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Various methods including X-ray photoelectron spectroscopy (XPS), UV-spectroelectrochemistry, infrared (IR) spectra and electrochemical techniques have been used to characterizing the modification. Clenbuterol can be modified at the electrode surface by carbon-nitrogen linkage or carbon-carbon linkage in 0. The 1 H NMR spectrum of clenbuterol hydrochloride was scanned in DMSO-d 6 on a Bruker NMR spectrometer operating at 500 MHz. Chemical shifts are expressed in δ-values (ppm) relative to TMS as an internal standard. Coupling constants (J) are expressed in Hz (Table 1 and Fig. 5 A and B). Clenbuterol (Broncodil and trade) is a direct-acting sympathomimetic agent with mainly beta-adrenergic activity and a selective action on β2 receptors (a β2 agonist). It has properties similar to those of salbutamol. It is used as a bronchodilator in the management of reversible airways obstruction, … Clenbuterol Hydrochloride. Using the high-resolution Terahertz Time-domain spectroscopy (THz-TDS) and the standard sample pellet technique, the far-infrared vibrational spectra of clenbuterol hydrochloride (CH), a β. 451 IUPAC Standard InChI: InChI=1S/C18H32Cl2N2OSi/c1-17 (2,3)22-11-15 (23-24 (7,8)18 (4,5)6)12-9-13 (19)16 (21)14 (20)10-12/h9-10,15,22H,11,21H2,1-8H3 IUPAC Standard InChIKey: JBSYMPUCORTAKN-UHFFFAOYSA-N Chemical structure: This structure is also available as a 2d Mol file. Clenbuterol – Optional [MS] – Spectrum – SpectraBase. John Wiley & Sons, Inc. SpectraBase; SpectraBase Compound ID=ABOSGHFGNtV SpectraBase Spectrum ID=F91QeBn5jDs. Com/spectrum/F91QeBn5jDs (accessed 10/22/2022 )
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