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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1708494
Assay:
≥99%
Form:
crystals
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
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.
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signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Related Content
Synthesis of novel mesoporous aluminum organophosphonate by using organically bridged diphosphonic acid.
Kimura T, et al.
Chemistry of Materials, 15(20), 3742-3744 (2003)
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.
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)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| M9508-250MG | 04061833285442 |
| M9508-10G | 04061834064343 |
| M9508-1G | 04061834064350 |
| M9508-5G | 04061835559565 |