Supplier: Merck

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid Hydrochlorid zur Synthese

Supplier: Apollo Scientific

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid Hydrochlorid

Supplier: Thermo Fisher Scientific

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid Hydrochlorid 98+%

Supplier: Biotium

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid Hydrochlorid

Supplier: Thermo Fisher Scientific

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid Hydrochlorid 98+%

Supplier: Apollo Scientific

EDAC is a water soluble condensing reagent.

Supplier: G-Biosciences

EDC is a heterobifunctional, water-soluble, zero-length carbodiimide crosslinker that is used to couple carboxyl groups to primary amines. EDC activates carboxyl groups first and forms amine reactive O-acylisourea imtermediate that spontaneously reacts with primary amines to form an amide bond and isourea by-product.

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce Premium Grade EDC is our highest quality formulation of this popular carbodiimide crosslinker, specially characterized for applications where product integrity and risk minimization are paramount.

Supplier: Thermo Fisher Scientific

Thermo Scientific Pierce EDC is a carboxyl- and amine-reactive zero-length crosslinker. EDC reacts with a carboxyl group first and forms an amine-reactive O-acylisourea intermediate that quickly reacts with an amino group to form an amide bond with release of an isourea by-product. The intermediate is unstable in aqueous solutions and so two-step conjugation procedures rely on N-hydroxysuccinimide (NHS) for stabilization. Failure to react with an amine will result in hydrolysis of the intermediate, regeneration of the carboxyl, and release of an N-substituted urea. A side reaction is the formation of an N-acylurea, which is usually restricted to carboxyls located in hydrophobic regions of proteins.

Supplier: Merck Millipore (Calbiochem‎)

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid Hydrochlorid, Sigma-Aldrich®

Supplier: Molekula

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid Hydrochlorid

Supplier: Molekula

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid Hydrochlorid

Supplier: BACHEM BIOCHEMICA

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimid Hydrochlorid