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• Basil
  ...he essential oils found in basil. Scientific studies have established that compounds in basil oil have potent antioxidant, anti-cancer, anti-viral, and anti-mic Basil, like other aromatic plants such as fennel and tarragon, contains estragole, a known carcinogen
  8 KB (1,351 words) - 23:10, 1 July 2010
• Wood Gas
  ...s into char, releasing methane (CH₄) and tar rich in polycyclic aromatic hydrocarbons (PAH). Other gasifiers are fed with previously pyrolysed char ...ng internal combustion engine may lead to problematic build-up of unburned compounds.
  11 KB (1,707 words) - 18:26, 24 June 2010
• Quinine
  ...[[anti-arrhythmic]]. Quinine contains two major fused-ring systems: the [[aromatic]] [[quinoline]] and the [[bicyclic]] [[quinuclidine]]. [[Category:Bitter compounds]]
  27 KB (3,844 words) - 16:41, 27 September 2010
• Rifampicin
  ...Journal 1999;319(7215):972 (9 October)}}</ref> they decided to call these compounds "rifamycins". After two years of attempts in order to obtain more stable se ...that replace [[phenylalanine]], [[tryptophan]], and [[tyrosine]] with non-aromatic amino acids result in poor bonding between rifampicin and the RNA polymeras
  18 KB (2,471 words) - 16:43, 27 September 2010
• 4-Aminosalicylic acid
  Like many commercially significant compounds, PAS has many names including ''para''-aminosalicylic acid, ''p''-aminosal [[Category:Aromatic amines]]
  7 KB (879 words) - 16:46, 27 September 2010
• Metformin
  66 KB (8,976 words) - 16:47, 27 September 2010
• Ampicillin
  [[Category:Aromatic compounds]]
  7 KB (881 words) - 16:47, 27 September 2010
• Ipratropium
  [[Category:Aromatic compounds]] [[Category:Quaternary ammonium compounds]]
  5 KB (580 words) - 16:49, 27 September 2010
• Paracetamol
  In ancient and medieval times, [[antipyretic|anti-fever]] compounds came from white [[willow]] bark (a family of chemicals known as [[salicin]] ...ake the benzene ring highly reactive toward [[electrophile|electrophilic]] aromatic substitution. As the substituents are ortho,para-directing and para with re
  54 KB (7,376 words) - 16:52, 27 September 2010
• Stinging nettle
  ...] or [[serotonin]], and possibly [[formic acid]]. This mixture of chemical compounds cause a painful sting or [[paresthesia]] from which the species derives its ...treatment of [[arthritis]] in Germany. Nettle leaf extract contains active compounds that reduce [[Tumor necrosis factor-alpha|TNF-α]] and other inflammatory [
  21 KB (3,099 words) - 12:28, 7 July 2010
• Coal tar
  ...black liquid of high [[viscosity]], which smells of [[naphthalene]] and [[aromatic hydrocarbon]]s. Coal tar is among the by-products when [[coal]] is .... Coal tars are complex and variable mixtures of [[phenols]], [[polycyclic aromatic hydrocarbon]]s (PAHs), and [[heterocyclic compound]]s. It is a mixture of a
  5 KB (781 words) - 10:07, 20 September 2010
• Primary Aromatic Amine
  '''Primary aromatic amines''' (PAA) are a group of compounds. They might be added to [[plastic]]s during production. ...%2FPAA_from_black_nylon_cooking_utentils_2004.pdf An acute case of primary aromatic amines migrating from cooking utensils]'', Memorandum for the Danish Veteri
