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

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

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

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

Bürkle single-use powder and liquid funnels

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A truly clean filling aid for your lab

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

Catalog Number: (59002.)
Supplier: Biotium
Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride)
UOM: 1 * 100 mg
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EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) 98+%

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

MSDS Certificates

Product Image-ACRO171440010

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

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

MSDS

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

Supplier: Apollo Scientific
Description: EDAC is a water soluble condensing reagent.

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EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) crosslinker

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.

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

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

Market Source Item This is a MarketSource item. Additional charges may apply

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

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

Market Source Item This is a MarketSource item. Additional charges may apply

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EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

Supplier: Merck Millipore (Calbiochem‎)
Description: EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Sigma-Aldrich®

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EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Premium Grade, Pierce™

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.

Product Image-PIER77149

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), Pierce™

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

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EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride), No-Weigh™ Format, Pierce™

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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1-(3-Dimethylaminopropyl)piperazine 97%

Supplier: Apollo Scientific
Description: 1-(3-Dimethylaminopropyl)piperazine 97%

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1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide methiodide 98%

Supplier: Thermo Scientific
Description: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide methiodide 98%

MSDS Certificates

Product Image-ACRO334120010

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide methiodide 98%

Supplier: Thermo Scientific
Description: Appearance: White to off-white Crystalline powder

MSDS

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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
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