You searched for: N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride

Supplier: MilliporeSigma

N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride, Cas: 25952-53-8, Chemical Formula: C8H18ClN3, for synthesis, Size: 500mg

Supplier: TCI America

[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

Crystalline.

Supplier: Bachem Americas

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

Supplier: Biotium

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

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: MilliporeSigma

EDAC HCl is a water-soluble derivative of carbodiimide useful for conjugating haptens to proteins and polypeptides.

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 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.