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472565

Sigma-Aldrich

Diethyl cyanophosphonate

90%

Synonym(s):

DEPC, Diethyl phosphoryl cyanide

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About This Item

Linear Formula:
(CH3CH2O)2P(O)CN
CAS Number:
Molecular Weight:
163.11
Beilstein/REAXYS Number:
1768938
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

assay

90%

refractive index

n20/D 1.403 (lit.)

bp

104-105 °C/19 mmHg (lit.)

density

1.075 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

CCOP(=O)(OCC)C#N

InChI

1S/C5H10NO3P/c1-3-8-10(7,5-6)9-4-2/h3-4H2,1-2H3

InChI key

ZWWWLCMDTZFSOO-UHFFFAOYSA-N

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General description

Diethyl cyanophosphonate (DCNP, a Tabun mimic,[1] DECP[2]) is a nerve agent simulant. Its detection by using fluorescein, a reversible fluorescent sensor, has been reported.[2] Its degradation in the presence of suitable organocatalysts (different amines, aminoalcohols and glycols) has been studied.[1]

Application

Coupling reagent for peptide synthesis.[3] Reagent for the phosphorylation of phenols.[4] Activating agent for fluorescent derivatization of carboxylic acids which allows separation by HPLC.[5]

Other Notes

Contains triethyl phosphate

pictograms

Skull and crossbonesCorrosion

signalword

Danger

Hazard Classifications

Acute Tox. 2 Dermal - Acute Tox. 2 Inhalation - Acute Tox. 2 Oral - Eye Dam. 1 - Skin Corr. 1B

supp_hazards

Storage Class

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk_germany

WGK 3

flash_point_f

176.0 °F - closed cup

flash_point_c

80 °C - closed cup

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter


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Synthetic Communications, 27, 3035-3035 (1997)
Farkhondeh Fathi et al.
Langmuir : the ACS journal of surfaces and colloids, 27(19), 12098-12105 (2011-08-27)
A simple electrochemical method has been proposed for the preparation of silver nanoparticles that can be used for the detection of cyanide. Both the electrochemical behavior and morphology of the Ag nanoparticles have been characterized in the presence of KCN
T C Bruice et al.
Proceedings of the National Academy of Sciences of the United States of America, 89(5), 1700-1704 (1992-03-01)
The structures of the compounds we call 3a, 3b, and 3c-compounds that incorporate (i) the tripyrrole peptide of the minor-groove-binding distamycin class of compounds and (ii) polyamine ligands that extend from the minor groove and can interact with phosphodiester bonds--were
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Organic nanoparticles made out of biodegradable and biocompatible materials have attracted increased attention in the therapeutic and diagnostic fields. In this study, we attempted to explore a new radiolabelling chelating free strategy for biodegradable sphingomyelin nanometric emulsions with fluorine-18 (18F)

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