D98203
N,N-二乙基甲胺
97%
别名:
N-甲基二乙胺
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关于此项目
线性分子式:
CH3N(C2H5)2
化学文摘社编号:
分子量:
87.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
210-480-5
Beilstein/REAXYS Number:
1730930
MDL number:
产品名称
N,N-二乙基甲胺, 97%
InChI
1S/C5H13N/c1-4-6(3)5-2/h4-5H2,1-3H3
InChI key
GNVRJGIVDSQCOP-UHFFFAOYSA-N
SMILES string
CCN(C)CC
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.)
Quality Level
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Application
- N,N-二乙基甲胺作为核磁共振130以上的线形标准 K：本研究探索了N,N-二乙基甲胺在130 K以上温度下作为核磁共振（NMR）光谱线形标准的使用，为其在高精度核磁共振分析中的应用提供了见解（Fritzsching et al., 2018）。
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
存储类别
3 - Flammable liquids
wgk
WGK 2
flash_point_f
-11.2 °F - closed cup
flash_point_c
-24 °C - closed cup
ppe
Faceshields, Gloves, Goggles
法规信息
危险化学品
此项目有
Lihua Huang et al.
Analytical chemistry, 81(2), 567-577 (2008-12-17)
PEGylation of peptides and proteins presents significant challenges for structural characterization due to the heterogeneity of the poly(ethylene glycol) (PEG), the number of PEG moieties attached, and the site(s) of PEGylation. In this work, a novel and powerful methodology using
P Roberts et al.
Biochemistry, 38(45), 14927-14940 (1999-11-11)
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
Ulderico Ulissi et al.
ChemSusChem, 11(1), 229-236 (2017-09-30)
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
L Huang et al.
The Journal of biological chemistry, 271(23), 13401-13406 (1996-06-07)
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
R J Rohlfs et al.
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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