  806 bytes (116 words) - 10:07, 20 September 2010
• Liquid crystal polymer
  '''Liquid-crystal polymers (LCPs)''' are a class of aromatic [[polyester]] [[polymer]]s. They are extremely [[Reactivity|unreactive]] a ...Kevlar. Chemical structure of this aramid consists of linearly substituted aromatic rings linked by amide groups. In a similar way, several series of thermotro
  4 KB (613 words) - 10:09, 20 September 2010
• Applied spectroscopy
  ...rs in a substance. Such groups are known as [[chromophores]] and include [[aromatic]] groups, [[conjugated system]] of bonds, [[carbonyl group]]s and so on. [[
  7 KB (1,065 words) - 10:09, 20 September 2010
• Polybutylene
  ...ethers. The pre-catalysts are activated by combinations of organoaluminum compounds and other types of organic or organometallic modifiers. Two most important ...ar solutions (including water).<ref name=b1/> It shows lower resistance to aromatic and chlorinated hydrocarbons as well as oxidising acids than other polymers
  12 KB (1,699 words) - 10:09, 20 September 2010
• Biopolymer
  ...erobic bacteria can be utilized by autotrophic bacteria to reduce oxidized compounds and CO₂ to form either acetic acid or methane. ...h monovalent cations, low molecular weight amines, and quaternary ammonium compounds. It becomes water-insoluble in the presence of polyvalent cations such as C
  68 KB (9,959 words) - 10:10, 20 September 2010
• Factors of polymer weathering
  ...al reactions involving oxygen differ in the inner and outer layers of both aromatic and aliphatic polymers due to their dependence on the diffusion of oxygen t ...CEEES Publication N°8, 2007, 487-500</ref> Unsaturated alkyl and aromatic compounds may act as catalysts in the photooxidation of polymers. In the presence of
  12 KB (1,716 words) - 10:10, 20 September 2010
• Fire-safe polymers
  === Linear, Single-Stranded Polymers With Cyclic Aromatic Components === ...[polymers]] made with aromatic heterocycles.]]<br />[[Polymers]] made with aromatic monomers have a tendency to condense into chars upon [[combustion]], decrea
  17 KB (2,260 words) - 10:10, 20 September 2010
• Conductive polymer
  ...[[Electrical conductance|conduct]] [[electricity]].<ref name=inzelt/> Such compounds may have metallic conductivity or be [[semiconductor]]s. The biggest advant ...cle: '''[[polythiophene|poly(thiophene)s]] (PT)'''... The S is outside the aromatic cycle: '''[[poly(p-phenylene sulfide)]] (PPS)'''
  22 KB (3,022 words) - 10:10, 20 September 2010
• Polyethylene terephthalate
  [[Category:Aromatic compounds]]
  43 KB (6,272 words) - 10:11, 20 September 2010
• Polymer
  ...g in 1811, [[Henri Braconnot]] did pioneering work in derivative cellulose compounds, perhaps the earliest important work in polymer science. The development of ...mer to degradation depends on its structure. Epoxies and chains containing aromatic functionality are especially susceptible to [[UV degradation]] while polyes
  45 KB (6,501 words) - 10:11, 20 September 2010
• Polyimide P84
  ...d of [[aromaticity|aromatic]] backbone units only. Despite the non melting aromatic, halogen free structure it is classified as non flammable with an LOI of 38 ...ient of [[thermal expansion]] or [[conductivity]] can be adjusted by using compounds with functional fillers.
