DBCO-PEG3-oxyamine-Boc hydrochloride

DBCO-PEG3-oxyamine-Boc hydrochloride Catalog number: BADC-01889

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DBCO-PEG3-oxyamine-Boc hydrochloride is an ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Category
ADCs Linker
Product Name
DBCO-PEG3-oxyamine-Boc hydrochloride
Catalog Number
BADC-01889
Molecular Formula
C34H45ClN4O9
Molecular Weight
689.20

Ordering Information

Catalog Number Size Price Quantity
BADC-01889 -- $-- Inquiry
Description
DBCO-PEG3-oxyamine-Boc hydrochloride is an ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
IUPAC Name
tert-butyl N-[2-[2-[2-[2-[2-[[4-(2-azatricyclo[10.4.0.04,9]hexadeca-1(16),4,6,8,12,14-hexaen-10-yn-2-yl)-4-oxobutanoyl]amino]ethoxy]ethoxy]ethoxy]ethylamino]-2-oxoethoxy]carbamate;hydrochloride
Canonical SMILES
CC(C)(C)OC(=O)NOCC(=O)NCCOCCOCCOCCNC(=O)CCC(=O)N1CC2=CC=CC=C2C#CC3=CC=CC=C31.Cl
InChI
InChI=1S/C34H44N4O9.ClH/c1-34(2,3)47-33(42)37-46-25-31(40)36-17-19-44-21-23-45-22-20-43-18-16-35-30(39)14-15-32(41)38-24-28-10-5-4-8-26(28)12-13-27-9-6-7-11-29(27)38;/h4-11H,14-25H2,1-3H3,(H,35,39)(H,36,40)(H,37,42);1H
InChIKey
XUYGSZLKYSJRGB-UHFFFAOYSA-N

DBCO-PEG3-oxyamine-Boc hydrochloride is a specialized reagent commonly used in bioconjugation and chemical biology. Here are some key applications of DBCO-PEG3-oxyamine-Boc hydrochloride:

Site-Specific Bioconjugation: This compound is employed to achieve precise bioconjugation of biomolecules, such as proteins and peptides, using click chemistry. The DBCO group reacts with azides in a copper-free “Click” reaction, ensuring biocompatibility. This application is critical for creating homogeneous and well-defined conjugates for diagnostic and therapeutic purposes.

Drug Delivery Systems: DBCO-PEG3-oxyamine-Boc hydrochloride can be used to modify nanoparticles and other drug carriers. The PEGylation offers increased solubility and reduced immunogenicity, while the DBCO group allows for the attachment of targeting ligands via click chemistry. This enhances the specificity and efficiency of drug delivery to targeted cells and tissues.

Biomolecular Labeling: Researchers utilize this reagent for the efficient labeling of biomolecules in various biological studies. The DBCO moiety facilitates conjugation with azide-labeled probes, enabling imaging and tracking of biomolecules in live cells and tissues. This is essential for studies in cellular dynamics and molecular interactions.

Polymer and Surface Modification: DBCO-PEG3-oxyamine-Boc hydrochloride is used to modify surfaces and polymers to introduce functional groups through click chemistry. This modification imparts desired biological or chemical properties to the materials, making them suitable for applications like biosensors, diagnostic devices, or biointerfaces. These functionalized materials can be utilized in a variety of biological and biomedical applications.

The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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