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Azido-dPEG®4-acid

ALDRICH/QBD10502

Synonym: 15-Azido-4,7,10,13-tetraoxapentadecanoic acid; 3-[2-[2-[2-(2-Azidoethoxy)ethoxy]ethoxy]ethoxy]propanoic acid; Polyethylene glycol

CAS Number: 1257063-35-6
Empirical Formula (Hill Notation): C11H21N3O6
Molecular Weight: 291.30
MDL Number: MFCD12406155
Linear Formula: C11H21N3O6
Product Type: Chemical
Catalog Number PKG Qty. Price Quantity
45-QBD10502-100MG 100 mg
 $315.00
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45-QBD10502-1000MG 1000 mg
 $787.00
1/EA		 Add To Favorites

 

assay >90%
form solid or viscous liquid
functional group azide
  carboxylic acid
InChI 1S/C11H21N3O6/c12-14-13-2-4-18-6-8-20-10-9-19-7-5-17-3-1-11(15)16/h1-10H2,(H,15,16)
InChI key BODPHGOBXPGJKO-UHFFFAOYSA-N
polymer architecture shape : linear
functionality : heterobifunctional
reaction suitability reaction type: click chemistry
  reagent type: cross-linking reagent
reaction type: click chemistry
shipped in ambient
SMILES string OC(CCOCCOCCOCCOCCN=[N+]=[N-])=O
storage temp. −20°C
Features and Benefits: The azido-dPEG®4 contains an azide function on one end of a single molecular weight dPEG® spacer (17.7 Å) and a reactive group on the other end of the spacer. The dPEG® spacer is hydrophilic and non-immunogenic and improves the water solubility of the target molecule while reducing the immunogenicity and increasing the hydrodynamic volume of the target. The acid function may be activated with 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC) or N,N′-dicyclohexylcarbodiimide (DCC) for conjugation to an amine. The azide group reacts with an alkyne in the well-known click chemistry reaction. The click chemistry reaction proceeds by copper(I) or ruthenium catalysis or in a strain-catalyzed reaction with certain types of alkyne partners.
Legal Information: dPEG is a registered trademark of Quanta BioDesign
Legal Information: Products Protected under U.S. Patents # 7,888,536 B2
RIDADR NONH for all modes of transport
WGK Germany WGK 3
Flash Point(F) Not applicable
Flash Point(C) Not applicable
Purity >90%
Storage Temp. −20°C
UNSPSC 12352106

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