N-ACETYLPROCAINAMIDE HYDROCHLORIDE

N-ACETYLPROCAINAMIDE HYDROCHLORIDE Basic information
Product Name:N-ACETYLPROCAINAMIDE HYDROCHLORIDE
Synonyms:N-ACETYLPROCAINAMIDE HCL;N-ACETYLPROCAINAMIDE HYDROCHLORIDE;N-ACETYLNOVOCAINAMIDE;N-ACETYLNOVOCAINAMIDE HYDROCHLORIDE;NAPA;N,N-diethyl-2-aminoethylcarbamoylacetanilide;N-ACETYLPROCAINAMIDE HYDROCHLORIDEAPPROX 97%;ACECAINIDE HYDROCHLORIDE
CAS:34118-92-8
MF:C15H24ClN3O2
MW:313.82
EINECS:251-831-2
Product Categories:A-AM;Amides;Bioactive Small Molecules;Building Blocks;Carbonyl Compounds;Cell Biology;Chemical Synthesis;Organic Building Blocks
Mol File:34118-92-8.mol
N-ACETYLPROCAINAMIDE HYDROCHLORIDE Structure
N-ACETYLPROCAINAMIDE HYDROCHLORIDE Chemical Properties
Melting point 184-186 °C(lit.)
storage temp. −20°C
solubility H2O: 50 mg/mL
form powder
color Light Beige to Beige
Merck 13,20
Stability:Very Hygroscopic
Safety Information
Safety Statements 24/25
RIDADR 3249
WGK Germany 3
HazardClass 6.1(b)
PackingGroup III
HS Code 29242998
MSDS Information
ProviderLanguage
SigmaAldrich English
ACROS English
N-ACETYLPROCAINAMIDE HYDROCHLORIDE Usage And Synthesis
Chemical Propertiesyellow-beige crystalline powder
UsesCardiac depressant (anti-arrhythmic).
UsesN-Acetylprocainamide Hydrochloride is an antiarrhythmic agent and a metabolite of Procainamide (P755130). Procainamide is a drug used for both supraventricular and ventricular arrhythmias. For example, it can be used to convert new-onset atrial fibrillation, though it is suboptimal for this purpose. It can also be used to treat Wolff-Parkinson-White syndrome by prolonging the refractory period of the accessory pathway.
General DescriptionThe GLC assay procedure was developed to study the stability of N-acetylprocainamide hydrochloride (acecainide hydrochloride) in rat feed.
Biochem/physiol ActionsClass III antiarrhythmic. Increases the duration of the action potential by decreasing the delayed outward potassium current, slightly decreasing the calcium current, and slightly depressing the inward rectifier potassium current. This is the active metabolite of procainamide that does not induce systemic lupus erythematosus.
N-ACETYLPROCAINAMIDE HYDROCHLORIDE Preparation Products And Raw materials
Triethylamine hydrochloride N1-BENZYL-N2-ETHYLETHANE-1,2-DIAMINE 4-Amino-N-methylbenzamide N-ACETYL PROCAINAMIDE HYDROCHLORIDE [ACETYL 1-14C] 4-Amino-N-methylbenzylamine 4-ACETAMIDOBENZYLAMINE 4-Acetamidobenzaldehyde p-Acetotoluidide N-{4-[(methylamino)methyl]phenyl}acetamide N-ACETYLPROCAINAMIDE HYDROCHLORIDE N-BENZYL-N'-METHYLETHYLENEDIAMINE procainamide Procainamide hydrochloride N-Benzylethylenediamine N'-Benzyl-N,N-diethylethylenediamine Cloxacepride 4-METHYLAMINO-BENZAMIDE 4-AMINO-N-ETHYLBENZAMIDE

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