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D98203

Sigma-Aldrich

N,N-Diethylmethylamine

97%

Sinônimo(s):

N-Methyldiethylamine

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About This Item

Fórmula linear:
CH3N(C2H5)2
Número CAS:
616-39-7
Peso molecular:
87.16
Beilstein:
1730930
Número CE:
210-480-5
Número MDL:
MFCD00009049
Código UNSPSC:
12352100
ID de substância PubChem:
24894115
NACRES:
NA.22

Ensaio

97%

Formulário

liquid

índice de refração

n20/D 1.389 (lit.)

p.e.

63-65 °C (lit.)

densidade

0.72 g/mL at 25 °C (lit.)

cadeia de caracteres SMILES

CCN(C)CC

InChI

1S/C5H13N/c1-4-6(3)5-2/h4-5H2,1-3H3

chave InChI

GNVRJGIVDSQCOP-UHFFFAOYSA-N

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Aplicação

  • 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).

Palavra indicadora

Danger

Frases de perigo

H225,H301,H314,H332

Classificações de perigo

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B

Código de classe de armazenamento

3 - Flammable liquids

Classe de risco de água (WGK)

WGK 2

Ponto de fulgor (°F)

-11.2 °F - closed cup

Ponto de fulgor (°C)

-24 °C - closed cup

Equipamento de proteção individual

Faceshields, Gloves, Goggles

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Certificados de análise (COA)

Lot/Batch Number
BCBV7595
BCBK9055V
BCBB1452V
BCBB1452
1374557

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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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