β-Phellandrene
- Formula: C10H16
- Molecular weight: 136.2340
- IUPAC Standard InChI: InChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,6,8,10H,3,5,7H2,1-2H3
- IUPAC Standard InChIKey: LFJQCDVYDGGFCH-UHFFFAOYSA-N
- CAS Registry Number: 555-10-2
- Chemical structure:
This structure is also available as a 2d Mol file - Stereoisomers:
- Other names: Cyclohexene, 3-methylene-6-(1-methylethyl)-; p-Mentha-1(7),2-diene; Phellandrene, β; beta-Phellandrene; 3-methylene-6-(1-methylethenyl)-cyclohexane; (-)-β-phellandrene; (+)-β-phellandrene; 3-methylene-6-(1-methylethenyl)-cyclohexane (β-phellandrene); 3-Isopropyl-6-methylenecyclohexene
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Kovats' RI, non-polar column, custom temperature program
Go To: Top, References, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director
| Column type | Capillary | Capillary | Capillary | Capillary | Capillary |
|---|---|---|---|---|---|
| Active phase | HP-5 | HP-5 | OV-1 | DB-5 | DB-5 |
| Column length (m) | 30. | 15. | 30. | 30. | |
| Carrier gas | He | He | He | H2 | |
| Substrate | |||||
| Column diameter (mm) | 0.25 | 0.317 | 0.20 | 0.26 | |
| Phase thickness (μm) | 0.25 | 0.25 | 0.25 | ||
| Program | 60C(5min) => 3C/min => 100C => 1C/min => 160C => 10C/min => 240C(10min) | 40C (3min) => 3C/min => 180C => 30C/min => 270C (5min) | 50C(4min) => (4C/min) => 90C => (10C/min)=300C(10min) | not specified | not specified |
| I | 1029. | 1030. | 1014. | 1031. | 1031. |
| Reference | de Marchese, de Heluani, et al., 2007 | Daferera, Ziogas, et al., 2003 | El-Shazly, Dorai, et al., 2002 | Moreira, Sousa, et al., 2001 | Adams, 1998 |
| Comment | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI |
| Column type | Capillary |
|---|---|
| Active phase | SF-96 |
| Column length (m) | 127. |
| Carrier gas | |
| Substrate | |
| Column diameter (mm) | 0.75 |
| Phase thickness (μm) | |
| Program | not specified |
| I | 1024. |
| Reference | Okamoto, Ellison, et al., 1981 |
| Comment | MSDC-RI |
References
Go To: Top, Kovats' RI, non-polar column, custom temperature program, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
de Marchese, de Heluani, et al., 2007
de Marchese, M.J.A.; de Heluani, C.S.; Catalán, C.A.N.; Griffin, C.A.; Vaughn, J.B., Jr.; Herz, W.,
Incisol, an alcohol with a novel sesquiterpene skeleton from Xenophyllum incisum,
Biochem. Syst. Ecol., 2007, 35, 3, 169-175, https://doi.org/10.1016/j.bse.2006.10.006
. [all data]
Daferera, Ziogas, et al., 2003
Daferera, D.J.; Ziogas, B.N.; Polissiou, M.G.,
The effectiveness of plant essential oils on the growth of Botrytis cinerea, Fusarium sp. and Clavibacter michiganensis subsp. michiganensis,
Crop Prot., 2003, 22, 1, 39-44, retrieved from http://www.elsevier.com/gej-ng/10/25/40/84/25/31/article.pdf, https://doi.org/10.1016/S0261-2194(02)00095-9
. [all data]
El-Shazly, Dorai, et al., 2002
El-Shazly, A.; Dorai, G.; Wink, M.,
Chemical composition and biological activity of the essential oils of Senecio aegyptus var. discoideus Boiss.,
Z. Naturforsch., 2002, 57c, 434-439. [all data]
Moreira, Sousa, et al., 2001
Moreira, D.L.; Sousa, P.O.; Pereira, N.A.; Cardoso, G.L.,
Effect of leaf essential oil from Piper solmsianum C.DC. in mice behaviour,
An. Acad. Bras. Cienc., 2001, 73, 1, 1-7, https://doi.org/10.1590/S0001-37652001000100004
. [all data]
Adams, 1998
Adams, R.P.,
The essential oils and chemotaxonomy of Juniperus sect. Juniperus,
Biochem. Syst. Ecol., 1998, 26, 6, 637-645, https://doi.org/10.1016/S0305-1978(98)00020-9
. [all data]
Okamoto, Ellison, et al., 1981
Okamoto, R.A.; Ellison, B.O.; Kepner, R.E.,
Volatile terpenes in Sequoia sempervirens foliage. Changes in composition during maturation,
J. Agric. Food Chem., 1981, 29, 2, 324-326, https://doi.org/10.1021/jf00104a026
. [all data]
Notes
Go To: Top, Kovats' RI, non-polar column, custom temperature program, References
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