China Biggest Factory Manufacturer Supply DIATRIZOIC ACID CAS 117-96-4 CAS NO.117-96-4

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DIATRIZOIC ACID Basic information Product Name: DIATRIZOIC ACID CAS: 117-96-4 MF: C11H9I3N2O4 MW: 613.91 EINECS: 204-223-6 Product Categories: UROVIST;Intermediates & Fine Chemicals;Organics;Pharmaceuticals Mol File: 117-96-4.mol   DIATRIZOIC ACID Chemical Properties Melting point  >300°C Boiling point  614.1±55.0 °C(Predicted) density  2.4079 (estimate) storage temp.  Keep in dark place,Inert atmosphere,Room temperature solubility  Soluble in Methanol. form  neat pka 0.92±0.10(Predicted) color  White to Off-White Water Solubility  500g/L(25 ºC) Merck  14,2992 Stability: Light Sensitive EPA Substance Registry System Benzoic acid, 3,5-bis(acetylamino)-2,4,6-triiodo- (117-96-4)   Safety Information WGK Germany  3 RTECS  DG5950000 Hazardous Substances Data 117-96-4(Hazardous Substances Data) Toxicity LD50 intravenous in mouse: 8900mg/kg MSDS Information Provider Language SigmaAldrich English   DIATRIZOIC ACID Usage And Synthesis Chemical Properties White Solid Originator Hypaque Sodium,Winthrop,US,1955 Uses Diatrizoic acid is a gradient reagent used for blood cell separation and diagnostic aid (radiopaque medium). Diatrizoic acid may be used as an alternative to barium sulfate for medical imaging of the gastrointestinal tract, such as upper gastrointestinal series and small bowel series. Uses Density gradient reagent for blood cell seperation. Diagnostic aid (radiopaque medium) Uses radiopaque agent Definition ChEBI: A member of the class of benzoic acids that is benzoic acid having iodo substituents at the 2-, 4- and 6-positions and acetamido substituents at the 3- and 5-positions. It is used, mainly as its N-methylglucamine and sodium salts, as an -ray contrast medium in gastrointestinal studies, angiography, and urography. Manufacturing Process 3,5-Dinitrobenzoic acid (15.9 g) was dissolved in an equivalent amount of sodium hydroxide solution, and the solution was diluted to 310 ml with water. The solution was refluxed with Raney nickel for fifteen minutes, filtered, and the filtrate was hydrogenated at elevated pressure using platinum oxide catalyst. After the amount of hydrogen calculated to reduce both nitro groups had been absorbed, the mixture was filtered, and the filtrate was acidified with an equal volume of concentrated hydrochloric acid. Iodine monochloride (17 ml) in 100 ml of 6N HCl was then added with stirring. The reaction mixture was allowed to stand for two and one-half hours at room temperature, then diluted with an equal amount of water with vigorous stirring, and the solid material was collected by filtration and recrystallized from dilute methanol, giving 18.5 g of 3,5-diamino-2,4,6-triiodobenzoic acid, MP about 135°C with decomposition. The 18.5 g of 3,5-diamino-2,4,6- triiodobenzoic acid was suspended in 150 ml of acetic anhydride containing 5 drops of 70% perchloric acid, and the mixture was heated on a steam bath for three and one-half hours. The reaction mixture was poured into 300 ml of ice water, and then heated on a steam bath until crystallization took place. The solid material was collected by filtration, dissolvedin dilute sodium hydroxide solution, filtered, and hydrochloric acid was added to the filtrate to reprecipitate the acid product. The latter was again dissolved in sodium hydroxide and reprecipitated with acid, giving 9 g of 3,5-diacetamido-2,4,6- triiodobenzoic acid, MP above 250°C. The acid may be used as the sodium salt or as the meglumate. Brand name Md (Mallinckrodt); Urovist Sodium (Berlex). Therapeutic Function Diagnostic aid (radiopaque medium) General Description Diatrizoate is a water-soluble, ionicmonomer. It is commercially available as the megluminesalt, sodium salt, or as fixed combinations of the two saltforms. These triiodobenzoic acid salts contain 47% organicallybound iodine. Numerous products with various concentrations of one ortwo of the salt forms are available for various imaging procedures.Indicated uses include angiography, venography,excretory urography, retrograde cystourethrography, retrogradeor ascending pyelography, operative, T-tube, or percutaneoustranshepatic cholangiography, splenoportography,arthrography; discography, radiographic examinationof the GI tract when barium sulfate is contraindicated (i.e.,suspected perforation of the GI tract), adjunct contrast enhancementin CT of the torso (dual contrast study), and hysterosalpingography.   DIATRIZOIC ACID Preparation Products And Raw materials Raw materials ACETYL IODIDE-->3,5-Diaminobenzoic acid-->Sodium hydroxide-->Hydrogen-->2-Chloro-3,5-dinitrobenzoic acid-->Iodine monochloride Preparation Products Diatrizoate sodium

