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Acidic agent

Fig. 12. Tryptic map of it-PA (mol wt = 66,000) showing peptides formed from hydrolysis of reduced, alkylated rt-PA. Separation by reversed-phase octadecyl (C g) column using aqueous acetonitrile with an added acidic agent to the mobile phase. Arrows show the difference between A, normal, and B, mutant rt-PA where the glutamic acid residue, D, has replaced the normal arginine residue, C, at position 275. Fig. 12. Tryptic map of it-PA (mol wt = 66,000) showing peptides formed from hydrolysis of reduced, alkylated rt-PA. Separation by reversed-phase octadecyl (C g) column using aqueous acetonitrile with an added acidic agent to the mobile phase. Arrows show the difference between A, normal, and B, mutant rt-PA where the glutamic acid residue, D, has replaced the normal arginine residue, C, at position 275.
A mixture of dimethyl sulfate with SO is probably dimethyl pyrosulfate [10506-59-9] CH2OSO2OSO2OCH2, and, with chlorobenzene, it yields the 4,4 -dichlorodiphenylsulfone (153). Trivalent rare earths can be separated by a slow release of acid into a solution of rare earth chelated with an ethylenediaminetetraacetic acid agent and iodate anion. As dimethyl sulfate slowly hydrolyzes and pH decreases, each metal is released from the chelate in turn and precipitates as the iodate, resulting in improved separations (154). [Pg.203]

Kost et al. have studied related reactions of 2-acyl-1-phenylpyrazolidines (422) and l-phenyl-2-thiocarbamoylpyrazolidines (423). The former are converted on reaction with phosphorus oxychloride into tetrahydropyrimido[l,2-a]indoles (424) (72CHE57) and the latter into tetrahydropyrimido[2,l-f ]benzothiazoles (425) under the influence of acidic agents (80CHE169). [Pg.257]

Elastomers, plastics, fabrics, wood and metals can be joined with themselves and with each other using nitrile rubber/epoxy resin blends cured with amines and/or acidic agents. Ethylene-propylene vulcanizates can also be joined using blends of carboxylated nitrile rubber, epoxy resin and a reactive metal filler (copper, nickel, cobalt). However, one of the largest areas of use of nitrile rubber modified epoxy systems is in the printed circuit board area [12]. [Pg.660]

Each component of Jessner s solution has specific effects (Fig. 3.1). Salicylic acid (ortho hydroxy benzoic acid) is a beta hydroxy acid agent... [Pg.23]

Salicylic acid (ortho hydroxybenzoic add) is a beta hydroxy acid agent. It is a lipophilic compound which produces desquamation of the stratum corneum via removal of intercellular lipids [3] (see salicylic acid section). Given its keratolytic effects, it has become an increasingly popular superficial peeling agent. Salicylic acid peels induce injury via thinning or removal of the stratum corneum. In addition, salicylic acid potentially enhances the penetration of TCA. [Pg.103]

Concerning anthropogenic sources, methyl arsenic compounds such as methyl arsonic acid and dimethylarsinic acid have been used as herbicides, and were once a significant source of environmental residues. Dimethyl-arsinic acid (Agent Blue) was used as a defoliant during the Vietnam War. [Pg.178]

In the cyclization of 7V-(het)arylaminomethylenemalonates, a wide variety of acidic agents have been used. Under such circumstances, not only iV-mono but also N /V-disubstituted derivatives could readily be cyclized. [Pg.158]

H. Bundgaard, N. M. Nielsen, Esters of /V,/V-Disubstiluted 2-Hydroxyacetamides as a Novel Highly Biolabile Prodrug Type for Carboxylic Acid Agents ,./. Med. Chem. 1987, 30,451-454. [Pg.538]

N. M. Nielsen, H. Bundgaard, Glycolamide Esters as Biolabile Prodrugs of Carboxylic Acid Agents Synthesis, Stabibty, Bioconversion and Physicochemical Properties , J. Pharm. Sci. 1988, 77, 285 - 298. [Pg.538]

Ion-radical reactions also open convenient routes to fused benzoheterocycles as a result of intramolecular cyclization. The fused heterocycles are useful as compounds of potential physiological activity. Many of them are used as medications. Certainly, only those syntheses that do not change the functional groups needed to provide or enforce the curative effect, are of interest. At the same time, it is desirable to exclude acidic agents that lead to the splitting of the final heterocycles, which... [Pg.372]

The elimination proceeds rapidly at room temperature with a catalytic amount of acid or fluoride, however, it has also been observed to occur upon distillation of the isoxazolidine (16,18). Because of the facile elimination, several procedures have been developed in which the reaction is quenched with an acidic agents, and the isoxazoline is isolated directly (108). Isoxazolines are useful in the preparation of p-hydroxy ketones and amino alcohols (138). [Pg.126]