  2 KB (264 words) - 10:11, 20 September 2010
• Polyethylene
  ...iupac/nomenclature/93/r93_683.htm A Guide to IUPAC Nomenclature of Organic Compounds (Recommendations 1993)] IUPAC, Commission on Nomenclature of Organic Chemis ...d a catalytic system based on [[titanium]] [[halide]]s and organoaluminium compounds that worked at even milder conditions than the Phillips catalyst. The Phill
  20 KB (2,802 words) - 10:11, 20 September 2010
• Bitumen
  ...arbon disulfide]], and composed primarily of highly condensed [[polycyclic aromatic hydrocarbon]]s. Vessels for the heating of bitumen or bituminous compounds are usually subject to specific conditions in public liability insurance po
  13 KB (1,945 words) - 10:12, 20 September 2010
• Petroleum
  ...cloalkane]]s and various [[aromatic hydrocarbon]]s while the other organic compounds contain [[nitrogen]], [[oxygen]] and [[sulfur]], and trace amounts of metal |[[Aromatic]]s || 15% || 3 to 30%
  69 KB (9,885 words) - 10:12, 20 September 2010
• Metallic bond
  ...s became accessible. Despite all this progress the nature of intermetallic compounds and alloys largely remained a mystery and their study was often empirical. ...t in [[boron]] chemistry. The principle can easily be extended over larger aromatic molecules like [[naphthalene]], [[anthracene]] and if the process is taken
  26 KB (4,024 words) - 10:13, 20 September 2010
• Polystyrene
  ...tandard '''PS''', is an [[Aromaticity|aromatic]] [[polymer]] made from the aromatic [[monomer]] [[styrene]], a liquid [[hydrocarbon]] that is commercially manu ...burns with an orange-yellow flame, giving off [[soot]], as opposed to non-aromatic hydrocarbon polymers such as [[polyethylene]], which burn with a light yell
  36 KB (5,017 words) - 10:14, 20 September 2010
• Coffea
  ...flavor of the coffee bean when it is roasted. Non-volatile [[nitrogen]]ous compounds (including [[alkaloid]]s, [[trigonelline]], proteins and free [[amino acid] ...the unpleasant taste making it impossible to prepare a beverage with such compounds. In fresh green coffee from Peru, these concentrations have been determined
  29 KB (4,179 words) - 10:14, 20 September 2010
• Wax
  ...s are components of fossil fuels or are synthesized from petroleum-derived compounds, such as [[paraffin]]. ''[[Earwax]]'' is an oily substance found in the hum ...and isoalkanes, naphthenes, and alkyl- and naphthene-substituted aromatic compounds. The degree of branching has an important influence on the properties. Mil
  11 KB (1,689 words) - 10:17, 20 September 2010
• Polyphenyl ether
  ...</ref>. Physical properties of a particular PPE depend upon the number of aromatic rings, their substitution pattern, and whether it is an ether or a thioethe ...ecause radiation attacks covalent bonds that are most prevalent in organic compounds. One result of ionization is that the organic molecules disproportionate t
  18 KB (2,654 words) - 10:18, 20 September 2010
• Lubricant
  * Aromatic Note that many of the basic chemical compounds used as detergents (example: calcium sulfonate) serve the purpose of the fi
  32 KB (4,626 words) - 10:18, 20 September 2010
• Aniline
  | Function = [[aromatic amine]]s ...It ignites readily, burning with a smoky flame characteristic of aromatic compounds. Aniline is colorless, but it slowly [[organic oxidation|oxidizes]] and re
  14 KB (2,008 words) - 13:10, 20 September 2010
• Dimethylaniline
  ...mposites Australia</ref> DMA is also used as a precursor to other organic compounds. [[Category:Aromatic amines]]
  4 KB (538 words) - 13:10, 20 September 2010
• Pentanitroaniline
  [[Category:Nitro compounds]] [[Category:Aromatic amines]]
  1 KB (162 words) - 13:10, 20 September 2010
• O-Phenylenediamine
  ...he formula C₆H₄(NH₂)₂. This [[aromatic]] [[diamine]] is an important precursor to many [[heterocyclic compound]]s. [[Category:Aromatic amines]]
