Trihexyltetradecylphosphonium chloride

Base Information

• Chemical Name: Trihexyltetradecylphosphonium chloride
• CAS No.: 258864-54-9
• Molecular Formula: C32H68ClP
• Molecular Weight: 519.319
• European Community (EC) Number: 684-206-1
• ChEMBL ID: CHEMBL3186883
• DSSTox Substance ID: DTXSID1047944
• Mol file: 258864-54-9.mol

Synonyms:CYPHOS 101;trihexyltetradecylphosphonium chloride

Chemical Property of Trihexyltetradecylphosphonium chloride

Chemical Property:

• Melting Point: -70 °C
• Refractive Index: 1.4818
• Flash Point: 118 °C
• PSA: 13.59000
• Density: 0.895 g/mL at 20 °C(lit.)
• LogP: 9.45000
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 28
• Exact Mass: 518.4747169
• Heavy Atom Count: 34
• Complexity: 319

Purity/Quality:

99%, ^*data from raw suppliers

TrihexyltetradecylphosphoniumChloride(TechnicalGrade) ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C
• Statements: 34
• Safety Statements: 26-36/37/39-45

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCCCCCCCCCCCC[P+](CCCCCC)(CCCCCC)CCCCCC.[Cl-]
• Uses: Trihexyltetradecylphosphonium chloride can be used as binder to develop a silver particle-modified carbon paste electrode, which can determine nitrite ions at low concentration.

Technology Process of Trihexyltetradecylphosphonium chloride

There total 3 articles about Trihexyltetradecylphosphonium chloride which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 90.0%

myristyl chloride (2425-54-9) + trihexylphosphine (4168-73-4) → trihexyl(tetradecyl)phosphonium chloride (258864-54-9)

Guidance literature:

at 145 ℃; for 24h;

DOI:10.2174/157017809789124966

Reference yield:

bis(tri(hexyl)tetradecylphosphonium) tetrachlorocobaltate(II) + water (7732-18-5) → trihexyl(tetradecyl)phosphonium chloride (258864-54-9) + cobalt(II) chloride hexahydrate

Guidance literature:

at 60 ℃; for 0.666667h;

DOI:10.1039/c2gc35246j

Reference yield:

→ trihexyl(tetradecyl)phosphonium chloride (258864-54-9)

Guidance literature:

upstream raw materials:

myristyl chloride

trihexylphosphine

water

Downstream raw materials:

tetradecyl(trihexyl)phosphonium bistriflamide

Heptanophenone

1-phenylpentadecan-1-one

1-(2-aminophenyl)pentadecan-1-one

Refernces

Chloroindate(III) ionic liquids: Recyclable media for Friedel-Crafts acylation reactions

10.1039/b413132k

This research explores the application of chloroindate(III) ionic liquids as a recyclable medium for Friedel–Crafts acylation reactions, which are crucial in the pharmaceutical and fine chemicals industry for synthesizing aromatic ketones. Traditionally, these reactions use strong Lewis acids like anhydrous aluminum(III) chloride, but they face issues such as catalyst deactivation and difficulty in separation. The study found that chloroindate(III) ionic liquids, synthesized by mixing organic chloride salts like 1-butyl-3-methylimidazolium chloride ([C4mim]Cl) or trihexyltetradecylphosphonium chloride ([P6,6,6,14]Cl) with anhydrous indium(III) chloride, offer a catalytic and completely recyclable system.

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