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1,2-distearoyl-sn-glycero-3-phosphoethanolaMine-N-[carboxy(polyethylene glycol)-2000] (aMMoniuM salt)

Basic information Safety Supplier Related

1,2-distearoyl-sn-glycero-3-phosphoethanolaMine-N-[carboxy(polyethylene glycol)-2000] (aMMoniuM salt) Basic information

Product Name:
1,2-distearoyl-sn-glycero-3-phosphoethanolaMine-N-[carboxy(polyethylene glycol)-2000] (aMMoniuM salt)
Synonyms:
  • 1,2-distearoyl-sn-glycero-3-phosphoethanolaMine-N-[carboxy(polyethylene glycol)-2000] (aMMoniuM salt)
  • DSPE-PEG(2000) Carboxylic Acid
  • DSPE-PEG2000-COOH
  • DSPE-PEG-2K-CH2COOH
  • 1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[carboxy(polyethylene glycol)-2000] (sodium salt)
  • Poly(oxy-1,2-ethanediyl), α-[(9R)-6-hydroxy-6-oxido-1,12-dioxo-9-[(1-oxooctadecyl)oxy]-5,7,11-trioxa-2-aza-6-phosphanonacos-1-yl]-ω-(carboxymethoxy)-, ammonium salt (1:1)
CAS:
474922-20-8
MF:
C134H267N2O57P
MW:
0
Mol File:
474922-20-8.mol
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1,2-distearoyl-sn-glycero-3-phosphoethanolaMine-N-[carboxy(polyethylene glycol)-2000] (aMMoniuM salt) Chemical Properties

solubility 
Ethanol: Sparingly soluble: 1-10 mg/ml
InChIKey
MFOLYTNLQCGGBD-UHFFFAOYSA-N
SMILES
C(COC(=O)CCCCCCCCCCCCCCCCC)(OC(=O)CCCCCCCCCCCCCCCCC)COP(O)(=O)OCCNC(=O)O{-}CC{+n}OCC(=O)O.N
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1,2-distearoyl-sn-glycero-3-phosphoethanolaMine-N-[carboxy(polyethylene glycol)-2000] (aMMoniuM salt) Usage And Synthesis

Description

DSPE-PEG-CH2COOH, MW 2,000 is a PEG polymer with DSPE and carboxylic acid end groups. The DSPE-PEGs have been FDA approved for medical applications. The hydrophobic properties of the DSPE allow for the encapsulation and congregation of other hydrophobic drugs. The -COOH group can react with primary amines in the presence of activator, such as EDC or HATU, to form a stable amide bond.

Uses

DSPE-PEG-Carboxylic Acid is a phospholipid PEG conjugate. DSPE-PEG-Carboxylic Acid can be widely used in the delivery of targeted agents and genes[1].

References

[1] Su H, et, al. A brightly red emissive AIEgen and its antibody conjugated nanoparticles for cancer cell targeting imaging. Materials Chemistry Frontiers. Issue 10, 2022.
[2] XUEMING LI . Targeted delivery of doxorubicin using stealth liposomes modified with transferrin[J]. International Journal of Pharmaceutics, 2009, 373 1: Pages 116-123. DOI: 10.1016/j.ijpharm.2009.01.023
[3] LINGWEI MENG . Improving glioblastoma therapeutic outcomes via doxorubicin-loaded nanomicelles modified with borneol[J]. International Journal of Pharmaceutics, 2019, 567: Article 118485. DOI: 10.1016/j.ijpharm.2019.118485

1,2-distearoyl-sn-glycero-3-phosphoethanolaMine-N-[carboxy(polyethylene glycol)-2000] (aMMoniuM salt)Supplier

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