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53166

Sigma-Aldrich

3-(Triphenylphosphonio)propane-1-sulfonate

≥99.0% (HPLC)

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About This Item

Empirical Formula (Hill Notation):
C21H21O3PS
CAS Number:
Molecular Weight:
384.43
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

≥99.0% (HPLC)

impurities

≤1.0% water
≤100 mg/kg halogene (as chloride)

functional group

phosphine
sulfonic acid

SMILES string

[O-]S(=O)(=O)CCC[P+](c1ccccc1)(c2ccccc2)c3ccccc3

InChI

1S/C21H21O3PS/c22-26(23,24)18-10-17-25(19-11-4-1-5-12-19,20-13-6-2-7-14-20)21-15-8-3-9-16-21/h1-9,11-16H,10,17-18H2

InChI key

CHVFGCXPLGAAQN-UHFFFAOYSA-N

General description

3-(Triphenylphosphonio)propane-1-sulfonate is a zwitterionic, sulfonic acid-functionalized ionic liquid.

Application

3-(Triphenylphosphonio)propane-1-sulfonate has been used as a zwitterion to study its effect on the work function of indium tin oxide (ITO) in inverted polymer solar cells (PSCs). It can be used in the preparation of triphenyl-(3-sulfopropyl)phosphonium phosphotungstate, an efficient green catalyst for esterification reactions.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Highly efficient, inverted polymer solar cells with indium tin oxide modified with solution-processed zwitterions as the transparent cathode.
Sun K, et al.
ACS Applied Materials & Interfaces, 4(4), 2009-2017 (2012)
Phosphotungstic acid salt of triphenyl (3-sulfopropyl) phosphonium: An efficient and reusable solid catalyst for esterification.
Zhang W, et al.
Catalysis Communications, 11(3), 151-154 (2009)
Task-Specific Ionic Liquids
Aldrich Chemfiles, 5(6), 17-17 (2006)

Articles

Functionalized imidazolium cations with thioether, urea, or thiourea derivatized side chains act as metal-ligating moieties, whereas the PF6– anions provide the desired water immiscibility.

Functionalized imidazolium cations with thioether, urea, or thiourea derivatized side chains act as metal-ligating moieties, whereas the PF6– anions provide the desired water immiscibility.

Functionalized imidazolium cations with thioether, urea, or thiourea derivatized side chains act as metal-ligating moieties, whereas the PF6– anions provide the desired water immiscibility.

Functionalized imidazolium cations with thioether, urea, or thiourea derivatized side chains act as metal-ligating moieties, whereas the PF6– anions provide the desired water immiscibility.

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