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289868

Sigma-Aldrich

Methylphosphonic acid

98%

Synonym(s):

MPA

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About This Item

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

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

Signal Word

Danger

Hazard Statements

H302,H314

Hazard Classifications

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

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 2

Flash Point(F)

>392.0 °F - Pensky-Martens closed cup

Flash Point(C)

> 200 °C - Pensky-Martens closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Vibrational analysis of methylphosphonic acid and its anions: I. Vibrational spectra.
Journal of Molecular Structure, 15(2), 225-236 (1973)
Co-oxidation of methylphosphonic acid and ethanol in supercritical water: II: Elementary reaction rate model.
Journal of Supercritical Fluids, 39(2), 239-245 (2006)
An Xie et al.
Molecular pharmacology, 80(6), 965-978 (2011-08-04)
2-Aminoethyl methylphosphonate (2-AEMP), an analog of GABA, has been found to exhibit antagonist activity at GABA(A)-ρ1 (also known as ρ1 GABA(C)) receptors. The present study was undertaken to elucidate 2-AEMP's action and to test the activities of 2-AEMP analogs. Whole-cell
Adrian Mermer et al.
Acta crystallographica. Section B, Structural science, 67(Pt 5), 399-408 (2011-09-21)
Two new crystal structures, calcium bis(hydrogen methylphosphonate), Ca(CH(3)PO(3)H)(2), and lithium hydrogen methylphosphonate, Li(CH(3)PO(3)H), have been obtained, and the experimental and theoretical charge densities, as well as their topological properties, are reported. Both compounds display layered structures. Each hydrogen methylphosphonate anion
Stephen P Hancock et al.
Journal of molecular biology, 406(2), 285-312 (2010-12-21)
DNA bending can be promoted by reducing the net negative electrostatic potential around phosphates on one face of the DNA, such that electrostatic repulsion among phosphates on the opposite face drives bending toward the less negative surface. To provide the
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