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Cyclohexanol

Cyclohexanol is a cyclic alcohol with the chemical formula C6H11OH.
It is a colorless, viscous liquid with a characteristic camphor-like odor.
Cyclohexanol is widely used as a solvent, in the manufacture of nylon, and as an intermediate in the production of various chemicals.
It can be obtained through the hydrogenation of benzene or the oxidation of cyclohexane.
Cyclohexanol is an importnat precursor for the synthesis of other compounds and has many industrial and research applications.
PubComapre.ai can help optimize your Cyclohexanol research by identifying the most reproducible and accurate protocols from literature, preprints, and patents, and streamlining your experiments.

Most cited protocols related to «Cyclohexanol»

The porous p(GMA-co-EDMA) particles were synthesized by seeded suspension polymerization using toluene and cyclohexanol as porogens. The polystyrene (PS) seeds were prepared according to the procedure provided in the Appendix A. 0.3 g PS seeds and 5 mL of a 2.0 g∙L−1 SDS solution were sonicated for 10 min. An emulsion containing 2.0 mL of the activator DBP and 150 mL of SDS (2.53 g∙L−1) were homogenized for 10 min at 5000 rpm and added to the seed particle suspension. The mixture was stirred for 24 h at 200 rpm at room temperature. Thereafter an emulsion (10 min, 5000 rpm) containing 150 mL of SDS (3.33 g∙L−1), initiator BPO (0.4 g), porogens and acrylate monomers was added. The relative amount of added monomers (GMA:EMDA) and porogens (toluene:cyclohexanol) was systematically varied according to the experimental design (Table 1). The absolute volume of added monomers and porogens was 30 mL for each synthesis.
To allow for complete swelling, the system was stirred at 200 rpm for another 24 h. 150 mL of a 23.3 g∙L−1 PVA solution was added to the mixture as stabilizer. The reaction mixture was heated to 70 °C and stirred at 200 rpm for 24 h for polymerization. After polymerization the porous particles were filtered off and washed three times with ethanol and three times with water. The porous copolymer particles were then dried prior to analysis.
Publication 2022
acrylate Anabolism Cyclohexanol Emulsions Ethanol GMA-EDMA ML 23 Polymerization Polystyrenes Suby's G solution Toluene
(−)-Nicotine hydrogen tartrate, (−)-menthol (cyclohexanol-5-methyl-2-[1-methylethyl), and dimethylsulfoxide (DMSO) were purchased from Sigma-Aldrich (St. Louis, MO, USA). Nicotine solutions for intravenous self-administration were prepared fresh each week by dissolving nicotine salt in physiological saline and adjusting the pH to 7.4 ± 0.4 with sodium hydroxide. The nicotine doses are reported as free-base concentrations. Menthol was dissolved in DMSO and diluted with deionized water to a final DMSO concentration being at 50% (V/V).
Publication 2016
Cyclohexanol Hydrogen Intravenous Infusion Menthol Nicotine Nicotine Bitartrate physiology Saline Solution Sodium Chloride Sodium Hydroxide Sulfoxide, Dimethyl
Two different GMA-EDMA monolith recipes were tested. Monolith 1 was prepared using 20% GMA, 10% EDMA, 25% cyclohexanol, 25% 1-dodecanol, and 20% Tween 20 [8 ]. Monolith 2 was prepared using 24% GMA, 11% EDMA, 10% cyclohexanol and 55% 1-dodecanol. Both mixtures were sonicated for 10 min, DMPA was added to make the solution 1% DMPA by mass, and the mixtures were sonicated for an additional 10 min. Prepolymer solution was loaded into one or more channels and the device was then placed under a SunRay 600 UV lamp (Uvitron, West Springfield, MA) for 10 min of UV exposure. The unpolymerized resin was then removed from the monolith by flushing the channel with IPA for 30 min. The monolith was emptied using vacuum and stored dry until use.
Monoliths were characterized by scanning electron microscopy (SEM) imaging. Specimens were prepared by removing 3D printed devices from the glass slide and cutting through the MPW using a razor blade. The pieces were then sputter coated with 80:20 Au:Pd, and images were taken using an ESEM XL30 (FEI, Thermo Fisher, Fair Lawn, NJ) in high vacuum mode at 10 kV electron beam potential. The nodule and pore sizes were analyzed from the SEM images using ImageJ (NUT, Bethesda, MD).
Publication 2018
Cyclohexanol Dodecanol Electrons GMA-EDMA Medical Devices N,N-dimethyl-4-anisidine Resins, Plant Scanning Electron Microscopy Tween 20 Vacuum
