONE TETRABUTYLAMMONIUM SALT is used as a reagent for the oxidation of sulfides and olefins, which are key processes in the production of various petrochemical products and intermediates.
Used in Fine Chemicals Industry:
OXONE TETRABUTYLAMMONIUM SALT is used as a reagent for the oxidation of alcohols, which is an important reaction in the synthesis of fine chemicals, fragrances, and flavor compounds.
Used in Dye and Pigment Industry:
OXONE TETRABUTYLAMMONIUM SALT is used as a reagent for the oxidation of aromatic amines, which is a critical step in the synthesis of azoxy arenes, a class of compounds used as intermediates in the production of dyes and pigments.

Check Digit Verification of cas no

The CAS Registry Mumber 104548-30-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,5,4 and 8 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104548-30:
(8*1)+(7*0)+(6*4)+(5*5)+(4*4)+(3*8)+(2*3)+(1*0)=103
103 % 10 = 3
So 104548-30-3 is a valid CAS Registry Number.

104548-30-3 Well-known Company Product Price

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  • Aldrich

  • (75920)  OXONE®tetrabutylammoniumsalt  technical, ~1.6% active oxygen basis

  • 104548-30-3

  • 75920-25G

  • 1,381.77CNY

  • Detail
  • Aldrich

  • (75920)  OXONE®tetrabutylammoniumsalt  technical, ~1.6% active oxygen basis

  • 104548-30-3

  • 75920-100G

  • 5,162.04CNY

  • Detail

104548-30-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name hydrogen sulfate,oxido hydrogen sulfate,tetrabutylazanium,sulfate

1.2 Other means of identification

Product number -
Other names Oxone tetrabutylammonium salt

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:104548-30-3 SDS

104548-30-3Relevant articles and documents

Catalytic epoxidation of cis-stilbene and naphthalene by tetra-n-butylammonium hydrogen monopersulfate in the presence of manganese(III) tetraarylporphyrins and various anionic co-catalysts

Solati, Zahra,Hashemi, Majid,Keshavarzi, Ahmad,Rafiee, Ezzat

, p. 149 - 153 (2012)

The epoxidation of cis-stilbene by n-Bu4NHSO5 was studied in the presence of two different manganese porphyrin complexes, [MnTPFPP(Cl) and MnTPP(Cl)], and various n-Bu4NX (X = OAc, F, Cl, Br, OCN, NO3, BF4). In general direct correlation was found between stereoselectivity of the epoxidation reaction and the nucleophilic properties of these anionic co-catalysts. Also epoxidation of naphthalene was carried out in high yield and good selectivity by n-Bu4NHSO 5 in the presence of MnTPFPP(Cl) in association with n-Bu 4NOAc or n-Bu4NF co-catalysts.

Tetra-n-butylammonium Oxone. Oxidations under Anhydrous Conditions

Trost, Barry M.,Braslau, Rebecca

, p. 532 - 537 (2007/10/02)

Tetra-n-butylammonium Oxone, readily prepared as a white solid from commercially available Oxone, performs oxidations in anhydrous methylene chloride.Under these conditions, sulfides are oxidized to sulfones in the presence of amines, ketones, esters, car

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