The Extractants. The extractants are classified into different groups, according to their reaction type solvating, salt forming (acidic agents) or ionic exchanging. [Pg.159]

CA 71, 51824v(1969) [Gelled nitric acid agent, such as contg HNOa (42°Be) 14.0,... [Pg.603]

Chloral condensations with aromatic hydrocarbons (and related derivatives) give rise to diaryltrichloroethane compounds, and are brought about in the presence of acid catalysts, proceeding with the formation of carbinol intermediates (Scheme 2.1). Commonly used catalysts include concentrated H2SO4 and its monohydrate, HCl, HF, I O,-, Lewis acids and a series of other acid agents [1, 2]. [Pg.5]

Another herbicide, 2,4,5-trichlorophenoxyacetic acid, is synthesized by starting with the chlorination of benzene to give 1,2,4,5-tetrachloroben-zene, which reacts with caustic to give 2,4,5-trichlorophenol. Conversion to the sodium salt followed by reaction with sodium chloroacetate and acidification gives 2,4,5-trichlorophenoxyacetic acid. Agent Orange is a 1-to-l mixture of the butyl esters of 2,4,5-trichlorophenoxyacetic acid and 2,4,-dichlorophenoxyacetic acid. [Pg.257]

Indole and its derivatives are acidophobic systems [55, 56], susceptible to the formation of products from dimerization and polymerization under the influence of acidic agents. This makes it possible to suppose that processes involving polymerization of phosphorus-containing indoles can occur at elevated temperatures under the influence of the acidic impurities present in amidophosphites. [Pg.10]

Nielson, N.M., Bundgaard, H. (1988) Glycolamide esters as biolabUe prodrugs of carboxylic acid agents synthesis, bioconversion and physicochemical properties. J. Pharm. Sci. 77(4), 285-298. [Pg.938]

Earlier we mentioned that a common measure of acidity is pH, which is a measure of the concentration of hydronium ions (H O", the acidic agent) in solution. Now we can be more specific a solution with a tenth of a mole of hydronium ions per liter has a pH of 1. A solution with a hundredth of a mole of hydronium ions per liter has a pH of 2. Every time the concentration of hydronium ions decreases by a multiple of ten, the pH goes up by one unit. [Pg.149]

Flavor enhancers are used imiversally in the food and pharmaceutical industries. Sugar, carboxylic acids (e.g., citric, malic, and tartaric), common salt (NaCl), amino acids, some amino acid derivatives (e.g., monosodium glutamate—MSG), and spices (e.g., peppers) are most often employed. Although extremely effective with proteins and vegetables, MSG has limited use in pharmaceuticals because it is not a sweetener. Citric acid is most frequently used to enhance taste performance of both liquid and solid pharmaceutical products, as well as a variety of foods. Other acidic agents, such as malic and tartaric acids, are also used for flavor enhancement. In oral liquids, these acids contribute unique and complex organoleptic effects, increasing overall flavor quality. Common salt provides similar effects at its taste threshold level in liquid pharmaceuticals. Vanilla, for example, has a delicate bland flavor, which is effectively enhanced by salt. [Pg.1770]

The compounds of formula II can be sjmthesized by condensing in the presence of an acid agent, a resorcinol of the formula ... [Pg.64]


See other pages where Acidic agent is mentioned: [Pg.354]    [Pg.493]    [Pg.49]    [Pg.363]    [Pg.49]    [Pg.18]    [Pg.540]    [Pg.72]    [Pg.156]    [Pg.43]    [Pg.336]    [Pg.339]    [Pg.142]    [Pg.44]    [Pg.160]    [Pg.2081]    [Pg.65]   
See also in sourсe #XX -- [ Pg.149 ]




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10-Camphorsulfonic acid resolving agent

2,2’-[ acid fluorescent whitening agent

2,4,5-Trichlorophenoxyacetic acid Agent orange)

