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Nicotinic acid hydrochloride

Nicotinic acid hydrochloride may be obtained directly from the nitrate by heating on a steam bath 460 g. of crude nitrate with 1000 cc. of concentrated hydrochloric acid (sp. gr. 1.19). After six to eight hours, the evolution of gas ceases and the liquid is evaporated under diminished pressure. The dry salt is again treated with 500 cc. of hydrochloric acid and heated for five hours and then evaporated as before. [Pg.51]

Hydroxylamine hydrochloride Lithium aluminum hydride Nicotinic acid chloride... [Pg.1068]

C7HJO 100-51-6) see Fluoxetine Gabapentin Ganciclovir Levocabastine Moexipril Nicotinic acid benzyl ester Perindopril Quinapril hydrochloride Ramipril Saquinavir Trandolapril benzylamine... [Pg.2304]

Stock solution 4. 100 x stock solution of vitamins was prepared by dissolving biotin (20 mg), folic acid (20 mg), pyrodoxine hydrochloride (100 mg), riboflavin (50 mg), thiamine hydrochloride (50 mg), nicotinic acid (50 mg), pantothenic acid (50 mg), vitamin B12 (1 mg), 4-aminobenzoic acid (50 mg) and thioctic acid (50 mg) in deionized water. The volume was adjusted to 1.0 L. The solution was filtered, sterilized and stored as 10 mL aliquots at —20 °C. [Pg.380]

Either acid or alkaline hydrolysis can be applied, converting nicotinamide to nicotinic acid. Alkaline hydrolysis releases also the unavailable vitamers providing the estimation of the total niacin content. Acid hydrolysis, instead, is slower than alkaline hydrolysis therefore the former is usually coupled with enzymatic digestion by using takadiastase, papain, and clarase. Extraction with water and dilute sulfuric or hydrochloride acid has been applied to release the vitamers from the matrix without degrading nicotinamide [598]. [Pg.626]

Hydroxylamine hydrochloride Nicotinic acid chloride Lithium aluminum hydride... [Pg.2425]

Niflumic acid is prepared as follows Nicotinic acid, m-trifluoromethylaniline, and potassium iodide are intimately mixed and heated on an oil bath at 140°C. The mixture melts to give a dark red liquid. The temperature of the oil bath is allowed to fall to 100°C and is maintained at this temperature for an hour and a half. The mixture puffs up and forms a yellow crystalline mass. After cooling to ordinary temperature, this mass is ground up in a mortar and extracted several times with small volumes of ether to remove excess m-trifluoromethylaniline. The residue is then washed twice with 10 ml of distilled water to remove m-trifluoromethylaniline hydrochloride and potassium iodide, and finally twice with 10 ml of 95% alcohol to remove colored resinous contaminants. After drying at 100°C, 2-(m-trifluoromethylanilino)nicotinic acid is obtained as pale yellow needles (from 70% ethanol) melting at 204°C (Kofler block). [Pg.2438]

Pyridoxine Hydrochloride, USP. Pyridoxine hydrochloride.. S-hydroxy-6-methyl-3.4-pyridinedimethanol hydrochloride. vitamin B, hydrochloride, rat antidermatitis factor. is a white, odorless, crystalline substance that is soluble l .S in water and 1 100 in alcohol and in.soluble in ether. It is relatively. stable to light and air in the solid form and in acid solutions at a pH no greater than S. at which pH it can be autoclaved at IS pounds at I20°C for 20 to 30 minutes. Pyridoxine is unstable when irradiated in aqueous solution.s at pH 6.8 or above. It is oxidized readily by hydrogen peroxide and other oxidizing agents. Pyridoxine is as stable in mixed vitamin preparations as riboflavin and nicotinic acid. A 1% aqueous solution has a pH of 3. The pK i values fur pyridoxine. pyridoxal. and pyridoxamine are S.OO. 4.22. and 3.40. respectively, and their pK 2 values are 8.96. 8.68. and 8.05. respectively. [Pg.894]

