Online Database of Chemicals from Around the World

1,3-Bis(diphenylphosphino)propane
[CAS# 6737-42-4]

List of Suppliers
Jiangsu B-Win Chemical Co., Ltd. China Inquire
www.jsbschem.com
+86 (510) 8584-0252
+86 18861806888
+86 (510) 8584-0253
huisongshu_2001@163.com
QQ Chat
Chemical manufacturer
chemBlink Standard supplier since 2008
HBCChem, Inc. USA Inquire
www.hbcchem-inc.com
+1 (510) 219-6317
+1 (510) 675-0318
sales@hbcchem-inc.com
Chemical manufacturer
chemBlink Standard supplier since 2008
Sinocompound Catalysts Co., Ltd. China Inquire
www.sinocompound.com
+86 (512) 6721-6630
+86 (512) 5631-6689
sales@sinocompound.com
Chemical manufacturer since 2008
chemBlink Standard supplier since 2010
Hefei TNJ Chemical Industry Co., Ltd. China Inquire
www.tnjchem.com
+86 (551) 6541-8684
+86 (551) 6541-8697
sales@tnjchem.com
Chemical manufacturer since 2001
chemBlink Standard supplier since 2010
BOC Sciences USA Inquire
www.bocsci.com
+1 (631) 485-4226
+1 (631) 614-7828
info@bocsci.com
Chemical manufacturer
chemBlink Standard supplier since 2010
Ereztech LLC USA Inquire
www.ereztech.com
+1 (888) 658-1221
sales@ereztech.com
Chemical distributor since 2010
chemBlink Standard supplier since 2011
Intatrade Chemicals GmbH Germany Inquire
www.intatrade.de
+49 (3493) 605-465
+49 (3493) 605-470
sales@intatrade.de
Chemical distributor
chemBlink Standard supplier since 2011
LOBA Feinchemie AG Austria Inquire
www.loba.co.at
+43 (223) 277-391
+43 (223) 276-677
sales@loba.co.at
Chemical distributor
chemBlink Standard supplier since 2012
Eastar Chemical Corporation USA Inquire
www.eastarchem.com
+1 800-898-2436
+1 (877) 898-2436
info@eastarchem.com
Chemical manufacturer since 1989
chemBlink Standard supplier since 2014
Forxine Pharmaceutical Co., Ltd. China Inquire
www.forxine.com
+86 (21) 6496-1699
+86 (21) 6496-1388 ex 8320
reagent@forxine.com
sales@forxine.com
QQ Chat
Chemical manufacturer since 2013
chemBlink Standard supplier since 2014
Labseeker Inc USA Inquire
www.labseeker.com
+1 (858) 750-1632
+1 (858) 412-1220
marketing@labseeker.com
Chemical manufacturer since 2002
chemBlink Standard supplier since 2015
Zhengzhou Kingorgchem Chemical Technology Co., Ltd. China Inquire
www.kingorgchem.com
+86 (371) 6551-1006
+86 (371) 6575-6965
sales@kingorgchem.com
QQ Chat
WeChat: 18625597674
Chemical manufacturer since 2015
chemBlink Standard supplier since 2016
Beijing Guofang Dingsheng Technology Co., Ltd. China Inquire
www.gfdschem.com
+86 (10) 8904-9254
5909-2859
+86 18610472091
+86 18031679351
+86 (10) 5909-2859
gfdskj@163.com
QQ Chat
Chemical manufacturer since 2012
chemBlink Standard supplier since 2016
Shanghai Fuxin Pharmaceutical Co., Ltd. China Inquire
www.fuxinpharm.com
+86 (21) 3130-0828
+86 18645121291
+86 (21) 3130-0828
contact@fuxinpharm.com
Chemical manufacturer since 2016
chemBlink Standard supplier since 2018
Gelest, Inc. USA Inquire
www.gelest.com
+1 (215) 547-1015
+1 (215) 547-2484
info@gelest.com
Chemical manufacturer
Kemprotec Limited UK Inquire
www.kemprotec.com
+44 (1642) 591-764
+44 (1845) 550-001
sales@kemprotec.co.uk
Chemical distributor since 1998
Digital Specialty Chemicals, Inc. USA Inquire
www.digitalchem.com
+1 (603) 563-5060
+1 (603) 563-9288
sales@digitalchem.com
Chemical manufacturer since 1987
Dalchem Russia Inquire
www.dalchem.com
+7 (8312) 753-772
+7 (8312) 750-799
dregichy@dalchem.com
Chemical manufacturer since 1997
Boulder Scientific Company USA Inquire
www.bouldersci.com
+1 (970) 535-4494
+1 (970) 535-4584
sales@bouldersci.com
Chemical manufacturer
Molekula Ltd UK Inquire
www.molekula.com
+44 (1747) 831-066
+44 (1747) 831-199
info@molekula.com
Chemical manufacturer
Anvia Chemicals, LLC USA Inquire
www.anviachem.com
+1 (414) 534-7845
+1 (414) 762-5539
sales@anviachem.com
Chemical manufacturer
Strem Chemicals, Inc. USA Inquire
www.strem.com
+1 (978) 499-1600
+1 (978) 465-3104
info@strem.com
Chemical manufacturer
Acros Organics Belgium Inquire
www.acros.com
+86 (21) 5258-1100
+86 (21) 5258-0119
info@acros.com
Chemical manufacturer

Identification
ClassificationOrganic raw materials >> Organic phosphine compound
Name1,3-Bis(diphenylphosphino)propane
SynonymsPropane-1,3-diylbis(diphenylphosphine)
Molecular StructureCAS # 6737-42-4, 1,3-Bis(diphenylphosphino)propane
Molecular FormulaC27H26P2
Molecular Weight412.45
CAS Registry Number6737-42-4
EC Number229-791-2
SMILESC1=CC=C(C=C1)P(CCCP(C2=CC=CC=C2)C3=CC=CC=C3)C4=CC=CC=C4
Properties
Melting point57-63 °C
Water solubilityinsoluble
Safety Data
Hazard Symbolssymbol symbol   GHS07;GHS09 Warning  Details
Risk StatementsH302-H315-H317-H319-H335-H400-H410  Details
Safety StatementsP261-P264-P264+P265-P270-P271-P272-P273-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P319-P321-P330-P332+P317-P333+P317-P337+P317-P362+P364-P391-P403+P233-P405-P501  Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Eye irritationEye Irrit.2H319
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Skin sensitizationSkin Sens.1H317
Acute toxicityAcute Tox.4H302
Acute hazardous to the aquatic environmentAquatic Acute1H400
Chronic hazardous to the aquatic environmentAquatic Chronic4H413
SDSAvailable
up Discovery and Applications
1,3-Bis(diphenylphosphino)propane, commonly abbreviated as dppp, is a bidentate ligand that has played a significant role in the field of organometallic chemistry and homogeneous catalysis. The molecule consists of a propane backbone with two diphenylphosphino groups attached to the first and third carbon atoms. This structure allows dppp to chelate metal centers, forming stable complexes that are widely utilized in various catalytic processes.

The discovery of 1,3-Bis(diphenylphosphino)propane dates back to the mid-20th century when researchers were exploring the synthesis and properties of phosphine ligands. The development of dppp was part of a broader effort to create ligands that could form stable complexes with transition metals, which are essential in catalysis. The synthesis of dppp involves the reaction of 1,3-dibromopropane with two equivalents of diphenylphosphine, typically in the presence of a base to facilitate the substitution reaction. The resulting product, dppp, is a white crystalline solid that is soluble in many organic solvents, making it easy to handle and use in various chemical reactions.

