Dibenzocyclooctyne-PEG4-N-hydroxysuccinimidyl ester
ALDRICH/764019 - ≥90%
Synonym: DBCO-PEG4-NHS ester; DBCO-PEG4-SE; DBCO-
Empirical Formula (Hill Notation): C34H39N3O10
Molecular Weight: 649.69
MDL Number: MFCD26793797
Linear Formula: C34H39N3O10
Product Type: Chemical
| assay | ≥90% |
| form | paste |
| functional group | NHS ester |
| InChI | 1S/C34H39N3O10/c38-30(11- |
| InChI key | RRCXYKNJTKJNTD-UHFFFAOYSA |
| Quality Level | 100 ![]() |
| reaction suitability | reaction type: click chemistry |
| reagent type: linker | |
| SMILES string | O=C(CCC(NCCOCCOCCOCCOCCC( |
| 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 |

