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(1S,2S)-(+)-N-Methylpseudoephedrine HCl
SpectraBase Compound ID D4bDHFgGB9r
InChI InChI=1S/C11H17NO.ClH/c1-9(12(2)3)11(13)10-7-5-4-6-8-10;/h4-9,11,13H,1-3H3;1H/t9-,11+;/m0./s1
InChIKey NTCYWJCEOILKNG-QLSWKGBWSA-N
Mol Weight 215.72 g/mol
Molecular Formula C11H18ClNO
Exact Mass 215.107692 g/mol

Attenuated Total Reflectance Infrared (ATR-IR) Spectrum

Attenuated Total Reflectance Infrared (ATR-IR) Spectrum

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SpectraBase Spectrum ID KAMArZCepFX
Name (1S,2S)-(+)-N-Methylpseudoephedrine HCl
Source of Sample Sigma-Aldrich Inc.
Catalog Number HCl salt of 290041
Lot Number HCl salt of 10917ED
Accessory DurasamplIR II
Compound Type Pure
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Formula C11H18ClNO
InChI InChI=1S/C11H17NO.ClH/c1-9(12(2)3)11(13)10-7-5-4-6-8-10;/h4-9,11,13H,1-3H3;1H/t9-,11+;/m0./s1
InChIKey NTCYWJCEOILKNG-QLSWKGBWSA-N
Instrument Name Bio-Rad FTS
SMILES O[C@@](c1ccccc1)([C@@](N(C)C)(C)[H])[H].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.
Source of Spectrum Forensic Spectral Research
Technique ATR-Neat (DuraSamplIR II)