| 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 Rotation]
[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). | [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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| Company Name: |
J & K SCIENTIFIC LTD.
|
| Telephone: |
18210857532 18210857532 |
| Website: |
https://www.jkchemical.com |
| Company Name: |
Energy Chemical
|
| Telephone: |
400-0056266 |
| Website: |
www.energy-chemical.com |
| Company Name: |
Sigma-Aldrich
|
| Telephone: |
021-61415566 800-8193336 |
| Website: |
https://www.sigmaaldrich.cn |
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