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4,4'-Bis(N-carbazolyl)-1,1'-biphenyl

CAS# 58328-31-7

4,4'-Bis(N-carbazolyl)-1,1'-biphenyl

Catalog No. BCC8660----Order now to get a substantial discount!

Product Name & Size Price Stock
4,4'-Bis(N-carbazolyl)-1,1'-biphenyl: 5mg $17 In Stock
4,4'-Bis(N-carbazolyl)-1,1'-biphenyl: 10mg Please Inquire In Stock
4,4'-Bis(N-carbazolyl)-1,1'-biphenyl: 20mg Please Inquire Please Inquire
4,4'-Bis(N-carbazolyl)-1,1'-biphenyl: 50mg Please Inquire Please Inquire
4,4'-Bis(N-carbazolyl)-1,1'-biphenyl: 100mg Please Inquire Please Inquire
4,4'-Bis(N-carbazolyl)-1,1'-biphenyl: 200mg Please Inquire Please Inquire
4,4'-Bis(N-carbazolyl)-1,1'-biphenyl: 500mg Please Inquire Please Inquire
4,4'-Bis(N-carbazolyl)-1,1'-biphenyl: 1000mg Please Inquire Please Inquire

Quality Control of 4,4'-Bis(N-carbazolyl)-1,1'-biphenyl

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Chemical structure

4,4'-Bis(N-carbazolyl)-1,1'-biphenyl

3D structure

Chemical Properties of 4,4'-Bis(N-carbazolyl)-1,1'-biphenyl

Cas No. 58328-31-7 SDF Download SDF
PubChem ID 11248716 Appearance Powder
Formula C36H24N2 M.Wt 484.6
Type of Compound N/A Storage Desiccate at -20°C
Solubility Soluble in Chloroform,Dichloromethane,Ethyl Acetate,DMSO,Acetone,etc.
Chemical Name 9-[4-(4-carbazol-9-ylphenyl)phenyl]carbazole
SMILES C1=CC=C2C(=C1)C3=CC=CC=C3N2C4=CC=C(C=C4)C5=CC=C(C=C5)N6C7=CC=CC=C7C8=CC=CC=C86
Standard InChIKey VFUDMQLBKNMONU-UHFFFAOYSA-N
Standard InChI InChI=1S/C36H24N2/c1-5-13-33-29(9-1)30-10-2-6-14-34(30)37(33)27-21-17-25(18-22-27)26-19-23-28(24-20-26)38-35-15-7-3-11-31(35)32-12-4-8-16-36(32)38/h1-24H
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.

4,4'-Bis(N-carbazolyl)-1,1'-biphenyl Dilution Calculator

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4,4'-Bis(N-carbazolyl)-1,1'-biphenyl Molarity Calculator

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Preparing Stock Solutions of 4,4'-Bis(N-carbazolyl)-1,1'-biphenyl

1 mg 5 mg 10 mg 20 mg 25 mg
1 mM 2.0636 mL 10.3178 mL 20.6356 mL 41.2712 mL 51.5889 mL
5 mM 0.4127 mL 2.0636 mL 4.1271 mL 8.2542 mL 10.3178 mL
10 mM 0.2064 mL 1.0318 mL 2.0636 mL 4.1271 mL 5.1589 mL
50 mM 0.0413 mL 0.2064 mL 0.4127 mL 0.8254 mL 1.0318 mL
100 mM 0.0206 mL 0.1032 mL 0.2064 mL 0.4127 mL 0.5159 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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References on 4,4'-Bis(N-carbazolyl)-1,1'-biphenyl

Investigation of the Charge Balance in Green Phosphorescent Organic Light-Emitting Diodes by Controlling the Mixed Host Emission Layer.[Pubmed:29677715]

J Nanosci Nanotechnol. 2018 Sep 1;18(9):5908-5912.

In this paper, we investigated the use of a mixed host emission layer (MH-EML) in green phosphorescent organic light-emitting diodes (OLEDs). The hole transport type (p-type) material (4,4'-Bis(N-carbazolyl)-1,1'-biphenyl (CBP)) and electron transport type (N-type) material (2,2',2''-(1,3,5-Benzinetriyl)-tris(1-phenyl-1-H-benzimidazole) (TPBi)) were mixed with different ratios. The electrons were easily injected through the lowest unoccupied molecular orbital (LUMO) of TPBi in the mixed host system. Also, holes were confined in the EML because of the deep highest occupied molecular orbital (HOMO) level of TPBi (6.7 eV). These results indicate that excitons were formed effectively and the recombination zone became wider under a high electric field in MH-EML devices. For these reasons, the lifetime of the MH-OLED device was 1.36 times higher than that of a single host emission layer (SH-EML) device and showed a reduction in Joule heating. Finally, the external quantum efficiency (EQE) roll-off ratio from 1 mA/cm2 to 100 mA/cm2 in the optimized device (30.46%) was 18.12%p lower than that of the SH-EML (48.58%).

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