2-Methyl-6-(p-tolyl)hept-2-en-4-ol

Formula: C₁₅H₂₂O
Molecular weight: 218.3346
IUPAC Standard InChI: InChI=1S/C15H22O/c1-11(2)9-15(16)10-13(4)14-7-5-12(3)6-8-14/h5-9,13,15-16H,10H2,1-4H3
IUPAC Standard InChIKey: NRBFEAZFHRHFFQ-UHFFFAOYSA-N
CAS Registry Number: 38142-57-3
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.
Species with the same structure:
- Turmerol isomer Unknown
Other names: Benzenepropanol,γ,4-dimethyl-α-(2-methyl-1-propen-1-yl)-; ar-Turmerol; ar-Tumerol; Turmerol (-ar)
Information on this page:
Other data available:
- Gas Chromatography
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Normal alkane RI, non-polar column, custom temperature program

Data compiled by: NIST Mass Spectrometry Data Center, William E. Wallace, director

Column type	Capillary	Capillary	Capillary	Capillary	Capillary
Active phase	HP-5	HP-5	HP-5	HP-5	HP-5
Column length (m)	30.	25.	25.	25.	25.
Carrier gas	Helium	Helium	Helium	Helium	Helium
Substrate
Column diameter (mm)	0.32	0.32	0.32	0.32	0.32
Phase thickness (μm)	0.25	0.17	0.17	0.17	0.17
Program	not specified	60 0C (5 min) 4 0C/min -> 220 0C 11 0C/min -> 280 0C (15 min)	60 0C (5 min) 4 0C/min -> 220 0C 11 0C/min -> 280 0C (15 min)	not specified	not specified
I	1583.	1579.	1579.	1583.	1583.
Reference	Kahriman, Tosun, et al., 2011	Custer, 2009	Custer, 2009	Custer, 2009	Custer, 2009
Comment	MSDC-RI	MSDC-RI	MSDC-RI	MSDC-RI	MSDC-RI

Column type	Capillary	Capillary
Active phase	SE-52	DB-5
Column length (m)	30.	30.
Carrier gas	He	He
Substrate
Column diameter (mm)	0.32	0.25
Phase thickness (μm)	0.15	0.1
Program	45C => 1C/min => 100C => 5C/min => 250C (10min)	35C => 4C/min => 180C => 20C/min => 280C
I	1583.	1578.
Reference	Tognolini, Barocelli, et al., 2006	Barros-Filho, Nunes, et al., 2004
Comment	MSDC-RI	MSDC-RI

References

Go To: Top, Normal alkane RI, non-polar column, custom temperature program, Notes

Kahriman, Tosun, et al., 2011
Kahriman, N.; Tosun, G.; Terzioglu, S.; Karaoglu, S.A.; Yayh, N., Chemical composition and antimicrobial activity of the essential oils from the flower, leaf, and stem of Senecio pandurifolis, Rec. Nat. Prod., 2011, 5, 2, 82-91. [all data]

Custer, 2009
Custer, Y., GC Volatile Components Analysis of Different Parts of Litchi chinensis (Dissertation), 2009. [all data]

Tognolini, Barocelli, et al., 2006
Tognolini, M.; Barocelli, E.; Ballabeni, V.; Bruni, R.; Bianchi, A.; Chiavarini, M.; Impicciatore, M., Comparative screening of plant essential oils: Phenylpropanoid moiety as basic core for antiplatelet activity, Life Sciences, 2006, 78, 13, 1419-1432, https://doi.org/10.1016/j.lfs.2005.07.020 . [all data]

Barros-Filho, Nunes, et al., 2004
Barros-Filho, B.A.; Nunes, F.M.; de Oliveira, M.C.F.; Mafezoli, J.; Andrade-Neto, M.; Silveira, E.R.; Pirani, J.R., Volatile constituents from Esenbeckia almawillia (Rutaceae), Biochem. Syst. Ecol., 2004, 32, 9, 817-821, https://doi.org/10.1016/j.bse.2004.02.003 . [all data]

Notes

Go To: Top, Normal alkane RI, non-polar column, custom temperature program, References

Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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