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2565-87-9

  • Product Name:phosphocitrate
  • Molecular Formula:C6H9O10P
  • Molecular Weight:272.105
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Product Details

pd_meltingpoint:>300℃

Purity:99%

Reputable manufacturer supply phosphocitrate 2565-87-9 in stock with high standard

  • Molecular Formula:C6H9O10P
  • Molecular Weight:272.105
  • Vapor Pressure:1.21E-09mmHg at 25°C 
  • Melting Point:>300℃ 
  • Refractive Index:1.589 
  • Boiling Point:457.6 °C at 760 mmHg 
  • Flash Point:230.5 °C 
  • PSA:188.47000 
  • Density:1.985 g/cm3 
  • LogP:-1.13150 

phosphocitrate(Cas 2565-87-9) Usage

General Description

Phosphocitrate is a novel biochemical compound, consisting of a phosphorylated form of citrate, which has shown promising potential as a therapeutic agent in the treatment of various musculoskeletal disorders. Phosphocitrate has been found to inhibit the formation and growth of hydroxyapatite crystals that are responsible for the development of conditions such as osteoarthritis and kidney stone formation. Additionally, phosphocitrate has demonstrated anti-inflammatory and anti-catabolic properties, making it a potential candidate for the management of joint diseases and other related disorders. Its ability to modulate bone and cartilage metabolism, as well as its safety profile, make phosphocitrate a valuable target for further research and development in the field of musculoskeletal medicine.

InChI:InChI=1/C6H9O10P/c7-3(8)1-6(5(11)12,2-4(9)10)16-17(13,14)15/h1-2H2,(H,7,8)(H,9,10)(H,11,12)(H2,13,14,15)

2565-87-9 Relevant articles

A novel strategy for the preparation of naturally occurring phosphocitrate and its partially esterified derivatives

Turhanen, Petri A.,Demadis, Konstantinos D.,Peraeniemi, Sirpa,Vepsaelaeinen, Jouko J.

, p. 1468 - 1471 (2007)

(Chemical Equation Presented) A novel me...

Synthesis via a cyclic dioxatrichlorophosphorane of 1,3-dibenzyl-2-phosphonooxy citrate

Pankowski, Andrew H.,Meehan, John D.,Sallis, John D.

, p. 927 - 930 (2007/10/02)

Phosphorylation of tribenzyl citrate wit...

CHEMICALLY MODIFIED PHOSPHOCITRATE AND ENTRAPMENT IN MICROPARTICLES FOR SUSTAINED INHIBITION OF BIOMINERALIZATION

Sallis, John,Meehan, John,Kamperman, Harold,Anderson, Maree

, p. 281 - 284 (2007/10/02)

Synthesis of glycolamide esters of phosp...

2565-87-9 Process route

tribenzyl citrate
631-25-4

tribenzyl citrate

2-phosphonooxy-1,2,3-propane tricarboxylic acid
2565-87-9

2-phosphonooxy-1,2,3-propane tricarboxylic acid

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1: PCl5 / benzene / 0.5 h / 5 °C
2: H2O / 0.5 h
3: H2 / Pd/C
With phosphorus pentachloride; water; hydrogen; palladium on activated charcoal; In benzene;
Multi-step reaction with 5 steps
1: 1.) NaOH
3: H2 / Pd/C
4: H2 / PtO2
5: 90 percent / 0.17 h / pseudo-cholinesterase
With sodium hydroxide; hydrogen; platinum(IV) oxide; palladium on activated charcoal;
Multi-step reaction with 5 steps
1: 1.) NaOH
3: H2 / Pd/C
4: H2 / PtO2
5: 90 percent / 0.17 h / pseudo-cholinesterase
With sodium hydroxide; hydrogen; platinum(IV) oxide; palladium on activated charcoal;
citric acid triethyl ester
77-93-0

citric acid triethyl ester

2-phosphonooxy-1,2,3-propane tricarboxylic acid
2565-87-9

2-phosphonooxy-1,2,3-propane tricarboxylic acid

Conditions
Conditions Yield
Multi-step reaction with 4 steps
1: 100 percent Spectr. / Et3N / diethyl ether / 24 h / 20 °C
2: Et3N / diethyl ether / 20 °C
3: SO2Cl2 / diethyl ether / 1 h / 20 °C
4: HCl / 20 h / 38 - 40 °C
With hydrogenchloride; sulfuryl dichloride; triethylamine; In diethyl ether;
Multi-step reaction with 3 steps
1: pyridine
2: platinum; ethanol / Hydrogenation
3: aq. NaOH solution / Hydrogenation
With pyridine; sodium hydroxide; ethanol; platinum;

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