BCN/Ethoxymethyl/Propargyl PEG reagent, N-(endo-BCN-PEG2-amido-PEG3)-N-bis-(PEG3-amino-Tri-(propargyl-PEG2-ethoxymethyl)-methane), Purity 95%

Cat. No.: X24-10-WXX124

BCN/Ethoxymethyl/Propargyl PEG reagent, N-(endo-BCN-PEG2-amido-PEG3)-N-bis-(PEG3-amino-Tri-(propargyl-PEG2-ethoxymethyl)-methane), Purity 95%

Synonym: BCN/Ethoxymethyl/Propargyl PEG reagent; N-(endo-BCN-PEG2-amido-PEG3)-N-bis-(PEG3-amino-Tri-(propargyl-PEG2-ethoxymethyl)-methane)

Size
50 mg; 100 mg
Price
Datasheet
MSDS
Properties
Description
N-(endo-BCN-PEG2-amido-PEG3)-N-bis-(PEG3-Amino-Tri-(Propargyl-PEG2-ethoxymethyl)-methane) is a reagent grade multi-functional PEG linker with six terminal propargyl groups and a BCN group. The propargyl groups enable the formation of triazole linkage with azide-bearing biomolecules or compounds in copper-catalyzed click chemistry. The BCN group reacts with azide-tagged compounds or biomolecules. The hydrophilic PEG spacer increases solubility in aqueous media.
Molecular Weight
2325.8
Molecular Formula
C112H185N11O40
Functional Group 1
BCN
Functional Group 2
Ethoxymethyl
Functional Group 3
Propargyl
Reactive Group 1
Azide
Form
Solid/liquid
Purity
95%
Identity
Confirmed by NMR.
Applications
N-(endo-BCN-PEG2-amido-PEG3)-N-bis-(PEG3-Amino-Tri-(Propargyl-PEG2-ethoxymethyl)-methane) integrates multiple functional moieties for enhanced bioconjugation strategies. The presence of propargyl groups allows for efficient click chemistry reactions, making it valuable for targeted drug delivery and functionalization of biomolecules.
Storage
Store at -20°C.
For Research Use Only. Not For Clinical Use.

Unleash the full potential of glycochemistry research with CD BioGlyco, the top CRO company committed to advancing the understanding of glycobiology through tailored solutions and exceptional expertise.

Copyright © CD BioGlyco. All Rights Reserved.
Top