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Merck
CN

T82600

Sigma-Aldrich

三亚苯

98%

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别名:
9,10-苯并菲
经验公式(希尔记法):
C18H12
CAS号:
分子量:
228.29
Beilstein:
1342908
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

98%

bp

438 °C (lit.)

mp

195-198 °C (lit.)

荧光

λex 265 nm; λem 372 nm in cyclohexane

SMILES字符串

c1ccc2c(c1)c3ccccc3c4ccccc24

InChI

1S/C18H12/c1-2-8-14-13(7-1)15-9-3-4-11-17(15)18-12-6-5-10-16(14)18/h1-12H

InChI key

SLGBZMMZGDRARJ-UHFFFAOYSA-N

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象形图

CorrosionEnvironment

警示用语:

Danger

危险声明

危险分类

Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1

WGK

WGK 3

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


分析证书(COA)

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  1. Which document(s) contains shelf-life or expiration date information for a given product?

    If available for a given product, the recommended re-test date or the expiration date can be found on the Certificate of Analysis.

  2. How do I get lot-specific information or a Certificate of Analysis?

    The lot specific COA document can be found by entering the lot number above under the "Documents" section.

  3. How do I find price and availability?

    There are several ways to find pricing and availability for our products. Once you log onto our website, you will find the price and availability displayed on the product detail page. You can contact any of our Customer Sales and Service offices to receive a quote.  USA customers:  1-800-325-3010 or view local office numbers.

  4. What is the Department of Transportation shipping information for this product?

    Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product. 

  5. What solvents can be used to dissolve Product T82600, Triphenylene?

    According to the chemicals encyclopedia published by the Royal Society of Chemistry, triphenylene is expected to be soluble in chloroform or ethanol.

  6. Is Product T82600, Triphenylene, fluorescently active?

    Yes. Triphenylene emits a blue fluorescence upon UV irradiation.

  7. How can Product T82600, Triphenylene, be used?

    Because of its stability towards hydrogenation, triphenylene has been used in optical and display devices.

  8. My question is not addressed here, how can I contact Technical Service for assistance?

    Ask a Scientist here.

Ozcan Kocyigit et al.
Journal of hazardous materials, 183(1-3), 334-340 (2010-08-10)
We presented the synthesis of a novel Schiff base and its complexation properties with some transition metal ions in this work. For this, the 2,3,4,6,7,10,11 hexahydroxytriphenylene (HHTP) as starting material was synthesized according to known procedure. Moreover, the 2-((2-chloroethylimino)methyl) phenol
Vandana Bhalla et al.
Dalton transactions (Cambridge, England : 2003), 41(37), 11413-11418 (2012-08-15)
The binding behavior of triphenylene based copper ensemble prepared in situ has been investigated toward various anions (F(-), Cl(-), Br(-), I(-), CH(3)COO(-), H(2)PO(4)(-), NO(3)(-), OH(-), ClO(4)(-), CN(-), CO(3)(-) and SO(4)(-)) by UV-vis and fluorescence spectroscopy. Among various anions tested, 1-Cu(2+)
Lucas A Haverkate et al.
The journal of physical chemistry. B, 116(43), 13098-13105 (2012-10-05)
Discotic liquid crystalline (DLC) charge transfer (CT) complexes, which combine visible light absorption with rapid charge transfer characteristics within the CT complex, can have a great potential for photovoltaic applications when they can be made to self-assemble in a bulk
Fabián Vaca Chávez et al.
The journal of physical chemistry. B, 116(8), 2339-2346 (2012-02-23)
The Larmor frequency and temperature dependence of the proton nuclear magnetic resonance (NMR) spin-lattice relaxation time was measured in the isotropic and columnar phases of both chain-end fluorinated triphenylene disk-like and fully hydrogenated molecules. In the columnar phase, the results
Mahuya Bagui et al.
The journal of physical chemistry. A, 115(9), 1579-1592 (2011-02-12)
A donor-acceptor charge transfer system based on two discotic mesogens has been synthesized. The donor is either a triphenylene (POG0) or a triphenylene-based conjugated dendron (POG1), while the acceptor is a perylene diimide (PDI) core. The donors are covalently linked

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