All Photos(3)
Synonym(s):
MPA
Linear Formula:
CH3P(O)(OH)2
CAS Number:
Molecular Weight:
96.02
Beilstein:
1739372
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
solid
mp
105-107 °C (lit.)
SMILES string
CP(O)(O)=O
InChI
1S/CH5O3P/c1-5(2,3)4/h1H3,(H2,2,3,4)
InChI key
YACKEPLHDIMKIO-UHFFFAOYSA-N
Gene Information
human ... ALPP(250)
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General description
The vibrational spectra of aqueous solutions of methylphosphonic acid and its anions were studied. The supercritical water co-oxidation elementary reaction rate mechanism for methylphosphonic acid was also studied.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
监管及禁止进口产品
Certificates of Analysis (COA)
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Co-oxidation of methylphosphonic acid and ethanol in supercritical water: II: Elementary reaction rate model.
Journal of Supercritical Fluids, 39(2), 239-245 (2006)
Vibrational analysis of methylphosphonic acid and its anions: I. Vibrational spectra.
Journal of Molecular Structure, 15(2), 225-236 (1973)
Edyta Proniewicz et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 103, 167-172 (2012-12-25)
Here, we report a systematic surface-enhanced Raman spectroscopy (SERS) study of the structures of five N-benzylamino(boronphenyl)-methylphosphonic acids: N-benzylamino-(3-boronphenyl)-S-methylphosphonic acid (m-PhS), N-benzylamino-(4-boronphenyl)-S-methylphosphonic acid (p-PhS), N-benzylamino-(2-boronphenyl)-R-methylphosphonic acid (o-PhR), N-benzylamino-(3-boronphenyl)-R-methyl-phosphonic acid (m-PhR), and N-benzylamino-(4-boronphenyl)-R-methylphosphonic acid (p-PhR) adsorbed on nanometer-sized colloidal particles (20-25 nm).
James Pratt et al.
Plant physiology, 151(3), 1646-1657 (2009-09-17)
In vivo (31)P-NMR analyses showed that the phosphate (Pi) concentration in the cytosol of sycamore (Acer pseudoplatanus) and Arabidopsis (Arabidopsis thaliana) cells was much lower than the cytoplasmic Pi concentrations usually considered (60-80 mum instead of >1 mm) and that
Nissan Ashkenazi et al.
The Journal of organic chemistry, 75(6), 1917-1926 (2010-02-16)
Potential energy surfaces for the nucleophilic displacements at phosphorus in dimethyl methyl-, chloromethyl-, dichloromethyl-, and trichloromethylphosphonates have been computed at the B3LYP/6-31+G* level of theory, using IEF-PCM to account for the solvent effect. The results reveal that sequential addition of
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