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Nom du produit
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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Catégories apparentées
1 of 4
Cet article | T84409 | 8.08270 | 8.00551 |
|---|---|---|---|
| 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 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
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1B - STOT RE 1 Inhalation
target_organs
Central nervous system,Peripheral nervous system
Classe de stockage
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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