Ticlopidine

Product Name: Ticlopidine
CAS No.: 55142-85-3
Chemical Name: Ticlopidine
Synonyms: pcr5332;PCR 5332;Ticlosin;Anagregal;Caudaline;TICIOPIDINE;TICLOPIDINE;PCR 5332|||Ticlid;5-(2-Chlorobenzyl);Ticlopidine USP/EP/BP
CBNumber: CB7674370
Molecular Formula: C14H14ClNS
Formula Weight: 263.79
MOL File: 55142-85-3.mol

More

Less

Ticlopidine Property

Melting point:: 210-212 °C
Boiling point:: 117-120 °C(Press: 0.5 Torr)
Density: 1.273±0.06 g/cm3(Predicted)
storage temp.: 2-8°C(protect from light)
solubility: Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly)
form: Solid
pka: 7.10±0.20(Predicted)
color: Off-White to Pale Yellow
CAS DataBase Reference: 55142-85-3(CAS DataBase Reference)
NIST Chemistry Reference: Thieno[3,2-c]pyridine, 5-[(2-chlorophenyl)methyl]-4,5,6,7-tetrahydro-(55142-85-3)
EPA Substance Registry System: Thieno[3,2-c]pyridine, 5-[(2-chlorophenyl)methyl]-4,5,6,7-tetrahydro- (55142-85-3)

More

Less

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Warning

Hazard statements

H315Causes skin irritation

H319Causes serious eye irritation

Precautionary statements

P264Wash hands thoroughly after handling.

P264Wash skin thouroughly after handling.

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.

P332+P313IF SKIN irritation occurs: Get medical advice/attention.

P337+P313IF eye irritation persists: Get medical advice/attention.

More

Less

N-Bromosuccinimide Price

TRC

Product number: T889915
Product name: Ticlopidine
Packaging: 25mg
Price: $55
Updated: 2021/12/16

TRC

Product number: T889915
Product name: Ticlopidine
Packaging: 100mg
Price: $145
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: API0004414
Product name: TICLOPIDINE
Purity: 95.00%
Packaging: 5MG
Price: $495
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: API0004414
Product name: TICLOPIDINE
Purity: 95.00%
Packaging: 1G
Price: $1290.45
Updated: 2021/12/16

American Custom Chemicals Corporation

Product number: API0004414
Product name: TICLOPIDINE
Purity: 95.00%
Packaging: 5G
Price: $1991.92
Updated: 2021/12/16

More

Less

Ticlopidine Chemical Properties,Usage,Production

Originator

Ticlid,Millot,France,1978

Uses

Ticlopidine is an antiplatelet drug for the treatment of ischemic heart diseases.

Uses

Ticlopidine suppresses aggregation of thrombocytes and possesses antiaggregant activity. It is believed that its action is connected to its effect on thrombocyte membranes and the reduction in quantity of released adenosine diphosphate and serotonin, which facilitate aggregation of thrombocytes. In wide-ranging clinical trials, ticlopidine presented a number of advantages compared to aspirin.

Definition

ChEBI: A thienopyridine that is 4,5,6,7-tetrahydrothieno[3,2-c]pyridine in which the hydrogen attached to the nitrogen is replaced by an o-chlorobenzyl group.

Manufacturing Process

A solution of thieno[3,2-c]pyridine (13.5 g; 0.1 mol) and 2-chlorobenzyl chloride (17.7 g) in acetonitrile (150 ml) is boiled during 4 hours. After evaporation of the solvent, the solid residue consists of 5-(2- chlorobenzyl)-thieno[3,2-c]pyridinium chloride which melts at 166°C (derivative n° 30). This compound is taken up into a solution comprising ethanol (300 ml) and water (100 ml). Sodium borohydride (NaBH4)(20 g) is added portionwise to the solution maintained at room temperature. The reaction medium is maintained under constant stirring during 12 hours and is then evaporated. The residue is taken up into water and made acidic with concentrated hydrochloric acid to destroy the excess reducing agent. The mixture is then made alkaline with ammonia and extracted with ether. The ether solution is washed with water, dried and evaporated. The oily residue is dissolved in isopropanol (50 ml) and hydrochloric acid in ethanol solution is then added thereto.
After filtration and recrystallization from ethanol, there are obtained 5-(2- chlorobenzyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine hydrochloride crystals (yield: 60%) having a melting point (Koefler block) of 190°C.

