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Disodium salt

Disodium salt of 6-hydroxy-5-[(2-methoxy-5-methyl-4-sulfophenyl)a2o]-2-naphthalenesulfonic acid... [Pg.336]

COLORANTS FORFOOD,DRUGS,COSTffiTICS AND TffiDICALDEVICES] (Vol 6) Disodium salt of tetrabromophthalate... [Pg.336]

Fluoro-llb,21-dihydroxy-16a-methyl-21-(phosphonooxy)-pregna-l,4-diene- 3,20-dione, disodium salt. See Dexamethasone sodium phospate. [Pg.413]

Treatment of this same 4, 5 -dibromofluorescein intermediate with mercuric acetate and conversion to the disodium salt yields the hydroxymercuric analogue merbromin or mercurochrome [129-16-8] (41). It was once a widely used antiseptic, especially for skin disinfection, and was even adrninistered internally. However, it has been replaced by more effective antibacterial agents. [Pg.404]

DSMA [144-21-8] disodium salt of methylarsonic acid CH3ASO3 -2Na... [Pg.41]

Iron(II) ediylenediaminetetraacetic acid [15651 -72-6] Fe(EDTA) or A/,Ar-l,2-ethaiiediylbis[A[-(carboxymethyl)glyciQato]ferrate(2—), is a colorless, air-sensitive anion. It is a good reducing agent, having E° = —0.1171, and has been used as a probe of outer sphere electron-transfer mechanisms. It can be prepared by addition of an equivalent amount of the disodium salt, Na2H2EDTA, to a solution of iron(II) in hydrochloric acid. Diammonium [56174-59-5] and disodium [14729-89-6] salts of Fe(EDTA) 2— are known. [Pg.439]

The first aromatic sulfone polymer produced commercially was introduced as Bakelite polysulfone but now is sold by Union Carbide under the trade name Udel. It is made by reaction of the disodium salt of bisphenol A (BPA) with 4,4 -dichIorodiphenyl sulfone in a mixed solvent of chlorobenzene and dimethyl sulfoxide (eq. 12). [Pg.331]

Economics vary, depending onlocation and country. In Japan, for example, the quinone of choice is the disodium salt of l,4-dihydto-9,10-dihydtoxyanthtacene (DDA). Unlike AQ, DDA is direcdy soluble in white Hquor and thus readily penetrates the chip. AQ works well with both hardwoods and softwoods. Addition rates as low as 0.025% by weight give satisfactory increases (ca 1—2%) in pulping rate and yield, especially for hardwoods. In the United States in 1987, the FDA put a limitation to the amount of AQ that can be added to most pulp to 0.11%. This typically is the amount added to softwoods lesser amounts ate employed with hardwoods. [Pg.271]

Benzenedisulfonic acid [831-59-4] (disodium salt), produced by the neutralization of the disulfonic acid with sodium sulfite [7757-83-7] is used in the manufacture of resorcinol [108-46-3] (1,3-benzenediol) (2), a chemical component found in mbber products and wood adhesives (72). The disodium salt is fused with sodium hydroxide, dissolved in water, and acidified to produce resorcinol, which is isolated via extraction (73). [Pg.100]

Solvent for Displacement Reactions. As the most polar of the common aprotic solvents, DMSO is a favored solvent for displacement reactions because of its high dielectric constant and because anions are less solvated in it (87). Rates for these reactions are sometimes a thousand times faster in DMSO than in alcohols. Suitable nucleophiles include acetyUde ion, alkoxide ion, hydroxide ion, azide ion, carbanions, carboxylate ions, cyanide ion, hahde ions, mercaptide ions, phenoxide ions, nitrite ions, and thiocyanate ions (31). Rates of displacement by amides or amines are also greater in DMSO than in alcohol or aqueous solutions. Dimethyl sulfoxide is used as the reaction solvent in the manufacture of high performance, polyaryl ether polymers by reaction of bis(4,4 -chlorophenyl) sulfone with the disodium salts of dihydroxyphenols, eg, bisphenol A or 4,4 -sulfonylbisphenol (88). These and related reactions are made more economical by efficient recycling of DMSO (89). Nucleophilic displacement of activated aromatic nitro groups with aryloxy anion in DMSO is a versatile and useful reaction for the synthesis of aromatic ethers and polyethers (90). [Pg.112]

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]

Sulfated Acids, Amides, and Esters. Reaction with sulfuric acid may be carried out on fatty acids, alkanolamides, and short-chain esters of fatty acids. The disodium salt of sulfated oleic acid is a textile additive and an effective lime soap dispersant. A typical sulfated alkanolamide stmcture is CiiH23C0NHCH2CH20S03Na. Others include the sulfates of mono and diethanolamides of fatty acids in the detergent range. The presence of... [Pg.244]

