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9-ANTHRALDEHYDE | ||
PRODUCT IDENTIFICATION |
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CAS NO. | 642-31-9 |
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EINECS NO. | 211-383-0 | |
FORMULA | C15H10O | |
MOL WT. | 206.25 | |
H.S. CODE | 2912.29 | |
TOXICITY | ||
SYNONYMS | 9-Anthracenecarbaldehyde; 9-Formylanthracene; | |
9-Anthrylaldehyde; 9-Anthrylcarboxaldehyde; Anthracene-9-carboxaldehyde; Anthracene-9-aldehyde; | ||
SMILES |
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CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | yellow crystalline powder | |
MELTING POINT | 101 - 105 C | |
BOILING POINT | ||
SPECIFIC GRAVITY | ||
SOLUBILITY IN WATER | Insoluble | |
pH |
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AUTOIGNITION | ||
VAPOR DENSITY | ||
NFPA RATINGS | Health: 1; Flammability: 0; Instability: 0 | |
FLASH POINT |
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STABILITY | Stable under ordinary conditions. Light sensitive | |
GENERAL DESCRIPTION AND APPLICATIONS |
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Anthracene is a tricyclic aromatic hydrocarbonn derived from coal tar; melts at 218°C,boils at 354°C, insoluble in water but is soluble in most organic solvents such as carbon disulfide, alcohols, benzene, chloroform, and hydronaphthalenes. Its molecular structure consists of three benzenelike rings joined side by side (the general formula CnH2n-18) and its oxidation yields anthraquinone, the parent substance of a large class of dyes and pigments. 9-Anthraldehyde is used as an intermedaite for dyes, pigment, pharmaceuticals and other organic compounds. Chemoluminescence (or chemiluminescence) is the luminescence (light emission) generated as the result of direct transformation of chemical energy into light energy without showing a corresponding degree of heat. When the reactants are oxidized in the presence of catalysts, they yield intermediate complexes which get rid of the extra energy quickly in the form of light (ultraviolet, visible, or infrared) photons to become a lower energy level products. Luminol (3-Aminophthalhydrazide) is a chemoluminescent dye. It is used for biological detection of metal cations and blood. The iron in haemoglobin acts as a catalyst to accelerate the process. Luciferins are bioluminescence emitting light pigments originated by an organism like bacteria, fungi, fireflies and deep sea fish. Enzymes and proteins associated with bioluminescence have been developed for biomedical research. Coelenterazine, substrate for luciferase and photoprotein, is used as a intracellular luminophore as to measure changes in oxide and Ca2+ levels in aequorin cells. Fluorescence such as fluorescein undergoes light-emission processes, but the energy source is light absorption from an external source. Some Chemoluminescence related compounds include:
Due to extended pi-electron cloud overlaps, organometallic molecules or aromatic oligometers such as anthracene exhibit semiconductor properties. Conductive polymers have extended delocalized bonds that creates electrical conductivity when charge carriers generated make positive charges (holes) and negative charges (electrons) move to opposite electrodes. Doping is the intentional impurities in a pure semiconductor to generate charge carriers. The transportation of charges is responsible for fluorescence and electrical energy. These can form well-ordered thin crystalline films. Organic semiconductors have some merits of self radiation, flexibility, light weight, easy fabrication, and low cost. Organic electroluminescence materials have lead to the rapid development of photovoltaic and display devices such as organic solar cells, biosensitizers, OLED(Organic Light Emiting Diode), OTFT(Organic Thin Film Transistor), Wearable Display, and e-Paper. Some examples of organic electroluminescence materials are:
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SALES SPECIFICATION | ||
APPEARANCE |
yellow crystalline powder | |
PURITY (G.C) | 99.0% min | |
LOSS ON DRYING |
0.5% max |
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MELTING POINT | 101 - 105 C | |
TRANSPORTATION | ||
PACKING | 25kgs in fiber drum | |
HAZARD CLASS | Not regulated | |
UN NO. | ||
OTHER INFORMATION | ||
Hazard Symbols: n/a, Risk Phrases: , Safety Phrases: 24/25-28A-37-45 |
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