Cas no 7368-65-2 (Phosphonium, tetraethyl-, chloride)

Tetraethylphosphonium chloride (C?H??P?Cl?) is a quaternary phosphonium salt characterized by its stable tetraethylphosphonium cation and chloride anion. This compound is valued for its ionic liquid properties, including high thermal stability and low volatility, making it suitable for applications in catalysis, electrolytes, and phase-transfer reactions. Its well-defined structure and ionic nature facilitate efficient charge transfer in electrochemical systems. The chloride counterion enhances solubility in polar solvents, broadening its utility in synthetic and material chemistry. Tetraethylphosphonium chloride is also employed as a precursor for other phosphonium-based ionic liquids or functional materials, offering consistent performance in demanding environments.
Phosphonium, tetraethyl-, chloride structure
7368-65-2 structure
Product Name:Phosphonium, tetraethyl-, chloride
CAS No:7368-65-2
MF:C8H20ClP
MW:182.671162605286
CID:542123
PubChem ID:21863291
Update Time:2025-09-28

Phosphonium, tetraethyl-, chloride Chemical and Physical Properties

Names and Identifiers

    • Phosphonium, tetraethyl-, chloride
    • tetraethylphosphanium,chloride
    • TETRAETHYLPHOSPHONIUM CHLORIDE
    • Tetraaethyl-phosphonium,Chlorid
    • Tetraaethyl-phosphonium,Tetraaethylphosphoniumchlorid
    • tetraethyl-phosphonium,chloride
    • FBOJNMRAZJRCNS-UHFFFAOYSA-M
    • DTXSID40618981
    • FT-0693994
    • tetraethylphosphanium chloride
    • SCHEMBL127178
    • TETRAETHYLPHOSPHONIUMCHLORIDE
    • 2-Cyano-3-(4-morpholinyl)-2-propenoicacidethylester
    • tetraethylphosphanium;chloride
    • 7368-65-2
    • Inchi: 1S/C8H20P.ClH/c1-5-9(6-2,7-3)8-4;/h5-8H2,1-4H3;1H/q+1;/p-1
    • InChI Key: FBOJNMRAZJRCNS-UHFFFAOYSA-M
    • SMILES: [Cl-].[P+](CC)(CC)(CC)CC

Computed Properties

  • Exact Mass: 182.09900
  • Monoisotopic Mass: 182.0991153g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 4
  • Complexity: 47.5
  • Covalently-Bonded Unit Count: 2
  • 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: nothing
  • XLogP3: nothing
  • Topological Polar Surface Area: 0?2

Experimental Properties

  • PSA: 13.59000
  • LogP: 0.08760

Phosphonium, tetraethyl-, chloride Security Information

  • WGK Germany:3
  • Hazard Category Code: 36/37/38
  • Safety Instruction: 26-37/39
  • Hazardous Material Identification: Xi
  • Risk Phrases:R36/37/38

Phosphonium, tetraethyl-, chloride Pricemore >>

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Additional information on Phosphonium, tetraethyl-, chloride

Phosphonium, tetraethyl-, chloride (CAS No. 7368-65-2): A Versatile Compound in Modern Chemical Research

The compound Phosphonium, tetraethyl-, chloride, identified by its CAS number 7368-65-2, is a significant chemical entity with a wide range of applications in various scientific and industrial fields. This organophosphorus compound, characterized by its tetraethylphosphonium cation and chloride anion, has garnered considerable attention due to its unique properties and functionalities. The following discussion delves into the chemical characteristics, synthesis methods, and recent advancements in the utilization of this compound, particularly in the context of pharmaceuticals and materials science.

In terms of chemical structure, Phosphonium, tetraethyl-, chloride consists of a central phosphorus atom bonded to four ethyl groups, forming the tetraethylphosphonium cation (Et?P?), which is stabilized by a counterbalancing chloride ion (Cl?). This structural configuration imparts remarkable stability and reactivity, making it an invaluable intermediate in organic synthesis. The compound's solubility in both polar and non-polar solvents further enhances its utility in diverse chemical reactions.

The synthesis of Phosphonium, tetraethyl-, chloride typically involves the reaction of phosphorus trichloride with ethyl Grignard reagents or ethyl lithium compounds. This process yields the desired tetraethylphosphonium salt upon subsequent treatment with hydrochloric acid. Recent studies have explored more efficient synthetic routes, including catalytic methods that reduce reaction times and improve yields. These advancements are crucial for large-scale production and industrial applications.

One of the most notable applications of Phosphonium, tetraethyl-, chloride is in the field of pharmaceutical research. Its ability to form stable complexes with various organic molecules has made it a valuable tool in drug design and development. For instance, researchers have utilized this compound to create novel phosphonate-based drugs that exhibit potent antimicrobial and anti-inflammatory properties. The unique electronic properties of the tetraethylphosphonium cation allow for precise modulation of drug activity, making it an attractive candidate for targeted therapies.

In materials science, Phosphonium, tetraethyl-, chloride has been employed as a precursor in the synthesis of advanced materials such as conductive polymers and liquid crystals. These materials find applications in electronic devices, including organic light-emitting diodes (OLEDs) and solar cells. The compound's ability to enhance charge transport properties makes it particularly useful in developing more efficient and sustainable energy technologies.

Recent research has also highlighted the role of Phosphonium, tetraethyl-, chloride in bioimaging techniques. Its luminescent derivatives have been used to develop contrast agents for medical imaging modalities such as fluorescence microscopy and positron emission tomography (PET). These imaging agents provide high-resolution visualization of biological processes, aiding in the diagnosis and monitoring of diseases.

The environmental impact of using Phosphonium, tetraethyl-, chloride has also been a subject of investigation. Studies have shown that this compound is biodegradable and does not accumulate in the environment under normal conditions. This characteristic makes it an environmentally friendly alternative to other synthetic reagents that may pose ecological risks. Furthermore, efforts are underway to develop greener synthetic methods that minimize waste generation and energy consumption.

In conclusion, Phosphonium, tetraethyl-, chloride (CAS No. 7368-65-2) is a multifaceted compound with significant implications across multiple scientific disciplines. Its unique chemical properties have enabled its use in pharmaceuticals, materials science, bioimaging, and environmental chemistry. As research continues to uncover new applications for this versatile compound, its importance in modern chemical research is likely to grow even further.

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