3-Cyclohexen-1-ol, 1-methyl-4-(1-methylethyl)-
- Formula: C10H18O
- Molecular weight: 154.2493
- IUPAC Standard InChI: InChI=1S/C10H18O/c1-8(2)9-4-6-10(3,11)7-5-9/h4,8,11H,5-7H2,1-3H3
- IUPAC Standard InChIKey: XJWZDXFFNOMMTD-UHFFFAOYSA-N
- CAS Registry Number: 586-82-3
- Chemical structure:
This structure is also available as a 2d Mol file - Other names: p-Menth-3-en-1-ol; 1-Terpinenol; 3-Terpinen-1-ol; 1-Terpineol; Terpin-1-ol; Terpin-3-en-1-ol; Terpinen-1-ol; Terpineol-1; 1-Methyl-4-isopropyl-3-cyclohexen-1-ol; 4-Isopropyl-1-methyl-3-cyclohexen-1-ol; 4-(isopropyl)-1-methylcyclohex-3-en-1-ol
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- Other data available:
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Normal alkane RI, non-polar column, temperature ramp
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 MS | HP-5 MS | DB-5 | DB-5 | DB-5 |
| Column length (m) | 60. | 30. | 30. | 50. | 30. |
| Carrier gas | Helium | Helium | Helium | Nitrogen | Helium |
| Substrate | |||||
| Column diameter (mm) | 0.25 | 0.25 | 0.25 | 0.20 | 0.25 |
| Phase thickness (μm) | 0.25 | 0.25 | 0.25 | 0.32 | 0.25 |
| Tstart (C) | 40. | 50. | 40. | 60. | 40. |
| Tend (C) | 250. | 180. | 240. | 220. | 240. |
| Heat rate (K/min) | 3. | 2. | 3. | 5. | 3. |
| Initial hold (min) | 1. | 1. | 3. | 1. | |
| Final hold (min) | 20. | 5. | |||
| I | 1099. | 1136. | 1141. | 1134. | 1141. |
| Reference | Sardashti, Valizadeh, et al., 2013 | Hammami, Kamoun, et al., 2011 | de Souza, Lopes, et al., 2010 | Shafaghat and Sadeghi, 2009 | de Souza, Lopes, et al., 2009 |
| Comment | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI |
| Column type | Capillary | Capillary | Capillary | Capillary | Capillary |
|---|---|---|---|---|---|
| Active phase | DBP-5 | HP-5 | HP-5MS | HP-5MS | HP-5 |
| Column length (m) | 25. | 30. | 30. | 30. | 25. |
| Carrier gas | Helium | He | He | He | N2 |
| Substrate | |||||
| Column diameter (mm) | 0.25 | 0.32 | 0.25 | 0.25 | 0.2 |
| Phase thickness (μm) | 0.22 | 0.25 | 0.25 | 0.25 | 0.33 |
| Tstart (C) | 40. | 60. | 50. | 50. | 30. |
| Tend (C) | 250. | 246. | 250. | 280. | 280. |
| Heat rate (K/min) | 3. | 3. | 2. | 5. | 3. |
| Initial hold (min) | 1. | 4. | |||
| Final hold (min) | 10. | 10. | |||
| I | 1096. | 1140. | 1134. | 1127. | 1140. |
| Reference | Sereshti and Samadi, 2007 | Coronel, Cerda-Garcia-Rojas, et al., 2006 | Farah, Afifi, et al., 2006 | Kim, Abd El-Aty, et al., 2006 | Shafi, Jose, et al., 2006 |
| Comment | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI |
| Column type | Capillary | Capillary | Capillary | Capillary | Capillary |
|---|---|---|---|---|---|
| Active phase | HP-5 | DB-1 | DB-5 | RTX-5Sil | DB-1 |
| Column length (m) | 30. | 50. | 30. | 30. | 30. |
| Carrier gas | He | N2 | He | He | He |
| Substrate | |||||
| Column diameter (mm) | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 |
| Phase thickness (μm) | 0.25 | 0.25 | 0.25 | 0.25 | 0.25 |
| Tstart (C) | 60. | 95. | 60. | 70. | 60. |
| Tend (C) | 250. | 240. | 240. | 200. | 250. |
| Heat rate (K/min) | 10. | 4. | 3. | 4. | 4. |
| Initial hold (min) | 2. | 10. | |||
