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

Aminooxy-PEG2-alcohol

  CAS No.: 185022-12-2   Cat No.: BADC-01012   Purity: ≥95% 4.5  

Aminooxy-PEG2-alcohol is a non-cleavable 2-unit PEG ADC linker that is used in the synthesis of antibody conjugated drugs (ADCs). Aminooxy-PEG2-alcohol is also a PROTAC linker, belonging to the PEG class, which can be used to synthesize PROTAC molecules.

Aminooxy-PEG2-alcohol

Structure of 185022-12-2

Quality
Assurance

Worldwide
Delivery

24/7 Customer
Support
Category
ADC Linker
Molecular Formula
C4H11NO3
Molecular Weight
121.14
Shipping
Room temperature
Shipping
Store at 2-8°C

* 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-[2-(aminooxy)ethoxy]ethan-1-ol; O-[2-(2-Hydroxyethoxy)ethyl]hydroxylamine; Ethanol, 2-[2-(aminooxy)ethoxy]-
IUPAC Name
2-(2-aminooxyethoxy)ethanol
Canonical SMILES
C(COCCON)O
InChI
InChI=1S/C4H11NO3/c5-8-4-3-7-2-1-6/h6H,1-5H2
InChIKey
CMECGOAFIHUPBI-UHFFFAOYSA-N
Density
1.116±0.06 g/cm3 (Predicted)
Solubility
10 mm in DMSO
Appearance
Pale Yellow or Colorless Oily Matter
Shelf Life
≥ 2 years
Shipping
Room temperature
Storage
Store at 2-8°C
Boiling Point
265.9±20.0°C (Predicted)
Form
Solid

Aminooxy-PEG2-alcohol, a versatile compound with diverse applications in biomedical and biotechnological research, presents numerous opportunities for advancement. Here are four key applications crafted with high perplexity and burstiness:

Bioconjugation: Functioning as a bioconjugation reagent, Aminooxy-PEG2-alcohol enables the precise attachment of various biomolecules, such as proteins, peptides, or antibodies, to surfaces or other molecules. Its unique reactivity with aldehyde or ketone groups allows for site-specific conjugation, a critical element in the development of diagnostic assays, therapeutic agents, and targeted drug delivery systems. The intricate capabilities of Aminooxy-PEG2-alcohol in facilitating such precise conjugations underscore its significance in the domains of biomedical research and biotechnology.

Protein Labeling: Within the realm of proteomics, Aminooxy-PEG2-alcohol assumes a pivotal role in selectively labeling proteins to track and analyze protein interactions, distribution, and function within biological systems. Through the modification of proteins with this compound, researchers can plunge into the dynamic realm of protein dynamics and interactions, shedding light on the complexities of cellular processes. This application emphasizes the importance of Aminooxy-PEG2-alcohol in unraveling the intricate tapestry of protein-related phenomena within biological systems.

Glycobiology: Aminooxy-PEG2-alcohol finds its niche in the exploration of glycoproteins and glycans, enabling the labeling and identification of crucial carbohydrate moieties. By engaging with oxidized sugars, this reagent empowers scientists to delve into protein glycosylation patterns and their implications in diverse biological functions and diseases. The realm of glycobiology, enriched by the capabilities of Aminooxy-PEG2-alcohol, holds the key to unraveling the enigmas surrounding immune responses, cell signaling, and disease biomarkers, showcasing the compound's significance in unlocking the mysteries of intricate biological systems.

Drug Delivery Development: In the landscape of drug delivery research, Aminooxy-PEG2-alcohol emerges as a pivotal component in attaching therapeutic agents to delivery vehicles like liposomes or nanoparticles through oxime bond formation. This strategic approach ensures the precise release of drugs at the designated target site, minimizing off-target effects and amplifying therapeutic efficacy. The precision and control offered by Aminooxy-PEG2-alcohol in drug delivery systems underscore its role in the advancement of sophisticated and safer drug delivery mechanisms.

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: N-(5-Hydroxypentyl)maleimide
Send Inquiry
Verification code
Inquiry Basket