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PAM (Phosphonoacetylaspartate)

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Identification
Molecular formula
C6H10NO7P
CAS number
5990-32-9
IUPAC name
2-[(2-phosphonoacetyl)amino]butanedioic acid
State
State

At room temperature, PAM is a solid compound. It remains stable under normal conditions, which makes it suitable for storage and handling. The solid form also facilitates its use in a variety of research and chemical applications.

Melting point (Celsius)
255.00
Melting point (Kelvin)
528.15
Boiling point (Celsius)
678.00
Boiling point (Kelvin)
951.15
General information
Molecular weight
241.12g/mol
Molar mass
241.1180g/mol
Density
2.0900g/cm3
Appearence

PAM is typically found as a white solid in its pure form. It is a crystalline compound, indicating a high degree of purity and homogeneity. The compound does not have any distinctive odor and is generally handled in crystalline or powdered form in laboratory settings.

Comment on solubility

Solubility of 2-[(2-phosphonoacetyl)amino]butanedioic acid

The compound 2-[(2-phosphonoacetyl)amino]butanedioic acid, with the chemical formula C6H10NO7P, exhibits interesting solubility characteristics that can be attributed to its unique molecular structure.

Key Characteristics of Solubility:

  • Hydrophilicity: The presence of multiple functional groups, particularly the phosphono group and carboxylic acids, lends the molecule a significant hydrophilic nature, which enhances its compatibility with polar solvents.
  • Aqueous Solubility: This compound is expected to be highly soluble in water due to its ionic character in aqueous environments. The ionic bonds formed can facilitate dissolution.
  • Temperature Effect: Solubility may increase with temperature as higher temperatures often lead to enhanced molecular interactions with solvent molecules.

In summary, 2-[(2-phosphonoacetyl)amino]butanedioic acid is likely to be highly soluble in polar solvents, with particular emphasis on water. Its functional groups dramatically influence its solubility properties, making it an intriguing compound for further studies regarding solubility dynamics in various environments.

Interesting facts

Interesting Facts about 2-[(2-Phosphonoacetyl)amino]butanedioic Acid

2-[(2-Phosphonoacetyl)amino]butanedioic acid, often referred to in scientific literature by its systematic name or abbreviated form, is a fascinating compound that exhibits unique properties and potential applications. Here are some intriguing aspects of this compound:

  • Complex Structure: The molecule contains both amino and phosphono groups, which contribute to its versatility in biochemical processes.
  • Role in Metabolic Pathways: Compounds similar to this one are often involved in metabolic and regulatory pathways, particularly in the synthesis of amino acids and other vital metabolites.
  • Potential Therapeutic Uses: Research continues into the use of phosphono-containing compounds in pharmaceuticals, where they may act as enzyme inhibitors or modulators of biochemical pathways.
  • Biochemistry and Agriculture: Phosphonate derivatives are used in agriculture for crop protection due to their ability to enhance plant defense mechanisms.
  • Analytical Interest: As a phosphonate, this compound presents analytical challenges and opportunities, particularly in detection techniques for phosphorous-dominated compounds.

In conclusion, 2-[(2-Phosphonoacetyl)amino]butanedioic acid represents a unique intersection of organic chemistry and biochemistry, emphasizing the importance of phosphonates in both nature and synthetic applications. Its complexity and multifunctionality make it an intriguing subject for ongoing research, and its potential implications in various fields of study highlight the significance of exploring such compounds.

Synonyms
N-(Phosphonoacetyl)aspartic acid
NSC632898
acido esparfosico
76338-95-9
2-[(2-phosphonoacetyl)amino]butanedioic acid
CHEMBL37681
SCHEMBL3514530
DTXSID30866191
NSC281263
L-Aspartic acid, calcium salt (2:3)
NSC-281263
NSC-632898
2-(2-phosphonoacetamido)butanedioic acid
NCI60_001849
2-(2-Phosphono-acetylamino)-succinic acid
EN300-11815753
BRD-A81539525-433-01-5