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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
biological source
synthetic
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).

in vivo

(-)-Myrtenal ((1R)-(-)-Myrtenal; orally; 80 mg/kg/day for 28 days) reveals decreased the levels of plasma glucose, improved the plasma insulin levels, up-regulation of IRS2, Akt and GLUT2 in liver and IRS2, Akt and GLUT4 protein expression in skeletal muscle in diabetic rats induced by single intraperitoneal injection of Streptozotocin (STZ) (40 mg/kg bw)[2].

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