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TOCAINIDE

CAS No.
41708-72-9
Chemical Name:
TOCAINIDE
Synonyms
W-36095;TOCAINIDE;Astra W-36095;TOCAINIDE USP/EP/BP;alanyl-2,6-xylidide;Naphthoic Acid Impurity 26;6'-propionoxylidide, 2-amino-2;2-amino-2',6'-propionoxylidide;N-(2-Aminopropionyl)-2,6-xylidine;N1-(2,6-dimethylphenyl)alaninamide
CBNumber:
CB8210193
Molecular Formula:
C11H16N2O
Molecular Weight:
192.26
MDL Number:
MFCD00072010
MOL File:
41708-72-9.mol
MSDS File:
SDS
Last updated:2023-09-20 16:43:00

TOCAINIDE Properties

Melting point 246-266 °C
Boiling point 328.25°C (rough estimate)
Density 1.0529 (rough estimate)
refractive index 1.5750 (estimate)
storage temp. Keep in dark place,Inert atmosphere,Room temperature
pka pKa 7.75(H2O t = 25.0±0.2 I = 0.01 (NaCl)) (Uncertain)
CAS DataBase Reference 41708-72-9(CAS DataBase Reference)
FDA UNII 27DXO59SAN
ATC code C01BB03

SAFETY

Risk and Safety Statements

Symbol(GHS)  GHS hazard pictograms
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P264-P270-P301+P312-P330-P501
Hazard Codes  Xn
Risk Statements  22

TOCAINIDE price More Price(6)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Activate Scientific AS146098 2-Amino-N-(2,6-dimethylphenyl)propanamide 97% 41708-72-9 250mg $207 2021-12-16 Buy
American Custom Chemicals Corporation API0004437 TOCAINIDE 95.00% 41708-72-9 1G $1358.28 2021-12-16 Buy
Ambeed A229662 2-Amino-N-(2,6-dimethylphenyl)propanamide 97% 41708-72-9 1g $320 2021-12-16 Buy
Crysdot CD12073305 Tocainide 97% 41708-72-9 1g $589 2021-12-16 Buy
Ambeed A229662 2-Amino-N-(2,6-dimethylphenyl)propanamide 97% 41708-72-9 100mg $83 2021-12-16 Buy
Product number Packaging Price Buy
AS146098 250mg $207 Buy
API0004437 1G $1358.28 Buy
A229662 1g $320 Buy
CD12073305 1g $589 Buy
A229662 100mg $83 Buy

TOCAINIDE Chemical Properties,Uses,Production

Originator

Tonocard,Astra,UK,1981

Uses

Tocainide is used for suppressing symptoms of ventricular arrhythmia and tachycardia, and for premature cardiac contractions.

Definition

ChEBI: A monocarboxylic acid amide in which 2,6-dimethylphenylaniline and isobutyric acid have combined to form the amide bond; used as a local anaesthetic.

Manufacturing Process

The compound 2-amino-2',6'-propionoxylidide was synthesized by saturating with gaseous ammonia at room temperature a suspension of 50 g (0.195 mol) of 2-bromo-2',6'-propionoxylidide in a mixture of 500 ml of 95% alcohol and 400 ml of concentrated aqueous ammonia. The saturation was carried out under mechanical stirring. After 25 hours the mixture was resaturated with ammonia gas. The stirring at room temperature was continued for a total period of 116 hours, and a sample was taken at that time. Gas chromatographic analysis indicated that about 95% of the bromo compound had been converted to the desired product.
The solvents were evaporated in vacuo, and the residue was taken up in 80 ml of 3 M hydrochloric acid. After addition of 220 ml of water, the insoluble material was filtered off, washed with 100 ml of water and then dried. The insoluble material weighed 9.5 g and was mainly unreacted bromo compound. The filtrate was reacted with 50 ml of 7 M NaOH, extracted three times with methylene chloride (50 ml + 2 x 25 ml portions), dried over potassium carbonate, and then evaporated. The yield of residue was 26.8 g which corresponds to 71.4% of the theoretical yield. This residue was a colorless solidifying oil and was dissolved in 200 ml chloroform. Hydrogen chloride was bubbled in until a sample of the solution tested acidic to wet pH indicator paper. A precipitate was obtained and recovered by filtration. The precipitate was washed with chloroform and dried. The melting point was determined to be from 246°C to 247.5°C.

brand name

Apx;Citocard;Taquidil;Tonocard;Toquidil;Xylotocan.

