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Spiro[4.5]dec-7-ene, 1,8-dimethyl-4-(1-methylethenyl)-, [1S-(1«alpha»,4«beta»,5«alpha»)]-


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

Van Den Dool and Kratz RI, non-polar column, temperature ramp

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Column type Active phase I Reference Comment
CapillaryDB-11440.de Feo, Bruno, et al., 200330. m/0.25 mm/0.25 «mu»m, He, 40. C @ 5. min, 2. K/min, 250. C @ 20. min
CapillaryHP-51462.Oprean, Tamas, et al., 1998He, 3. K/min; Column diameter: 0.26 mm; Phase thickness: 0.25 «mu»m; Tstart: 60. C; Tend: 240. C

Normal alkane RI, non-polar column, temperature ramp

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Column type Active phase I Reference Comment
CapillaryVF-1 MS1474.Marchesini, Prada, et al., 200930. m/0.25 mm/0.25 «mu»m, Helium, 60. C @ 5. min, 4. K/min, 280. C @ 10. min
CapillaryDB-51421.Chagonda and Chalchat, 200550. m/0.3 mm/0.25 «mu»m, 2. K/min; Tstart: 60. C; Tend: 240. C
CapillaryDB-51471.Abreu, Reis, et al., 200430. m/0.25 mm/0.25 «mu»m, H2, 4. K/min; Tstart: 50. C; Tend: 290. C
CapillaryHP-5MS1459.Li and Jiang, 200430. m/0.25 mm/0.25 «mu»m, He, 50. C @ 2. min, 5. K/min, 230. C @ 10. min

Normal alkane RI, non-polar column, custom temperature program

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Column type Active phase I Reference Comment
CapillaryVF-51479.Shivashankar, Roy, et al., 201230. m/0.25 mm/0.25 «mu»m, Helium; Program: 50 0C (2 min) 3 0C/min -> 200 0C (3 min) 10 0C/min -> 220 0C (8 min)
CapillaryVF-51471.Shivashankar, Roy, et al., 201230. m/0.25 mm/0.25 «mu»m, Helium; Program: not specified
CapillaryHP-5MS1483.Demyttenaere, Moriña, et al., 200430. m/0.25 mm/0.25 «mu»m, He; Program: 40C (2min) => 10C/min => 200C => 15C/min => 250C (5min)
CapillaryHP-5MS1483.Demyttenaere, Moriña, et al., 200430. m/0.25 mm/0.25 «mu»m, He; Program: 40C (2min) => 10C/min => 200C => 15C/min => 250C (5min)
CapillaryCP Sil 8 CB1464.Judpentienë and Mockutë, 200450. m/0.32 mm/0.25 «mu»m, He; Program: 60C(2min) => 5C/min => 160C(1min) => 10C/min => 250C (5min)
CapillaryDB-51476.Jelen H.H., Mirocha C.J., et al., 199530. m/0.25 mm/0.25 «mu»m; Program: 35C(1min) => 5C/min => 230C => 20C/min => 280C
CapillaryDB-51474.Jelen H.H., Mirocha C.J., et al., 199530. m/0.25 mm/0.25 «mu»m; Program: 35C(1min) => 5C/min => 230C => 20C/min => 280C

Normal alkane RI, polar column, temperature ramp

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Column type Active phase I Reference Comment
CapillaryDB-Wax1689.Guo, Wu, et al., 200830. m/0.25 mm/0.25 «mu»m, Helium, 60. C @ 2. min, 10. K/min, 250. C @ 10. min
CapillaryTC-Wax1698.Miyazawa, Kurose, et al., 2001He, 4. K/min, 250. C @ 47. min; Column length: 60. m; Column diameter: 0.25 mm; Tstart: 80. C

References

Go To: Top, Gas Chromatography, Notes

Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

de Feo, Bruno, et al., 2003
de Feo, V.; Bruno, M.; Tahiri, B.; Napolitano, F.; Senatore, F., Chemical composition and antibacterial activity of essential oils from Thymus spinulosus Ten. (Lamiaceae), J. Agric. Food Chem., 2003, 51, 13, 3849-3853, https://doi.org/10.1021/jf021232f . [all data]