Acetic acid flavoring agent

Acid neutralization agents

Acidic curing agents

Acidic extracting agent

Acidic halogenating agent

Acidic resolving agents

Acidifying agents hydrochloric acid

Acidifying agents lactic acid

Acidifying agents phosphoric acid

Acidifying agents sulfuric acid

Acids antistaling agents

Acids as oxidant agents

Acids, Bases, and Etching Agents

Acids, resolving agents, brucine

Acrylic acid Coupling agents, silanes

Acrylic acid biological agents

Acylating agents acid esters

Acylating agents from carboxylic acids

Additives acidic agents

Agents which act on nucleic acid transcription and replication

Alkylating agents acid esters

Amino Acid, Chelating Agent

Amino acids acylating agents

Antibacterial agents benzoic acid

Antibacterial agents nucleic acid synthesis inhibition

Antifungal agents benzoic acid

Aromatic sulfonation by halosulfuric acids and other sulfonating agents

Ascorbic acid (vitamin reducing agent

Ascorbic acid developing agents

Benzoic acid agent

Bile acid sequestrating agents

Boric acid dehydrating agent

Buffering agents malic acid

Buffering agents phosphoric acid

Carboxylic acids acylating agent

Carboxylic acids conversion into acylating agents

Carboxylic acids, as acylating agents

Carboxylic acids, conversion dehydrating agents

Chain transfer polymerization agents Methacrylic acid

Chelating agents acidic

Chelating agents citric acid

Chelating agents edetic acid

Chelating agents fumaric acid

Chelating agents malic acid

Chelating agents tartaric acid

Complexing agent acetic acid

Contrast agents amino acids

Conversion of Carboxylic Acids into Isolable Acylating Agents

Corrosion by Acids and with Complexing Agents

Coupling agents acid-functionalized polymers

Coupling agents acrylic acid

Coupling agents unsaturated acids

Cross-linking agent sulfuric acid

Dehydrogenating agents sulfuric acid

Delivery Agents for Nucleic Acids and Drugs

Emulsifying agents lauric acid

Emulsifying agents linoleic acid

Emulsifying agents myristic acid

Emulsifying agents oleic acid

Emulsifying agents palmitic acid

Emulsifying agents stearic acid

Esterifying agents, propionic acid

Fatty acid reducing agents

Fatty acids agents

Flavoring agents fumaric acid

Flavoring agents malic acid

Flavoring agents phosphoric acid

Flavoring agents propionic acid

Gastric acid agents

Glycolic acid chemical peeling agent

Hydroxamic acids sequestering agents

Inorganic agents, with Acids

Inositolpolyphosphoric acid antistain agent

Interaction of Platinum Agents with Amino Acids, Peptides and Proteins

Lactic acid bacteria as antifungal agents

Latent acid curing agents

Lewis acid reducing agent

Lewis acids acylating agent activation

Methylphosphonic acids agents

Nerve agents alkyl methylphosphonic acids

Nitrating agent acidic” mixture

Nitrating agent nitric acid

Nitrating agent nitric acid/trifluoroacetic anhydride

Nitrating agent sulfuric-nitric acid mixture

Nitrilotriacetic acid chelating agent

Nucleic acid denaturing agents

Nucleic-acid-based therapeutic agents

Organic Acid, Chelating Agent

Other Agents Targeting Mucosal Bile Acid Exposure

Oxidation agents organic peroxy acids

Oxidizing agents arsenic acid

Oxidizing agents selenic acid

Oxidizing agents sulfuric acid (cone

Peracetic acid bleaching agent

Peracetic acid epoxidizing agent

Peracetic acid, trifluoroanti hydroxylation epoxidizing agent

Perbenzoic acid, 3,5-dinitroepoxidizing agent

Perbenzoic acid, 4-nitroepoxidizing agent

Perbenzoic acid, 4-nitroepoxidizing agent ethers

Perbenzoic acid, 4-nitroepoxidizing agent oxidation

Performic acid epoxidizing agent

Phosphonic acid, methylenedilabelled with technetium bone scanning agent

Phosphoric acid ester tube, nerve agents

Polylactic Acid and Polyethylene Glycol as Antimicrobial Agents

Propionic acid derivatives agents

Reaction CXI.—Action of Dehydrating Agents on a Free Acid

Reactions with acidic condensing agents

Reducing agent, ascorbic acid

Resolving agents carboxylic acids

Salicylic acid uricosuric agent

Scavenging agents acid scavengers

Solubilizing agents stearic acid

Stabilizing agents ascorbic acid

Sulfonates, dialkylaminotrifluorohalogen transfer agents acid fluoride synthesis

Sulfonating Agents and Derivatives Based on Sulfuric Acid

Sulfosalicylic Acid as a Masking Agent

Sulfuric acid as cyclizing agent

Sulfuric acid as dehydrating agent

Sulfuric acid dehydrating agent

Supported Lewis acids oxidizing agents

Surface active agents fatty acid based

Synthesis with C-acyl Meldrums Acid as the A-Acylating Agent

Tartaric Acid amino acids resolution agent

Therapeutic agents ascorbic acid

Therapeutic agents benzoic acid

Therapeutic agents lactic acid

Therapeutic agents sulfuric acid

Triazole-Substituted Oleanolic Acid Derivatives as Anticancer Agents

Triterpene betulinic acid derivatives, as anti-HIV agents

Wetting acid agents

With Acids, Electrophiles, and Oxidizing Agents

With Acylating Agents Followed by Acids, Bases, or Hydrogen Peroxide (for Pyrimidin-4-ones)

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