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线性分子式:
C2H5NH2
化学文摘社编号:
分子量:
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
bp
16.6 °C (lit.)
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
存储类别
2A - Gases
wgk
WGK 1
flash_point_f
-34.6 °F - closed cup
flash_point_c
-37 °C - closed cup
法规信息
新产品
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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
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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
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Biochemistry, 47(29), 7726-7733 (2008-07-17)
During the catalytic reaction of copper amine oxidase, one of the two prochiral hydrogen atoms at the C1 position of substrate amine is stereoselectively abstracted by a conserved Asp residue serving as a general base. Using stereospecifically deuterium-labeled enantiomers of
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