
2,2''-Dimethyl-p-terphenyl | CAS 53092-64-1
| Catalog Number | A17-0086 |
| Category | Laser Dyes |
| Molecular Formula | C20H18 |
| Molecular Weight | 258.36 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
High-efficiency blue fluor with excellent scintillation yield. Used in radiation detection, wavelength shifters, and optical materials.
Chemical Information
Application
Computed Properties
Patents
Chemical Information
| Synonyms | 2,2''-dimethyl-1,1':4'1''-terphenyl; BM-Terphenyl; BMT; 1,2-Bis(2-methylphenyl)benzene |
| IUPAC Name | 1,4-bis(2-methylphenyl)benzene |
| SMILES | CC1=CC=CC=C1C2=CC=C(C=C2)C3=CC=CC=C3C |
| InChI | InChI=1S/C20H18/c1-15-7-3-5-9-19(15)17-11-13-18(14-12-17)20-10-6-4-8-16(20)2/h3-14H,1-2H3 |
| InChIKey | MSMADJZSMBWBTF-UHFFFAOYSA-N |
| Appearance | White Crystalline Solid |
Application
2,2''-Dimethyl-p-terphenyl is an aromatic, conjugated small molecule commonly used as a fluorescent material in organic optoelectronic and photophysical research contexts. Its rigid, extended pi-system supports light absorption and emission behavior that makes it useful as a scintillator or wavelength-shifting component, and it is also used in fluorescence-based imaging and sensing material development where stable organic emission is required.
1. Scintillator And Wavelength Shifting
2,2''-Dimethyl-p-terphenyl is used in scintillation and radiation-detection development as a wavelength shifter and fluorescent component in composite scintillator formulations. Researchers and industrial R&D groups incorporate it into polymer or solid matrices to convert higher-energy excitation into emission that better matches downstream optical readout, supporting material-level tuning of emission color for photodetector coupling.
2. Organic Light-Emitting Materials
2,2''-Dimethyl-p-terphenyl finds application in organic electroluminescent material research where aromatic fluorescent emitters are needed to build light-emitting layers and host-dopant systems. Device and materials scientists use it to explore emission characteristics and charge/energy transfer behavior within organic thin-film architectures, including studies aimed at optimizing color and emission stability in electroluminescent stacks.
3. Fluorescent Polymer And Coating Formulations
2,2''-Dimethyl-p-terphenyl is applied in the development of fluorescent polymers, doped films, and coating materials for optical readout experiments. Materials engineers and analytical developers use it to create solid-state fluorescence standards and to prototype visualization layers for imaging setups where an organic emissive component is embedded into a bulk or surface coating to enable repeatable optical response under controlled illumination.
Computed Properties
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 2 |
| Exact Mass | 258.140850574 g/mol |
| Monoisotopic Mass | 258.140850574 g/mol |
| Topological Polar Surface Area | 0Ų |
| Heavy Atom Count | 20 |
| Formal Charge | 0 |
| Complexity | 256 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| Covalently-Bonded Unit Count | 1 |
| Compound Is Canonicalized | Yes |
Patents
| Publication Number | Title | Priority Date |
|---|---|---|
| CA-3059584-A1 | Methods for assessing cell surface glycosylation | 2017-04-14 |
| CN-110709700-A | Methods for Assessing Cell Surface Glycosylation | 2017-04-14 |
| EP-3610261-A1 | Methods for assessing cell surface glycosylation | 2017-04-14 |
| WO-2018191723-A1 | Methods for assessing cell surface glycosylation | 2017-04-14 |
| US-2021255173-A1 | Methods for assessing cell surface glycosylation | 2017-04-14 |
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry