webinar
Oct. 27-28, 2025, Boston, MA, USA - Booth 114.
Read More

DBCO-PEG3-oxyamine-Boc hydrochloride

  CAS No.:   Cat No.: BADC-01889 4.5  

DBCO-PEG3-oxyamine-Boc hydrochloride is a bifunctional ADC linker combining strain-promoted DBCO click group and oxyamine for oxime ligation, improving payload attachment and stability in antibody-drug conjugates. Keywords: ADC linker, DBCO linker, PEG spacer, oxyamine, bioorthogonal chemistry.

DBCO-PEG3-oxyamine-Boc hydrochloride

Structure of

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C34H45ClN4O9
Molecular Weight
689.20

* For research and manufacturing use only. We do not sell to patients.

Size Price Stock Quantity
-- $-- In stock

Looking for different specifications? Click to request a custom quote!

Capabilities & Facilities

Popular Publications Citing BOC Sciences Products
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

Related Products

Contact our experts today for pricing and comprehensive details on our ADC offerings.

You May Also Be Interested In

From cytotoxin synthesis to linker design, discover our specialized services that complement your ADC projects.

ADC Linker Development Enzyme Cleavable Linker Cathepsin B Cleavable Linker Phosphatase Cleavable Linker β-Glucuronide Linker β-Galactosidase Cleavable Linker Sulfatase Cleavable Linker Chemically Cleavable Linker Non-Cleavable Linker Services Acid Cleavable Linker

Unlock Deeper ADC Insights

Learn more about payload design, linker strategies, and integrated CDMO support through our curated ADC content.

Linkers - A Crucial Factor in Antibody–Drug Conjugates In-Depth Review of ADC Linkers: Types, Mechanisms, and Research Progress New Structural Insights Solve Instability Issues of Maleimide Linkers in ADCs PEG Linkers in Antibody-Drug Conjugates Peptide Linkers in Antibody-Drug Conjugates Disulfide Linkers in Antibody-Drug Conjugates Biotinylation Reagents in Antibody-Drug Conjugates Maleimide Linkers in Antibody-Drug Conjugates Current ADC Linker Chemistry SPDB Linkers in Antibody-Drug Conjugates

Explore More ADC Products

Find exactly what your project needs from our expanded range of ADCs, offering flexible options to fit your timelines and goals.

ADC Cytotoxin

Powerful Targeted Cancer Solutions

ADC  Cytotoxin with Linker

Enhanced Stability And Efficacy

ADC Linker

Precise Conjugation For Success

Antibody-Drug  Conjugates (ADCs)

Maximized Therapeutic Performance

Auristatins

Next-Level Tubulin Inhibition

Calicheamicins

High-Impact DNA Targeting

Camptothecins

Advanced Topoisomerase Inhibition

Daunorubicins / Doxorubicins

Trusted Anthracycline Payloads

Duocarmycins

Potent DNA Alkylation Agents

Maytansinoids

Superior Microtubule Disruption

Pyrrolobenzodiazepines

Ultra-Potent DNA Crosslinkers

Traditional Cytotoxic Agents

Proven Chemotherapy Solutions

Cleavable Linker

Precise Intracellular Drug Release

Non-Cleavable Linker

Exceptional Long-Term Stability

Historical Records: 1-Amino-8-azido-3,6-dioxaoctane tosylate | 8-Azido-3,6-dioxaoctanoyl-AEEA | Nα-Fmoc-Nε-(propargyloxy)carbonyl-L-lysine | Propargyl-PEG9-bromide | H-D-Lys(N3)-OH | DBCO-PEG4-GGFG-DMEA-PNU159682 | Boc-L-4-trans-hydroxyproline methyl ester | OSu-Glu-vc-PAB-MMAE | (2S,4R)-H-L-Pro(4-N3)-OH hydrochloride | NH2-MPAA-NODA | DBCO-PEG3-oxyamine-Boc hydrochloride
Send Inquiry
Verification code
Inquiry Basket