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(-)-MYRTENAL

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(-)-MYRTENAL Basic information

Product Name:
(-)-MYRTENAL
Synonyms:
  • FEMA 3395
  • (1R)-2-PINEN-10-AL
  • (1R)-(-)-MYRTENAL
  • (1R)-6,6-DIMETHYLBICYCLO[3.1.1]HEPT-2-EN-2-CARBOXAL-DEHYDE
  • (-)-MYRTENAL
  • MYRTENAL
  • MYRTENAL, -(-)-
  • (1β,5β)-6,6-Dimethylbicyclo[3.1.1]hepta-2-ene-2-carbaldehyde
CAS:
18486-69-6
MF:
C10H14O
MW:
150.22
EINECS:
209-274-8
Product Categories:
  • Aldehydes
  • Asymmetric Synthesis
  • Building Blocks
  • C10-C12
  • Carbonyl Compounds
  • Chamaemelum nobile (Chamomile tea)
  • Chemical Synthesis
  • Chiral Building Blocks
  • Nutrition Research
  • Organic Building Blocks
  • Phytochemicals by Plant (Food/Spice/Herb)
  • Zingiber officinale (Ginger)
Mol File:
18486-69-6.mol
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(-)-MYRTENAL Chemical Properties

Boiling point:
220-221 °C(lit.)
Density 
0.988 g/mL at 20 °C(lit.)
refractive index 
n20/D 1.504
Flash point:
174 °F
storage temp. 
2-8°C
solubility 
Insoluble in water, soluble in alcohol and oils.
form 
Liquid
color 
Clear colorless to yellow
Specific Gravity
0.99
Odor
at 100.00 %. sweet cinnamon tonka spicy terpene camphor jam
Odor Type
spicy
optical activity
[α]22/D 15°, neat
BRN 
2961587
LogP
2.520 (est)
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Safety Information

Safety Statements 
23-24/25-16
WGK Germany 
2
RTECS 
DT5180000
10-23
HS Code 
29122900

MSDS

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(-)-MYRTENAL Usage And Synthesis

Uses

(-)-Myrtenal is used in the synthesis of antiviral adamantanamine and monoterpene fragments.

Preparation

By Chromic acid oxidation of Myrtenol or by isolation from the higher-than-Cineole fractions in the process of rectifying Eucalyptus oil.

Biochem/physiol Actions

Taste at 30 ppm

Anticancer Research

Anticancer activity of myrtenal was tested against the diethylnitrosamine-inducedhepatocellular carcinoma in Wistar albino rats. The apoptosis protein pattern wastaken into account and resulted in upregulation of proteins anti-apoptotic (Ziechet al. 2012; Gautam et al. 2014).

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