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93092

Triphenylphosphine

≥95.0% (GC), crystals

Synonym(s):

Phosphorustriphenyl

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250 g

Available to ship TODAYfromMILWAUKEE

$120.00
1 kg

Available to ship TODAYfromMILWAUKEE

$225.00
$168.75

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)

vapor density

9 (vs air)

Quality Segment

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

SMILES string

c1ccc(cc1)P(c2ccccc2)c3ccccc3

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

InChI key

RIOQSEWOXXDEQQ-UHFFFAOYSA-N

General description

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

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).

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This Item
T844098.082708.00551
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, reaction type: Negishi Coupling, reagent type: ligand

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

-

assay

≥95.0% (GC)

assay

99%

assay

≥99.0% (GC)

assay

≥97.0% (GC)

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

bp

377 °C (lit.)

bp

377 °C (lit.)

bp

377 °C/1013 hPa

bp

360 °C/1013 hPa (decomposes)


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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)
Booth HS.
Inorganic Syntheses, 48-48 (2009)



Global Trade Item Number

SKUGTIN
93092-250G04061833274880
93092-1KG04061833274859

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