2,7-Octadiene-1,6-diol, 2,6-dimethyl-, (E)-
- Formula: C10H18O2
- Molecular weight: 170.2487
- IUPAC Standard InChI: InChI=1S/C10H18O2/c1-4-10(3,12)7-5-6-9(2)8-11/h4,6,11-12H,1,5,7-8H2,2-3H3/b9-6+
- IUPAC Standard InChIKey: NSMIMJYEKVSYMT-RMKNXTFCSA-N
- CAS Registry Number: 75991-61-6
- Chemical structure:
This structure is also available as a 2d Mol file - Species with the same structure:
- Stereoisomers:
- Other names: 2,6-dimethyl-2(E),7-octadiene-1,6-diol; (E)-2,6-Dimethyl-2,7-octadien-1,6-diol; (E)-2,6-dimethyl-2,7-octadiene-1,6-diol; (E)-2,6-Dimethyl-octa-2,7-dien-1,6-diol; (E)-2,6-dimethylocta-2,7-diene-1,6-diol; (E)-2,6-Dimethyl-octa-2.7-dien-1,6-diol; E-8-Hydroxylinalol; (E)-8-hydroxylinalool; trans-8-hydroxylinalool (trans-3,7-dimethyl-1,6-octadiene-3,8-diol); (E)-9-Hydroxylinalool; trans-2,6-Dimethyl-2,7-octadien-1,6-diol; trans-2,6-dimethyl-2,7-octadiene-1,6-diol; (2E)-2,6-Dimethyl-2,7-octadiene-1,6-diol
- Information on this page:
- Other data available:
- Options:
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 | Capillary |
|---|---|---|---|---|
| Active phase | DB-Wax | CP-Wax 52CB | CP-Wax 52 CB | DB-Wax |
| Column length (m) | 30. | 25. | 30. | 30. |
| Carrier gas | He | H2 | H2 | |
| Substrate | ||||
| Column diameter (mm) | 0.25 | 0.3 | 0.32 | 0.25 |
| Phase thickness (μm) | 0.5 | 1.2 | 0.25 | |
| Program | 30C => 70C/min => 60C (3min) => 3C/min => 245C (20min) | 60C(3min) => 2C/min => 220C => 3C/min => 245C | 60 0C 2 0C/min -> 220 0C 3 0C/min -> 245 0C | not specified |
| I | 2275. | 2298. | 2266. | 2296. |
| Reference | Schneider, Razungles, et al., 2001 | López-Tamames, Carro-Mariño, et al., 1997 | Carro Marino, López Tamames, et al., 1995 | Marlatt, Ho, et al., 1992 |
| Comment | MSDC-RI | 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.
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]
López-Tamames, Carro-Mariño, et al., 1997
López-Tamames, E.; Carro-Mariño, N.; Gunata, Y.Z.; Sapis, C.; Baumes, R.; Bayonove, C.,
Potential aroma in several varieties of Spanish grapes,
J. Agric. Food Chem., 1997, 45, 5, 1729-1735, https://doi.org/10.1021/jf960572w
. [all data]
Carro Marino, López Tamames, et al., 1995
Carro Marino, N.; López Tamames, E.; García Jares, C.M.,
Contribution to the study of the aromatic potential of three muscat Vitis vinifera varieties: identification of new compounds,
Food Sci. Technol. Int., 1995, 1, 2-3, 105-116, https://doi.org/10.1177/108201329500100206
. [all data]
Marlatt, Ho, et al., 1992
Marlatt, C.; Ho, C.-T.; Chien, M.,
Studies of aroma constituents bound as glycosides in tomato,
J. Agric. Food Chem., 1992, 40, 2, 249-252, https://doi.org/10.1021/jf00014a016
. [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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