Skip to Content
Merck
CN

239356

N,N-Dimethylethylamine

99%

Synonym(s):

N-Ethyldimethylamine, DMEA

Sign In to View Organizational & Contract Pricing.

Select a Size


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:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

N,N-Dimethylethylamine, 99%

InChI key

DAZXVJBJRMWXJP-UHFFFAOYSA-N

InChI

1S/C4H11N/c1-4-5(2)3/h4H2,1-3H3

SMILES string

CCN(C)C

vapor pressure

8.09 psi ( 20 °C)

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

Quality Level

Looking for similar products? Visit Product Comparison Guide

Related Categories

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

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
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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
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 Sollenberg et al.
Journal of chromatography, 390(1), 133-140 (1987-03-18)
Eight different isotachophoretic systems for the analysis of 27 aliphatic amines are described. Complete methods including sampling and analysis procedures for the determination of eight amines in workroom air are also given. Different systems for the generation of gaseous amine
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
B Ståhlbom et al.
International archives of occupational and environmental health, 63(5), 305-310 (1991-01-01)
Dimethylethylamine (DMEA) is an aliphatic tertiary amine, which is used as a catalyst in the mould core manufacturing. During 8 h, four healthy volunteers were exposed to four different DMEA air concentrations (10, 20, 40 and 50 mg/m3; 20 mg/m3

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service