mPEG4-thiol

 CAS No.: 52190-55-3  Cat No.: BP-501244  Purity: >95% 4.5  

mPEG4-thiol is a methoxy-capped PEG thiol linker component containing an ether-rich spacer and a terminal sulfhydryl group. Its thiol handle enables chemoselective conjugation with maleimide, haloacetamide, activated disulfide, and related thiol-reactive partners, allowing researchers to introduce PEGylated thioether or disulfide-linked segments into PROTAC-related intermediates. The PEG chain can contribute hydrophilicity and conformational mobility. This product is useful for preparing linker-modified degrader analogues, constructing probe-oriented conjugates, and evaluating how sulfur-containing PEG linker motifs affect molecular presentation, conjugation efficiency, and targeted degradation research workflows.

mPEG4-thiol

Structure of 52190-55-3

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Category
PROTAC Linker
Molecular Formula
C9H20O4S
Molecular Weight
224.32
Appearance
Colorless Liquid

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

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Purity
>95%
Appearance
Colorless Liquid
Storage
Please store the product under the recommended conditions in the Certificate of Analysis.
Shipping
Room temperature in continental US; may vary elsewhere.
IUPACName
2-[2-[2-(2-methoxyethoxy)ethoxy]ethoxy]ethanethiol
Synonyms
2,5,8,11-Tetraoxatridecane-13-thiol
Boiling Point
293.5±30.0 °C at 760 mmHg
InChI Key
VXEBAWYHFQRROQ-UHFFFAOYSA-N
InChI
InChI=1S/C9H20O4S/c1-10-2-3-11-4-5-12-6-7-13-8-9-14/h14H,2-9H2,1H3
SMILES
COCCOCCOCCOCCS

mPEG4-thiol is a methoxy PEG thiol linker that combines hydrophilic PEG spacing with thiol-directed conjugation chemistry. It is suitable for PROTAC designs requiring thioether connectivity and improved polar character without introducing a long spacer. The molecule is described below.

Structure: The linker contains a methoxy-terminated PEG chain and a terminal thiol group. It features flexible ether bonds, a polar nonionic backbone, and a sulfur nucleophile for selective coupling.

Reactivity: The thiol can undergo Michael addition with maleimide-functional fragments or nucleophilic substitution with activated haloalkyl partners. Reactions are commonly conducted under mild, non-oxidizing conditions in polar organic or aqueous-organic solvents. Fresh thiol solutions, compatible base, and minimized competing electrophiles support clean PROTAC intermediate formation.

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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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g/mol
Tip: Chemical formula is case sensitive. C22H30N4O c22h30n40
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