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1,3,5-Tris(1-phenyl-1H-benzimidazol-2-yl)benzene - 99.5% (HPLC), high purity , CAS No.192198-85-9

    Grade & Purity:
  • ≥99.5%(HPLC)
In stock
Item Number
T168233
Grouped product items
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
View related series
Organic light emitting diode (18)

Basic Description

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.

Taxonomic Classification

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

Names and Identifiers

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

Certificates(CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

7 results found

Lot Number Certificate Type Date Item
J22111424 Certificate of Analysis Jul 08, 2024 T168233
J22111407 Certificate of Analysis Jul 08, 2024 T168233
J22111408 Certificate of Analysis Jul 08, 2024 T168233
L2118106 Certificate of Analysis Oct 08, 2023 T168233
L2118095 Certificate of Analysis Oct 08, 2023 T168233
I2114353 Certificate of Analysis Jun 16, 2023 T168233
I2114354 Certificate of Analysis Jun 16, 2023 T168233

Chemical and Physical Properties

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

Citations of This Product

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,  (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,     

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