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239356

Sigma-Aldrich

N,N-Dimethylethylamine

99%

Sinónimos:

N-Ethyldimethylamine, DMEA

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About This Item

Fórmula lineal:
(CH3)2NC2H5
Número de CAS:
598-56-1
Peso molecular:
73.14
Beilstein/REAXYS Number:
1696893
EC Number:
209-940-8
MDL number:
MFCD00009039
UNSPSC Code:
12352100
PubChem Substance ID:
24854372
NACRES:
NA.22

vapor pressure

8.09 psi ( 20 °C)

Quality Level

200

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.)

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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Categorías relacionadas

Application

N,N-Dimethylethylamine was used in the preparation of pH and reduction dual-responsive polypeptide nanogels with self-reinforced endocytoses.

signalword

Danger

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_germany

WGK 1

flash_point_f

-18.4 °F - closed cup

flash_point_c

-28 °C - closed cup

ppe

Faceshields, Gloves, Goggles

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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
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
Charles E Hudson et al.
Journal of the American Society for Mass Spectrometry, 19(10), 1491-1499 (2008-07-29)
1,2-Eliminations are a varied and extensive set of dissociations of ions in the gas phase. To understand better such dissociations, elimination of CH(2)=CH(2) and CH(3)CH(3) from (CH(3))(2)NH(+)CH(2)CH(3) (1) and of CH(4) from (CH(3))(2)NH(2)(+) are characterized by quantum chemical calculations. Stretching
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