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Hefei TNJ chemical industry co.,ltd

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Orotic acid vitamin B13 CAs 65-86-1

CAS NO.65-86-1

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Product Details

Keywords

  • Orotic acid
  • 65-86-1
  • vitamin B13

Quick Details

  • ProName: Orotic acid vitamin B13 CAs 65-86-1
  • CasNo: 65-86-1
  • Molecular Formula: C5H4N2O4
  • Appearance: White crystalline powder
  • Application: food additive
  • DeliveryTime: 1 week
  • PackAge: 25kg per drum
  • Port: shanghai
  • ProductionCapacity: 200 Metric Ton/Year
  • Purity: 99-101%
  • Storage: dry and cool place avoid fire and heat
  • Transportation: by sea/air
  • LimitNum: 25 Kilogram
  • Heavy Metal: not more than 20ppm
  • Limited Quantity: N/A
  • Valid Period: 2 years
  • pH: 2.8
  • loss on dry: 9.0-10.5
  • assay: 99-101
  • CAs: 65-86-1

Superiority

Link person Albert yu
Cellphone +8613696510409
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Product specification:                                                
Enterprise standard
Appearance                White to off-white crystalline powder
Assay                        99.0-102.0 %
Loss on drying           (140℃) ≤1.0 %
Chloride                      ≤150ppm
Residue on ignition      ≤0.2%
Heavy Metals(lead)  ≤20ppm
 
 
Orotic acid Chemical Properties
MP >300°C
Water Solubility Slightly soluble
 
Stability:
Stable. Incompatible with strong oxidizing agents.

Shelf life:

in conform to the specified storage conditions and packaging is complete, shelf life is 2 years.Usage:Nutrition or food additive。

Packing:
Carton or Carton or drum with 2 inner PE bags。

Details

Orotic acid

CAS: 65-86-1

MF: C5H4N2O4
MW: 156.1
EINECS: 200-619-8
 
appearance               white powder
loss on dry(140℃) ≤1.0%
assay                       99.0-102.0 %
chloride                     ≤150ppm
residue on ignition      ≤0.2%
heavy metal               ≤20ppm
 
Packing 25kg per drum
 
Orotic acid Usage And Synthesis
Chemical Properties     white crystalline powder
Usage                         Hepatoprotectant, uricosuric agent
General Description      White crystals or crystalline powder.
Air & Water Reactions  Slightly soluble in water.
 
Reactivity Profile 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.
 
Fire Hazard     Flash point data for Orotic acid are not available; however, Orotic acid is probably combustible.