291145
N-Ethylmethylamine
97%
Synonym(s):
N-Methylethylamine, NMEA
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About This Item
Linear Formula:
C2H5NHCH3
CAS Number:
Molecular Weight:
59.11
Beilstein:
1730786
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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vapor pressure
8.53 psi ( 20 °C)
Quality Level
Assay
97%
refractive index
n20/D 1.374 (lit.)
bp
36-37 °C (lit.)
density
0.688 g/mL at 25 °C (lit.)
functional group
amine
storage temp.
2-8°C
SMILES string
CCNC
InChI
1S/C3H9N/c1-3-4-2/h4H,3H2,1-2H3
InChI key
LIWAQLJGPBVORC-UHFFFAOYSA-N
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General description
The kinetics of reaction of guanosine 5′-phospho-2-methylimidazolide with N-ethylmethylamine has been studied in water at 37°C.
Application
N-Ethylmethylamine has been used in the synthesis of N-ethylmethylacrylamide via reaction with acryloyl chloride.
related product
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Flam. Liq. 2 - Skin Corr. 1A
Storage Class Code
3 - Flammable liquids
WGK
WGK 2
Flash Point(F)
<-29.2 °F - closed cup
Flash Point(C)
< -34 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Absolute intensities of NH-stretching fundamental and overtone transitions of gas phase aniline, methylamine, ethylamine, cyclopropylamine, methylethylamine, diethylamine and pyrrolidine have been measured with long path length conventional absorption spectroscopy. To support the assignments of NH-stretching transitions, transition frequencies and intensities
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The Journal of organic chemistry, 60(3), 632-637 (1995-02-10)
Aliphatic amines react with phosphoimidazolide-activated derivatives of guanosine and cytidine (ImpN) by replacing the imidazole group. The kinetics of reaction of guanosine 5'-phospho-2-methylimidazolide (2-MeImpG) with glycine ethyl ester, glycinamide, 2-methoxyethylamine, n-butylamine, morpholine, dimethylamine (Me2NH), ethylmethylamine (EtNHMe), diethylamine (Et2NH), pyrrolidine, and
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