CAS 873310-31-7

Atomoxetine Related Compound C (N-methyl-3-phenyl-3-(p-tolyloxy)propan-1-amine hydrochloride)

CAS : 873310-31-7

Amino-alcohols, other than those containing more than one kind of oxygen function, their ethers and esters, salts therof, nesoi

Formule : C₁₇H₂₁NO·HCl

Couleur et forme : Off-White Solid

Masse moléculaire : 255.16231

Ref: 45-1044491

rac-Atomoxetine EP Impurity C HCl (Atomoxetine USP Related Compound C)

CAS : 873310-31-7

Formule : C₁₇H₂₁NO·HCl

Couleur et forme : White To Off-White Solid

Masse moléculaire : 255.36 36.46

Ref: 4Z-A-2520

Atomoxetine USP Related Compound C

CAS : 873310-31-7

Formule : C₁₇H₂₁NOHCl

Masse moléculaire : 255.4 : 36.46

Ref: ST-EA-CP-A30020

p-Methyl Atomoxetine Hydrochloride

Produit contrôlé

CAS : 873310-31-7

Impurity Atomoxetine EP Impurity C
Applications p-Methyl Atomoxetine Hydrochloride (Atomoxetine EP Impurity C) is an impurity of Atomoxetine (A791400), a norepinephrine reuptake inhibitor.
References Farid, N.A., et al.: J. Clin. Pharmacol., 25, 296 (1985), Gehlert, D.R., et al.: J. Neurochem., 64, 2792 (1995), Hwamg. et al.: Neurosci. Lett., 265, 151 (1999), Ring, B.J., et al.: Drug Metab. Dispos., 30, 319 (2002),

Formule : C₁₇H₂₁NO·ClH

Couleur et forme : Neat

Masse moléculaire : 291.82

Ref: TR-M288280

p-Methyl atomoxetine hydrochloride

CAS : 873310-31-7

p-Methyl atomoxetine hydrochloride is a selective norepinephrine reuptake inhibitor, which is synthesized from chemical precursors typically through a series of organic reactions proceeding under controlled conditions. It functions by inhibiting the reuptake of norepinephrine in the synaptic cleft, resulting in increased concentrations of this neurotransmitter in the central nervous system.

Formule : C₁₇H₂₂ClNO

Degré de pureté : Min. 95%

Masse moléculaire : 291.8 g/mol

Ref: 3D-YJB31031