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Glutathionylspermidine

Base Information Edit
  • Chemical Name:Glutathionylspermidine
  • CAS No.:33932-35-3
  • Molecular Formula:C17H34N6O5S
  • Molecular Weight:434.56
  • Hs Code.:
  • DSSTox Substance ID:DTXSID10955517
  • Nikkaji Number:J669.049A
  • Wikidata:Q3772542
  • Metabolomics Workbench ID:50566
  • Mol file:33932-35-3.mol
Glutathionylspermidine

Synonyms:glutathionylspermidine;N'-glutathionylspermidine disulfide

Suppliers and Price of Glutathionylspermidine
Supply Marketing:Edit
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 1 raw suppliers
Chemical Property of Glutathionylspermidine Edit
Chemical Property:
  • Vapor Pressure:1.4E-30mmHg at 25°C 
  • Boiling Point:643.3°Cat760mmHg 
  • Flash Point:342.8°C 
  • PSA:227.47000 
  • Density:1.256g/cm3 
  • LogP:0.50830 
  • XLogP3:-5
  • Hydrogen Bond Donor Count:8
  • Hydrogen Bond Acceptor Count:9
  • Rotatable Bond Count:17
  • Exact Mass:434.23113938
  • Heavy Atom Count:29
  • Complexity:523
Purity/Quality:

98% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C(CCNCCCNC(=O)CNC(=O)C(CS)NC(=O)CCC(C(=O)O)N)CN
  • Isomeric SMILES:C(CCNCCCNC(=O)CNC(=O)[C@H](CS)NC(=O)CC[C@@H](C(=O)O)N)CN
Technology Process of Glutathionylspermidine

There total 7 articles about Glutathionylspermidine 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:
Multi-step reaction with 3 steps
1: isobutylchloroformate / dimethylformamide / 8 h / 4 °C
2: TFA / 0.75 h / Ambient temperature
3: aq. dithiothreitol
With trifluoroacetic acid; diothiothreitol; isobutyl chloroformate; In N,N-dimethyl-formamide;
DOI:10.1039/c39860000593
Guidance literature:
Multi-step reaction with 5 steps
1: 70 percent / dimethylformamide / 10 h / Ambient temperature
2: 80 percent / dicyclohexylcarbodiimide / tetrahydrofuran / 8 h / 4 °C
3: dimethylformamide / 8 h / 4 °C
4: TFA / 0.75 h / Ambient temperature
5: aq. dithiothreitol
With dicyclohexyl-carbodiimide; trifluoroacetic acid; diothiothreitol; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1039/c39860000593
Guidance literature:
Multi-step reaction with 4 steps
1: 80 percent / dicyclohexylcarbodiimide / tetrahydrofuran / 8 h / 4 °C
2: dimethylformamide / 8 h / 4 °C
3: TFA / 0.75 h / Ambient temperature
4: aq. dithiothreitol
With dicyclohexyl-carbodiimide; trifluoroacetic acid; diothiothreitol; In tetrahydrofuran; N,N-dimethyl-formamide;
DOI:10.1039/c39860000593
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