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Merck
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주요 문서

ERM-038

Supelco

Methylphosphonic acid solution

1000 μg/mL in methanol, ampule of 1.2 mL, certified reference material

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About This Item

실험식(Hill 표기법):
CH5O3P
CAS Number:
Molecular Weight:
96.02
EC Number:
UNSPSC 코드:
41116107

Grade

certified reference material

특징

Snap-N-Spike®/Snap-N-Shoot®

포장

ampule of 1.2 mL

농도

1000 μg/mL in methanol

응용 분야

environmental

형식

single component solution

저장 온도

−20°C

SMILES string

CP(O)(O)=O

법적 정보

Snap-N-Shoot is a registered trademark of Cerilliant Corporation
Snap-N-Spike is a registered trademark of Merck KGaA, Darmstadt, Germany

픽토그램

FlameSkull and crossbonesHealth hazard

신호어

Danger

유해 및 위험 성명서

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Flam. Liq. 2 - STOT SE 1

표적 기관

Eyes,Central nervous system

Storage Class Code

3 - Flammable liquids

WGK

WGK 2

Flash Point (°F)

49.5 °F - closed cup

Flash Point (°C)

9.7 °C - closed cup


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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문

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
William W Metcalf et al.
Science (New York, N.Y.), 337(6098), 1104-1107 (2012-09-01)
Relative to the atmosphere, much of the aerobic ocean is supersaturated with methane; however, the source of this important greenhouse gas remains enigmatic. Catabolism of methylphosphonic acid by phosphorus-starved marine microbes, with concomitant release of methane, has been suggested to
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

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