potassium butyrate

Base Information

• Chemical Name: potassium butyrate
• CAS No.: 589-39-9
• Molecular Formula: C4H7KO2
• Molecular Weight: 126.197
• Hs Code.: 2915600000
• Mol file: 589-39-9.mol

Synonyms:potassium n-butanoate;potassium n-butyrate;potassium butyrate (n);Butanoic acid,potassium salt;EINECS 209-647-5;potassium butanoate;Potassium butyrate;butyric acid,potassium butyrate;butyric acid,potassium salt;

Chemical Property of potassium butyrate

Chemical Property:

• Vapor Pressure: 1.35mmHg at 25°C
• Boiling Point: 164.3°Cat760mmHg
• Flash Point: 69.7°C
• PSA: 40.13000
• Density: g/cm³
• LogP: -0.46360

Purity/Quality:

99%, ^*data from raw suppliers

POTASSIUM BUTYRATE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of potassium butyrate

There total 5 articles about potassium butyrate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 96.0%

butan-1-ol (71-36-3) → potassium n-butyrate (589-39-9)

Guidance literature:

With C₁₈H₂₃IrN₃⁽¹⁺⁾*CF₃O₃S^(1-); potassium hydroxide; In toluene; at 120 ℃; for 40h;

DOI:10.1021/acscatal.8b00105

Reference yield:

C4H4F3O2(1-)*K(1+) (1449571-40-7) → potassium n-butyrate (589-39-9)

Guidance literature:

With ruthenium(III) chloride trihydrate; hydrogen; potassium hydroxide; In water; at 200 ℃; for 5h; under 20686.5 Torr;

DOI:10.1002/adsc.201200870

Reference yield:

di(4-butanoyloxybenzyl) methoxycarbonylmethylphosphonate (144758-72-5) → (4-hydroxyphenyl)methanol (623-05-2) + potassium n-butyrate (589-39-9) + C14H18O7P(1-)*K(1+)

Guidance literature:

In [D₃]acetonitrile; water-d2; at 37 ℃; Mechanism; potassium phosphate buffer, porcine liver carboxyesterase; half-live; also with human plasma;

upstream raw materials:

di(4-butanoyloxybenzyl) methoxycarbonylmethylphosphonate

lithium 4-butanoyloxybenzyl methoxycarbonylmethylphosphonate

water

1,1-dinitro-butane; potassium salt

Downstream raw materials:

propene

isopropyl alcohol

2-hydroxyethyl butanoate

hexanoic acid

Refernces

• 1、 Cherepakhin, Valeriy,Williams, Travis J.. "Iridium catalysts for acceptorless dehydrogenation of alcohols to carboxylic acids: Scope and mechanism". . p. 3754 - 3763. Retrieved 2018/05/23.
• 2、 Mitchell, Anthony G.,Thomson, William,Nicholls, Dave,Irwin, William J.,Freeman, Sally. "Bioreversible Protection for the Phospho Group: Bioactivation of the Di(4-acyloxybenzyl) and Mono(4-acyloxybenzyl) Phosphoesters of Methylphosphonate and Phosphonoacetate". . p. 2345 - 2354. Retrieved 2007/10/02.