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Heretic multi armed polyethylene glycol (NH2) 7-8ARM-PEG-N3

NegotiableUpdate on 05/06
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Overview

Heterologous Dobby Polyethylene Glycol (NH2) 7-8ARM-PEG-N3 $r $n Hydrogel cross-linking or network construction (Dobby NH ₂ participates in cross-linking, N ≮ directionally introduces functional molecules) $r $n Biomolecule coupling (protein/polypeptide/nucleic acid/targeted ligand modification) $r $n Nanomaterials or surface modification (electric regulation, functional grafting) $r $n Drug carrier functionalization or multi module material construction

Product Details

Heretic multi armed polyethylene glycol (NH2) 7-8ARM-PEG-N3


keyProduct Information

Chinese name:Eight arm polyethylene glycol, seven arm amino, one arm azide

English name:8arm PEG,1arm-Azide,7arm-Amine

Abbreviation: (NH2)7-8ARM-PEG-N3

Brand: MeloPEG Technology

Structure:

异端多臂聚乙二醇 (NH2)7-8ARM-PEG-N3


Purity:Over 95%

定制:NH2and The proportion of N3 can be customized at any ratio

Molecular weight: PEG2K、PEG5K、PEG10K、PEG20k, Other molecular weight consultation customer service

noteIntentional mattersitem

Keep dry

Storage conditions

-Freezing and drying below 20 ℃


Heretic multi armed polyethylene glycol (NH2) 7-8ARM-PEG-N3

application

1. Basic Definition

An asymmetric multifunctional derivative of 8-arm star shaped polyethylene glycol (8-arm PEG)

End group composition: 7 amino groups (NH ₂)+1 azide (N ∝)

Mainly used for click coupling, cross-linking construction, and targeted functionalization

2. Structural features

Star shaped eight arm core provides high-density reaction platform

7: Asymmetric end group design enables selective reactions of different arms, suitable for constructing complex bifunctional or multifunctional systems

PEG backbone has excellent water solubility, flexibility, and biocompatibility

3. Terminal function

NH ₂ (amino, 7):Can participate in amidation, grafting modification, electrostatic binding, surface charge regulation, commonly used to connect targeted molecules, dyes, peptides, etc., or participate in multi-point crosslinking

N3 (azide, 1):Classic click reactive groups are used for efficient coupling of CuAAC or SPAAC (copper free click) with alkynyl molecules, characterized by high specificity, mildness, rapidity, and high yield

4. Typical applications

Hydrogel cross-linking or network construction (Dobby NH ₂ participates in cross-linking, and N ∨ directionally introduces functional molecules)

Biomolecular coupling (protein/peptide/nucleic acid/targeted ligand modification)

Nanomaterials or surface modification (charge control, functional grafting)

Functionalization of drug carriers or construction of multi module materials

5. Main advantages

Multiple reaction sites with high density (eight arm structure)

Click to separate from conventional chemical modification sites, with strong controllability

Has high water solubility, low toxicity, low immunogenicity, and good in vivo compatibility

Accurate functional design suitable for complex systems

Related directories:

(NH2)7-8ARM-PEG-COOH Eight arm polyethylene glycol, seven arm amino, one arm carboxyl

(HO)7-8ARM-PEG-N3 Eight arm polyethylene glycol, seven arm hydroxyl, one arm azide

(NH2)7-8ARM-PEG-N3 Eight arm polyethylene glycol, seven arm amino, one arm azide

(NH2)7-8ARM-PEG-BocNH Eight arm polyethylene glycol, seven arm amino, one arm tert butoxycarbonylamino

(Nor)7-8ARM-PEG-Biotin Eight arm polyethylene glycol, seven arm de icing, graphene, and one arm biotin

(NH2)7-8ARM-PEG-Biotin Eight arm polyethylene glycol, seven arm amino, one arm biotin