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Technology Process of 6-Amino-4-((4-(diethylamino)-1-methylbutyl)amino)quinoline diphosphate

6-Amino-4-((4-(diethylamino)-1-methylbutyl)amino)quinoline diphosphate

Base Information
  • Chemical Name:6-Amino-4-((4-(diethylamino)-1-methylbutyl)amino)quinoline diphosphate
  • CAS No.:78703-85-2
  • Molecular Formula:C18H28 N4
  • Molecular Weight:0
  • Hs Code.:
  • DSSTox Substance ID:DTXSID20999962
  • Mol file:78703-85-2.mol
6-Amino-4-((4-(diethylamino)-1-methylbutyl)amino)quinoline diphosphate

Synonyms:78703-85-2;6-Amino-4-((4-(diethylamino)-1-methylbutyl)amino)quinoline diphosphate;Quinoline, 6-amino-4-((4-(diethylamino)-1-methylbutyl)amino)-, diphosphate;N4-(5-(Diethylamino)pentan-2-yl)quinoline-4,6-diamine;C18H28N4.2H3O4P;C18-H28-N4.2H3-O4-P;DTXSID20999962;LS-141307;4-{[5-(Diethylamino)pentan-2-yl]imino}-1,4-dihydroquinolin-6-amine

Suppliers and Price of 6-Amino-4-((4-(diethylamino)-1-methylbutyl)amino)quinoline diphosphate
Supply Marketing:
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
  • American Custom Chemicals Corporation
  • 6-AMINO-4-((4-(DIETHYLAMINO)-1-METHYLBUTYL)AMINO)QUINOLINE DIPHOSPHATE 95.00%
  • 5MG
  • $ 505.90
Total 3 raw suppliers
Chemical Property of 6-Amino-4-((4-(diethylamino)-1-methylbutyl)amino)quinoline diphosphate
Chemical Property:
  • Vapor Pressure:1.1E-09mmHg at 25°C 
  • Boiling Point:488.3°C at 760 mmHg 
  • Flash Point:249.1°C 
  • PSA：57.41000 
  • Density:1.079g/cm3 
  • LogP:3.74250 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:8
  • Exact Mass:300.23139691
  • Heavy Atom Count:22
  • Complexity:306
Purity/Quality:

6-AMINO-4-((4-(DIETHYLAMINO)-1-METHYLBUTYL)AMINO)QUINOLINE DIPHOSPHATE 95.00% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCN(CC)CCCC(C)NC1=C2C=C(C=CC2=NC=C1)N
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