Sodium references

The difference between the two titrations represents the volume of 0.02 N iodine equivalent to the total penicillins present in the given sample of benzylpenicillin. An assay may be carried out simultaneously by benzylpenicillin sodium (reference sample) so as to determine the exact equivalent of each ml of 0.02 N iodine. 

Calculations Calculate the potency in Units of penicillin from the declared number of Units of pencillin in benzylpenicillin sodium (reference sample). 

Identification The infrared absorption spectrum of a film of the sample between two salt plates exhibits relative maxima at the same wavelengths as those of a similar preparation of USP Docusate Sodium Reference Standard. 

Atomic Weight.—In connexion with the atomic weight of sodium, reference has been made to the general methods employed by Berzelius, by Stas, and by Marignac in determining the atomic weights of sodium, potassium, silver, chlorine, bromine, and iodine. At this point it will suffice to summarize the results obtained by these methods, and those derived from the work of modem investigators. 

The term very low sodium refers to which of the following ... 

Flame atomic emission spectrometry Basic information on FAES is presented elsewhere in this encyclopedia. Sodium measurements are performed at 590 nm with the use of a propane flame (1925°C). Physiological samples for sodium determination are highly diluted before measurement. The diluent and the calibrator solution contain the same concentration of lithium ions so as to balance flame instability by a concomitant measurement of lithium in the reference beam (the so-called lithium guideHne). At the same time, lithium ions inhibit the ionization of sodium atoms. This procedure cannot be used in the case of therapy with lithium salts. That is why some authors prefer the concomitant measurement of caesium to that of lithium. Dilution adjusts the viscosity of the sample to that of the calibrator solution to produce identical aspiration rate and drop size on nebulization. As other electrolytes interfere with sodium measurement, their concentration in the caH-brator solution must be similar to their concentration in the sample. For the measurement of sodium in urine, calibrator solutions different from those for serum measurement are needed as the electrolyte concentrations in urine samples are quite different from those in serum and their relations are very variable. As the concentration of the electrolytes in serum is rather constant, calibrator solutions for serum measurements can fulfill their function better than those for urine in other words, urine determinations are usually less accurate. FAES proved to be sufficiently reliable to be used as the basic principle of the sodium reference measurement procedure. In routine use, however, FAES is less accurate. Its application is given up by most clinical laboratories in favor of potentiometric measurements... 

Pentoses (CXXXII) may be converted to hexoses by the addition of hydrocyanic acid to the carbonyl group and hydrolysis of the two C-2 epimeric cyanhydrins (CXXXIII) to the next higher C-2 epimeric pair of acids (CXXXIV). Separation of the two acids, conversion to the lactones (CXXXV) and reduction yields the respective sugars (CXXXVI) . Reaction of a sugar (CXXXVI I) with nitromethane in the presence of sodium methoxide produces the C-nitro-alcohols which are converted into the acid sodium References p. 63... 

Equation V-64 is that of a parabola, and electrocapillary curves are indeed approximately parabolic in shape. Because E ax tmd 7 max very nearly the same for certain electrolytes, such as sodium sulfate and sodium carbonate, it is generally assumed that specific adsorption effects are absent, and Emax is taken as a constant (-0.480 V) characteristic of the mercury-water interface. For most other electrolytes there is a shift in the maximum voltage, and is then taken to be Emax 0.480. Some values for the quantities are given in Table V-5 [113]. Much information of this type is due to Gouy [125], although additional results are to be found in most of the other references cited in this section. 

Acetals are usually liquid they are almost unaffected by alkalis and are not attacked by metallic sodium nor by Fehling s solution. They are identified by reference to the alcohol and aldehyde (or ketone if a ketal) which they yield when hydrolysed in acid solution. Hydrolysis proceeds readily in dilute acid solution e.g., with 3-5 per cent, acid). ... 

The refractive index of a liquid is recorded as where t is the temperature at which the measurement is made, and D refers to the wave length of the D line of sodium. As already pointed out, it is usual to determine both the refractive index and the density of the liquid at 20° in any case they should be determined at the same temperatme. These two constants are useful in assisting the characterisation of a pure hquid they are particularly valuable for ahphatic hydrocarbons and similar compounds where the methods of characterisation by the formation of solid derivatives are not entirely satisfactory. 

The production of both an alcohol and the sodium salt of an acid might easily be confused with the hydrolysis products of an ester (in the above instance benzyl benzoate). Such an error would soon be discovered (e.g., by reference to the b.p. and other physical properties), but it would lead to an unnecessary expenditure of time and energy. The above example, however, emphasises the importance of conducting the class reactions of neutral oxygen-containing compounds in the proper order, viz., (1) aldehydes and ketones, (2) esters and anhydrides, (3) alcohols, and (4) ethers. 