One of the most important applications of dppp is in the field of palladium-catalyzed cross-coupling reactions, such as the Heck, Suzuki-Miyaura, and Stille reactions. In these reactions, dppp acts as a ligand that coordinates to the palladium center, stabilizing the metal and enhancing its catalytic activity. The chelating nature of dppp, with its two phosphine groups, allows it to form a stable five-membered ring with the palladium center, which is crucial for the catalytic cycle. The use of dppp in these reactions has enabled the efficient formation of carbon-carbon and carbon-heteroatom bonds, which are fundamental steps in the synthesis of a wide range of organic molecules, including pharmaceuticals, agrochemicals, and materials.

In addition to its role in cross-coupling reactions, dppp has been employed in hydrogenation and hydroformylation reactions. In hydrogenation, dppp is used as a ligand in catalysts that promote the addition of hydrogen to unsaturated substrates, such as alkenes and alkynes, converting them into saturated products. This reaction is of great industrial importance in the production of fine chemicals and pharmaceuticals. In hydroformylation, dppp is part of the catalytic system that adds a formyl group to alkenes, producing aldehydes. This reaction is particularly valuable in the synthesis of aldehydes that serve as intermediates in the production of alcohols, acids, and other functionalized organic compounds.

Beyond catalysis, 1,3-Bis(diphenylphosphino)propane has been studied for its coordination chemistry with various metal centers. The ability of dppp to form stable complexes with metals such as ruthenium, rhodium, and platinum has led to its use in the study of metal-ligand interactions and the development of new metal-based materials. These complexes are often characterized by their interesting electronic and structural properties, which can be fine-tuned by varying the metal and the ancillary ligands. This versatility has made dppp an important ligand in the design of metal complexes for applications in materials science, including the development of conductive polymers, catalysts for polymerization reactions, and photochemical systems.

The role of dppp in organometallic chemistry is further highlighted by its use in the stabilization of low-coordinate metal centers. The chelating nature of dppp helps to stabilize reactive metal species, allowing for the exploration of unusual oxidation states and coordination environments. These studies have provided valuable insights into the behavior of metals in catalysis and have led to the discovery of new catalytic processes and reaction mechanisms.

1,3-Bis(diphenylphosphino)propane continues to be a ligand of great interest in both academic research and industrial applications. Its ability to form stable metal complexes, combined with its effectiveness in catalysis, ensures its continued use in the development of new synthetic methods and the exploration of new chemical reactivity. As the field of catalysis evolves, dppp is likely to remain a key player in the design and implementation of catalytic systems that enable the efficient and sustainable production of a wide range of chemical products.

References

2023. Pincer Ru with a single stereogenic identity for highly efficient asymmetric transfer hydrogenation of ketones. Science China Chemistry, 66(5).
DOI: 10.1007/s11426-022-1535-7

2023. Development of a Synthetic Method for Tridentate Phosphine Ligands. Iron-Catalyzed C-H/C-H Coupling for Synthesis of Functional Small Molecules and Polymers, 3.
DOI: 10.1007/978-981-99-4121-6_3

1975. Phosphine-Nickel Complexes as Catalysts for Cross-Coupling Reaction of Grignard Reagents with Vinylic, Aromatic and Heteroaromatic Halides. Organotransition-Metal Chemistry, 19.
DOI: 10.1007/978-1-4684-2142-2_19
Market Analysis Reports
List of Reports Available for 1,3-Bis(diphenylphosphino)propane
Related Products
1,8-Bis(dipheny...  (R)-(-)-4,12-Bi...  1,5-Bis(dipheny...  (2S,4S)-2,4-Bis...  (2R,4R)-2,4-Bis...  4,6-Bis(dipheny...  Bis(2-diphenylp...  cis-[Bis[2-(dip...  (S,S)-1,2-Bis[[...  (3R-trans)-3,4-...  (2R)-1,2-Bis(di...  [1,3-Bis(diphen...  1,3-Bis(dipheny...  [1,3-Bis(diphen...  2,6-Bis(dipheny...  12,12'-Bis(diph...  (3R)-4,4'-Bis(d...  (OC-6-22)-[(3R)...  Bis(Diphenylpho...  2,7-Bis(dipheny...