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1,5-Bis(diphenylphosphino)pentane

CAS No.
27721-02-4
Chemical Name:
1,5-Bis(diphenylphosphino)pentane
Synonyms
DPPPE;DPPENT;1,5-Bis(diphenyL;phosphino)pentane;98% Ph2P(CH2)5PPh2;1,5-BIS(DIPHENYPHOSPHINO);1,5-Bis(Diphenylphosphino);Bis(diphenylphosphino)pentane;1,5-bis(diphenylphosphino)pent;1,5-Bis(diphenyphosphino)Pentane
CBNumber:
CB6429845
Molecular Formula:
C29H30P2
Molecular Weight:
440.5
MDL Number:
MFCD00003052
MOL File:
27721-02-4.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 05:24:00

1,5-Bis(diphenylphosphino)pentane Properties

Melting point 43-47 °C (lit.)
Boiling point 230 C
Flash point >230 °F
storage temp. Inert atmosphere,Room Temperature
solubility Soluble in N,N-dimethyl formamide.
form Powder to Crystals or Chunks
color White to light yellow
BRN 2953640
InChI 1S/C29H30P2/c1-6-16-26(17-7-1)30(27-18-8-2-9-19-27)24-14-5-15-25-31(28-20-10-3-11-21-28)29-22-12-4-13-23-29/h1-4,6-13,16-23H,5,14-15,24-25H2
InChIKey MZFPAWGWFDGCHP-UHFFFAOYSA-N
SMILES C(CCP(c1ccccc1)c2ccccc2)CCP(c3ccccc3)c4ccccc4
CAS DataBase Reference 27721-02-4(CAS DataBase Reference)
UNSPSC Code 12352002
NACRES NA.22

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P264-P271-P280-P302+P352-P305+P351+P338
target organs Respiratory system
PPE dust mask type N95 (US), Eyeshields, Gloves
Hazard Codes  Xi,F
Risk Statements  36/37/38-10
Safety Statements  26-37/39-36-16
WGK Germany  3
10-23
TSCA  No
HS Code  29319090
Storage Class 11 - Combustible Solids
Hazard Classifications Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
NFPA 704
1
2 0

1,5-Bis(diphenylphosphino)pentane price More Price(61)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich 287997 1,5-Bis(diphenylphosphino)pentane 97% 27721-02-4 1g $31.68 2024-03-01 Buy
Sigma-Aldrich 287997 1,5-Bis(diphenylphosphino)pentane 97% 27721-02-4 5g $61.8 2024-03-01 Buy
TCI Chemical B1960 1,5-Bis(diphenylphosphino)pentane >96.0%(GC)(T) 27721-02-4 1g $27 2026-04-30 Buy
Strem Chemicals 15-0430 1,5-Bis(diphenylphosphino)pentane, min. 98% min.98% 27721-02-4 1g $43 2026-04-30 Buy
Strem Chemicals 15-0430 1,5-Bis(diphenylphosphino)pentane, min. 98% min.98% 27721-02-4 5g $162 2026-04-30 Buy
Product number Packaging Price Buy
287997 1g $31.68 Buy
287997 5g $61.8 Buy
B1960 1g $27 Buy
15-0430 1g $43 Buy
15-0430 5g $162 Buy

1,5-Bis(diphenylphosphino)pentane Chemical Properties, Uses, Production

Chemical Properties

white to light yellow crystal powde

Uses

1,5-Bis(diphenylphosphino)pentane is used as a ligand for the cross coupling reactions. It is used in the manufacturing of glass bottle PTFE bottle, aluminum foil bag and in cardboard drum. combination of a 1,5-bis(diphenylphosphino)pentane ligand and the addition of N,N,N,N-tetramethylethylenediamine (TMEDA) as a co-catalyst are the key factors in obtaining the corresponding aryl nitriles with improved catalyst productivities and selectivities.

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

Synthesis

1,5-Dichloropentane

628-76-2

Lithium

7439-93-2

Triphenylphosphine

603-35-0

1,5-Bis(diphenylphosphino)pentane

27721-02-4

In a 2-liter four-necked flask equipped with an effective condenser, stirrer, and dropping funnel, 500 mL of anhydrous tetrahydrofuran (THF) was added and deoxygenated by drying nitrogen for 1 hour. Subsequently, 100 g (0.382 mol) of triphenylphosphine was added and the mixture was stirred until a clarified solution was formed. During this process, 6 g (0.856 mol) of freshly prepared, ultrafine lithium rinsed with THF was added in small amounts in batches while keeping the reaction temperature below 50 °C to control the exothermic nature of the reaction. After the lithium addition was completed, the resulting dark red solution was cooled to 0 °C and a THF solution (50 mL) of 50 g (0.442 mol) of 1,5-dichloropentane was prepared and similarly cooled to 0 °C. This solution was added dropwise to the reaction mixture, keeping the temperature at 0°C. Upon completion of the dropwise addition, the color of the reaction mixture changed to light brown. Subsequently, the mixture was refluxed at 80°C for 3 hours. After completion of the reaction, it was cooled to room temperature and 750 ml of deoxy methanol was added. The mixture was again cooled to 0 °C and 125 ml of oxygen-free water was added rapidly and dropwise to the vigorously stirred mixture. After standing at 0 °C for some time, the upper solution was decanted. The residue was filtered under nitrogen protection, washed with 5 x 25 ml of cold ether and dried under vacuum for 20 hours. 29.4 g (35% yield as triphenylphosphine) of 1,5-bis(diphenylphosphino)pentane was finally obtained as a white amorphous powder with a melting point of 41-44 °C, which is consistent with literature data. The 1H and 31P NMR spectra of the product were consistent with the structure, and the data are listed in Table 3.If the synthesis is carried out using undeoxygenated methanol and water, the oxidation of 1,5-bis(diphenylphosphino)pentane to 1,5-bis(diphenylphosphino)pentoxide is observed, at which point the product is a caramelized, amorphous mixture, which needs to be separated by graded recrystallization from the mixed benzene/methanol solvent.

References

[1] Journal of Organometallic Chemistry, 2011, vol. 696, # 10, p. 2238 - 2251

1,5-Bis(diphenylphosphino)pentane Preparation Products And Raw materials

Raw materials

Preparation Products

Global Suppliers ( 267)
Supplier Tel Email Country ProdList Advantage
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
future industrial shanghai co., ltd 400-0066400 13621662912 sales@jonln.com China 1989 65
Alfa Aesar 400-6106006 saleschina@alfa-asia.com China 30103 84
TCI (Shanghai) Development Co., Ltd. 021-67121386 Sales-CN@TCIchemicals.com China 24512 81
ShangHai DEMO Chemical Co.,Ltd 400-021-7337 2355568890 sales@demochem.com China 2569 57
Beijing HwrkChemical Technology Co., Ltd 89508211 18501085097 sales.bj@hwrkchemical.com China 9407 55
Energy Chemical 400-0056266 sales8178@energy-chemical.com China 44850 61

View Latest Price from 1,5-Bis(diphenylphosphino)pentane manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
1,5-Bis(diphenylphosphino)pentane   pictures 2026-08-07 1,5-Bis(diphenylphosphino)pentane
27721-02-4
$1.00 1KG 99% 20 tons Shaanxi Dideu Medichem Co. Ltd
1,5-Bis(diphenylphosphino)pentane pictures 2019-07-06 1,5-Bis(diphenylphosphino)pentane
27721-02-4
$1.00 1KG 99% 1000KG Career Henan Chemical Co
98% Ph2P(CH2)5PPh2 1,5-bis(diphenylphosphino)pent 1,5-Bis(diphenylphosphino)pentane (DPPPe) 1,5-Bis(diphenylphosphino)pentane 97% 1,5-Bis(diphenyL phosphino)pentane 5-diphenylphosphanylpentyl(diphenyl)phosphane 1,5-BIS(DIPHENYLPHOSPHINO)PENTANE PENTAMETHYLENEBIS(DIPHENYLPHOSPHINE) 1,5-Bis(diphenyphosphino)Pentane 1,5-Bis(Diphenylphosphino) 1,5-Bis(diphenylphosphino)pentane,min.98% DPPPE/1,5-BIS(DIPHENYLPHOSPHINO) PENTANE 1,5-BIS(DIPHENYPHOSPHINO) 1,5-Bis(diphenylphosphino)pentane ,98% 1,5-Bis(diphenylphosphino)pentane, min. 98% (Pentane-1,5-diyl)bis(diphenylphosphine) 1,5-Pentanediylbis(diphenylphosphine) Bis(diphenylphosphino)pentane 1,5-Bis(diphenylphosphino)pentane,97% 1,5-Bis(diphenylphosphino)pentane> Phosphine, 1,1'-(1,5-pentanediyl)bis[1,1'-diphenyl- DPPENT DPPPE 27721-02-4 C28H30P2 C6H52PCH25PC6H52 Phosphine Ligands Phosphorus Compounds Polydentate Phosphine Ligands Catalysis and Inorganic Chemistry phosphine ligand Pyrimidines Achiral Phosphine Aryl Phosphine Phosphines Ligand Phosphine Ligands Synthetic Organic Chemistry