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Ethylenediaminetetraacetic acid salts

Buffers can also be provided in parenteral formulations to ensure the required pH needed for solubility and/or stability considerations. Other excipients included in parenteral products are preservatives (e.g., benzyl alcohol, p-hydroxybenzoate esters, and phenol), antioxidants (e.g., ascorbic acid, sodium bisulfite, sodium metabisulfite, cysteine, and butyl hydroxy anisole), surfactants (e.g., polyoxyethylene sorbitan monooleate), and emulsifying agents (e.g., polysorbates). An inert gas (such as nitrogen) can also be used to enhance drug stability. Stability and solubility can also be enhanced by the addition of complexation and chelating agents such as the ethylenediaminetetraacetic acid salts. For a more detailed list of approved excipients in parenteral products, the reader should consult the monographs within the USP. [Pg.1006]

B. Preparation of Disodium Ethylenediaminetetraacetic Acid Salt Solution... [Pg.222]

Other Additives. To provide and maintain the clarity of clear shampoos, the use of either ethyl or isopropyl alcohol maybe employed. Perfumes are added to make shampoos more pleasing in terms of odor, while dyes are incorporated to give visual aesthetics to the products. Salts of ethylenediaminetetraacetic acid are found to sequester and prevent formation of insoluble alkaline-earth metal salts. [Pg.450]

The lanthanides form many compounds with organic ligands. Some of these compounds ate water-soluble, others oil-soluble. Water-soluble compounds have been used extensively for rare-earth separation by ion exchange (qv), for example, complexes form with citric acid, ethylenediaminetetraacetic acid (EDTA), and hydroxyethylethylenediaminetriacetic acid (HEEDTA) (see Chelating agents). The complex formation is pH-dependent. Oil-soluble compounds ate used extensively in the industrial separation of rate earths by tiquid—tiquid extraction. The preferred extractants ate catboxyhc acids, otganophosphoms acids and esters, and tetraaLkylammonium salts. [Pg.541]

A method suitable for analysis of sulfur dioxide in ambient air and sensitive to 0.003—5 ppm involves aspirating a measured air sample through a solution of potassium or sodium tetrachloromercurate, with the resultant formation of a dichlorosulfitomercurate. Ethylenediaminetetraacetic acid (EDTA) disodium salt is added to this solution to complex heavy metals which can interfere by oxidation of the sulfur dioxide. The sample is also treated with 0.6 wt % sulfamic acid to destroy any nitrite anions. Then the sample is treated with formaldehyde and specially purified acid-bleached rosaniline containing phosphoric acid to control pH. This reacts with the dichlorosulfitomercurate to form an intensely colored rosaniline—methanesulfonic acid. The pH of the solution is adjusted to 1.6 0.1 with phosphoric acid, and the absorbance is read spectrophotometricaHy at 548 nm (273). [Pg.147]

EDA reacts with formaldehyde and sodium cyanide under the appropriate alkaline conditions to yield the tetrasodium salt of ethylenediaminetetraacetic acid (24). By-product ammonia is removed at elevated temperatures under a partial vacuum. The free acid or its mono-, di-, or trisodium salts can be produced by the appropriate neutrali2ation using a strong mineral acid. This same reaction with other amines is used to produce polyamino acetic acids and their salts. These products are used widely as chelating agents. [Pg.42]

Metal Content. Two common analytical methods for determining metal content are by titration and by atomic absorption spectrophotometry (aas). The titration method is a complexiometric procedure utilizing the disodium salts of ethylenediaminetetraacetic acid (EDTA). The solvent, indicator. [Pg.219]

Until recent years the only syntheses of 3-hydroxy quinoline involved multistep processes, the last step of which consisted of the conversion of 3-aminoquinoline to 3-hydroxyquinoline via the diazonium salt. " Small quantities of quinoline have been oxidized to 3-hydroxyquinoline in low yields by using oxygen in the presence of ascorbic acid, ethylenediaminetetraacetic acid, ferrous sulfate, and i)hosi)halc buffer. The decarboxylation of 3-hydroxycinchoninic, acid in boiling nitrobenzene has been re-... [Pg.59]

From this material, samples are cut and swelled to constant weight in a buffered saline solution prepared from 8.43 g sodium chloride (NaCl), 9.26 g boric acid (H3BO3), 1.0 g sodium borate (Na3B03), and 0.1 g of the disodium salt of the dihydrate of ethylenediaminetetraacetic acid [Na2 EDTA -(/ 0)21 ini L of distilled water. [Pg.251]

Iron can be controlled with certain complexing agents, in particular glucono-5-lactone, citric acid, ethylenediaminetetraacetic acid, nitrilotriacetic acid, hydroxyethylethylene diaminetriacetic acid, hydroxyethyliminodiacetic acid, and the salts from the aforementioned compounds. These compounds must be added together with nitrogen-containing compounds such as hydroxylamine salts or hydrazine salts [486,643,1815]. [Pg.273]

