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Dibenzocyclooctyne-PEG4-N-hydroxysuccinimidyl ester

ALDRICH/764019 - ≥90%

Synonym: DBCO-PEG4-NHS ester; DBCO-PEG4-SE; DBCO-PEG4-succinimidyl ester

Empirical Formula (Hill Notation): C34H39N3O10
Molecular Weight: 649.69
MDL Number: MFCD26793797
Linear Formula: C34H39N3O10
Product Type: Chemical

Catalog Number PKG Qty. Price Quantity
45-764019-1MG 1 mg
$39.70
1/EA
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45-764019-5MG 5 mg
$127.00
1/EA
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45-764019-50MG 50 mg
$547.00
1/EA
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assay ≥90%
form paste
functional group NHS ester
InChI 1S/C34H39N3O10/c38-30(11-12-31(39)36-25-28-7-2-1-5-26(28)9-10-27-6-3-4-8-29(27)36)35-16-18-44-20-22-46-24-23-45-21-19-43-17-15-34(42)47-37-32(40)13-14-33(37)41/h1-8H,11-25H2,(H,35,38)
InChI key RRCXYKNJTKJNTD-UHFFFAOYSA-N
reaction suitability reaction type: click chemistry
  reagent type: linker
SMILES string O=C(CCC(NCCOCCOCCOCCOCCC(ON1C(CCC1=O)=O)=O)=O)N2CC3=C(C=CC=C3)C#CC4=C2C=CC=C4
storage temp. −20°C
Application: Dibenzocyclooctyne-PEG4-N-hydroxysuccinimidyl ester may be used in the synthesis of a prostate-specific membrane antigen (PSMA)-targeted single photon emission computed tomography (SPECT) agent via copper-less click chemistry.
Application: Succinimidyl ester (NHS, amine reactive) functionalized cyclooctyne derivative for incorporation of the cyclooctyne moiety into amine containing compounds or biomolecules. Cyclooctynes are useful in strain-promoted copper-free click chemistry cycloaddition reactions. This dibenzocyclooctyne will react with azide functionalized compounds or biomolecules without the need for a Cu(I) catalyst to result in a stable triazole linkage.

Applications Include:
• Protein-peptide conjugates
• Antibody-enzyme or antibody-drug conjugates
• Protein or peptide-oligonucleotide conjugates
• Surface modification
Packaging: 1, 5, 50 mg in clear glass bottle
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 12352108

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