295663
丙烯
≥99%
别名:
Propene
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线性分子式:
CH3CH=CH2
化学文摘社编号:
分子量:
42.08
UNSPSC Code:
12142100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-062-1
Beilstein/REAXYS Number:
1696878
MDL number:
Assay:
≥99%
General description
丙烯是一种非极性烯烃。它通常用作合成异丙基苯、环氧丙烷、丙烯腈和异丙醇的前体。研究人员已经报道过Au/TiO2 催化剂作用下含氧和氢气体中丙烯的选择性氧化。研究人员已经研究过以齐格勒-纳塔催化剂进行丙烯的聚合。研究人员已经提及金属催化的非极性烯烃（乙烯和丙烯）与烷基丙烯酸酯的共聚合。研究人员已经研究过丙烯与线性α-烯烃1-辛烯、1-癸烯、1-十四碳烯和1-十八碳烯的共聚合。
Application
在钛硅沸石催化剂存在下，丙烯可用于通过用过氧化氢环氧化合成环氧丙烷。
Packaging
Legal Information
Aldrich is a registered trademark of Sigma-Aldrich Co. LLC
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signalword
Danger
hcodes
pcodes
Hazard Classifications
Flam. Gas 1 - Press. Gas Liquefied gas
存储类别
2A - Gases
wgk
WGK 3
flash_point_f
-162.4 °F - closed cup
flash_point_c
-108 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)
法规信息
监管及禁止进口产品
此项目有
Lei Ma et al.
Environmental science & technology, 46(3), 1747-1754 (2012-01-14)
Application of Fe-zeolites for urea-SCR of NO(x) in diesel engine is limited by catalyst deactivation with hydrocarbons (HCs). In this work, a series of Fe-zeolite catalysts (Fe-MOR, Fe-ZSM-5, and Fe-BEA) was prepared by ion exchange method, and their catalytic activity
One-step propylene formation from bio-glycerol over molybdena-based catalysts
Green Chemistry
Green Chemistry, 17, 903-912 (2015)
Manab Sharma et al.
Journal of the American Chemical Society, 134(41), 17234-17244 (2012-09-21)
The use of bis(1,3-di-tert-butylimidazolin-2-iminato) titanium dichloride (1) and dimethyl (2) complexes in the polymerization of propylene is presented. The complexes were activated using different amounts of methylalumoxane (MAO), giving in each case a very active catalytic mixture and producing polymers
Synthesis of propylene oxide from propylene and hydrogen peroxide catalyzed by titanium silicalite.
Clerici MG, et al.
J. Catal., 129(1), 159-167 (1991)
Thomas Hampel et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 18(33), 10382-10392 (2012-07-19)
The title compounds were synthesized in a longest sequence of 27 linear steps and with an overall yield of 2.9 and 3.9%. In the course of the synthesis, two aldehydes representing carbon fragments C1-C7 (Eastern fragment) and C9-C21 (Western fragment)
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