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N,N-Diethylmethylamine

Names

[ CAS No. ]:
616-39-7

[ Name ]:
N,N-Diethylmethylamine

[Synonym ]:
N-ethyl-N-methylethanamine
MFCD00009049
EINECS 210-480-5

Chemical & Physical Properties

[ Density]:
0.72 g/mL at 25 °C(lit.)

[ Boiling Point ]:
63-65 °C(lit.)

[ Melting Point ]:
-196 °C

[ Molecular Formula ]:
C5H13N

[ Molecular Weight ]:
87.16340

[ Flash Point ]:
−11 °F

[ Exact Mass ]:
87.10480

[ PSA ]:
3.24000

[ LogP ]:
0.95800

[ Index of Refraction ]:
n20/D 1.389(lit.)

[ Storage condition ]:
Flammables area

MSDS

Safety Information

[ Symbol ]:

GHS02, GHS05, GHS06

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H225-H301-H314-H332

[ Precautionary Statements ]:
P210-P280-P305 + P351 + P338-P310

[ Personal Protective Equipment ]:
Faceshields;full-face respirator (US);Gloves;Goggles;multi-purpose combination respirator cartridge (US)

[ Hazard Codes ]:
F:Flammable;C:Corrosive;

[ Risk Phrases ]:
R11;R20/22;R34

[ Safety Phrases ]:
S16-S26-S36/37/39-S45

[ RIDADR ]:
UN 2733 3/PG 1

[ WGK Germany ]:
2

[ Packaging Group ]:
I

[ Hazard Class ]:
3.1

Synthetic Route

Precursor & DownStream

Articles

Characterization of poly(ethylene glycol) and PEGylated products by LC/MS with postcolumn addition of amines.

Anal. Chem. 81(2) , 567-77, (2009)

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, an...

The reaction of trimethylamine dehydrogenase with diethylmethylamine.

J. Biol. Chem. 269(49) , 30869-79, (1994)

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...

Reaction of the C30A mutant of trimethylamine dehydrogenase with diethylmethylamine.

J. Biol. Chem. 271(23) , 13401-6, (1996)

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 diethylmethy...


More Articles


Related Compounds