Hexopar inositol nicotinate nicotinic acid, hexoprenaline [ban, inn] (hexoprenaline hydrochloride [jan]) is a P-ADRENOCEPTOR agonist selective for the P2-subtype that therapeutically can be used as a BRONCHODIIATOR in ANTIASTHMATIC treatment, hexoprenaline hydrochloride hexoprenaline. hexuronic acid ascorbic acid, hexylcaine [inn] (hexylcaine hydrochloride [usan]) is an ester series LOCAL ANAESTHETIC, used by topical application for the local relief of pain, hexylcaine hydrochloride hexylcaine. hexylresorcinol [usan] is a urinary ANTISEPTIC and an ANTHELMINTIC. It inhibits melanosis (blackspot) in shrimps, and is used as a food additive for prevention of enzymic browning in shrimps and fruits, hexyltheobromine pentifylline. [Pg.141]

An alternate synthesis was developed by E. Smissman and G. Hite2, using a modified Favorski rearrangement. Iso-nicotinic acid was methylated, reduced to 1-methyl-U-piperi-dinecarboxylic acid hydrochloride, and converted to the acid chloride hydrochloride. This was then condensed with benzene, chlorinated, treated with alkali, esterfied, and converted to the hydrochloride (See Figure 8). [Pg.186]

Plasma free fatty acids (FFA) are elevated during the early phase of myocardial infarction. Rapid reduction of FFA following the administration of the nicotinic acid analog 5"fluoro-3 hydroxymethylpyridine hydrochloride (6) to patients with infarction was associated with decreased incidence of ventricular arrhythmias.10 Amiodarone (j) was reported to be effective in the treatment of atrial and ventricular arrhythmias in a recent trial.19... [Pg.41]

Anabasine (3-pyridyl-2-piperidine) appears to be the sole constituent of N. glauca R. Grah., and this plant has been used for the study of the biogenesis of the alkaloid. Anabasine isolated from N. glauca cultured in hydroponic solution containing lysine-2-C hydrochloride is radioactive (53). The alkaloid when oxidized with nitric acid gives nicotinic acid which by decarboxylation yields pyridine and carbon dioxide isolated as barium carbonate. Whereas the activity of anabasine is... [Pg.130]

Nicotinic acid converted to the acid chloride hydrochloride with... [Pg.152]

He considers A a disguised form of a /9-aldehyde acid and as such readily loses carbon dioxide. When nicotinic acid was reduced in dilute hydrochloride acid only 10% of piperidine was obtained, indicating a small amount of decarboxylation. Decarboxylation has been observed during the hydrogenation of nicotinic acid in aqueous solution in the presence of ruthenium (8), rhodium (16), and platinum oxide (49). It has been... [Pg.214]


See other pages where Nicotinic acid hydrochloride is mentioned: [Pg.137]    [Pg.213]    [Pg.45]    [Pg.137]    [Pg.213]    [Pg.45]    [Pg.849]    [Pg.92]    [Pg.53]    [Pg.1078]    [Pg.1391]    [Pg.90]    [Pg.849]    [Pg.143]    [Pg.379]    [Pg.74]    [Pg.74]    [Pg.849]    [Pg.2430]    [Pg.3071]    [Pg.46]    [Pg.153]    [Pg.101]    [Pg.422]    [Pg.92]    [Pg.197]    [Pg.849]    [Pg.354]    [Pg.1034]    [Pg.1593]    [Pg.849]    [Pg.85]    [Pg.176]   
See also in sourсe #XX -- [ Pg.4 , Pg.51 ]

See also in sourсe #XX -- [ Pg.4 , Pg.51 ]

See also in sourсe #XX -- [ Pg.4 , Pg.51 ]

See also in sourсe #XX -- [ Pg.4 , Pg.51 ]




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Nicotinic acid

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