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Disopyramid phosphate

Product Name
Disopyramid phosphate
CAS No.
22059-60-5
Chemical Name
Disopyramid phosphate
Synonyms
norpace;sc13957;RYTHMODAN;norpace cr;disopyramid phosphate;DISOPYRAMIDE PHOSPHATE;Disopyramide phosphate CRS;DISOPYRAMIDE PHOSPHATE SALT;Disopyramid phosphate USP/EP/BP;Disopyramide Phosphate (200 mg)
CBNumber
CB7263617
Molecular Formula
C21H32N3O5P
Formula Weight
437.47
MOL File
22059-60-5.mol
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Disopyramid phosphate Property

Melting point:
202-204°C
storage temp. 
2-8°C
solubility 
DMSO (Slightly, Heated, Sonicated), Methanol (Slightly), Water (Slightly)
color 
White to Off-White
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Safety

Hazard Codes 
Xn
Risk Statements 
22
Safety Statements 
36
WGK Germany 
3
RTECS 
UR8440000
HS Code 
2933399090
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Hazard and Precautionary Statements (GHS)

Symbol(GHS)
Signal word
Warning
Hazard statements

H302Harmful if swallowed

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
D6035
Product name
Disopyramide phosphate salt
Packaging
1g
Price
$55.4
Updated
2024/03/01
Sigma-Aldrich
Product number
1222501
Product name
Disopyramide phosphate
Purity
United States Pharmacopeia (USP) Reference Standard
Packaging
200mg
Price
$261.6
Updated
2024/03/01
Sigma-Aldrich
Product number
D6035
Product name
Disopyramide phosphate salt
Packaging
10g
Price
$107.4
Updated
2024/03/01
Sigma-Aldrich
Product number
D2922000
Product name
Disopyramide phosphate
Purity
European Pharmacopoeia (EP) Reference Standard
Packaging
d2922000
Price
$150
Updated
2024/03/01
TRC
Product number
D493455
Product name
Disopyramide phosphate
Packaging
100mg
Price
$50
Updated
2021/12/16
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Disopyramid phosphate Chemical Properties,Usage,Production

Originator

Rythmodan,Cassenne,France,1969

Uses

Disopyramide Phosphate is an antiarrhythmic (class IA). Sodium channel blocker.

Uses

Disopyramide phosphate salt has been used as an internal standard for plasma sample analysis by mass spectrometry. It might be used as a test compound in a teratogenicity study.

Uses

Cardiac depressant (anti-arrhythmic).

Definition

ChEBI: Disopyramide phosphate is an organoammonium phosphate. It is functionally related to a disopyramide.

Manufacturing Process

To a solution of 35.3 parts of phenylacetonitrile and 47.6 parts of 2- bromopyridine in 175 parts of dry toluene is added 53.4 parts of sodamide slowly with stirring over a period of 45 minutes. The resultant mixture is stirred at 100°C for 2 hours before it is cooled and the excess sodamide is decomposed by the addition of water. The toluene layer is separated and washed with water to remove excess alkali. The toluene solution is extracted with 6 N hydrochloric acid and the acid extract is made alkaline and then extracted with toluene. The toluene solution is dried over sodium sulfate and the solvent is evaporated. Recrystallization of the residue from alcohol-hexane gives α-phenyl-2-pyridineacetonitrile melting at about 87-88°C.
To a solution of 41 parts of α-phenyl-2-pyridineacetonitrile in 350 parts of dry toluene is added 9.2 parts of sodamide and the mixture is stirred and heated at 90°C for 30 minutes. Heating is stopped and a solution of 38.5 parts of 2- diisopropylaminoethyl chloride in 110 parts of dry toluene is added slowly over a period of 30 minutes. The mixture is stirred and refluxed for 6 hours before it is cooled and decomposed by the addition of water. The toluene layer is separated and washed with water and extracted with 6 N hydrochloric acid. The acid extract is made alkaline and extracted with toluene. The toluene solution is washed with water and dried and the solvent is evaporated. Distillation of the residue gives 4-diisopropylamino-2-phenyl-2-(2-pyridyl)- butyronitrile boiling at about 145°-160°C at 0.3 mm pressure.
A solution of 27.2 parts of 4-diisopropylamino-2-phenyl-2-(2- pyridyl)butyronitrile in 200 parts of concentrated sulfuric acid is heated on a steam bath for 4 hours and then poured onto ice. The resultant mixture is alkalized with 10 N sodium hydroxide, and the pH is adjusted to 6 by the addition of acetic acid. The solution is washed once with benzene before it is alkalized again with 10 N sodium hydroxide solution. The resultant mixture is extracted with benzene, and the solvent is evaporated from the benzene extract. The resultant residue is dissolved in ethanol and the alcohol solution is treated with charcoal and filtered. Evaporation of the solvent leaves a residue which is recrystallized from hexane to give 4-diisopropylamino-2- phenyl-2-(2-pyridyl)butyramide melting at about 94.5-95°C. It may be converted to the phosphate with phosphoric acid.

brand name

Norpace (Searle).

Therapeutic Function

Antiarrhythmic

General Description

Disopyramide phosphate, -[2(diisopropylamino)ethyl]- -phenyl-2-pyridineacetamidephosphate (Norpace), is an oral and intravenousclass IA antiarrhythmic agent. It is quite similar to quinidineand procainamide in its electrophysiological properties, inthat it decreases phase 4 diastolic depolarization, decreasesconduction velocity, and has vagolytic properties.31 It is usedclinically in the treatment of refractory, life-threatening ventriculartachyarrhythmias. Oral administration of the drugproduces peak plasma levels within 2 hours. The drug isbound approximately 50% to plasma protein and has a halflifeof 6.7 hours in humans. More than 50% is excretedunchanged in the urine. Therefore, patients with renal insufficiencyshould be monitored carefully for evidence ofoverdose. Disopyramide phosphate commonly exhibits sideeffects of dry mouth, constipation, urinary retention, andother cholinergic blocking actions because of its structuralsimilarity to anticholinergic drugs.

Biochem/physiol Actions

Class IA antiarrhythmic; sodium channel blocker

Disopyramid phosphate Preparation Products And Raw materials

Raw materials

Preparation Products

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Disopyramid phosphate Suppliers

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View Lastest Price from Disopyramid phosphate manufacturers

Career Henan Chemical Co
Product
Disopyramid phosphate 22059-60-5
Price
US $1.00/KG
Min. Order
1KG
Purity
≥98%
Supply Ability
200KG
Release date
2019-08-30

22059-60-5, Disopyramid phosphate Related Search:


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