E3754
Ethylamine solution
70% in H2O
Synonym(s):
Aminoethane, Monoethylamine
Sign In to View Organizational & Contract Pricing.
About This Item
Linear Formula:
C2H5NH2
CAS Number:
Molecular Weight:
45.08
PubChem Substance ID:
UNSPSC Code:
12352100
Beilstein/REAXYS Number:
505933
MDL number:
Skip To
SMILES string
CCN
InChI
1S/C2H7N/c1-2-3/h2-3H2,1H3
InChI key
QUSNBJAOOMFDIB-UHFFFAOYSA-N
concentration
70% in H2O
density
0.81 g/mL at 20 °C
storage temp.
2-8°C
Looking for similar products? Visit Product Comparison Guide
comparable product
Product No.
Description
Pricing
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Liq. 2 - Skin Corr. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk
WGK 1
flash_point_f
71.6 °F
flash_point_c
22 °C
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
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
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
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
Tracy A LeGreve et al.
The journal of physical chemistry. A, 113(2), 399-410 (2008-12-23)
Neutral serotonin-(H(2)O)(n) clusters with n = 1,2 have been studied under jet-cooled conditions using a combination of resonant two-photon ionization (R2PI), UV-UV hole-burning (UVHB), and resonant ion-dip infrared (RIDIR) spectroscopy. Serotonin (5-hydroxytryptamine, SERO) is a close analogue of tryptamine, differing
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