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8.02954

Sigma-Aldrich

N,N′-Dicyclohexylcarbodiimide

for peptide synthesis

Sinonimo/i:

N,N′-Dicyclohexylcarbodiimide, DCC

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About This Item

Formula condensata:
C(NC6H11)2
Numero CAS:
Peso molecolare:
206.33
Codice UNSPSC:
12352111
Numero indice EU:
208-704-1
NACRES:
NA.22

product name

N,N′-Dicyclohexylcarbodiimide, for synthesis

Livello qualitativo

Forma fisica

solid

Potenza

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

Impiego in reazioni chimiche

reaction type: Coupling Reactions

P. eboll.

148-152 °C/15 hPa

Punto di fusione

35-36 °C

Temp. transizione

flash point 113 °C

Densità

0.95 g/cm3 at 40 °C

Densità bulk

920 kg/m3

applicazioni

peptide synthesis

Temperatura di conservazione

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
QOSSAOTZNIDXMA-UHFFFAOYSA-N

Descrizione generale

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.

Applicazioni

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.

Pittogrammi

CorrosionSkull and crossbones

Avvertenze

Danger

Indicazioni di pericolo

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

235.4 °F - closed cup

Punto d’infiammabilità (°C)

113 °C - closed cup


Certificati d'analisi (COA)

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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)
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)
N, N-dicyclohexylcarbodiimide assisted synthesis and characterization of poly (vinyl alcohol-co-vinyl levulinate
Wang YM, et al.
Polymer, 9793-9802 (2005)

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