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289868

Sigma-Aldrich

Methylphosphonic acid

98%

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Synonym(s):
MPA
Linear Formula:
CH3P(O)(OH)2
CAS Number:
993-13-5
Molecular Weight:
96.02
Beilstein/REAXYS Number:
1739372
EC Number:
213-607-2
MDL number:
MFCD00002137
UNSPSC Code:
12352100
PubChem Substance ID:
24857412
NACRES:
NA.22

Quality Level

100

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.

pictograms

CorrosionExclamation mark
GHS05,GHS07

signalword

Danger

hcodes

H302,H314

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

wgk_germany

WGK 2

ppe

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges

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Sigma-Aldrich

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Sigma-Aldrich

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Sigma-Aldrich

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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
Chien-Hui Ma et al.
The EMBO journal, 28(12), 1745-1756 (2009-05-15)
Water, acting as a rogue nucleophile, can disrupt transesterification steps of important phosphoryl transfer reactions in DNA and RNA. We have unveiled this risk, and identified safeguards instituted against it, during strand cleavage and joining by the tyrosine site-specific recombinase
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