Acetic acid, hydroxyphosphono-

Base Information

• Chemical Name: Acetic acid, hydroxyphosphono-
• CAS No.: 23783-26-8
• Deprecated CAS: 115469-15-3,153733-51-8
• Molecular Formula: C2H5O6P
• Molecular Weight: 156.032
• Hs Code.: 2931900090
• DSSTox Substance ID: DTXSID40865115
• Nikkaji Number: J211.538G
• Mol file: 23783-26-8.mol

Synonyms:2-hydroxy-2-phosphonoacetic acid;Acetic acid, hydroxyphosphono-;Acetic acid, 2-hydroxy-2-phosphono-;2-Hydroxyphosphonoacetic Acid;2-hydroxy-2-phosphono-acetic acid;Phosphono-hydroxy-acetic acid;SCHEMBL254667;2-hydroxy-2-phosphonoaceticacid;2-Hydroxyphosphonocarboxylic Acid;DTXSID40865115;.alpha.-Hydroxyphosphonoacetic acid;.alpha.-Hydroxyl phosphonoacetic acid;AKOS015892863;CS-0158494;FT-0694552;E77112;EC 405-710-8

Chemical Property of Acetic acid, hydroxyphosphono-

Chemical Property:

• Appearance/Colour: Dark brown liquid
• Vapor Pressure: 0.000278mmHg at 25°C
• Melting Point: 108-110oC
• Boiling Point: 557.7 °C at 760 mmHg
• PKA: 2.05±0.10(Predicted)
• Flash Point: 291.1 °C
• PSA: 134.10000
• Density: 2.131 g/cm³
• LogP: -1.50130
• Storage Temp.: -20°C
• XLogP3: -2.6
• Hydrogen Bond Donor Count: 4
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 2
• Exact Mass: 155.98237487
• Heavy Atom Count: 9
• Complexity: 156

Purity/Quality:

99% ^*data from raw suppliers

HPSE ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C
• Statements: 22-34-43-48/22
• Safety Statements: 1/2-22-26-36/37/39-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(C(=O)O)(O)P(=O)(O)O
• Uses: Hydroxyphosphono-acetic acid - 50% in water (cas# 23783-26-8) is used in preparation method of salt-resistant calcium-magnesium resistant polymer colloid system and its application in oil reservoir oil displacement.

Technology Process of Acetic acid, hydroxyphosphono-

There total 3 articles about Acetic acid, hydroxyphosphono- 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: 85.0%

dimethoxyphosphinyl-hydroxy-acetic acid butyl ester (17151-69-8) → 2-hydroxy-2-phosphonoacetic acid (23783-26-8)

Guidance literature:

With hydrogenchloride;

Reference yield:

Glyoxilic acid (298-12-4) → 2-hydroxy-2-phosphonoacetic acid (23783-26-8)

Guidance literature:

With P₄O₆; Yield given; inert solvent;

Reference yield:

→ 2-hydroxy-2-phosphonoacetic acid (23783-26-8)

Guidance literature:

upstream raw materials:

Glyoxilic acid

dimethoxyphosphinyl-hydroxy-acetic acid butyl ester

Refernces

• 1、 -. "Phosphonohydroxyacetonitrile, a process for its preparation and its use as an intermediate product for the preparation of medicaments". . . Retrieved 2008/06/13.