| Final hold (min) | 10. | 10. | |||
| I | 1142. | 1130. | 1133. | 1146. | 1141. |
| Reference | Wang, Yang, et al., 2006 | Palá-Paúl, Pérez-Alonso, et al., 2005 | Tellez, Khan, et al., 2004 | Dudai, Larkov, et al., 2003 | Norouzi-Arasi, Yavari, et al., 2002 |
| Comment | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI | MSDC-RI |
| Column type | Capillary | Capillary |
|---|---|---|
| Active phase | CBP-1 | OV-101 |
| Column length (m) | 25. | 25. |
| Carrier gas | Nitrogen | He |
| Substrate | ||
| Column diameter (mm) | 0.25 | 0.20 |
| Phase thickness (μm) | 0.25 | |
| Tstart (C) | 50. | 80. |
| Tend (C) | 210. | 240. |
| Heat rate (K/min) | 3. | 6. |
| Initial hold (min) | 2. | |
| Final hold (min) | ||
| I | 1145. | 1133. |
| Reference | Ly, Yamauchi, et al., 2001 | Zenkevich, Kosman, et al., 1999 |
| Comment | MSDC-RI | MSDC-RI |
References
Go To: Top, Normal alkane RI, non-polar column, temperature ramp, Notes
Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.
Sardashti, Valizadeh, et al., 2013
Sardashti, A.R.; Valizadeh, J.; Adhami, Y.,
Variations in the essential oil composition of Peroskia abrotonolides of different growth stage in Baluchestan,
Middle-East J. Sci. Res., 2013, 13, 6, 781-784. [all data]
Hammami, Kamoun, et al., 2011
Hammami, I.; Kamoun, N.; Rebai, A.,
Biocontrol of Botrytis cinerea with essential oil and methanol extract of Viola odorata flowers,
Archives of Appl. Sci. Res., 2011, 3, 5, 44-51. [all data]
de Souza, Lopes, et al., 2010
de Souza, A.; Lopes, E.M.C.; da Silva, M.C.; Cordeiro, I.; Young, M.C.M.; Sobral, M.E.G.; Moreno, P.R.H.,
Chemical composition and acetylcholinesterase inhibitory activity of essential oils of Myrceugenia myrciolides (Cambess.) O. Berg and Eugenia riedelliana O. Berg, Myrtaceae,
Braz. J. Pharmacognosy, 2010, 20, 2, 175-179. [all data]
Shafaghat and Sadeghi, 2009
Shafaghat, A.; Sadeghi, H.,
Composition and antibacterial activity of essentia; oils from leaf, stem and root of Chrysanthemum parthenium (L.) Bernh. from Iran,
Electronic J. of Environ., Agriculture and Food Chem. (EJEAFChe), 2009, 8, 9, 766-771. [all data]
de Souza, Lopes, et al., 2009
de Souza, A.; Lopes, E.M.C.; da Silva, M.C.; Cordeiro, I.; Young, M.C.M.; Sobral, M.E.G.; Moreno, P.R.H.,
Chemical composition and acetylcholinesterase inhibitory activity of essential oils of Myrceugenia myrcioides (Chambess.) O. Berg and Eugenia riedeliana O. Berg, Myrtaceae,
Braz. J. Pharmacognosy, 2009, 20, 2, 175-179. [all data]
Sereshti and Samadi, 2007
Sereshti, H.; Samadi, S.,
Comparison of hydrodistillation-headspace liquid phase microextraction techniques with hydrodistillation in determination of essential oils in Artemisia Haussknechtii Boiss,
JSUT, 2007, 33, 2, 7-17. [all data]
Coronel, Cerda-Garcia-Rojas, et al., 2006
Coronel, A. del.C.; Cerda-Garcia-Rojas, C.M.; Joseph-Nathan, P.; Catalán, C.A.N.,
Chemical composition, seasonal variation and a new sesquiterpene alcohol from the essential oil of Lippia integrifolia,
Flavour Fragr. J., 2006, 21, 5, 839-847, https://doi.org/10.1002/ffj.1736
. [all data]
Farah, Afifi, et al., 2006
