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N-ACETYLPROCAINAMIDE

Product Name
N-ACETYLPROCAINAMIDE
CAS No.
32795-44-1
Chemical Name
N-ACETYLPROCAINAMIDE
Synonyms
acekainid;acecainide;TIMTEC-BB SBB005970;N-ACETYLPROCAINAMIDE;n-acetyloprokainamid;N-ACETYLPROCAINAMIDE, 99+%;N-ACETYLPROCAINAMIDE USP/EP/BP;4-acetamido-N-(2-(diethylamino)ethyl)benzamide;4’-((2-(diethylamino)ethyl)carbamoyl)acetanilide;4’-((2-(diethylamino)ethyl)carbamoyl)-acetanilid
CBNumber
CB8432449
Molecular Formula
C15H23N3O2
Formula Weight
277.36
MOL File
32795-44-1.mol
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N-ACETYLPROCAINAMIDE Property

Melting point:
138-140 °C(lit.)
Boiling point:
500.0±35.0 °C(Predicted)
Density 
1.097±0.06 g/cm3(Predicted)
storage temp. 
-20°C
solubility 
soluble1%, clear, colorless to faintly yellow (1N HCl)
form 
Solid
pka
14.54±0.46(Predicted)
color 
White to off-white
Merck 
13,20
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Safety

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
RIDADR 
3249
WGK Germany 
3
RTECS 
AE1974350
HazardClass 
6.1(b)
PackingGroup 
III
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

H335May cause respiratory irritation

Precautionary statements

P261Avoid breathing dust/fume/gas/mist/vapours/spray.

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

P271Use only outdoors or in a well-ventilated area.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P302+P352IF ON SKIN: wash with plenty of soap and water.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
269476
Product name
N-Acetylprocainamide
Purity
≥99%
Packaging
250mg
Price
$62.4
Updated
2024/03/01
Sigma-Aldrich
Product number
269476
Product name
N-Acetylprocainamide
Purity
≥99%
Packaging
1g
Price
$176
Updated
2024/03/01
ChemScene
Product number
CS-4707
Product name
N-Acetylprocainamide
Purity
≥98.0%
Packaging
100mg
Price
$60
Updated
2021/12/16
American Custom Chemicals Corporation
Product number
CHM0031256
Product name
N-ACETYLPROCAINAMIDE
Purity
95.00%
Packaging
1G
Price
$681.09
Updated
2021/12/16
CSNpharm
Product number
CSN11506
Product name
N-Acetylprocainamide
Packaging
100mg
Price
$48
Updated
2021/12/16
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N-ACETYLPROCAINAMIDE Chemical Properties,Usage,Production

Originator

Acecainide ,ZYF Pharm Chemical

Uses

antiprotozoal

Uses

N-acetylprocainamide (NAPA) was used as a model drug in the study of establishing a quantitative approach to predict the renal clearances of basic drugs using N-1-methylnicotinamide (NMN).

Definition

ChEBI: A benzamide obtained via formal condensation of 4-acetamidobenzoic acid and 2-(diethylamino)ethylamine.

Manufacturing Process

1.0 g of p-amino-N-(2-diethylaminoethyl)benzamide is dissolved in chloroform. A few ice cubes are added to the solution. Acetyl chloride is added dropwise with stirring until no more white precipitate forms; the latter is separated by filtering under suction. The precipitate is washed with cold acetone and dried overnight in a vacuum oven at room temperature. The product is dissolved in a minimum amount of hot isopropanol and allowed to precipitate in the cold. The p-acetamido-N-(2-diethylaminoethyl)benzamide hydrochloride, is recrystallized a second time from hot isopropanol, melting point 190°-193°C. The free base is obtained from the hydrochloride by dissolving the latter in water, adjusting the pH to greater than 10 with dilute sodium hydroxide, and adding an equal volume of benzene. After shaking in a separatory funnel, the benzene layer is recovered and evaporated to dryness. So the p-acetamido-N- (2-diethylaminoethyl)benzamide is obtained.

Therapeutic Function

Antiarrhythmic

General Description

The relaxant effects of N-acetylprocainamide on bovine tracheal smooth muscle was studied.

N-ACETYLPROCAINAMIDE Preparation Products And Raw materials

Raw materials

Preparation Products

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N-ACETYLPROCAINAMIDE Suppliers

Energy Chemical
Tel
021-021-58432009 400-005-6266
Fax
021-58436166
Email
sales8178@energy-chemical.com
Country
China
ProdList
44689
Advantage
61
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Country
China
ProdList
42958
Advantage
64
MedChemexpress LLC
Tel
021-58955995
Fax
609-228-5909
Email
sales@medchemexpress.cn
Country
United States
ProdList
4861
Advantage
58
EnliPharma Technology Co., Ltd
Tel
0551-66399836 18955197623
Email
sales@enlipharma.com
Country
China
ProdList
1874
Advantage
55
ShangHai Caerulum Pharma Discovery Co., Ltd.
Tel
18149758185 18149758185
Email
sales-cpd@caerulumpharma.com
Country
China
ProdList
3466
Advantage
58
Wuxi Zhongkun Biochemical Technology Co., Ltd.
Tel
0510-85629785 18013409632
Fax
051085625359
Email
sales@reading-chemicals.com
Country
China
ProdList
15178
Advantage
58
Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51456
Advantage
80
Guangzhou QiYun Biotechnology Co., Ltd.
Tel
020-61288194 61288195
Fax
020-61288700
Email
505721671@qq.com
Country
China
ProdList
3866
Advantage
58
ShangHai Biochempartner Co.,Ltd
Tel
177-54423994 17754423994
Fax
QQ:2853530913
Email
2853530910@QQ.com
Country
China
ProdList
8011
Advantage
62
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131957
Advantage
58

32795-44-1, N-ACETYLPROCAINAMIDERelated Search:


  • 4-(acetylamino)-n-(2-(diethylamino)ethyl)-benzamid
  • 4-(acetylamino)-n-[2-(diethylamino)ethyl]-benzamid
  • 4-acetamido-N-(2-(diethylamino)ethyl)benzamide
  • 4’-((2-(diethylamino)ethyl)carbamoyl)-acetanilid
  • 4’-((2-(diethylamino)ethyl)carbamoyl)acetanilide
  • acecainide
  • acekainid
  • n-acetyloprokainamid
  • N-ACETYLPROCAINAMIDE
  • TIMTEC-BB SBB005970
  • N-ACETYLPROCAINAMIDE, 99+%
  • 4-(Acetylamino)-N-[2-(diethylamino)ethyl]benzamide
  • Benzamide, 4-(acetylamino)-N-[2-(diethylamino)ethyl]-
  • N-ACETYLPROCAINAMIDE USP/EP/BP
  • KcsA,N Acetylprocainamide,N-Acetylprocainamide,inhibit,Potassium Channel,NAcetylprocainamide,Inhibitor,Drug Metabolite
  • 32795-44-1
  • C15H23N3O2
  • 4CH3CONHC6H4CONHCH2CH2NC2H52
  • Carbonyl Compounds
  • Amides
  • Building Blocks
  • Organic Building Blocks
  • TINDAMAX
  • Amides
  • Carbonyl Compounds
  • Organic Building Blocks