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880228P

Avanti

DSPE-PEG(2000) Azide

Avanti Research™ - A Croda Brand, powder

Synonym(s):

1,2-distearoyl-sn-glycero-3-phosphoethanolamine-N-[azido(polyethylene glycol)-2000] (ammonium salt)

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About This Item

CAS Number:
1938081-40-3
UNSPSC Code:
12352211
NACRES:
NA.25

form

powder

packaging

pkg of 1 × 10 mg (880228P-10mg)
pkg of 1 × 100 mg (880228P-100mg)
pkg of 1 × 25 mg (880228P-25mg)
pkg of 1 × 50 mg (880228P-50mg)
pkg of 1 × 500 mg (880228P-500mg)

manufacturer/tradename

Avanti Research™ - A Croda Brand

lipid type

click reagents
polymerizable lipids

shipped in

dry ice

storage temp.

−20°C

SMILES string

[H][C@@](COP([O-])(OCCNC(OCC)=O)=O)(OC(CCCCCCCCCCCCCCCCC)=O)COC(CCCCCCCCCCCCCCCCC)=O.[N-]=[N+]=NCCO.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOOCC.CCOO(CC)OCC.[NH

General description

DSPE-PEG(2000) azide is used to prepare conjugated polymer nanoparticles.

Packaging

20 mL Clear Glass Screw Cap Vial (880228P-500mg)
5 mL Amber Glass Screw Cap Vial (880228P-100mg)
5 mL Amber Glass Screw Cap Vial (880228P-10mg)
5 mL Amber Glass Screw Cap Vial (880228P-25mg)
5 mL Amber Glass Screw Cap Vial (880228P-50mg)

Legal Information

Avanti Research is a trademark of Avanti Polar Lipids, LLC

Storage Class Code

11 - Combustible Solids

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Conjugated Polymers for Biological and Biomedical Applications, 29-29 (2018)
Elizabeth D Hood et al.
Bioconjugate chemistry, 29(11), 3626-3637 (2018-09-22)
Liposomes are a proven, versatile, and clinically viable technology platform for vascular delivery of drugs and imaging probes. Although targeted liposomes have the potential to advance these applications, complex formulations and the need for optimal affinity ligands and conjugation strategies
John C Jewett et al.
Journal of the American Chemical Society, 132(11), 3688-3690 (2010-03-02)
Bioorthogonal chemical reactions, those that do not interact or interfere with biology, have allowed for exploration of numerous biological processes that were previously difficult to study. The reaction of azides with strained alkynes, such as cyclooctynes, readily forms a triazole

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