ChemicalBook > Product Catalog > Flavors and fragrances > Synthetic fragrances > Aldehydes spices > Terpene aldehyde > (-)-MYRTENAL
(-)-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
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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
- F
- 10-23
- HS Code
- 29122900
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
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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).
(-)-MYRTENALSupplier
J & K SCIENTIFIC LTD.
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- 010-82848833 400-666-7788
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- 800-810-5118
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