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14518-69-5

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14518-69-5 Usage

Uses

Different sources of media describe the Uses of 14518-69-5 differently. You can refer to the following data:
1. Tetrabutylphosphonium Hydroxide (TBPH) is a quaternary phosphonium salt. It is an effective catalyst in a variety of reactions. It is a strong base that can be used as a strong organic base catalyst. Its basicity combined with its function as phase transfer catalyst makes it a versatile catalyst in many biphasic organic transitions used in the manufacture of polymers, pharmaceuticals, agrochemicals, flavors and fragrances. Also it finds use as (trans)esterification catalyst for the preparation of several monomers,polymers and a cleaning agent for printed circuit boards and semiconductor wafers. Applications: Glycidyl Ether Intermediates used in pharmaceutical applications. Chemicals for Polymer Applications.
2. Tetrabutylphosphonium Hydroxide is a phase transfer catalyst for the etherification of thiosalicylic acid and analogs. Tetrabutylphosphonium Hydroxide is a pretreatment for rice husks that enhances enzymic and acid hydrolysis yields. Tetrabutylphosphonium Hydroxide is used in the synthesis of tetrabutylphosphonium carboxylate as a recyclable and highly selective catalysts for alcoholysis reaction of propylene oxide.

Check Digit Verification of cas no

The CAS Registry Mumber 14518-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,5,1 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 14518-69:
(7*1)+(6*4)+(5*5)+(4*1)+(3*8)+(2*6)+(1*9)=105
105 % 10 = 5
So 14518-69-5 is a valid CAS Registry Number.
InChI:InChI=1/C16H36P.H2O/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;/h5-16H2,1-4H3;1H2/q+1;/p-1

14518-69-5 Well-known Company Product Price

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  • Alfa Aesar

  • (41718)  Tetra-n-butylphosphonium hydroxide, 40% w/w aq. soln.   

  • 14518-69-5

  • 50ml

  • 486.0CNY

  • Detail
  • Alfa Aesar

  • (41718)  Tetra-n-butylphosphonium hydroxide, 40% w/w aq. soln.   

  • 14518-69-5

  • 250ml

  • 1916.0CNY

  • Detail
  • Alfa Aesar

  • (41718)  Tetra-n-butylphosphonium hydroxide, 40% w/w aq. soln.   

  • 14518-69-5

  • 1L

  • 5376.0CNY

  • Detail
  • Aldrich

  • (438294)  Tetrabutylphosphoniumhydroxidesolution  40 wt. % in H2O

  • 14518-69-5

  • 438294-100ML

  • 1,070.55CNY

  • Detail

14518-69-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetra-n-Butylphosphonium Hydroxide

1.2 Other means of identification

Product number -
Other names Tetra-n-butylphosphonium hydroxide

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:14518-69-5 SDS

14518-69-5Relevant articles and documents

Enhanced CO2 uptake by intramolecular proton transfer reactions in amino-functionalized pyridine-based ILs

Pan, Mingguang,Vijayaraghavan,Zhou, Fengling,Kar, Mega,Li, Haoran,Wang, Congmin,MacFarlane, Douglas R.

, p. 5950 - 5953 (2017)

This work presents a new strategy for the promotion of CO2 uptake by an intramolecular proton transfer reaction in amino functionalized hydroxypyridine based anions.

Peroxotantalate-Based Ionic Liquid Catalyzed Epoxidation of Allylic Alcohols with Hydrogen Peroxide

Ma, Wenbao,Chen, Chen,Kong, Kang,Dong, Qifeng,Li, Kun,Yuan, Mingming,Li, Difan,Hou, Zhenshan

, p. 7287 - 7296 (2017/05/31)

The efficient and environmentally benign epoxidation of allylic alcohols has been attained by using new kinds of monomeric peroxotantalate anion-functionalized ionic liquids (ILs=[P4,4,4,n]3[Ta(O)3(η-O2)], P4,4,4,n=quaternary phosphonium cation, n=4, 8, and 14), which have been developed and their structures determined accordingly. This work revealed the parent anions of the ILs underwent structural transformation in the presence of H2O2. The formed active species exhibited excellent catalytic activity, with a turnover frequency for [P4,4,4,4]3[Ta(O)3(η-O2)] of up to 285 h?1, and satisfactory recyclability in the epoxidation of various allylic alcohols under very mild conditions by using only one equivalent of hydrogen peroxide as an oxidant. NMR studies showed the reaction was facilitated through a hydrogen-bonding mechanism, in which the peroxo group (O–O) of the peroxotantalate anion served as the hydrogen-bond acceptor and hydroxyl group in the allylic alcohols served as the hydrogen-bond donor. This work demonstrates that simple monomeric peroxotantalates can catalyze epoxidation of allylic alcohols efficiently.

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