D98203
N,N-Diethylmethylamine
97%
Synonym(s):
N-Methyldiethylamine
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About This Item
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Quality Level
Assay
97%
form
liquid
refractive index
n20/D 1.389 (lit.)
bp
63-65 °C (lit.)
density
0.72 g/mL at 25 °C (lit.)
SMILES string
CCN(C)CC
InChI
1S/C5H13N/c1-4-6(3)5-2/h4-5H2,1-3H3
InChI key
GNVRJGIVDSQCOP-UHFFFAOYSA-N
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Application
- N,N-Diethylmethylamine as lineshape standard for NMR above 130 K.: This study explores the use of N,N-Diethylmethylamine as a lineshape standard for nuclear magnetic resonance (NMR) spectroscopy at temperatures above 130 K, providing insights into its applications in high-precision NMR analysis (Fritzsching et al., 2018).
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
-11.2 °F - closed cup
Flash Point(C)
-24 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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The steady-state reaction of trimethylamine dehydrogenase (TMADH) with the artificial electron acceptor ferricenium hexafluorophosphate (Fc(+)) has been studied by stopped-flow spectroscopy, with particular reference to the mechanism of inhibition by trimethylamine (TMA). Previous studies have suggested that the presence of
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The room-temperature molten salt mixture of N,N-diethyl-N-(2-methoxyethyl)-N-methylammonium bis(trifluoromethanesulfonyl) imide ([DEME][TFSI]) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt is herein reported as electrolyte for application in Li-O
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The role played by the 6-S-cysteinyl-FMN bond of trimethylamine dehydrogenase in the reductive half-reaction of the enzyme has been studied by following the reaction of the slow substrate diethylmethylamine with a C30A mutant of the enzyme lacking the covalent flavin
The Journal of biological chemistry, 269(49), 30869-30879 (1994-12-09)
The reductive half-reaction of trimethylamine dehydrogenase has been studied using the substrate diethylmethylamine over the pH range 6-10. It is found that the reaction occurs with three distinct and, under most conditions, fully resolved kinetic phases. The hyperbolic substrate concentration
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