| Weight | 154.253 g/mol |
|---|---|
| Formula | C10H18O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
nerol (106-25-2)
geraniol · geraniol, (E)-isomer · geraniol, titanium (4+) salt
Score:
#278 in Biochemistry
,
#1063 in Biology
,
#1190 in Chemistry
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- Antibacterial Activity of Carvacrol, Citral, and Geraniol against Salmonella typhimurium in Culture Medium and on Fish Cubes (Journal of Food Science, 1995)
- Geraniol 10-hydroxylase1, a cytochrome P450 enzyme involved in terpenoid indole alkaloid biosynthesis (FEBS Letters, 2001)
- Inhibition of pancreatic cancer growth by the dietary isoprenoids farnesol and geraniol. (Lipids, 1997)
- Characterization of Geraniol Synthase from the Peltate Glands of Sweet Basil (Plant Physiology, 2004)
- Co-expression of three MEP pathway genes and geraniol 10-hydroxylase in internal phloem parenchyma of Catharanthus roseus implicates multicellular translocation of intermediates during the biosynthesis of monoterpene indole alkaloids and isoprenoid-derived primary metabolites (Plant Journal, 2004)
- Volatile ester formation in roses. Identification of an acetyl-coenzyme A. Geraniol/Citronellol acetyltransferase in developing rose petals. (Plant Physiology, 2003)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - geraniol
- geraniol, (E)-isomer
- geraniol, titanium (4+) salt
- geraniol, 2-(14)C-labeled, (E)-isomer
- geraniol, 1-(14)C-labeled, (E)-isomer
- geraniol, (Z)-isomer
-
SMILESCC(=CCCC(=CCO)C)C
-
InChIKeyGLZPCOQZEFWAFX-UHFFFAOYSA-N
- Pubchem - nerol
- Wikipedia - nerol
Nerol is a monoterpene found in many essential oils such as lemongrass and hops. It was originally isolated from neroli oil, hence its name. This colourless liquid is used in perfumery.
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nerol
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