Determine the necessary mass, volume, or concentration for preparing a solution.
This is a demo store. No orders will be fulfilled.
| SKU | Size | Availability |
Price | Qty |
|---|---|---|---|---|
|
T168233-250mg
|
250mg |
3
|
$87.90
|
|
|
T168233-1g
|
1g |
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
|
$270.90
|
|
|
T168233-5g
|
5g |
1
|
$1,218.90
|
|
| Synonyms | TPBi | 2-[3,5-bis(1-phenylbenzimidazol-2-yl)phenyl]-1-phenylbenzimidazole | A851976 | DTXSID70620299 | 2,2,2-(1,3,5-Benzenetriyl)tris[1-phenyl-1H-benzimidazole] | TPBi, AldrichCPR | AKOS005145755 | 2,2',2'-(1,3,5-Benzinetriyl)-tris(1-phenyl-1-H-benzimidaz |
|---|---|
| Specifications & Purity | ≥99.5%(HPLC) |
| Storage Temp | Room temperature |
| Shipped In | Normal |
| Product Description |
Used in OLED′s devices as electron transport and exciton blocking materials. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Benzimidazoles |
| Subclass | Phenylbenzimidazoles |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenylbenzimidazoles |
| Alternative Parents | Phenylimidazoles N-substituted imidazoles Benzene and substituted derivatives Heteroaromatic compounds Azacyclic compounds Organonitrogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Phenylbenzimidazole - 1-phenylimidazole - 2-phenylimidazole - Benzenoid - N-substituted imidazole - Monocyclic benzene moiety - Heteroaromatic compound - Imidazole - Azole - Azacycle - Organic nitrogen compound - Hydrocarbon derivative - Organonitrogen compound - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as phenylbenzimidazoles. These are compounds containing a phenylbenzimidazole skeleton, which consists of a benzimidazole moiety where its imidazole ring is attached to a phenyl group. |
| External Descriptors | Not available |
|
|
|
| IUPAC Name | 2-[3,5-bis(1-phenylbenzimidazol-2-yl)phenyl]-1-phenylbenzimidazole |
|---|---|
| INCHI | InChI=1S/C45H30N6/c1-4-16-34(17-5-1)49-40-25-13-10-22-37(40)46-43(49)31-28-32(44-47-38-23-11-14-26-41(38)50(44)35-18-6-2-7-19-35)30-33(29-31)45-48-39-24-12-15-27-42(39)51(45)36-20-8-3-9-21-36/h1-30H |
| InChIKey | GEQBRULPNIVQPP-UHFFFAOYSA-N |
| Smiles | C1=CC=C(C=C1)N2C3=CC=CC=C3N=C2C4=CC(=CC(=C4)C5=NC6=CC=CC=C6N5C7=CC=CC=C7)C8=NC9=CC=CC=C9N8C1=CC=CC=C1 |
| Isomeric SMILES | C1=CC=C(C=C1)N2C3=CC=CC=C3N=C2C4=CC(=CC(=C4)C5=NC6=CC=CC=C6N5C7=CC=CC=C7)C8=NC9=CC=CC=C9N8C1=CC=CC=C1 |
| PubChem CID | 21932919 |
| Molecular Weight | 654.76 |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Jul 08, 2024 | T168233 | |
| Certificate of Analysis | Jul 08, 2024 | T168233 | |
| Certificate of Analysis | Jul 08, 2024 | T168233 | |
| Certificate of Analysis | Oct 08, 2023 | T168233 | |
| Certificate of Analysis | Oct 08, 2023 | T168233 | |
| Certificate of Analysis | Jun 16, 2023 | T168233 | |
| Certificate of Analysis | Jun 16, 2023 | T168233 |
| Sensitivity | light sensitive |
|---|---|
| Melt Point(°C) | 272-277°C |
| Molecular Weight | 654.800 g/mol |
| XLogP3 | 10.400 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 6 |
| Exact Mass | 654.253 Da |
| Monoisotopic Mass | 654.253 Da |
| Topological Polar Surface Area | 53.500 Ų |
| Heavy Atom Count | 51 |
| Formal Charge | 0 |
| Complexity | 980.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Hongyu Lv, Xin Tang, Menglu Chen. (2023) Ionic Doping of CsPbI3 Perovskite Nanocrystals Improves Luminescence and Stability in Patterned Large-Area Light-Emitting Diodes. ACS Applied Nano Materials, 6 (20): (18918–18925). |
| 2. Man Li, Xin Li, Ying-Feng Han. (2025) Achieving a Record Photoluminescence Quantum Yield in Green Light-Emitting Carbon-Centered Radicals with Nanosecond Emission Lifetimes. ADVANCED MATERIALS, (2418324). |
| 3. Jiaxin Sun, Wenjie Xu, Yixiang Liu, Bin Sun, Jie Xiong, Yongfu Lian, Yanhui Lou, Lai Feng. (2024) Precursor engineering towards orange- and red-emissive carbon dots for LEDs with tunable emission colors. Nanoscale, |
| 4. Yangyang Cai, Siyu Yan, Yue-jian Lin, Tingting Lin, Longzhen Qiu, Xiaoyong Pan, Weizhi Wang. (2025) Quantum Wells in Magnesium–Manganese Bimetallic Antiperovskites for High Luminescence. ACS Applied Materials & Interfaces, |