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Melem
In chemistry, melem is a compound with formula ; specifically, 2,5,8-triamino-heptazine or 2,5,8-triamino-tri-''s''-triazine, whose molecule can be described as that of heptazine with the three hydrogen atoms replaced by amino groups. It is a white crystalline solid. Preparation Melem can be prepared by thermal decomposition of various C−N−H compounds, such as melamine C3N3(NH2)3, dicyandiamide H4C2N4, ammonium dicyanamide NH4 (CN)2 cyanamide H2CN2, at 400 to 450 °C. Structure and properties Crystal structure Melem crystallizes in the group P21/c (No. 14), with parameters a = 739.92(1) pm, b = 865.28(3) pm, c = 1338.16(4) pm, β = 99.912(2)°, and Z = 4. The almost-planar molecules are arranged in parallel layers spaced 327 pm apart. The molecule is in the triamino form, rather than one of the possible tautomers. Thermal decomposition When heated above 560°, melem transforms into a graphite-like C−N material. Melemium cations Melem accepts up to three protons yie ...
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Melemium Sulfate
In chemistry, melem is a chemical compound, compound with formula ; specifically, 2,5,8-triamino-heptazine or 2,5,8-triamino-tri-''s''-triazine, whose molecule can be described as that of heptazine with the three hydrogen atoms replaced by amino groups. It is a white crystalline solid. Preparation Melem can be prepared by thermal decomposition of various C−N−H compounds, such as melamine C3N3(NH2)3, dicyandiamide H4C2N4, ammonium dicyanamide NH4[N(CN)2], cyanamide H2CN2, at 400 to 450 °C. Structure and properties Crystal structure Melem crystallizes in the crystallographic group, group P21/c (No. 14), with parameters a = 739.92(1) picometre, pm, b = 865.28(3) pm, c = 1338.16(4) pm, β = 99.912(2)°, and Z = 4. The almost-planar molecules are arranged in parallel layers spaced 327 pm apart. The molecule is in the triamino form, rather than one of the possible tautomers. Thermal decomposition When heated above 560°, melem transforms into a graphite-like C−N material. ...
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Melemium Methylsulfonate
In chemistry, melem is a compound with formula ; specifically, 2,5,8-triamino-heptazine or 2,5,8-triamino-tri-''s''-triazine, whose molecule can be described as that of heptazine with the three hydrogen atoms replaced by amino groups. It is a white crystalline solid. Preparation Melem can be prepared by thermal decomposition of various C−N−H compounds, such as melamine C3N3(NH2)3, dicyandiamide H4C2N4, ammonium dicyanamide NH4 (CN)2 cyanamide H2CN2, at 400 to 450 °C. Structure and properties Crystal structure Melem crystallizes in the group P21/c (No. 14), with parameters a = 739.92(1) pm, b = 865.28(3) pm, c = 1338.16(4) pm, β = 99.912(2)°, and Z = 4. The almost-planar molecules are arranged in parallel layers spaced 327 pm apart. The molecule is in the triamino form, rather than one of the possible tautomers. Thermal decomposition When heated above 560°, melem transforms into a graphite-like C−N material. Melemium cations Melem accepts up to three protons yiel ...
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Melemium Perchlorate
In chemistry, melem is a compound with formula ; specifically, 2,5,8-triamino-heptazine or 2,5,8-triamino-tri-''s''-triazine, whose molecule can be described as that of heptazine with the three hydrogen atoms replaced by amino groups. It is a white crystalline solid. Preparation Melem can be prepared by thermal decomposition of various C−N−H compounds, such as melamine C3N3(NH2)3, dicyandiamide H4C2N4, ammonium dicyanamide NH4 (CN)2 cyanamide H2CN2, at 400 to 450 °C. Structure and properties Crystal structure Melem crystallizes in the group P21/c (No. 14), with parameters a = 739.92(1) pm, b = 865.28(3) pm, c = 1338.16(4) pm, β = 99.912(2)°, and Z = 4. The almost-planar molecules are arranged in parallel layers spaced 327 pm apart. The molecule is in the triamino form, rather than one of the possible tautomers. Thermal decomposition When heated above 560°, melem transforms into a graphite-like C−N material. Melemium cations Melem accepts up to three protons yiel ...
