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Arginylproline

Base Information
  • Chemical Name:Arginylproline
  • CAS No.:2418-69-1
  • Molecular Formula:C11H21N5O3
  • Molecular Weight:271.319
  • Hs Code.:
  • DSSTox Substance ID:DTXSID70178886
  • Nikkaji Number:J1.481.854E
  • Metabolomics Workbench ID:78690
  • ChEMBL ID:CHEMBL48223
  • Mol file:2418-69-1.mol
Arginylproline

Synonyms:Arg-Pro;arginylproline;arginylproline diacetate, (L)-isomer

Suppliers and Price of Arginylproline
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
  • Biosynth Carbosynth
  • H-Arg-Pro-OH sulfate salt
  • 500 mg
  • $ 1430.00
  • Biosynth Carbosynth
  • H-Arg-Pro-OH sulfate salt
  • 250 mg
  • $ 822.50
  • Biosynth Carbosynth
  • H-Arg-Pro-OH sulfate salt
  • 100 mg
  • $ 411.00
  • Biosynth Carbosynth
  • H-Arg-Pro-OH sulfate salt
  • 50 mg
  • $ 236.00
  • Biosynth Carbosynth
  • H-Arg-Pro-OH sulfate salt
  • 25 mg
  • $ 136.00
Total 9 raw suppliers
Chemical Property of Arginylproline
Chemical Property:
  • Vapor Pressure:8.48E-15mmHg at 25°C 
  • Boiling Point:576.6°Cat760mmHg 
  • PKA:3.16±0.20(Predicted) 
  • Flash Point:302.5°C 
  • PSA:228.51000 
  • Density:1.51g/cm3 
  • LogP:0.90970 
  • Storage Temp.:-15°C 
  • XLogP3:-4.3
  • Hydrogen Bond Donor Count:4
  • Hydrogen Bond Acceptor Count:5
  • Rotatable Bond Count:6
  • Exact Mass:271.16443955
  • Heavy Atom Count:19
  • Complexity:367
Purity/Quality:

99% *data from raw suppliers

H-Arg-Pro-OH sulfate salt *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC(N(C1)C(=O)C(CCCN=C(N)N)N)C(=O)O
  • Isomeric SMILES:C1C[C@H](N(C1)C(=O)[C@H](CCCN=C(N)N)N)C(=O)O
Technology Process of Arginylproline

There total 1 articles about Arginylproline 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:
at 37 ℃; for 0.166667h; 0.1 M Tris HCl buffer pH 8.0, X-prolyl dipeptidyl aminopeptidase from Lactococcus lactis subsp. cremoris nTR;
DOI:10.1271/bbb.56.704
Guidance literature:
Multi-step reaction with 4 steps
2: HCl / diethyl ether
4: 1.) EEDQ
With hydrogenchloride; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In diethyl ether;
Guidance literature:
Multi-step reaction with 4 steps
2: HCl / diethyl ether
4: 1.) EEDQ
With hydrogenchloride; N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline; In diethyl ether;
upstream raw materials:

Arg-Pro-pNA

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