19781-07-8

Usage

Diol

Two hydroxyl (OH) groups This indicates that the compound has two hydroxyl groups, which contribute to its solubility and reactivity.

Octanediol

Carbon chain length of eight The compound has an eight-carbon chain, which influences its physical and chemical properties.

Fragrance ingredient

Commonly used in cosmetic and personal care products 2,7-DIMETHYL-2,7-OCTANEDIOL is added to various products to provide a pleasant scent.

Viscosity controlling agent

Regulates the flow and consistency of products This property helps to maintain the desired texture in products like lotions and creams.

Skin conditioning agent

Improves the appearance and feel of the skin The compound helps to moisturize and soften the skin, making it smoother and more supple.

Solvent

Dissolves other substances in cosmetic and personal care products 2,7-DIMETHYL-2,7-OCTANEDIOL can act as a solvent for various ingredients, allowing them to be evenly distributed throughout a product.

Humectant

Retains moisture in products such as lotions and creams This property helps to keep products hydrated and maintain their effectiveness over time.

InChI:InChI=1/C10H22O2/c1-9(2,11)7-5-6-8-10(3,4)12/h11-12H,5-8H2,1-4H3

Upstream product

• 5929-72-6 2,7-dimethyl-octa-3,5-diyne-2,7-diol 
• 67-64-1 acetone 
• 23708-47-6 1,4-bis(bromomagnesium)butane 
• 106-99-0 buta-1,3-diene 
• 141-78-6 ethyl acetate 
• 141-28-6 diethyl adipate 
• 627-93-0 hexanedioic acid dimethyl ester 
• 75-16-1 methylmagnesium bromide 
• 74-88-4 methyl iodide 
• 115-19-5 2-methyl-but-3-yn-2-ol 
• 57155-32-5 5-(3,3-dimethyl-oxiranyl)-2-methyl-pent-3-yn-2-ol 
• 917-54-4 methyllithium 
• 25462-04-8 2-Methyl-2-(tert-butylperoxy)cyclohexanon 
• 110-52-1 1,4-dibromo-butane 

Downstream Products

• 16736-42-8 2,7-dimethyl-octa-2,6-diene 
• 59840-10-7 2,7-Dimethyl-octa-1,7-diene 
• 72535-89-8 1-isopropyl-5,5-dimethylcyclopent-1-ene 
• 72535-87-6 2-isopropylidene-1,1-dimethyl-cyclopentane 
• 40195-09-3 2,7-dimethyl-1,6-octadiene 
• 73331-73-4 5-isopropyl-1,5-dimethylcyclopent-1-ene 
• 72535-88-7 2-isopropenyl-1,1-dimethyl-cyclopentane 

Relevant academic research and scientific papers

The Development of Synthetic Routes to 1,1,n,n-Tetramethyl[n](2,11)teropyrenophanes

A concise synthetic approach to 1,1,n,n-tetramethyl[n](2,11)teropyrenophanes has been developed. It involves the construction of triply-bridged pyrenophanes, during which the three bridges are installed successively using Friedel-Crafts alkylation, Wurtz coupling and McMurry reactions. At the same time, the innate regiochemical preferences of pyrene toward electrophilic aromatic substitution are relied upon to control the substitution pattern. A cyclodehydrogenation reaction is then employed to generate the teropyrene system directly in a nonplanar conformation. The crystal structure of 1,1,7,7-tetramethyl[7](2,11)teropyrenophane was determined and the teropyrene system was found to have an end-to-end bend angle of 177.9°.

A Grignard-type phase-vanishing method: Generation of organomagnesium reagent and its subsequent addition to carbonyl compounds

Abstract A quadraphasic phase-vanishing system comprised of diethyl ether, magnesium, perfluoropolyether, and iodoalkane efficiently generated the corresponding Grignard reagents, which subsequently added to carbonyl compounds in the ether layer to afford alkylated alcohols in good yields.

Boron trifluoride-mediated alkylation of diphenylphosphine with tert-alkyl fluoride

(Chemical Equation Presented) Treatment of tertiary alkyl fluoride with diphenylphosphine in the presence of a stoichiometric amount of boron trifluoride etherate yields the corresponding tert-alkyldiphenylphosphine despite the coexistence of the strong L

Acyclic monomers which when cured are reworkable through thermal decomposition

Compounds containing unsaturated aliphatic moieties which are linked to each other by a tertiary oxycarbonyl containing acyclic moiety are basis for compositions which are cured to polymer networks which are thermally decomposable to provide residue which can be dissolved to allow repair of inoperative assemblies by replacement of inoperative components or recovery or recycling of operative elements which are affixed in assemblies by the cured compositions.

A Convenient Synthesis of Acyclic 1,n-Diketones (n=5-8) from 2-t-Butylperoxycycloalkanones

The reaction of organolithium with 2-alkyl-2-t-butylperoxycycloalkanones, readily available from t-butylperoxylation of 2-alkylcycloalkanones, gave 2-t-butylperoxy-1-cycloalkanol derivatives quantitatively, thermal decomposition of which with or without an acid afforded 1,n-diketones (n=5-8) in excellent yields.