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  • ...ation. The fats are hydrolyzed by the base, yielding alkali salts of fatty acids (crude soap) and [[glycerol]]. Soaps made from vegetable oils (such as olive oil), aromatic oils (such as thyme oil) and lye (''al-Soda al-Kawia'') were first produced
    20 KB (3,140 words) - 21:41, 17 June 2010
  • ...gh its 7 modules. Before Vancomycin is assembled through NRPS, the [[amino acids]] are first modified. L-tyrosine is modified to become the β-hydroxychloro ...omycin.png|thumb|Figure 2: Linear heptapeptide, which consists of modified aromatic rings]]
    31 KB (4,198 words) - 15:43, 27 September 2010
  • ...[phenylalanine]], [[tryptophan]], and [[tyrosine]] with non-aromatic amino acids result in poor bonding between rifampicin and the RNA polymerase.<ref name=
    18 KB (2,471 words) - 15:43, 27 September 2010
  • [[Category:Aromatic amines]] [[Category:Salicylic acids]]
    7 KB (879 words) - 15:46, 27 September 2010
  • [[Category:Benzoic acids]] [[Category:Aromatic amines]]
    12 KB (1,678 words) - 15:48, 27 September 2010
  • ...sine hydroxylase]], and then by the [[decarboxylation]] of [[L-DOPA]] by [[aromatic L-amino acid decarboxylase]] (which is often referred to as dopa decarboxyl ...ly co-administered with an inhibitor of peripheral decarboxylation (DDC, [[Aromatic-L-amino-acid decarboxylase|dopa decarboxylase]]), such as [[carbidopa]] or
    48 KB (6,470 words) - 15:48, 27 September 2010
  • ...es, and as an [[asbestos]] substitute. The name is a shortened form of "[[aromatic]] [[polyamide]]". They are fibers in which the chain molecules are highly Aromatic polyamides were first introduced in commercial applications in the early 19
    10 KB (1,313 words) - 09:07, 20 September 2010
  • ...isture barrier. HDPE is compatible with a wide range of products including acids and caustics but is not compatible with [[solvents]]. It is supplied in FDA ...arance to HDPE and have exceptional barrier properties to hydrocarbons and aromatic solvents. Fluorine treated bottles are excellent for use with insecticides,
    9 KB (1,285 words) - 14:54, 15 April 2013
  • '''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) - 09:09, 20 September 2010
  • ...t unit, Kisco product), Parylene VT-4 (generic name, fluorine atoms on the aromatic ring), Parylene CF (VT-4, Kisco product), and Parylene X (a cross-linkable ...ating with good barrier properties for inorganic and organic media, strong acids, caustic solutions, gases and water vapor
    8 KB (1,048 words) - 09:09, 20 September 2010
  • ...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) - 09:09, 20 September 2010
  • ...r resistance to aromatic and chlorinated hydrocarbons as well as oxidising acids than other polymers such aspolysulfone and polyamide 6/6.<ref name=j1/> Add
    12 KB (1,699 words) - 09:09, 20 September 2010
  • ...de-esterification and decomposition of the resulting cellulose and organic acids. Cellulose acetate is currently used in high volume applications ranging fr ...Resonance]] structures of the [[peptide bond]] that links individual amino acids to form a protein [[polymer]].]]
    68 KB (9,959 words) - 09:10, 20 September 2010
  • ...it is rugged and unusually resistant to many chemical solvents, bases and acids. ...ygen]], followed by chain scission to yield [[aldehydes]] and [[carboxylic acids]]. In external applications, it shows up as a network of fine cracks and [[
    25 KB (3,657 words) - 09:10, 20 September 2010
  • ..., recommending its use under high pressures. It is also stable in aqueous acids and bases and many non-polar solvents; however it is soluble in dichloromet
    5 KB (716 words) - 09:10, 20 September 2010
  • ...nd [[ammonium chloride]], [[ammonium phosphate]], [[borax]], and various [[acids]]. These early attempts found application in reducing the flammability of w === Linear, Single-Stranded Polymers With Cyclic Aromatic Components ===
    17 KB (2,260 words) - 09:10, 20 September 2010
  • ...H- end groups with mono-functional degradation products like mono-carbonic acids or alcohols. Results are decreased reactivity during re-polycondensation or [[Category:Aromatic compounds]]
    43 KB (6,272 words) - 09:11, 20 September 2010
  • ...een used for centuries. [[Biopolymers]] such as [[proteins]] and [[nucleic acids]] play crucial roles in biological processes. A variety of other natural po ...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) - 09:11, 20 September 2010
  • <tr><td>[[Aromatic hydrocarbon]]s</td><td bgcolor="#ffcccc">Poor</td></tr>
    20 KB (2,772 words) - 09:11, 20 September 2010
  • ...made in the description of the salts that can be formed in reactions with acids. With the advent of [[electrochemistry]] it became clear that metals genera ...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) - 09:13, 20 September 2010

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