The following reagents were purchased from the indicated sources: Recombinant HIV-1 gp120LAV (IIIB), which has clade B origins (Protein Sciences, Meriden, CT); cannabinoid agonists and antagonists: WIN55,212-2, WIN55,212-3 (S(-)-[2,3-dihydro-5-methyl-3-[(4-morpholinyl)methyl]pyrrolo-[1,2,3-de]-1,4-benzoxazinyl]-(1-naphthalenyl) methanone mesylate, an inactive enantiomer of WIN55,212-2), CP55,940 ((-)-cis-3-[2-hydroxy-4-(1,1-dimethylheptyl)phenyl]-trans-4-(3-hydroxypropyl) cyclohexanol) and JWH 015 ((2-methyl-1-propyl-1H-indol-3-yl)-1-naphthalenylmethanone) (Tocris, Ellisville, MO), SR141716A (5-(4-chlorophenyl)-1-(2,4-dichlorophenyl)-4- methyl-N-(1-piperidyl)pyrazole-3-carboxamide hydrochloride), SR144528 ((1S-endo)-5-(4-chloro-3-methylphenyl)-1-((4-methylphenyl)methyl)-N-(1,3,3-trimethylbicyclo(2.2.1)hept-2-yl)-1H-pyrazole-3-carboxamide) (NIDA, National Institutes of Health, Bethesda, MD); Dulbecco’s modified Eagle’s medium (DMEM), Hank’s balanced salt solution (HBSS), penicillin, streptomycin, trypsin, glucose, bovine serum albumin, polyoxyethylenesorbitan monolaurate (Tween 20), PBS, Krebs-Ringer buffer, paraformaldehyde, uridine, fluorodeoxyuridine, poly-D-lysine, superoxide dismutase (SOD) and mazindol (Sigma-Aldrich, St. Louis, MO); rabbit anti-tyrosine hydroxylase (TH) antibody (Pel-Freez, Rogers, AR); fetal bovine serum (FBS) (Hyclone Laboratories, Logan, UT); rabbit anti-dopamine β-hydroxylase (DBH) antibodies (Millipore, Billerica, MA); mouse anti-CD68 antibody (DAKO, Carpinteria, CA); donkey anti-rabbit or anti-mouse IgG rhodamine- conjugated secondary antibodies (Jackson ImmunoResearch, West Grove, PA); propidium iodide (PI) and Hoechst stain 33342 (Roche, Indianapolis, IN); [7,8-3H]dopamine (DA, 50 Ci/mmol) (GE Healthcare, Piscataway, NJ).
Publication 2013
antagonists anti-IgG Antibodies Antibodies, Anti-Idiotypic Buffers Cannabinoid Receptor Agonists Cyclohexanol Dopamine Dopamine beta Monooxygenase Eagle Endometriosis Equus asinus Fetal Bovine Serum Floxuridine Glucose HIV-1 HOE 33342 Hypromellose JWH 015 Lysine Mazindol Mesylates Mice, House N-nitrosoiminodiacetic acid paraform Penicillins Poly A Polysorbates Propidium Iodide Proteins pyrazole Rabbits Rhodamine Salts Serum Albumin, Bovine SR 141716A SR 144528 Stains Streptomycin Superoxide Dismutase Trypsin Tween 20 Tyrosine 3-Monooxygenase Uridine
Two kinds of microdevices were utilized in this study (Figure 1): extractor and separation chips. The fabrication protocol was adapted from our previous work [26 (link)]. Briefly, the designed pattern was photolithographically transferred to silicon wafers, which were wet etched with 40% KOH and served as templates. PMMA substrates were imprinted by hot embossing using etched Si templates. The patterned PMMA was thermally bonded to an unimprinted PMMA substrate with drilled holes for reservoirs. Channel widths at half height were 50 µm, and channel depths were 20 µm.
Porous polymer monoliths (0.5-cm long) were prepared in the extraction microchip (Figure 1a) by photoinitiated in situ polymerization. Monoliths were made from GMA and EDMA monomers with DMPA as the photoinitiator. Cyclohexanol and 1-dodecanol were used as the porogen. The monolith preparation followed published procedures [27 –29 (link)]. Briefly, 0.005 g DMPA, 0.4 g GMA and 0.6 g EDMA were mixed in a 4-mL glass vial. Porogen (0.3 g cyclohexanol and 0.7 g 1-dodecanol) was added slowly to the mixture. Before polymerization, the solution was sonicated in a water bath for 3 min followed by nitrogen purging for 3 min to remove dissolved oxygen. The degassed mixture was aspirated into the microchannels by vacuum, and excess monomer in the reservoir was removed by pipet to minimize siphoning during polymerization [30 (link)]. Next, the microchip was partially covered with electrical tape or aluminum foil to provide spatial control over polymerization. The microchip was then put on a cooled aluminum plate and exposed to UV light (200 mW/cm2) in the wavelength range of 320–390 nm for 10 min. Cooling the device helped eliminate undesired thermal polymerization [30 (link)]. Finally, unreacted monomer and porogen were removed by flushing isopropanol through the microchannels using a syringe pump.
Publication 2008
Aluminum Bath Cyclohexanol DNA Chips Dodecanol Electricity Isopropyl Alcohol Medical Devices N,N-dimethyl-4-anisidine Nitrogen Oxygen Polymerization Polymers Polymethyl Methacrylate Silicon Syringes Ultraviolet Rays Vacuum

