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8.02954

Sigma-Aldrich

N,N′-Dicyclohexylcarbodiimide

for peptide synthesis

Synonym(e):

DCC

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About This Item

Lineare Formel:
C(NC6H11)2
CAS-Nummer:
Molekulargewicht:
206.33
UNSPSC-Code:
12352111
EG-Index-Nummer:
208-704-1
NACRES:
NA.22

product name

N,N′-Dicyclohexylcarbodiimide, for synthesis

Qualitätsniveau

Form

solid

Wirksamkeit

1110 mg/kg LD50, oral (Rat)
71 mg/kg LD50, skin (Rat)

Eignung der Reaktion

reaction type: Coupling Reactions

bp

148-152 °C/15 hPa

mp (Schmelzpunkt)

35-36 °C

Übergangstemp.

flash point 113 °C

Dichte

0.95 g/cm3 at 40 °C

Schüttdichte

920 kg/m3

Anwendung(en)

peptide synthesis

Lagertemp.

2-30°C

InChI

1S/C13H22N2/c1-3-7-12(8-4-1)14-11-15-13-9-5-2-6-10-13/h12-13H,1-10H2

InChIKey

QOSSAOTZNIDXMA-UHFFFAOYSA-N

Allgemeine Beschreibung

N,N′-Dicyclohexylcarbodiimide (DCC) is a highly versatile dehydrating reagent with varied applications in organic chemistry. It is most frequently used as a coupling agent for the synthesis of amides, esters and thioesters from carboxylic acids and amines, alcohol and thiols, respectively. In peptide synthesis applications, DCC is used in conjunction with auxiliary nucleophiles such as Oxyma Pure and HOBt, to minimize side reactions such as racemization, N-acylurea or oxazolone formation. It is used as a dehydration reagent in the Moffatt oxidation of primary alcohols to aldehydes and in the conversion of amides to nitriles. The by-product of the dehydration reaction, dicyclohexylurea, is sparingly soluble in most reaction solvents and can be removed by filtration.

Anwendung

Recent applications of N,N′-Dicyclohexylcarbodiimide include:
  • The synthesis of optically pure N-acyl-N,N′-dicyclohexylureas.
  • The activation of the carboxylic acid groups in aromatic carboxylic acids to facilitates their reaction with (N-isocyanimino)trifluoroacetamide to form the corresponding 1,3,4-oxadiazole derivatives.
  • The synthesis of poly (vinyl alcohol-co-vinyl levulinate) copolymers for use in biomedical applications.

Piktogramme

CorrosionSkull and crossbones

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 4 Oral - Eye Dam. 1 - Skin Sens. 1

Lagerklassenschlüssel

6.1D - Non-combustible, acute toxic Cat.3 / toxic hazardous materials or hazardous materials causing chronic effects

WGK

WGK 3

Flammpunkt (°F)

235.4 °F - closed cup

Flammpunkt (°C)

113 °C - closed cup


Analysenzertifikate (COA)

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Die Dokumentenbibliothek aufrufen

Formation of optically pure N-acyl-N, N?-dicyclohexylurea in N, N?-dicyclohexylcarbodiimide-mediated peptide synthesis
SLEBIODA, M, et al.
International Journal of Peptide and Protein Research, 35, 539-541 (1990)
Dicyclohexylcarbodiimide
Albert, J. S. et al.
Encyclopedia of Reagents for Organic Synthesis, Second Edition, 1-9 (2017)
N, N-dicyclohexylcarbodiimide assisted synthesis and characterization of poly (vinyl alcohol-co-vinyl levulinate
Wang YM, et al.
Polymer, 9793-9802 (2005)
Synthesis of sterically congested 1, 3, 4-oxadiazole derivatives from aromatic carboxylic acids, N, N-dicyclohexylcarbodiimide and (N-isocyanimino) triphenylphosphorane
Nasrabadi FZ, et al.
Molecular Diversity, 791-798 (2011)

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