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HENAN SUNLAKE ENTERPRISE CORPORATION

Country: China (Mainland)

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ARECAIDINE BUT-2-YNYL ESTER TOSYLATE

CAS NO.499-04-7

  • FOB Price: USD: /Metric Ton Get Latest Price
  • Min.Order: 100 Kilogram
  • Payment Terms: L/C,D/A,D/P,T/T,Other
  • Available Specifications:

    1(10-100)Metric Ton1(10-100)Metric Ton

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Product Details

Keywords

  • ARECAIDINE BUT-2-YNYL ESTER TOSYLATE
  • 499-04-7
  • C18H23NO5S

Quick Details

  • ProName: ARECAIDINE BUT-2-YNYL ESTER TOSYLATE
  • CasNo: 499-04-7
  • Molecular Formula: C18H23NO5S
  • Appearance: powder
  • Application: 499-04-7
  • DeliveryTime: Within 3-7 days
  • PackAge: Depended
  • Port: China Main Port
  • ProductionCapacity: 300 Kilogram/Month
  • Purity: 99%
  • Storage: Store in dry, dark and ventilated plac...
  • Transportation: by air or by sea
  • LimitNum: 100 Kilogram
  • Application: Multipurpose intermediate
  • Application: ISO/9001 Certificate

Superiority

ARECAIDINE BUT-2-YNYL ESTER TOSYLATE Basic information
Product Name: ARECAIDINE BUT-2-YNYL ESTER TOSYLATE
Synonyms: N-METHYL-1,2,5,6-TETRAHYDROPYRIDINE-3-CARBOXYLIC ACID BUT-2-YNYL ESTER TOSYLATE;1,2,5,6-tetrahydro-1-methyl-3-pyridinecarboxylicaci;1,2,5,6-tetrahydro-1-methyl-3-pyridinecarboxylicacid;1,2,5,6-tetrahydro-1-methyl-nicotinicaci;arecaidine;arecaine;methylguvacine;ARECAIDINE BUT-2-YNYL ESTER TOSYLATE
CAS: 499-04-7
MF: C18H23NO5S
MW: 365.44
EINECS:  
Product Categories: Various Metabolites and Impurities;Intermediates & Fine Chemicals;Metabolites & Impurities;Neurochemicals;Pharmaceuticals;Acetylcholine receptor
Mol File: 499-04-7.mol
ARECAIDINE BUT-2-YNYL ESTER TOSYLATE Structure
 
ARECAIDINE BUT-2-YNYL ESTER TOSYLATE Chemical Properties
mp  232°C (dec.)
bp  104-112℃ (14-16 Torr)
density  1.166±0.06 g/cm3 (20 ºC 760 Torr)
Fp  115.1±25.9℃
storage temp.  Store at RT
 
Safety Information
MSDS Information
 
 
ARECAIDINE BUT-2-YNYL ESTER TOSYLATE Usage And Synthesis
Chemical Properties Crystalline Solid
Usage A metabolite of Arecoline, a cholinergic agonist.
Biological Activity Potent muscarinic agonist, 4.6-fold selective for M 2 receptors in the atrium versus those in the ileum.

 

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