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Tizanidine

Base Information Edit
  • Chemical Name:Tizanidine
  • CAS No.:51322-75-9
  • Molecular Formula:C9H8ClN5S
  • Molecular Weight:253.715
  • Hs Code.:2934999090
  • European Community (EC) Number:610-648-1
  • UNII:6AI06C00GW
  • DSSTox Substance ID:DTXSID9023679
  • Nikkaji Number:J11.180E
  • Wikipedia:Tizanidine
  • Wikidata:Q423538
  • NCI Thesaurus Code:C61976
  • RXCUI:57258
  • Pharos Ligand ID:UVBAZLFK7DQV
  • Metabolomics Workbench ID:43008
  • ChEMBL ID:CHEMBL1079
  • Mol file:51322-75-9.mol
Tizanidine

Synonyms:5-chloro-4-(2-imidazolin-2-yl-amino)-2,1,3-benzothiadiazole;DS 103-282;Sirdalud;tizanidine;tizanidine hydrochloride;tizanidine monohydrochloride;Zanaflex

Suppliers and Price of Tizanidine
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • Crysdot
  • Tizanidine 98+%
  • 50mg
  • $ 57.00
  • Crysdot
  • Tizanidine 98+%
  • 100mg
  • $ 77.00
  • ApexBio Technology
  • Tizanidine
  • 50mg
  • $ 77.00
  • ApexBio Technology
  • Tizanidine
  • 500mg
  • $ 553.00
  • American Custom Chemicals Corporation
  • TIZANIDINE 95.00%
  • 2.5G
  • $ 983.88
  • American Custom Chemicals Corporation
  • TIZANIDINE 95.00%
  • 1G
  • $ 721.57
  • AHH
  • 5-Chloro-N-(4,5-dihydro-1H-imidazol-2-yl)-2,1,3benzothiadiazole-4-aminehydrochloride 98%
  • 5g
  • $ 456.00
Total 40 raw suppliers
Chemical Property of Tizanidine Edit
Chemical Property:
  • Appearance/Colour:White Solid 
  • Melting Point:221-223° 
  • Boiling Point:391.2 °C at 760 mmHg 
  • PKA:7.48±0.10(Predicted) 
  • Flash Point:190.4 °C 
  • PSA:90.44000 
  • Density:1.821 g/cm3 
  • LogP:2.35520 
  • Solubility.:H2O: ~29 mg/mL 
  • XLogP3:1.1
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:253.0188941
  • Heavy Atom Count:16
  • Complexity:300
Purity/Quality:

99.9% *data from raw suppliers

Tizanidine 98+% *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn 
  • Hazard Codes:Xn 
  • Statements: 22-36/37/38 
  • Safety Statements: 26-36 
MSDS Files:

SDS file from LookChem

Useful:
  • Drug Classes:Autonomic Agents: Muscle Relaxants, Central
  • Canonical SMILES:C1CN=C(N1)NC2=C(C=CC3=NSN=C32)Cl
  • Recent ClinicalTrials:Clinical Study on the Effect of Tizanidine on the Function and Pain of Patients After Shoulder Arthroscopy
  • Recent EU Clinical Trials:A phase III, multicenter, randomized, parallel groups study to assess the efficacy and safety of 0,5 mg Tizaspray? administered intranasally versus Sirdalud? 2 mg tablets, in patients with acute low back pain
  • Description Tizanidine is a centrally-acting muscle relaxant useful in the treatment of muscle spasms and a variety of spastic conditions.
  • Uses Labeled Tizanidine, intended for use as an internal standard for the quantification of Tizanidine by GC- or LC-mass spectrometry. Tizanidine could have therapeutic use as a SARS-CoV-2 main protease inhibitor.
  • Therapeutic Function Muscle relaxant, Spasmolytic
  • Clinical Use Tizanidine is a centrally acting adrenergic α2 receptor agonist used to treat chronic muscle spasticity conditions, such as multiple sclerosis.
  • Drug interactions Potentially hazardous interactions with other drugs Anti-arrhythmics: enhanced muscle relaxant effect with procainamide. Antibacterials: concentration increased by ciprofloxacin - avoid; concentration possibly increased by norfloxacin; concentration possibly reduced by rifampicin. Antidepressants: concentration increased by fluvoxamine - avoid. Antihypertensives: enhanced hypotensive effect. Oral contraceptives: clearance of tizanidine reduced by 50%.
Technology Process of Tizanidine

There total 7 articles about Tizanidine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With water; sodium hydroxide; In methanol; at 60 - 65 ℃; for 2h;
Guidance literature:
With pyridine; In iso-butanol; at 65 - 70 ℃; for 8h; Temperature; Solvent; Reagent/catalyst;
Guidance literature:
With trichlorophosphate; In methanol; sodium hydroxide; water;
Refernces Edit
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