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You Searched For: 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide+methiodide


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Image Unavailable-76219-918

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide methiodide ≥98.0% (by titrimetric analysis)

Catalog Number: (76219-918)
Supplier: TCI America
Description: 1-[3-(Dimethylamino)propyl]-3-ethylcarbodiimide Methiodide, Purity: >98.0%(T), CAS: 22572-40-3, Molecular Formula: C9H20IN3, Molecular Weight: 297.18, Synonyms: EDC Methiodide, Form: Crystal - Powder, White - Almost white, Size: 5G
Image Unavailable-CAAAA10962-03

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

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

Certificates

Image Unavailable-Q-1955.0025BA

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

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

Image Unavailable-CAAAAB25057-06

EDC (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide) 98%

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

Certificates

Image Unavailable-TCD1601-005G

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) ≥98.0% (by titrimetric analysis)

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

SDS Certificates

Image Unavailable-89139-284

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

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
Image Unavailable-CA8.00907.8500

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

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

SDS Certificates


Image Unavailable-CAAAA10807-06

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

Supplier: Thermo Scientific Chemicals
Description: Crystalline.

Certificates

Image Unavailable-CA80051-568

EDC-HCl (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride) ≥98%, Calbiochem®

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

Certificates

Image Unavailable-CA82021-610

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.

Product Image-CAPIPG82073

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

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.

SDS Certificates

Product Image-CAPI22981

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

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.

SDS Certificates

Image Unavailable-CAAAJ62298-MC

4-Diphenylacetoxy-N-methylpiperidine methiodide

Catalog Number: (CAAAJ62298-MC)
Supplier: Thermo Scientific Chemicals
Description: Powder

Certificates


Image Unavailable-89157-518

(-)-Bicuculline methiodide (synthetic) ≥98% (by HPLC)

Catalog Number: (89157-518)
Supplier: Enzo Life Sciences
Description: GABAA receptor agonist.
Product Image-89156-694

4-Diphenylacetoxy-N-methylpiperidine methiodide ≥98% (by HPLC)

Catalog Number: (89156-694)
Supplier: Enzo Life Sciences
Description: Acetylcholine receptor ligand.
Product Image-89166-030

Propidium iodide ≥95% (by HPLC), Ultrapure

Catalog Number: (89166-030)
Supplier: Enzo Life Sciences
Description: DNA dye
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