| 產(chǎn)品編號 | C-0026 |
| 英文名稱 | EDC |
| 中文名稱 | 碳二亞胺 (進(jìn)口分裝) |
| 別 名 | EDC?HCl; N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride; EDAC; WSC; N-Ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride; EDC hydrochloride; WSC hydrochloride; Carbodiimide; 偶聯(lián)劑; N-乙基-N′-(3-二甲基氨丙基)碳二亞胺鹽酸鹽; EDC 鹽酸鹽; WSC 鹽酸鹽; 1-(3-二甲氨基丙基)-3-乙基碳二亞胺鹽酸鹽; |
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Specific References (3) | C-0026 has been referenced in 3 publications.
[IF=8.758] Lei Bi. et al. Microwave-Assisted Synthesis of Hollow Microspheres with Multicomponent Nanocores for Heavy-Metal Removal and Magnetic Sensing. Acs Appl Mater Inter. 2020;12(41):46779–46787
[IF=4.601] Hanjiao He. et al. Multi-component immune knockout: A strategy for studying the effective components of traditional Chinese medicine. J CHROMATOGR A. 2023 Mar;1692:463853
[IF=2.397] Binze Ma. et al. All-Dielectric Metasurface for Sensing Microcystin-LR. Electronics-Switz. 2021 Jan;10(11):1363 Other ;
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| 保存條件 | Store at 2-8℃. |
| 產(chǎn)品介紹 |
1-Ethyl-3-(3-dimethylaminopropyl)carbodiimide (EDC, EDAC or EDCI) is a water-soluble carbodiimide usually obtained as the hydrochloride. It is typically employed in the 4.0-6.0 pH range. It is generally used as a carboxyl activating agent for the coupling of primary amines to yield amide bonds. Additionally, EDC can also be used to activate phosphate groups in order to form phosphomono-esters and phosphodiesters. Common uses for this carbodiimide include peptide synthesis, protein crosslinking to nucleic acids, but also in the preparation of immunoconjugates. EDC is often used in combination with N-hydroxysuccinimide (NHS) for the immobilisation of large biomolecules. 碳二亞胺含有N=C=N官能團(tuán)，是一類常用的脫水劑。主要用于活化羧基，促使酰胺和酯的生成。此外，它還會與磷酸基發(fā)生反應(yīng)。EDC用于肽合成、蛋白質(zhì)與核酸的交聯(lián)以及免疫偶聯(lián)物的制備。通常情況下，EDC的使用pH值范圍為4.0-6.0（無緩沖液）。尤其應(yīng)避免使用胺和羧酸緩沖液。CAS號: 25952-53-8，化學(xué)式 C8H17N3·HCl。 水溶性冷凝劑。EDAC通常用作羧基活化劑，用于與伯胺的酰胺鍵合。此外，它還會與磷酸基發(fā)生反應(yīng)。EDAC已被用于肽合成、蛋白質(zhì)與核酸的交聯(lián)以及免疫偶聯(lián)物的制備等。通常，EDAC在pH范圍為4.0-6.0（無緩沖液）時使用。尤其應(yīng)避免使用胺和羧酸緩沖液。 分子結(jié)構(gòu)式：
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