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3-Penten-2-one occurs naturally in the berries of two species of Aronia melanocarpa. [7] It has also been found in other plants and foods such as tomatoes, cocoa, tea, and potato chips. [5] 3-Penten-2-one can be used for the synthesis of other compounds such as the alkaloids senepodine G and cermizine C, for example. [7]
1-Octen-3-ol, octenol for short and also known as mushroom alcohol, [1] is a chemical that attracts biting insects such as mosquitoes. It is contained in human breath and sweat, and it is believed that insect repellent DEET works by blocking the insects' octenol odorant receptors .
Oct-1-en-3-one (CH 2 =CHC(=O)(CH 2) 4 CH 3), also known as 1-octen-3-one or amyl vinyl ketone, is the odorant that is responsible for the typical "metallic" smell of metals and blood coming into contact with skin. [2] Oct-1-en-3-one has a strong metallic mushroom-like odor with an odor detection threshold of 0.03–1.12 μg/m 3 and it is the ...
Most often, 1-pentene is made as a byproduct of catalytic or thermal cracking of petroleum or during the production of ethylene and propylene via thermal cracking of hydrocarbon fractions. As of 2010s, the only commercial manufacturer of 1-pentene was Sasol Ltd. , where it is separated from crude by the Fischer-Tropsch process .
1-Octen-3-yl acetate is a chemical compound with molecular formula C 10 H 18 O 2. It is an ester of acetic acid and oct-1-en-3-ol. It exists as two enantiomers and can be obtained as a racemic mixture. It is a component of lavender oil.
This Halloween, don't overlook a box of good ol' Good & Plenty. This tasty candy is a surprisingly old American treat. You may be old enough to remember the "Choo Choo Charlie" commercials on TV ...
3-Methyl-1-pentanol (IUPAC name: 3-methylpentan-1-ol) is an organic chemical compound. It occurs naturally in Capsicum frutescens, the tabasco pepper. [2] References
3-Methyl-3-penten-2-one is an unsaturated aliphatic ketone. It is an isomer of mesityl oxide and isomesityl oxide. It is a precursor of 3-methyl-2-pentanone (methyl sec-butyl ketone) and is obtained by acid-catalyzed dehydration of 4-hydroxy-3-methyl-2-pentanone. It is used as an intermediate in organic chemistry syntheses. [1]