China Largest Manufacturer factory sales DCDMH CAS 118-52-5 CAS NO.118-52-5

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1,3-Dichloro-5,5-dimethylhydantoin Basic information Product Name: 1,3-Dichloro-5,5-dimethylhydantoin Synonyms: DCDMH;DANTOIN;DACTIN;DICHLORO-DIMETHYL-HYDANTOINE;1,3-DICHLORO-5,5-DIMETHYL-2,4-IMIDAZOLIDINEDIONE;1,3-DICHLORO-5,5-DIMETHYLHYDANTOIN;1,3-DICHLORO-5,5-DIMETHYLHYDANTOINE;1,3-dichloro-5,5’-methylhydantoin CAS: 118-52-5 MF: C5H6Cl2N2O2 MW: 197.02 EINECS: 204-258-7 Product Categories: Water Ttreatment Chemicals;Imidazolines/ImidazolidinesBuilding Blocks;Water treatment chemicals;Halogenated Heterocycles;Heterocyclic Building Blocks;Imidazolines/Imidazolidines;Miscellaneous;water treatment;Pyridines Mol File: 118-52-5.mol   1,3-Dichloro-5,5-dimethylhydantoin Chemical Properties Melting point  132-134 °C (lit.) Boiling point  214.7±23.0 °C(Predicted) density  1,5 g/cm3 refractive index  1.5720 (estimate) Fp  171 °C storage temp.  Keep in dark place,Sealed in dry,Room Temperature solubility  water: soluble0.21% at 25°C(lit.) form  Crystalline Powder pka -3.44±0.40(Predicted) color  White PH 4.4 (H2O)(HSDB) Water Solubility  0.21 g/100 mL (25 ºC) Sensitive  Moisture Sensitive Sublimation  100 ºC Merck  14,3065 BRN  146013 Exposure limits NIOSH REL: TWA 0.2, STEL 0.4, IDLH 5; OSHA PEL: TWA 0.2, STEL/C 0.4 (adopted). Stability: Stable, but a strong oxidizer - contact with combustible material may lead to fire. Incompatible with reducing agents, acids, strong bases. Moisture sensitive. InChIKey KEQGZUUPPQEDPF-UHFFFAOYSA-N CAS DataBase Reference 118-52-5(CAS DataBase Reference) EPA Substance Registry System 1,3-Dichloro-5,5-dimethylhydantoin (118-52-5)   Safety Information Hazard Codes  Xn,C,O,N Risk Statements  22-36/37/38-34-8-50-43-31-20/21/22 Safety Statements  26-36-45-36/37/39-17-61 RIDADR  UN 1479 5.1/PG 2 WGK Germany  3 RTECS  MU0700000 TSCA  Yes HazardClass  5.1 PackingGroup  II HS Code  29332100 Hazardous Substances Data 118-52-5(Hazardous Substances Data) Toxicity LD50 oral in rabbit: 1520mg/kg IDLA 5 mg/m3 MSDS Information Provider Language 1,3-Dichloro-5,5-dimethylhydantoin English ACROS English SigmaAldrich English ALFA English   1,3-Dichloro-5,5-dimethylhydantoin Usage And Synthesis Chemical Properties DCDMH is a combustible, white powder. Chlorine-like odor. Physical properties White powder or four-sided crystals from chloroform with a chlorine-like odor. Aqueous solutions are acidic. Uses Chlorinating agent; disinfectant; laundry bleach; in water treatment; intermediate for drugs; insecticides; polymerization catalyst Uses Dantoin(R) DCDMH is an industrial bleaching agent based on dimethyl hydantoin. This product finds application wherever solid bleach is desired. Uses Dantoin(R) DCDMH LD (low dust) is an industrial bleaching agent based on dimethyl hydantoin. This product finds application wherever solid bleach is desired. Definition Methionine hydroxy analog c. 90%. General Description White powder with a weak chlorine odor. Conflagrates at 414°F (turns brown). Chlorine gas evolves > 410°F. Air & Water Reactions Sensitive to exposure to light, air, and moisture. Reacts with water or steam to produce toxic and corrosive fumes. Reactivity Profile 1,3-Dichloro-5,5-dimethylhydantoin reacts violently with xylene. 1,3-Dichloro-5,5-dimethylhydantoin is incompatible with strong acids, easily oxidized materials, ammonia salts and sulfides. 1,3-Dichloro-5,5-dimethylhydantoin will react with water or steam to produce toxic and corrosive fumes. At a pH of 9, 1,3-Dichloro-5,5-dimethylhydantoin decomposes completely. Health Hazard 1,3-Dichloro-5,5-dimethylhydantoin powder in contact with water yields hypochlorous acid, which is an irritant of the eyes and mucous membranes. Fire Hazard Flash point data for 1,3-Dichloro-5,5-dimethylhydantoin are not available. 