The sodium and calcium salts of EDTA (ethylenediaminetetraacetic acid, Fig. 9.3.1.) are common sequestrants in food products. A three-dimensional representation of EDTA is shown in color Fig. 9.3.2. The EDTA ion is an especially effective sequestrant, forming up to six coordinate covalent bonds with a metal ion. These bonds are so named because a lone pair of electrons on a single atom serves as the source of the shared electrons in the bond between the metal ion and EDTA. The two nitrogen atoms in the amino groups and the oxygen... [Pg.120]

Corynantheidol (255) has been prepared by Hanaoka et al. (155), who started from piperideine derivative 268 and tryptophyl bromide (197). The key cyclization step, resulting in indolo[2,3-a]quinolizine 270 as the major product besides 271, was carried out by mercuric acetate oxidation in the presence of the disodium salt of ethylenediaminetetraacetic acid (EDTA), followed by sodium borohydride reduction. Finally, lithium aluminum hydride reduction of 270 provided ( )-corynantheidol in good yield (155). [Pg.190]

The usual source of EDTA for use in metal analysis is the disodium dihydrogen salt of ethylenedi-aminetetraacetic acid (Figure 5.20). This is the partially neutralized salt of ethylenediaminetetraacetic acid. [Pg.120]

Ethylenediaminetetraacetic acid is frequently symbolized H4Y, and the disodium salt, Na2H2Y. The hydrogens in these formulas are the acidic hydrogens associated with the carboxyl groups, as in any weak organic carboxylic acid they dissociate from the EDTA ion in a series of equilibrium steps ... [Pg.120]

FIGURE 5.20 The disodium dihydrogen salt of ethylenediaminetetraacetic acid. [Pg.121]

Ethylenediaminetetraacetic acid, calcium disodium salt hydrate [23411-34-9] Fenpropidin [67306-00-7] Fenpropimorph [67564-91-4] Flupropadin 81613-59-41 Haloperidol [52-86-8] 1605D EV7700000, USP EU1575000, USP... [Pg.1056]

Tetrakis(triphenylphosphine)palladium(0) Palladium, tetrakis(triphenylphosphine) (8) Palladium, tetrakis(triphenylphosphine)-, (T-4)- (9) (14221-01-3) Ethylenediaminetetraacetic acid, tetrasodium salt , Glycine, N,N -1,2-ethanediylbis[N (carboxymethyl)-, tetrasodium salt, trihydrate (9) (67401-50-7)... [Pg.209]

Concerns about the effect of TPP on eutrophication have led many states, cities, and regional governments to ban the use of the compound in syndets. Such bans have caused serious problems for detergent manufacturers, however, because no entirely satisfactory substitute for TPP has yet been found. Two promising candidates are the sodium salt of nitrilotriacetic acid, 3Na, N(CH2C02)3 , or NTA and ethylenediaminetetraacetic acid (EDTA). Both of these compounds act in much the same way as TPP, that is, by sequestering metal ions. Other builders that have been incorporated into syndet formulations include sodium carbonate, synthetic zeolites, borates, and organic polymers known as polycarboxylates. [Pg.108]

Ethylenediaminetetraacetic acid, tetrasodium salt Glydne, N,N -1,2-ethanediylbis[N-(carboxymethyl)]-, tetrasodium salt, trihydrate (67401-50-7), 65, 166... [Pg.124]

Secondary antioxidants, i.e., sequestrants or chelators, are important compounds in the prevention of lipid oxidation. The effect of chelators tested varied with the different compounds. Of those chelators tested, ethylenediaminetetraacetic acid (EDTA, tetrasodium salt) and sodium phytate were the most effective inhibitors of lipid oxidation (so indicated by low hexanal and TEARS values) and MFD (as seen by high CBB and low PIT and CBD intensity values), see Table 5. Sodium phytate was previously shown to chelate iron and thus, was proposed as a food antioxidant(7J). Sodium citrate at a concentration of 500... [Pg.65]

Ethylenediaminetetraacetic acid disodium salt dehydrate (EDTA) buffer solution... [Pg.208]

Ethylenediaminetetraacetic acid (Figure 57-2) is an efficient chelator of many divalent and trivalent metals in vitro. To prevent potentially life-threatening depletion of calcium, the drug should be administered only as the calcium disodium salt. [Pg.1241]

The phosphane analogue of ethylenediaminetetraacetic acid is obtained as an air-stable monohydrate of the tetrasodium salt (30). The phosphory-lated derivative of maleic acid 4 was synthesized in 1993 (31). [Pg.479]


See other pages where Ethylenediaminetetraacetic acid salts is mentioned: [Pg.227]    [Pg.227]    [Pg.154]    [Pg.132]    [Pg.497]    [Pg.439]    [Pg.150]    [Pg.233]    [Pg.127]    [Pg.157]    [Pg.103]    [Pg.392]    [Pg.537]    [Pg.119]    [Pg.147]    [Pg.825]    [Pg.334]    [Pg.284]    [Pg.570]    [Pg.54]    [Pg.41]    [Pg.143]    [Pg.56]    [Pg.150]    [Pg.226]    [Pg.386]   
See also in sourсe #XX -- [ Pg.485 ]




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Ethylenediaminetetraacetic acid dipotassium salt

Ethylenediaminetetraacetic acid disodium salt dihydrate

Ethylenediaminetetraacetic acid, tetrasodium salt: Glycine

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