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Home > Organic Chemistry > Phosphines (Find 726 items)

Phosphines

Phosphines are compounds of organophosphine and phosphine gas(PH3) which are essential chemicals that are used widely owing to their reactivity. These compounds are applied in the synthesis of agrochemical products, pharmaceuticals, and semiconductors as such products need quality raw materials for quality output in their production. Learn more about phosphines such as the CAS No., as well as properties and information of materials and products from our suppliers available on ECHEMI.

Diphenylphosphine

(829-85-6)
Diphenylphosphine is used in the synthesis of aminophosphines for application as catalysts. It is also used in the preparation of chiral palladacycles with N-heterocyclic carbene ligands as catalysts.

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Tricyclohexylphosphine

(2622-14-2)
Tricyclohexyl Phosphine is a ligand catalyst used primarily in organometallic chemistry. Ligand used in the Pd-catalyzed coupling of malononitrile with aryl halides. suzuki reaction: Bulky phosphine ligand used with a Pd(0)-triolefinic macrocycle catalyst for Suzuki coupling of aryl bromides and chlorides. This ligand is applied with Ni as a key intermediate in the formation of cylcopentane compounds. As a reagent, Tricyclohexylphosphine is used for a range of metal-catalyzed organic transformat

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Tributylphosphine

(998-40-3)
Usually used as catalyst for Domino reactions of activated conjugated dienes with β,γ?unsaturated-α-ketoesters, [3+2]-Cycloadditions,Umpolung addition reactions,Reductive carbonylation, Allylation reactions.

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Tri-tert-butylphosphine

(13716-12-6)
The preferred ligand for the palladium-catalyzed coupling reaction between arylboronic acid and hydroxyquinone phenyl iodide. It can also be used together with Pd(dba) for α-arylation of trimethylsilyl enol ether and aryl halide.

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BINAP

(98327-87-8)
racemic-2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl ( (+/-)-BINAP ) is an essential role in the organic synthesis of enantioselective transformations catalyzed by the complexes of ruthenium, rhodium and palladium. It is also employed in palladium-catalyzed arylamine coupling in the preparation of demethylthiocholchines. used with Cu(II) to catalyze the addition of arylsulfonamides to styrenes and olefins.

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Benzyltriphenylphosphonium chloride

(1100-88-5)
Benzyltriphenylphosphonium chloride is used as an organic synthesis reagent for several compounds, including stable phosphine ylides containing saturated oxygen heterocycles, and is also used to synthesize new substituted cis-stilbene derivatives with antibacterial activity. Benzyltriphenylphosphonium chloride is used in combination with bisphenol AF as a vulcanizing agent for fluororubber.

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Fosetyl aluminum

(39148-24-8)
It is a systemic fungicide suitable for the prevention and treatment of diseases caused by Monoaxial mold and Peronospora on fruit trees, vegetables, flowers, and economic crops. It is effective against many diseases of the genus Peronospora, Phytophthora, and Frostaceae, and has a longer duration. Mainly used for cucumber, vegetables, lettuce, grape downy mildew, spray with 40% wettable powder 400-600 times, once a week, 3 to 4 times in total. In addition, it is also used for tomato, potato, eg

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[1,1′-Bis(diphenylphosphino)ferrocene]dichloropalladium

(72287-26-4)
Catalyst for carbonylation reaction, cross-coupling reaction, Suzuki reaction. C-C and C-N coupling reaction catalyst [1,1'-Bis(diphenylphosphino)ferrocene]palladium dichloride (PdCl2(dppf)) as a catalyst is mainly used to catalyze the cross-coupling reaction. Similar to other Pd(II) and Ni(II) complexes, PdCl2(dppf) can effectively catalyze the cross-coupling reaction between halogenated olefins, halogenated aromatic hydrocarbons or trifluoromethanesulfonate aromatic hydrocarbons and Grignard

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Phosphine is a general term for phosphorus hydrides and their alkyl and aryl substituents. Among them, relatively stable trialkyl and triaryl substituents have been widely used in industry. Phosphines can form a large number of coordination compounds with various metals, have a catalytic effect on many chemical reactions, and have been applied in industry.

