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Triphenylphosphin

≥95.0% (GC), crystals

Synonym(e):

Phosphortriphenyl

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Größe/SKUVerfügbarkeitPreis
250 g
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€ 98,40
€ 73,80
1 kg
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Über diesen Artikel

Lineare Formel:
(C6H5)3P
CAS-Nummer:
Molekulargewicht:
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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Produktname

Triphenylphosphin, ≥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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T84409216666
description

≥95.0% (GC)

description

ReagentPlus®, 99%

description

99%

assay

≥95.0% (GC)

assay

99%

assay

99%

reaction suitability

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

reaction suitability

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

reaction suitability

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

functional group

phosphine

functional group

phosphine

functional group

-

form

crystals

form

-

form

solid

Quality Level

200

Quality Level

200

Quality Level

200

bp

377 °C (lit.)

bp

377 °C (lit.)

bp

-


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Piktogramme

Health hazardExclamation mark

Signalwort

Danger

Zielorgane

Central nervous system,Peripheral nervous system

Lagerklasse

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

Flammpunkt (°F)

356.0 °F - closed cup

Flammpunkt (°C)

180 °C - closed cup

PSA (Persönliche Schutzausrüstung)

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

Gefahrencodes

Hazard Classifications

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



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