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Iminodisuccinic acid

Figure 10.11 Conditional stability constant graphs for (a) ethylenediaminedisuccinic acid [(S,S)-EDS], (b) ethylenediaminetetraacetic acid (EDTA), (c) iminodisuccinic acid (IDS), (d) glutamic acid N,N-diacetic acid (CLDA), and (e) methylglycinediacetic acid (MGDA). Figure 10.11 Conditional stability constant graphs for (a) ethylenediaminedisuccinic acid [(S,S)-EDS], (b) ethylenediaminetetraacetic acid (EDTA), (c) iminodisuccinic acid (IDS), (d) glutamic acid N,N-diacetic acid (CLDA), and (e) methylglycinediacetic acid (MGDA).
Katata, L., Nagaraju, V., and Crouch, A.M. Determination of ethylenediaminetetraacetic acid, ethylenediaminedisuccinic acid and iminodisuccinic acid in cosmetic products by capillary electrophoresis and high performance liquid chromatography. Anal. Chim. Acta 2006, 579, 177-184. [Pg.180]

Bis(carboxvmethvl)iminodiacetic acid (iminodisuccinic acid) (Other values in Vol.5, p.60)... [Pg.71]

Sodium iminodisuccinate belongs to the aminocarboxylate class of chelating agents. Nearly all anoinocarboxylates in use today are acetic acid derivatives produced from amines, formaldehyde, sodium hydroxide, and hydrogen cyanide. The industrial use of thousands of tons of hydrogen cyanide is an extreme toxicity hazard. In contrast, sodium iminodisuccinate is produced from maleic anhydride (a raw material also produced by Bayer), water, sodium hydroxide, and ammonia. The only solvent used in the production process is water, and the only side product formed—ammonia dissolved in water—is recycled back into sodium iminodisuccinate production or used in other Bayer processes. [Pg.36]

See other pages where Iminodisuccinic acid is mentioned: [Pg.293]    [Pg.307]    [Pg.60]    [Pg.61]    [Pg.293]    [Pg.307]    [Pg.60]    [Pg.61]    [Pg.183]   
See also in sourсe #XX -- [ Pg.60 ]



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