4209-91-0

Usage

Uses

Used in Flavors and Fragrances Industry:
3,5-DIMETHYL-3-HEXANOL is used as a key ingredient in the production of flavors and fragrances for its pleasant and slightly sweet, floral aroma, enhancing the sensory experience of various consumer products.
Used as a Solvent:
In various industrial applications, 3,5-DIMETHYL-3-HEXANOL serves as a solvent, leveraging its ability to dissolve other substances, which is crucial for processes in industries such as pharmaceuticals, cosmetics, and coatings.
Used in Organic Synthesis:
3,5-DIMETHYL-3-HEXANOL is utilized as an intermediate in the synthesis of other organic compounds, playing a vital role in the creation of a wide range of chemical products, from specialty chemicals to active pharmaceutical ingredients.

InChI:InChI=1/C8H18O/c1-5-8(4,9)6-7(2)3/h7,9H,5-6H2,1-4H3/t8-/m0/s1

Upstream product

• 10467-10-4 ethylmagnesium iodide 
• 108-10-1 4-methyl-2-pentanone 
• 925-90-6 ethylmagnesium bromide 
• 926-62-5 isobutylmagnesium bromide 
• 78-93-3 butanone 
• 1569-43-3 3,5-dimethyl-hex-4-en-3-ol 
• 17123-64-7 dimethyl-3,5 hexadiene-1-5 ol-3 
• 56640-44-9 (R)-2-ethyl-4-methyl-pent-4-enylamine 
• 75-00-3 chloroethane 
• 3329-48-4 3,5-dimethyl-hex-1-en-3-ol 
• 1522-46-9 ethyl 2-isopropylacetoacetate 
• 141-79-7 4-methyl-pent-3-en-2-one 
• 56640-39-2 ethyl-(2-methyl-allyl)-malonic acid diethyl ester 
• 87635-77-6 2-Ethyl-4-methyl-4-pentensaeureethylester 

Downstream Products

• 589-43-5 2,4-dimethylhexane 
• 54059-76-6 4-Chlor-2,4-dimethyl-hexan 
• 66225-12-5 3,5-dimethyl-hex-2-ene 
• 123-42-2 4-Hydroxy-4-methyl-2-pentanone 
• 78-84-2 isobutyraldehyde 
• 108-10-1 4-methyl-2-pentanone 
• 78-93-3 butanone 
• 253185-03-4 tert-butylbenzene 
• 75-28-5 Isobutane 
• 686350-55-0 (1-ethyl-1,3-dimethyl-butyl)-benzene 
• 855412-93-0 4-(1-ethyl-1,3-dimethyl-butyl)-phenol 

Relevant academic research and scientific papers

Effect of the Structure of Unsaturated Aliphatic Alcohols on the Hydrogenation Rate over Pd-Ru Membrane Catalyst

It is shown that the rate of hydrogenation of substituted propargyl and allyl alcohols, as measured in the liquid phase on a membrane Pd-Ru alloy catalyst is described by the two-parameter Taft equation, which accounts for the induction and steric substituent effects.A positive induction effect of the substituent group promotes the reaction, whereas a negative one slows it down; an enhancement in the steric factor decreases the rate of conversion.Both induction and steric effects are stronger in reactions with ethylenic rather than acetylenic alcohols and for trans rather than cis isomers.

Oxidizing Action of Hydroperoxides. Oxidation of Alkyl Aryl Ketones by Hydroperoxides

The oxidation of alkyl aryl ketones by t-butyl hydroperoxide under basic conditions gave products which resulted from the fission of the carbon-carbon bond between carbonyl carbon and alkyl carbon.The reaction was investigated using chiral alkyl aryl ketones.On the basis of the results, a probable reaction mechanism is proposed.