추천 제품
Quality Level
분석
97%
양식
liquid
refractive index
n20/D 1.431 (lit.)
bp
155 °C/0.5 mmHg (lit.)
density
1.08 g/mL at 25 °C (lit.)
작용기
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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일반 설명
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.
애플리케이션
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
신호어
Danger
유해 및 위험 성명서
예방조치 성명서
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
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Extraction of europium and americium into nitrobenzene by using synergistic mixture of hydrogen dicarbollylcobaltate and tetraisopropyl methylene diphosphonate.
Makrlik E, et al.
J. Radioanal. Nucl. Chem., 283(3), 727-733 (2010)
Synthesis of novel bisphosphonate polyamine conjugates and their affinity to hydroxyapatite.
Sankala E, et al.
ARKIVOC (Gainesville, FL, United States), 4, 233-241 (2012)
Synthesis of Tetraisopropyl Methyenediphosphonate.
Jian-ming XU.
Jing Xi Hua Gong Zhong Jian Ti / Fine Chemical Intermediates, 4, 007-007 (2002)
Electron paramagnetic resonance studies of some copper (II) complexes with organophosphorus chelates.
Joesten MD, et al.
Journal of the American Chemical Society, 93(5), 1138-1140 (1971)
L Gil et al.
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
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