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Leader Biochemical Group is a large leader incorporated industry manufacturers and suppliers of advanced refined raw materials From the year of 1996 when our factory was put into production to year of 2020, our group has successively invested in more than 52 factories with shares and subordinates.We focus on manufacture Pharm & chemicals, functional active ingredients, nutritional Ingredients, health care products, cosmetics, pharmaceutical and refined feed, oil, natural plant ingredients industries to provide top quality of GMP standards products.All the invested factories' product lines cover API and intermediates, vitamins, amino acids, plant extracts, daily chemical products, cosmetics raw materials, nutrition and health care products, food additives, feed additives, essential oil products, fine chemical products and agricultural chemical raw materials And flavors and fragrances. Especially in the field of vitamins, amino acids, pharmaceutical raw materials and cosmetic raw materials, we have more than 20 years of production and sales experience. All products meet the requirements of high international export standards and have been recognized by customers all over the world. Our manufacture basement & R&D center located in National Aerospace Economic & Technical Development Zone Xi`an Shaanxi China. Now not only relying on self-cultivation and development as well as maintains good cooperative relations with many famous research institutes and universities in China. Now, we have closely cooperation with Shanghai Institute of Organic Chemistry of Chinese Academy of Science, Beijing Institute of Material Medical of Chinese Academy of Medical Science, China Pharmaceutical University, Zhejiang University. Closely cooperation with them not only integrating Science and technology resources, but also increasing the R&D speed and improving our R&D power. Offering Powerful Tech supporting Platform for group development. Keep serve the manufacture and the market as the R&D central task, focus on the technical research.  Now there are 3 technology R & D platforms including biological extract, microorganism fermentation and chemical synthesis, and can independently research and develop kinds of difficult APIs and pharmaceutical intermediates. With the strong support of China State Institute of Pharmaceutical Industry (hereinafter short for CSIPI), earlier known as Shanghai Institute of Pharmaceutical Industry (SIPI), we have unique advantages in the R & D and industrialization of high-grade, precision and advanced products.  Now our Group technical force is abundant, existing staff more that 1000 people, senior professional and technical staff accounted for more than 50% of the total number of employees, including 15 PhD research and development personnel, 5 master′ S degree in technical and management personnel 9 people. We have advanced equipment like fermentation equipment and technology also extraction, isolation, purification, synthesis with rich production experience and strict quality control system, According to the GMP required, quickly transforming the R&D results to industrial production in time, it is our advantages and our products are exported to North and South America, Europe, Middle East, Africa, and other five continents and scale the forefront in the nation, won good international reputation.  We believe only good quality can bring good cooperation, quality is our key spirit during our production, we are warmly welcome clients and partner from all over the world contact us for everlasting cooperation, Leader will be your strong, sincere and reliable partner in China.