Most recents protocols related to «Cyclohexanol»

Not available on PMC !

Example 8

    • A composition comprising:
    • a plurality of metallic nanofibers, substantially all of the metallic nanofibers having at least a partial coating of polyvinyl pyrrolidone;
    • a first solvent comprising about 1% to 10% 1-butanol, ethanol, 1-pentanol, n-methylpyrrolidone, 1-hexanol, or acetic acid, or mixtures thereof;
    • a viscosity modifier, resin, or binder comprising about 0.75% to 5.0% PVP, polyvinyl alcohol, or a polyimide, or mixtures thereof; and
    • with the balance comprising a second solvent such as cyclohexanol, cyclohexanone, cyclopentanone, cyclopentanol, butyl lactone, or mixtures thereof.

Patent 2024
1-hexanol 1-methyl-2-pyrrolidinone Acetic Acid Butyl Alcohol Cyclohexanol cyclohexanone cyclopentanol cyclopentanone Ethanol Lactones Metals n-pentanol Polyvinyl Alcohol Povidone Resins, Plant Solvents Viscosity

Example 18

    • A composition comprising:
    • about 0.01% to 3.0% of a plurality of functionalized metallic nanofibers 100;
    • a first solvent comprising about 2.0% to 10.0% n-methylpyrrolidone, 2-propanol (isopropyl alcohol or IPA), 1-methoxy-2-propanol,1-butanol, ethanol, diethylene glycol, 1-pentanol, n-methylpyrrolidone, or 1-hexanol, or mixtures thereof.
    • a first viscosity modifier, resin, or binder comprising about 0.75% to 5.0% PVP, polyvinyl alcohol, or a polyimide, or mixtures thereof;
    • a second viscosity modifier, resin, or binder comprising about 7% to 12% alpha-terpineol;
    • a second solvent comprising about 1% to 5% of n-propanol, 2-propanol, or diethylene glycol, or mixtures thereof; and
    • with the balance comprising a third solvent such as n-methylpyrrolidone, cyclohexanol, cyclohexanone, cyclopentanone, cyclopentanol, butyl lactone, or mixtures thereof.

