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93092

Triphenylphosphine

≥95.0% (GC), crystals

Synonym(s):

Phosphorustriphenyl

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250 G

$118.00

1 KG

$221.00

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About This Item

Linear Formula:
(C6H5)3P
CAS Number:
Molecular Weight:
262.29
NACRES:
NA.21
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
210-036-0
MDL number:
Beilstein/REAXYS Number:
610776

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Product Name

Triphenylphosphine, ≥95.0% (GC)

InChI key

RIOQSEWOXXDEQQ-UHFFFAOYSA-N

InChI

1S/C18H15P/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h1-15H

SMILES string

c1ccc(cc1)P(c2ccccc2)c3ccccc3

vapor density

9 (vs air)

vapor pressure

5 mmHg ( 20 °C)

assay

≥95.0% (GC)

form

crystals

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: ligand

impurities

~3% triphenylphosphine oxide

bp

377 °C (lit.)

mp

77-84 °C
79-81 °C (lit.)

solubility

water: soluble 0.00017 g/L at 22 °C

functional group

phosphine

Quality Level

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1 of 4

This Item
T844098.082708.00551
assay

≥95.0% (GC)

assay

99%

assay

≥99.0% (GC)

assay

≥97.0% (GC)

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Hiyama Coupling, reaction type: Sonogashira Coupling, reaction type: Suzuki-Miyaura Coupling, reaction type: Heck Reaction, reaction type: Stille Coupling, reagent type: ligand, reaction type: Negishi Coupling

reaction suitability

reaction type: Buchwald-Hartwig Cross Coupling Reaction, reaction type: Heck Reaction, reaction type: Hiyama Coupling, reaction type: Negishi Coupling, reaction type: Sonogashira Coupling, reaction type: Stille Coupling, reaction type: Suzuki-Miyaura Coupling, reagent type: ligand
reaction type: Cross Couplings

reaction suitability

-

reaction suitability

-

functional group

phosphine

functional group

phosphine

functional group

-

functional group

-

form

crystals

form

-

form

solid

form

solid

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

200

mp

77-84 °C, 79-81 °C (lit.)

mp

79-81 °C (lit.)

mp

78.5-81.5 °C

mp

-

Application


  • The palladium-based complexes bearing 1, 3-dibenzylbenzimidazolium with morpholine, triphenylphosphine, and pyridine derivate ligands: This study discusses the synthesis and characterization of new palladium-based complexes incorporating triphenylphosphine, providing insights into their potential catalytic activities (Aktaş et al., 2022).

  • Polymer-supported triphenylphosphine: This review highlights the diverse applications of polymer-supported triphenylphosphine in organic synthesis and its significant role in promoting more sustainable and efficient chemical processes (Moussa et al., 2019).

  • Application prospects of triphenylphosphine-based mitochondria-targeted cancer therapy: The review focuses on the utilization of triphenylphosphine for developing mitochondria-targeted drugs, emphasizing its potential in cancer therapy (Cheng et al., 2023).

General description

Triphenylphosphine, also referred to as PPH3, is an organophosphorous compound. It readily forms complexes with platinum-metal group salts.[1]

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1B - STOT RE 1 Inhalation

target_organs

Central nervous system,Peripheral nervous system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 2

flash_point_f

356.0 °F - closed cup

flash_point_c

180 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Booth HS.
Inorganic Syntheses, 54-54 (2009)
Booth HS.
Inorganic Syntheses, 46-46 (2009)
Alexandra Madeira et al.
Nanomaterials (Basel, Switzerland), 9(6) (2019-06-23)
Silver nanowire (AgNW) transparent electrodes show promise as an alternative to indium tin oxide (ITO). However, these nanowire electrodes degrade in air, leading to significant resistance increases. We show that passivating the nanowire surfaces with small organic molecules of 11-mercaptoundecanoic
Booth HS.
Inorganic Syntheses, 48-48 (2009)
Booth HS.
Inorganic Syntheses, 51-51 (2009)

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