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258864-54-9

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258864-54-9 Usage

Conductivity

4.63 mS/cm (25 °C)

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.

General Description

Trihexyltetradecylphosphonium chloride is a hydrophobic ionic liquid, which is soluble in carbon dioxide.

Check Digit Verification of cas no

The CAS Registry Mumber 258864-54-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,8,8,6 and 4 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 258864-54:
(8*2)+(7*5)+(6*8)+(5*8)+(4*6)+(3*4)+(2*5)+(1*4)=189
189 % 10 = 9
So 258864-54-9 is a valid CAS Registry Number.
InChI:InChI=1/C32H68P.ClH/c1-5-9-13-17-18-19-20-21-22-23-24-28-32-33(29-25-14-10-6-2,30-26-15-11-7-3)31-27-16-12-8-4;/h5-32H2,1-4H3;1H/q+1;/p-1

258864-54-9 Well-known Company Product Price

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  • Aldrich

  • (89744)  Trihexyltetradecylphosphoniumchloride  ≥95.0% (NMR)

  • 258864-54-9

  • 89744-5G-F

  • 200.07CNY

  • Detail
  • Aldrich

  • (89744)  Trihexyltetradecylphosphoniumchloride  ≥95.0% (NMR)

  • 258864-54-9

  • 89744-50G-F

  • 680.94CNY

  • Detail

258864-54-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name trihexyl(tetradecyl)phosphanium,chloride

1.2 Other means of identification

Product number -
Other names Trihexyltetradecylphosphonium chloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:258864-54-9 SDS

258864-54-9Synthetic route

myristyl chloride
2425-54-9

myristyl chloride

trihexylphosphine
4168-73-4

trihexylphosphine

trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

Conditions
ConditionsYield
at 145℃; for 24h;90%
at 145℃; Inert atmosphere;90%
at 80℃; for 48h; Inert atmosphere;
myristyl chloride
2425-54-9

myristyl chloride

trihexylphosphine
4168-73-4

trihexylphosphine

trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

Conditions
ConditionsYield
at 145℃; for 24h;90%
at 145℃; Inert atmosphere;90%
at 80℃; for 48h; Inert atmosphere;
bis(tri(hexyl)tetradecylphosphonium) tetrachlorocobaltate(II)

bis(tri(hexyl)tetradecylphosphonium) tetrachlorocobaltate(II)

water
7732-18-5

water

A

trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

B

cobalt(II) chloride hexahydrate

cobalt(II) chloride hexahydrate

Conditions
ConditionsYield
at 60℃; for 0.666667h;
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

dimethyl sulfate
77-78-1

dimethyl sulfate

trihexyl(tetradecyl)phosphonium methylsulfate

trihexyl(tetradecyl)phosphonium methylsulfate

Conditions
ConditionsYield
at 20℃; for 1h;100%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

dimethylsulfite
616-42-2

dimethylsulfite

trihexyltetradecylphosphonium methanesulfonate

trihexyltetradecylphosphonium methanesulfonate

Conditions
ConditionsYield
at 110 - 115℃; under 750.075 - 1125.11 Torr; for 72h;100%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

sodium salicylate
54-21-7

sodium salicylate

trihexyl(tetradecyl)phosphonium salicylate
1228997-35-0

trihexyl(tetradecyl)phosphonium salicylate

Conditions
ConditionsYield
In acetone for 72h;100%
In water; acetone at 20℃; for 24h; Inert atmosphere;95%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

trimethylsilyl trifluoromethanesulfonate
27607-77-8

trimethylsilyl trifluoromethanesulfonate

trihexyl tetradecylphosphonium trifluoromethanesulfonate

trihexyl tetradecylphosphonium trifluoromethanesulfonate

Conditions
ConditionsYield
at 20℃; for 4h;100%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

methyl trifluoromethanesulfonate
333-27-7

methyl trifluoromethanesulfonate

trihexyl tetradecylphosphonium trifluoromethanesulfonate

trihexyl tetradecylphosphonium trifluoromethanesulfonate

Conditions
ConditionsYield
at 20℃; for 0.5h;100%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

C32H68P(1+)*Br2Cl(1-)

C32H68P(1+)*Br2Cl(1-)

