Orotic Acid High-Purity Pyrimidine Precursor for Nucleotide Biosynthesis and Nutritional Supplementation

Orotic acid

4-Pyrimidinecarboxylic acid,1,2,3,6-tetrahydro-2,6-dioxo-;Orotic acid;1,2,3,6-Tetrahydro-2,6-dioxo-4-pyrimidinecarboxylic acid;Animal galactose factor;6-Carboxyuracil;6-Uracilcarboxylic acid;Whey factor;2,6-Dihydroxy-4-pyrimidinecarboxylic acid;Oroturic;Orotyl;Orodin;Orotonin;2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid;NSC 79560;NSC 9791;Vitamin B13;2,4-Dihydroxypyrimidine-6-carboxylic acid;2,4-Dioxo-1H-pyrimidine-6-carboxylic acid;2-Hydroxy-6-oxo-1,6-dihydropyrimidine-4-carboxylic acid;6784-70-9;58915-47-2

65-86-1

C5H4N2O4

InChIKey=PXQPEWDEAKTCGB-UHFFFAOYSA-N

156.09600

156.10

200-619-8

61H4T033E5

758903|9791

DTXSID0025814

Crystals

29335990

Nutrition Supplements

103.02000

-1.4

Orotic acid appears as white crystals or crystalline powder. (NTP, 1992)

1.642 g/cm3

345-346 °C

656.9ºC at 760 mmHg

351.1ºC

1.705

H2O: Slightly soluble

Keep in a cool, dry, dark location in a tightly sealed container or cylinder. Keep away from incompatible materials, ignition so

1X10-8 mm Hg at 25 deg C (est)

pic-esc 1 g/L ZAPOAK12,583,72

Henry's Law constant = 8.1X10-15 atm-cu m/mol at 25 °C (est)

pKa1 = 2.07; pKa2 = 9.45

138.85 Ų [M+H]+ [CCS Type: DT, Method: stepped-field]|181.87 Ų [M+Na]+ [CCS Type: DT, Method: stepped-field]|125.2 Ų [M-H]- [CCS Type: DT, Method: stepped-field]|121.7 Ų [M-H]-

Hydroxyl radical reaction rate constant = 8.9X10-12 cu cm/molec-sec at 25 °C (est)

Slightly soluble in water.

Acids, Carboxylic

Carboxylic acids, such as OROTIC ACID, donate hydrogen ions if a base is present to accept them. They react in this way with all bases, both organic (for example, the amines) and inorganic. Their reactions with bases, called "neutralizations", are accompanied by the evolution of substantial amounts of heat. Neutralization between an acid and a base produces water plus a salt. Carboxylic acids with six or fewer carbon atoms are freely or moderately soluble in water; those with more than six carbons are slightly soluble in water. Soluble carboxylic acid dissociate to an extent in water to yield hydrogen ions. The pH of solutions of carboxylic acids is therefore less than 7.0. Many insoluble carboxylic acids react rapidly with aqueous solutions containing a chemical base and dissolve as the neutralization generates a soluble salt. Carboxylic acids in aqueous solution and liquid or molten carboxylic acids can react with active metals to form gaseous hydrogen and a metal salt. Such reactions occur in principle for solid carboxylic acids as well, but are slow if the solid acid remains dry. Even "insoluble" carboxylic acids may absorb enough water from the air and dissolve sufficiently in it to corrode or dissolve iron, steel, and aluminum parts and containers. Carboxylic acids, like other acids, react with cyanide salts to generate gaseous hydrogen cyanide. The reaction is slower for dry, solid carboxylic acids. Insoluble carboxylic acids react with solutions of cyanides to cause the release of gaseous hydrogen cyanide. Flammable and/or toxic gases and heat are generated by the reaction of carboxylic acids with diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides. Carboxylic acids, especially in aqueous solution, also react with sulfites, nitrites, thiosulfates (to give H2S and SO3), dithionites (SO2), to generate flammable and/or toxic gases and heat. Their reaction with carbonates and bicarbonates generates a harmless gas (carbon dioxide) but still heat. Like other organic compounds, carboxylic acids can be oxidized by strong oxidizing agents and reduced by strong reducing agents. These reactions generate heat. A wide variety of products is possible. Like other acids, carboxylic acids may initiate polymerization reactions; like other acids, they often catalyze (increase the rate of) chemical reactions.