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Oxycodone
SpectraBase Compound ID JxB1Av4IM3I
InChI InChI=1S/C18H21NO4/c1-19-8-7-17-14-10-3-4-12(22-2)15(14)23-16(17)11(20)5-6-18(17,21)13(19)9-10/h3-4,13,16,21H,5-9H2,1-2H3/t13-,16+,17+,18-/m1/s1
InChIKey BRUQQQPBMZOVGD-XFKAJCMBSA-N
Mol Weight 315.37 g/mol
Molecular Formula C18H21NO4
Exact Mass 315.147058 g/mol

Transmission Infrared (IR) Spectrum

Transmission Infrared (IR) Spectrum

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SpectraBase Spectrum ID 6g04fPyXOhY
Name Oxycodone
Source of Sample Lipomed AG
Catalog Number Free base of C-404-HC
Lot Number Free base of 404.1B0.3
Apodization Function Triangular
CAS Registry Number 76-42-6
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DEA Schedule II
Formula C18H21NO4
InChI InChI=1S/C18H21NO4/c1-19-8-7-17-14-10-3-4-12(22-2)15(14)23-16(17)11(20)5-6-18(17,21)13(19)9-10/h3-4,13,16,21H,5-9H2,1-2H3/t13-,16+,17+,18-/m1/s1
InChIKey BRUQQQPBMZOVGD-XFKAJCMBSA-N
Instrument Name Bio-Rad FTS
SMILES O[C@]12[C@]3(Cc4ccc(c5c4[C@]1([C@](C(CC2)=O)(O5)[H])CCN3C)OC)[H]
Sample Preparation Procedure The HCl salt was dissolved in 0.5 ml water in a test tube, and 1 drop of 30% NaOH solution was added, causing the clear solution to turn cloudy white. 1 ml dichloromethane was added to the test tube, which was shaken thoroughly using a vortex mixer. The test tube was spun in a centrifuge to separate the organic and aqueous layers. The bottom organic layer was retrieved with a pipette and placed in another clean test tube. The solvent was evaporated from the tube using a flow of nitrogen gas, and the sample was run in a crystalline state.
Scan Speed (number) 5
Source of Spectrum Forensic Spectral Research
Technique KBr0