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8.02954

Sigma-Aldrich

N,N′-Dicyclohexylcarbodiimide

for peptide synthesis

Synonyme(s) :

N,N′-Dicyclohexylcarbodiimide, DCC

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About This Item

Formule linéaire :
C(NC6H11)2
CAS Number:
Poids moléculaire :
206.33
Numéro MDL:
Code UNSPSC :
12352111
Numéro de classement CE :
208-704-1
Nomenclature NACRES :
NA.22
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Product Name

N,N′-Dicyclohexylcarbodiimide, for synthesis

Niveau de qualité

Forme

solid

Puissance

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

Capacité de réaction

reaction type: Coupling Reactions

pb

148-152 °C/15 hPa

Pf

35-36 °C

Température de transition

flash point 113 °C

Densité

0.95 g/cm3 at 40 °C

Masse volumique apparente

920 kg/m3

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Cet article
D1980000BP899D2521
manufacturer/tradename

USP

manufacturer/tradename

EDQM

manufacturer/tradename

BP

manufacturer/tradename

-

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

grade

pharmaceutical primary standard

grade

-

format

neat

format

neat

format

mixture

format

-

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical (small molecule)

application(s)

pharmaceutical
pharmaceutical small molecule

application(s)

-

API family

diltiazem

API family

diltiazem

API family

diltiazem

API family

-

Gene Information

human ... CACNA1C(775), CACNA1D(776), CACNA1F(778), CACNA1S(779)

Gene Information

human ... CACNA1C(775), CACNA1D(776), CACNA1F(778), CACNA1S(779)

Gene Information

human ... CACNA1C(775), CACNA1D(776), CACNA1F(778), CACNA1S(779)

Gene Information

human ... CACNA1C(775), CACNA1D(776), CACNA1F(778), CACNA1S(779)

Description générale

N,N′-Dicyclohexylcarbodiimide (DCC) is a highly versatile dehydrating reagent with varied applications in organic chemistry.[1] 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.

Application

Recent applications of N,N′-Dicyclohexylcarbodiimide include:
  • The synthesis of optically pure N-acyl-N,N′-dicyclohexylureas.[2]
  • 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.[3]
  • The synthesis of poly (vinyl alcohol-co-vinyl levulinate) copolymers for use in biomedical applications.[4]

Pictogrammes

CorrosionSkull and crossbones

Mention d'avertissement

Danger

Mentions de danger

Classification des risques

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

Code de la classe de stockage

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

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

235.4 °F - closed cup

Point d'éclair (°C)

113 °C - closed cup


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