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Phosphoserine

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Identification
Molecular formula
C4H10NO6P
CAS number
407-41-0
IUPAC name
2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid
State
State

Phosphoserine is typically encountered as a solid at room temperature.

Melting point (Celsius)
220.00
Melting point (Kelvin)
493.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
169.10g/mol
Molar mass
169.0730g/mol
Density
0.7125g/cm3
Appearence

Phosphoserine is a crystalline solid that is generally white in appearance. It is commonly available in the form of a powder and is noted for its high solubility in water, contributing to its utility in biochemical applications.

Comment on solubility

Solubility of 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid (C4H10NO6P)

The solubility of 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid is an intriguing subject due to its complex structure that includes both amino and phosphonic acid functionalities. This compound is primarily characterized by its high solubility in polar solvents, particularly in water, due to the presence of multiple hydrophilic groups.

Key Factors Influencing Solubility:

  • Ionization: The amino group may become ionized under physiological conditions, enhancing its solubility in aqueous environments.
  • Hydrophilic Groups: The hydroxyl and phosphoryl functional groups significantly contribute to its ability to interact with water molecules.
  • Concentration: At higher concentrations, the solubility may exhibit saturation effects, thus necessitating precise measurements.
  • Temperature: Like many compounds, an increase in temperature can enhance solubility, as the kinetic energy of molecules increases, promoting dissolution.

In summary, the solubility of 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid is primarily governed by its ionic nature and the presence of polar functional groups. As a result, it demonstrates a strong propensity to dissolve in water, making it an accessible compound for various applications in biochemical contexts. Emphasizing the solubility properties can lead to deeper insights into its functionality and interactions in biological systems.

Interesting facts

Facts About 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic Acid

2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid, commonly referred to as a derivative of amino acids with a phosphonate group, exhibits some fascinating characteristics that make it an interesting subject for both chemical research and application in biochemistry.

Key Characteristics

  • Biological Importance: This compound is closely related to vital biochemical pathways and can play a role as a potential building block for various biosynthetic processes.
  • Phosphorylation: The presence of the phosphoryl group indicates its potential involvement in phosphorylation reactions, which are fundamental in cellular signaling.
  • Analytical Interest: The unique structure of this compound makes it a subject of interest in analytical chemistry, often utilized in studies involving mass spectrometry and NMR spectroscopy.

Potential Applications

  • Pharmaceuticals: Given its structural characteristics, it can serve as a lead compound in designing medications targeting metabolic disorders.
  • Research Tool: Researchers can utilize this compound to study enzyme interactions and metabolic pathways, particularly those involving amino acid metabolism.
  • Agricultural Chemistry: As a phosphonate, it may also have applications in the development of fertilizers or pest control agents.

In the words of renowned chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." With compounds like 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid, the interplay between structure and function provides a rich vein of ideas waiting to be explored. As scientists delve deeper into its properties, the compound continues to "give" in terms of potential discoveries and advancements in various fields.

Overall, 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid embodies the elegance of chemistry, bridging the gap between fundamental chemical principles and real-world applications.

Synonyms
GLUFOSINATE
phosphinothricin
51276-47-2
2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid
Glufosinate [ISO]
DL-Phosphinothricin
Basta
3-Amino-3-carboxypropylmethylphosphinic acid
DL-2-Amino-4-(methylphosphino)butanoic acid
2-Amino-4-(hydroxymethylphosphinyl)butyric acid
ammonium glufosinate
C8W4FP6BTY
Butanoic acid, 2-amino-4-(hydroxymethylphosphinyl)-
EINECS 257-102-5
Ruthenium104
GLUFOSINATE AMMONIUM
Glufosinate (ammonium)
DTXSID0043973
CHEBI:52136
HOE 39866
2-Amino-4-(hydroxymethylphosphinyl)butanoic acid
2-Amino-4-(hydroxy-methyl-phosphoryl)butanoic acid
HOE 35956
HOE-35956
77182-82-2
phosphinothricin hydrochloride
(+-)-Phosphinothricin
PHOSPHINOTHRICIN [MI]
2-amino-4-(hydroxy(methyl)phosphoryl)butanoic acid
UNII-C8W4FP6BTY
2-amino-4-methylphosphinobutyric acid
glufosin
Glufosinic acid
72P470U27C
DL-Phosphinotricin
MFCD00211362
(-)-phosphinothricin
L-PHOPHINOTHRICIN
SCHEMBL17697
NChemBio.2007.9-comp2
CHEMBL450298
(+/-)-PHOSPHINOTHRICIN
DTXCID8023973
SCHEMBL14826101
UNII-72P470U27C
CHEBI:142851
HMS3741K13
HY-W019870A
PHOSPHINOTHRICIN DL-FORM [MI]
AKOS016344180
FP16278
NCGC00160382-01
AS-15138
DA-63802
CS-0111198
NS00005957
C05042
EN300-7466514
2-amino-4-[hydroxy(methyl)phosphoryl]butyric acid
Q302204
(2S)-2-amino-4-(hydroxy-methylphosphoryl)butanoic acid
Z2737639744
(2RS)-2-AMINO-4-(HYDROXY(METHYL)PHOSPHINOYL)BUTYRIC ACID