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Phosphines are one of the most vital classes of phosphorus-based compounds with their application in several industries. Phosphine, the simplest of these compounds, is a colorless, very reactive gas used in many manufacturing processes. Phosphine gas is used in industries that need high-purity materials for their state-of-the-art products. Due to its reactivity, it is suitable for use in chemical reactions that produce important intermediate products.

Phosphines are a class of compounds widely used in the synthesis of various industries including agrochemicals, pharmaceuticals and electronics. Phosphine and its derivatives are widely used in the synthesis of flame retardants that are indispensable for producing safer materials. Furthermore, they are used in the semiconductor industry where the role of chemical reactions is decisive in creating high-quality semiconductors. Phosphines are also employed in chemical vapour deposition processes, which prove their involvement in the synthesis of the latest materials.

Key Applications of Phosphines:

Applied in making flame retardants for safer materials.

Applied in the production of semiconductors for manufacturing of semiconductor devices.

Used in the manufacture of pharmaceuticals, especially the intermediates.

Used in the synthesis of pesticides and herbicides.

Applied in chemical vapour deposition in the production of electronic components.

Function as ligands in catalytic activities in various reactions.

Frequently Asked Questions

What are phosphines and what are they used for?

Phosphines are organophosphorus compounds containing a trivalent phosphorus atom bonded to three organic substituents. They are widely used as ligands in transition metal catalysis, particularly in cross-coupling reactions such as Suzuki, Heck, and Stille couplings. Phosphines also play essential roles in pharmaceutical synthesis, agrochemical manufacturing, and materials science due to their electron-donating properties and ability to modulate catalyst activity and selectivity.

How do I choose the right phosphine ligand for my catalytic reaction?

Selecting the appropriate phosphine ligand depends on several factors:1. The type of metal catalyst being used (e.g., palladium, nickel, rhodium).2. The desired reaction outcome—bulky or electron-rich phosphines may enhance reactivity or selectivity.3. Air and moisture sensitivity; some phosphines (like triphenylphosphine) are stable, while others (e.g., trialkylphosphines) require inert handling.4. Solubility and compatibility with your reaction solvent.Consulting literature precedents for similar transformations is a reliable starting point.

Are phosphines hazardous to handle?

Many phosphines can pose health and safety risks. Tertiary phosphines, especially low-molecular-weight alkylphosphines, are often pyrophoric (ignite spontaneously in air) and toxic if inhaled or absorbed through the skin. Aromatic phosphines like triphenylphosphine are generally more stable but still require proper handling under inert atmosphere when high purity is needed. Always use appropriate personal protective equipment (PPE), work in a fume hood, and follow SDS guidelines for safe storage and disposal.

What are common types of phosphine ligands used in industrial applications?

Common phosphine ligands in industrial settings include triphenylphosphine (PPh₃), tricyclohexylphosphine (PCy₃), tri(o-tolyl)phosphine, and bidentate phosphines like 1,2-bis(diphenylphosphino)ethane (dppe) and Xantphos. These ligands are selected based on steric bulk (measured by Tolman cone angle) and electronic properties (Tolman electronic parameter). For large-scale processes, air-stable and recyclable phosphine derivatives are preferred to ensure operational safety and cost efficiency.

How should phosphines be stored to maintain stability and purity?

To preserve stability and prevent oxidation, phosphines should be stored under an inert atmosphere (argon or nitrogen) in tightly sealed, amber glass bottles at low temperatures (typically 2–8°C or –20°C for sensitive types). Avoid exposure to light, moisture, and oxygen. For long-term storage, consider using glovebox conditions or ampoule-sealed formats. Always check for discoloration or precipitate formation before use, as these may indicate degradation to phosphine oxides.

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