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N-ETHYLCARBAZOLE | ||
PRODUCT IDENTIFICATION |
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CAS NO. | 86-28-2 | |
EINECS NO. | 201-660-4 | |
FORMULA | C14H13N | |
MOL WT. | 195.26 | |
H.S. CODE |
2933.90 | |
TOXICITY | ||
SYNONYMS | 9-Ethyl-9H-Carbazole; 9-Ethylcarbazole; | |
SMILES |
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CLASSIFICATION |
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PHYSICAL AND CHEMICAL PROPERTIES |
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PHYSICAL STATE | White to Grey Crystalline Powder | |
MELTING POINT | 66 - 70 C | |
BOILING POINT | ||
SPECIFIC GRAVITY |
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SOLUBILITY IN WATER | Insoluble | |
pH | ||
VAPOR DENSITY | ||
AUTOIGNITION |
620 C | |
NFPA RATINGS | Health: 1; Flammability: 0; Reactivity: 0 | |
REFRACTIVE INDEX |
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FLASH POINT |
185 C | |
STABILITY | Stable under ordinary conditions | |
APPLICATIONS |
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Carbazole, azafluorene, is a group of organic heterocyclic compounds containing nitrogen atom in dibenzopyrrole system; white crystalline solid, insoluble in water, melts at 244 C. Carbazole and its derivatives are widely used as an intermediate in synthesis of pharmaceuticals, agrochemicals, dyes, pigments and other organic compounds. | ||
SALES SPECIFICATION | ||
APPEARANCE |
White to Grey Crystalline Powder | |
CONTENT | 97.0% | |
MELTING POINT | 66 - 70 C | |
TRANSPORTATION | ||
PACKING | 25kgs in fiber drum | |
HAZARD CLASS | ||
UN NO. | ||
OTHER INFORMATION | ||
Hazard Symbols: , Risk Phrases: , Safety Phrases:24/25-28A-37-45 | ||
GENERAL DESCRIPTION OF PYRROLE | ||
Pyrrole is one of a class of organic heterocyclic compounds of five-membered diunsaturated ring structure composed of four carbon atoms and one nitrogen atom. The simplest member of the pyrrole family is Pyrrole itself; colorless to pale yellow oil with with pungent taste and similar to chloroform odor; insoluble in water; soluble in alcohol, ether, and dilute acids; boils at 129 - 131 C; polymerizes in light. Pyrrole rings are components of larger aromatic rings including the amino acids proline and hydroxyproline; and in coloured natural products as joined rings and attached to straight chains. Pyrrole and its derivatives are widely used as an intermediate in synthesis of pharmaceuticals, medicines, agrochemicals, dyes, photographic chemicals, perfumes and other organic compounds. | ||
GENERAL DESCRIPTION OF PAHs |
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Polycyclic aromatic hydrocarbons (also called polynuclear hydrocarbons) have two
or more single or fused aromatic rings if a pair of carbon atoms is shared
between rings in their molecules. In particular, the term 'PAH' refers to the
compounds consisting of only carbon and hydrogen atoms while the wider term
'polycyclic aromatic compounds' includes the alkyl-substituted derivatives and
functional derivatives such as nitro- and hydroxy-PAH as well as the
heterocyclic analogues, which contain one or more hetero atoms in the aromatic
structure. PAHs exist in various combinations that manifest various functions
such as light sensitivity, heat resistance, conductivity, emittability,
corrosion resistance and physiological action. The simplest examples are
naphthalene having two benzene rings side by side and biphenyl having two
bond-connected benzene rings. PAHs are not found in synthetic products and
are non-essential for the growth of living cells. The general
characteristics of PAH describe high melting- and boiling-points (they are
solid), low vapour pressure, and very low water solubility, decreasing with
increasing molecular weight whereas resistance to oxidation, reduction, and
vapourization increases. Vapour pressure tends to decrease with increasing
molecular weight. PAHs are highly lipophilic and readily soluble in organic
solvents. The lower molecular weight PAHs of 2 or 3 ring groups such as
naphthalenes, fluorenes, phenanthrenes, and anthracenes have toxicity which
tends to decrease with increasing molecular weight. PAHs are not synthesized
chemically for industrial purposes but are isolated from concentrated coal-tar
products (or from pyrolysis of coal hydrocarbons) followed by subsequent
purification through repeated distillation and crystallization. Some PAHs such
as naphthalene are also obtained from the concentration of the high boiling
residual oil (and asphalt) derived from crude petroleum refinery processing.
These PAHs are mostly used as intermediaries in pharmaceuticals, agricultural
products,
photographic products, thermosetting plastics, lubricating materials, and other
chemical
industries. General uses are;
Precise PAHs, specific refined products are used also in the field of electronics, functional plastics and liquid crystals. Pharmaceutical and agricultural PAHs obtained coal tar are such materials as indole, indolizine, indene, quinoline, quinalidine, isoquinoline and their derivatives. High boiling-point special solvent are such materials as tetoralin, decaline, methyl-naphthalenes. Coumarins and dihydrocoumarins which can be obtained coal tar are PAHs used in perfumery. Thermosensitive paper sensitizer PAHs are such materials as p-benzylbiphenyl and ethylbiphenyl. |
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