902683

BocNH-PEG5-acid

• Sinonimo/i: 2,2-Dimethyl-4-oxo-3,8,11,14,17,20-hexaoxa-5-azadocosan-22-oic acid, Boc-NH-PEG5-CH₂COOH
• Formula empirica (notazione di Hill): C₁₇H₃₃NO₉
• Numero CAS: 890152-41-7
• Peso molecolare: 395.45
• Numero MDL: MFCD31656900
• Codice UNSPSC: 12352106
• NACRES: NA.22

Proprietà

• Stato: liquid
• Impiego in reazioni chimiche: reaction type: Pegylations; reagent type: cross-linking reagent
• Gruppo funzionale: Boc; amine; carboxylic acid
• Temperatura di conservazione: −20°C
• Stringa SMILE: OC(COCCOCCOCCOCCOCCNC(OC(C)(C)C)=O)=O
• InChI: 1S/C17H33NO9/c1-17(2,3)27-16(21)18-4-5-22-6-7-23-8-9-24-10-11-25-12-13-26-14-15(19)20/h4-14H2,1-3H3,(H,18,21)(H,19,20); OLLNIAGWMCSEJB-UHFFFAOYSA-N

Descrizione

Applicazioni

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-PEG5-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.

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Note legali

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

Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 10 - Combustible liquids
• Classe di pericolosità dell'acqua (WGK): WGK 3
• Punto d’infiammabilità (°F): Not applicable
• Punto d’infiammabilità (°C): Not applicable