Skip to Content
Merck

724033

Ethylamine

99.0%

Synonym(s):

Aminoethane, Monoethylamine

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
C2H5NH2
CAS Number:
Molecular Weight:
45.08
UNSPSC Code:
12142100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-834-7
Beilstein/REAXYS Number:
505933
MDL number:
Assay:
99.0%
Form:
gas
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

InChI

1S/C2H7N/c1-2-3/h2-3H2,1H3

InChI key

QUSNBJAOOMFDIB-UHFFFAOYSA-N

SMILES string

CCN

vapor density

1.56 (15 °C, vs air)

vapor pressure

874 mmHg ( 20 °C)

assay

99.0%

form

gas

autoignition temp.

721 °F

expl. lim.

14 %, 3.5-14 %

Quality Level

mp

-81 °C (lit.)

density

0.680 g/mL at 20 °C (lit.), 0.689 g/mL at 25 °C (lit.)

functional group

amine

Looking for similar products? Visit Product Comparison Guide

Packaging

Supplied in a Sure/Pac cylinder and has a 316 stainless steel needle valve with a male 1/4" NPTF outlet thread installed . Before using the cylinder, ensure that the valve is closed, then remove the galvanized steel hex cap that seals the outlet valve.

Compatible with the following:

Legal Information

Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
Sure/Pac is a trademark of Sigma-Aldrich Co. LLC

signalword

Danger

Hazard Classifications

Acute Tox. 4 Inhalation - Eye Irrit. 2 - Flam. Gas 1 - Press. Gas Liquefied gas - STOT SE 3

target_organs

Respiratory system

Storage Class

2A - Gases

wgk

WGK 1

flash_point_f

-34.6 °F - closed cup

flash_point_c

-37 °C - closed cup


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

Câline Christine et al.
Organic & biomolecular chemistry, 10(46), 9183-9190 (2012-10-23)
The synthesis of a phosphonated acyclic bifunctional chelate L* for the labeling of biomaterial is described. L* is based on a pyridine backbone, functionalized in ortho positions by aminomethyl-bis-methylphosphonic acids, and, in the para position, by a side chain containing
Zhixiong Zhong et al.
Analytica chimica acta, 715, 49-56 (2012-01-17)
A new multi-channel purge and trap system coupled with ion chromatography for the determination of six alkylamines in cosmetics was developed. The proposed method, based on purge and trap of the volatile alkylamines, involved in a miniaturization and multi-channel integration
Yuying Shuai et al.
Journal of the science of food and agriculture, 90(15), 2563-2567 (2010-08-26)
Theanine, a unique amino acid found almost exclusively in tea plants, has various favourable physiological and pharmacological functions in humans. Gamma-glutamyltranspeptidase (GGT, EC 2.3.2.2) is considered to be the most effective enzyme for the production of theanine. In fact, GGT
Lisa Vasicek et al.
Analytical chemistry, 81(19), 7876-7884 (2009-09-03)
Electron transfer dissociation (ETD) has proven to be a promising new ion activation method for proteomics applications due to its ability to generate c- and z-type fragment ions in comparison to the y- and b-type ions produced upon the more
Song Yang et al.
Journal of chromatography. A, 1216(15), 3280-3289 (2009-03-10)
Complementary methods using liquid chromatography-tandem quadrupole mass spectrometry (LC-MS/MS) and comprehensive two-dimensional gas chromatography-time-of-flight mass spectrometry (GCxGC-TOF-MS) were developed and applied to determine targeted metabolites involved in central carbon metabolism [including tricarboxylic acid cycle, serine cycle, ethylmalonyl-coenzyme A (ethylmalonyl-CoA) pathway

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