Passa al contenuto
Merck
Tutte le immagini(8)

Documenti

D80002

Sigma-Aldrich

DCC

99%

Sinonimo/i:

N,N′-Dicyclohexylcarbodiimide

Autenticatiper visualizzare i prezzi riservati alla tua organizzazione & contrattuali
Tutte le immagini(8)

About This Item

Formula condensata:
C6H11N=C=NC6H11
Numero CAS:
538-75-0
Peso molecolare:
206.33
Beilstein:
610662
Numero CE:
208-704-1
Numero MDL:
MFCD00011659
Codice UNSPSC:
12352111
ID PubChem:
24894174
NACRES:
NA.22

Livello qualitativo

200

Saggio

99%

Forma fisica

solid

Impiego in reazioni chimiche

reaction type: Coupling Reactions

P. eboll.

122-124 °C/6 mmHg (lit.)

Punto di fusione

34-35 °C (lit.)

Stringa SMILE

C1CCC(CC1)N=C=NC2CCCCC2

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

Informazioni sul gene

human ... EPHX2(2053)
mouse ... Ephx2(13850)

Cerchi prodotti simili? Visita Guida al confronto tra prodotti

Descrizione generale

DCC is the acronym for N,N′-dicyclohexylcarbodiimide. In peptide synthesis, it is utilized for the activation of carboxyl group. The structure of DCC has been analyzed based on IR and Raman spectral data. It mediates the esterification of poly(vinyl alcohol) with free levulinic acid to form poly(vinyl alcohol-co-vinyl levulinate).

Applicazioni

Carboxy group activating reagent for peptide synthesis.
DCC has been used in the preparation of titanate nanotubes-phthalocyanine(TiONts-Pc) nanohybrids and 7-((tert-butyldimethylsilyl)oxy)hepta-2,4-diyn-1-yl propynoate.
DCC may be used to promote the esterification of
7-((tert-butyldimethylsilyl)oxy)hepta-2,4-diyn-1-ol with propiolic acid to form 7-((tert-butyldimethylsilyl)oxy)hepta-2,4-diyn-1-yl propynoate.
It can also used to synthesize:
  • 1,3-Thiazetedine derivatives via [2+2] cycloaddition with 2-phenylethenyl- and 2-(4-nitrophenyl)ethenyl isothiocyanates.
  • 1,3,5-Oxadiazine-4-thiones via [4+2] cycloaddition with benzoyl isothiocyanates.
  • Sterically hindered 1,3,4-oxadiazole derivatives by reacting with (N-isocyanimino)triphenylphosphorane in the presence of aromatic (or heteroaromatic) carboxylic acids.

Pittogrammi

CorrosionSkull and crossbones
GHS05,GHS06

Avvertenze

Danger

Indicazioni di pericolo

H302 - H311 - H317 - H318

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

Dispositivi di protezione individuale

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Certificati d'analisi (COA)

Cerca il Certificati d'analisi (COA) digitando il numero di lotto/batch corrispondente. I numeri di lotto o di batch sono stampati sull'etichetta dei prodotti dopo la parola ‘Lotto’ o ‘Batch’.

Possiedi già questo prodotto?

I documenti relativi ai prodotti acquistati recentemente sono disponibili nell’Archivio dei documenti.

Visita l’Archivio dei documenti

I clienti hanno visto anche

Slide 1 of 2

1 of 2

N-(3-Dimethylaminopropyl)-N′-ethylcarbodiimide ≥97.0% (T)

Sigma-Aldrich

39391

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

4-(Dimethylamino)pyridine for synthesis

Sigma-Aldrich

8.20499

4-(Dimethylamino)pyridine

N,N-dicyclohexylcarbodiimide assisted synthesis and characterization of poly (vinyl alcohol-co-vinyl levulinate).
Wang, YM, et al.
Polymer, 46(23), 9793-9802 (2005)
Vibrational spectroscopy and DFT calculations of N,N'-dicyclohexylcarbodiimide.
Chowdhry BZ, et al.
Journal of Raman Spectroscopy, 42(2), 230-238 (2011)
Jones, J.
The Chemical Synthesis of Peptides, International Series of Monographs on Chemistry, 23 (1994)
Phthalocyanine-titanate nanotubes: a promising nanocarrier detectable by optical imaging in the so-called imaging window.
Paris J, et al.
Royal Society of Chemistry Advances, 5(9), 6315-6322 (2015)
Reaction of 4-substituted benzoyl isothiocyanates with N, N'-dicyclohexylcarbodiimide and N, N'-diphenylcarbodiimide
Hritzova O
Collection of Czechoslovak Chemical Communications, 43(12), 3258-3262 (1978)
Visualizza tutti i documenti correlati

Articoli

Carbodiimide-mediated peptide coupling

Carbodiimide-mediated peptide coupling remains to the most frequently used technique.

Properties and Applications of Functionalized Graphene Oxide

Professor Aran (Claremont University, USA) thoroughly discusses the engineering of graphene based materials through careful functionalization of graphene oxide, a solution processable form of graphene.

Il team dei nostri ricercatori vanta grande esperienza in tutte le aree della ricerca quali Life Science, scienza dei materiali, sintesi chimica, cromatografia, discipline analitiche, ecc..

Contatta l'Assistenza Tecnica.