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Merck
CN

295663

Sigma-Aldrich

丙烯

≥99%

别名:

Propene

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关于此项目

线性分子式:
CH3CH=CH2
CAS Number:
分子量:
42.08
Beilstein:
1696878
EC 号:
MDL编号:
UNSPSC代码:
12142100
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽密度

1.48 (vs air)

质量水平

蒸汽压

15.4 atm ( 37.7 °C)

方案

≥99%

自燃温度

860 °F

expl. lim.

11.1 %

沸点

−47.7 °C (lit.)

mp

−185 °C (lit.)

SMILES字符串

CC=C

InChI

1S/C3H6/c1-3-2/h3H,1H2,2H3

InChI key

QQONPFPTGQHPMA-UHFFFAOYSA-N

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相关类别

一般描述

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。

应用

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。

包装

以Sure/Pac 气瓶供货,并具有配备 1/4" NPTF出口外螺纹的青铜针阀。使用气瓶前,务必确认阀门是关闭的,然后取下密封出口阀的镀锌钢六角螺帽。

兼容以下设备:

法律信息

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

象形图

FlameGas cylinder

警示用语:

Danger

危险声明

预防措施声明

危险分类

Flam. Gas 1 - Press. Gas Liquefied gas

储存分类代码

2A - Gases

WGK

WGK 3

闪点(°F)

-162.4 °F - closed cup

闪点(°C)

-108 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, multi-purpose combination respirator cartridge (US)

法规信息

监管及禁止进口产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A reducible MIL-100(Fe) metal-organic framework (MOF) was investigated for the separation of a propane/propene mixture. An operando methodology was applied (for the first time in the case of a MOF) in order to shed light on the separation mechanism. Breakthrough
Selective vapor-phase epoxidation of propylene over Au/TiO2 catalysts in the presence of oxygen and hydrogen.
Hayashi T, et al.
J. Catal., 178(2), 566-575 (1998)
Fee Pitsch et al.
Advanced materials (Deerfield Beach, Fla.), 24(31), 4306-4310 (2012-06-22)
An adaptive self-healing ionic liquid nanocomposite membrane comprising a multi-layer support structure hosting the ionic salt [Ag](+) [Tf(2) N](-) is used for the separation of the olefin propylene and the paraffin propane. The ionic salt renders liquid like upon complexation
Thomas Hampel et al.
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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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