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factory lower price64461-82-1
factory lower price64461-82-1
factory lower price64461-82-1

factory lower price64461-82-1

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100 Kilogram

Negotiable

  • Min.Order :100 Kilogram
  • Purity: 99%
  • Payment Terms : L/C,D/A,D/P,T/T,Other

Keywords

Tizanidine hydrochloride 64461-82-1 C9H9Cl2N5S

Quick Details

  • Appearance:powder
  • Application:64461-82-1
  • PackAge:Depended
  • ProductionCapacity:300|Kilogram|Month
  • Storage:Refrigerator
  • Transportation:by air or by sea

Superiority:

Tizanidine hydrochloride Basic information
Product Name: Tizanidine hydrochloride
Synonyms: 1,3-benzothiadiazol-4-amine,5-chloro-n-(4,5-dihydro-1h-imidazol-2-yl)-mono;5-chloro-4-(2-imidazolin-2-ylamino)-2,1,3-benzothiadiazolehydrochloride;SIRDALUD;TERNELIN;TIZANIDINE HCL;TIZANIDINE HYDROCHLORIDE;ZANAFLEX;DS-103-282
CAS: 64461-82-1
MF: C9H9Cl2N5S
MW: 290.17
EINECS:  
Product Categories: Muscle relaxant (skeletal);Inhibitors;Intermediates & Fine Chemicals;Pharmaceuticals;Adrenoceptor;Bases & Related Reagents;Heterocycles;Nucleotides;Sulfur & Selenium Compounds;Zanaflex, Sirdalud
Mol File: 64461-82-1.mol
Tizanidine hydrochloride Structure
 
Tizanidine hydrochloride Chemical Properties
mp  280 °C
storage temp.  Desiccate at RT
solubility  H2O: ~29 mg/mL
form  solid
color  white
Merck  9485
CAS DataBase Reference 64461-82-1(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xn,Xi
Risk Statements  22-36/37/38
Safety Statements  26-36-37/39
WGK Germany  3
RTECS  DK9910000
MSDS Information
Provider Language
SigmaAldrich English
 
Tizanidine hydrochloride Usage And Synthesis
Chemical Properties Off-White to pale Yellow Solid
Usage Tizanidine (Zanaflex) is a drug that is used as a muscle relaxant. It is a centrally acting α-2 adrenergic agonist. It is used to treat the spasms, cramping, and tightness of muscles caused by medical problems such as multiple sclerosis, spastic diplegia,
Usage Anticoagulant
Usage An α2-adrenergic agonist; centrally active myotonolytic. A muscle relaxant (skeletal).
Biological Activity α 2 -adrenergic receptor agonist. Antinociceptive upon epidural administration in rats (IC 50 = 48 nM). Also binds to imidazoline receptor.

 

 

 

 

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