CarbazoleCAS# 86-74-8 |
Quality Control & MSDS
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Number of papers citing our products
| 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. |
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| 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. |
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| 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. | ||
| Description | 1. Some carbazole derivatives show antibacterial and antifungal activities. |
| Targets | Antifection |
Carbazole Dilution Calculator
Carbazole Molarity Calculator
| 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. | |||||
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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.