Properties. Thienamycin is isolated as a colorless, hygroscopic, zwitterionic soHd, although the majority of carbapenems have been obtained as sodium salts and, in the case of the sulfated olivanic acids, as disodium salts (12). Concentrated aqueous solutions of the carbapenems are generally unstable, particularly at low pH. AH the substituted natural products have characteristic uv absorption properties that are often used in assay procedures. The ir frequency of the P-lactam carbonyl is in the range 1760 1790 cm . ... [Pg.4]

The reaction of toluene-3,4-dithiol(3,4-dimercaptotoluene) and antimony trichloride ia acetone yields a yeUow soHd Sb2(tdt)2, where tdt is the toluene-3,4-dithiolate anionic ligand (51). With the disodium salt of maleonitnledithiol ((Z)-dimercapto-2-butenedinitrile), antimony trichloride gives the complex ion [Sb(mnt)2] , where mat is the maleonitnledithiolate anionic ligand. This complex has been isolated as a yeUow, crystalline, tetraethyl ammonium salt. The stmctures of these antimony dithiolate complexes have apparendy not been unambiguously determiaed. [Pg.206]

The Chemicaly3.bstractIndexis 2,7-naphthalene-disulfonic acid, 4-amino-5-hydroxy-3-[[4 -[(4-hydroxyphenyl)azo] [l,l -biphenyl]-4-yl]azo]-6-(phenylazo)-, disodium salt. [Pg.430]

Ethylenediamine tetraacetic acid (EDTA) [60-00-4] (Sequestrene), an anticoagulent at 1 mg of the disodium salt per mL blood, complexes with and removes calcium, Ca ", from the blood. Oxalate, citrate, and fluoride ions form insoluble salts with Ca " and chelate calcium from the blood. Salts containing these anticoagulants include lithium oxalate [553-91-3] 1 mg/mL blood sodium oxalate [62-76-0]2 mg/mL blood ... [Pg.176]

Eosin [15086-94-9] (tetrabromofluorescein), C2QHgBi40, made by the bromination of fluorescein, is both a dye and an adsorption indicator. Eosin Y /7 7372-87-17, C2QH Br40 2Na, the disodium salt, is a biological stain. 475 -Dibromofluorescein [596-03-2], C2QH2QBr20, is used in D C Orange No. [Pg.298]

FD C Red No. 40. This monoa2o dye (5) is manufactured by coupling dia2oti2ed 5-amino-4-methoxy-2-toluenesulfonic with 6-hydroxy-2-naphtha-lenesulfonic acid. FD C Red No. 40 is also known as Allura Red or Cl Food Red 17. Its chemical identity is principally the disodium salt of 6-hydroxy-5-[(2-methoxy-5-methyl-4-sulfophenyl)a2o]-2-naphthalenesulfonic acid, which has the formula C gH 4N20gS2Na2, and mol wt 496.43. [Pg.442]

Disodium salt of 6,6 -oxybis(2-naphthalenesulfonic acid)—not more than 1.0%... [Pg.442]

It is prepared from the polycondensation of the disodium salt of bisphenol A and 4,4-dichlorodiphenyl sulfone in a polar aprotic solvent such as dimethyl sulfoxide (26). [Pg.39]

Hexacyanobutadiene [5104-27-4] (4), 1,3-butadiene-1,1,2,3,4,4-hexacarbonitrile, is prepared in good yield by a two-step process from the disodium salt of tetracyanoethane (30). It is like TCNE in forming colored TT-complexes and an anion radical. [Pg.404]

EDA reacts readily with two moles of CS2 in aqueous sodium hydroxide to form the bis sodium dithiocarbamate. When aqueous ammonia and 2inc oxide (or manganese oxide or its hydrate) is used with a basic catalyst, the 2inc (or manganese) dithiocarbamate salt is isolated. Alternatively, the disodium salt can react with ZnSO or MnSO followed by dehydration in an organic solvent to yield the same salts (48—50). [Pg.43]

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]


See other pages where Disodium salt is mentioned: [Pg.143]    [Pg.304]    [Pg.327]    [Pg.490]    [Pg.98]    [Pg.115]    [Pg.410]    [Pg.475]    [Pg.970]    [Pg.1024]    [Pg.95]    [Pg.470]    [Pg.472]    [Pg.115]    [Pg.116]    [Pg.366]    [Pg.297]    [Pg.335]    [Pg.430]    [Pg.224]    [Pg.519]    [Pg.467]    [Pg.127]    [Pg.298]    [Pg.301]    [Pg.37]    [Pg.318]   
See also in sourсe #XX -- [ Pg.216 ]

See also in sourсe #XX -- [ Pg.256 ]

See also in sourсe #XX -- [ Pg.107 , Pg.108 , Pg.117 ]




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Disodium

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