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BICYCLOHEXYL

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BICYCLOHEXYL Basic information

Product Name:
BICYCLOHEXYL
Synonyms:
  • 1,1’-bicyclohexyl
  • 1,1-Bicyclohexyl
  • 1,1'-Biphenyl, dodecahydro-
  • Bicyclohexane
  • cis,cis-bicyclohexyl
  • Cyclohexane, cyclohexyl-
  • Cyclohexylcyclohexane
  • Dicyclohexane
CAS:
92-51-3
MF:
C12H22
MW:
166.3
EINECS:
202-161-4
Mol File:
92-51-3.mol
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BICYCLOHEXYL Chemical Properties

Melting point:
3-4 °C(lit.)
Boiling point:
227 °C(lit.)
Density 
0.864 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.478(lit.)
Flash point:
92 °C
storage temp. 
Store below +30°C.
solubility 
Difficult to mix.
form 
Liquid
Specific Gravity
0.864
color 
Colorless to nearly colorless
BRN 
1848266
Stability:
Stable. Flammable. Incompatible with strong oxidizing agents.
InChIKey
WVIIMZNLDWSIRH-UHFFFAOYSA-N
CAS DataBase Reference
92-51-3(CAS DataBase Reference)
NIST Chemistry Reference
1,1'-Bicyclohexyl(92-51-3)
EPA Substance Registry System
1,1'-Bicyclohexyl (92-51-3)
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Safety Information

Hazard Codes 
Xi,N
Risk Statements 
50-50/53
Safety Statements 
23-24/25-61-60
RIDADR 
UN3082 - class 9 - PG 3 - DOT NA1993 - Environmentally hazardous substances, liquid, n.o.s. HI: all (not BR)
WGK Germany 
3
Autoignition Temperature
473 °F
TSCA 
T
HazardClass 
IRRITANT
HS Code 
29021990

MSDS

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BICYCLOHEXYL Usage And Synthesis

Chemical Properties

Bicyclohexyl is a colourless liquid. Solidifies in the cold, melts at 3° C. B.P. 214° C. Sp.Gr. 0.89. Insoluble in water, soluble in alcohol and oils. Sweet, mild-aromatic, but rather “chemical” odor.

Uses

Bicyclohexyl can be used high-boiling solvent and penetrant. It Has been suggested for use in perfume compositions, mainly as a modifier in low-cost Geranium, New Mown Hay, Lavender, Rose and other bases.

Uses

Bicyclohexyl is used as process media or solvent in many industries including chemicals, petrochemicals, polymers, coatings, photography. And it is also used to produce 1-fluorobicyclohexyl at temperature of -75°C.

Preparation

By catalytic reduction of Diphenyl.

Purification Methods

Shake bicyclohexyl repeatedly with aqueous KMnO4 and with conc H2SO4, wash it with water, dry, first with CaCl2 then with sodium, and distil it. [Mackenzie J Am Chem Soc 77 2214 1955, Beilstein 5 IV 334.]

BICYCLOHEXYLSupplier

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