p-Menth-1-en-3,8-diol, cis
- Formula: C10H18O2
- Molecular weight: 170.2487
- IUPAC Standard InChI: InChI=1S/C10H18O2/c1-7-4-5-8(9(11)6-7)10(2,3)12/h6,8-9,11-12H,4-5H2,1-3H3/t8-,9+/m0/s1
- IUPAC Standard InChIKey: MUTBSGZZTDPVPZ-DTWKUNHWSA-N
- Chemical structure:
This structure is also available as a 2d Mol file or as a computed 3d SD file
The 3d structure may be viewed using Java or Javascript. - Stereoisomers:
- Other names: cis-p-menth-1-ene-3,8-diol
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Gas Chromatography
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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
Normal alkane RI, non-polar column, temperature ramp
| Column type | Active phase | I | Reference | Comment |
|---|---|---|---|---|
| Capillary | DB-1 | 1351. | Ueno, Masuda, et al., 2004 | 60. m/0.25 mm/0.25 μm, N2, 3. K/min, 210. C @ 15. min; Tstart: 80. C |
| Capillary | SE-30 | 1362. | Peacock and Kuneman, 1985 | N2, 45. C @ 1. min, 4. K/min; Column length: 100. m; Column diameter: 0.25 mm; Tend: 250. C |
References
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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Ueno, Masuda, et al., 2004
Ueno, T.; Masuda, H.; Ho, C.-T.,
Formation mechanism of p-methylacetophenone from citral via a tert-alkoxy radical intermediate,
J. Agric. Food Chem., 2004, 52, 18, 5677-5684, https://doi.org/10.1021/jf035517j
. [all data]
Peacock and Kuneman, 1985
Peacock, V.E.; Kuneman, D.W.,
Inhibition of the formation of α-p-dimethylstyrene and p-cymen-8-ol in a carbonated citral-containing beverage system,
J. Agric. Food Chem., 1985, 33, 3, 330-335, https://doi.org/10.1021/jf00063a003
. [all data]
Notes
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- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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