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

Supplier: MilliporeSigma

Description: N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride for synthesis, CAS number 25952-53-8, Chemical formula C8H17N3*HCl 5g

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Supplier: Bachem Americas

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

Supplier: Thermo Scientific Chemicals

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

Supplier: Thermo Scientific Chemicals

Description: Crystalline.

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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

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Supplier: APOLLO SCIENTIFIC

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

Supplier: Spectrum Chemicals

Description: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride, purity: 98 %, CAS number: 25952-53-8, Molecular Formula: C8H17N3.HCl, Molecular weight: 191.71, Form: Solid, synonyms: monohydrochloride, EDAP, size: 5 g

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Supplier: BeanTown Chemical

Description: CAS: 25952-53-8; EC No: 247-361-2; MDL No: MFCD00012503; RTECS: FF2200000 Crystalline/Powder; Molecular Formula: C8H17N3·HCl; MW: 191.70 Melting Point: 110-115° Moisture Sensitive

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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: 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: Ambeed

Description: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride, Purity: 99%, CAS number: 25952-53-8, Appearance: Form: Crystal - Powder/ Colour: White - pale yellow, Storage: Keep in dark place, Sealed in dry, Store in freezer, under -20C, Size: 5G

Supplier: Matrix Scientific

Description: MF=C8H18CLN3 MW=191.71 CAS=25952-53-8 MDL=MFCD00012503 100G

Catalog Number: (103523-940)

Supplier: Invitrogen

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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Supplier: Chem Impex International

Description: A carbodiimide coupling reagent that generates a urea by-product which can be easily removed from the reaction media by extraction with water

Supplier: Invitrogen

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.

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Supplier: Invitrogen

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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