C5132
Carbazole
≥95% purity (GC), powder
Sinónimos:
Dibenzopyrrole; Diphenylenimine
Iniciar sesión para ver los precios por organización y contrato.
Seleccione un Tamaño
Cambiar Vistas
Acerca de este artículo
Fórmula empírica (notación de Hill):
C12H9N
Número CAS:
Peso molecular:
167.21
NACRES:
NA.47
PubChem Substance ID:
UNSPSC Code:
12171500
EC Number:
201-696-0
MDL number:
Beilstein/REAXYS Number:
3956
Servicio técnico
¿Necesita ayuda? Nuestro equipo de científicos experimentados está aquí para ayudarle.
Permítanos ayudarleNombre del producto
Carbazole, ≥95% (GC)
vapor pressure
400 mmHg ( 323 °C)
Quality Level
assay
≥95% (GC)
form
powder
technique(s)
titration: suitable
color
white to tan
bp
355 °C (lit.)
mp
243-246 °C (lit.)
solubility
acetone: 50 mg/mL
density
1.1 g/cm3 at 18 °C
application(s)
diagnostic assay manufacturing
hematology
histology
storage temp.
room temp
SMILES string
c1ccc2c(c1)[nH]c3ccccc23
InChI
1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H
InChI key
UJOBWOGCFQCDNV-UHFFFAOYSA-N
General description
Carbazole is an aromatic heterocyclic organic molecule.
Application
Carbazole has been used in the uronic acid assay.
Biochem/physiol Actions
Carbazole mainly interacts with DNA and damages it. These events suppress the synthesis of new DNA or RNA. Carbazole derivatives are involved in antimicrobial, antitumor, antiepileptic, antihistaminic, antioxidant, anti-inflammatory, antidiarrhoeal, analgesic, neuroprotective, and pancreatic lipase suppression activities.
Analysis Note
May contain dark particles.
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 4 - Carc. 2 - Muta. 2
Clase de almacenamiento
11 - Combustible Solids
flash_point_f
428.0 °F - closed cup
flash_point_c
220.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Elija entre una de las versiones más recientes:
¿Ya tiene este producto?
Encuentre la documentación para los productos que ha comprado recientemente en la Biblioteca de documentos.
CARBAZOLE DERIVATIVES IN CANCER TREATMENT-A REVIEW.
Kanneti Naga M, et al.
World Journal of Pharmacy and Pharmaceutical Sciences (2015)
A complete set of hyaluronan fragments obtained from hydrolysis catalyzed by hyaluronidase: Application to studies of hyaluronan mass distribution by simple HPLC devices.
Tranchepain F, et al.
Analytical Biochemistry, 348, 232-242 (2006)
Guodong Ji et al.
Journal of hazardous materials, 225-226, 1-7 (2012-05-23)
We examined the effects of power and treatment time on the ultrasonically enhanced ozonation of carbazole dissolved in APG(1214) surfactant solutions, including an analysis of the mechanism of OH radical formation, the zeta potential of the colloidal suspension, the influence