Conditions
ConditionsYield
With bromine In neat (no solvent) for 1h;100%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

tris(pentafluoroethyl)difluorophosphorane
91543-32-7

tris(pentafluoroethyl)difluorophosphorane

trihexyltetradecylphosphonium tris(pentafluoroethyl)difluorochlorophosphate

trihexyltetradecylphosphonium tris(pentafluoroethyl)difluorochlorophosphate

Conditions
ConditionsYield
In acetonitrile at 20℃; for 3h;99.6%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

dodecatungstosilic acid

dodecatungstosilic acid

O40SiW12(4-)*4C32H68P(1+)

O40SiW12(4-)*4C32H68P(1+)

Conditions
ConditionsYield
In water at 20℃; for 3.25h; Sonication;99.6%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

phosphotungstic acid

phosphotungstic acid

trihexyl(tetradecyl)phosphonium 12-tungstophosphate

trihexyl(tetradecyl)phosphonium 12-tungstophosphate

Conditions
ConditionsYield
In water at 20℃; for 3.25h; Sonication;99.3%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

trihexyl(tetradecyl)phosphonium nitrate

trihexyl(tetradecyl)phosphonium nitrate

Conditions
ConditionsYield
With potassium nitrate In water99%
With potassium nitrate In water for 1h;98%
With potassium nitrate In water for 5h;94.9%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

Bis(2-ethylhexyl)phosphoric acid
298-07-7

Bis(2-ethylhexyl)phosphoric acid

trihexyltetradecylphosphonium bis(2-ethylhexyl) phosphate

trihexyltetradecylphosphonium bis(2-ethylhexyl) phosphate

Conditions
ConditionsYield
With sodium hydroxide In water; toluene at 70℃;99%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

ammonium 8-anilino-1-naphthalenesulfonate
28836-03-5

ammonium 8-anilino-1-naphthalenesulfonate

trihexyltetradecylphosphonium 8-anilinonaphthalene-1-sulfonate

trihexyltetradecylphosphonium 8-anilinonaphthalene-1-sulfonate

Conditions
ConditionsYield
In dichloromethane at 20℃; for 24h;99%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

trihexyl(tetradecyl)phosphonium trichloride

trihexyl(tetradecyl)phosphonium trichloride

Conditions
ConditionsYield
With chlorine In neat (no solvent) under 1500.15 Torr; for 0.5h; Darkness;99%
With chlorine at 20℃; under 1500.15 Torr;
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

tris(pentafluoroethyl)trifluorophosphoric acid

tris(pentafluoroethyl)trifluorophosphoric acid

tris(P-hexyl)tetradecylphosphonium trifluorotris(pentafluoroethyl) phosphate
883860-35-3

tris(P-hexyl)tetradecylphosphonium trifluorotris(pentafluoroethyl) phosphate

Conditions
ConditionsYield
In methanol at 20℃; for 0.5h;98.2%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

(phenylthio)acetic acid
103-04-8

(phenylthio)acetic acid

trihexyl(tetradecyl)phosphonium 2-(phenylthio)acetate
1228997-38-3

trihexyl(tetradecyl)phosphonium 2-(phenylthio)acetate

Conditions
ConditionsYield
With sodium hydroxide In water; acetonitrile at 60℃; for 12h; Inert atmosphere;98%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

sodium tetraphenyl borate
143-66-8

sodium tetraphenyl borate

trihexyl(tetradecyl)phosphonium tetraphenylborate

trihexyl(tetradecyl)phosphonium tetraphenylborate

Conditions
ConditionsYield
In water; acetone at 20℃; for 12h; Inert atmosphere;98%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

benzoic acid
65-85-0

benzoic acid

trihexyl(tetradecyl)phosphonium benzoate
920759-13-3

trihexyl(tetradecyl)phosphonium benzoate

Conditions
ConditionsYield
With sodium hydroxide In ethanol; water at 60℃; for 5h; Inert atmosphere;98%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

Octanoic acid
124-07-2

Octanoic acid

trihexyl(tetradecyl)phosphonium octanoate

trihexyl(tetradecyl)phosphonium octanoate

Conditions
ConditionsYield
With sodium hydroxide In hexane; water at 20℃;98%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

stearic acid
57-11-4

stearic acid

trihexyltetradecylphosphonium octadecanoate

trihexyltetradecylphosphonium octadecanoate

Conditions
ConditionsYield
With sodium hydroxide In hexane; water at 20℃;97%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

