3809-32-3

Basic information

• Product Name: 2,5-DIMETHYLCYCLOHEXANOL
• Synonyms: Cyclohexanol, 2,5-dimethyl-;2,5-dimethylcyclohexan-1-ol;2,5-DIMETHYLCYCLOHEXANOL, MIXTURE OFISOM ERS;1-HYDROXY-2,5-DIMETHYLCYCLOHEXANE 97%;2,5-DIMETHYLCYCLOHEXANOL 97%;Einecs 223-281-3;Hexahydro-p-xylenol;2,5-DiMethylcyclohexanol
• CAS NO: 3809-32-3
• Molecular Formula: C₈H₁₆O
• Molecular Weight: 128.21
• EINECS: 223-281-3
• Product Categories: Alpha Sort;D;Volatiles/ Semivolatiles
• Mol File: 3809-32-3.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 179 °C
• Flash Point: 69 °C
• Appearance: /
• Density: 0.908 g/mL at 20 °C(lit.)
• Vapor Pressure: 0.236mmHg at 25°C
• Refractive Index: n20/D 1.458
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2,5-DIMETHYLCYCLOHEXANOL(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-DIMETHYLCYCLOHEXANOL(3809-32-3)
• EPA Substance Registry System: 2,5-DIMETHYLCYCLOHEXANOL(3809-32-3)

Safety Data

• Safety Statements: 23-24/25
• WGK Germany: 3
• Hazardous Substances Data: 3809-32-3(Hazardous Substances Data)

Usage

General Description

2,5-DIMETHYLCYCLOHEXANOL is a chemical compound with the molecular formula C8H16O. It is a colorless liquid with a faint odor, and it is insoluble in water but soluble in organic solvents. 2,5-DIMETHYLCYCLOHEXANOL is widely used in the synthesis of other organic compounds and as a solvent in various industrial processes, including the production of paints, coatings, and adhesives. It also has potential applications in the pharmaceutical and fragrance industries. 2,5-DIMETHYLCYCLOHEXANOL is considered to be relatively safe, with low toxicity and minimal environmental impact, making it a versatile and valuable chemical in various industrial and commercial applications.

InChI:InChI=1/C8H16O/c1-6-3-4-7(2)8(9)5-6/h6-9H,3-5H2,1-2H3/t6-,7+,8-/m1/s1

Upstream product

• 95-87-4 2,5-Dimethylphenol 
• 932-51-4 2,5-dimethylcyclohexanone 
• 7647-01-0 hydrogenchloride 
• 64-19-7 acetic acid 
• 589-90-2 1,4 dimethylcyclohexane 
• 2207-04-7 trans-1,4-dimethylcyclohexane 
• 6610-21-5 6-methylcyclohex-2-en-1-one 
• 583-60-8 2-Methylcyclohexanone 
• 36504-12-8 2-bromo-6-methylcyclohexanone 
• 15329-10-9 3,6-dimethylcyclohex-2-enone 
• 66395-23-1 (+-)-trans-2,5-dimethyl-cyclohexanone 
• 15359-12-3 trans-3,6-dimethyl-2-cyclohexen-1-ol 
• 36099-51-1 3-methyl-7-oxabicyclo[4.1.0]heptane 
• 917-64-6 methyl magnesium iodide 

Downstream Products

• 109805-47-2 phenyl-carbamic acid-(2,5-dimethyl-cyclohexyl ester) 
• 932-51-4 2,5-dimethylcyclohexanone 
• 4500-14-5 (+/-)-trans-2,5-dimethyl-cyclohexanone oxime 
• 1224935-93-6 C₁₁H₂₀O₂ 
• 95-87-4 2,5-Dimethylphenol 
• 922512-01-4 1-(4-methylphenyl)-1,4-dimethylcyclohexane 
• 14845-35-3 2,5-dimethyl-cyclohex-2-enone 
• 19550-40-4 trans-3,6-dimethylcyclohexene 
• 59356-67-1 cis-3,6-dimethylcyclohexene 
• 66395-23-1 (+-)-trans-2,5-dimethyl-cyclohexanone 
• 932-51-4 (+/-)-cis-2,5-dimethyl-cyclohexanone 
• 58626-26-9 cis-1,1-Dichloro-2,2-difluoro-3,6-dimethylcyclohexan 

Relevant articles and documents

Upgrading of aromatic compounds in bio-oil over ultrathin graphene encapsulated Ru nanoparticles

Fast pyrolysis of biomass for bio-oil production is a direct route to renewable liquid fuels, but raw bio-oil must be upgraded in order to remove easily polymerized compounds (such as phenols and furfurals). Herein, a synthesis strategy for graphene encapsulated Ru nanoparticles (NPs) on carbon sheets (denoted as Ru@G-CS) and their excellent performance for the upgrading of raw bio-oil were reported. Ru@G-CS composites were prepared via the direct pyrolysis of mixed glucose, melamine and RuCl3 at varied temperatures (500-800 °C). Characterization indicated that very fine Ru NPs (2.5 ± 1.0 nm) that were encapsulated within 1-2 layered N-doped graphene were fabricated on N-doped carbon sheets (CS) in Ru@G-CS-700 (pyrolysis at 700 °C). And the Ru@G-CS-700 composite was highly active and stable for hydrogenation of unstable components in bio-oil (31 samples including phenols, furfurals and aromatics) even in aqueous media under mild conditions. This work provides a new protocol to the utilization of biomass, especially for the upgrading of bio-oil.

Raney Ni-Al alloy-mediated reduction of alkylated phenols in water

Raney Ni-Al alloy in a dilute aqueous alkaline solution has been shown to be a very powerful reducing agent in the hydrogenation of phenol and alkylated phenols to the corresponding cyclohexanol derivatives.

Cycloalkyl esters of mercaptoalkanoic acids

Described are the cycloalkyl esters of mercaptoalkanoic acids defined according to the structure: STR1 wherein R1 represents hydrogen or methyl; R2 represents mono C1 -C4 alkyl substituted or unsubstituted C5 -C8 cycloalkyl; R3 represents hydrogen or methyl; and N represents 0, 1 or 2 and uses thereof in augmenting or enhancing the aroma or taste of foodstuffs.