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Merck

8.00907

N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride

for peptide synthesis

Synonym(s):

N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride

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About This Item

Empirical Formula (Hill Notation):
C8H17N3 · xHCl
CAS Number:
25952-53-8
Molecular Weight:
155.24 (free base basis)
UNSPSC Code:
12352107
EC Index Number:
247-361-2
NACRES:
NA.22
MDL number:
MFCD00012503

Product Name

N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride, for synthesis

SMILES string

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

form

solid

reaction suitability

reaction type: Coupling Reactions

mp

110-115 °C

application(s)

peptide synthesis

storage temp.

−20°C (−15°C to −25°C)

Quality Level

200

Related Categories

Application

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.

General description

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.

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Danger

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT RE 2 Oral

Storage Class

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Effects of amounts of additives on peptide coupling mediated by a water-soluble carbodiimide in alcohols
Nozaki S
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
Yang Q, et al.
Journal of Biomaterials Science. Polymer Edition, 25, 1717-1729 (2014)
EDC-promoted one-step synthesis of teriflunomide at the industrial scale
Wang L, et al.
Reaction Chemistry & Engineering, 2493-2496 (2022)

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