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Azo Coupling
In organic chemistry, an azo coupling is an reaction between a diazonium compound () and another aromatic compound that produces an azo compound (). In this electrophilic aromatic substitution reaction, the aryldiazonium cation is the electrophile, and the activated carbon (usually from an arene, which is called coupling agent), serves as a nucleophile. Classical coupling agents are phenols and naphthols. Usually the diazonium reagent attacks at the para position of the coupling agent. When the para position is occupied, coupling occurs at a ortho position, albeit at a slower rate. Uses of the reaction Aromatic azo compounds tend to be brightly colored due to their extended conjugated systems. Many are useful dyes (see azo dye). Important azo dyes include methyl red and pigment red 170. Azo printing exploits this reaction as well. In this case, the diazonium ion is degraded by light, leaving a latent image in undegraded diazonium salt which is made to react with a phe ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Dye Coupler
Dye coupler is present in Chromogen, chromogenic photographic film, film and photographic paper, paper used in photography, primarily color photography. When a color developer Redox, reduces ionized (exposed) silver halide crystals, the developer is oxidized, and the oxidized molecules react with dye coupler molecules to form a dye ''in situ.'' The silver image is removed by subsequent bleach and Photographic fixer, fix processes, so the final image will consist of the dye image. Dye coupler technology has seen considerable advancement since the beginning of modern color photography. Major film and paper manufacturers have continually improved the stability of the image dye by improving couplers, particularly since the 1980s, so that Archive, archival properties of images are enhanced in newer color papers and films. Generally speaking, dye couplers for paper use are given more emphasis on the image permanence than those for film use, but some modern films (such as Fujifilm, Fujic ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Pigment Red 170
Naphthol Red (Pigment red 170 or PR170) is an organic pigment extensively used in automotive coatings and painting. It is produced synthetically by converting p-aminobenzamide into the corresponding diazonium compound followed by coupling with 3-hydroxy-2-naphththoic acid (2-ethoxy)anilide ("Naphtol AS-PH" dye precursor). : In the solid state the hydrazo tautomer forms and several crystal structures exist. In the initial α polymorph the molecules are arranged in a herringbone pattern with extensive hydrogen bonding. The φ polymorph is more dense and more stable and produced industrially by thermal treatment in water at 130°C under pressure. In this phase the molecules are planar and arranged in layers. Extensive hydrogen bonding exists within the layer but between layers the only interactions are Van der Waals forces. Dense crystal structures are preferred for pigments used in coatings because in the event of photochemical decomposition the fragments are locked in place ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Phenyldiazonium
Benzenediazonium tetrafluoroborate is an organic compound with the chemical formula, formula [C6H5N2]BF4. It is a salt of a diazonium compound, diazonium cation and tetrafluoroborate. It exists as a colourless solid that is soluble in polar solvents. It is the parent member of the aryldiazonium compounds, which are widely used in organic chemistry. Synthesis Diazotization of aniline: : C6H5NH2 + HNO2 (from NaNO2 and HCl) + HCl → [C6H5N2]Cl + 2 H2O The tetrafluoroborate can be obtained from crude benzenediazonium chloride by salt metathesis using tetrafluoroboric acid. : [C6H5N2]Cl + HBF4 → [C6H5N2]BF4 + HCl The tetrafluoroborate is more stable than the chloride. Properties The diazo group (N2) can be replaced by many other groups, usually anions, giving a variety of substituted phenyl derivatives: :C6H5N2+ + Nu− → C6H5Nu + N2 These transformations are associated with many named reactions including the Schiemann reaction, Sandmeyer reaction, and Gomberg–Bachmann r ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
β-naphthol
2-Naphthol, or β-naphthol, is a fluorescence, fluorescent colorless (or occasionally yellow) crystalline solid with the formula C10H7OH. It is an isomer of 1-Naphthol, 1-naphthol, differing by the location of the hydroxide, hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol, but more reactive. Both isomers are soluble in simple Alcohol (chemistry), alcohols, ethers, and chloroform. 2-Naphthol is a widely used intermediate for the production of dyes and other compounds. Production Traditionally, 2-naphthol is produced by a two-step process that begins with the sulfonation of naphthalene in sulfuric acid:full-text PDF/ref> :C10H8 + H2SO4 → C10H7SO3H + H2O The sulfonic acid group is then cleaved in molten sodium hydroxide: :C10H7(SO3H) + 3 NaOH → C10H7ONa + Na2SO3 + 2 H2O Neutralization of the product with acid gives 2-naphthol. 2-Naphthol can also be produced by a method analogous to the cumene process. 2-Naphthol-deri ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Synthesis Of Organol Brown N
Synthesis or synthesize may refer to: Science Chemistry and biochemistry *Chemical synthesis, the execution of chemical reactions to form a more complex molecule from chemical precursors **Organic synthesis, the chemical synthesis of organic compounds ***Total synthesis, the complete organic synthesis of complex organic compounds, usually without the aid of biological processes ***Convergent synthesis or linear synthesis, a strategy to improve the efficiency of multi-step chemical syntheses **Dehydration synthesis, a chemical synthesis resulting in the loss of a water molecule *Biosynthesis, the creation of an organic compound in a living organism, usually aided by enzymes **Photosynthesis, a biochemical reaction using a carbon molecule to produce an organic molecule, using sunlight as a catalyst **Chemosynthesis, the synthesis of biological compounds into organic waste, using methane or an oxidized molecule as a catalyst **Amino acid synthesis, the synthesis of an amino acid ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
