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22987-21-9

22987-21-9 Structure

22987-21-9 Structure
IdentificationBack Directory
[Name]

2-HYDROXYETHYL PHOSPHONIC ACID
[CAS]

22987-21-9
[Synonyms]

BRN 1751212
Einecs 245-370-6
2-HYDROXYETHYL PHOSPHONIC ACID
(2-hydroxyethyl)-phosphonicaci
2-Hydroxyethanephosphonic acid
Phosphonic acid, (2-hydroxyethyl)-
P-(2-Hydroxyethyl)-phosphonic Acid
Phosphonic acid, P-(2-hydroxyethyl)-
2-Hydroxyethyl phosphonic acid, 97 %
[EINECS(EC#)]

245-370-6
[Molecular Formula]

C2H7O4P
[MDL Number]

MFCD00043865
[MOL File]

22987-21-9.mol
[Molecular Weight]

126.05
Chemical PropertiesBack Directory
[Boiling point ]

398.8±44.0 °C(Predicted)
[density ]

1.611±0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,2-8°C
[solubility ]

DMSO (Sparingly), Methanol (Slightly)
[form ]

Colourless to Red Thick Oil to Semi-Solid
[pka]

2.25±0.10(Predicted)
[Appearance]

Colorless to light yellow Viscous Liquid
[Stability:]

Hygroscopic
[InChI]

InChI=1S/C2H7O4P/c3-1-2-7(4,5)6/h3H,1-2H2,(H2,4,5,6)
[InChIKey]

SEHJHHHUIGULEI-UHFFFAOYSA-N
[SMILES]

P(CCO)(=O)(O)O
Safety DataBack Directory
[Symbol(GHS) ]

Corrosion (GHS05)
GHS05
[Signal word ]

Danger
[Hazard statements ]

H314
[Precautionary statements ]

P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P363-P405-P501
Hazard InformationBack Directory
[Uses]

2-Hydroxyethanephosphonic acid is an substrate used in the study of 2-hydroxyethylphosphonate dioxygenase reaction mechanism. 2-Hydroxyethanephosphonic Acid is also a required intermediate in labelled Fosfomycin (F727502) biosynthesis.
[Uses]

2-Hydroxyethanephosphonic acid is an substrate used in the study of 2-hydroxyethylphosphonate dioxygenase reaction mechanism. 2-Hydroxyethanephosphonic Acid is also a required intermediate in labelled Fosfomycin (F727502) biosynthesis.
[Definition]

ChEBI: A phosphonic acid consisting of ethanol with the phospho group at the 2-position.
[Synthesis]

DIMETHYL 2-ACETOXYETHYLPHOSPHONATE

39118-50-8

2-HYDROXYETHYL PHOSPHONIC ACID

22987-21-9

The general procedure for the synthesis of (2-hydroxyethyl)phosphonic acid from ethyl 2-(dimethoxyphosphono)acetate was as follows: to a 500 mL four-necked round-bottomed flask equipped with a heating jacket, thermocouples, a 10-pallet old Shore column and distillation head, were added sequentially dimethyl-2-(acetoxy)ethyl phosphonate (293 g, 1.5 mol), AMBERLYST-15 ion exchange resin (48 g) and water (72 g, 4 mol). The reaction mixture was heated to 100 °C. After 15 hours of reaction, the reaction temperature was raised to 105°C. During this process, the vapor temperature frequently reached 95 °C and the distillate was mainly water. Subsequently, about 150 g of additional water was added to the reaction system and the volatile components were removed under vacuum, resulting in 168 g (89% yield) of hydroxyethylphosphonic acid. The method avoids the use of stoichiometric HCl, thereby reducing the generation of corrosive and carcinogenic by-products (e.g., hydrochloric acid and methyl chloride), which are mainly methanol and methyl acetate, as compared to conventional methods. In addition, the method offers the advantage of easy recovery and reuse of the ion exchange resin.

[References]

[1] Patent: US2015/361117, 2015, A1. Location in patent: Paragraph 0009
[2] Phosphorus and Sulfur and the Related Elements, 1982, vol. 13, p. 363 - 370
Spectrum DetailBack Directory
[Spectrum Detail]

2-HYDROXYETHYL PHOSPHONIC ACID(22987-21-9)1HNMR
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