(-)-MYRTENAL
(-)-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
(-)-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)
Safety Information
- Safety Statements
- 23-24/25-16
- WGK Germany
- 2
- RTECS
- DT5180000
- F
- 10-23
- HS Code
- 29122900
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
(-)-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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