652571
N,N-Dimethylethylamine
≥99%
Synonym(s):
N-Ethyldimethylamine, DMEA
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About This Item
Linear Formula:
(CH3)2NC2H5
CAS Number:
Molecular Weight:
73.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-940-8
Beilstein/REAXYS Number:
1696893
MDL number:
Assay:
≥99%
vapor pressure
8.09 psi ( 20 °C)
Quality Level
assay
≥99%
refractive index
n20/D 1.372 (lit.)
bp
36-38 °C (lit.)
mp
−140 °C (lit.)
density
0.675 g/mL at 25 °C (lit.)
functional group
amine
SMILES string
CCN(C)C
InChI
1S/C4H11N/c1-4-5(2)3/h4H2,1-3H3
InChI key
DAZXVJBJRMWXJP-UHFFFAOYSA-N
Application
N,N-Dimethylethylamine (DMEA) is generally used to prepare water-soluble quaternary ammonium salts. It facilitates lithium hexamethyldisilazide (LiHMDS) mediated enolization of highly substituted aryl ketones. Additionally, DMEA is also used as an organic solvent in synthetic chemistry.
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
-18.4 °F - closed cup
flash_point_c
-28 °C - closed cup
ppe
Faceshields, Gloves, Goggles
Regulatory Information
危险化学品
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Highly Stereoselective Synthesis of Tetrasubstituted Acyclic All-Carbon Olefins via Enol Tosylation and Suzuki-Miyaura Coupling.
Li BX, et al.
Journal of the American Chemical Society, 139(31), 10777-10783 (2017)
A theophylline based copper N-heterocyclic carbene complex: synthesis and activity studies in green media.
Szadkowska A, et al.
Royal Society of Chemistry Advances, 6(50), 44248-44253 (2016)
Lithium Hexamethyldisilazide-Mediated Enolization of Highly Substituted Aryl Ketones: Structural and Mechanistic Basis of the E/Z Selectivities.
Mack KA, et al.
Journal of the American Chemical Society, 139(35), 12182-12189 (2017)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 652571-2L | 04061836827779 |
| 652571-500ML | 04061832732701 |