ChemicalBook >> CAS DataBase List >>Diphenylphosphine

Diphenylphosphine

CAS No.
829-85-6
Chemical Name:
Diphenylphosphine
Synonyms
HPPh2;PH2PH;Diphenylphosphin;98% Ph2PH;AURORA KA-1107;DIPHENYLPHOSPHINE;Diphenyl phospine;Diphenyl-phosphane;PHOSPHINE, DIPHENYL;DPP/DIPHENYLPHOSPHIN
CBNumber:
CB0720195
Molecular Formula:
C12H11P
Molecular Weight:
186.19
MDL Number:
MFCD00003040
MOL File:
829-85-6.mol
MSDS File:
SDS
Last updated:2025-09-25 17:15:13
Product description Number Pack Size Price
Diphenylphosphine 98% 252964 10g $88.3
Diphenylphosphine 98% 252964 1kg $1490
Diphenylphosphine, 99% 15-1700 10g $68
Diphenylphosphine, 99% 15-1700 50g $254
Diphenylphosphine min. 97% (30 wt% in 2-methyltetrahydrofuran) Diphenylphosphine min. 97% (30 wt% in 2-methyltetrahydrofuran) 15-1701 100g $423
More product size

Diphenylphosphine Properties

Melting point -14.5 °C
Boiling point 280 °C(lit.)
Density 1.07 g/mL at 25 °C(lit.)
vapor pressure 2 mm Hg ( 110 °C)
refractive index n20/D 1.625(lit.)
Flash point -18°C (Hexane)
storage temp. 2-8°C
solubility Chloroform
pka diphenylphosphine is weakly basic. The pKa of the protonated derivative is 0.03.
form liquid
color colorless
Specific Gravity 0.68
Water Solubility Miscible with ethanol, ether, benzene, concentrated hydrochloric acid. Immiscible with water.
Sensitive Air & Moisture Sensitive
Hydrolytic Sensitivity 8: reacts rapidly with moisture, water, protic solvents
BRN 742504
InChIKey GPAYUJZHTULNBE-UHFFFAOYSA-N
CAS DataBase Reference 829-85-6(CAS DataBase Reference)
FDA UNII F9B5T7O7ZY
NIST Chemistry Reference Phosphine, diphenyl-(829-85-6)

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictogramsGHS hazard pictograms
GHS02,GHS07
Signal word  Danger
Hazard statements  H250-H315-H319-H335
Precautionary statements  P210-P222-P231+P232-P302+P352-P305+P351+P338-P370+P378
Hazard Codes  F,Xi
Risk Statements  17-36/37/38
Safety Statements  26-36
RIDADR  UN 2845 4.2/PG 1
WGK Germany  3
8-10-13-23
HazardClass  4.2
PackingGroup  I
HS Code  29319090
Limited Quantities 0.5 L (0.1 gallon)
Excepted Quantities Max Inner Pack (30g or 30ml) and Max Outer Pack (300g or 300ml)
NFPA 704
4
2 2

Diphenylphosphine price More Price(19)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 252964 Diphenylphosphine 98% 829-85-6 10g $88.3 2025-07-31 Buy
Sigma-Aldrich 252964 Diphenylphosphine 98% 829-85-6 1kg $1490 2025-07-31 Buy
Strem Chemicals 15-1700 Diphenylphosphine, 99% 829-85-6 10g $68 2024-03-01 Buy
Strem Chemicals 15-1700 Diphenylphosphine, 99% 829-85-6 50g $254 2024-03-01 Buy
Strem Chemicals 15-1701 Diphenylphosphine min. 97% (30 wt% in 2-methyltetrahydrofuran) Diphenylphosphine min. 97% (30 wt% in 2-methyltetrahydrofuran) 829-85-6 100g $423 2021-12-16 Buy
Product number Packaging Price Buy
252964 10g $88.3 Buy
252964 1kg $1490 Buy
15-1700 10g $68 Buy
15-1700 50g $254 Buy
15-1701 100g $423 Buy

Diphenylphosphine Chemical Properties,Uses,Production

Organophosphorus compound

Diphenylphosphine is commonly used in laboratory as organic phosphorus compound, it is unpleasant odor colorless liquid, and it is pungent, it is easily oxidized in air and can cause spontaneous combustion, it is sensitive to air and light, it need the protection of nitrogen. It can be used as precursor to synthesize some organic phosphine ligand. By deprotonation, it can be converted to diphenylphosphine compound: Ph2PH + nBuLi → Ph2PLi + nBuH, such as 1,2-bis (diphenylphosphino) ethane and 1,3-bis (diphenylphosphino) propane phosphine ligands etc, Wittig-Horner reagents and the synthesis of quaternary phosphonium salt is usually by means of diphenylphosphino alkylation to achieve.
Diphenylphosphine such as sodium and lithium diphenylphosphine and diphenylphosphine compound can add to carbon heteroatom double bond as nucleophile. For example, in the condition of concentrated hydrochloric acid at 100℃, diphenylphosphine can add to aldehyde carbon atoms of benzaldehyde: Ph2PH + PhCHO → Ph2P (O) CH2Ph, when compares with tertiary phosphine, alkalinity of diphenylphosphine is weaker. The pKa of conjugate acid diphenylphosphine is 0.03: Ph2PH2 + → Ph2PH + H +
Preparation: Lithium diphenylphosphine can generated by inexpensive triphenylphosphine and the with the cancellation of water can obtain diphenylphosphine: (1) PPh3 + 2 Li → LiPPh2 + LiPh (2) LiPPh2 + H2O → Ph2PH + LiOH.
The above information is edited by the chemicalbook of Wang Xiaodong.

