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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
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
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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:
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
hcodes
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
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Paige E Mahaney et al.
Journal of medicinal chemistry, 51(13), 4038-4049 (2008-06-19)
Further exploration of the cycloalkanol ethylamine scaffold, of which venlafaxine ( 1) is a member, was undertaken to develop novel and selective norepinephrine reuptake inhibitors (NRIs) for evaluation in a variety of predictive animal models. These efforts led to the
Veronica Sandgren et al.
Bioorganic & medicinal chemistry, 20(14), 4377-4389 (2012-06-16)
A series of P1-P3 linked macrocyclic BACE-1 inhibitors containing a hydroxyethylamine (HEA) isostere scaffold has been synthesized. All inhibitors comprise a toluene or N-phenylmethanesulfonamide P2 moiety. Excellent BACE-1 potencies, both in enzymatic and cell-based assays, were observed in this series
Riccardo Di Corato et al.
ACS nano, 5(2), 1109-1121 (2011-01-12)
Trifunctional polymer nanobeads are prepared by destabilization of a mixture of magnetic nanoparticles, quantum dots, and an amphiphilic polymer, followed by functionalization of the bead surface with folic acid molecules. The distribution of the nanoparticles within the nanobeads can be
Stacey F Bent et al.
Proceedings of the National Academy of Sciences of the United States of America, 108(3), 956-960 (2010-11-12)
Surface functionalization of semiconductors has been the backbone of the newest developments in microelectronics, energy conversion, sensing device design, and many other fields of science and technology. Over a decade ago, the notion of viewing the surface itself as a
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
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