propene

Total world production of propene is currently about half that of ethylene.

"The work opens a new chapter in the field of silver as a catalyst for propene epoxidation."

One strategy that has been explored (but thus far failed) is reaction of propene with atomic carbon.

This method is advantageous because propene is inexpensive and "green."

The correct root for this compound is "propene".

This compound is primarily produced by combining water and propene in a hydration reaction.

Vinyl acetate is produced similarly, using ethylene in place of propene.

Allyl chloride is generally produced directly by the chlorination of propene.

HD-5 is a specification which establishes a maximum concentration of 5% propene in propane.

In 1920, Standard Oil first produced isopropyl alcohol by hydrating propene.

Isobutyraldehyde is manufactured, often as a side-product, by the hydroformylation of propene.

The conversion rate of propene is 98% and the selectivity to the n-butanal is high.

A large amount of methanol is required to make a world-scale ethylene and/or propene plant.

The propene molecules assemble randomly into three unique molecules.

Industrially, the most important nonenes are trimers of propene.

Since propene is volatile and flammable, precautions must be taken to avoid fire hazards in the handling of the gas.

Likewise, 1-chloropropane and 2-chloropropane give propene.

It is a byproduct in the chlorination of propene to make allyl chloride.

Propane containing too much propene (also called propylene) is not suited for most vehicle fuels.

So we simply write propene.

Propenyl is a chemical radical of propene (propylene).

The structure is like propene, but in this compound, 3 hydrogen atoms are changed into chlorine atoms.

The current industrial route involves dimerization of propene followed by dehydration of the 2,3-dimethylbutene.

One case study monitored the dehydrogenation of propane to propene using micro-GC.

The simplest alkenes, ethene, propene and butene are gases.