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ALPHA-PINENE OXIDE

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ALPHA-PINENE OXIDE Basic information

Product Name:
ALPHA-PINENE OXIDE
Synonyms:
  • alpha-Pinene oxide 97%
  • .alpha.-Pinene epoxide (Isomer 1)
  • .alpha.-Pinene epoxide (Isomer 2)
  • 2,3-epoxy-pinan
  • 2,7,7-trimethyl-3-oxatricyclo(4.1.1.0(sup2,4))octane
  • A-PINENEOXIDE WITH GC
  • 2,6,6-Trimethyl-2,3-epoxybicyclo[3.1.1]heptane
  • Nsc5609
CAS:
1686-14-2
MF:
C10H16O
MW:
152.23
EINECS:
216-869-6
Product Categories:
  • Bicyclic Monoterpenes
  • Biochemistry
  • Terpenes
  • Epoxide Monomers
  • Monomers
  • Polymer Science
Mol File:
1686-14-2.mol
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ALPHA-PINENE OXIDE Chemical Properties

Boiling point:
102-103 °C/50 mmHg (lit.)
Density 
0.964 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.469(lit.)
Flash point:
150 °F
storage temp. 
Keep in dark place,Inert atmosphere,Room temperature
solubility 
Chloroform (Sparingly), Dichloromethane (Sparingly), Ethanol (Slightly)
form 
Oil
color 
Colourless
Specific Gravity
0.97
Stability:
Moisture Sensitive
LogP
2.339 (est)
CAS DataBase Reference
1686-14-2(CAS DataBase Reference)
EPA Substance Registry System
3-Oxatricyclo[4.1.1.02,4]octane, 2,7,7-trimethyl- (1686-14-2)
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Safety Information

RIDADR 
2810
WGK Germany 
3
RTECS 
TK4565000
HS Code 
2910.90.9100
HazardClass 
6.1
PackingGroup 
III

MSDS

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ALPHA-PINENE OXIDE Usage And Synthesis

Definition

ChEBI: Alpha-pinene oxide is an epoxide of alpha-pinene. It has a role as a fragrance, a bacterial xenobiotic metabolite and a human metabolite. It is a pinane monoterpenoid and an epoxide. It derives from a hydride of an alpha-pinene.

Preparation

a-Pinene oxide is prepared industrially by using percarboxylic acid. Processes based on air oxidation are also known.

Uses

An industrially important reaction of optically active a-pinene oxide is rearrangement to campholene aldehyde (e.g., in the presence of zinc bromide). Subsequent aldol condensation with lower aliphatic aldehydes or ketones (e.g., propionaldehyde, butyraldehyde, or acetone) provides unsaturated aldehydes or ketones that can be reduced to the corresponding saturated alcohols. These are used in the fragrance industry as a sandalwood scent.

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