239356
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
Beilstein:
1696893
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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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
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Application
N,N-Dimethylethylamine was used in the preparation of pH and reduction dual-responsive polypeptide nanogels with self-reinforced endocytoses.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1B
Storage Class Code
3 - Flammable liquids
WGK
WGK 1
Flash Point(F)
-18.4 °F - closed cup
Flash Point(C)
-28 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Jianxun Ding et al.
Journal of controlled release : official journal of the Controlled Release Society, 172(2), 444-455 (2013-06-08)
The pH and reduction dual-responsive polypeptide nanogels with self-reinforced endocytoses were prepared through ring-opening polymerization of l-glutamate N-carboxyanhydrides, deprotection of benzyl group and subsequent quaternization reaction between γ-2-chloroethyl-l-glutamate unit in polypeptide block and 2,2'-dithiobis(N,N-dimethylethylamine). The nanogels were revealed to exhibit
T Lundh et al.
British journal of industrial medicine, 48(3), 203-207 (1991-03-01)
The exposure and metabolism of dimethylethylamine (DMEA) was studied in 12 mould core makers in four different foundries using the Ashland cold box technique. The mean time weighted average (TWA) full work shift DMEA exposure concentration was 3.7 mg/m3. Inhaled
Paul Gee et al.
Annals of emergency medicine, 60(4), 431-434 (2012-05-12)
Dimethylamylamine (DMAA) was a forgotten pharmaceutical that was patented in 1944 as a nasal decongestant. DMAA has recently gained popularity as a dietary supplement, with claims of effectiveness as an athletic performance enhancer and weight loss aid. It is also
J A Post et al.
The American journal of physiology, 268(2 Pt 2), H773-H780 (1995-02-01)
Phosphatidylethanolamine (PE) is a nonbilayer-preferring and fusogenic phospholipid. It is kept in the bilayer configuration by interaction with other phospholipids in biologic membranes. However, reorganization of the membrane phospholipids could lead to expression of the nonbilayer nature of PE and
T Lundh et al.
International archives of occupational and environmental health, 70(5), 309-313 (1997-01-01)
The aims of the study were three-fold: to assess the skin uptake of the industrial catalyst dimethylethylamine (DMEA) (a) in vitro from water solutions by fresh guinea-pig and human skin specimens, (b) in gaseous form in vivo in human volunteers
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