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

16-Iodo-2,5,8,11,14-pentaoxahexadecane

  CAS No.: 104518-24-3   Cat No.: BADC-01548   Purity: 98% +(stabilized with Copper chip) 4.5  

16-Iodo-2,5,8,11,14-pentaoxahexadecane is a PEG-based halogenated ADC linker for site-specific cysteine conjugation, improving solubility, stability, and targeted delivery in antibody-drug conjugates.

16-Iodo-2,5,8,11,14-pentaoxahexadecane

Structure of 104518-24-3

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C11H23IO5
Molecular Weight
362.2

* 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
16-iodo-2,5,8,11,14-pentaoxahexadecane
IUPAC Name
1-[2-[2-[2-(2-iodoethoxy)ethoxy]ethoxy]ethoxy]-2-methoxyethan
Canonical SMILES
COCCOCCOCCOCCOCCI
InChI
InChI=1S/C11H23IO5/c1-13-4-5-15-8-9-17-11-10-16-7-6-14-3-2-12/h2-11H2,1H3
InChIKey
WPAHNAZXLUHBBI-UHFFFAOYSA-N
Solubility
Soluble
Pictograms
Harmful
Signal Word
Warning

16-Iodo-2,5,8,11,14-pentaoxahexadecane, a compound with exceptional chemical characteristics, finds diverse applications in the realm of bioscience. Here are four key applications presented with high perplexity and burstiness:

Radiolabeling: Playing a pivotal role in radiolabeling endeavors, 16-Iodo-2,5,8,11,14-pentaoxahexadecane is utilized for imaging and tracking studies. Through the substitution of the iodine atom with a radioactive isotope, researchers gain the ability to monitor the distribution and dynamics of the labeled molecule within biological systems. This technique proves invaluable for investigating pharmacokinetics, biodistribution, and receptor-ligand interactions.

Synthetic Chemistry: Serving as a crucial intermediate in organic synthesis, this compound facilitates the construction of intricate molecular architectures. Its iodine atom renders it a versatile precursor for various coupling reactions, such as Suzuki or Sonogashira couplings, empowering chemists to synthesize novel compounds with potential biological activities.

Drug Delivery Systems: Within the realm of drug delivery systems, 16-Iodo-2,5,8,11,14-pentaoxahexadecane plays a vital role, particularly in the design of liposomes and micelles. Thanks to its amphiphilic nature, the compound can interact with both hydrophilic and hydrophobic molecules, aiding in the encapsulation and targeted delivery of therapeutic agents. This capability enhances the bioavailability and efficacy of drugs, revolutionizing drug delivery strategies.

Polymer Chemistry: In the domain of polymer chemistry, this compound emerges as a valuable component capable of being incorporated as a monomer or functional group in the creation of advanced materials. Its unique structure presents opportunities for developing polymers with specific properties, such as enhanced solubility, biocompatibility, and responsiveness to stimuli. These innovative materials find applications in medical devices, coatings, and responsive hydrogels, showcasing the versatility and potential of 16-Iodo-2,5,8,11,14-pentaoxahexadecane in polymer science.

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: 13-Iodo-2,5,8,11-tetraoxatridecane | 23-Hydroxy-3,6,9,12,15,18,21-heptaoxatricosyl 4-methylbenzenesulfonate | 3-Oxo-1-phenyl-2,7,10,13,16-pentaoxa-4-azaoctadecan-18-oic acid | O-(2-(2-(2-(Prop-2-yn-1-yloxy)ethoxy)ethoxy)ethyl)hydroxylamine | 3,6,9,12,15,18,21,24,27-Nonaoxanonatriacontan-1-ol | N-(35-amino-3,6,9,12,15,18,21,24,27,30,33-undecaoxapentatriacontyl)-4-formylbenzamide | 2,5-Dioxopyrrolidin-1-yl 4-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)benzoate | (E)-Cyclooct-4-en-1-yl (2,5-dioxopyrrolidin-1-yl) carbonate | O-(3,6,9,12-Tetraoxapentadec-14-yn-1-yl)hydroxylamine | 2,5,8,11-Tetraoxatridecan-13-yl 4-methylbenzenesulfonate | 16-Iodo-2,5,8,11,14-pentaoxahexadecane
Send Inquiry
Verification code
Inquiry Basket