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363596

Sigma-Aldrich

Diethyl phosphoramidate

98%

Synonym(s):

(Diethoxyphosphoryl)amine, Amidophosphoric acid diethyl ester, Diethyl amidophosphonate, Diethyl aminophosphonate, Diethyl phosphorylamide, O,O′-Diethylphosphoramidate

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About This Item

Linear Formula:
H2NP(O)(OC2H5)2
CAS Number:
1068-21-9
Molecular Weight:
153.12
MDL number:
MFCD00015676
UNSPSC Code:
12352100
PubChem Substance ID:
24862205
NACRES:
NA.22

Quality Level

100

Assay

98%

bp

140 °C/3 mmHg (lit.)

mp

51-53 °C (lit.)

SMILES string

CCOP(N)(=O)OCC

InChI

1S/C4H12NO3P/c1-3-7-9(5,6)8-4-2/h3-4H2,1-2H3,(H2,5,6)

InChI key

MCQILDHFZKTBOD-UHFFFAOYSA-N

General description

Diethyl phosphoramidate is a chemical and biological toxin and its ultra-low level detection by Surface-Enhanced Raman Spectroscopy (SERS) is reported. It is reported as chemical warfare simulant.

Application

Diethyl phosphoramidate may be employed as reagent which mimics or imitates the actual chemical warfare agents. It may be used in the preparation of α-aminoalkyl phosphonates, via three-component Mannich type reaction.

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCS6955
MKCS1014
MKCN2165
MKCB0585V
MKBS4023V

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Surface-enhanced Raman scattering detection of chemical and biological agents using a portable Raman integrated tunable sensor.
Yan F and Vo-Dinh T.
Sensors and Actuators B, Chemical, 121(1), 61-66 (2007)
Mehmet Yilmaz et al.
Physical chemistry chemical physics : PCCP, 16(12), 5563-5570 (2014-02-12)
The detection of molecules at an ultralow level by Surface-Enhanced Raman Spectroscopy (SERS) has recently attracted enormous interest for various applications especially in biological, medical, and environmental fields. Despite the significant progress, SERS systems are still facing challenges for practical
Mannich type reactions of chlorophosphites, phosphoramides and aldehydes (ketones) under solvent-free and catalyst-free conditions-synthesis of N-phosphoramino a-aminophosphonates.
Zhang J, et al.
Green Chemistry, 9(12), 1341-1345 (2007)
Jialu Liu et al.
Pesticide biochemistry and physiology, 163, 31-38 (2020-01-25)
Amidase is an important hydrolytic enzyme in detoxification metabolism. Amidase hydrolyzes a wide variety of nonpeptide carbon‑nitrogen bonds by attacking a cyano group or carbonyl carbon. However, little is known about the relationship between amidase and insecticides. In this study
Surface detection of chemical warfare agent simulants and degradation products.
Kanu AB, et al.
Analytica Chimica Acta, 553(1), 148-159 (2001)

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