Patent 2024
1-hexanol 1-methyl-2-pyrrolidinone 1-Propanol alpha-terpineol Butyl Alcohol Cyclohexanol cyclohexanone cyclopentanol cyclopentanone diethylene glycol Ethanol Isopropyl Alcohol Lactones Metals methoxyisopropanol n-pentanol Polyvinyl Alcohol Resins, Plant Solvents Viscosity
Not available on PMC !

Example 15

    • A composition comprising:
    • about 0.01% to 3.0% of a plurality of functionalized metallic nanofibers;
    • a first solvent comprising about 3.0% to 7% 1-butanol, ethanol, 1-pentanol, n-methylpyrrolidone, 1-hexanol, or acetic acid, or mixtures thereof;
    • a viscosity modifier, resin, or binder comprising about 1.4% to 3.75% PVP, polyvinyl alcohol, or a polyimide, or mixtures thereof;
    • a second solvent comprising about 0.001% to 2% of 1-octanol, acetic acid, diethylene glycol, dipropylene glycol, propylene glycol, potassium hydroxide or sodium hydroxide, or mixtures thereof; and
    • with the balance comprising a third solvent such as cyclohexanol, cyclohexanone, cyclopentanone, cyclopentanol, butyl lactone, or mixtures thereof.

Patent 2024
1-hexanol 1-methyl-2-pyrrolidinone Acetic Acid Butyl Alcohol Cyclohexanol cyclohexanone cyclopentanol cyclopentanone diethylene glycol Ethanol Glycols Lactones Metals n-pentanol Octanols Polyvinyl Alcohol potassium hydroxide Propylene Glycol Resins, Plant Sodium Hydroxide Solvents Viscosity

Example 12

    • A composition comprising:
    • about 0.01% to 3.0% of a plurality of functionalized metallic nanofibers, substantially all of the metallic nanofibers having at least a partial coating of a polyvinyl pyrrolidone polymer;
    • a first solvent comprising about 2.5% to 8% 1-butanol, ethanol, 1-pentanol, n-methylpyrrolidone, or 1-hexanol, or mixtures thereof;
    • a second solvent comprising about 0.01% to 5% of an acid or bases, including organic acids such as carboxylic acids, dicarboxylic acids, tricarboxylic acids, alkyl carboxylic acids, acetic acid, oxalic acid, mellitic acid, formic acid, chloroacetic acid, benzoic acid, trifluoroacetic acid, propanoic acid, butanoic acid, or bases such as ammonium hydroxide, sodium hydroxide, potassium hydroxide, or mixtures thereof;
    • a viscosity modifier, resin, or binder comprising about 1.0% to 4.5% PVP, polyvinyl alcohol, or a polyimide, or mixtures thereof; and
    • with the balance comprising a third solvent such as cyclohexanol, cyclohexanone, cyclopentanone, cyclopentanol, butyl lactone, or mixtures thereof.

Patent 2024
1-hexanol 1-methyl-2-pyrrolidinone Acetic Acid Acids Ammonium Hydroxide Benzoic Acid Butanols Butyric Acid Carboxylic Acids chloroacetic acid Cyclohexanol cyclohexanone cyclopentanol cyclopentanone Dicarboxylic Acids Ethanol formic acid Lactones mellitic acid Metals n-pentanol Oxalic Acids Polymers Polyvinyl Alcohol potassium hydroxide Povidone propionic acid Resins, Plant Sodium Hydroxide Solvents Tricarboxylic Acids Trifluoroacetic Acid Viscosity

