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Diphenylphosphinic Chloride

CAS No.
1499-21-4
Chemical Name:
Diphenylphosphinic Chloride
Synonyms
DPPC;DPP-CL;DIPHENYLPHOSPHINIC CHLORIDE;Ph2POCl;DIPHENYLPHOSPHINYL CHLORIDE;Diphenylphosphinoyl chloride;CHLORODIPHENYLPHOSPHINE OXIDE;Diphenylphosphinic acid chloride;phosphinic chL;Diphenylphoshinic
CBNumber:
CB8273899
Molecular Formula:
C12H10ClOP
Molecular Weight:
236.63
MDL Number:
MFCD00002077
MOL File:
1499-21-4.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 06:11:28

Diphenylphosphinic Chloride Properties

Melting point 20°C
Boiling point 222 °C/16 mmHg (lit.)
Density 1.24 g/mL at 25 °C (lit.)
refractive index n20/D 1.609(lit.)
Flash point 79 °F
storage temp. 2-8°C
solubility soluble in Chloroform, methanol
form Liquid
color Clear colorless to yellow
Specific Gravity 1.24
Water Solubility decomposes
Sensitive Moisture Sensitive
BRN 975191
InChI 1S/C12H10ClOP/c13-15(14,11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H
InChIKey QPQGTZMAQRXCJW-UHFFFAOYSA-N
SMILES ClP(=O)(c1ccccc1)c2ccccc2
CAS DataBase Reference 1499-21-4(CAS DataBase Reference)
FDA UNII 5GP30GY04V
NIST Chemistry Reference Diphenylphosphinic chloride(1499-21-4)
UNSPSC Code 12352002
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Flame (GHS02)Corrosion (GHS05)
GHS02,GHS05
Signal word  Danger
Hazard statements  H226-H314
Precautionary statements  P210-P280-P303+P361+P353-P305+P351+P338+P310
PPE Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Hazard Codes  C,F
Risk Statements  10-34
Safety Statements  16-26-36/37/39-45
RIDADR  UN 2920 8/PG 2
WGK Germany  3
10-21
Hazard Note  Flammable/Corrosive
HazardClass  8
PackingGroup  II
HS Code  29310095
Storage Class 3 - Flammable liquids
Hazard Classifications Eye Dam. 1
Flam. Liq. 3
Skin Corr. 1B
Skin Sens. 1A
REACH Registrations Active
NFPA 704
2
3 0

Diphenylphosphinic Chloride price More Price(48)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 230235 Diphenylphosphinic chloride 98% 1499-21-4 10g $82.8 2026-04-30 Buy
Sigma-Aldrich 230235 Diphenylphosphinic chloride 98% 1499-21-4 50g $325 2026-04-30 Buy
TCI Chemical C1415 Diphenylphosphinic Chloride >98.0%(GC)(T) 1499-21-4 25g $121 2026-04-30 Buy
Strem Chemicals 15-1740 Diphenylphosphinic chloride, 98% 98% 1499-21-4 5g $41 2026-04-30 Buy
Strem Chemicals 15-1740 Diphenylphosphinic chloride, 98% 98% 1499-21-4 25g $147 2026-04-30 Buy
Product number Packaging Price Buy
230235 10g $82.8 Buy
230235 50g $325 Buy
C1415 25g $121 Buy
15-1740 5g $41 Buy
15-1740 25g $147 Buy

Diphenylphosphinic Chloride Chemical Properties, Uses, Production

Chemical Properties

clear colorless to yellow liquid

Uses

Diphenylphosphinic chloride (Ph2POCl) is widely used as a precursor to synthesize various chiral phosphine bidentate ligands for asymmetric synthesis, in addition to several peptide coupling agents.

Application

Diphenylphosphinic chloride is a reagent that is used in the synthesis of bidentate ligands and peptide coupling agents. It is used as flame retardants. It also act as pharmaceutical adjuvant.

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

Synthesis

To an oven-dried 100 mL, a two-necked flask fitted with a reflux condenser was added Et2O (depending on the Grignard reagent solution's concentration) and POCl3. The solution was cooled in an ice-salt mixture, and a Grignard reagent solution in Et2O was slowly added. After stirring with cooling for 30 min, the reaction mixture was brought to rt and stirred for the indicated time. The mixture was then cooled in an ice-salt mixture, and the alcohol and pyridine were slowly added. Stirring with cooling for 5 min was followed by reaction at rt. The reaction was quenched after the indicated time by cooling in an ice-salt mixture and adding sat aq NH4Cl. The crude mixture was then poured into CH2Cl2, washed three times with HCl, dried, filtered, and evaporated to dryness. The excess alcohol was removed using a short-path vacuum distillation apparatus, and the resulting crude product Diphenylphosphinic Chloride was purified by column chromatography.Diphenylphosphinic Chloride

