Search results
Results from the WOW.Com Content Network
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 main compound responsible for the "smell of metal", followed by decanal (smell: orange skin, flowery) and nonanal (smell: tallowy, fruity). [3] Oct-1-en-3-one is the degradative reduction product of the chemical reaction ...
Pentan-3-ol. Other names 3-Pentanol, diethyl carbinol. ... 1.2 – 9% Except where otherwise noted, data are given for materials in their standard state ...
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-Pentanol, (or n-pentanol, pentan-1-ol), is an organic compound with the formula CH 3 CH 2 CH 2 CH 2 CH 2 OH and is classified as a primary alcohol. [2] It is a colourless liquid with a distinctive aroma. It is one of 8 isomeric alcohols with the formula C 5 H 11 OH. It is used as a solvent, a biological drying agent and in the synthesis of ...
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. [2] [3] [4]
3-Methyl-3-pentanol (IUPAC name: 3-methylpentan-3-ol) is an organic chemical compound and a tertiary hexanol. It is used in the synthesis of the tranquilizer emylcamate , [ 2 ] and has similar sedative and anticonvulsant actions itself.
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
The bond lengths in the molecule are for the three equatorial As−C bonds 1.975 Å and the two axial As−C bonds 2.073 Å. [ 8 ] The infrared spectrum of pentamethylarsenic shows strong bands at 582 and 358 cm −1 due to axial C-As vibration, and weaker bands at 265 and 297 cm −1 due to equatorial C-As vibration. [ 9 ]