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CAS-Nr. | 65-86-1 |
Bezeichnung: | Orotsure |
Englisch Name: | Orotic acid |
Synonyma: | Orotsure Orodin;Oropur;orotic;Orotyl;Orotonin;Oroturic;H-ORO-OH;Orotonsan;Orotsaure;orodin[qr] |
CBNumber: | CB5691265 |
Summenformel: | C5H4N2O4 |
Molgewicht: | 156.1 |
MOL-Datei: | 65-86-1.mol |
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Orotsure physikalisch-chemischer Eigenschaften |
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Wasserlöslichkeit: |
Slightly soluble |
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Stabilität:: |
Stable. Incompatible with strong oxidizing agents. |
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Orotsure Chemische Eigenschaften,Einsatz,Produktion Methoden |
Chemische Eigenschaften white crystalline powder |
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Verwenden hepatoprotectant, uricosuric agent |
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Allgemeine Beschreibung White crystals or crystalline powder. |
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Air & Water Reaktionen Slightly soluble in water. |
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Reaktivität anzeigen 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 Orotic acid 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. |
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Brandgefahr Flash point data for Orotic acid are not available; however, Orotic acid is probably combustible. |
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R-Sätze Betriebsanweisung: R22:Gesundheitsschädlich beim Verschlucken. R36/37/38:Reizt die Augen, die Atmungsorgane und die Haut. |
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S-Sätze Betriebsanweisung: S26:Bei Berührung mit den Augen sofort gründlich mit Wasser abspülen und Arzt konsultieren. S36/37/39:Bei der Arbeit geeignete Schutzkleidung,Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen. S22:Staub nicht einatmen. S37/39:Bei der Arbeit geeignete Schutzhandschuhe und Schutzbrille/Gesichtsschutz tragen. |
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Orotsure Upstream-Materialien And Downstream Produkte |
Upstream-Materialien
6-Methyluracil
Natriumdichromat Dihydrat
1,3-Dibenzyl-2-oxoimidazolidin-4,5-dicarbonsure
Diethylethoxymethylenmalonat
Diethyloxalat
Harnstoff
Essigsure
Selendioxid
Schwefelsure
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Downstream Produkte
5-Amino-2,6-dioxo-1,2,3,4-tetrahydropyrimidin-4-carbonsure
1,2,3,6-Tetrahydro-2,6-dioxopyrimidin-4-carbonsure, Verbindung mit 5-Amino-1H-imidazol-4-carboxamid (1:1)
Hydantoin
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Orotsure Anbieter Lieferant Produzent Hersteller Vertrieb Händler. Global( 151)Lieferanten |
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65-86-1(Orotsure)Verwandte Suche: |
1,2,3,6-Tetrahydro-2,6-dioxopyrimidin-4-carbonsure, Verbindung mit 5-Amino-1H-imidazol-4-carboxamid (1:1)
Bis(1,2,3,6-tetrahydro-2,6-dioxopyrimidin-4-carboxylato-N3,O4)zink
Methyl-1,2,3,6-tetrahydro-2,6-dioxopyrimidin-4-carboxylat
Zink-1,2,3,6-tetrahydro-2,6-dioxopyrimidin-4-carboxylat (1:2)
Kalium-1,2,3,6-tetrahydro-2,6-dioxopyrimidin-4-carboxylat
URACIL
Orotsure
ACETIC ACID
CARBOXYLIC ACID
Selendioxid
Hyaluronsure
5-Fluoruracil-4-carbonsure
DIOXOPROMETHAZINE HCL
Folsure
Zitronensure
Stearinsure
DIOXOPROMETHAZINE
1,4-Dioxan
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1,2,3,6-tetrahydro-2,6-dioxo-4-pyrimidecarboxylicacid[qr]
1,2,3,6-tetrahydro-2,6-dioxo-4-pyrimidinecarboxylicaci
2,6-Dihydroxy-4-pyrimidinecarboxylic acid
4-Pyrimidinecarboxylic acid, 1,2,3,6-tetrahydro-2,6-dioxo-
4-pyrimidinecarboxylicacid,1,2,3,6-tetrahydro-2,6-dioxo-[qr]
6-carboxyuracil[qr]
acideorotique(french)[qr]
acidoorotico[qr]
acidumoroticum(latin)[qr]
ai3-25478[qr]
Animal galactose factor
animalgalactosefactor
animalgalactosefactor[qr]
Dioxotetrahydropyrimidine-6-car-boxylicacid
Orodin
orodin[qr]
Oropur
orotic
Orotonin
orotonin[qr]
Orotonsan
Orotsaure
orotsaure[qr]
Oroturic
oroturic[qr]
Orotyl
orotyl[qr]
uracil-6-carboxylicacid[qr]
Whey factor
wheyfactor
wheyfactor[qr]
AKOS MSC-0707
6-URACILCARBOXYLIC ACID
65-86-1
6-CARBOXYURACIL
6-CARBOXY-2,4-DIHYDROXYPYRIMIDINE
4-CARBOXYURACIL
2,6-DIHYDROXYPYRIMIDINE-4-CARBOXYLIC ACID
2 6-DIOXO-1 2 3 6-TETRAHYDRO-4-PYRIMIDINECARBOXYLIC ACID
2,6-DIOXO-1,2,3,6-TETRAHYDROPYRIMIDINE-4-CARBOXYLIC ACID
2,6-DIOXY-1,2,3,6-TETRAHYDRO-4-PYRIMIDINECARBOXYLIC ACID
2 4-DIHYDROXYPYRIMIDINE-4-CARBOXYLIC ACID
1,2,3,6-TETRAHYDRO-2,6-DIOXO-4-PYRIMIDINECARBOXYLIC ACID
BioChemical
Building Blocks
H-ORO-OH
URACIL-4-CARBOXYLIC ACID
URACIL-6-CARBOXYLIC ACID
VITAMIN B13
TIMTEC-BB SBB004017
Metabolomics
Metabolites and Cofactors on the Metabolic Pathways Chart
Metabolic Pathways
Heterocyclic Building Blocks
Pyrimidines
Nucleotide
OROTIC ACID
1,2,3,6-tetrahydro-2,6-dioxopyrimidine-4-carboxylic acid
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