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Biotin-PEG3-NHS ester

Base Information
  • Chemical Name:Biotin-PEG3-NHS ester
  • CAS No.:1253286-56-4
  • Molecular Formula:C23H36N4O9S
  • Molecular Weight:544.626
  • Hs Code.:2934999090
  • Mol file:1253286-56-4.mol
Biotin-PEG3-NHS ester

Synonyms:

Suppliers and Price of Biotin-PEG3-NHS ester
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
  • purepeg
  • (+)-Biotin-PEG3-NHSEster min.97%
  • 1 g
  • $ 530.00
  • BroadPharm
  • Biotin-PEG3-NHSester 98%
  • 1 G
  • $ 540.00
Total 8 raw suppliers
Chemical Property of Biotin-PEG3-NHS ester
Chemical Property:
  • PKA:13.90±0.40(Predicted) 
  • Density:1.35±0.1 g/cm3(Predicted) 
Purity/Quality:

98%,99%, *data from raw suppliers

(+)-Biotin-PEG3-NHSEster min.97% *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:
Useful:
  • Description Biotin-PEG3-NHS ester is an biotinylation compound that can couple with primary amino groups (-NH2). The NHS group reacts specifically and efficiently with lysine and N-terminal amino groups at pH 7-9 to form stable amide bonds.
Technology Process of Biotin-PEG3-NHS ester

There total 7 articles about Biotin-PEG3-NHS ester 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: dichloromethane / 20 °C
2: trifluoroacetic acid / dichloromethane / 20 °C
3: diisopropyl-carbodiimide / dichloromethane / 20 °C
With trifluoroacetic acid; diisopropyl-carbodiimide; In dichloromethane;
Guidance literature:
Multi-step reaction with 4 steps
1: diisopropyl-carbodiimide / N,N-dimethyl-formamide / 45 °C
2: dichloromethane / 20 °C
3: trifluoroacetic acid / dichloromethane / 20 °C
4: diisopropyl-carbodiimide / dichloromethane / 20 °C
With trifluoroacetic acid; diisopropyl-carbodiimide; In dichloromethane; N,N-dimethyl-formamide;
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