Cyclohexanol

Cyclohexanol

Cyclohexanol

Min.Order / FOB Price:Get Latest Price

1 Kilogram

Negotiable

  • Min.Order :1 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,T/T,

Keywords

Cyclohexanol 108-93-0 1-Cyclohexanol;Adronal

Quick Details

  • Appearance:colourless liquid
  • Application:Mainly used as organic solvents, pharmaceutical and pesticide intermediate
  • PackAge:in drums
  • ProductionCapacity:1|Metric Ton|Day
  • Storage:
  • Transportation:by sea

Superiority:

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Details:

Cyclohexanol Chemical Properties
mp  23 °C
bp  161 °C
density  0.96
vapor density  3.5 (vs air)
vapor pressure  0.98 mm Hg ( 25 °C)
refractive index  n20/D 1.465(lit.)
Fp  67 °C
storage temp.  Store at RT.
Water Solubility  3.6 g/100 mL (20 ºC)
Sensitive  Hygroscopic
Merck  14,2725
BRN  906744
Stability: Stable. Incompatible with oxidizing agents. Reacts violently with oxidizing agents such as hydrogen peroxide and nitric acid, even at room temperature, to form an explosive material. Hygroscopic. Combustible.
CAS DataBase Reference 108-93-0(CAS DataBase Reference)
NIST Chemistry Reference Cyclohexanol(108-93-0)
EPA Substance Registry System Cyclohexanol(108-93-0)
 
Safety Information
Hazard Codes  Xn
Risk Statements  20/22-37/38
Safety Statements  24/25
RIDADR  1993
WGK Germany  1
RTECS  GV7875000
21
Hazardous Substances Data 108-93-0(Hazardous Substances Data)
MSDS Information
Provider Language
SigmaAldrich English
ACROS English
ALFA English
 
Cyclohexanol Usage And Synthesis
Chemical Properties colourless liquid
General Description A colorless liquid with a camphor-like odor. Soluble in most organic liquids. Flash point 154°F. May be toxic by inhalation or skin exposure. Vapors are narcotic in high concentrations. Irritates skin, eyes and mucus membranes. Used in making soap, lacquers, and plastics.
Air & Water Reactions Less dense than water and slightly soluble in water.
Reactivity Profile Cyclohexanol is an alcohol. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides. Violent reaction with nitric acid. Incompatible with strong oxidizers (chromium trioxide, nitric acid, etc.).
Health Hazard Narcosis-depression of the central nervous system tending to produce sleep or unconsciousness.

 

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