Recall that the term kinetics refers to how the rate of a reaction varies with changes m concentration Consider the nucleophilic substitution m which sodium hydroxide reacts with methyl bromide to form methyl alcohol and sodium bromide... 

An excephon to this type of nomenclature is NaC CH which is normally referred to as sodium acetylide Both sodium acetyhde and ethynylsodium are acceptable lUPAC names... 

The sign of optical rotation is placed in parentheses, (-f) for dextrorotary, (—) for levorotary, and ( ) for racemic, and placed before the formula. The wavelength (in nanometers is indicated by a right subscript unless indicated otherwise, it refers to the sodium D-line. 

Molar concentrations are used so frequently that a symbolic notation is often used to simplify its expression in equations and writing. The use of square brackets around a species indicates that we are referring to that species molar concentration. Thus, [Na ] is read as the molar concentration of sodium ions. ... 

The ubiquitous use of the word Tine to describe an experimentally observed transition goes back to the early days of observations of visible spectra with spectroscopes in which the lines observed in, say, the spectmm of a sodium flame are images, formed at various wavelengths, of the entrance slit. Although, nowadays, observations tend to be in the form of a plot of some measure of the intensity of the transition against wavelength, frequency or wavenumber, we still refer to peaks in such a spectmm as lines. 

Furfural can be oxidized to 2-furoic acid [88-14-2] reduced to 2-furanmethanol [98-00-0] referred to herein as furfuryl alcohol, or converted to furan by decarbonylation over selected catalysts. With concentrated sodium hydroxide, furfural undergoes the Cannizzaro reaction yielding both 2-furfuryl alcohol and sodium 2-furoate [57273-36-6]. 

Nitdles may be prepared by several methods (1). The first nitrile to be prepared was propionitdle, which was obtained in 1834 by distilling barium ethyl sulfate with potassium cyanide. This is a general preparation of nitriles from sulfonate salts and is referred to as the Pelou2e reaction (2). Although not commonly practiced today, dehydration of amides has been widely used to produce nitriles and was the first commercial synthesis of a nitrile. The reaction of alkyl hahdes with sodium cyanide to produce nitriles (eq. 1) also is a general reaction with wide appHcabiUty ... 

The first commercial production of fatty alcohol ia the 1930s employed the sodium reduction process usiug a methyl ester feedstock. The process was used ia plants constmcted up to about 1950, but it was expensive, hazardous, and complex. By about 1960 most of the sodium reduction plants had been replaced by those employing the catalytic hydrogenolysis process. Catalytic hydrogenation processes were investigated as early as the 1930s by a number of workers one of these is described ia reference 26. 

Articles fabricated from FEP resins can be made bondable by surface treatment with a solution of sodium in Hquid ammonia, or naphthalenyl sodium in tetrahydrofuran (64) to faciUtate subsequent wetting. Exposing the surface to corona discharge (65) or amines at elevated temperatures in an oxidizing atmosphere (66) also makes the resins bondable. Some of the more recent work is described in References 67—69. 

The earhest frothing process developed was the Dunlop process, which made use of chemical gelling agents, eg, sodium fluorosiUcate, to coagulate the mbber particles and deactivate the soaps. The Talalay process, developed later, employs freeze-coagulation of the mbber followed by deactivation of the soaps with carbon dioxide. The basic processes and a multitude of improvements are discussed extensively in Reference 3. A discussion more oriented to current use of these processes is given in Reference 115. 

The concentration of aqueous solutions of the acid can be deterrnined by titration with sodium hydroxide, and the concentration of formate ion by oxidation with permanganate and back titration. Volatile impurities can be estimated by gas—Hquid chromatography. Standard analytical methods are detailed in References 37 and 38. 

Sucralfate. Sucralfate [54182-58-0] (Carafate) (6) is a white amorphous powder soluble in dilute hydrochloric acid and sodium hydroxide. It is practically insoluble in water, ethanol, and carbon tetrachloride. Dissolution of aluminum occurs at pH <3. It may be prepared by the method described in Reference 7. 

Humic acids are alkaH-extractable materials and total humic acid content is a term that refers to the humic acid content of coal that has had its carboxylate cations removed with sodium pyrophosphate. Values for some typical AustraHan brown coals range from 24—92% (13). Treatment of lignitic coals with mineral acid to release the alkaH and alkaline cations may dissolve up to 20% of the coal. The naturally moist coals are slightly acidic and have a pH of 3.5—6.5. 

Functional Blends. The term functional blend refers to various ingredient blends formulated to achieve a certain objective such as fat reduction. An example of this blend consists of water, partially hydrogenated canola oil, hydrolyzed beef plasma, tapioca flour, sodium alginate, and salt. This blend is designed to replace animal fat and is typically used at less than 25% of the finished product. Another functional blend is composed of modified food starch, rice flour, salt, emulsifier, and flavor. A recommended formula is 90% meat (with 10% fat), 7% added water, and 3% seasoning blend... 

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