SINFACHEM LIMITED

SINFACHEM LIMITED
Country:  China (Mainland)
Business Type:  Lab/Research institutions
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Mr.Wang
Tel: 86-25-84683399
Fax:  86-25-84683112
City:  Nanjing
Street:  605, Phoenix Herui Plaza, No.389, South Taiping Road, Nanjing, China 210002
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Amlodipine Besylate

Amlodipine Besylate CAS NO.111470-99-6

  • Min.Order: 1 Metric Ton
  • Payment Terms: L/C,D/A,D/P,T/T
  • Product Details

Keywords

  • Amlodipine Besylate
  • Intermediates of Glibenclamide
  • competitive price

Quick Details

  • ProName: Amlodipine Besylate
  • CasNo: 111470-99-6
  • Molecular Formula: C26H31ClN2O8S
  • Appearance: White Solid
  • Application: Intermediates of Glibenclamide
  • DeliveryTime: 15 days after order confirmed
  • PackAge: 25kg/drum
  • Port: shanghai or hangzhou
  • ProductionCapacity: 1 Metric Ton/Day
  • Purity: 98%
  • Storage: Store at RT
  • Transportation: by sea/air/courier
  • LimitNum: 1 Metric Ton

Superiority

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Details

 
Amlodipine besilate Chemical Properties
mp  199-201°C
storage temp.  Store at RT
solubility  DMSO: 20 mg/mL
form  solid
color  white
CAS DataBase Reference 111470-99-6(CAS DataBase Reference)
 
Safety Information
Hazard Codes  Xn
Risk Statements  22-36/37/38-20/21/22
Safety Statements  26-36
WGK Germany  3
RTECS  US7967700
Hazardous Substances Data 111470-99-6(Hazardous Substances Data)
MSDS Information
Provider Language
SigmaAldrich English
 
Amlodipine besilate Usage And Synthesis
Chemical Properties White Crystalline Solid
Usage A dihydropyridine calcium channel blocker. Used as an antianginal and antihypertensive
Usage Angiotensin II inhibitor prodrug, antihypertensive
Usage Amlodipine besylate is a L-type calcium channel blocker which may be used for the treatment of angina pectoris and hypertension. Amlodipine also inhibits growth of human epidermoid carcinoma A431 cells and has antireproductive effects in male rats.
Biological Activity L-type calcium channel blocker that displays antihypertensive properties. Inhibits Ca 2+ -induced contractions in depolarized rat aorta (IC 50 = 1.9 nM) and displays vasoprotective effects in cardiovascular disease. Inhibits proliferation of human vascular smooth muscle cells and epidermoid carcinoma A431 cells (IC 50 = 25 μ M).

 

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