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产品名称:EDC.HCL 1-乙基-(3-二甲基氨基丙基)碳酰二亚胺盐酸盐
英文名称:1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
CAS编号:25952-53-8
英文别名: EDCI; 1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide Hydrochloride; EDAC; EDC; WS.HCl; EDAC,HCl; N-Ethyl-N-(3-dimethylaminopropyl)carbodiimide hydrochloride; WSC; EDC (WSC-HCl); N-(3-Dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride; EDC.HCL; EDAC.HCL; EDC HCL; EDAC HCL; 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride; 1-[3-Dimethylamino propyl]-3-ethyl carbodiimide Hcl; 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride; (3-dimethylaminopropyl)ethyl-carbodiimidmonohydrochloride; 3-propanediamine,n'-(ethylcarbonimidoyl)-n,n-dimethyl-monohydrochloride; 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide hydrochloride;
EDC.HCL 1-乙基-(3-二甲基氨基丙基)碳酰二亚胺盐酸盐
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基本信息
分子式:
C8H17N3.HCl
分子量:
191.70162
理化性质
安全信息
产品用途和参考文献
中文名称:EDC.HCL 1-乙基-(3-二甲基氨基丙基)碳酰二亚胺盐酸盐
CAS号:25952-53-8
中文别名:1-(3-二甲氨基丙基)-3-乙基碳二亚胺盐酸盐; 1-乙基-(3-二甲基氨基丙基)碳酰二亚胺盐酸盐; 1-(3-二甲氨基丙基)-3-乙基-碳二亚胺盐酸盐; 1-(3-二甲基氨基丙基)-3-乙基碳化二亚胺盐酸盐; 1-乙基-3-(3-二甲氨丙基)碳二亚胺盐酸盐; 1-(3-二甲胺丙基)-3-乙基碳二亚胺盐酸盐; 1-乙基-3-(3-二甲基銨丙基)碳銨; 1-乙基-(3-二甲基氨基丙基)碳酰二亚胺
英文名称:1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
英文别名: EDCI; 1-Ethyl-3-(3-dimethylaminopropyl) carbodiimide Hydrochloride; EDAC; EDC; WS.HCl; EDAC,HCl; N-Ethyl-N-(3-dimethylaminopropyl)carbodiimide hydrochloride; WSC; EDC (WSC-HCl); N-(3-Dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride; EDC.HCL; EDAC.HCL; EDC HCL; EDAC HCL; 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride; 1-[3-Dimethylamino propyl]-3-ethyl carbodiimide Hcl; 1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride; (3-dimethylaminopropyl)ethyl-carbodiimidmonohydrochloride; 3-propanediamine,n'-(ethylcarbonimidoyl)-n,n-dimethyl-monohydrochloride; 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide hydrochloride;
EINECS:247-361-2
分子式:C8H17N3.HCL
分子量:191.70162

 

属性

敏感性 对湿度和热敏感;白色结晶粉末
密度 0.8770
熔点 115-118°C
存贮条件 储存温度2-8℃,充氩保存

描述

产品介绍 EDC.HCl是水溶性碳二亚胺,分子呈线性结构,用于羧基与伯胺的缩合反应,并已获得广泛的用途。如在多肽合成中形成酰胺健、将半抗原结合于载体蛋白形成免疫抗原、通过与核酸5'位的磷酸基团反应形成氨基反应活性的NHS-酯等。EDC 通过与氨基反应形成可与氨基反应的O-酰基脲中间体。如果该中间体不与氨基反应,则会很快水解并重新释放出羧基基团。在N-羟基硫代琥珀酰亚胺(Sulfo-NHS)存在的情况下,EDC.HCl可以将羧基转变为氨基反应活性的Sulfo-NHS酯。这步反应通过将EDC.HCl、含羧基分子以及Sulfo-NHS混合即可实现。
别名 1-乙基-(3-二甲基氨基丙基)碳酰二亚胺盐酸盐; 1-(3-二甲氨基丙基)-3-乙基碳二亚胺盐酸盐; N-乙基-N′-(3-二甲基氨丙基)碳二亚胺盐酸盐; EDAC EDC 盐酸盐; EDC WSC 盐酸盐; 1-乙基-3-(3-二甲基銨丙基)碳銨; 1-乙基-3-(3-二甲氨丙基)碳二亚胺盐酸盐; 1-(3-二甲氨基丙基)-3-乙基-碳二亚胺盐酸盐;1-Ethyl-3-(3-dimethyllaminopropyl)carbodiimide hydrochloride; 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide Hydrochloride; EDC·HCl; EDAC·HCL; EDCI·HCl
生化机理 Water soluble condensing reagent. EDAC is generally utilized as a carboxyl activating agent for amide bonding with primary amines. In addition, it will react with phosphate groups. EDAC has been used in peptide synthesis; crosslinking proteins to nucleic acids; and preparation of immunoconjugates as examples. Typically, EDAC is utilized in the pH range 4.0-6.0 without buffers. In particular, amine and carboxylate buffers should be avoided.
应用 用于多肽缩合剂和交联剂,该品是水溶性碳二亚胺,主要用作多肽、蛋白质、核苷酸合成中的脱水剂,可实现快速多肽缩合反应的水溶性碳二亚胺型缩合剂。
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