Farah, A.; Afifi, A.; Fechtal, M.; Chhen, A.; Satrani, B.; Talbi, M.; Chaouch, A.,
Fractional distillation effect on the chemical composition of Moroccan myrtle (Myrtus communis L.) essential oils,
Flavour Fragr. J., 2006, 21, 2, 351-354, https://doi.org/10.1002/ffj.1651
. [all data]
Kim, Abd El-Aty, et al., 2006
Kim, M.R.; Abd El-Aty, A.M.; Kim, I.S.; Shim, J.H.,
Determination of volatile flavor components in danggui cultivars by solvent free injection and hydrodistillation followed by gas chromatographic-mass spectrometric analysis,
J. Chromatogr. A, 2006, 1116, 1-2, 259-264, https://doi.org/10.1016/j.chroma.2006.03.060
. [all data]
Shafi, Jose, et al., 2006
Shafi, P.M.; Jose, B.; Radhamani, K.T.; Clery, R.A.,
Influence of pH on essential oil composition of Zanthoxylum rhetsa seeds obtained by steam distillation,
Flavour Fragr. J., 2006, 21, 2, 317-318, https://doi.org/10.1002/ffj.1598
. [all data]
Wang, Yang, et al., 2006
Wang, Q.; Yang, Y.; Zhao, X.; Zhu, B.; Nan, P.; Zhao, J.; Wang, L.; Chen, F.; Liu, Z.; Zhong, Y.,
Chemical variation in the essential oil of Ephedra sinica from Northeastern China,
Food Chem., 2006, 98, 1, 52-58, https://doi.org/10.1016/j.foodchem.2005.04.033
. [all data]
Palá-Paúl, Pérez-Alonso, et al., 2005
Palá-Paúl, J.; Pérez-Alonso, M.; Velasco-Negueruela, A.; Vadaré, J.; Villa, A.M.; Sanz, J.; Brophy, J.J.,
Analysis of the essential oil composition from the different parts of Eryngium glaciale Boiss. from Spain,
J. Chromatogr. A, 2005, 1094, 1-2, 179-182, https://doi.org/10.1016/j.chroma.2005.09.029
. [all data]
Tellez, Khan, et al., 2004
Tellez, M.R.; Khan, I.A.; Schaneberg, B.T.; Crockett, S.L.; Rimando, A.M.; Kobaisy, M.,
Steam distillation-solid-phase microextraction for the detection of Ephedra sinica in herbal preparations,
J. Chromatogr. A, 2004, 1025, 1, 51-56, https://doi.org/10.1016/S0021-9673(03)01035-5
. [all data]
Dudai, Larkov, et al., 2003
Dudai, N.; Larkov, O.; Chaimovitsh, D.; Lewinsohn, E.; Freiman, L.; Ravid, U.,
Essential oil compounds of Origanum dayi Post,
Flavour Fragr. J., 2003, 18, 4, 334-337, https://doi.org/10.1002/ffj.1237
. [all data]
Norouzi-Arasi, Yavari, et al., 2002
Norouzi-Arasi, H.; Yavari, I.; Ghaffarzadeh, F.; Mortazavi, M.-S.,
Volatile constituents of Cymbopogon olivieri (Boiss.) Bor from Iran,
Flavour Fragr. J., 2002, 17, 4, 272-274, https://doi.org/10.1002/ffj.1096
. [all data]
Ly, Yamauchi, et al., 2001
Ly, T.N.; Yamauchi, R.; KAto, K.,
Volatile components of the essential oils in Galanga (Alpina officinarum Hance) from Vietnam,
Food Sci. Technol. Res., 2001, 7, 4, 303-306, https://doi.org/10.3136/fstr.7.303
. [all data]
Zenkevich, Kosman, et al., 1999
Zenkevich, I.G.; Kosman, V.M.; Tkachenko, K.G.,
Some Features of Quantitative Analysis of Essential Oil's Components in High Performance Liquid Chromatography,
Rastitelnye Resursy (Plant resources), 1999, 35, 1, 128-137. [all data]
Notes
Go To: Top, Normal alkane RI, non-polar column, temperature ramp, References
- Symbols used in this document:
Tend Final temperature Tstart Initial temperature - Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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