China Biggest Manufacturer factory sales Sulfamethazine CAS 57-68-1

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Sulfamethazine Basic information Brand Name(s) in US Product Name: Sulfamethazine Synonyms: (p-Aminobenzolsulfonyl)-2-amino-4,6-dimethylpyrimidin;2-(4-Aminobenzenesulfonamido)-4,6-dimethylpyrimidine;6-(4’-aminobenzol-sulfonamido)-2,4-dimethylpyrimidin;6-(4'-Aminobenzol-sulfonamido)-2,4-dimethylpyrimidin;A-502;Azolmetazin;Benzenesulfonamide, 4-amino-N-(4,6-dimethyl-2-pyrimidinyl)-;benzenesulfonamide,4-amino-N-(4,6-dimethyl-2-pyrimiidinyl)- CAS: 57-68-1 MF: C12H14N4O2S MW: 278.33 EINECS: 200-346-4 Product Categories: Active Pharmaceutical Ingredients;Intermediates & Fine Chemicals;Antibiotics for Research and Experimental Use;Biochemistry;Pharmaceuticals;Sulfur & Selenium Compounds;Sulfonamides (Antibiotics for Research and Experimental Use);Pharmaceutical intermediate;SULFASURE;Animal medication Mol File: 57-68-1.mol   Sulfamethazine Chemical Properties Melting point  197 °C Boiling point  294°C (rough estimate) density  1.2997 (rough estimate) refractive index  1.6440 (estimate) storage temp.  2-8°C solubility  acetone: soluble50mg/mL pka 7.4, 2.65(at 25℃) form  Crystalline Powder color  white to off-white Water Solubility  150mg/100mL (29 ºC) Merck  14,8905 BRN  261304 Stability: Stable, but light sensitive. Incompatible with strong oxidizing agents. CAS DataBase Reference 57-68-1(CAS DataBase Reference) NIST Chemistry Reference Sulfamethazine(57-68-1) IARC 3 (Vol. 79) 2001 EPA Substance Registry System Sulfamethazine (57-68-1)   Safety Information Hazard Codes  Xi Risk Statements  36/37/38 Safety Statements  23-24/25-36-26 WGK Germany  2 RTECS  WO9275000 F  10 TSCA  Yes HS Code  29350090 Hazardous Substances Data 57-68-1(Hazardous Substances Data) Toxicity LD50 i.p. in mice: 1.06 g/kg (Bobranski) MSDS Information Provider Language 2-(p-Aminobenzenesulfonamido)-4,6-dimethylpyrimidine English SigmaAldrich English ACROS English ALFA English   Sulfamethazine Usage And Synthesis Brand Name(s) in US Brand Name(s) in US Description Sulfamethazine is an antibacterial sulfonamide. Like other sulfonamides, sulfamethazine is bacteriostatic, competitively inhibiting dihydropteroate synthase to block folate synthesis and inhibit growth and multiplication. Sulfamethazine is metabolized by cytochrome P450 isoforms and arylamine N-acetyltransferase 2 in a sex-dependent manner. Chemical Properties White to Off-Solid Originator Cremomethazine,MSD,US,1947 Uses Antibacterial Uses Sulfamethazine is an antibacterial.This compound is a contaminant of emerging concern (CECs). Definition ChEBI: A sulfonamide consisting of pyrimidine with methyl substituents at the 4- and 6-positions and a 4-aminobenzenesulfonamido group at the 2-position. Manufacturing Process A flask heated in an oil bath is filled with 600 ml water and 60 g (1 mol) glacial acetic acid (or an equivalent quantity of diluted acetic acid). While stirring 235 g (1.1 mols) anhydrous p-aminobenzenesulfonamidoguanidine (or an equivalent quantity of a nonanhydrous product) and 122 g (1 mol) sodium acetylacetonate 100% purity (or an equivalent quantity of product of a lower purity) are introduced into the flask while stirring. The temperature of the reaction mixture is brought to 102°C to 103°C, the mixture is further stirred at this temperature during 24 hours. The pH value of the mixture, which should range between 5 and 6 is checked during the reaction. On expiry of the reaction period heating is cut off, the mass being cooled or allowed to cool down to 60°C. Filtering under suction is effected, the solids on the filter being washed with 100 ml water at 80°C. After drying of the product on the filter 256 g of 2-paminobenzenesulfonamido- 4,6-dimethylpyrimidine, melting point 196°C to 197°C, purity 99.5% are obtained. The output is 92% of the theory calculated with respect to the sodium acetylacetonate employed. Brand name Calfspan Tablets [Veterinary] (Fort Dodge Animal Health); Sulka S Boluses [Veterinary] (Fort Dodge Animal Health); SulfaSURE SR Bolus [Veterinary] (Boehringer Ingelheim Animal Health);Crermomethazine;Deladine;Dimezathine;Hava-span;Intradin;Neotrizine;Rigesol;Rivodin;S-dimidine;Spanbolet;Sulka-s;Sulphamezathine;Sulphfmezatine;Superseptyl;Sustain iii;Tersulpha;Trisulfaminic;Trisulfaminie. Therapeutic Function Antimicrobial World Health Organization (WHO) Sulfadimidine, a sulfonamide anti-infective agent, was introduced in 1942 for the treatment of bacterial infections. The importance of sulfonamides has subsequently decreased as a result of increasing resistance and their replacement by antibiotics which are generally more active and less toxic. The sulfonamides are known to cause serious adverse effects such as renal toxicity, sometimes fatal exfoliative dermatitis and erythema multiforma and dangerous adverse reactions affecting blood formation such as agranulocytosis and haemolytic or aplastic anaemia. Sulfadimidine is still used in some countries as a injectable or oral antimicrobial for susceptible infections. Antimicrobial activity This drug is used for pneumococcal, staphylococcal, and streptococcal infections as well as for sepsis, gonorrhea, and other infectious diseases. Synonyms of this drug are sulfadiamezin and sulfadimidin. General Description Sulfamethazine’splasma half-life is 7 hours. This compound is similar inchemical properties to sulfamerazine and sulfadiazine butdoes have greater water solubility than either. Its pKa is 7.2.Because it is more soluble in acid urine than sulfamerazineis, the possibility of kidney damage from use of the drug isdecreased. The human body appears to handle the drugunpredictably; hence, there is some disfavor to its use in thiscountry except in combination sulfa therapy (in trisulfapyrimidines,USP) and in veterinary medicine. General Description Odorless sticky, white or creamy-white crystalline powder. Slightly bitter taste. An antibacterial. Air & Water Reactions Water solubility increases rapidly with increasing pH [Merck]. Insoluble in water. Reactivity Profile Sulfamethazine is sensitive to light and may also be sensitive to heat. The presence of oxygen and moisture may accelerate the effects of heat and light . Fire Hazard Flash point data for Sulfamethazine are not available; however, Sulfamethazine is probably combustible. Pharmaceutical Applications 2-Sulfanilamido-4,6-methylpyrimidine (syn: sulphamethazine, sulfamezathine). A water-soluble compound, unstable on exposure to light. It is usually administered by mouth and is a component of some triple sulfonamide combinations. The spectrum is typical of the group, but sulfadimidine exhibits relatively low potency. It is well absorbed after oral administration. It is extensively metabolized, predominantly by acetylation. The mean plasma half-life (1.5–5 h) varies with acetylator status. In addition to side effects common to the group, a serious interaction between ciclosporin (cyclosporin A) and sulfadimidine, leading to reduced ciclosporin levels, has been reported. Biochem/physiol Actions Sulfamethazine is an antimicrobial sulfur drug that blocks the synthesis of dihydrofolic acid by inhibiting the enzyme dihydropteroate synthase. Sulfamethazine is a competitive inhibitor of bacterial para-aminobenzoic acid (PABA), which is required for bacterial synthesis of folic acid. It induces CYP3A4 expression and is acetylated by N-acetyltransferase. It exhibits sex dependent pharmacokinetics, metabolized by the male specific isoform CYP2C11. Sulfamethazine is bacteriostatic. Safety Profile Moderately toxic by intravenous and intraperitoneal routes. Experimental teratogenic and reproductive effects. Questionable carcinogen with experimental tumorigenic data. When heated to decomposition it emits very toxic fumes of SOx and NOx. Chemical Synthesis Sulfamethazine, N1 -(4,6-dimethyl-2-pyrimidinyl)sulfanilamide (33.1.13), is also synthesized in the aforementioned manner by reacting 4-acetylaminobenzenesulfonyl chloride with 2-amino-4,6-dimethylpyrimidine, which is in turn synthesized by condensing acetylacetone with guanidine followed by hydrolysis of the acetylamino group using a base. Purification Methods Crystallise it from dioxane or aqueous dioxane. [Caldwell et al. J Am Chem Soc 63 2188 1941, Roblin et al. J Am Chem Soc 64 567 1942, Beilstein 25 III/IV 2215.]   Sulfamethazine Preparation Products And Raw materials Raw materials Sodium carbonate-->Acetylacetone-->Cyclohexanone-->Sulfaguanidine-->SODIUM 2,4-PENTANEDIONATE Preparation Products 2-Amino-4,6-dimethylpyrimidine Tag:Sulfamethazine(57-68-1) Related Product Information

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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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