Example 17

    • A composition comprising:
    • about 0.01% to 3.0% of a plurality of functionalized metallic nanofibers 100;
    • a first solvent comprising about 18% to 28% 2-propanol (isopropyl alcohol or IPA), 1-methoxy-2-propanol, 1-butanol, ethanol, diethylene glycol, 1-pentanol or 1-hexanol, or mixtures thereof;
    • a viscosity modifier, resin, or binder comprising about 1.5% to 2.5% cellulose resin such as propoxymethyl cellulose, methoxyl cellulose or hydroxypropyl cellulose resin, or mixtures thereof;
    • a second solvent comprising about 15% to 25% of n-propanol, 2-propanol, or diethylene glycol, or mixtures thereof; and
    • with the balance comprising a third solvent such as (deionized) water, 1-methoxy-2-propanol, cyclohexanol, cyclohexanone, cyclopentanone, cyclopentanol, butyl lactone, or mixtures thereof.

Patent 2024
1-hexanol 1-Propanol Butyl Alcohol Cellulose Cyclohexanol cyclohexanone cyclopentanol cyclopentanone diethylene glycol Ethanol hydroxypropylcellulose Isopropyl Alcohol Lactones Metals methoxyisopropanol n-pentanol Resins, Plant Solvents Viscosity

Top products related to «Cyclohexanol»

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Cyclohexanol is a chemical compound with the formula C6H11OH. It is a colorless, viscous liquid with a mild, pleasant odor. Cyclohexanol is used as an intermediate in the production of various chemicals and pharmaceuticals.
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Methanol is a clear, colorless, and flammable liquid that is widely used in various industrial and laboratory applications. It serves as a solvent, fuel, and chemical intermediate. Methanol has a simple chemical formula of CH3OH and a boiling point of 64.7°C. It is a versatile compound that is widely used in the production of other chemicals, as well as in the fuel industry.
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Acetonitrile is a colorless, volatile, flammable liquid. It is a commonly used solvent in various analytical and chemical applications, including liquid chromatography, gas chromatography, and other laboratory procedures. Acetonitrile is known for its high polarity and ability to dissolve a wide range of organic compounds.
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Glycidyl methacrylate is a chemical compound used in the production of various synthetic polymers. It is a bifunctional monomer, containing both an epoxide group and a methacrylate group, which allows it to participate in a range of polymerization reactions. The core function of glycidyl methacrylate is to serve as a building block in the synthesis of specialty polymers and copolymers, which find applications in diverse industries.
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Cyclohexane is a colorless, flammable liquid chemical compound with the molecular formula C6H12. It is commonly used as a solvent and as an intermediate in the production of various industrial chemicals.
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Cyclohexanone is a chemical compound with the formula C6H10O. It is a colorless liquid with a characteristic odor. Cyclohexanone is used as a solvent and as an intermediate in the production of various chemicals and materials.
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1-dodecanol is a long-chain primary alcohol with the molecular formula of C12H26O. It is a colorless, waxy solid at room temperature. 1-dodecanol is commonly used as a starting material in the production of various chemical compounds and as a component in personal care products and industrial applications.
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Ethylene glycol dimethacrylate is a chemical compound used as a cross-linking agent in various applications. It is a colorless, viscous liquid with a characteristic odor. The primary function of ethylene glycol dimethacrylate is to create a three-dimensional network structure in polymeric materials, enhancing their mechanical and thermal properties.
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Ethanol is a clear, colorless liquid chemical compound commonly used in laboratory settings. It is a key component in various scientific applications, serving as a solvent, disinfectant, and fuel source. Ethanol has a molecular formula of C2H6O and a range of industrial and research uses.
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Toluene is a colorless, flammable liquid with a distinctive aromatic odor. It is a common organic solvent used in various industrial and laboratory applications. Toluene has a chemical formula of C6H5CH3 and is derived from the distillation of petroleum.

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