163119-16-2

Basic information

• Product Name: 2,6-Bis-tert-butyl-4-methylcyclohexanol
• Synonyms: 2,6-Bis-tert-butyl-4-methylcyclohexanol;2,6-bis(1,1-dimethylethyl)-4-methylcyclohexanol;2,6-Di-tert-butyl-4-methylcyclohexanol;2,6-Bis-tert-butyl-4;1,3-Di(tert-butyl)-2-hydroxy-5-methylcyclohexane;4-METHYL-2,6-BIS(2-METHYL-2-PROPANYL)CYCLOHEXANOL;Cyclohexanol, 2,6-bis(1,1-dimethylethyl)-4-methyl
• CAS NO: 163119-16-2
• Molecular Formula: C₁₅H₃₀O
• Molecular Weight: 226.4
• EINECS: 1312995-182-4
• Mol File: 163119-16-2.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 270°C
• Flash Point: 112°C
• Appearance: /
• Density: 0.884
• Vapor Pressure: 0.000937mmHg at 25°C
• Refractive Index: 1.462
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 15.36±0.70(Predicted)
• CAS DataBase Reference: 2,6-Bis-tert-butyl-4-methylcyclohexanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Bis-tert-butyl-4-methylcyclohexanol(163119-16-2)
• EPA Substance Registry System: 2,6-Bis-tert-butyl-4-methylcyclohexanol(163119-16-2)

Safety Data

• Hazardous Substances Data: 163119-16-2(Hazardous Substances Data)

Usage

Physical Form

Solid or liquid

Uses

2,6-ditert-butyl-4-methylcyclohexan-1-ol is a useful research chemical.

InChI:InChI=1/C15H30O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h10-13,16H,8-9H2,1-7H3

Upstream product

• 608-48-0 2,4-di-t-butyl-3-methyl phenol 
• 23790-39-8 2,6-di-tert-butyl-4-methylcyclohexanone 
• 128-37-0 2,6-di-tert-butyl-4-methyl-phenol 

Downstream Products

• 217955-03-8 C₂₆H₃₈N₂O₂ 
• 1015700-86-3 C₃₇H₄₇N₅O₄ 
• 1015700-85-2 C₂₄H₃₈N₂O₄ 
• 1015700-84-1 C₂₃H₃₈N₂O₃ 
• 1018968-39-2 C₄₇H₇₄N₄O₆ 
• 1015700-83-0 C₄₃H₇₀N₄O₄ 
• 1276654-20-6 C₄₉H₇₆N₄O₈Zn 
• 217956-11-1 cyanoacetic acid 2,6-di-t-butyl-4-methylcyclohexyl ester 

Relevant articles and documents

Synthesis method of 2,6-di-tert-butyl-4-methylcyclohexanol compound

The invention discloses a synthetic method of a 2,6-di-tert-butyl-4-methylcyclohexanol compound, and belongs to the technical field of chemical products. The synthetic method specifically comprises the steps: adding ethyl acetate and 2,6-di-tert-butyl-4-methylphenol into an autoclave, and stirring for 15 min at normal temperature until the ethyl acetate and the 2,6-di-tert-butyl-4-methylphenol arecompletely dissolved; then adding palladium on carbon and potassium tert-butoxide, sealing the autoclave, replacing with nitrogen, and introducing hydrogen; carrying out hydrogenation reaction underthe conditions that the temperature is 80-100 DEG C and the hydrogen pressure is 0.2-0.4 MPa, and stopping hydrogenation when hydrogen is not absorbed in the autoclave; discharging and filtering palladium carbon; adding a diluted hydrochloric acid solution, adjusting to be neutral, and removing lower-layer water; distilling the supernatant liquid until all ethyl acetate is distilled out, so as toobtain colorless and transparent 2,6-di-tert-butyl-4-methylcyclohexanol liquid. According to the method, the 2,6-di-tert-butyl-4-methylcyclohexanol is directly obtained through hydrogenation at low temperature and pressure, and the method is suitable for industrial production.

Method of preparing 2,6-di-tert-butyl-4-methylcyclohexanol through catalytic hydrogenation

The invention discloses a method of preparing 2,6-di-tert-butyl-4-methylcyclohexanol through catalytic hydrogenation. Di-tert-butyl-4-methylphenol (BHT) and a supported catalyst are fed into a high pressure reaction kettle; after the reaction is finished,

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.