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Gluconic acid sodium salt

Citric acid and other hydroxycarboxylic acids, such as gluconic acid. Also, derivatives such as sodium gluconate (D-gluconic acid, sodium salt), HOCH2[CH(OH)]4 COONa. [Pg.432]

SYNS GLONSEN GLUCONATO di SODIO (ITALIAN) GLUCONIC ACID SODIUM SALT MONOSODIUM GLUCONATE PASEXON lOOT PMP SODIUM GLUCONATE SODIUM d-GLUCONATE... [Pg.1255]

D-Ghiconk acid monosodium salt Gluconic acid sodium salt See Sodium gluconate... [Pg.1127]

Synonyms D-Gluconic acid monosodium salt Gluconic acid sodium salt Monosodium gluconate Monosodium D(-)-pentahydroxy capronate Sodium D-gluconate Classification Nonaromatic acid salt Definition Sodium salt of D-gluconic acid Empirical CsH NaQ,... [Pg.1346]

Gluconic acid sodium salt Monosodium gluconate Monosodium D(-)-pentahydroxy capronate Sodium D-gluconate... [Pg.4028]

Gluconic acid sodium salt As a detergent in bottle washing In metallurgy (alkaline derusting) Additive in cement As a derusting agent Textile (iron deposits prevention) industry Paper industry Blom et al. (1952)... [Pg.239]

The most common chelants include EDTA (ethylenediaminetetraacetic acid) and its salts, NTA (nitrilotriacetic acid) and its salts, gluconic acid, sodium gluconate, sodium glucoheptonate (sodium heptonate), as well as the various phosphonates, polyphosphates, lignin sulfonates, and citric acid. [Pg.145]

Hydroxycar-boxyl acids and their salts gluconic acid, sodium, potassium, calcium citric acid, gluconates 0.0005-0.002 As for saccharides... [Pg.236]

Lactic acid, alkyl fatty acids (salicylic acid, glycolic add, benzoic add Chlorhexidine gluconate/acetate Fatty alkyl 1,3-diaminopropane A-Fatty alkyl 3-aminopropionate, A-hydroxyethyl-A-carboxymethyl fatty acid sodium salt of amidoethylamine Ethyl alcohol, propyl alcohol, benzyl alcohol, pine oil Sodium hypochlorite (liquid chlorine bleach), chlorine dioxide, hypochlorous acid, trichloro- and dichloroisocyanuric acids and their salts, sodium perborate and activator, peroxy acid (per acid), magnesium salt of peroxy phthalic acid, oxygen bleach generated from ozone... [Pg.257]

The reduced catalyst deactivation compared to the analogous oxidations of glycerol and tartronic acid was attributed to the use of the calcium salt rather than the free acid. A recent publication describes a similar observation for the oxidation of sodium gluconate [15]. Sodium ions were assumed to counter catalyst deactivation by neutralizing the acid species responsible. [Pg.167]

Oxalate is found to be a frequent impurity in pharmaceutical substances belonging to the category of either organic acids e.g.. anhydrous citric acid, tartaric acid or salts of organic acids e.g., ferrous gluconate, sodium citrate, potassium citrate and sodium cromoglycate. The presence of this impurity is due to the following two prime factors, namely ... [Pg.36]

In the form of sodium salts all are very soluble and have low freezing points, so that solidification in winter conditions is unlikely. Figure 1.8 shows the types and formulae of materials which have been reported to find application in the formulation of this type of water-reducing admixture. However, the only materials finding widescale application in formulations are the salts of gluconic and heptonic acids. [Pg.36]

Of all these products, sodium glucoheptonate has been the most widely used chelant in cooling water formulations. It shows a greater stability than sodium gluconate and retains the ability to chelate ions effectively in high pH water, which citrates and EDTA do not do so well. Sodium glucoheptonate is a sodium salt of polyhydroxymonocarboxylic acid (2,3,4,5,6,7-hexahydroxy-s-heptonic acid). It is a reaction product of sodium cyanide and sucrose. [Pg.146]

An unusual classification of hexonic acids described by Levene21 was based on the differences in optical rotation between the free acid and its sodium salt. For example, in the D-gluconic acid series the sodium salt has the more positive rotation whereas in the D-mannonic acid group the reverse is the case and the acid has the more positive rotation. In comparison with these results glucosaminic acid was found to have a rotation of —15° (and its sodium salt +1.3°) and therefore these derivatives were in conformity with the D-gluconic acid series. [Pg.251]

See other pages where Gluconic acid sodium salt is mentioned: [Pg.843]    [Pg.167]    [Pg.146]    [Pg.1705]    [Pg.1362]    [Pg.565]    [Pg.167]    [Pg.346]    [Pg.843]    [Pg.167]    [Pg.146]    [Pg.1705]    [Pg.1362]    [Pg.565]    [Pg.167]    [Pg.346]    [Pg.1350]    [Pg.281]    [Pg.281]    [Pg.52]    [Pg.1885]    [Pg.49]    [Pg.148]    [Pg.99]    [Pg.196]    [Pg.105]    [Pg.20]    [Pg.9]    [Pg.21]    [Pg.303]    [Pg.577]    [Pg.331]    [Pg.370]    [Pg.49]    [Pg.16]    [Pg.148]    [Pg.132]    [Pg.272]    [Pg.330]   
See also in sourсe #XX -- [ Pg.66 ]



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Glucon

Gluconate

Gluconate salt

Gluconic

Gluconic acid

Sodium acids

Sodium gluconate

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