112062
N-Ethyldiethanolamine
98%
Sinónimos:
2,2′-Ethyliminodiethanol
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About This Item
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Quality Level
assay
98%
refractive index
n20/D 1.4665 (lit.)
bp
246-252 °C (lit.)
mp
−50 °C (lit.)
density
1.014 g/mL at 25 °C (lit.)
functional group
amine
hydroxyl
SMILES string
CCN(CCO)CCO
InChI
1S/C6H15NO2/c1-2-7(3-5-8)4-6-9/h8-9H,2-6H2,1H3
InChI key
AKNUHUCEWALCOI-UHFFFAOYSA-N
Categorías relacionadas
General description
N-Ethyldiethanolamine can be identified in water, urine and blood samples by gas chromatography-mass spectrometry (GC-MS).
N-Ethyldiethanolamine is a precursor of VX type nerve agent.
Application
N-Ethyldiethanolamine was used in the analysis of urine for assaying nitrogen mustard metabolites.
Storage Class
10 - Combustible liquids
wgk_germany
WGK 2
flash_point_f
255.2 °F - closed cup
flash_point_c
124 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Rapid communications in mass spectrometry : RCM, 34(3), e8586-e8586 (2019-09-12)
Nitrogen mustards (NMs) are vesicant class of chemical warfare agents. From the viewpoint of the Chemical Weapons Convention partially hydrolyzed products of nitrogen mustards (pHpNMs) are considered as important markers of nitrogen mustard exposure. The detection of pHpNMs from biological
Journal of chromatography. A, 1216(45), 7906-7914 (2009-10-03)
N,N-Dialkylamino alcohols, N-methyldiethanolamine, N-ethyldiethanolamine and triethanolamine are the precursors of VX type nerve agents and three different nitrogen mustards respectively. Their detection and identification is of paramount importance for verification analysis of chemical weapons convention. GC-FTIR is used as complimentary
Analytical methods : advancing methods and applications, 12(36), 4447-4456 (2020-08-29)
The development and optimization of an analytical method for the detection and identification of reactive metabolite of organochlorine chemical warfare agent nitrogen mustards (NMs), 2-[(2-chloroethyl)(alkyl)amino]ethanol (CEAAE), known as half nitrogen mustard, in blood samples is presented, herein. In this study
Rapid communications in mass spectrometry : RCM, 34(12), e8777-e8777 (2020-03-08)
Analytical methods for the detection and identification of half nitrogen mustards (halfNMs), i.e., partially hydrolyzed products of nitrogen mustards (pHpNMs), using silyl derivatives are often associated with low sensitivity and selectivity. In order to overcome these limitations, the derivatization of
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