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1-(α,α,α-Trifluoro-m-tolyl)piperazine HCl
SpectraBase Compound ID 7hLTZoe63mg
InChI InChI=1S/C11H13F3N2.ClH/c12-11(13,14)9-2-1-3-10(8-9)16-6-4-15-5-7-16;/h1-3,8,15H,4-7H2;1H
InChIKey DGNLGWJZZZOYPT-UHFFFAOYSA-N
Mol Weight 266.7 g/mol
Molecular Formula C11H14ClF3N2
Exact Mass 266.079761 g/mol

Attenuated Total Reflectance Infrared (ATR-IR) Spectrum

Attenuated Total Reflectance Infrared (ATR-IR) Spectrum

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SpectraBase Spectrum ID 84QaMLcPgaK
Name 1-(α,α,α-Trifluoro-m-tolyl)piperazine HCl
Source of Sample Sigma-Aldrich Company Llc
Catalog Number HCl salt of T9073
Lot Number HCl salt of 102K3742V
Accessory DurasamplIR II
Classification Serotonin receptor agonist with preference for 5-HT1B serotonin receptors
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Formula C11H14ClF3N2
InChI InChI=1S/C11H13F3N2.ClH/c12-11(13,14)9-2-1-3-10(8-9)16-6-4-15-5-7-16;/h1-3,8,15H,4-7H2;1H
InChIKey DGNLGWJZZZOYPT-UHFFFAOYSA-N
Instrument Name Bio-Rad FTS
SMILES N1CCN(c2cc(ccc2)C(F)(F)F)CC1.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
Synonyms TFMPP HCl; 1-(3-(Trifluoromethyl)phenyl)piperazine hydrochloride
Technique ATR-Neat (DuraSamplIR II)