Amino-PEG12-Tris(-PEG24-acid)3

 Cat No.: BP-502158 4.5  

Amino-PEG12-Tris(-PEG24-acid)3 is a multifunctional, water-soluble polyethylene glycol (PEG)-based linker featuring a terminal primary amine for conjugation and a central trisubstituted architecture that presents three long PEG24-acid arms. The extended PEG12 segment provides conformational flexibility and spacing, while the three PEG24-acid termini (carboxylate-bearing) enable multivalent attachment or further derivatization, supporting stable coupling chemistries commonly used in PROTAC construction. In targeted protein degradation designs, such linkers help position a ligand-bearing moiety and the recruiting element with reduced steric interference, improving the probability of productive ternary complex formation and thereby supporting efficient ubiquitin–ligase engagement. The high hydrophilicity and extended chain length can also mitigate aggregation and enhance handling in aqueous assay conditions. This compound is valuable for researchers optimizing linker geometry and attachment strategies in PROTACs and related bifunctional degraders, particularly when multivalent or acid-functional conjugation handles are required.

Amino-PEG12-Tris(-PEG24-acid)3

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PROTAC Linker
Molecular Formula
C204H403N5O97
Molecular Weight
4478.41

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

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Amino-PEG12-Tris(-PEG24-acid)3 is a multifunctional, PEG-based linker engineered for PROTAC assembly, offering high aqueous solubility, conformational flexibility, and efficient spacing between binding elements. Its terminal amino functionality supports robust conjugation strategies, while the multiple PEG arms and carboxylated termini enable stable, well-defined attachment chemistries for targeted protein degradation workflows. The detailed structural and reactivity considerations are provided below.

Structure: The linker is built from repeating ethylene glycol units that form a flexible, hydrophilic PEG scaffold. It contains a primary amino group for coupling and a tris-substituted architecture bearing multiple carboxylic acid–terminated PEG arms. The structure features ether linkages within PEG and amide-forming potential at the amino terminus.

Reactivity: Suitable PROTAC construction typically relies on amine-reactive coupling at the amino terminus, followed by carboxyl-directed conjugation where needed. Common approaches include amide bond formation using activated carboxylic acids (for example, NHS/EDC-type activation) under mildly basic conditions, or orthogonal chemistries that preserve other functional groups. Solvents such as aqueous buffers with compatible organic co-solvents are commonly used to maintain PEG solubility and reaction efficiency.

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L

* 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

* Total Molecular Weight:
g/mol
Tip: Chemical formula is case sensitive. C22H30N4O √ c22h30n40 ╳
g/mol
g

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