824-72-6
108-90-7
1499-21-4
Synthesis of Diphenylphosphinic Chloride from Phenylphosphonic dichloride and Chlorobenzene

Diphenylphosphinic Chloride Preparation Products And Raw materials

Global Suppliers ( 406)
Supplier Tel Email Country ProdList Advantage
xinxiang runyu material co.,Ltd 03737759608 15690792173 sales@runvmat.com China 300 58
Hubei Jusheng Technology Co.,Ltd 027-59599241 18871490274 1400878000@qq.com China 9506 58
Shaoxing Fangxiao Chemical Co., LTD +86-13456999252; 13456999252 shellyhouse39@126.com China 41 58
Jiangsu Huaweisite Pharmaceutical Technology Co., Ltd. 0519-88721112 supporting@harvechem.com China 84 58
BEIJING ODYSSEY CHEMICALS CO.,LTD 10-88018188-315 17502279376 kallisto@bj-odyssey.com China 32 58
Shijiazhuang Benchu Technology Co., Ltd. 0311-680150596798-6798 17367983103 925646462@qq.com China 29 58
J & K SCIENTIFIC LTD. 18210857532 18210857532 jkinfo@jkchemical.com China 96815 76
Meryer (Shanghai) Chemical Technology Co., Ltd. 4006356688 18621169109 market03@meryer.com China 40202 62
Beijing Donghualituo Techonlogy Development Co.,Ltd. 010-88425576 sales@dhltchem.com China 793 59
INTATRADE GmbH +49 3493/605464 sales@intatrade.de Germany 3563 66

View Latest Price from Diphenylphosphinic Chloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Diphenylphosphinic chloride, 98% pictures 2026-09-18 Diphenylphosphinic chloride, 98%
1499-21-4
$20.00 1KG 98% 200tons/ year Speranza Chemical Co., Ltd.
Diphenylphosphinic Chloride pictures 2026-06-30 Diphenylphosphinic Chloride
1499-21-4
1KG 99.0% 10000KGS Shaanxi Dideu New Materials Co. Ltd
Diphenylphosphinic Chloride pictures 2025-12-23 Diphenylphosphinic Chloride
1499-21-4
1KG 99%+ 250KG XINXIANG RUNYU MATERIAL CO., LTD.
Diphenyl phosphilic chloride Diphenylphoshinic DIPHENYLPHOSHINIC CHLORIDE Diphenylchlorophosphine oxide Diphenylphosphinyl chloride,98% (Chloro-phenylphosphoryl)benzene Diphenylphosphinicchloride,98% DIPHENYLPHOSPHINYL CHLORIDE OR CHLORODIPHENYLPHOSPHINE OXIDE ORDIPHENYLPHOSPHINIC CHLORIDE Diphenylphosphinic chloride,Chloro Diphenylphosphinic chloride,Chlorodiphenylphosphine oxide Bis(phenyl)phosphinic chloride Diphenylphosphinyl choloride Bis(phenyl)chlorophosphine oxide Diphenylphosphinyl chloride, 98% 50GR Diphenylphosphinic chloride, 97+% Diphenylphosphinic chlorid Two phenylphosphinicchloride Diphenylphosphinochloridic acid Phosphine oxide, chlorodiphenyl- PHOSPHINIC CHLORIDE, DIPHENYL- DIPHENYLPHOSPHINIC CHLORIDE CHLORODIPHIOSPHINE OXIDE phosphinic chL DiphenylphosphinicChloride> Phosphinic chloride, P,P-diphenyl- Diphenylphosphinyl chloride 1499-21-4 diphenylhypophosphinoacylchloro DPPC CHLORODIPHENYLPHOSPHINE OXIDE Diphenylphosphinic acid chloride Diphenylphosphinoyl chloride DIPHENYLPHOSPHINYL CHLORIDE DPP-CL Ph2POCl 1499-21-4 C6H5POCl C12H10CIO C12H10ClOP C6H52POCl C12H10POCl Catalysis and Inorganic Chemistry Organic Building Blocks Phosphorus Compounds Phosphorus Halides Phosphorus Precursors Reagents for Oligosaccharide Synthesis Peptide Synthesis Protection & Derivatization Reagents (for Synthesis) Coupling Reactions (Peptide Synthesis) Building Blocks Biochemistry Coupling Reactions (Peptide Synthesis) Peptide Synthesis Protection & Derivatization Reagents (for Synthesis) Reagents for Oligosaccharide Synthesis Synthetic Organic Chemistry Phosphorus compounds Pharmaceutical Intermediates