1,3-Dichloro-5,5-dimethylhydantoin is probably combustible. Safety Profile Moderately toxic by ingestion. Mildly toxic by inhalation. A severe slun irritant. Mutation data reported. Avoid excessive contact because of effects of active chlorine on skin. Some of the hydantoins are central nervous system depressants. Mixtures with xylene may explode. Wdl react with water or steam to produce toxic and corrosive fumes. When heated to decomposition it emits toxic fumes of Cl and NOx. See also CHLORIDES. Potential Exposure It is used as a chlorinating agent, disinfectant, biocide, and laundry bleach. It is also used as a polymerization catalyst in making vinyl chloride; and in drug and pesticide synthesis. Environmental fate Chemical/Physical. Reacts with water (pH 7.0) releasing hypochlorous acid. At pH 9, nitrogen chloride is formed (Windholz et al., 1983). Shipping UN1479 Oxidizing solid, n.o.s., Hazard Class: 5.1; Labels: 5.1-Oxidizer, Technical Name Required Purification Methods Purify it by dissolving in conc H2SO4 and diluting with ice H2O, collect the solid, dry it in a vacuum and recrystallise it from CHCl3. It sublimes at 100o in a vacuum. It exhibits time-dependent hydrolysis at pH 9. [Petterson & Grzeskowiak J Org Chem 24 1414 1959, Beilstein 24 III/IV 1100.] Incompatibilities A strong oxidizer. Contact with water forms poisonous and corrosive gases. Mixtures with xylene may explode. Not compatible with moisture (especially hot water, steam), strong acids; easily oxidized materials (such as ammonia salts; sulfides, etc.); reducing agents; strong bases; ammonium salts; sulfides. Compounds of the carboxyl group react with all bases, both inorganic and organic (i.e., amines) releasing substantial heat, water and a salt that may be harmful. Incompatible with arsenic compounds (releases hydrogen cyanide gas), diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides (releasing heat, toxic and possibly flammable gases), thiosulfates and dithionites (releasing hydrogen sulfate and oxides of sulfur) Waste Disposal Incineration (815.5C/816C, 0.5 second for primary combustion; 104.4C/220F, 1.0 second for secondary combustion). The formation of elemental chlorine can be prevented by injection of steam or methane into the combustion process. Any nitrogen oxides may be abated by the use of thermal or catalytic devices   1,3-Dichloro-5,5-dimethylhydantoin Preparation Products And Raw materials Raw materials Hydrochloric acid-->Sodium hypochlorite Preparation Products florpyrauxifen-benzyl

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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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1,3-Dichloro-5,5-dimethylhydantoin Basic information Product Name: 1,3-Dichloro-5,5-dimethylhydantoin Synonyms: DCDMH;DANTOIN;DACTIN;DICHLORO-DIMETHYL-HYDANTOINE;1,3-DICHLORO-5,5-DIMETHYL-2,4-IMIDAZOLIDINEDIONE;1,3-DICHLORO-5,5-DIMETHYLHYDANTOIN;1,3-DICHLORO-5,5-DIMETHYLHYDANTOINE;1,3-dichloro-5,5’-methylhydantoin CAS: 118-52-5 MF: C5H6Cl2N2O2 MW: 197.02 EINECS: 204-258-7 Product Categories: Water Ttreatment Chemicals;Imidazolines/ImidazolidinesBuilding Blocks;Water treatment chemicals;Halogenated Heterocycles;Heterocyclic Building Blocks;Imidazolines/Imidazolidines;Miscellaneous;water treatment;Pyridines Mol File: 118-52-5.mol   1,3-Dichloro-5,5-dimethylhydantoin Chemical Properties Melting point  132-134 °C (lit.) Boiling point  214.7±23.0 °C(Predicted) density  1,5 g/cm3 refractive index  1.5720 (estimate) Fp  171 °C storage temp.  Keep in dark place,Sealed in dry,Room Temperature solubility  water: soluble0.21% at 25°C(lit.) form  Crystalline Powder pka -3.44±0.40(Predicted) color  White PH 4.4 (H2O)(HSDB) Water Solubility  0.21 g/100 mL (25 ºC) Sensitive  Moisture Sensitive Sublimation  100 ºC Merck  14,3065 BRN  146013 Exposure limits NIOSH REL: TWA 0.2, STEL 0.4, IDLH 5; OSHA PEL: TWA 0.2, STEL/C 0.4 (adopted). Stability: Stable, but a strong oxidizer - contact with combustible material may lead to fire. Incompatible with reducing agents, acids, strong bases. Moisture sensitive. InChIKey KEQGZUUPPQEDPF-UHFFFAOYSA-N CAS DataBase Reference 118-52-5(CAS DataBase Reference) EPA Substance Registry System 1,3-Dichloro-5,5-dimethylhydantoin (118-52-5)   Safety Information Hazard Codes  Xn,C,O,N Risk Statements  22-36/37/38-34-8-50-43-31-20/21/22 Safety Statements  26-36-45-36/37/39-17-61 RIDADR  UN 1479 5.1/PG 2 WGK Germany  3 RTECS  MU0700000 TSCA  Yes HazardClass  5.1 PackingGroup  II HS Code  29332100 Hazardous Substances Data 118-52-5(Hazardous Substances Data) Toxicity LD50 oral in rabbit: 1520mg/kg IDLA 5 mg/m3 MSDS Information Provider Language 1,3-Dichloro-5,5-dimethylhydantoin