Carbazole

CAS# 86-74-8

Carbazole

Catalog No. BCN6903----Order now to get a substantial discount!

Product Name & Size Price Stock
Carbazole: 5mg Please Inquire In Stock
Carbazole: 10mg Please Inquire In Stock
Carbazole: 20mg Please Inquire Please Inquire
Carbazole: 50mg Please Inquire Please Inquire
Carbazole: 100mg Please Inquire Please Inquire
Carbazole: 200mg Please Inquire Please Inquire
Carbazole: 500mg Please Inquire Please Inquire
Carbazole: 1000mg Please Inquire Please Inquire

Quality Control of Carbazole

Number of papers citing our products

Chemical structure

Carbazole

3D structure

Chemical Properties of Carbazole

Cas No. 86-74-8 SDF Download SDF
PubChem ID 6854 Appearance Powder
Formula C12H9N M.Wt 167.21
Type of Compound Alkaloids Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 9H-carbazole
SMILES C1=CC=C2C(=C1)C3=CC=CC=C3N2
Standard InChIKey UJOBWOGCFQCDNV-UHFFFAOYSA-N
Standard InChI InChI=1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H
General tips For obtaining a higher solubility , please warm the tube at 37 ℃ and shake it in the ultrasonic bath for a while.Stock solution can be stored below -20℃ for several months.
We recommend that you prepare and use the solution on the same day. However, if the test schedule requires, the stock solutions can be prepared in advance, and the stock solution must be sealed and stored below -20℃. In general, the stock solution can be kept for several months.
Before use, we recommend that you leave the vial at room temperature for at least an hour before opening it.
About Packaging 1. The packaging of the product may be reversed during transportation, cause the high purity compounds to adhere to the neck or cap of the vial.Take the vail out of its packaging and shake gently until the compounds fall to the bottom of the vial.
2. For liquid products, please centrifuge at 500xg to gather the liquid to the bottom of the vial.
3. Try to avoid loss or contamination during the experiment.
Shipping Condition Packaging according to customer requirements(5mg, 10mg, 20mg and more). Ship via FedEx, DHL, UPS, EMS or other couriers with RT, or blue ice upon request.

Source of Carbazole

The coal tar.

Biological Activity of Carbazole

Description1. Some carbazole derivatives show antibacterial and antifungal activities.
TargetsAntifection

Carbazole Dilution Calculator

Concentration (start)
x
Volume (start)
=
Concentration (final)
x
Volume (final)
 
 
 
C1
V1
C2
V2

calculate

Carbazole Molarity Calculator

Mass
=
Concentration
x
Volume
x
MW*
 
 
 
g/mol

calculate

Preparing Stock Solutions of Carbazole

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 5.9805 mL 29.9025 mL 59.805 mL 119.6101 mL 149.5126 mL
5 mM 1.1961 mL 5.9805 mL 11.961 mL 23.922 mL 29.9025 mL
10 mM 0.5981 mL 2.9903 mL 5.9805 mL 11.961 mL 14.9513 mL
50 mM 0.1196 mL 0.5981 mL 1.1961 mL 2.3922 mL 2.9903 mL
100 mM 0.0598 mL 0.299 mL 0.5981 mL 1.1961 mL 1.4951 mL
* Note: If you are in the process of experiment, it's necessary to make the dilution ratios of the samples. The dilution data above is only for reference. Normally, it's can get a better solubility within lower of Concentrations.

Organizitions Citing Our Products recently

 
 
 

Calcutta University

University of Minnesota

University of Maryland School of Medicine

University of Illinois at Chicago

The Ohio State University

University of Zurich

Harvard University

Colorado State University

Auburn University

Yale University

Worcester Polytechnic Institute

Washington State University

Stanford University

University of Leipzig

Universidade da Beira Interior

The Institute of Cancer Research

Heidelberg University

University of Amsterdam

University of Auckland
TsingHua University
TsingHua University
The University of Michigan
The University of Michigan
Miami University
Miami University
DRURY University
DRURY University
Jilin University
Jilin University
Fudan University
Fudan University
Wuhan University
Wuhan University
Sun Yat-sen University
Sun Yat-sen University
Universite de Paris
Universite de Paris
Deemed University
Deemed University
Auckland University
Auckland University
The University of Tokyo
The University of Tokyo
Korea University
Korea University
Featured Products
New Products
 

References on Carbazole

Carbazole compounds as host materials for triplet emitters in organic light-emitting diodes: polymer hosts for high-efficiency light-emitting diodes.[Pubmed:15198620]

J Am Chem Soc. 2004 Jun 23;126(24):7718-27.

A Carbazole homopolymer and Carbazole copolymers based on 9,9'-dialkyl-[3,3']-bicarbazolyl, 2,5-diphenyl-[1,3,4]-oxadiazole and 9,9-bis(4-[3,7-dimethyloctyloxy]phenyl)fluorene were synthesized and their electrical and photophysical properties were characterized with respect to their application as host in phosphorescent polymer light-emitting diodes. It is shown that the triplet energy of a polymer depends on the specific connections between its building blocks. Without changing the composition of the polymer, its triplet energy can be increased from 2.3 to 2.6 eV by changing the way in which the different building blocks are coupled together. For poly(9-vinylCarbazole) (PVK), a Carbazole polymer often used as host for high-energy triplet emitters in polymer light-emitting diodes, a large hole-injection barrier of about 1 eV exists due to the low-lying HOMO level of PVK. For all Carbazole polymers presented here, the HOMO levels are much closer to the Fermi level of a commonly used anode such as ITO and/or a commonly used hole-injection layer such as PEDOT:PSS. This makes high current densities and consequently high luminance levels possible at moderate applied voltages in polymer light-emitting diodes. A double-layer polymer light-emitting diode is constructed comprising a PEDOT:PSS layer as hole-injection layer and a Carbazole-oxadiazole copolymer doped with a green triplet emitter as emissive layer that shows an efficacy of 23 cd/A independent of current density and light output.

Synthesis, antibacterial and antifungal activities of some carbazole derivatives.[Pubmed:20176480]

Bioorg Med Chem Lett. 2010 Mar 15;20(6):1881-4.

A series of N-substituted Carbazole derivatives were synthesized and evaluated for antibacterial and antifungal activities against Staphylococcus aureus, methicillin-resistant Staphylococcus aureus (MRSA), Bacillus subtilis, Escherichia coli, Pseudomonas aeruginosa, Bacillus proteus, Candida albicans and Aspergillus fumigatus by two fold serial dilution technique. Some of the synthesized compounds displayed comparable or even better antibacterial and antifungal activities than reference drugs fluconazole, chloramphenicol and norfloxacin against tested strains.

Keywords:

Carbazole,86-74-8,Natural Products, buy Carbazole , Carbazole supplier , purchase Carbazole , Carbazole cost , Carbazole manufacturer , order Carbazole , high purity Carbazole

Online Inquiry for:

      Fill out the information below

      • Size:Qty: - +

      * Required Fields

                                      Result: