High quality Manidi...

High quality Manidipine hydrochloride powder supplier

High quality Manidipine hydrochloride powder supplier

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10 Gram

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  • Min.Order :10 Gram
  • Purity: 99%
  • Payment Terms : L/C,D/P,T/T,Other

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High quality Manidipine HCl Manidipine hydrochloride powder Manidipine hydrochloride supplier

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  • Appearance:powder
  • Application:Used as medical and organic intermediates, an important amino protective agent. Pharmaceutical and synthetic organic makes intermediates, organic synthesis used to introduce t-Boc protect gene. Speci
  • PackAge:custom-made
  • ProductionCapacity:1|Metric Ton|Month
  • Storage:store in dry and cool place
  • Transportation:air or ocean or rail or parcel post

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High quality Manidipine hydrochloride powder supplier

CAS No.:89226-75-5

Other Names:Manidipine hydrochloride

MF:C35H40Cl2N4O6

Place of Origin: Anhui, China (Mainland)

Type:Central Nervous System Agents, Vitamins, Amino Acids and Coenzymes

Grade Standard:Food Grade, Medicine Grade, Tech Grade

Usage:Animal Pharmaceuticals

Brand Name:Joye

Model Number:CV 4093

Purity:99%min

Appearance: Yellow crystalline powder

MW:683.62

SUNSANTA
  We are one of the leading exporters in China in the fields of active pharma
ingredients including oncology drug, prostaglandin, anti-HIV drug, cardiovascular
drug, diabetes drug, anti-inflammatory drug, urinary system drug, cosmetics peptide
and intermediate, dyestuff & pigment and kinds of package materials. 
  We specialize in synthesis of novel organic compounds, process development
and manufacturing of pharmaceutical and fine organic chemicals from gram to kilogram quantity.
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High quality Manidipine hydrochloride powder supplier

SSDa00268    Manidipine dihydrochloride CAS 89226-75-5

Manidipine dihydrochloride

CAS 89226-75-5

 CAS 89226-75-5 Brand: SUNSANTA
MF C35H38N4O6•2HCl  MSDS:  Aviable
MW 683.62 EINECS:ND
 Speification: In-house/USP  
Usage Manidipine dihydrochloride is a dihydropyridine compound and calcium channel protein inhibitor and antagonist. Manidipine is described to block T-type Ca2+ channels specifically and is also described to have a high selectivity for the vasculature, presenting negligible cardiodepression as compared to other Ca2+ channel antagonists. Manidipine is also described to not significantly affect norepinephrine levels, suggesting a lack of sympathetic activation with this compound.
Applications Pharmaceutical  raw material

 

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