The molecular structure image of GERANIOL is available in chemical structure page of GERANIOL, which provides the molecular geometry information, i.e., the spatial arrangement of atoms in GERANIOL and the chemical bonds that hold the atoms together.
Geranylgeraniol is a diterpenoid that is hexadeca-2,6,10,14-tetraene substituted by methyl groups at positions 3, 7, 11 and 15 and a hydroxy group at position 1. backward compatibility problems in GMD's mass spectra, chemical compound structure
A mixture of [2H7]-geraniol, [2H7]-nerol, [2H7]-linalool and [2H7]-α-terpineol was prepared for use as internal standards in a rapid and accurate analytical method, employing gas chromatography–mass spectrometry (GC/MS), to determine the concentration of geraniol, nerol, linalool and α-terpineol in wine. The atomic mass takes into account the isotopic distribution of the element in a given sample.
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Thus, the hypothesis was correct. 1H Nuclear Magnetic Resonance (NMR) Chemical Shifts of Geraniol with properties. poor, not helpful . trans-3,7-DIMETHYL-2,6-OCTADIEN-1-OL
The GERANIOL molecule consists of 18 Hydrogen atom(s), 10 Carbon atom(s) and 1 Oxygen atom(s) - a total of 29 atom(s). SpectraBase Compound ID=AuQh3kfYvNv
(accessed Nov 12, 2020). This spectrum was 0 times rated; on average=0.0, service last updated 17/02/2017 © 2008-2014 Golm Metabolome Database -, InChI=1S/C13H26OSi/c1-12(2)8-7-9-13(3)10-11-14-15(4,5)6/h8,10H,7,9,11H2,1-6H3/b13-10+, SpectrumJcampDx.ashx?id=3a24b562-4124-4405-af12-a5ab43c97740, SpectrumMsp.ashx?id=3a24b562-4124-4405-af12-a5ab43c97740, Boelling C, Liebig F, Erban A, Kopka J, Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany, retention index (VAR5 method, n-alkanes C10–C36), Kopka J, Max Planck Institute of Molecular Plant Physiology, Department of Molecular Plant Physiology (Prof. Willmitzer L), Am Muehlenberg 1, D-14476 Golm, Germany, OFFSET: "just above noise"; SMOOTHING: 20; PEAK WIDTH: 6; S/N: 2, METHOXYAMINATION: 90min at 30°C; TRIMETHYLSILYLATION: 30min at 37°C, m/z = 70-600; scans:20/s; Pegasus III TOF mass spectrometer, C10, C12, C15, C18, C19, C22, C28, C32, C36, COLUMN:5%phenyl-95%dimethylpolysiloxane, 30+10m, ID:0.25mm, DF:0.25µm, 5PDM VF-5ms (Varian, Darmstadt, Germany); PROGRAM:iso1min 70°C, ramp 9°C/min, iso 5min 350°C; FLOW:Helium, 0.6mL/min; INJECTION:1µL, splitless, 230°C; TRANSFER:250°C; IONSOURCE:250°C, 30+10m (analytical column + guard column), isotherm 1min 70°C, ramp 9°C/min, isotherm 5min 350°C. SpectraBase Spectrum ID: JEi5SWCcFdb: SpectraBase Batch ID: 4jj0toMTxNK: Name: GERANIOL: Source of Sample: Aldrich Chemical Company, Inc., Milwaukee, Wisconsin: Boiling Point: 229-230C: CAS … Structure, properties, spectra, suppliers and links for: Geraniol, 106-24-1.
View the Full Spectrum for FREE! Geranyl geraniol (E,E,E)-Geranylgeraniol.
View the Full Spectrum for FREE! There may be different names of the GERANIOL compound depending on the various situations of industrial applications, which are given below including the registry numbers if available: Visit ChemTopia for further professional chemical information on the basis of a comprehensive intelligence networking platform for experts in the discipline around the globe. Copyright © 1980, 1981-2020 John Wiley & Sons, Inc. All Rights Reserved. This message indicates
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How would you rate the quality of this mass spectrum? Conversion of complicated chemical-related units is no longer sophisticated with the aid of UnitPot. The GERANIOL structure data file can be imported to most of the chemistry-related software, providing three-dimensional visualization and further analysis. outstanding, most helpful. (2) (b) The mass spectrum of geraniol is shown.
The structure of geraniol is OH Deduce the molecular formula of geraniol. and metabolite profile visualizations.
© 2020 ChemEssen, Inc. All rights reserved. Source: Mol-Instincts Chemical Database, Predicted on Quantum. Use your answer to calculate the molar mass of geraniol in g mol–1. Molecular masses are calculated from the standard atomic weights of each nuclide, while molar masses are calculated from the atomic mass of each element. Heat of Vaporization at Normal Boiling Point, LogP (Octanol-Water Partition Coefficient), Ghose-Crippen Octanol-Water Partition Coefficient (logP), Moriguchi Octanol-Water Partition Coefficient (logP), Activity Score for Ion Channel Modulators, Activity Score for Nuclear Receptor Ligands, Structure Data File (SDF/MOL File) of GERANIOL, 29 atom(s) - 18 Hydrogen atom(s), 10 Carbon atom(s) and 1 Oxygen atom(s), 28 bond(s) - 10 non-H bond(s), 2 multiple bond(s), 4 rotatable bond(s), 2 double bond(s), 1 hydroxyl group(s) and 1 primary alcohol(s), 3,7-Dimethyloctan-1-ol, tetradehydro derivative. Need to identify active compounds in your natural products?
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The full standard InChI of GERANIOL is given below: InChI=1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7+.
This site uses cookies. For physicochemical, thermodynamic, transport, spectra, and other property data & information, the followings are available from “Mol-Instincts”, a chemical database based on quantum mechanics: The structure data file (SDF/MOL File) of GERANIOL is available for download in the SDF page of GERANIOL, which provides the information on atoms, bonds, connectivity and coordinates of GERANIOL. How would you rate the quality of this mass spectrum? LEMONOL. Geraniol (1TMS) Replica Mass Spectra of Geraniol (1TMS) replica lib entry date detection method species; 3: 30 March 2011 : Fiehn_GC_2010 : 1 spectrum(a) rotate: click+drag; translate: alt+click+drag; zoom: mousewheel; save: mol. http://spectrabase.com/spectrum/JEi5SWCcFdb, View entire compound with free spectra: 7 NMR, 6 FTIR, and 1 Raman, InChI=1S/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7+, Aldrich Chemical Company, Inc., Milwaukee, Wisconsin. Relative intensity 100 80 60 40 20 0.0 0.0 40 80 120 160 m / z (i) Show that this mass spectrum can be used to confirm the molar mass of geraniol.