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F6270

Supelco

Fipexide hydrochloride

analytical standard

Synonym(s):

1-(2-[4-Chlorophenoxy]acetyl)-4-(3,4-methylenedioxybenzyl)piperazine

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About This Item

Empirical Formula (Hill Notation):
C20H21ClN2O4 · HCl
CAS Number:
34161-24-5
Molecular Weight:
425.31
EC Number:
251-857-4
MDL number:
MFCD00133323
UNSPSC Code:
41116107
PubChem Substance ID:
329799752
NACRES:
NA.24

grade

analytical standard

Quality Level

200

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

application(s)

forensics and toxicology
pharmaceutical (small molecule)
veterinary

format

neat

SMILES string

Cl.Clc1ccc(OCC(=O)N2CCN(CC2)Cc3ccc4OCOc4c3)cc1

InChI

1S/C20H21ClN2O4.ClH/c21-16-2-4-17(5-3-16)25-13-20(24)23-9-7-22(8-10-23)12-15-1-6-18-19(11-15)27-14-26-18;/h1-6,11H,7-10,12-14H2;1H

InChI key

MVOWQBJZZKOQNU-UHFFFAOYSA-N

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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[Fipexide: a new drug for the regulation of dopaminergic system at the macromolecular level].
C Missale et al.
Bollettino chimico farmaceutico, 122(2), 79-85 (1983-02-01)
F Durand et al.
Journal of hepatology, 15(1-2), 144-146 (1992-05-01)
Fipexide belongs to a new class of cognition activators and is noted for its lack of amphetamin-like side effects. We describe three patients who developed fulminant hepatic failure less than 2 months after beginning fipexide administration. The mean interval from
M Genkova-Papasova et al.
Acta physiologica et pharmacologica Bulgarica, 14(4), 36-41 (1988-01-01)
Experiments on albino rats were carried out to study the effects of the nootropic drugs piracetam, aniracetam, meclofenoxate and fipexide on the DA-beta-hydroxylase inhibitor diethyldithiocarbamate- and the alpha 2-adrenoceptor agonist clonidine-impaired cognitive functions. The changes in memory were studied by
André Leblanc et al.
Rapid communications in mass spectrometry : RCM, 24(9), 1241-1250 (2010-04-15)
Drug bioactivation leading to the formation of reactive species capable of covalent binding to proteins represents an important cause of drug-induced toxicity. Reactive metabolite detection using in vitro microsomal incubations is a crucial step in assessing potential toxicity of pharmaceutical
Roland F Staack et al.
Journal of chromatography. B, Analytical technologies in the biomedical and life sciences, 804(2), 337-343 (2004-04-15)
Qualitative studies are described on the metabolism and the toxicological analysis of the nootropic fipexide (FIP) in rat urine using gas chromatography-mass spectrometry (GC-MS). FIP was extensively metabolized to 1-(3,4-methylenedioxybenzyl)piperazine (MDBP), 4-chlorophenoxyacetic acid, 1-[2-(4-chlorophenoxy)acetyl]piperazine, N-(4-hydroxy-3-methoxy-benzyl)piperazine, piperazine, N-(3,4-methylenedioxybenzyl)ethylenediamine, and N-[2-(4-chlorophenoxy)acetyl]ethylenediamine. The
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