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What is the formula for 1-hexanol in Wikipedia?

What is the formula for 1-hexanol in Wikipedia?

1-Hexanol From Wikipedia, the free encyclopedia 1-Hexanol (IUPAC name hexan-1-ol) is an organic alcohol with a six- carbon chain and a condensed structural formula of CH 3 (CH 2) 5 OH. This colorless liquid is slightly soluble in water, but miscible with diethyl ether and ethanol.

What kind of metabolite is Hexan-1-ol?

Hexan-1-ol is a primary alcohol that is hexane substituted by a hydroxy group at position 1. It has a role as a plant metabolite. It is a primary alcohol and a hexanol.

Are there any other isomers of 1-hexanol?

Two additional straight chain isomers of 1-hexanol exist, 2-hexanol and 3-hexanol, both of which differ by the location of the hydroxyl group. Many isomeric alcohols have the formula C6H13OH. 1-hexanol is believed to be a component of the odour of freshly mown grass. It is used in the perfume industry.

Which is the SMILES string of 1-hexanol?

The SMILES string of 1-Hexanol is CCCCCCO, which can be can be imported by most molecule editors for conversion back into two-dimensional drawings or three-dimensional models of the 1-Hexanol.

Where does 1-hexanol get its energy from?

1-Hexanol is a fatty alcohol and is derived from natural fats, oils, and waxes from a number of animal (1), vegetable (1-3), fruit (4) and marine sources (1,8). 1-Hexanol is released to the atmosphere in emissions from vegetation (5-6).

Is the colorless liquid 1 hexanol soluble in water?

This colorless liquid is slightly soluble in water, but miscible with diethyl ether and ethanol. Two additional straight chain isomers of 1-hexanol, 2-hexanol and 3-hexanol, exist, both of which differing by the location of the hydroxyl group.

Where is the OH group located in 2-hexanol?

Description. 2-Hexanol (or hexan-2-ol) is a six carbon alcohol in which the OH group is located on the second carbon atom. Its chemical formula is C6H14O or C6H13OH. It is an isomer of the other hexanols. 2-Hexanol has a chiral center and can be resolved into enantiomers.

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Ruth Doyle