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N-ACETYLPROCAINAMIDE HYDROCHLORIDE

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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
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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
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Safety Information

Safety Statements 
24/25
RIDADR 
3249
WGK Germany 
3
HazardClass 
6.1(b)
PackingGroup 
III
HS Code 
29242998

MSDS

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N-ACETYLPROCAINAMIDE HYDROCHLORIDE Usage And Synthesis

Description

Acecainide, a main metabolite of procainamide, is a class I a antiarrhythmic agent .

Chemical Properties

yellow-beige crystalline powder

Uses

Cardiac depressant (anti-arrhythmic).

Uses

N-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 Description

The GLC assay procedure was developed to study the stability of N-acetylprocainamide hydrochloride (acecainide hydrochloride) in rat feed.

Biochem/physiol Actions

Class 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 HYDROCHLORIDESupplier

J & K SCIENTIFIC LTD.
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Meryer (Shanghai) Chemical Technology Co., Ltd.
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Energy Chemical
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Shanghai Hanhong Scientific Co.,Ltd.
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Thermo Fisher Scientific
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800-810-5118
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cnchemical@thermofisher.com