3-methoxy-4-hydroxybenzoic acid
121-34-6

3-methoxy-4-hydroxybenzoic acid

trihexyl(tetradecyl)phosphonium vanillate
1228997-36-1

trihexyl(tetradecyl)phosphonium vanillate

Conditions
ConditionsYield
With sodium hydroxide In water; acetone at 40℃; for 24h; Inert atmosphere;96%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

4-Methylnonanoic acid
45019-28-1

4-Methylnonanoic acid

trihexyltetradecylphosphonium 4-methylnonanoate

trihexyltetradecylphosphonium 4-methylnonanoate

Conditions
ConditionsYield
With sodium hydroxide In hexane; water at 20℃;96%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

[trihexyl(tetradecyl)phosphonium hexafluorophosphate]

[trihexyl(tetradecyl)phosphonium hexafluorophosphate]

Conditions
ConditionsYield
With hexafluorophosphoric acid at 20℃; Inert atmosphere; Cooling with ice;95%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

europium(III) chloride hexahydrate

europium(III) chloride hexahydrate

4,4,4-trifluoro-1-(2-naphthyl)-1,3-butanedione
893-33-4

4,4,4-trifluoro-1-(2-naphthyl)-1,3-butanedione

C56H32EuF12O8(1-)*C32H68P(1+)

C56H32EuF12O8(1-)*C32H68P(1+)

Conditions
ConditionsYield
Stage #1: 4,4,4-trifluoro-1-(2-naphthyl)-1,3-butanedione With sodium hydroxide In ethanol at 20℃;
Stage #2: europium(III) chloride hexahydrate In ethanol at 50℃; for 4h;
Stage #3: trihexyl(tetradecyl)phosphonium chloride In ethanol at 20℃; for 2h;
95%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

silver(I) α-oximido-(acetamide)acetonitrile
474651-28-0

silver(I) α-oximido-(acetamide)acetonitrile

trihexyl(tetradecyl)phosphonium carbamoylcyano(nitroso)methanide

trihexyl(tetradecyl)phosphonium carbamoylcyano(nitroso)methanide

Conditions
ConditionsYield
In water; acetone for 16h; Reflux;95%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

C35H69N2O2(1-)*Na(1+)

C35H69N2O2(1-)*Na(1+)

trihexyl(tetradecyl)phosphonium N,N,N′,N′-tetra-(2-ethylhexyl)malonate

trihexyl(tetradecyl)phosphonium N,N,N′,N′-tetra-(2-ethylhexyl)malonate

Conditions
ConditionsYield
In toluene for 6 - 7h; Reflux;95%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

trihexyltetradecylphosphonium sulfate

trihexyltetradecylphosphonium sulfate

Conditions
ConditionsYield
Stage #1: trihexyl(tetradecyl)phosphonium chloride With sodium hydrogen sulfate In water; toluene for 0.833333h;
Stage #2: With sodium hydroxide In water; toluene for 1h;
95%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

methyl orange
547-58-0

methyl orange

[P(6,6,6,14)][MO]
1198363-83-5

[P(6,6,6,14)][MO]

Conditions
ConditionsYield
In acetone at 20℃; for 48h;94%
In dichloromethane; water
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

L-Lactic acid
79-33-4

L-Lactic acid

trihexyl(tetradecyl)phosphonium L-lactate
1370552-04-7

trihexyl(tetradecyl)phosphonium L-lactate

Conditions
ConditionsYield
With sodium hydroxide In dichloromethane; water94%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

