| Identification | Back Directory | [Name]
DBCO-C6-NHS ester | [CAS]
1384870-47-6 | [Synonyms]
DBCO-C6-NHS
DBCO-NHS ester 2
DBCO-C6-NHS ester
DBCO-(CH2)2-NH2-CO-(CH2)4COOH-NHS
Dibenzoazacyclooctyne-carboxylic acid succinimidyl ester
2,5-Dioxo-1-pyrrolidinyl 11,12-didehydro-ε-oxodibenz[b,f]azocine-5(6H)-hexanoate
Dibenz[b,f]azocine-5(6H)-hexanoic acid, 11,12-didehydro-ε-oxo-, 2,5-dioxo-1-pyrrolidinyl ester | [Molecular Formula]
C25H22N2O5 | [MDL Number]
MFCD22380763 | [MOL File]
1384870-47-6.mol | [Molecular Weight]
430.45 |
| Chemical Properties | Back Directory | [Boiling point ]
685.5±65.0 °C(Predicted) | [density ]
1.37±0.1 g/cm3(Predicted) | [form ]
Solid | [pka]
-0.17±0.20(Predicted) | [color ]
White to light yellow |
| Hazard Information | Back Directory | [Description]
DBCO-C6-NHS ester is an amine-reactive compound, which can be used to modify an amine-containing molecule in organic media. This reagent isn't soluble in aqueous media. The extended 6-carbon atom spacer arm improves solubility in commonly used organic solvents including dichloromethane, chloroform, THF, and ethyl acetate and it also improves derivatization efficiency and stability of conjugates. DBCO is commonly used for copper-free Click Chemistry reactions. | [Uses]
DBCO-C6-NHS Ester is a useful research chemical compound used in the synthesis of polar red-emitting rhodamine dyes with reactive groups. |
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