brand name

4-c-32 53-32-c;Aplaquette;Derivatives;Klodin;Opteron;Panaldine;Tcp;Ticlidan;Ticlodix;Ticlodone;Ticlopedine;Ticlosan;Tiklid;Tiklyd;Tilcid.

Therapeutic Function

Platelet aggregation inhibitor

World Health Organization (WHO)

Ticlopidine, an inhibitor of platelet aggregation, was introduced in 1978 for use as an antithrombotic agent. By 1982 its use had been associated with cases of agranulocytosis, severe leucopenia and impaired haemostasis. The drug remains available in most countries in which it was approved with appropriate warnings in the product information.

General Description

Ticlopidine, 5-[(2-chlorophenyl)methyl]-4,5,6,7-tetrahydrothieno [3,2-c]pyridine hydrochloride(Ticlid), is useful in reducing cardiac events in patients withunstable angina and cerebrovascular events in secondaryprevention of stroke. It belongs to the thienopyridine classand facilitated the development of clopidogrel. One of thedrawbacks to this agent is its side effect profile, whichincludes neutropenia, and patients receiving this antithromboticshould have their blood levels monitored. Its mechanismof action is similar to that of clopidogrel, in that itinhibits the purinergic receptors on platelets.

Synthesis

Ticlopidine, 5-(o-chlorobenzyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine (24.2.1), is synthesized in many different ways. The first way consists of N-alkylation of 4,5,6,7-tetrahydrothieno[3,2-c]pyridine with 2-chlorobenzylchloride.

Ticlopidine Preparation Products And Raw materials

Raw materials

Lithium tert-butoxide Ticlopidine hydrochloride Nitroethylene 2-Thiophenecarboxaldehyde Nitromethane Tosyl chloride Diethyl ether Potassium borohydride Sodium hydroxide ethylthiolphene Diisopropyl ether n-Butyllithium

Preparation Products

More

Less

Ticlopidine Suppliers

China 76 Europe 2 Germany 1 India 5 United Kingdom 2 United States 17 Global 103

LGM Pharma

Tel: 1-(800)-881-8210
Fax: 615-250-9817
Email: inquiries@lgmpharma.com
Country: United States
ProdList: 2123
Advantage: 70

TargetMol Chemicals Inc.

Tel: +1-781-999-5354 +1-00000000000
Email: marketing@targetmol.com
Country: United States
ProdList: 32161
Advantage: 58

Aladdin Scientific

Tel: +1-+1(833)-552-7181
Email: sales@aladdinsci.com
Country: United States
ProdList: 57505
Advantage: 58

TargetMol Chemicals Inc.

Tel
Email: support@targetmol.com
Country: United States
ProdList: 38631
Advantage: 58

Alfa Chemistry

Tel: --
Fax: --
Email: info@Alfa-Chemistry.com
Country: United States
ProdList: 6814
Advantage: 0

CarboMer, Inc.

Tel: --
Fax: --
Email: sales@carbomer.com
Country: United States
ProdList: 4026
Advantage: 67

SynFine Research

Tel: --
Fax: --
Email: research@synfine.com
Country: United States
ProdList: 1024
Advantage: 68

AlliChem, LLC

Tel: --
Fax: --
Email: sales@allichemllc.com
Country: United States
ProdList: 6516
Advantage: 60

Combi-Blocks Inc.