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DIATRIZOIC ACID Basic information Product Name: DIATRIZOIC ACID CAS: 117-96-4 MF: C11H9I3N2O4 MW: 613.91 EINECS: 204-223-6 Product Categories: UROVIST;Intermediates & Fine Chemicals;Organics;Pharmaceuticals Mol File: 117-96-4.mol   DIATRIZOIC ACID Chemical Properties Melting point  >300°C Boiling point  614.1±55.0 °C(Predicted) density  2.4079 (estimate) storage temp.  Keep in dark place,Inert atmosphere,Room temperature solubility  Soluble in Methanol. form  neat pka 0.92±0.10(Predicted) color  White to Off-White Water Solubility  500g/L(25 ºC) Merck  14,2992 Stability: Light Sensitive EPA Substance Registry System Benzoic acid, 3,5-bis(acetylamino)-2,4,6-triiodo- (117-96-4)   Safety Information WGK Germany  3 RTECS  DG5950000 Hazardous Substances Data 117-96-4(Hazardous Substances Data) Toxicity LD50 intravenous in mouse: 8900mg/kg MSDS Information Provider Language SigmaAldrich English   DIATRIZOIC ACID Usage And Synthesis Chemical Properties White Solid Originator Hypaque Sodium,Winthrop,US,1955 Uses Diatrizoic acid is a gradient reagent used for blood cell separation and diagnostic aid (radiopaque medium). Diatrizoic acid may be used as an alternative to barium sulfate for medical imaging of the gastrointestinal tract, such as upper gastrointestinal series and small bowel series. Uses Density gradient reagent for blood cell seperation. Diagnostic aid (radiopaque medium) Uses radiopaque agent Definition ChEBI: A member of the class of benzoic acids that is benzoic acid having iodo substituents at the 2-, 4- and 6-positions and acetamido substituents at the 3- and 5-positions. It is used, mainly as its N-methylglucamine and sodium salts, as an -ray contrast medium in gastrointestinal studies, angiography, and urography. Manufacturing Process 3,5-Dinitrobenzoic acid (15.9 g) was dissolved in an equivalent amount of sodium hydroxide solution, and the solution was diluted to 310 ml with water. The solution was refluxed with Raney nickel for fifteen minutes, filtered, and the filtrate was hydrogenated at elevated pressure using platinum oxide catalyst. After the amount of hydrogen calculated to reduce both nitro groups had been absorbed, the mixture was filtered, and the filtrate was acidified with an equal volume of concentrated hydrochloric acid. Iodine monochloride (17 ml) in 100 ml of 6N HCl was then added with stirring. The reaction mixture was allowed to stand for two and one-half hours at room temperature, then diluted with an equal amount of water with vigorous stirring, and the solid material was collected by filtration and recrystallized from dilute methanol, giving 18.5 g of 3,5-diamino-2,4,6-triiodobenzoic acid, MP about 135°C with decomposition. The 18.5 g of 3,5-diamino-2,4,6- triiodobenzoic acid was suspended in 150 ml of acetic anhydride containing 5 drops of 70% perchloric acid, and the mixture was heated on a steam bath for three and one-half hours. The reaction mixture was poured into 300 ml of ice water, and then heated on a steam bath until crystallization took place. The solid material was collected by filtration, dissolvedin dilute sodium hydroxide solution, filtered, and hydrochloric acid was added to the filtrate to reprecipitate the acid product. The latter was again dissolved in sodium hydroxide and reprecipitated with acid, giving 9 g of 3,5-diacetamido-2,4,6- triiodobenzoic acid, MP above 250°C. The acid may be used as the sodium salt or as the meglumate. Brand name Md (Mallinckrodt); Urovist Sodium (Berlex). Therapeutic Function Diagnostic aid (radiopaque medium) General Description Diatrizoate is a water-soluble, ionicmonomer. It is commercially available as the megluminesalt, sodium salt, or as fixed combinations of the two saltforms. These triiodobenzoic acid salts contain 47% organicallybound iodine. Numerous products with various concentrations of one ortwo of the salt forms are available for various imaging procedures.Indicated uses include angiography, venography,excretory urography, retrograde cystourethrography, retrogradeor ascending pyelography, operative, T-tube, or percutaneoustranshepatic cholangiography, splenoportography,arthrography; discography, radiographic examinationof the GI tract when barium sulfate is contraindicated (i.e.,suspected perforation of the GI tract), adjunct contrast enhancementin CT of the torso (dual contrast study), and hysterosalpingography.   DIATRIZOIC ACID Preparation Products And Raw materials Raw materials ACETYL IODIDE-->3,5-Diaminobenzoic acid-->Sodium hydroxide-->Hydrogen-->2-Chloro-3,5-dinitrobenzoic acid-->Iodine monochloride Preparation Products Diatrizoate sodium