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Merck

910007

20-Azido-3,6,9,12,15,18-hexaoxaicosanoic acid

95%

동의어(들):

Azido-PEG6-CH2CO2H, Azido-PEG6-acid, N3-PEG6-CH2COOH

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제품정보 (DICE 배송 시 비용 별도)

실험식(Hill 표기법):
C14H27N3O8
CAS 번호:
Molecular Weight:
365.38
UNSPSC Code:
12352106
Assay:
95%
Form:
(Liquid or Semi-Solid or Paste or Solid)
기술 서비스
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assay

95%

form

(Liquid or Semi-Solid or Paste or Solid)

reaction suitability

reaction type: click chemistry, reagent type: cross-linking reagent

functional group

azide, carboxylic acid

storage temp.

2-8°C

SMILES string

OC(COCCOCCOCCOCCOCCOCCN=[N+]=[N-])=O

Application

This heterobifunctional, PEGylated crosslinker 20-Azido-3,6,9,12,15,18-hexaoxaicosanoic acid features a carboxyl group at one end and azide at the other. The hydrophillic PEG linker facilitates solubility in biological applications. This azido-PEG6-acid linker can be used for bioconjugation or as a building block for synthesis of small molecules, conjugates of small molecules and/or biomolecules, or other tool compounds for chemical biology and medicinal chemistry that require ligation. Examples of applications include its synthetic incorporation into antibody-drug conjugates or proteolysis-targeting chimeras (PROTAC® molecules) for targeted protein degradation.

Legal Information

PROTAC is a registered trademark of Arvinas Operations, Inc., and is used under license


저장 등급

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable



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시험 성적서(COA)

Lot/Batch Number

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문서 라이브러리 방문



Yong Ma et al.
Bioconjugate chemistry, 21(11), 1994-1999 (2010-10-14)
A surface-bound cytomimetic assembly based on chemically selective and biocompatible immobilization and further modification of intact liposome is described. Liposomes carrying PEG-triphenylphosphine were chemoselectively immobilized onto azide-modified glass slides through Staudinger ligation, followed by modification with azide-modified lactose as a
Joel Hwang et al.
Chemical communications (Cambridge, England), 50(24), 3159-3162 (2014-01-30)
Oligo(ethylene glycol)-linked light fluorous tags have been found to be optimal for conjugating to glycans for both high-yield enzymatic glycosylation reactions using one-pot multienzyme (OPME) systems and quick product purification using fluorous solid-phase extraction (FSPE) cartridges. The combination of OPME
Souad Kachbi-Khelfallah et al.
Beilstein journal of organic chemistry, 12, 1366-1371 (2016-08-26)
The use of nanotechnologies for biomedical applications took a real development during these last years. To allow an effective targeting for biomedical imaging applications, the adsorption of plasmatic proteins on the surface of nanoparticles must be prevented to reduce the