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Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)
Catalog Number: APOSOR5163-500G
UOM: 1 * 500 g
Supplier: Apollo Scientific

Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) 98+%
Catalog Number: A10807.14
UOM: 1 * 25 g
Supplier: Thermo Fisher Scientific

Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)
Catalog Number: 59002.
UOM: 1 * 100 mg
Supplier: Biotium


Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) for synthesis
Catalog Number: MERC8.00907.0025
UOM: 1 * 25 g
Supplier: Merck

Description: EDAC is a water soluble condensing reagent.
Catalog Number: APOSBIE1308-500G
UOM: 1 * 500 g
Supplier: Apollo Scientific

Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) 98+%
Catalog Number: ACRO171440010
UOM: 1 * 1 g
Supplier: Thermo Fisher Scientific

MSDS


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.
Catalog Number: BC25-5
UOM: 1 * 5 g
Supplier: G-Biosciences


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.
Catalog Number: PIERPG82074
UOM: 1 * 500 g
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.
Catalog Number: PIER22981
UOM: 1 * 25 g
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.
Catalog Number: PIERA35391
UOM: 1 * 10 mg
Supplier: Thermo Fisher Scientific


Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®
Catalog Number: 341006-25
UOM: 1 * 25 g
Supplier: Merck Millipore (Calbiochem‎)


Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)
Catalog Number: MOLE71674020-25G
UOM: 1 * 25 g
Supplier: Molekula


Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)
Catalog Number: MOLEM10152267
UOM: 1 * 100 g
Supplier: Molekula


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