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Lecithin

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Identification
Molecular formula
C6H15ClNO3P
CAS number
60-00-4
IUPAC name
trimethyl(2-phosphonooxyethyl)ammonium;chloride
State
State

At room temperature, it is typically a solid.

Melting point (Celsius)
241.00
Melting point (Kelvin)
514.15
Boiling point (Celsius)
230.00
Boiling point (Kelvin)
503.15
General information
Molecular weight
181.68g/mol
Molar mass
181.6840g/mol
Density
1.1124g/cm3
Appearence

Usually found as a white or off-white crystalline powder. It may also be hygroscopic, meaning it can absorb moisture from the air.

Comment on solubility

Solubility of trimethyl(2-phosphonooxyethyl)ammonium chloride

When discussing the solubility of trimethyl(2-phosphonooxyethyl)ammonium chloride, it's essential to consider several key aspects:

  • Nature of the Compound: This compound is a quaternary ammonium salt, typically known for its ionic properties. Such compounds usually exhibit good solubility in polar solvents.
  • Solvent Compatibility: Trimethyl(2-phosphonooxyethyl)ammonium chloride is likely to be highly soluble in water due to its ionic nature, which facilitates interaction with water molecules.
  • Temperature Influence: As with many salts, solubility can increase with temperature. Hence, higher temperatures may enhance the dissolution process.
  • Concentration Considerations: The concentration of the solution can also impact solubility; at high concentrations, solubility might reach a limit due to precipitation.

Overall, one might say that the solubility of trimethyl(2-phosphonooxyethyl)ammonium chloride is generally favorable in water, making it an effective compound for various applications that require soluble species. The interplay of its ionic structure and interactions with solvents increases its potential utility in fields such as biochemistry and materials science.

Interesting facts

Interesting Facts about Trimethyl(2-phosphonooxyethyl)ammonium Chloride

Trimethyl(2-phosphonooxyethyl)ammonium chloride is a fascinating compound that plays a significant role in various fields of chemistry and biochemistry. Below are some interesting points that highlight its importance and unique characteristics:

  • Versatile Utility: This compound is primarily employed as a reagent in organic synthesis, particularly in the development of phosphonate derivatives, which are crucial in medicinal chemistry.
  • Biological Significance: Structurally, phosphonates, including this compound, possess a phosphorus-carbon bond that mimics natural phosphates, allowing them to be involved in biological processes in a way that can inhibit enzymatic functions.
  • Potential Applications: The unique chemical reactivity of this compound paves the way for its use in pharmaceuticals, agriculture (as a herbicide) and environmental science (bioremediation processes).
  • Inhibition Mechanism: Due to its phosphate analog structure, it can inhibit enzymes such as kinases and phosphatases, which are involved in numerous signaling pathways, making it an attractive target for drug discovery.

As a chemistry student or a scientist, the exploration of trimethyl(2-phosphonooxyethyl)ammonium chloride provides not just an insight into its functionality but also opens doors to innovate new compounds that can lead to groundbreaking discoveries. The ability to design compounds that can influence biological systems is a testament to the intricate balance between chemistry and life sciences.

In summary, the multifaceted nature of trimethyl(2-phosphonooxyethyl)ammonium chloride exemplifies the importance of phosphorus-containing compounds in modern science, which blend the realms of synthetic chemistry and biological relevance.

Synonyms
107-73-3
Phosphorylcholine Chloride
PHOSPHORYLCHOLINE
choline phosphate
Choline phosphate chloride
Trimethyl-(2-Phosphonooxyethyl)Azanium Chloride
phosphocholine chloride
N,N,N-trimethyl-2-(phosphonooxy)ethanaminium chloride
trimethyl(2-phosphonooxyethyl)azanium;chloride
Ethanaminium, N,N,N-trimethyl-2-(phosphonooxy)-, chloride
Phosphorylcholine (chloride)
[2-(trimethylazaniumyl)ethoxy]phosphonic acid chloride
96AN057F7A
Trimethyl(2-(phosphonooxy)ethyl)ammonium chloride
UNII-96AN057F7A
Ethanaminium, N,N,N-trimethyl-2-(phosphonooxy)-, chloride (1:1) (ACI); Choline, chloride, dihydrogen phosphate (7CI, 8CI); Ethanaminium, N,N,N-trimethyl-2-(phosphonooxy)-, chloride (9CI); Choline phosphate; Choline phosphate chloride; Choline phosphochlor
EINECS 203-516-6
MFCD00871728
FOSFORYLCHOLINE
Choline phosphochloride
PC-Cl
SCHEMBL24426
PHOSPHORYLCHOLINE [MI]
FOSFORYLCHOLINE [MART.]
CHEBI:61040
DTXSID90910205
MSK2067
AAA10773
HY-B2233
AKOS027327289
CS-7829
WS-03268
DB-257203
NS00041278
E85458
[2-(phosphonooxy)ethyl]trimethylammonium chloride
(2-HYDROXYETHYL)TRIMETHYLAMMONIUM CHLORIDE DIHYDROGEN PHOSPHATE