M9508
Methylenediphosphonic acid
≥99%
Synonym(s):
MDP, Medronic acid
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About This Item
Linear Formula:
CH2[P(O)(OH)2]2
CAS Number:
Molecular Weight:
176.00
Beilstein:
1708494
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
≥99%
form
crystals
mp
197-199 °C (lit.)
storage temp.
−20°C
SMILES string
OP(O)(=O)CP(O)(O)=O
InChI
1S/CH6O6P2/c2-8(3,4)1-9(5,6)7/h1H2,(H2,2,3,4)(H2,5,6,7)
InChI key
MBKDYNNUVRNNRF-UHFFFAOYSA-N
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Application
Methylenediphosphonic acid can be used as a precursor in the synthesis of:
- Mesoporous aluminum organophosphonate in the presence of alkyltrimethylammonium as a surfactant.
- Tetraester of methylenediphosphonic acids which are used as metal ion extractants for actinides in all oxidation states.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Megan H Ryan et al.
Plant, cell & environment, 42(6), 1987-2002 (2019-02-09)
Crops with improved uptake of fertilizer phosphorus (P) would reduce P losses and confer environmental benefits. We examined how P-sufficient 6-week-old soil-grown Trifolium subterraneum plants, and 2-week-old seedlings in solution culture, accumulated P in roots after inorganic P (Pi) addition.
Synthesis of novel mesoporous aluminum organophosphonate by using organically bridged diphosphonic acid.
Kimura T, et al.
Chemistry of Materials, 15(20), 3742-3744 (2003)
Metal extraction by silyl-substituted diphosphonic acids. III. Ester group substituent effects on phosphoryl oxygen basicity.
Zalupski PR, et al.
Solvent Extr. Ion Exch., 21(3), 331-345 (2003)
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Journal of clinical microbiology, 53(3), 777-781 (2014-12-19)
Prosthetic joint infection (PJI) is a rare but refractory complication of arthroplasty. Accurate identification of pathogens is a key step for successful treatment of PJI, which remains a challenge for clinicians and laboratory workers. We designed a combined culture method
Domenick A Prosdocimo et al.
American journal of physiology. Cell physiology, 296(4), C828-C839 (2009-02-06)
Extracellular inorganic pyrophosphate (PP(i)) is a potent suppressor of physiological calcification in bone and pathological calcification in blood vessels. Ectonucleotide pyrophosphatase/phosphodiesterases (eNPPs) generate PP(i) via the hydrolysis of ATP released into extracellular compartments by poorly understood mechanisms. Here we report
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