English ACROS English SigmaAldrich English ALFA English   1,3-Dichloro-5,5-dimethylhydantoin Usage And Synthesis Chemical Properties DCDMH is a combustible, white powder. Chlorine-like odor. Physical properties White powder or four-sided crystals from chloroform with a chlorine-like odor. Aqueous solutions are acidic. Uses Chlorinating agent; disinfectant; laundry bleach; in water treatment; intermediate for drugs; insecticides; polymerization catalyst Uses Dantoin(R) DCDMH is an industrial bleaching agent based on dimethyl hydantoin. This product finds application wherever solid bleach is desired. Uses Dantoin(R) DCDMH LD (low dust) is an industrial bleaching agent based on dimethyl hydantoin. This product finds application wherever solid bleach is desired. Definition Methionine hydroxy analog c. 90%. General Description White powder with a weak chlorine odor. Conflagrates at 414°F (turns brown). Chlorine gas evolves > 410°F. Air & Water Reactions Sensitive to exposure to light, air, and moisture. Reacts with water or steam to produce toxic and corrosive fumes. Reactivity Profile 1,3-Dichloro-5,5-dimethylhydantoin reacts violently with xylene. 1,3-Dichloro-5,5-dimethylhydantoin is incompatible with strong acids, easily oxidized materials, ammonia salts and sulfides. 1,3-Dichloro-5,5-dimethylhydantoin will react with water or steam to produce toxic and corrosive fumes. At a pH of 9, 1,3-Dichloro-5,5-dimethylhydantoin decomposes completely. Health Hazard 1,3-Dichloro-5,5-dimethylhydantoin powder in contact with water yields hypochlorous acid, which is an irritant of the eyes and mucous membranes. Fire Hazard Flash point data for 1,3-Dichloro-5,5-dimethylhydantoin are not available. 1,3-Dichloro-5,5-dimethylhydantoin is probably combustible. Safety Profile Moderately toxic by ingestion. Mildly toxic by inhalation. A severe slun irritant. Mutation data reported. Avoid excessive contact because of effects of active chlorine on skin. Some of the hydantoins are central nervous system depressants. Mixtures with xylene may explode. Wdl react with water or steam to produce toxic and corrosive fumes. When heated to decomposition it emits toxic fumes of Cl and NOx. See also CHLORIDES. Potential Exposure It is used as a chlorinating agent, disinfectant, biocide, and laundry bleach. It is also used as a polymerization catalyst in making vinyl chloride; and in drug and pesticide synthesis. Environmental fate Chemical/Physical. Reacts with water (pH 7.0) releasing hypochlorous acid. At pH 9, nitrogen chloride is formed (Windholz et al., 1983). Shipping UN1479 Oxidizing solid, n.o.s., Hazard Class: 5.1; Labels: 5.1-Oxidizer, Technical Name Required Purification Methods Purify it by dissolving in conc H2SO4 and diluting with ice H2O, collect the solid, dry it in a vacuum and recrystallise it from CHCl3. It sublimes at 100o in a vacuum. It exhibits time-dependent hydrolysis at pH 9. [Petterson & Grzeskowiak J Org Chem 24 1414 1959, Beilstein 24 III/IV 1100.] Incompatibilities A strong oxidizer. Contact with water forms poisonous and corrosive gases. Mixtures with xylene may explode. Not compatible with moisture (especially hot water, steam), strong acids; easily oxidized materials (such as ammonia salts; sulfides, etc.); reducing agents; strong bases; ammonium salts; sulfides. Compounds of the carboxyl group react with all bases, both inorganic and organic (i.e., amines) releasing substantial heat, water and a salt that may be harmful. Incompatible with arsenic compounds (releases hydrogen cyanide gas), diazo compounds, dithiocarbamates, isocyanates, mercaptans, nitrides, and sulfides (releasing heat, toxic and possibly flammable gases), thiosulfates and dithionites (releasing hydrogen sulfate and oxides of sulfur) Waste Disposal Incineration (815.5C/816C, 0.5 second for primary combustion; 104.4C/220F, 1.0 second for secondary combustion). The formation of elemental chlorine can be prevented by injection of steam or methane into the combustion process. Any nitrogen oxides may be abated by the use of thermal or catalytic devices   1,3-Dichloro-5,5-dimethylhydantoin Preparation Products And Raw materials Raw materials Hydrochloric acid-->Sodium hypochlorite Preparation Products florpyrauxifen-benzyl