Oprean, Tamas, et al., 1998
Oprean, R.; Tamas, M.; Sandulescu, R.; Roman, L., Essential oils analysis. I. Evaluation of essential oils composition using both GC and MS fingerprints, J. Pharm. Biomed. Anal., 1998, 18, 4-5, 651-657, https://doi.org/10.1016/S0731-7085(98)00283-0 . [all data]

Marchesini, Prada, et al., 2009
Marchesini, A.M.; Prada, G.G.; Messiano, G.B.; Machado, M.B.; Lopes, L.M.X., Chemical constituents of Aristolochia giberti, J. Braz. Chem. Soc., 2009, 20, 9, 1598-1608, https://doi.org/10.1590/S0103-50532009000900006 . [all data]

Chagonda and Chalchat, 2005
Chagonda, L.S.; Chalchat, J.-C., The essential oil of wild and cultivated Hoslundia opposita Vahl. from Zimbabwe, Flavour Fragr. J., 2005, 20, 2, 193-195, https://doi.org/10.1002/ffj.1402 . [all data]

Abreu, Reis, et al., 2004
Abreu, I.N.; Reis, M.G.; Marsaioli, A.J.; Mazzafera, P., Essential oil composition of Hypericum brasiliense choise, Flavour Fragr. J., 2004, 19, 1, 80-82, https://doi.org/10.1002/ffj.1319 . [all data]

Li and Jiang, 2004
Li, R.; Jiang, Z.-T., Chemical composition of the essential oil of Cuminum cyminum L. from China, Flavour Fragr. J., 2004, 19, 4, 311-313, https://doi.org/10.1002/ffj.1302 . [all data]

Shivashankar, Roy, et al., 2012
Shivashankar, S.; Roy, T.K.; Moorthy, P.N.R., Headspace solid phase micro extraction and GC/MS analysis of the volatile components in seed and cake of Azadirachta indica A. juss, Chem. Bull. of Politechnika Univ. Timisoara, Romania, 2012, 57(71), 1, 1-6. [all data]

Demyttenaere, Moriña, et al., 2004
Demyttenaere, J.C.R.; Moriña, R.M.; De Kimpe, N.; Sandra, P., Use of headspace solid-phase microextraction and headspace sorptive extraction for the detection of the volatile metabolites produced by toxigenic Fusarium species, J. Chromatogr. A, 2004, 1027, 1-2, 147-154, https://doi.org/10.1016/j.chroma.2003.08.105 . [all data]

Judpentienë and Mockutë, 2004
Judpentienë, A.; Mockutë, D., Chemical composition of essential oils of Artemisia absinthium L. (wormwood) growing wild in Vilnius, Chemija, 2004, 15, 4, 64-68. [all data]

Jelen H.H., Mirocha C.J., et al., 1995
Jelen H.H.; Mirocha C.J.; Wasowicz E.; Kaminski E., Production of volatile sesquiterpenes by Fusarium sambucinum strans with different abilities to synthesize trichlothecenes, Appl. Environ. Microbiol., 1995, 61, 11, 3815-3820. [all data]

Guo, Wu, et al., 2008
Guo, L.; Wu, J.-Z.; Han, T.; Cao, T.; Rahman, K.; Qin, L.-P., Chemical composition, antifungal and antitumor properties of ether extracts of Scapania verrucosa Heeg. and its endophytic fungus Chaetomium fusiforme, Molecules, 2008, 13, 9, 2114-2125, https://doi.org/10.3390/molecules13092114 . [all data]

Miyazawa, Kurose, et al., 2001
Miyazawa, M.; Kurose, K.; Itoh, A.; Hiraoka, N., Comparison of the essential oils of Glehnia littoralis from Northern and Southern Japan, J. Agric. Food Chem., 2001, 49, 11, 5433-5436, https://doi.org/10.1021/jf010219c . [all data]


Notes

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