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p-Terphenyl | CAS 92-94-4
| Catalog Number | A17-0125 |
| Category | Laser Dyes |
| Molecular Formula | C18H14 |
| Molecular Weight | 230.30 |
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Product Introduction
p-Terphenyl is a detector of neutron. It can be used in analytical studies.
Chemical Information
Product Specification
Application
QC Data
Computed Properties
Literatures
Patents
| Synonyms | 1,4-diphenylbenzene |
| Purity | 98% |
| IUPAC Name | 1,4-diphenylbenzene |
| Canonical SMILES | C1=CC=C(C=C1)C2=CC=C(C=C2)C3=CC=CC=C3 |
| InChI | InChI=1S/C18H14/c1-3-7-15(8-4-1)17-11-13-18(14-12-17)16-9-5-2-6-10-16/h1-14H |
| InChIKey | XJKSTNDFUHDPQJ-UHFFFAOYSA-N |
| Solubility | Insoluble |
| Density | 1.23 g/cm3 |
| Appearance | White to off-white solid |
| Boiling Point | 383 °C |
| Vapor Pressure | Very low (NIOSH, 2022) |
| LogP | 5.02060 |
| Storage | RT. Keep in the tight container. |
| Signal | Warning |
| GHSHazardStatements | H315 (97.96%): Causes skin irritation [Warning Skin corrosion/irritation] H319 (97.96%): Causes serious eye irritation [Warning Serious eye damage/eye irritation] H335 (93.88%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation] H400 (85.71%): Very toxic to aquatic life [Warning Hazardous to the aquatic environment, acute hazard] |
| Precautionary Statement Codes | P261, P264, P264+P265, P271, P273, P280, P302+P352, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P391, P403+P233, P405, and P501 (The corresponding statement to each P-code can be found at the GHS Classification page.) |
p-Terphenyl is an organic compound with a wide range of applications in various fields. Here are some key applications of p-Terphenyl:
Fluorescent Probes: p-Terphenyl is employed as a fluorescent probe in scientific research due to its strong fluorescence properties. It is used to label biomolecules in fluorescence microscopy and spectroscopy studies. Researchers can leverage its fluorescence for visualizing cellular components and molecular interactions in real-time.
Organic Semiconductors: p-Terphenyl serves as a valuable material in the development of organic semiconductors for electronic devices. It is used in organic light-emitting diodes (OLEDs) and organic photovoltaic cells due to its good charge transport properties. These applications are crucial for advancing flexible and wearable electronic technologies.
Antioxidants: p-Terphenyl and its derivatives can act as antioxidants, scavenging free radicals and preventing oxidative damage in various applications. In the food and cosmetic industries, p-Terphenyl is added to products to enhance shelf life and stability. It helps protect ingredients from degradation caused by exposure to oxygen and light.
Analytical Chemistry: p-Terphenyl is used as an internal standard and reference compound in analytical chemistry. Its well-characterized properties make it an ideal choice for calibrating instruments such as gas chromatographs and mass spectrometers. This ensures accurate and reliable analytical measurements in various research and industrial settings.
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 2 |
| Exact Mass | 230.109550447 g/mol |
| Monoisotopic Mass | 230.109550447 g/mol |
| Topological Polar Surface Area | 0Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 198 |
| 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 |
| PMID | Publication Date | Title | Journal |
|---|---|---|---|
| 23040979 | 2012-11-09 | Synthesis of polychlorinated terphenyl mixtures and gas chromatography with mass spectrometry data of tetra- to octachlorinated ortho-, meta-, and para-terphenyls | Journal of chromatography. A |
| 23061916 | 2012-11-02 | Phenyl shifts in substituted arenes via ipso arenium ions | The Journal of organic chemistry |
| 22996418 | 2012-10-22 | Efficient synthesis of oxygenated terphenyls and other oligomers: sequential arylation reactions through phenol oxidation-rearomatization | Chemistry (Weinheim an der Bergstrasse, Germany) |
| 22931365 | 2012-10-11 | Organization of T-shaped facial amphiphiles at the air/water interface studied by infrared reflection absorption spectroscopy | The journal of physical chemistry. B |
| 22859218 | 2012-09-21 | Synthesis, structure and luminescence properties of Cu(II), Zn(II) and Cd(II) complexes with 4'-terphenylterpyridine | Dalton transactions (Cambridge, England : 2003) |
| Publication Number | Title | Priority Date |
|---|---|---|
| CN-115109236-A | A kind of piperidine tertiary amine group polymer containing sp3 carbon-based skeleton structure and its application | 2022-07-29 |
| CN-115236720-A | A multi-type ray detection device | 2022-07-21 |
| CN-115094454-A | Electrolyzer and method for urea electrolytic hydrogen production and carbon reduction | 2022-07-01 |
| CN-217869103-U | Electrolytic cells for hydrogen production and carbon reduction by electrolysis of urea | 2022-07-01 |
| CN-115201887-A | An ultra-low background alpha particle detector and method for measuring alpha particles | 2022-06-23 |
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