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Melemium Hydrogensulfate
In chemistry, melem is a compound with formula ; specifically, 2,5,8-triamino-heptazine or 2,5,8-triamino-tri-''s''-triazine, whose molecule can be described as that of heptazine with the three hydrogen atoms replaced by amino groups. It is a white crystalline solid. Preparation Melem can be prepared by thermal decomposition of various C−N−H compounds, such as melamine C3N3(NH2)3, dicyandiamide H4C2N4, ammonium dicyanamide NH4 (CN)2 cyanamide H2CN2, at 400 to 450 °C. Structure and properties Crystal structure Melem crystallizes in the group P21/c (No. 14), with parameters a = 739.92(1) pm, b = 865.28(3) pm, c = 1338.16(4) pm, β = 99.912(2)°, and Z = 4. The almost-planar molecules are arranged in parallel layers spaced 327 pm apart. The molecule is in the triamino form, rather than one of the possible tautomers. Thermal decomposition When heated above 560°, melem transforms into a graphite-like C−N material. Melemium cations Melem accepts up to three protons yiel ...
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Melon (chemistry)
In chemistry, melon is a compound of carbon, nitrogen, and hydrogen of still somewhat uncertain composition, consisting mostly of heptazine units linked and closed by amine groups and bridges (, , , etc.). It is a pale yellow solid, insoluble in most solvents. A careful 2001 study indicates the formula , that consists of ten imino-heptazine units connected into a linear chain by amino bridges; that is, . However, other researchers are still proposing different structures. Melon is the oldest known compound with the heptazine core, having been described in the early 19th century. It has been little studied until recently, when it has been recognized as a notable photocatalyst and as a possible precursor to carbon nitride. History In 1834 Liebig described the compounds that he named melamine, melam, and melon. The compound received little attention for a long time, due to its insolubility. In 1937 Linus Pauling showed by x-ray crystallography that the structure of melon and ...
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Melamine
Melamine is an organic compound with the formula C3H6N6. This white solid is a trimer of cyanamide, with a 1,3,5-triazine skeleton. Like cyanamide, it contains 67% nitrogen by mass, and its derivatives have fire retardant properties due to its release of nitrogen gas when burned or charred. Melamine can be combined with formaldehyde and other agents to produce melamine resins. Such resins are characteristically durable thermosetting plastic used in high pressure decorative laminates such as Formica, melamine dinnerware, laminate flooring, and dry erase boards. Melamine foam is used as insulation, soundproofing material and in polymeric cleaning products, such as Magic Eraser. Melamine was once illegally added to baby formula in China, in order to increase the apparent protein content. Ingestion of melamine may lead to reproductive damage, or bladder or kidney stones, and bladder cancer. It is also an irritant when inhaled or in contact with the skin or eyes. The United N ...
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Heptazine
Heptazine, or tri-''s''-triazine or cyamelurine, is a chemical compound with formula , that consist of a planar triangular core group or three fused triazine rings, with three hydrogen atoms at the corners. It is a yellow, weakly fluorescent solid with melting point over 300 °C. It is soluble in organic solvents such as acetonitrile, but is decomposed by water in the presence of light. The name "heptazine" is also used for derivative compounds, which have the three hydrogens substituted by other functional groups. Heptazine oligomers and polymers were discovered in the 19th century but their study has long been hampered by their general insolubility. They are used as flame retardants. Heptazine derivatives have been the object of interest recently for potential applications in electronics materials, explosives, and more. The synthesis of heptazine proper was reported only in 1982. History Berzelius discovered in 1815 that the ignition of mercuric thiocyanate yielded, ...
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Melamine
Melamine is an organic compound with the formula C3H6N6. This white solid is a trimer of cyanamide, with a 1,3,5-triazine skeleton. Like cyanamide, it contains 67% nitrogen by mass, and its derivatives have fire retardant properties due to its release of nitrogen gas when burned or charred. Melamine can be combined with formaldehyde and other agents to produce melamine resins. Such resins are characteristically durable thermosetting plastic used in high pressure decorative laminates such as Formica, melamine dinnerware, laminate flooring, and dry erase boards. Melamine foam is used as insulation, soundproofing material and in polymeric cleaning products, such as Magic Eraser. Melamine was once illegally added to baby formula in China, in order to increase the apparent protein content. Ingestion of melamine may lead to reproductive damage, or bladder or kidney stones, and bladder cancer. It is also an irritant when inhaled or in contact with the skin or eyes. The United N ...
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Melam (chemistry)
, Section2={{Chembox Properties , Formula = C6H9N11 , MolarMass = 235.21 g/mol , Appearance = white powder , Density = , MeltingPt = , MeltingPt_notes = , BoilingPt = , BoilingPt_notes = , Solubility = insoluble , SolubleOther = slightly soluble in acids , Solvent = , pKa = , pKb = , Section7={{Chembox Hazards , MainHazards = , NFPA-H = , NFPA-F = , NFPA-R = , NFPA-S = , FlashPt = , AutoignitionPt = , ExploLimits = , PEL = Melam (''N2''-(4,6-diamino-1,3,5-triazin-2-yl)-1,3,5-triazine-2,4,6-triamine) is a condensation product of melamine. Synthesis Melam was discovered by Liebig in 1834 from the residue of heating ammonium thiocyanate. Chemical property In the presence of 30% ammonia, melam undergoes hydrolysis to form ammeline and melamine. It also reacts with concentrated nitric acid, producing cyanuric acid. Upon heating, melam first loses ammonia to form melem, and then melon. References * B. Bann and S.A. Miller, "Melamines and deriva ...
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Nitrogen Heterocycles
Nitrogen is the chemical element with the symbol N and atomic number 7. Nitrogen is a nonmetal and the lightest member of group 15 of the periodic table, often called the pnictogens. It is a common element in the universe, estimated at seventh in total abundance in the Milky Way and the Solar System. At standard temperature and pressure, two atoms of the element bond to form N2, a colorless and odorless diatomic gas. N2 forms about 78% of Earth's atmosphere, making it the most abundant uncombined element. Nitrogen occurs in all organisms, primarily in amino acids (and thus proteins), in the nucleic acids ( DNA and RNA) and in the energy transfer molecule adenosine triphosphate. The human body contains about 3% nitrogen by mass, the fourth most abundant element in the body after oxygen, carbon, and hydrogen. The nitrogen cycle describes the movement of the element from the air, into the biosphere and organic compounds, then back into the atmosphere. Many industrially importa ...
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Heterocyclic Compounds With 3 Rings
A heterocyclic compound or ring structure is a cyclic compound that has atoms of at least two different elements as members of its ring(s). Heterocyclic chemistry is the branch of organic chemistry dealing with the synthesis, properties, and applications of these heterocycles. Examples of heterocyclic compounds include all of the nucleic acids, the majority of drugs, most biomass (cellulose and related materials), and many natural and synthetic dyes. More than half of known compounds are heterocycles. 59% of US FDA-approved drugs contain nitrogen heterocycles. Classification The study of heterocyclic chemistry focuses especially on unsaturated derivatives, and the preponderance of work and applications involves unstrained 5- and 6-membered rings. Included are pyridine, thiophene, pyrrole, and furan. Another large class of heterocycles refers to those fused to benzene rings. For example, the fused benzene derivatives of pyridine, thiophene, pyrrole, and furan are quinol ...
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Ludwig-Maximilians-Universität München
The Ludwig Maximilian University of Munich (simply University of Munich or LMU; german: Ludwig-Maximilians-Universität München) is a public research university in Munich, Germany. It is Germany's sixth-oldest university in continuous operation. Originally established in Ingolstadt in 1472 by Duke Ludwig IX of Bavaria-Landshut, the university was moved in 1800 to Landshut by King Maximilian I of Bavaria when the city was threatened by the French, before being relocated to its present-day location in Munich in 1826 by King Ludwig I of Bavaria. In 1802, the university was officially named Ludwig-Maximilians-Universität by King Maximilian I of Bavaria in honor of himself and Ludwig IX. LMU is currently the second-largest university in Germany in terms of student population; in the 2018/19 winter semester, the university had a total of 51,606 matriculated students. Of these, 9,424 were freshmen while international students totalled 8,875 or approximately 17% of the student popu ...
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