Thiosalicylic acid
147-93-3

Thiosalicylic acid

trihexyl(tetradecyl)phosphonium thiosalicylate
1228997-33-8

trihexyl(tetradecyl)phosphonium thiosalicylate

Conditions
ConditionsYield
With sodium hydroxide In water; acetone at 20℃; for 48h; Inert atmosphere;93%
trihexyl(tetradecyl)phosphonium chloride
258864-54-9

trihexyl(tetradecyl)phosphonium chloride

1-decanoic acid
334-48-5

1-decanoic acid

tetradecyl(trihexyl)phosphonium decanoate

tetradecyl(trihexyl)phosphonium decanoate

Conditions
ConditionsYield
With sodium hydroxide In water; toluene at 70℃;93%

258864-54-9Relevant articles and documents

An environmentally friendlier approach to hydrometallurgy: Highly selective separation of cobalt from nickel by solvent extraction with undiluted phosphonium ionic liquids

Wellens, Sil,Thijs, Ben,Binnemans, Koen

, p. 1657 - 1665 (2012)

A green solvent extraction process for the separation of cobalt from nickel, magnesium and calcium in chloride medium was developed, using undiluted phosphonium-based ionic liquids as extractants. Cobalt was extracted to the ionic liquid phase as the tetrachlorocobaltate(ii) complex, leaving behind nickel, magnesium and calcium in the aqueous phase. Manganese is interfering in the separation process. The main advantage of this ionic liquid extraction process is that no organic diluents have to be added to the organic phase, so that the use of volatile organic compounds can be avoided. Separation factors higher than 50 000 were observed for the cobalt/nickel separation from 8 M HCl solution. After extraction, cobalt can easily be stripped using water and the ionic liquid can be reused as extractant, so that a continuous extraction process is possible. Up to 35 g L-1 of cobalt can be extracted to the ionic liquid phase, while still having a distribution coefficient higher than 100. Instead of hydrochloric acid, sodium chloride can be used as a chloride source. The extraction process has been upscaled to batch processes using 250 mL of ionic liquid. Tri(hexyl)tetradecylphosphonium chloride, tri(butyl) tetradecylphosphonium chloride, tetra(octyl)phosphonium bromide, tri(hexyl)tetradecylphosphonium bromide and Aliquat 336 have been tested for their performance to extract cobalt from an aqueous chloride phase to an ionic liquid phase. Tri(hexyl)tetradecylphosphonium chloride (Cyphos IL 101) turned out to be the best option as the ionic liquid phase, compromising between commercial availability, separation characteristics and easiness to handle the ionic liquid. The Royal Society of Chemistry.

Highly stable noble-metal nanoparticles in tetraalkylphosphonium ionic liquids for in situ catalysis

Banerjee, Abhinandan,Theron, Robin,Scott, Robert W. J.

experimental part, p. 109 - 116 (2012/06/30)

Gold and palladium nanoparticles were prepared by lithium borohydride reduction of the metal salt precursors in tetraalkylphosphonium halide ionic liquids in the absence of any organic solvents or external nanoparticle stabilizers. These colloidal suspensions remained stable and showed no nanoparticle agglomeration over many months. A combination of electrostatic interactions between the coordinatively unsaturated metal nanoparticle surface and the ionic-liquid anions, bolstered by steric protection offered by the bulky alkylated phosphonium cations, is likely to be the reason behind such stabilization. The halide anion strongly absorbs to the nanoparticle surface, leading to exceptional nanoparticle stability in halide ionic liquids; other tetraalkylphosphonium ionic liquids with non-coordinating anions, such as tosylate and hexafluorophosphate, show considerably lower affinities towards the stabilization of nanoparticles. Palladium nanoparticles stabilized in the tetraalkylphosphonium halide ionic liquid were stable, efficient, and recyclable catalysts for a variety of hydrogenation reactions at ambient pressures with sustained activity. Aerial oxidation of the metal nanoparticles occurred over time and was readily reversed by re-reduction of oxidized metal salts. Stable morsels of metal: Palladium nanoparticles stabilized in tetraalkylphosphonium halide ionic liquids are stable, efficient, and recyclable catalysts for a variety of hydrogenation reactions at ambient pressures with sustained activity (see picture). Copyright

Organic salt conditioner, organic salt-containing composition, and uses thereof

-

, (2008/06/13)

The present invention relates to the use of, and a composition containing, at least one non-polymeric organic salt with a melting point of less than 60° C. These organic salts may be imidazolium, pyrazolium, pyridinium, pyrimidinium or tetraalkylphosphonium salts. The inventinon composition may be used for washing (cleaning) and/or conditioning keratin materials, and especially the hair.

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