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Merck
CN

289868

甲基膦酸

98%

别名:

MPA

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线性分子式:
CH3P(O)(OH)2
化学文摘社编号:
分子量:
96.02
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
213-607-2
Beilstein/REAXYS Number:
1739372
MDL number:
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产品名称

甲基膦酸, 98%

InChI key

YACKEPLHDIMKIO-UHFFFAOYSA-N

InChI

1S/CH5O3P/c1-5(2,3)4/h1H3,(H2,2,3,4)

SMILES string

CP(O)(O)=O

assay

98%

form

solid

mp

105-107 °C (lit.)

Quality Level

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

signalword

Danger

hcodes

Hazard Classifications

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

存储类别

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

ppe

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

法规信息

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历史批次信息供参考:

分析证书(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)
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
Luis Briseño-Roa et al.
Protein engineering, design & selection : PEDS, 24(1-2), 151-159 (2010-11-03)
The most lethal organophosphorus nerve agents (NA), like sarin, soman, agent-VX and Russian-VX, share a methylphosphonate moiety. Pseudomonas diminuta phosphotriesterase (PTE) catalyses the hydrolysis of methylphosphonate NA analogues with a catalytic efficiency orders of magnitude lower than that towards the
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).

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