Isopropyldiphenylphosphine
Isopropyldiphenylphosphine (CAS 6372-40-3) is an organophosphorus compound with the linear formula (C6H5)2PCH(CH3)2 and a molecular weight of 228.27 g/mol. It serves as a valuable ligand and catalyst in various organic synthesis reactions, particularly in transition metal catalysis. Its applications span cyanation, carbonylation, and cross-coupling methodologies, making it a key reagent for chemists.
- IUPAC
- NSC 244305

Nickel/Lewis Acid-Catalyzed Reactions
Utilised as a catalyst in nickel/Lewis acid-mediated aryl- and alkenylcyanation of unsaturated bonds, as well as in the cyanoesterification and cyanocarbamoylation of alkynes.
Palladium-Catalyzed Transformations
Functions as a ligand in palladium-catalyzed methoxycarbonylation reactions and decarboxylative cross-coupling processes. It is also employed in the hydroesterification of vinylarenes.
Asymmetric Hydrogenation
A component in iridium complexes for the asymmetric hydrogenation of quinolines, utilising BINOL-derived diphosphonites.
Heck Coupling Reactions
Acts as a ligand precatalyst enabling Heck coupling reactions to proceed effectively at room temperature.
| Molecular weight | 228.27 |
|---|---|
| Linear formula | (C6H5)2PCH(CH3)2 |
| Assay | 97% |
| Boiling point | 165 °C/11 mmHg(lit.) |
| Application | Catalyst in:• Nickel/Lewis acid-catalyzed aryl- and alkenylcyanation of unsaturated bonds1• Nickel/Lewis Acid-Catalyzed Cyanoesterification and Cyanocarbamoylation of Alkynes2• Methoxycarbonylation reactions (palladium complex)3• Decarboxylative cross-coupling in the presence of palladium4• Asymmetric hydrogenation of quinolines catalyzed by iridium complexes of BINOL-derived diphosphonites5• Hydroesterification of vinylarenes in complex with palladium6• Ligand precatalyst for room-temperature Heck coupling reactions7 |
| Melting point | 40-43 °C(lit.) |

Hazard statements
- H315Causes skin irritation
- H319Causes serious eye irritation
- H335May cause respiratory irritation
Precautionary statements
- P261Avoid breathing dust, fume, gas or vapours
- P305IF IN EYES
| Protective equipment | dust mask type N95 (US), Eyeshields, Gloves |
|---|---|
| Flash point | 113 °C / 235.4 °F |
| Water hazard class (WGK, DE) | 3 |
| Hazard codes (EU) | Xi |
| Risk statements (R) | 36/37/38 |
| Safety statements (S) | 26-37/39 |
Hazard information is provided for guidance. Always consult the product Safety Data Sheet (SDS), available on request, before handling.
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is Isopropyldiphenylphosphine used for?
+
Isopropyldiphenylphosphine is used as a catalyst and ligand in various organic synthesis reactions, including cyanation, carbonylation, and cross-coupling methodologies, particularly in transition metal catalysis.
What is the CAS number and formula for Isopropyldiphenylphosphine?
+
The CAS number for Isopropyldiphenylphosphine is 6372-40-3 and its linear formula is (C6H5)2PCH(CH3)2.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies Isopropyldiphenylphosphine with a purity of 97%. We do not represent this product as USP, BP, or EP grade.
How should Isopropyldiphenylphosphine be handled?
+
Isopropyldiphenylphosphine is classified as a Warning substance, with hazards including skin irritation (H315), serious eye irritation (H319), and respiratory irritation (H335). Appropriate personal protective equipment, including a dust mask (N95), eyeshields, and gloves, should be used. Ensure adequate ventilation.
How is Isopropyldiphenylphosphine packed and shipped?
+
Isopropyldiphenylphosphine is carefully packed and exported globally by Tech Serve Solutions, adhering to all relevant shipping regulations for chemical compounds.
How can I request a quote or sample for Isopropyldiphenylphosphine?
+
To request a quote or sample for Isopropyldiphenylphosphine, please contact the Tech Serve Solutions sales department through our website or by phone.
▶ Related products

Benzeneruthenium(II) chloride dimer
Ru2(C6H6)2Cl4
Catalysis & Inorganic
Benzoylferrocene
C17H14FeO
Catalysis & Inorganic
Benzyldiphenylphosphine
C6H5CH2P(C6H5)2
Catalysis & Inorganic
Beryllium
Be
Catalysis & Inorganic
Beryllium oxide
BeO
Catalysis & Inorganic![Bicyclo[2.2.1]hepta-2,5-diene-rhodium(I) chloride dimer — chemical structure, CAS 12257-42-0; Catalysis & Inorganic, fine chemical supplied by Tech Serve Solutions](/_next/image?url=https%3A%2F%2Fpub-f4d920c906024441a773a96f7098e551.r2.dev%2Fimages%2Fproducts%2F12257-42-0.png&w=3840&q=75)
Bicyclo[2.2.1]hepta-2,5-diene-rhodium(I) chloride dimer
Catalysis & Inorganic
![Bis[(10,11-η)-5-[(11bS)-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-yl- κP4]-5H-dibenz[b,f]azepine]rhodium(I) tetrafluorobo — chemical structure, CAS 1228149-03-8; Catalysis & Inorganic, fine chemical supplied by Tech Serve Solutions](/_next/image?url=https%3A%2F%2Fpub-f4d920c906024441a773a96f7098e551.r2.dev%2Fimages%2Fproducts%2F1228149-03-8.png&w=3840&q=75)
Bis[(10,11-η)-5-[(11bS)-dinaphtho[2,1-d:1′,2′-f][1,3,2]dioxaphosphepin-4-yl- κP4]-5H-dibenz[b,f]azepine]rhodium(I) tetrafluorobo
1-d:1′
Catalysis & Inorganic![Bis[(2-dimethylamino)phenyl]amine nickel(II) chloride (C16H20ClN3Ni) — chemical structure, CAS 1033772-47-2; Catalysis & Inorganic, fine chemical supplied by Tech Serve Solutions](/_next/image?url=https%3A%2F%2Fpub-f4d920c906024441a773a96f7098e551.r2.dev%2Fimages%2Fproducts%2F1033772-47-2.png&w=3840&q=75)
Bis[(2-dimethylamino)phenyl]amine nickel(II) chloride
C16H20ClN3Ni
Catalysis & Inorganic▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis