exo-2-Hydroxycineole
- Formula: C10H18O2
- Molecular weight: 170.2487
- IUPAC Standard InChI: InChI=1S/C10H18O2/c1-9(2)7-4-5-10(3,12-9)8(11)6-7/h7-8,11H,4-6H2,1-3H3/t7?,8-,10?/m0/s1
- IUPAC Standard InChIKey: YVCUGZBVCHODNB-ZCUBBSJVSA-N
- CAS Registry Number: 92999-78-5
- Chemical structure:
This structure is also available as a 2d Mol file - Stereoisomers:
- Other names: 1,3,3-Trimethyl-2-oxabicyclo[2.2.2]octan-6-ol, (1α,4α,6β)-; 2α-Hydroxy-1,8-cineole; 2-exo-Hydroxy-1,8-cineole; 2-Hydroxycineole, exo-; trans-2-Hydroxy-1,8-cineole; exo-2-Hydroxycineol; exo-2-Hydroxy-1,8-cineole; 2α-Hydroxy-1,8-cineol; exo-2-Hydroxy-8-cineole; 1,8-cineole, 2α hydroxy
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Normal alkane RI, polar column, custom temperature program
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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 |
|---|---|---|---|
| Active phase | CP-Wax 52 CB | HP-Innowax | DB-Wax |
| Column length (m) | 50. | 60. | 30. |
| Carrier gas | Helium | He | |
| Substrate | |||
| Column diameter (mm) | 0.25 | 0.25 | 0.25 |
| Phase thickness (μm) | 0.20 | 0.25 | 0.5 |
| Program | 60 0C (5 min) 3 0C/min -> 250 0C (20 min) 1 0C/min -> 255 0C | 60C(10min) => 4C/min => 220C(10min) => 1C/min => 240C | 30C => 70C/min => 60C (3min) => 3C/min => 245C (20min) |
| I | 1857. | 1875. | 1840. |
| Reference | Genisheva and Oliveira, 2009 | Viljoen, van Vuuren, et al., 2003 | Schneider, Razungles, et al., 2001 |
| Comment | MSDC-RI | MSDC-RI | MSDC-RI |
References
Go To: Top, Normal alkane RI, 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.
Genisheva and Oliveira, 2009
Genisheva, Z.; Oliveira, J.M.,
Monoterpenic characterization of white cultivars from Vinhos Verdes appelation of origin (North Portugal),
J. Inst. Brewing, 2009, 115, 4, 308-317, https://doi.org/10.1002/j.2050-0416.2009.tb00386.x
. [all data]
Viljoen, van Vuuren, et al., 2003
Viljoen, A.; van Vuuren, S.; Ernst, E.; Klepser, M.; Demirci, B.; Baser, H.; van Wyk, B.-E.,
Osmitopsis asteriscoides (Asteraceae)-the antimicrobial activity and essential oil composition of a Cape-Dutch remedy,
J. Ethnopharmacol., 2003, 88, 2-3, 137-143, https://doi.org/10.1016/S0378-8741(03)00191-0
. [all data]
Schneider, Razungles, et al., 2001
Schneider, R.; Razungles, A.; Augier, C.; Baumes, R.,
Monoterpenic and norisoprenoidic glycoconjugates of Vitis vinifera L. cv. Melon B. as precursors of odorants in Muscadet wines,
J. Chromatogr. A, 2001, 936, 1-2, 145-157, https://doi.org/10.1016/S0021-9673(01)01150-5
. [all data]
Notes
Go To: Top, Normal alkane RI, polar column, custom temperature program, References
- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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