Amino-PEG5-alcohol

 CAS No.: 34188-11-9  Cat No.: BP-500067  Purity: ≥95% 4.5  

Amino-PEG5-alcohol is a bifunctional polyethylene glycol linker featuring a terminal primary amine and a terminal hydroxyl group, providing a flexible, hydrophilic chain of five ethylene glycol units. The ether-rich PEG backbone confers conformational mobility and improves aqueous solubility, while the amine and alcohol termini serve as orthogonal handles for chemical conjugation. In PROTAC and targeted protein degradation workflows, such linkers are used to spatially separate the ligand-binding warhead from the E3 ligase–recruiting moiety, tuning effective intramolecular geometry and thereby influencing ternary complex formation and degradation potency. The PEG segment can also reduce non-specific hydrophobic interactions and help maintain solubility of larger conjugates during synthesis and biological testing. This linker is therefore valuable for constructing modular PROTACs, enabling systematic optimization of linker length and attachment chemistry to support reproducible, structure–function studies in targeted degradation research.

Amino-PEG5-alcohol

Structure of 34188-11-9

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Category
PROTAC Linker
Molecular Formula
C10H23NO5
Molecular Weight
237.29
Related CAS
933789-97-0 (polymer)
Appearance
Pale Yellow or Colorless Oily Matter

* For research and manufacturing use only. Not for human or clinical use.

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Purity
≥95%
Solubility
Soluble in DMSO (10 mm)
Appearance
Pale Yellow or Colorless Oily Matter
Storage
Store at 2-8°C
Shipping
Room temperature, or blue ice upon request.
IUPACName
2-[2-[2-[2-(2-aminoethoxy)ethoxy]ethoxy]ethoxy]ethanol
Synonyms
NH2-PEG5-OH; 14-Amino-3,6,9,12-tetraoxatetradecan-1-ol
Boiling Point
346.3±0.0 °C at 760 mmHg
Density
1.1±0.0 g/cm3
InChI Key
DEOUHEFHTMMUCM-UHFFFAOYSA-N
InChI
InChI=1S/C10H23NO5/c11-1-3-13-5-7-15-9-10-16-8-6-14-4-2-12/h12H,1-11H2
SMILES
C(COCCOCCOCCOCCO)N
Biological Activity
NH2-PEG5-OH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs[1]. NH2-PEG5-OH is also a noncleavable 5 unit PEG ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[2] . In Vitro: PROTACs contain two different ligands connected by a linker; one is a ligand for an E3 ubiquitin ligase and the other is for the target protein. PROTACs exploit the intracellular ubiquitin-proteasome system to selectively degrade target proteins[1] . ADCs are comprised of an antibody to which is attached an ADC cytotoxin through an ADC linker[2] .
ConcentrationVolumeMass1 mg5 mg10 mg
1 mM4.2143 mL21.0713 mL42.1425 mL
5 mM0.8429 mL4.2143 mL8.4285 mL
10 mM0.4214 mL2.1071 mL4.2143 mL

Amino-PEG5-alcohol is a PEG-based bifunctional linker designed for modular assembly in targeted protein degradation (PROTAC) workflows. Its flexible polyether backbone supports productive ternary complex formation, while the terminal amino and alcohol functionalities enable robust conjugation to ligands under standard bioconjugation and coupling strategies. This linker is well suited for constructing PROTACs where controlled spacing and aqueous compatibility are important, and the following sections describe its structure and practical reactivity for experimental use.

Structure: The linker comprises a flexible polyethylene glycol chain terminated by an amino group and a primary alcohol. It contains repeating ether linkages that confer conformational mobility and hydrophilicity, alongside a carbon–oxygen bond at the alcohol terminus. The amino functionality provides a reactive handle for amide or carbamate formation.

Reactivity: The amino group can be employed in amide coupling (via activated carboxylic acids) or carbamate formation (via activated carbonyl derivatives), while the alcohol can participate in esterification or conversion to leaving-group derivatives for subsequent substitution. Typical conditions use coupling reagents such as carbodiimides or activated chloroformates, with polar aprotic solvents and base to promote nucleophilic acyl substitution. Protecting-group strategies are often used to maintain chemoselectivity during stepwise PROTAC synthesis.

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* Our calculator is based on the following equation:
Concentration (start) x Volume (start) = Concentration (final) x Volume (final)
It is commonly abbreviated as: C1V1 = C2V2

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Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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