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DSPE-PDP//Cas No.: 144735-79-5

December 19, 2025

DSPE-PDP(cas no: 144735-79-5)

DSPE-PDP is a functional phospholipid-PEG conjugate used to stabilize lipid nanoparticles and provide a reducible disulfide linkage for thiol-containing molecules, enabling reversible conjugation for targeted and functionalized drug delivery systems.

Product Name DSPE-PDP
Synonyms DSPE-PDP;1,2-distearoyl-sn-glycero-3-phosphoethanolamine–N-[3-(2-pyridyldithio)propionate](sodiumsalt);1,2-distearoyl-sn-glycero-3-phosphoethanolamine–N-[3-(2-pyridyldithio)propionate](sodiumsalt)(DSPE-PDP);Octadecanoicacid,1-[3-hydroxy-3-oxido-8-oxo-10-(2-pyridinyldithio)-2,4-dioxa-7-aza-3-phosphadec-1-yl]-1,2-ethanediylester,(R)-(9CI);DSPE-SPDP;DSPE-PDP(SodiumSalt)FolicacidPEGDSPE
CAS NO 144735-79-5
Purity 98% above
Appearance White Powder
MF C49H89N2O9PS2
MW 945.34
Contact selina@coreychem.com

Key Functions

1. Stabilization of lipid nanocarriers

  • DSPE anchors the molecule into lipid bilayers of liposomes, LNPs, or micelles.

  • PEG provides a steric hydration layer that improves particle stability, dispersity, and in vivo circulation.

  • Widely applied in nucleic acid therapeutics, protein delivery, and vaccine systems.


2. Reducible disulfide–thiol conjugation (core advantage)

  • The PDP group contains an active disulfide bond that reacts with thiol groups (–SH) under mild conditions.

  • Compatible with:

    • Cysteine-containing peptides (e.g., RGD, CPP)

    • Thiolated antibodies or antibody fragments

    • Thiol-modified proteins, sugars, or small molecules

  • Features:

    • High selectivity and mild reaction conditions

    • Reversible linkage that can release the conjugated molecule in reductive environments (e.g., intracellular)


3. Construction of targeted and functionalized delivery systems

  • Enables targeted liposomes or LNPs

  • Supports:

    • Tumor- or cell-specific targeting

    • Controlled intracellular release

    • Fluorescent or imaging labeling

    • Conjugation of proteins, peptides, or drugs


4. PEGylation effect

  • PEG forms a hydrated layer on the particle surface

  • Reduces plasma protein adsorption and immune clearance

  • Extends circulation time and improves bioavailability

  • Enhances biocompatibility for in vivo applications

Functional DSPE‑PEG Analogues and CAS Numbers    
Product Name Function / Application CAS Number
DSPE‑PEG‑Maleimide (e.g., DSPE‑PEG2000‑Maleimide) Terminal Maleimide group allows selective conjugation with thiol (‑SH) containing molecules, used for targeted or functionalized nanocarriers. 474922‑22‑0
DSPE‑PEG‑NH₂ (DSPE‑PEG‑Amine) Terminal amine (‑NH₂) can react with activated carboxyl/NHS ester groups, used for conjugating proteins, peptides, antibodies, etc. 474922‑26‑4
DSPE‑PEG‑COOH (DSPE‑PEG‑Carboxylic acid) Terminal carboxyl (‑COOH) can be activated via EDC/NHS chemistry to conjugate amine-containing ligands. 1403744‑37‑5
DSPE‑PEG‑Azide (DSPE‑PEG‑N₃) Terminal azide group allows Click chemistry (e.g., conjugation with alkyne-containing ligands). 1938081‑39‑0
DSPE‑PEG‑Biotin (DSPE‑PEG‑Biotinyl) Terminal biotin enables labeling or capture via the biotin‑streptavidin system. 385437‑57‑0

 

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