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Indospicine

Base Information
  • Chemical Name:Indospicine
  • CAS No.:16377-00-7
  • Molecular Formula:C7H15N3O2
  • Molecular Weight:173.215
  • Hs Code.:
  • UNII:X29Q4D9671
  • DSSTox Substance ID:DTXSID70167659
  • Nikkaji Number:J16.050D
  • Wikipedia:Indospicine
  • Wikidata:Q1661793
  • Metabolomics Workbench ID:68092
  • Mol file:16377-00-7.mol
Indospicine

Synonyms:6-amidino-2-aminohexanoic acid;indospicine;indospicine, (+-)-isomer

Suppliers and Price of Indospicine
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
Total 4 raw suppliers
Chemical Property of Indospicine
Chemical Property:
  • Vapor Pressure:7.77E-06mmHg at 25°C 
  • Boiling Point:350.1°Cat760mmHg 
  • PKA:2.52±0.24(Predicted) 
  • Flash Point:165.5°C 
  • PSA:113.19000 
  • Density:1.33g/cm3 
  • LogP:1.39500 
  • XLogP3:-3.2
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:6
  • Exact Mass:173.116426730
  • Heavy Atom Count:12
  • Complexity:170
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C(CCC(=N)N)CC(C(=O)O)N
  • Isomeric SMILES:C(CCC(=N)N)C[C@@H](C(=O)O)N
  • Uses Indospicine combined with arginine deprivation triggers cancer cell death via caspase-dependent apoptosis.
Technology Process of Indospicine

There total 24 articles about Indospicine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With hydrogenchloride; at 20 ℃; for 72h;
DOI:10.1081/SCC-120004860
Guidance literature:
Multi-step reaction with 7 steps
1.1: 52.2 percent / 4M NaOH; sodium nitroprusside dihydrate / H2O / 6.5 h / 60 °C / pH 9.5
2.1: 73 percent / H2SO4 / 5 h / Heating
3.1: 77 percent / pyridine / 6 h / 4 °C
4.1: 60 percent / ethanol; H2O / 2 h / 90 °C
5.1: HCl gas / ethanol / 20 °C
5.2: NH3 gas / 0 - 4 °C
6.1: 6M HCl / 20 °C
With pyridine; hydrogenchloride; sodium nitroprusside; sodium hydroxide; sulfuric acid; In ethanol; water;
DOI:10.1081/SCC-120004860
Guidance literature:
Multi-step reaction with 9 steps
1.1: 1M NaOH / ethanol / -20 - -5 °C
2.1: 0.275 mol / HCl / ethanol / 0.08 h / 50 °C
3.1: 52.2 percent / 4M NaOH; sodium nitroprusside dihydrate / H2O / 6.5 h / 60 °C / pH 9.5
4.1: 73 percent / H2SO4 / 5 h / Heating
5.1: 77 percent / pyridine / 6 h / 4 °C
6.1: 60 percent / ethanol; H2O / 2 h / 90 °C
7.1: HCl gas / ethanol / 20 °C
7.2: NH3 gas / 0 - 4 °C
8.1: 6M HCl / 20 °C
With pyridine; hydrogenchloride; sodium nitroprusside; sodium hydroxide; sulfuric acid; In ethanol; water;
DOI:10.1081/SCC-120004860
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