Tel: --
Fax: --
Email: sales@combi-blocks.com
Country: United States
ProdList: 6618
Advantage: 69

Waterstone Technology, LLC

Tel: --
Fax: --
Email: sales@waterstonetech.com
Country: United States
ProdList: 6786
Advantage: 30

2A PharmaChem USA

Tel: --
Fax: --
Email: sales@2apharmachem.com
Country: United States
ProdList: 6137
Advantage: 39

3B Scientific Corporation

Tel: --
Fax: --
Email: sales@3bsc.com
Country: United States
ProdList: 6718
Advantage: 47

AK Scientific, Inc.

Tel: --
Fax: --
Email: sales@aksci.com
Country: United States
ProdList: 6347
Advantage: 65

APAC Pharmaceutical, LLC

Tel: --
Fax: --
Email: sales@apacpharma.com
Country: United States
ProdList: 6322
Advantage: 38

ASDI Incorporated

Tel: --
Fax: --
Email: customerservice@asdi.net
Country: United States
ProdList: 6922
Advantage: 67

BOSCHE SCIENTIFIC, LLC

Tel: --
Fax: --
Email: Sales@BoscheSci.com
Country: United States
ProdList: 6477
Advantage: 55

ChemPacific Corporation

Tel: --
Fax: --
Email: sales@chempacific.com
Country: United States
ProdList: 6891
Advantage: 51

More

Less

View Lastest Price from Ticlopidine manufacturers

Career Henan Chemical Co

Product: Ticlopidine 55142-85-3
Price: US $1.00/KG
Min. Order: 1KG
Purity: 85.0-99.8%
Supply Ability: 20tons
Release date: 2020-01-08

55142-85-3, TiclopidineRelated Search:

Benzyl chloroformate Clopidol Pizotifen Cephaloridine Benzyl chloride 2-Chloro-5-chloromethylpyridine 4,5,6,7-Tetrahydrothieno[3,2-c]pyridine PIPERACILLIN Tetrahydrothiophene Pyridine Benzyl chloromethyl ether Hydrochlorothiazide TICLOPIDINE,TICLOPIDINE HCL,TICLOPIDINE HYDROCHLORIDE,Ticlopidine HCl ( EDMF /COS) TICLOPIDINE IMPURITY F TICLOPIDINE IMPURITY B Ticlopidine TICLOPIDINE HYDROCHLORIDE IMP. H (EP) AS HYDROCHLORIDE: 5-(4-CHLOROBENZYL)-4,5,6,7-TETRAHYDROTHIENO[3,2-C]PYRIDINE HYDROCHLORIDE TICLOPIDINE HYDROCHLORIDE IMP. C (EP) AS HYDROCHLORIDE: (2-CHLOROPHENYL)METHANAMINE HYDROCHLORIDE

2-c)pyridine,4,5,6,7-tetrahydro-5-((2-chlorophenyl)methyl)-thieno(

5-((2-Chlorophenyl)methyl)-4,5,6,7-tetrahydrothieno(3,2-c)pyridine

5-(O-Chlorobenzyl)-4,5,6,7-tetrahydrothieno-[3,2-c]pyridine

PCR 5332

pcr5332

Thieno(3,2-c)pyridine, 4,5,6,7-tetrahydro-5-((2-chlorophenyl)methyl)-

Thieno[3,2-c]pyridine, 5-[(2-chlorophenyl)methyl]-4,5,6,7-tetrahydro-

5-(2-CHLORO-BENZYL)-4,5,6,7-TETRAHYDRO-THIENO[3,2-C]PYRIDINE

TICLOPIDINE

TICIOPIDINE

Ticlopidine (base and/or unspecified salts)

2-[N-Methyl-N-(2-chlorobenzyl)aMinoethyl]thiophene

Ticlopidine IMpurity (N-Methyl)

5-(2-Chlorobenzyl)

Anagregal

Caudaline

Ticlosin

Ticlopidine hydrochloride CRS

Ticlopidine USP/EP/BP

PCR 5332|||Ticlid

55142-85-3

C14H14ClNS

TF - TO

Analytical Standards

Alphabetic

Analytical Chromatography Product Catalog