You Searched For: N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride

Supplier: Merck

Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) for synthesis

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Supplier: Thermo Scientific

Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) 98+%

MSDS

Supplier: Thermo Scientific

Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) 98+%

MSDS Certificates

Catalog Number: (59002.)

Supplier: Biotium

Description: N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride

UOM: 1 * 100 mg

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Supplier: Apollo Scientific

Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)

Supplier: Apollo Scientific

Description: EDAC is a water soluble condensing reagent.

Supplier: G-Biosciences

Description: 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

Description: 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

Description: 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.

MSDS Certificates

Catalog Number: (PIERA35391)

Supplier: Thermo Fisher Scientific

Description: 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.

UOM: 1 * 10 mg

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Supplier: Merck Millipore (Calbiochem‎)

Description: N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride, Sigma-Aldrich®

Catalog Number: (MOLEM10152267)

Supplier: Molekula

Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)

UOM: 1 * 100 g

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Catalog Number: (MOLE71674020-25G)

Supplier: Molekula

Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)

UOM: 1 * 25 g

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 This is a MarketSource item. Additional charges may apply