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Propargyl-PEG5-CH2CO2H

Base Information Edit
  • Chemical Name:Propargyl-PEG5-CH2CO2H
  • CAS No.:1429934-37-1
  • Molecular Formula:C13H22O7
  • Molecular Weight:290.313
  • Hs Code.:
  • Mol file:1429934-37-1.mol
Propargyl-PEG5-CH2CO2H

Synonyms:3,6,9,12,15-pentaoxaoctadec-17-ynoic acid

Suppliers and Price of Propargyl-PEG5-CH2CO2H
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
  • BroadPharm
  • Propargyl-PEG5-CH2CO2H 98%
  • 100 MG
  • $ 280.00
  • BroadPharm
  • Propargyl-PEG5-CH2CO2H 98%
  • 250 MG
  • $ 480.00
  • BroadPharm
  • Propargyl-PEG5-CH2CO2H 98%
  • 1 G
  • $ 1450.00
  • BroadPharm
  • Propargyl-PEG5-CH2CO2H 98%
  • 500 MG
  • $ 780.00
  • Activate Scientific
  • Propargyl-PEG4-CH2COOH 95+%
  • 5 g
  • $ 1498.00
  • Activate Scientific
  • Propargyl-PEG4-CH2COOH 95+%
  • 1 g
  • $ 588.00
  • Activate Scientific
  • Propargyl-PEG4-CH2COOH 95+%
  • 250 mg
  • $ 294.00
  • Acrotein
  • Propargyl-PEG4-CH2COOH 97%
  • 0.25g
  • $ 220.00
Total 8 raw suppliers
Chemical Property of Propargyl-PEG5-CH2CO2H Edit
Chemical Property:
Purity/Quality:

99.3% *data from raw suppliers

Propargyl-PEG5-CH2CO2H 98% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Description Propargyl-PEG5-CH2CO2H is an alkyne linker with a carboxylic acid. The carboxylic acid can react with primary amines to form stable amide bonds; activator (e.g. EDC, or HATU) is needed. The alkyne group can participate in copper catalyzed azide-alkyne Click Chemistry to form stable triazole linkage.
Technology Process of Propargyl-PEG5-CH2CO2H

There total 6 articles about Propargyl-PEG5-CH2CO2H 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 sodium hydroxide; In methanol; water;
DOI:10.1002/chem.201700607
Guidance literature:
With lithium hydroxide; In tetrahydrofuran; water; at 20 ℃; for 2h;
Guidance literature:
Multi-step reaction with 2 steps
1: potassium tert-butylate / tetrahydrofuran
2: sodium hydride / tetrahydrofuran
With potassium tert-butylate; sodium hydride; In tetrahydrofuran;
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