1-Naphthol
1-Naphthol, or α-naphthol, is an organic compound with the formula . It is a fluorescent white solid. 1-Naphthol differs from its isomer 2-naphthol by the location of the hydroxyl group on the naphthalene ring. The naphthols are naphthalene homologues of phenol. Both isomers are soluble in simple organic solvents. They are precursors to a variety of useful compounds. Production 1-Naphthol is prepared by two main routes. In one method, naphthalene is nitrated to give 1-nitronaphthalene, which is hydrogenated to the amine followed by hydrolysis: : : : Alternatively, naphthalene is hydrogenated to tetralin, which is oxidized to 1-tetralone, which undergoes dehydrogenation. Reactions Some reactions of 1-naphthol are explicable with reference to its tautomerism, which produces a small amount of the keto tautomer. : One consequence of this tautomerism is the Bucherer reaction, the ammonolysis of 1-naphthol to give 1-aminonaphthalene. 1-Naphthol biodegrades via format ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Aniline
Aniline (From , meaning ' indigo shrub', and ''-ine'' indicating a derived substance) is an organic compound with the formula . Consisting of a phenyl group () attached to an amino group (), aniline is the simplest aromatic amine. It is an industrially significant commodity chemical, as well as a versatile starting material for fine chemical synthesis. Its main use is in the manufacture of precursors to polyurethane, dyes, and other industrial chemicals. Like most volatile amines, it has the odor of rotten fish. It ignites readily, burning with a smoky flame characteristic of aromatic compounds. It is toxic to humans. Relative to benzene, aniline is "electron-rich". It thus participates more rapidly in electrophilic aromatic substitution reactions. Likewise, it is also prone to oxidation: while freshly purified aniline is an almost colorless oil, exposure to air results in gradual darkening to yellow or red, due to the formation of strongly colored, oxidized impurities. Ani ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Solvent Yellow 7
Solvent Yellow 7 is an aromatic organic molecule and a common azo dye with a formula of C6H5N2C6H4OH. It has a phenolic hydroxyl and an azo group in the same molecule. Synthesis Like most azobenzenes, Solvent Yellow 7 can be synthesized by the reaction of the phenyldiazonium salt with phenol. The optimal pH value for this azo coupling is 8.5-10. The reaction is carried out in water, since sodium chloride (or potassium chloride) formed in the reaction is soluble in water, while the product precipitates. As azo dyes are not usually water soluble, the effect of various solvents on them has been studied analytically, and likewise analytical methods and calculations for the color concentration developed. Further reactions The molecule can be further reacted including with bromine, and other halogens. Other reactions include nitration. The reactivity with Grignard reagents has also been studied. Toxicology The toxicology has been extensively studied, including IARC studies. T ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Benzenediazonium Chloride
Benzenediazonium tetrafluoroborate is an organic compound with the formula 6H5N2F4. It is a salt of a diazonium cation and tetrafluoroborate. It exists as a colourless solid that is soluble in polar solvents. It is the parent member of the aryldiazonium compounds, which are widely used in organic chemistry. Synthesis Diazotization of aniline: : C6H5NH2 + HNO2 (from NaNO2 and HCl) + HCl → 6H5N2l + 2 H2O The tetrafluoroborate can be obtained from crude benzenediazonium chloride by salt metathesis using tetrafluoroboric acid. : 6H5N2l + HBF4 → 6H5N2F4 + HCl The tetrafluoroborate is more stable than the chloride. Properties The diazo group (N2) can be replaced by many other groups, usually anions, giving a variety of substituted phenyl derivatives: :C6H5N2+ + Nu− → C6H5Nu + N2 These transformations are associated with many named reactions including the Schiemann reaction, Sandmeyer reaction, and Gomberg–Bachmann reaction. A wide range of groups that can b ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Phenol
Phenol (also known as carbolic acid, phenolic acid, or benzenol) is an aromatic organic compound with the molecular formula . It is a white crystalline solid that is volatile and can catch fire. The molecule consists of a phenyl group () bonded to a hydroxy group (). Mildly acidic, it requires careful handling because it can cause chemical burns. It is acutely toxic and is considered a health hazard. Phenol was first extracted from coal tar, but today is produced on a large scale (about 7 million tonnes a year) from petroleum-derived feedstocks. It is an important industrial commodity as a precursor to many materials and useful compounds, and is a liquid when manufactured. It is primarily used to synthesize plastics and related materials. Phenol and its chemical derivatives are essential for production of polycarbonates, epoxies, explosives such as picric acid, Bakelite, nylon, detergents, herbicides such as phenoxy herbicides, and numerous pharmaceuti ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
Pauly Reaction
The Pauly reaction is a chemical test used for detecting the presence of tyrosine or histidine in proteins. It is named after German chemist Hermann Pauly, who first described the reaction. When proteins containing either tyrosine or histidine are reacted with diazotized sulfanilic acid under alkaline conditions, a red color is formed by a coupling reaction In organic chemistry, a coupling reaction is a type of reaction in which two reactant molecules are bonded together. Such reactions often require the aid of a metal catalyst. In one important reaction type, a main group organometallic compound o .... References Protein methods Biochemistry detection reactions {{analytical-chemistry-stub ... [...More Info...] [...Related Items...] OR: [Wikipedia] [Google] [Baidu] |
