N-(3-Dimethylaminopropyl)-N'-Ethylcarbodiimide Hydrochloride 98% - 1 Gr - Sigma
Código: 17556
N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride
purum, ≥98.0% (AT)
Sinônimo(s):
EDC, WSC hydrochloride, N-Ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride, EDAC, EDC hydrochloride
Empirical Formula (Hill Notation):
C8H17N3 · HCl
Número CAS:
Peso molecular:
191.70
Beilstein:
5764110
Beilstein:
1718733
Número EC:
Número EC:
Número MDL:
Número MDL:
ID de substância PubChem:
ID de substância PubChem:
NACRES:
NA.31
Nível de qualidade
200
densidade de vapor
1.59 (vs air)
grau
purum
pressão de vapor
44.6 mmHg ( 20 °C)
teor
≥98.0% (AT)
≥99.8% (based on denaturant-free substance)
temperatura de autoignição
683 °F
pf
110-115 °C (lit.)
110-115 °C
−114 °C (lit.)
qualidade
absolute alcohol, denaturated with 1% diethyl phthalate, A15 DEP1
Lim. expl.
19 %, 60 °F
solubilidade
H2O: soluble 1 gm/10 ml, clear to very slightly hazy, colorless to very faintly yellow
temperatura de armazenamento
−20°C
índice de refração
n20/D 1.3600 (lit.)
n20/D 1.363
pb
78 °C (lit.)
densidade
0.789 g/mL at 25 °C (lit.)
SMILES string
CCO
Cl.CCN=C=NCCCN(C)C
InChI
1S/C2H6O/c1-2-3/h3H,2H2,1H3
1S/C8H17N3.ClH/c1-4-9-8-10-6-5-7-11(2)3;/h4-7H2,1-3H3;1H
InChI key
LFQSCWFLJHTTHZ-UHFFFAOYSA-N
FPQQSJJWHUJYPU-UHFFFAOYSA-N
Aplicação
N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride has been used modify the cell surface of Escherichia coli to covalently couple substances. It has also been used as an activator to modify microfluidic chips to capture Escherichia coli.
Ações bioquímicas/fisiológicas
N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide is a water soluble condensing reagent. EDAC is generally utilized as a carboxyl activating agent for amide bonding with primary amines. Additionally, it reacts with phosphate groups. It has been utilized in peptide synthesis, crosslinking proteins to nucleic acids as well as preparation of immunoconjugates.
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.
Outras notas
Sales restrictions may apply
Nota de rodapé
1Distribution and use of ethyl alcohol in Switzerland require a license from the Swiss Federal Alcohol Administration
Informações legais
Honeywell is a registered trademark of Honeywell International Inc.