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

Azide-PEG5-Tos

  CAS No.: 236754-49-7   Cat No.: BADC-01105   Purity: >98.0% 4.5  

Azide-PEG5-Tos is an ADC linker with PEG5 spacer and azide reactive group, designed for strain-promoted azide-alkyne cycloaddition. It enhances conjugation efficiency and improves stability in targeted antibody-drug conjugate synthesis.

Azide-PEG5-Tos

Structure of 236754-49-7

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C17H27N3O7S
Molecular Weight
417.48
Shipping
Room temperature, or blue ice upon request.
Shipping
Store at -20 °C, keep in dry and avoid sunlight.

* 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
Synonyms
14-Azido-3,6,9,12-tetraoxatetradecyl 4-methylbenzenesulfonate
IUPAC Name
2-[2-[2-[2-(2-azidoethoxy)ethoxy]ethoxy]ethoxy]ethyl 4-methylbenzenesulfonate
Canonical SMILES
CC1=CC=C(C=C1)S(=O)(=O)OCCOCCOCCOCCOCCN=[N+]=[N-]
InChI
InChI=1S/C17H27N3O7S/c1-16-2-4-17(5-3-16)28(21,22)27-15-14-26-13-12-25-11-10-24-9-8-23-7-6-19-20-18/h2-5H,6-15H2,1H3
InChIKey
RCRFPWKHJGMATE-UHFFFAOYSA-N
Solubility
10 mm in DMSO
Appearance
Solid Power
Shelf Life
≥ 2 years
Shipping
Room temperature, or blue ice upon request.
Storage
Store at -20 °C, keep in dry and avoid sunlight.
Form
Solid

Azide-PEG5-Tos is a versatile chemical reagent with diverse applications in bioconjugation and chemical synthesis. Here are four key applications of Azide-PEG5-Tos presented with a high degree of perplexity and burstiness:

Bioconjugation: At the forefront of biomolecular attachment, Azide-PEG5-Tos is a staple reagent for linking proteins, peptides, and nucleic acids to surfaces or other molecules through click chemistry reactions. This ingenious method gives rise to functionalized nanoparticles, biosensors, and diagnostic tools, pushing the boundaries of biofunctional material engineering. The inclusion of a polyethylene glycol (PEG) spacer not only enhances solubility but also mitigates steric hindrance, streamlining the conjugation process with finesse and precision.

Drug Delivery: Unveiling new horizons in drug transportation, Azide-PEG5-Tos plays a pivotal role in modifying drugs or drug carriers with azide groups, paving the way for subsequent conjugation with targeting ligands or therapeutic agents using click chemistry tactics. This groundbreaking approach catalyzes the creation of targeted drug delivery systems that hold the promise of heightened treatment efficacy and reduced adverse effects. The biocompatible nature of the PEG spacer further optimizes the pharmacokinetics of drug carriers, propelling advancements in therapeutic interventions to unparalleled heights.

Surface Modification: Embarking on the frontier of biomaterial surfaces, Azide-PEG5-Tos emerges as a transformative agent for enhancing biocompatibility and biofunctionality. By leveraging its capabilities to functionalize surfaces of biomaterials, profound improvements are witnessed in the performance of implants and medical devices. The strategic modification of these surfaces with PEG and biologically active molecules not only curtails protein adsorption and bacterial adhesion but also fosters robust tissue integration, heralding a new era of advanced implants and medical devices endowed with superior performance and longevity.

Molecular Imaging: Enter the realm of molecular imaging, where Azide-PEG5-Tos takes center stage in the synthesis of imaging probes tailored for cutting-edge applications. Utilizing Azide-PEG5-Tos to conjugate imaging agents to specific biomolecules, molecular imaging probes can be precisely directed to target tissues or cells within the intricate biological landscape. This precision enables the visualization of dynamic biological processes and disease states through innovative techniques like fluorescence imaging and positron emission tomography (PET).

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/Peptide Linker Phosphatase Cleavable Linker β-Glucuronide Linker β-Galactosidase Cleavable Linker Sulfatase Cleavable Linker Chemically Cleavable Linker Non-Cleavable Linker Services Acid Cleavable Linker/Hydrazone 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: C3-Amide-C4-NH2 | Boc-D-Dap(N3) CHA salt | Fmoc-N-amido-PEG4-propionic acid | Amine-PEG3-Lys(PEG3-N3)-PEG3-N3 | EC1167 | Methyltetrazine-PEG5-nhs ester | Asn-Pro-Val-PABC-MMAE (TFA) | Methyltetrazine-PEG12-acid | MDTF (free acid) | MC-GGFG-NH-CH2-O-CH2-(s-cyclopropane)-COOH | Azide-PEG5-Tos
Send Inquiry
Verification code
Inquiry Basket