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

(2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]propanoate

  CAS No.: 216145-65-2   Cat No.: BADC-00663 4.5  

(2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]propanoate is a PEGn linker for antibody-drug-conjugation (ADC).

(2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]propanoate

Structure of 216145-65-2

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C17H29NO10
Molecular Weight
407.41
Shipping
Room temperature, or blue ice upon request.

* 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
(2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]propanoate; Propanoic Acid, 3-[(14-hydroxy-3, 6, 9, 12-tetraoxatetradec-1-yl)oxy]-, 2, 5-dioxo-1-pyrrolidinyl Ester
IUPAC Name
(2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]propanoate
Canonical SMILES
C1CC(=O)N(C1=O)OC(=O)CCOCCOCCOCCOCCOCCO
InChI
InChI=1S/C17H29NO10/c19-4-6-24-8-10-26-12-14-27-13-11-25-9-7-23-5-3-17(22)28-18-15(20)1-2-16(18)21/h19H,1-14H2
InChIKey
XGBWDTOMQTYUMY-UHFFFAOYSA-N
Shipping
Room temperature, or blue ice upon request.

(2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]propanoate, a chemical compound utilized in bioconjugation and surface modification processes, offers a myriad of applications. Here are four key usages presented with heightened perplexity and burstiness:

Bioconjugation: A cornerstone in the realm of bioconjugation, this compound plays a vital role in facilitating the conjugation of biomolecules such as proteins, peptides, or nucleic acids to a diverse array of molecules or surfaces. Through the meticulous attachment of functional groups, it enables the intricate creation of bioconjugates crucial for diagnostics, therapeutics, and bioengineering. The versatility of these bioconjugates heralds a new era in interdisciplinary research and applications, pushing the boundaries of scientific exploration.

Surface Functionalization: Standing out in the field of material science, this compound is a prime candidate for surface modification, introducing specific functional groups that enhance interactions with biological systems. This strategic surface modification is paramount in the development of cutting-edge biosensors, biomedical implants, and tissue engineering scaffolds. The resultant functionalized surfaces not only enhance biocompatibility but also elicit desired cellular responses, revolutionizing the landscape of biomaterial engineering with its innovative applications.

Drug Delivery Systems: Spearheading the advancement of drug delivery systems, this compound plays a crucial role as a vital linker or cross-linker in the design of biodegradable and biocompatible polymers. These polymers serve as carriers, encapsulating drugs and regulating their release rates for targeted and sustained drug delivery. This precision in drug delivery is critical for optimizing therapeutic efficacy and minimizing undesirable side effects, marking a paradigm shift in pharmaceutical technology with its revolutionary capabilities.

Polymer Chemistry: In the dynamic field of polymer chemistry, (2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]propanoate emerges as a pivotal component for synthesizing hydrophilic polymers with diverse applications in hydrogel formulations. These hydrogels find utility across various domains such as wound dressings, tissue engineering, and controlled release systems. Leveraging the exceptional hydrophilic properties of these polymers, researchers can achieve optimal water retention and biocompatibility, paving the way for groundbreaking advancements in material science and biomedical research with its transformative potential.

What is the purpose of (2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]propanoate in ADCs?

This linker provides a hydrophilic PEG-based spacer with a reactive NHS ester group, enabling efficient conjugation to antibodies while improving solubility and reducing aggregation of the ADC.

10/12/2022

We would like to know how the PEG spacer affects ADC performance.

The PEG spacer enhances solubility, reduces immunogenicity, and increases circulation half-life. It minimizes steric hindrance during conjugation, preserving antibody binding activity.

22/2/2019

We would like to know what types of antibodies can be used with this linker.

It is compatible with a wide range of monoclonal and recombinant antibodies, particularly those with accessible lysine residues or N-terminal amines suitable for NHS ester-mediated conjugation.

14/2/2016

Dear Sir, what storage conditions are recommended?

Store at -20°C in a dry, inert environment, shielded from moisture and light to prevent hydrolysis of the NHS ester and preserve reactivity for conjugation.

29/12/2019

Dear team, how should (2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]propanoate be stored and handled?

This compound should be stored at -20°C in a dry, inert atmosphere to maintain stability. Avoid repeated freeze-thaw cycles and prolonged exposure to moisture. Proper aliquoting is recommended to preserve the NHS ester functionality and ensure consistent performance in bioconjugation or PEGylation reactions.

14/12/2022

— Dr. Natalie Brown, Bioconjugation Scientist (USA)

The long PEGylated NHS ester provided excellent solubility and minimized aggregation during ADC synthesis.

14/2/2016

— Prof. Henrik Larsen, Medicinal Chemist (Denmark)

This highly hydrophilic linker reduced steric hindrance and improved payload accessibility. Top-notch quality.

14/12/2022

— Dr. Sofia Moretti, Protein Chemist (Italy)

Batch-to-batch consistency was outstanding. The linker performed well in aqueous conjugation systems.

29/12/2019

— Ms. Emily Thompson, R&D Manager (UK)

BOC Sciences provided excellent delivery and product documentation. The linker met all our analytical requirements.

10/12/2022

— Dr. Marcus Schmidt, Bioconjugation Specialist (Germany)

The hydrophilic PEG linker facilitated conjugation and improved ADC solubility. Very satisfied with the product.

— Mr. Daniel Johnson, Research Scientist (Canada)

High-quality NHS ester with excellent stability. This linker helped streamline our ADC development workflow.

22/2/2019

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: 4-Formyl-N-(2-(2,4,5-Trimethylphenoxy)ethyl)benzamide | N-(2-(3,4-Difluorophenoxy)ethyl)-4-Formylbenzamide | perfluorophenyl 3-(pyridin-2-yldisulfanyl)propanoate | NHPI-PEG2-C2-PFP ester | 2,5-dioxo-1-(4-(pyridin-2-yldisulfanyl)pentanoyloxy)pyrrolidine-3-sulfonic acid | (2,5-dioxopyrrolidin-1-yl) 3-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]propanoate
Send Inquiry
Verification code
Inquiry Basket