1-ethyl-3-(3-dimethylaminopropyl)carbodiimide suppliers USA
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Commonly known as EDAC, EDC or EDCI, this carbodiimide HCl salt is used as a coupling reagent in the synthesis of amides and carboxylic esters. EDAC is highly soluble in water and in most organic solvents, it can be employed in liquid and solid-phase and synthesis. The major advantage of EDCI over other carbodiimides such as DCC and DIC is the ease of purification of the product from the water-soluble urea by-product by washing the crude mixture with water or mild acid and extracting in the organic phase. The main applications of EDAC are in peptide synthesis, Steglich esterification reactions in presence of catalytic DMAP, immunoconjugate synthesis, synthesis of sulfo-NHS esters and coupling of biomolecules onto solid supports. Group: Biochemicals. Alternative Names: EDC.HCl; EDAC. HCl; Water Soluble Carbodiimide; N-Ethyl-N'- (3-dimethylaminopropyl) carbodiimide HCl; 1-Ethyl-3- (3-dimethylaminopropyl) carbodiimide HCl. Grades: Highly Purified. CAS No. 25952-53-8. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C8H17N3·HCl, Molecular Weight: 191.7. US Biological Life Sciences.
It is being used for the synthesis of amides. EDC HCl is also used as a coupling agent in the preparation of esters from carboxylic acids using dimethylaminopyridine as the catalyst. It is water-soluble carbodiimide, widely used for peptide coupling. Synonyms: EDC.HCL; 1-Ethyl-3-(3-dimethyllaminopropyl)carbodiimide hydrochloride; EDC hydrochloride; EDCI; 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride; 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride [Coupling Agent; EDAP; 1-Ethyl-3-(3-dimethyllaminopropyl)carbodiimide hydrochloride; edac hcl; wsc hcl; N1-((Ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine hydrochloride. Grades: 98%. CAS No. 25952-53-8. Molecular formula: C8H17N3·HCl. Mole weight: 191.70.
3-(Ethylthio)-butanoic Acid
3-(Ethylthio)-butanoic Acid is a reagent in the synthesis of amide using polyer-bound EDC (1-ethyl-3- (3-dimethylaminopropyl) carbodiimide) as coupling reagent. Group: Biochemicals. Grades: Highly Purified. CAS No. 89534-40-7. Pack Sizes: 100mg, 1g. Molecular Formula: C6H12O2S, Molecular Weight: 148.22. US Biological Life Sciences.
Worldwide
Carboxylic Acid-Doxorubicin Liposome (PEGylated)
This formulation is Doxorubicin Liposome (PEGylated) with the carboxyl group, which can be activated by EDC (1-ethyl-3-[3-dimethylaminopropyl] carbodiimide) and react with sulfo-NHS (N-hydroxysulfosuccinimide) to produce a significantly more stable and more soluble active intermediate (NHS ester). The intermediate can covalently conjugate to the amine group on the proteins, peptides or antibodies through displacement of sulfo-NHS group by amine. Group: Drug-loaded liposome. Categories: liposomes, niosomes, ethosomes, and transfersomes.
N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide
N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide. Uses: Designed for use in research and industrial production. Additional or Alternative Names: 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide; N-(3-Dimethylaminopropyl)-N-ethylcarbodiimide; N-[(dimethylamino)propyl]-N-ethylcarbodiimide; N-(3-Dimethylaminopropyl)-N-ethylcarbodiimide; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N-3-(N,N-dimethylamino)propylcarbodiimide; 3-dimethylaminopropyl ethyl carbodiimide; N1-((Ethylimino)methylene)-N3,N3-dimethylpropane-1,3-diamine; EDC polymer-bound; 1,3-Propanediamine,N-(ethylcarbonimidoyl)-N,N-dimethyl; 3-(ethyliminomethyleneamino)-N,N-dimethyl-propan-1-amine; EDAC; 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide; 1-(3-DIMETHYLAMINOPROPYL)-3-ETHYLCARBODIIMIDE. Appearance: clear, liquid. CAS No. 1892-57-5. Molecular formula: C8H17N3. Mole weight: 155.24. Purity: 97%+. IUPACName: 3-(ethyliminomethylideneamino)-N,N-dimethylpropan-1-amine. Canonical SMILES: CCN=C=NCCCN(C)C. Density: 0.877. ECNumber: 217-579-2. Product ID: ACM1892575. Alfa Chemistry ISO 9001:2015 Certified.
Succinyl-Doxorubicin Liposome (PEGylated)
This formulation is Doxorubicin Liposome (PEGylated) with the carboxyl group, which can be activated by EDC (1-ethyl-3-[3-dimethylaminopropyl] carbodiimide) and react with sulfo-NHS (N-hydroxysulfosuccinimide) to produce a significantly more stable and more soluble active intermediate (NHS ester). The intermediate can covalently conjugate to the amine group on the proteins, peptides or antibodies through displacement of sulfo-NHS group by amine. Group: Drug-loaded liposome. Categories: liposomes, niosomes, ethosomes, and transfersomes.
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