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Merck
모든 사진(1)

주요 문서

D98203

Sigma-Aldrich

N,N-Diethylmethylamine

97%

동의어(들):

N-Methyldiethylamine

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About This Item

Linear Formula:
CH3N(C2H5)2
CAS Number:
Molecular Weight:
87.16
Beilstein:
1730930
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22

분석

97%

양식

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

유사한 제품을 찾으십니까? 방문 제품 비교 안내

애플리케이션

  • 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).

픽토그램

FlameSkull and crossbonesCorrosion

신호어

Danger

유해 및 위험 성명서

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

개인 보호 장비

Faceshields, Gloves, Goggles


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시험 성적서(COA)

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문서 라이브러리 방문

이미 열람한 고객

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
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
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
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
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

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