Uses

It can be used the intermediates of organic, catalysts.

Chemical Properties

Diphenylphosphine is an organophosphorus compound commonly used in laboratories. It is a clear colorless to slightly yellow liquid with unpleasant odor, irritating, easily oxidized in air and spontaneously combusts, sensitive to air and light, and needs to be protected by nitrogen. It can be used as a precursor for the synthesis of a variety of organophosphine ligands. These ligands, in turn, are used in homogeneous catalysis for many applications including: asymmetric hydrogenation, coupling chemistry, ethylene oligomerization, hydroformylation, hydration of nitriles, and polymerization of alkenes.

Uses

suzuki reaction

Uses

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.

Uses

Diphenylphosphine acts as an intermediate in the preparation of diphenylphosphide derivatives, phosphonium salts, phosphine ligands and Wittig-Horner reagents. The presence of hydrogen atom bonded to phosphorus undergoes Michael-like addition to activated alkenes. It is involved in the preparation of 1,2-bis(diphenylphosphino)ethane and (phenyl-(phenylmethyl)phosphoryl)benzene. Further, it is used in the synthesis of aminophosphines and chiral palladacycles with N-heterocyclic carbene ligands as catalysts.

Preparation

Diphenylphosphine can be prepared from triphenylphosphine by reduction to lithium diphenylphosphide, which can be protonated to give the title compound:
PPh3 + 2 Li → LiPPh2 + LiPh
LiPPh2 + H2O → Ph2PH + LiOH

24630-80-6
1707-03-5
829-85-6
Synthesis of Diphenylphosphine from Phosphinous acid, P,P-diphenyl- and Diphenylphosphinic acid
Global( 340)Suppliers
Supplier Tel Email Country ProdList Advantage
Puyang Huicheng Electronic Materials Co., Ltd.
+86-0393-+86-0393-8910800 +8615839383373 info@huichengchem.com China 529 58
Shanghai Bojing Chemical Co.,Ltd.
+86-86-02137122233 +8613795318958 bj1@bj-chem.com China 299 55
Hebei Chuanghai Biotechnology Co., Ltd
+8615350571055 Sibel@chuanghaibio.com China 8753 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21597 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
AB PharmaTech,LLC
323-480-4688 sales@acrospharmatech.com United States 989 55
career henan chemical co
+86-0371-86658258 +8613203830695 sales@coreychem.com China 29831 58
Changzhou Ditong Chemical Co.,Ltd
+86-0519-88298848 info@edengenechem.com China 2176 58
Shandong chuangyingchemical Co., Ltd.
18853181302 sale@chuangyingchem.com CHINA 5906 58
Changzhou Carman Chemical Co., Ltd.
15061933924 CHINA 514 58

Related articles

View Lastest Price from Diphenylphosphine manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Diphenylphosphine pictures 2026-01-30 Diphenylphosphine
829-85-6
US $0.00-0.00 / KG 1KG 99% 20 mt Hebei Chuanghai Biotechnology Co., Ltd
Diphenylphosphine  pictures 2025-12-12 Diphenylphosphine
829-85-6
US $1.00-0.00 / KG 1KG 99% 20 Tons Shaanxi Dideu Medichem Co. Ltd
Diphenylphosphine pictures 2025-04-04 Diphenylphosphine
829-85-6
US $0.00-0.00 / kg 1kg 98% 1Ton Henan Aochuang Chemical Co.,Ltd.
  • Diphenylphosphine pictures
  • Diphenylphosphine
    829-85-6
  • US $0.00-0.00 / KG
  • 99%
  • Hebei Chuanghai Biotechnology Co., Ltd
PHOSPHINE, DIPHENYL Diphenyl-phosphane Diphenylphosphin Diphenyl phospine Diphenylphosphine,99% Diphenylphosphine,99%(10wt%inhexane) DIPHENYLPHOSPHINE AURORA KA-1107 Diphenylphosphine, 99% 20% in heptane Diphenylphosphine, 99% 10% thf DIPHENYLPHOSPHINE OR PHOSPHINE, DIPHENYL DPP/DIPHENYLPHOSPHIN PH2PH DIPHENYLPHOSPHINE, 10% SOLUTION IN HEXANE Diphenylphosphine ,98% Diphenylphosphine,95% Diphenyl phosphine (DPP) Diphenylphosphine, AcroSeal, 95% Diphenylphosphine, 98% (20% in hexanes) Diphenylphosphine, 99% (20% in hexanes) 98% Ph2PH Diphenylphosphine, 95%, AcroSeal Diphenylphosphine,98% Ph2PH HPPh2 Diphenylphosphine, 10 wt.% sulution in hexanes Diphenylphosphine, 99% (10 wt% in hexanes) Diphenylphosphine, 10 wt.% sulution in hexanes, J&KSeal 20% Diphenylphosphine Hexane Solution Diphenylphosphine (UK sale only) 829-85-6 C12H11P Phosphorus Compounds Phosphorus Precursors Catalysis and Inorganic Chemistry organophosphorus ligand organophosphine ligand Pyrazoles Catalysis and Inorganic Chemistry Phosphorus Compounds Phosphorus Precursors