Hydroxy-PEG13-Boc

 Cat No.: BP-501748 4.5  

Hydroxy-PEG13-Boc is a heterobifunctional polyethylene glycol linker bearing a terminal hydroxyl group and a tert-butyl ester-protected carboxyl handle, providing a chemically versatile, water-compatible chain for PROTAC and related targeted protein degradation constructs. Structurally, it consists of a PEG oligomer of moderate length that confers flexibility, improved solubility, and reduced steric bias, while the tert-butyl ester protects the carboxyl group and can be selectively deprotected under suitable conditions to enable subsequent amide or ester coupling to ligands. In PROTAC design, PEG linkers act as spacers that position the two binding elements—typically an E3 ligase recruiter and a target-binding moiety—so that productive ternary complex formation can occur with minimal unfavorable contacts. This linker is valuable for researchers seeking to tune linker length and hydrophilicity, optimize conjugation chemistry, and systematically evaluate how linker-mediated geometry influences degradation efficiency and cellular activity.

Hydroxy-PEG13-Boc

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Category
PROTAC Linker
Molecular Formula
C₃₃H₆₆O₁₆
Molecular Weight
718.87

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

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Please store the product under the recommended conditions in the Certificate of Analysis.
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Room temperature in continental US; may vary elsewhere.
IUPACName
tert-butyl 3-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-[2-(2-hydroxyethoxy)ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]ethoxy]propanoate
InChI Key
VCMFXOTTYDVNJC-UHFFFAOYSA-N
InChI
InChI=1S/C33H66O16/c1-33(2,3)49-32(35)4-6-36-8-10-38-12-14-40-16-18-42-20-22-44-24-26-46-28-30-48-31-29-47-27-25-45-23-21-43-19-17-41-15-13-39-11-9-37-7-5-34/h34H,4-31H2,1-3H3
SMILES
CC(C)(C)OC(=O)CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO

Hydroxy-PEG13-Boc is a polyethylene glycol-based linker that provides a defined spacer length and terminal hydroxyl group for modular conjugation workflows. The tert-butyl ester-protected carboxyl functionality enables stepwise assembly of conjugates under standard organic synthesis conditions. Its PEG character helps tune hydrophilicity and conformational presentation, which can improve practical handling and downstream coupling strategies. The following sections describe its structure and the reactivity considerations relevant to PROTAC construction.

Structure: The linker comprises a hydrophilic PEG chain terminated by a hydroxyl group and a tert-butyl ester-protected carboxyl handle. It contains repeating ether linkages, a tert-butyl ester-protected carboxyl group, and a terminal alcohol. These features confer strong hydrogen-bonding capacity and favorable aqueous compatibility.

Reactivity: The tert-butyl ester can be cleaved using acid-mediated conditions to reveal the carboxylic acid when that handle is needed during PROTAC synthesis. The terminal hydroxyl supports formation of activated derivatives or coupling partners, commonly via standard functional-group interconversion routes. For assembly, the hydroxyl group can be functionalized independently, while the carboxylic acid can be revealed by controlled ester deprotection and activated for subsequent coupling. Solvent choice and temperature are selected to maintain linker stability and minimize side reactions.

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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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