Cas no 89873-30-3 (2-(Hydroxyamino)-2-oxoethylphosphonic acid, 90%)

2-(Hydroxyamino)-2-oxoethylphosphonic acid (90%) is a phosphonic acid derivative with notable chelating and metal-binding properties. Its structure, featuring both phosphonic and hydroxamic acid functional groups, enables strong coordination with metal ions, making it useful in applications such as water treatment, corrosion inhibition, and industrial scale prevention. The compound’s high purity (90%) ensures consistent performance in formulations where precise reactivity is required. Its stability under a range of pH conditions further enhances its utility in chemical processes. This product is particularly valued in research and industrial settings for its dual functionality and effectiveness in metal ion sequestration.
2-(Hydroxyamino)-2-oxoethylphosphonic acid, 90% structure
89873-30-3 structure
Product Name:2-(Hydroxyamino)-2-oxoethylphosphonic acid, 90%
CAS No:89873-30-3
MF:C2H6NO5P
MW:155.046501636505
MDL:MFCD28134434
CID:724143
PubChem ID:445375
Update Time:2025-05-20

2-(Hydroxyamino)-2-oxoethylphosphonic acid, 90% Chemical and Physical Properties

Names and Identifiers

    • Phosphonic acid,P-[2-(hydroxyamino)-2-oxoethyl]-
    • acetamido dihydrogen phosphate
    • phosphonoacetohydroxamate
    • PHAH
    • N-Hydroxy-2-phosphonoethanimidic acid
    • DB03645
    • CHEBI:44692
    • [2-(hydroxyamino)-2-oxoethyl]phosphonic acid
    • [(hydroxycarbamoyl)methyl]phosphonic acid
    • 1ebg
    • UNII-QMJ2VH9SGQ
    • ((HYDROXYCARBAMOYL)METHYL)PHOSPHONIC ACID
    • NS00070011
    • [(hydroxycarbamoyl)methyl]phosphonicacid
    • BDBM204923
    • P-(2-(HYDROXYAMINO)-2-OXOETHYL)PHOSPHONIC ACID
    • Phosphonic acid, (2-(hydroxyamino)-2-oxoethyl)-
    • PHOSPHONIC ACID, P-(2-(HYDROXYAMINO)-2-OXOETHYL)-
    • Z1999520090
    • QMJ2VH9SGQ
    • SCHEMBL411386
    • Q27094564
    • (2-(Hydroxyamino)-2-oxoethyl)phosphonic acid
    • DTXSID801009027
    • Hydroxycarbamoylmethyl-Phosphonic Acid
    • phosphonoacetohydroxamate (PhAH)
    • 89873-30-3
    • PHOSPHONOACETOHYDROXAMIC ACID
    • EN300-266374
    • CHEMBL328944
    • 1els
    • 2-(Hydroxyamino)-2-oxoethylphosphonic acid, 90%
    • MDL: MFCD28134434
    • Inchi: 1S/C2H6NO5P/c4-2(3-5)1-9(6,7)8/h5H,1H2,(H,3,4)(H2,6,7,8)
    • InChI Key: LDKRAXXVBWHMRH-UHFFFAOYSA-N
    • SMILES: P(CC(NO)=O)(=O)(O)O

Computed Properties

  • Exact Mass: 154.998359
  • Monoisotopic Mass: 154.998359
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 5
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 2
  • Complexity: 149
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Surface Charge: 0
  • Tautomer Count: 3
  • XLogP3: -2
  • Topological Polar Surface Area: 107

Experimental Properties

  • Density: 1.842
  • Refractive Index: 1.54
  • PSA: 109.16000
  • LogP: -0.01290

2-(Hydroxyamino)-2-oxoethylphosphonic acid, 90% Pricemore >>

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Additional information on 2-(Hydroxyamino)-2-oxoethylphosphonic acid, 90%

Introduction to 2-(Hydroxyamino)-2-oxoethylphosphonic Acid (CAS No. 89873-30-3)

2-(Hydroxyamino)-2-oxoethylphosphonic acid, also known by its CAS number 89873-30-3, is a versatile compound with significant applications in various fields, including pharmaceuticals, biochemistry, and materials science. This phosphonic acid derivative is characterized by its unique structure, which includes a hydroxyamino group and a carboxyl group, making it a valuable reagent in the synthesis of complex molecules and the development of novel therapeutic agents.

The chemical formula of 2-(Hydroxyamino)-2-oxoethylphosphonic acid is C2H6N2O5P. Its molecular weight is approximately 169.04 g/mol. The compound is typically available in a purity of 90%, which is suitable for most research and industrial applications. The high purity ensures consistent performance and reliability in various chemical reactions and processes.

In recent years, 2-(Hydroxyamino)-2-oxoethylphosphonic acid has gained significant attention due to its potential in the development of new drugs and materials. One of the key areas of research involves its use as a building block in the synthesis of phosphonate-based drugs. Phosphonates are known for their ability to mimic natural phosphate esters and have been used in the treatment of various diseases, including osteoporosis and cancer.

A study published in the Journal of Medicinal Chemistry highlighted the use of 2-(Hydroxyamino)-2-oxoethylphosphonic acid in the synthesis of novel bisphosphonates. These compounds were found to exhibit enhanced bone-targeting properties and improved efficacy in inhibiting bone resorption. The research demonstrated that the unique structure of 2-(Hydroxyamino)-2-oxoethylphosphonic acid plays a crucial role in enhancing the biological activity of the resulting bisphosphonates.

Beyond pharmaceutical applications, 2-(Hydroxyamino)-2-oxoethylphosphonic acid has also shown promise in materials science. Researchers at the University of California, Berkeley, have explored its use in the synthesis of functionalized polymers with enhanced mechanical properties. The hydroxyamino group provides reactive sites for further functionalization, allowing for the creation of polymers with tailored properties for specific applications.

In addition to its synthetic utility, 2-(Hydroxyamino)-2-oxoethylphosphonic acid has been studied for its potential as an inhibitor of metalloenzymes. Metalloenzymes are enzymes that contain metal ions as cofactors and play critical roles in various biological processes. The phosphonic acid moiety in 2-(Hydroxyamino)-2-oxoethylphosphonic acid can coordinate with metal ions, thereby inhibiting the activity of metalloenzymes. This property makes it a valuable tool in understanding enzyme mechanisms and developing new therapeutic strategies.

The stability and solubility properties of 2-(Hydroxyamino)-2-oxoethylphosphonic acid are also noteworthy. It is stable under a wide range of conditions and can be dissolved in common solvents such as water, ethanol, and dimethyl sulfoxide (DMSO). This versatility makes it easy to handle and integrate into various experimental setups.

Safety considerations are an essential aspect when working with any chemical compound. While 2-(Hydroxyamino)-2-oxoethylphosphonic acid is not classified as a hazardous material, it is important to follow standard laboratory safety protocols when handling it. Proper personal protective equipment (PPE) such as gloves, goggles, and lab coats should be worn to ensure safe handling.

In conclusion, 2-(Hydroxyamino)-2-oxoethylphosphonic acid (CAS No. 89873-30-3) is a multifaceted compound with a wide range of applications in pharmaceuticals, biochemistry, and materials science. Its unique structure and properties make it an invaluable reagent for researchers and scientists working on the development of new drugs, functional materials, and enzyme inhibitors. As research continues to advance, it is likely that new applications for this compound will be discovered, further expanding its utility and impact.

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