QBD11205

Bromoacetamido-dPEG ^®₂₃-azide

• Empirical Formula (Hill Notation): C₅₀H₉₉BrN₄O₂₄
• Molecular Weight: 1220.24
• UNSPSC Code: 12352101
• NACRES: NA.22

Properties

• assay: >90%
• form: solid or viscous liquid
• reaction suitability: reagent type: cross-linking reagent; reaction type: click chemistry
• polymer architecture: shape: linear; functionality: heterobifunctional
• shipped in: ambient
• storage temp.: −20°C
• SMILES string: BrCC(NCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCN=[N+]=[N-])=O
• InChI: 1S/C50H99BrN4O24/c51-49-50(56)53-1-3-57-5-7-59-9-11-61-13-15-63-17-19-65-21-23-67-25-27-69-29-31-71-33-35-73-37-39-75-41-43-77-45-47-79-48-46-78-44-42-76-40-38-74-36-34-72-32-30-70-28-26-68-24-22-66-20-18-64-16-14-62-12-10-60-8-6-58-4-2-54-55-52/h1-49H2,(
• InChI key: CUORTMALVRPNBL-UHFFFAOYSA-N

Description

Features and Benefits

Bromoacetamido-dPEG^®₂₃-azide is can be used to conjugate two different proteins or an antibody with a payload by reaction of the bromoacetamido with a free thiol and by using copper-catalyzed "click" chemistry with the azide to react with terminal alkynes or strained alkynes.

Legal Information

Products Protected under U.S. Patents # 7,888,536 B2

dPEG is a registered trademark of Quanta BioDesign

Safety Information

• Storage Class: 11 - Combustible Solids
• wgk_germany: WGK 3
• flash_point_f: Not applicable
• flash_point_c: Not applicable