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Methaqualone HCl
SpectraBase Compound ID Fe6GNzBGuxj
InChI InChI=1S/C16H14N2O.ClH/c1-11-7-3-6-10-15(11)18-12(2)17-14-9-5-4-8-13(14)16(18)19;/h3-10H,1-2H3;1H
InChIKey KJUHIXIWKSVBKB-UHFFFAOYSA-N
Mol Weight 286.76 g/mol
Molecular Formula C16H15ClN2O
Exact Mass 286.087291 g/mol

Raman Spectrum

Raman Spectrum

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SpectraBase Spectrum ID 68CxrKHJSDW
Name Methaqualone hydrochloride
Source of Sample Lipomed AG
Catalog Number HCl salt of MTQ-765-1LM
Lot Number HCl salt of 765.1B1.1L4
CAS Registry Number 340-56-7
Cell Type NMR tube
Compound Type Pure
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Formula C16H15ClN2O
InChI InChI=1S/C16H14N2O.ClH/c1-11-7-3-6-10-15(11)18-12(2)17-14-9-5-4-8-13(14)16(18)19;/h3-10H,1-2H3;1H
InChIKey KJUHIXIWKSVBKB-UHFFFAOYSA-N
Raman Corrections Referenced to internal white light source; 180 degree backscatter
Raman Laser Power 804 mW
Raman Laser Source Nd:YAG
Raman Laser Wavelength 1064 nm
SMILES c1cc2c(cc1)C(N(\C(=N/2)C)c1ccccc1C)=O.Cl
Sample Preparation Procedure The free amine was added to a test tube, and a minimum amount of dichloromethane (several drops) was added to completely dissolve the sample. The test tube was then filled halfway with anhydrous diethyl ether or hexane. Hydrochloric acid gas was bubbled through the solution, which led to the precipitation of the HCl salt of amine. The test tube was spun in a centrifuge to separate the HCl salt precipitate from the organic solvent. The organic solvent was removed from the tube, and the precipitate was dried with nitrogen gas.
Scans Performed 1536
Source of Spectrum Forensic Spectral Research
Synonyms Methaqualone HCl
Technique FT-Raman