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Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.431 (lit.)
bp
155 °C/0.5 mmHg (lit.)
density
1.08 g/mL at 25 °C (lit.)
functional group
phosphonate
SMILES string
CC(C)OP(=O)(CP(=O)(OC(C)C)OC(C)C)OC(C)C
InChI
1S/C13H30O6P2/c1-10(2)16-20(14,17-11(3)4)9-21(15,18-12(5)6)19-13(7)8/h10-13H,9H2,1-8H3
InChI key
ODTQUKVFOLFLIQ-UHFFFAOYSA-N
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General description
Tetraisopropyl methylenediphosphonate (IPCP) is a tetraisopropyl ester of methylenediphosphonic acid. It is an electroneutral ligand, reported to be synthesized from triisopropyl phosphate. Powder electron paramagnetic resonance (EPR) studies of tris complexes of Cu(II) complexes with IPCP has been analyzed.
Application
Tetraisopropyl methylenediphosphonate [T(iPr)MDP] forms a synergistic mixture with hydrogen dicarbollylcobaltate in nitrobenzene which was used in the extraction of europium and americium.
It may be used in the synthesis of the following:
It may be used in the synthesis of the following:
- tetraisopropyl ethenylidenebisphosphonate.
- tetraisopropyl 4-acetylthiobutane-1,1-diphosphonate
- tetraisopropyl 2-(3,5-bis(bromomethyl)phenyl)ethane-1,1-diphosphonate
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
320.0 °F - closed cup
Flash Point(C)
160 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Electron paramagnetic resonance studies of some copper (II) complexes with organophosphorus chelates.
Journal of the American Chemical Society, 93(5), 1138-1140 (1971)
Extraction of europium and americium into nitrobenzene by using synergistic mixture of hydrogen dicarbollylcobaltate and tetraisopropyl methylene diphosphonate.
J. Radioanal. Nucl. Chem., 283(3), 727-733 (2010)
Synthesis of Tetraisopropyl Methyenediphosphonate.
Jing Xi Hua Gong Zhong Jian Ti / Fine Chemical Intermediates, 4, 007-007 (2002)
Bioorganic & medicinal chemistry, 7(5), 901-919 (1999-07-10)
Conjugates of bisphosphonates (potential bone resorption inhibitors) and prostaglandin E2 (a bone formation enhancer) were prepared and evaluated for their ability to bind to bone and to liberate, enzymatically, free PGE2. The conjugate 3, an amide at C-1 of PGE2
Synthesis of novel bisphosphonate polyamine conjugates and their affinity to hydroxyapatite.
ARKIVOC (Gainesville, FL, United States), 4, 233-241 (2012)
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