Cyclohexene, 3-methyl-6-(1-methylethyl)-
- Formula: C10H18
- Molecular weight: 138.2499
- IUPAC Standard InChIKey: WHNGPXQYYRWQAS-UHFFFAOYSA-N
- CAS Registry Number: 5256-65-5
- Chemical structure:
This structure is also available as a 2d Mol file - Stereoisomers:
- Other names: p-Menth-2-ene; 2-Menthene; 3-Isopropyl-6-methylcyclohexene; 3-Isopropyl-6-methyl-1-cyclohexene; Δ2-menthene; p-Ment-2-ene
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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
Kovats' RI, non-polar column, isothermal
Column type | Active phase | Temperature (C) | I | Reference | Comment |
---|---|---|---|---|---|
Capillary | Apiezon L | 100. | 1004. | Morishita, Okano, et al., 1980 | Column length: 45. m; Column diameter: 0.25 mm |
Packed | SE-30 | 160. | 985. | Hedin, Thompson, et al., 1972 | N2, Chromosorb W; Column length: 6.145 m |
Kovats' RI, non-polar column, temperature ramp
Column type | Active phase | I | Reference | Comment |
---|---|---|---|---|
Capillary | DB-5 | 1009. | Buchin, Salmon, et al., 2002 | 60. m/0.32 mm/1. μm, He, 40. C @ 5. min, 3. K/min, 230. C @ 2. min |
Capillary | HP-5 | 985. | Ramos, Siani, et al., 2000 | 30. m/0.32 mm/0.25 μm, He, 3. K/min; Tstart: 70. C; Tend: 250. C |
Kovats' RI, polar column, isothermal
Column type | Active phase | Temperature (C) | I | Reference | Comment |
---|---|---|---|---|---|
Capillary | PEG-20M | 100. | 1091. | Morishita, Okano, et al., 1980 | Column length: 75. m; Column diameter: 0.25 mm |
Normal alkane RI, non-polar column, temperature ramp
Column type | Active phase | I | Reference | Comment |
---|---|---|---|---|
Capillary | HP-1 | 982. | Antoniotti, Alezra, et al., 2004 | 50. m/0.2 mm/0.33 μm, 2. K/min, 250. C @ 10. min; Tstart: 60. 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.
Morishita, Okano, et al., 1980
Morishita, F.; Okano, T.; Kojima, T.,
Retention indices of monocyclic monoterpene hydrocarbons,
Bunseki Kagaku, 1980, 29, 1, 48-53, https://doi.org/10.2116/bunsekikagaku.29.48
. [all data]
Hedin, Thompson, et al., 1972
Hedin, P.A.; Thompson, A.C.; Gueldner, R.C.,
Application of a Sequential Reduction Regimen to Fractionation of Essential Oils,
Anal. Chem., 1972, 44, 7, 1254-1257, https://doi.org/10.1021/ac60315a030
. [all data]
Buchin, Salmon, et al., 2002
Buchin, S.; Salmon, J.-C.; Carnat, A.-P.; Berger, T.; Bugaud, C.; Bosset, J.O.,
Identification de composés monoterpéniques, sesquiterpéniques et benzéniques dans un lait d'alpage très riche en ces substances,
Mitt. Lebensmittelunters. Hyg., 2002, 93, 199-216. [all data]
Ramos, Siani, et al., 2000
Ramos, M.F.S.; Siani, A.C.; Tappin, M.R.R.; Guimaraes, A.C.; Lahoz, J.E.; Ribeiro, J.E.L.S.,
Essential oils from oleoresins of Protium spp. of the Amazon region,
Flavour Fragr. J., 2000, 15, 6, 383-387, https://doi.org/10.1002/1099-1026(200011/12)15:6<383::AID-FFJ927>3.0.CO;2-X
. [all data]
Antoniotti, Alezra, et al., 2004
Antoniotti, S.; Alezra, N.; Fernandez, X.; Duñach, E.,
Catalytic epoxide oxidation: a novel access to flavouring and odorant α-diketones,
Flavour Fragr. J., 2004, 19, 5, 373-381, https://doi.org/10.1002/ffj.1371
. [all data]
Notes
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- Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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