1H-Cycloprop[e]azulen-4-ol, decahydro-1,1,4,7-tetramethyl-, [1aR-(1aα,4β,4aβ,7α,7aβ,7bα)]-

Formula: C₁₅H₂₆O
Molecular weight: 222.3663
IUPAC Standard InChI: InChI=1S/C15H26O/c1-9-5-6-10-12(9)13-11(14(13,2)3)7-8-15(10,4)16/h9-13,16H,5-8H2,1-4H3/t9-,10?,11?,12?,13?,15+/m1/s1
IUPAC Standard InChIKey: AYXPYQRXGNDJFU-JDBZYWECSA-N
CAS Registry Number: 552-02-3
Chemical structure:
This structure is also available as a 2d Mol file
Stereoisomers:
Other names: Viridiflorol; 1,1,4,7-Tetramethyldecahydro-1H-cyclopropa[e]azulen-4-ol-, [1aR-(1aα,4β,4aβ,7α,7aβ,7bα)]-; (+)-Viridiflorol; d-Viridiflorol; Himbaccol; Viridflorol; Virdiflorol; [1aR-(1aα,4β,4aβ,7α,7aβ,7bα)]-decahydro-1,1,4,7-tetramethyl-1H-cycloprop[e]azulen-4-ol
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Other data available:
- Mass spectrum (electron ionization)
- Gas Chromatography
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Van Den Dool and Kratz 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-5MS	CBP-5	SPB-1	DB-5MS	CP Sil 8 CB
Column length (m)	30.	30.	27.	30.	50.
Carrier gas	He	He	He	He	He
Substrate
Column diameter (mm)	0.25	0.25	0.25	0.25	0.32
Phase thickness (μm)	0.25	0.25	0.25	0.25
Program	60C (1 min) => 5 C/min => 210C => 10 C/min => 280C (15 min)	60C => 3C/min => 246C => 10C/min => 270C (5min)	60C => 3C/min => 180C => 8C/min => 250C (5min)	40C(5min) => 4C/min => 160C => 8C/min => 240C (15min)	60C (2min) => 5C/min => 160C (1min) => 10C/min => 250C (2min)
I	1609.	1592.	1580.	1600.	1590.
Reference	Andriamaharavo, 2014	Silva, Oliveira, et al., 2007	Sanz, Soria, et al., 2004	Kim, Lee, et al., 2003	Mockute and Judzentiene, 2003
Comment	MSDC-RI	MSDC-RI	MSDC-RI	MSDC-RI	MSDC-RI

Column type	Capillary
Active phase	DB-5
Column length (m)	30.
Carrier gas	He
Substrate
Column diameter (mm)	0.25
Phase thickness (μm)	0.25
Program	60C(2min) => 3C/min => 240C => 10C/min => 270C (4.5min)
I	1587.
Reference	Passos X.S., Castro A.C.M., et al., 2003
Comment	MSDC-RI

References

Go To: Top, Van Den Dool and Kratz RI, non-polar column, custom temperature program, Notes

Andriamaharavo, 2014
Andriamaharavo, N.R., Retention Data. NIST Mass Spectrometry Data Center., NIST Mass Spectrometry Data Center, 2014. [all data]

Silva, Oliveira, et al., 2007
Silva, F.G.; Oliveira, C.B.A.; Pinto, J.E.B.P.; Nascimento, V.E.; Santos, S.C.; Seraphin, J.C.; Ferri, P.H., Seasonal Variability in the Essential Oils of Wild and Cultivated Baccharis trimera, J. Braz. Chem. Soc., 2007, 18, 5, 990-997, https://doi.org/10.1590/S0103-50532007000500017 . [all data]

Sanz, Soria, et al., 2004
Sanz, J.; Soria, A.C.; García-Vallejo, M.C., Analysis of volatile components of Lavandula luisieri L. by direct thermal desorption-gas chromatography-mass spectrometry, J. Chromatogr. A, 2004, 1024, 1-2, 139-146, https://doi.org/10.1016/j.chroma.2003.10.024 . [all data]

Kim, Lee, et al., 2003
Kim, T.H.; Lee, S.M.; Kim, Y.-S.; Kim, K.H.; Oh, S.; Lee, H.J., Aroma dilution method using GC injector split ratio for volatile compounds extracted by headspace solid phase microextraction, Food Chem., 2003, 83, 1, 151-158, https://doi.org/10.1016/S0308-8146(03)00221-8 . [all data]

Mockute and Judzentiene, 2003
Mockute, D.; Judzentiene, A., Variability of the essential oils composition of Achillea millefolium ssp. millefolium growing wild in Lithuania, Biochem. Syst. Ecol., 2003, 31, 9, 1033-1045, https://doi.org/10.1016/S0305-1978(03)00066-8 . [all data]

Passos X.S., Castro A.C.M., et al., 2003
Passos X.S.; Castro A.C.M.; Pires J.S.; Garcia A.C.F.; Campos F.C.; Fernandes O.F.L.; Paula J.R.; Ferreira H.D.; Santos S.C.; Ferri P.H.; Silva M.D.R., Composition and antifungal activity of the essential oils of Caryocar brasiliensis, Pharm. Biol., 2003, 41, 5, 319-324, https://doi.org/10.1076/phbi.41.5.319.15936 . [all data]

Notes

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Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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