QBD10213

Fmoc-N-amido-dPEG^®₄-acid

• Formula empirica (notazione di Hill): C₂₆H₃₃NO₈
• Numero CAS: 557756-85-1
• Peso molecolare: 487.54
• Numero MDL: MFCD06656472
• Codice UNSPSC: 51171641
• ID PubChem: 329823895
• NACRES: NA.22

Proprietà

• Saggio: >90%
• Stato: solid or viscous liquid
• Impiego in reazioni chimiche: reaction type: Pegylations; reagent type: cross-linking reagent
• Gruppo funzionale: Fmoc; amine; carboxylic acid
• Architettura del polimero: shape: linear; functionality: heterobifunctional
• Condizioni di spedizione: ambient
• Temperatura di conservazione: −20°C
• Stringa SMILE: OC(CCOCCOCCOCCOCCNC(OCC1C(C=CC=C2)=C2C3=C1C=CC=C3)=O)=O
• InChI: 1S/C26H33NO8/c28-25(29)9-11-31-13-15-33-17-18-34-16-14-32-12-10-27-26(30)35-19-24-22-7-3-1-5-20(22)21-6-2-4-8-23(21)24/h1-8,24H,9-19H2,(H,27,30)(H,28,29); NUHRPLKTAAVHCZ-UHFFFAOYSA-N

Descrizione

Caratteristiche e vantaggi

Fmoc-N-amido-dPEG^®₄-acid is a novel Fmoc-protected amino acid containing a single molecular weight PEG (dPEG^®) spacer arm. These reagents are used to introduce a hydrophilic, non-immunogenic spacer into a peptide. Three different lengths of dPEG^® allow precise control of spacing and hydrophilicity. The Fmoc group can be removed, exposing the terminal amine, using piperidine as with standard peptide synthesis.Fmoc-N-amido-dPEG^®n-acid reagents are novel Fmoc-protected amino acids containing a single molecular weight PEG (dPEG^®) spacer arm (18.1 Å). This reagents is used to introduce a hydrophilic, non-immunogenic spacer into a peptide. Fmoc group can be removed, exposing the terminal amine, using piperidine as with standard peptide synthesis.

Note legali

Products Protected under U.S. Patents # 7,888,536 B2

dPEG is a registered trademark of Quanta BioDesign

Informazioni sulla sicurezza

• Codice della classe di stoccaggio: 11 - Combustible Solids
• Punto d’infiammabilità (°F): Not applicable
• Punto d’infiammabilità (°C): Not applicable