| Identification | Back Directory | [Name]
(-)-MYRTENAL | [CAS]
18486-69-6 | [Synonyms]
MYRTENAL
FEMA 3395
l-Myrtenal
(-)-MYRTENAL
JACS-18486-69-6
MYRTENAL, -(-)-
(1R)-(-)-MYRTENAL
(1R)-2-PINEN-10-AL
MYRTENAL, -(-)-(SG)
(1R)-(-)-Myrtenal 98%
(-)-MYRTENAL USP/EP/BP
(1R)-6,6-DIMETHYLBICYCLO[3.1.1]HEPT-2-EN-2-CARBOXAL-DEHYDE
(1β,5β)-6,6-Dimethylbicyclo[3.1.1]hepta-2-ene-2-carbaldehyde
[1R,5S,(-)]-6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-carbaldehyde
Bicyclo[3.1.1]hept-2-ene-2-carboxaldehyde, 6,6-dimethyl-, (1R,5S)- | [EINECS(EC#)]
209-274-8 | [Molecular Formula]
C10H14O | [MDL Number]
MFCD00074768 | [MOL File]
18486-69-6.mol | [Molecular Weight]
150.22 |
| Chemical Properties | Back Directory | [Boiling point ]
220-221 °C(lit.)
| [density ]
0.988 g/mL at 20 °C(lit.)
| [refractive index ]
n20/D 1.504
| [Fp ]
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 | [biological source]
synthetic | [Odor Type]
spicy | [optical activity]
[α]22/D 15°, neat | [BRN ]
2961587 | [LogP]
2.520 (est) |
| Hazard Information | Back Directory | [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). |
|
| Company Name: |
Energy Chemical
|
| Tel: |
021-021-58432009 400-005-6266 |
| Website: |
http://www.energy-chemical.com |
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