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Merck

902551

Sigma-Aldrich

BocNH-PEG4-acid

Synonym(e):

2,2-Dimethyl-4-oxo-3,8,11,14,17-pentaoxa-5-azanonadecan-19-oic acid, Boc-NH-PEG4-CH2COOH

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About This Item

Empirische Formel (Hill-System):
C15H29NO8
CAS-Nummer:
Molekulargewicht:
351.39
UNSPSC-Code:
12352106
NACRES:
NA.22

Form

liquid

Eignung der Reaktion

reaction type: Pegylations
reagent type: cross-linking reagent

Brechungsindex

n/D 1.4641

Dichte

1.1395 g/mL

Funktionelle Gruppe

Boc
amine
carboxylic acid

Lagertemp.

−20°C

SMILES String

OC(COCCOCCOCCOCCNC(OC(C)(C)C)=O)=O

Verwandte Kategorien

Anwendung

This heterobifunctional, PEGylated crosslinker features a carboxylic acid at one end and Boc-protected amino group at the other, which can be deprotected with mildly acidic conditions. The hydrophilic PEG linker facilitates solubility in biological applications. BocNH-PEG4-acid 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

Technology Spotlight: Degrader Building Blocks for Targeted Protein Degradation

Rechtliche Hinweise

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

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Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable


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Shirude P S, et sl.
European Journal of Organic Chemistry, 2005, 5207-5215 (2005)
A biocompatible condensation reaction for the labeling of terminal cysteine residues on proteins.
Hongjun Ren et al.
Angewandte Chemie (International ed. in English), 48(51), 9658-9662 (2009-11-20)
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Rosnizeck I C, et al.
Inorgorganica Chimica Acta, 365 (1), 38-48 (2011)

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