Therapeutic Function

Antiarrhythmic

World Health Organization (WHO)

Tocainide, an antidysrhythmic agent, was introduced in 1981 for the treatment of ventricular dysrhythmias. By 1984 its use was associated with cases of agranulocytosis, aplastic anaemia and thrombocytopenia, some of which were fatal. This led some regulatory authorities to restrict the indications for its use. The major manufacturer has subsequently restricted its use on a worldwide basis to the treatment of symptomatic ventricular dysrhythmias not responding to other therapy, or when other therapy is contraindicated.

Pharmacokinetics

The α-methyl group is believed to slow the rate of metabolism and, thereby, to contribute to oral activity. The plasma half-life of tocainide is approximately 12 hours, and nearly 50% of the drug may be excreted unchanged in the urine. Adverse effects associated with tocainide are like those observed with lidocaine—specifically, gastrointestinal disturbances and central nervous system effects.

Clinical Use

Tocainide (Tonocard) is an orally effective antiarrhythmic agent with close structural similarities to lidocaine. Tocainide is indicated for the treatment of symptomatic ventricular arrhythmias refractory to more conventional therapy. Serious noncardiac adverse effects limit its use to patients with life-threatening arrhythmias.

Side effects

Light-headedness, dizziness, or nausea occurs in approximately 15% of patients, paresthesias and numbness in 9%, and tremor in 8%.These adverse effects are generally mild in intensity, transient, and dose related. Overall, however, approximately 20% of patients prescribed tocainide discontinue therapy because of such effects. Serious immune-based side effects, such as pulmonary fibrosis, have been reported, and blood dyscrasias, such as agranulocytosis and thrombocytopenia, may occur in up to 0.2% of patients.

Synthesis

Tocainide, 2-amino-2,6-dimethylpropionanilide (18.1.8), is synthesized by reacting 2,6-dimethylaniline with 2-bromopropionic acid bromide and subsequent substitution of the bromine atom in the resulting amide (18.1.7) with an amino group.

Synthesis_41708-72-9

Drug interactions

When used with other class IB antiarrhythmic drugs, tocainide toxicity may be increased without significant gain in antiarrhythmic efficacy.

Precautions

Patients who are hypersensitive to tocainide or to local anesthetics of the amide type should not be exposed to tocainide.The presence of second- or third-degree heart block in the absence of an artificial pacemaker also contraindicates the use of tocainide.

TOCAINIDE Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 60)Suppliers
Supplier Tel Email Country ProdList Advantage
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 32480 60
Hubei Jusheng Technology Co.,Ltd.
18871490254 linda@hubeijusheng.com CHINA 28180 58
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Wuxi Rejoys chemical Technology Co., Ltd.
0510-86103381 sales@rejoyschem.com CHINA 976 58
Shaanxi Dideu Medichem Co. Ltd
+86-029-89586680 +86-18192503167 1026@dideu.com China 9320 58
Dideu Industries Group Limited
+86-29-89586680 +86-15129568250 1026@dideu.com China 29220 58
ZHEJIANG JIUZHOU CHEM CO., LTD
+86-0576225566889 +86-13454675544 admin@jiuzhou-chem.com;jamie@jiuzhou-chem.com;alice@jiuzhou-chem.com China 20000 58
Shanghai Acmec Biochemical Technology Co., Ltd.
+undefined18621343501 product@acmec-e.com China 33349 58
Aladdin Scientific
+1-833-552-7181 sales@aladdinsci.com United States 57511 58
Mainchem Co., Ltd. +86-0592-6210733 sale@mainchem.com China 32360 55

View Lastest Price from TOCAINIDE manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
TOCAINIDE USP/EP/BP pictures 2021-08-12 TOCAINIDE USP/EP/BP
41708-72-9
US $1.10 / g 1g 99.9% 100 Tons min Dideu Industries Group Limited

TOCAINIDE Spectrum

TOCAINIDE 2-amino-2',6'-propionoxylidide 2-amino-n-(2,6-dimethylphenyl)-propanamid 6'-propionoxylidide, 2-amino-2 alanyl-2,6-xylidide Astra W-36095 W-36095 2-Amino-N-(2,6-dimethylphenyl)propanamide N-(2-Aminopropionyl)-2,6-xylidine N1-(2,6-dimethylphenyl)alaninamide TOCAINIDE USP/EP/BP Sodium Channel,Na+ channels,Tocainide,tinnitus,lidocaine,Na channels,Inhibitor,inhibit Naphthoic Acid Impurity 26 41708-72-9 Cell Signaling and Neuroscience Sodium Channel Modulators Voltage-gated Ion Channels Other Sodium Channel Modulators Ion Channels Monovalent Ion Channels BioChemical Cell Biology Active Pharmaceutical Ingredients