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


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Catalog Number: (CA8.00907.8500)
Supplier: MilliporeSigma
Description: N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride, Cas: 25952-53-8, Chemical Formula: C8H18ClN3, for synthesis, Size: 500mg

Supplier: Bachem Americas
Description: Synonym(s): EDAC · HCl#EDC · HCl#N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide · HCl#Water-soluble Carbodiimide#WSC

Supplier: TCI America
Description: [Coupling Agent for Peptides Synthesis]
CAS Number: 25952-53-8
MDL Number: MFCD00012503
Molecular Formula: C8H17N3
Molecular Weight: 191.70
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 115
Storage Temperature: 0-10°C
Supplier: Thermo Scientific Chemicals
Description: Crystalline.
Catalog Number: (89139-284)
Supplier: Biotium
Description: has recently been found to be very useful for fixing chelators or fluorescent ion indicators in situ, thus making it useful for post histological studies following the physiological experiments


Supplier: Thermo 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: 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: MilliporeSigma
Description: EDAC HCl is a water-soluble derivative of carbodiimide useful for conjugating haptens to proteins and polypeptides.
Supplier: Thermo 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.
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