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COMMON NAME | : | Geraniol |
SYMBOL | : | GOH |
FORMULA | : | C10H18O MOL.WT (average) : 154.249 |
BIOLOGICAL ACTIVITY |
PHYSICAL AND CHEMICAL PROPERTIES |
MELTING POINT | : | |
BOILING POINT | : | |
REFRACTIVE INDEX | : | |
OPTICAL ROTATION | : | |
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SPECTRAL DATA |
UV SPECTRA | : | |
IR SPECTRA | : | |
NMR SPECTRA | : | The 2H-labeled geraniol gave rise to 2H NMR powder patterns interpretable in terms of quadrupole splittings and splin-lattice relaxation times. Spin-lattice relaxation time measurements revealed high rates of motion for geraniol relative to cholesterol in similar membrane hosts and revealed correlation times close to the fatty acyl methyl termini in phosphatidylcholine.(Ref. 0038) |
MASS SPECTRA | : | |
OTHER SPECTRA | : | |
CHROMATOGRAM DATA |
SOURCE |
CHEMICAL SYNTHESIS |
METABOLISM |
GENETIC INFORMATION |
NOTE |
REFERENCES |
AUTHOR | : | de Ropp, J. S., and Troy, F. A. |
TITLE | : | 2H NMR investigation of the organization and dynamics of polyisoprenols in membranes PubMed ID:4066690 |
JOURNAL | : | J Biol Chem. |
VOL | : | 260 PAGE : 15669-15674 (1985) |
AUTHOR | : | Hinson, D. D., Chambliss, K. L., Toth, M. J., Tanaka, R. D., and Gibson, K. M. |
TITLE | : | Post-translational regulation of mevalonate kinase by intermediates of the cholesterol and nonsterol isoprene biosynthetic pathways PubMed ID:9392419 |
JOURNAL | : | J Lipid Res. |
VOL | : | 38 PAGE : 2216-2223 (1997) |