  5 KB (609 words) - 13:10, 20 September 2010
• 4-Aminobiphenyl
  ...oxicology Program]</ref> and so it has been largely replaced by less toxic compounds. It is similar to [[benzidine]]. [[Category:Aromatic amines]]
  2 KB (180 words) - 13:10, 20 September 2010
• 2-Naphthylamine
  ...s a known human [[carcinogen]] and has largely been replaced by less toxic compounds. 2-Naphthylamine is prepared by heating 2-[[naphthol]] with [[ammonium]] [[ [[Category:Aromatic amines]]
  3 KB (377 words) - 13:10, 20 September 2010
• Bromethalin
  [[Category:Nitro compounds]] [[Category:Aromatic amines]]
  2 KB (308 words) - 13:11, 20 September 2010
• Padimate A
  ...nt in some [[sunscreen]]s. It is an [[ester]] derivative of [[PABA]]. This aromatic chemical absorbs [[ultraviolet]] rays thereby preventing sunburn. However, ...of padimate O and padimate A resemble that of [[Michler's ketone]]. These compounds have been shown to increase the lethal effects of UV-radiation on cells.<re
  2 KB (228 words) - 13:11, 20 September 2010
• 2-Nitrodiphenylamine
  ...''-nitroaniline''', is an [[organic chemical]], a [[nitration|nitrated]] [[aromatic amine]], a derivate of [[diphenylamine]]. Its chemical formula is C<sub>12< [[Category:Aromatic amines]]
  3 KB (363 words) - 13:11, 20 September 2010
• Pendimethalin
  [[Category:Aromatic amines]] [[Category:Nitro compounds]]
  2 KB (253 words) - 13:11, 20 September 2010
• 4-Nitroaniline
  ...[[aniline]]. The key step in this reaction sequence is an [[electrophilic aromatic substitution]] to install the nitro group ''para'' to the amino group. Afte [[Category:Aromatic amines]]
  4 KB (480 words) - 13:11, 20 September 2010
• 2-Nitroaniline
  [[Category:Aromatic amines]] [[Category:Nitro compounds]]
  2 KB (153 words) - 13:11, 20 September 2010
• 3-Nitroaniline
  [[Category:Aromatic amines]] [[Category:Nitro compounds]]
  2 KB (233 words) - 13:11, 20 September 2010
• Sulfanilic acid
  ...nzene sulfonic acid''' ) is a colourless crystalline solid produced from [[aromatic sulfonation|sulfonation]] of [[aniline]].<ref name="DOC">"Sulphanilic acid" It readily forms [[diazo]] compounds and is used to make dyes and [[Sulfonamide (medicine)|sulpha drugs]]. <ref
  2 KB (272 words) - 13:11, 20 September 2010
• 2-Aminophenol
  ...l-complex dyes when diazotized and coupled to a phenol, naphthol, or other aromatic or resonant dye species. Metal complex dyes using copper or chromium are co [[Category:Aromatic amines]]
  4 KB (476 words) - 13:11, 20 September 2010
• Toluidine
  ...ar to [[aniline]] except that a [[methyl group]] is substituted onto the [[aromatic ring]]. The difference between these three isomers is the position where t ...tly referred to as aromatic) amines. Due to the amino group bonded to the aromatic ring, the toluidines are [[weak base|weakly basic]]. None of the toluidine
  4 KB (551 words) - 13:11, 20 September 2010
• Trifluralin
  ...lly related herbicides (dinitroanilines) as well as a variety of energetic compounds (explosives).<ref>Tor, J., C. Xu, J. M. Stucki, M. Wander, G. K. Sims. 2000 [[Category:Nitro compounds]]
  3 KB (361 words) - 13:11, 20 September 2010
• 3-(Trifluoromethyl)aniline
  ...formula CF₃C₆H₄NH₂. It is an [[aromatic amine]]. ...herbicide [[fluometuron]].<ref name=Ullmann>Siegemund, Günter “Aromatic Compounds with Fluorinated Side-Chains” in Ullmann’s Encyclopedia of Industrial C
  1 KB (170 words) - 13:11, 20 September 2010
• 3,3',5,5'-Tetramethylbenzidine
  ...ed). On that evidence, it has been used as a replacement for carcinogenic compounds such as [[benzidine]]<ref>{{cite journal|title=One-pot synthesis of silver [[Category:Aromatic amines]]
  4 KB (524 words) - 13:11, 20 September 2010

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