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DSPE-PEG-ICG

  Cat. No.:  DC66168   Featured
Chemical Structure
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More than 5000 active chemicals with high quality for research!
Field of application
DSPE phospholipids can be used as pharmaceutical excipients for emulsification and drug solubilization, and are important materials for slow release drug preparations such as liposomes, fat milk and nanoparticles in recent years. Modification of phospholipid molecules can make these preparations have the ability of release and targeting under specific conditions. Common modification methods include: disintegration time; Introducing immune factors to enhance targeting; Introduce markers for diagnosis and tracking.
Chemicals PropertiesBiological activity Related products COA MSDS Datasheet
Cas No.:
Chemical Name: DSPE-PEG-ICG
Synonyms: DSPE PEG ICG
SMILES: CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](COP(=O)(O)OCCNC(=O)COCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOS(=O)(=O)CCCCN1/C(=C\C=C\C=C\C=C\C2=[N+](CCCCS(=O)(=O)[O-])C3=CC=C4C=CC=CC4=C3C2(C)C)C(C)(C)C2=C1C=CC1=C2C=CC=C1)OC(=O)CCCCCCCCCCCCCCCCC
Formula: C166H290O55N3PS2
M.Wt: 3303.21
Purity: >98%
Sotrage: 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO
Cat. No. Product name Field of application
DC68215 DSG-PEG3400-N3 DSG-PEG3400-N3 is a conjugate composed of DSG, PEG chains, and terminal azido groups (-N3). DSG-PEG3400-Azide is a click chemistry reagent used for the targeted modification of liposomes/nanoparticles.
DC68214 DSG-PEG3400-Mal DSG-PEG3400-Mal is a conjugate composed of DSG, PEG chains, and maleimide (Mal). The maleimide group in DSG-PEG3400-Mal can undergo a specific Michael addition reaction with thiol-containing (-SH) biomolecules (such as peptides, antibodies, and aptamers), enabling targeted modification of liposomes/nanoparticles.
DC68163 DSPE-PEG-DSS6 DSS6-PEG-DSPE,DSPE-PEG-DSS6 is a composite molecule composed of phospholipids(DSPE),polyethylene glycol(PEG),and bone targeting peptide DSS6,mainly used for bone targeted drug delivery and bone tissue repair. Its core structure achieves precise targeting and efficient delivery through the synergistic effect of three parts.The DSS6 peptide consists of six Asp-Ser-Ser amino acid repeat sequences and can specifically recognize hydroxyapatite(HAp)in bone tissue.
DC68155 DMG-PEG2000-Biotin DMG-PEG2000-Biotin is a synthetic amphiphilic molecule composed of dimyristoyl glycerol (DMG), polyethylene glycol (PEG2000), and biotin functionalities. It is commonly employed in biomedical research for surface modification of lipid-based delivery platforms, such as lipid nanoparticles (LNPs) and liposomes. The PEG moiety enhances colloidal stability, prolongs circulation time, and reduces rapid clearance in vivo. The biotin termination facilitates conjugation to streptavidin-tagged biomolecules, exploiting the highly specific biotin-streptavidin interaction. Thus, DMG-PEG2000-Biotin is valuable for drug-delivery optimization, targeted therapeutic approaches, and in vitro diagnostic assay development.
DC68154 Thiol-PEG2000-DMG Thiol-PEG2000-DMG is a phospholipid polyPEG which can be used to prepare liposomes or nanoparticles. The terminal thiol group reacts with maleimide, OPSS, vinylsulfone and transition metal surfaces including gold, silver, etc.
DC68153 DMG-PEG2000-OH DMG-PEG2000-OH is a PEG derivative that can be used to construct drug delivery vehicles.
DC68152 DMG-PEG2000-SH DMG-PEG2000-SH is a PEG derivative that can be used to construct drug delivery vehicles.
DC67619 DMG-PEG-TCO (MW2000) DMG-PEG2000-TCO offer the ability to easily conjugate to specific biomolecules via metal free click chemistry to tetrazines. By changing the PEG length, one can change the micelle size, immunological safety, and change the drug release rate.
DC67603 DMG-PEG-Mal, MW 2,000 DMG-PEG-Mal, MW 2,000 is a lipid PEG consisting of DMG and maleimide for reacting with thiols between pH 6.5 to 7.5
DC67571 DMG-PEG-Mannose DMG-PEG-Mannose is a specialized functionalized lipid used primarily for the targeted delivery of lipid nanoparticles (LNPs) and liposomes to cells expressing mannose receptors, such as macrophages and dendritic cells. It combines a 1,2-dimyristoyl-sn-glycerol (DMG) lipid anchor with a polyethylene glycol (PEG) spacer and a terminal mannose sugar moiety.
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Products are chemical reagents for research use only and are not intended for human use. We do not sell to patients.
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