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  • | Name = <small>D</small>-Gluconic acid | ImageName = Skeletal formula of gluconic acid
    6 KB (794 words) - 20:14, 21 September 2010
  • |ImageFile=Nitrilotriacetic-acid-2D-skeletal.png |ImageName=[[Skeletal formula]] of nitrilotriacetic acid
    2 KB (302 words) - 20:14, 21 September 2010
  • | IUPACName = Trisodium citrate<br/>Trisodium 2-hydroxypropane-1,2,3-tricarboxylate | OtherNames = Citrosodine<br/>Citric acid, trisodium salt<br/>Sodium citrate
    5 KB (649 words) - 20:14, 21 September 2010
  • | IUPACName = Benzene-1,2-diol ...OtherNames = pyrocatechol<br />1,2-benzenediol<br />2-hydroxyphenol<br />1,2-dihydroxybenzene
    11 KB (1,437 words) - 20:14, 21 September 2010
  • | Formula = C<sub>12</sub>H<sub>8</sub>N<sub>2</sub> | OtherCpds = [[2,2'-bipyridine]]<br />ferroin<br />[[phenanthrene]]
    6 KB (660 words) - 20:14, 21 September 2010
  • | IUPACName = 1,2-diaminoethane | OtherNames = en; ethane-1,2-diamine; Edamine<ref>http://eur-lex.europa.eu/smartapi/cgi/sga_doc?smartapi
    9 KB (1,089 words) - 20:14, 21 September 2010
  • | ImageFile = Dimercaptosuccinic-acid-2D-skeletal.png | IUPACName = ''meso''-2,3-dimercaptosuccinic acid
    5 KB (629 words) - 20:15, 21 September 2010
  • | InChI = 1/C8H20N4/c1-2-10-5-6-12-8-7-11-4-3-9-1/h9-12H,1-8H2 ...yclization. In the final step the tosyl groups are removed with [[sulfuric acid]].
    4 KB (531 words) - 20:15, 21 September 2010
  • | IUPACName = Bis(2-aminoethyl)amine | OtherNames = ''N''-(2-aminoethyl)-1,2-ethanediamine<br />1,4,7-triazaheptane<br />3-azapentane-1,5-diamine
    2 KB (215 words) - 20:15, 21 September 2010
  • ...-bis(6-oxo-1-cyclohexa-2,4-<br>dienylidene)-1,2,4-triazolidin-1-yl]benzoic acid | InChI = 1/C21H15N3O4/c25-17-7-3-1-5-15(17)19-22-20(16-6-2-4-8-18(16)26)24(23-19)14-11-9-13(10-12-14)21(27)28/h1-12,22-23H,(H,27,28)/b
    5 KB (703 words) - 20:15, 21 September 2010
  • | IUPACName = 1,1,1,5,5,5-Hexafluoro-2,4-pentanedione | Formula = C<sub>5</sub>H<sub>2</sub>F<sub>6</sub>O<sub>2</sub>
    2 KB (256 words) - 20:15, 21 September 2010
  • | IUPACName = 2-[bis[2-[bis(carboxymethyl)amino]ethyl]amino]acetic acid ...es = DTPA, H<sub>5</sub>dtpa, Pentetic acid, Diethylenetriaminepentaacetic acid
    6 KB (825 words) - 20:15, 21 September 2010
  • {{DISPLAYTITLE:''trans''-1,2-Diaminocyclohexane}} |Name=''trans''-1,2-Diaminocyclohexane
    2 KB (253 words) - 20:15, 21 September 2010
  • | IUPACName = 2-[4-(bis(carboxymethyl)amino)-3-[2-[2-(bis(carboxymethyl)amino)- 5-methylphenoxy]ethoxy]phenyl]-1H-indole-6-carboxylic acid
    3 KB (410 words) - 20:15, 21 September 2010
  • |IUPACName=Pentane-2,4-dione |Formula=C<sub>5</sub>H<sub>8</sub>O<sub>2</sub>
    16 KB (2,268 words) - 20:15, 21 September 2010
  • | OtherNames = 1H-Benzotriazol, 1,2,3-Benzotriazol, btaH Benzotriazole is classified as an 1,2,3-[[triazole]], i.e. a cyclic compound with the linkage -N=N-NH-. Benzotria
    4 KB (469 words) - 20:15, 21 September 2010
  • [[Image:Phosphonate.png|thumb|right|General ester of phosphonic acid.]] ...lity of the metal complexes increases with increasing number of phosphonic acid groups. Phosphonates are highly water-soluble while the phosphonic acids ar
    8 KB (1,135 words) - 20:15, 21 September 2010
  • | ImageFile = Iminodiacetic acid.png | IUPACName = 2-(carboxymethylamino)acetic acid
    2 KB (202 words) - 20:15, 21 September 2010
  • ...c]]. That is, they obey [[Hückel's rule]] for aromaticity, possessing 4n+2 = &pi; electrons (n=4 for the shortest cyclic path) that are delocalized ov ...omplex (chemistry)|complexes]]. The metal [[ion]] usually has a charge of 2+ or 3+. A schematic equation for these syntheses is shown:
    12 KB (1,605 words) - 20:15, 21 September 2010
  • | IUPACName = ethylenediamine-N,N’-disuccinic acid | C = 10 | H = 16 | N = 2 | O = 8
    10 KB (1,372 words) - 20:15, 21 September 2010

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