mPEG2-SH, namely Methyl Diethylene Glycol Thiol (2-(2-methoxyethoxy)ethane-1-thiol), is a monodisperse, short-chain polyethylene glycol (PEG) derivative. It features a well-defined molecular structure and a single molecular weight, consisting of a methoxy cap, two ethylene glycol units, and a terminal thiol (-SH) group. Compared to polydisperse PEG, monodisperse PEG offers advantages such as uniform molecular weight, high batch-to-batch reproducibility, and ease of purification and characterization, making it valuable for applications including gold nanoparticle modification, bioconjugation, and molecular linker design.
I. Basic Information
| Item | Content |
|---|---|
| Name | 2-(2-methoxyethoxy)ethane-1-thiol |
| Abbreviation | mPEG2-SH |
| CAS Number | 88778-21-6 |
| Purity | ≥98% |
| Solubility | Soluble in water and most organic solvents |
II. Structural Characteristics and Mechanism of Action
mPEG2-SH consists of precisely two ethylene glycol units with a single molecular weight, minimizing the impact of PEG molecular weight distribution variability on experimental result analysis. The terminal thiol (-SH) group serves as the core functional site with dual conjugation capabilities:
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Gold–Sulfur (Au–S) Bonding:Exhibits high affinity for noble metal surfaces such as gold and silver, forming stable surface modification layers suitable for gold nanoparticle modification and biosensor construction.
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Thioether Bond Formation:Undergoes thiol–maleimide coupling reactions (typically at pH 6.5–7.5) with maleimide groups, enabling site-specific PEGylation of biomacromolecules such as proteins and antibodies.
The PEG segment imparts good water solubility and biocompatibility to the molecule. The short-chain PEG structure helps reduce steric hindrance and is suitable for applications requiring precise control over modification layer thickness.
III. Main Applications
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Gold Nanoparticle Modification:Forms stable covalent conjugation through Au–S bonds, improving nanoparticle dispersion stability, biocompatibility, and reducing particle aggregation.
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Site-Specific Protein PEGylation:The thiol group undergoes specific coupling with maleimide, enabling site-directed modification of proteins, antibodies, and other biomacromolecules.
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Bioconjugation and Molecular Linkers:Serves as a short PEG connecting unit for modulating spatial distance and flexibility between biomolecules and functional small molecules, with potential applications in ADC, PROTAC, and chemical biology molecular design.
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Self-Assembled Monolayers and Biosensors:Utilizes the binding capability of thiol groups to metal surfaces to construct functionalized surfaces, reducing non-specific adsorption and enhancing detection signal stability.
IV. Related PEG Derivatives
| Name | Abbreviation | CAS # |
|---|---|---|
| Methyl Hexaethylene Glycol Azide | mPEG6-N3 | 1043884-49-6 |
| Methyl Diethylene Glycol Thiol | mPEG2-SH | 88778-21-6 |
| Methyl Heptaethylene Glycol | mPEG7-OH | 4437-01-8 |
| Methyl Octaethylene Glycol Amine | mPEG8-NH2 | 869718-81-0 |
| Methyl Hexatriacontaethylene Glycol Propionic Acid | mPEG36-PA | — |
| Methyl Pentaethylene Glycol Bromide | mPEG5-Br | 854601-80-2 |
| Methyl Triethylene Glycol Tosylate | mPEG3-OTs | 518012-62-9 |
| Methyl Pentaethylene Glycol Acetic Acid | mPEG5-CH2COOH | 16142-03-3 |
| Methyl Heptaethylene Glycol Succinimidyl Carbonate | mPEG7-SC | — |
| Methyl Nonaethylene Glycol Succinimidyl Propionate | mPEG9-SPA | — |










