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製品名
N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride, for synthesis
品質水準
フォーム
solid
反応適合性
reaction type: Coupling Reactions
mp
110-115 °C
アプリケーション
peptide synthesis
保管温度
−20°C (−15°C to −25°C)
SMILES記法
Cl.N(CCCN(CC)C#N)(C)C
InChI
1S/C8H17N3.ClH/c1-4-11(8-9)7-5-6-10(2)3;/h4-7H2,1-3H3;1H
InChI Key
FDXPUDRRFDHONO-UHFFFAOYSA-N
詳細
N-(3-Dimethylaminopropyl)-N-ethylcarbodiimide hydrochloride, also known as EDAC HCl or WSC, is a water-soluble condensing reagent. EDAC HCl is generally used to couple carboxylic acids with amines to form amides. The by-product urea is water-soluble and can be removed from immiscible reaction milieux by extraction with water. It is principally utilized in solution-phase peptide synthesis and as a zero-length crosslinker for protein modification.
アプリケーション
N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (EDC hydrochloride) can be used as:
- A water-soluble carbodiimide to facilitate peptide coupling reactions in alcohols.
- A coupling agent along with HOBt to synthesize poly(glutamic acid) (PGA) polypeptides for the creation of non-fouling polypeptides that could be useful in a variety of biomedical applications.
- A coupling reagent for the efficient synthesis of teriflunomide at the industrial scale.
シグナルワード
Danger
危険有害性の分類
Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Oral
保管分類コード
6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
WGK
WGK 3
引火点(°F)
Not applicable
引火点(℃)
Not applicable
試験成績書(COA)
製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。
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Effects of amounts of additives on peptide coupling mediated by a water-soluble carbodiimide in alcohols
The Journal of Peptide Research, 54, 162-167 (1999)
Investigation of nonfouling polypeptides of poly (glutamic acid) with lysine side chains synthesized by EDCHCl/HOBt chemistry
Journal of Biomaterials Science. Polymer Edition, 25, 1717-1729 (2014)
EDC-promoted one-step synthesis of teriflunomide at the industrial scale
Reaction Chemistry & Engineering, 2493-2496 (2022)
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