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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:
116154-22-4
Molecular Weight:
384.43
MDL number:
MFCD07784455
UNSPSC Code:
12352100
PubChem Substance ID:
57651398
NACRES:
NA.22

Assay

≥99.0% (HPLC)

impurities

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

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
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
Task-Specific Ionic Liquids
Aldrich Chemfiles, 5(6), 17-17 (2006)
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)

Articles

Task-Specific Ionic Liquids

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.

Task-Specific Ionic Liquids

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.

Task-Specific Ionic Liquids

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.

Task-Specific Ionic Liquids

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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