ISO.HACCP.GMP.FDA.SGS.BV-China Largest Manufacturer factory Supply DL-1,2-Hexanediol CAS 6920-22-5 CAS NO.6920-22-5

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DL-1,2-Hexanediol Basic information Product Name: DL-1,2-Hexanediol Synonyms: dl-hexane-1,2-diol;DL-1,2-Hexanediol, 98+%;1,2-HEXANEDIOL, 98.5%;DL-Hexan-1,2-diol;hexane-1,2-diol;DL-1,2-Hexanediol, GC 98%;DL-1,2-HEXANEDIOL;1,2-HEXANEDIOL CAS: 6920-22-5 MF: C6H14O2 MW: 118.17 EINECS: 230-029-6 Product Categories: Organic Building Blocks;Oxygen Compounds;Polyols;Organic solvents Mol File: 6920-22-5.mol   DL-1,2-Hexanediol Chemical Properties Melting point  45°C alpha  [α]D20 -0.3～+0.3゜ (neat) Boiling point  223-224 °C (lit.) density  0.951 g/mL at 25 °C (lit.) refractive index  n20/D 1.442(lit.) Fp  >230 °F storage temp.  Inert atmosphere,Room Temperature solubility  Chloroform (Slightly), Methanol (Slightly) pka 14.49±0.20(Predicted) form  Liquid color  Clear colorless to light yellow Specific Gravity 0.951 Water Solubility  Miscible with water, lower aliphatic hydrocarbons and fatty acids. Sensitive  Hygroscopic BRN  1719244 InChIKey FHKSXSQHXQEMOK-UHFFFAOYSA-N CAS DataBase Reference 6920-22-5(CAS DataBase Reference) EPA Substance Registry System 1,2-Hexanediol (6920-22-5)   Safety Information Hazard Codes  Xi Risk Statements  36/37/38 Safety Statements  26-36-37/39 WGK Germany  2 F  3 TSCA  Yes HS Code  29053990 MSDS Information Provider Language DL-1,2-Hexanediol English ACROS English SigmaAldrich English ALFA English   DL-1,2-Hexanediol Usage And Synthesis Chemical Properties CLEAR COLORLESS TO LIGHT YELLOW LIQUID Uses DL-1,2-Hexanediol is a solvent used to dissolve other compounds in a formulation. Uses 1,2-Hexanediol can be used in the ruthenium-catalyzed synthesis of oxazolidin-2-ones from urea. It can undergo ruthenium-hydride catalyzed dehydrative coupling with anilines to form substituted indole and quinoline products. General Description 1,2-Hexanediol acts as cosurfactant, used for modifying the sodium dodecyl sulfate micelles. Solubility of 1,2-hexanediol in supercritical CO2 has been reported. It has a tendency of self-association to form micelle-like aggregates. Purification Methods Fractionally distil it, preferably in a vacuum. Alternatively, dissolve it in Et2O, dry with K2CO3 then Na2SO4, filter, evaporate and distil it in a vacuum. The bis-4-nitrobenzoyl derivative has m 101.5-102.5o. [Rudloff Can J Chem 36 486 1958, Beilstein 1 I 251, 1 III 2200, 1 IV 2554.]   DL-1,2-Hexanediol Preparation Products And Raw materials

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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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DL-1,2-Hexanediol Basic information Product Name: DL-1,2-Hexanediol Synonyms: dl-hexane-1,2-diol;DL-1,2-Hexanediol, 98+%;1,2-HEXANEDIOL, 98.5%;DL-Hexan-1,2-diol;hexane-1,2-diol;DL-1,2-Hexanediol, GC 98%;DL-1,2-HEXANEDIOL;1,2-HEXANEDIOL CAS: 6920-22-5 MF: C6H14O2 MW: 118.17 EINECS: 230-029-6 Product Categories: Organic Building Blocks;Oxygen Compounds;Polyols;Organic solvents Mol File: 6920-22-5.mol   DL-1,2-Hexanediol Chemical Properties Melting point  45°C alpha  [α]D20 -0.3～+0.3゜ (neat) Boiling point  223-224 °C (lit.) density  0.951 g/mL at 25 °C (lit.) refractive index  n20/D 1.442(lit.) Fp  >230 °F storage temp.  Inert atmosphere,Room Temperature solubility  Chloroform (Slightly), Methanol (Slightly) pka 14.49±0.20(Predicted) form  Liquid color  Clear colorless to light yellow Specific Gravity 0.951 Water Solubility  Miscible with water, lower aliphatic hydrocarbons and fatty acids. Sensitive  Hygroscopic BRN  1719244 InChIKey FHKSXSQHXQEMOK-UHFFFAOYSA-N CAS DataBase Reference 6920-22-5(CAS DataBase Reference) EPA Substance Registry System 1,2-Hexanediol (6920-22-5)   Safety Information Hazard Codes  Xi Risk Statements  36/37/38 Safety Statements  26-36-37/39 WGK Germany  2 F  3 TSCA  Yes HS Code  29053990 MSDS Information Provider Language DL-1,2-Hexanediol English ACROS English SigmaAldrich English ALFA English   DL-1,2-Hexanediol Usage And Synthesis Chemical Properties CLEAR COLORLESS TO LIGHT YELLOW LIQUID Uses DL-1,2-Hexanediol is a solvent used to dissolve other compounds in a formulation. Uses 1,2-Hexanediol can be used in the ruthenium-catalyzed synthesis of oxazolidin-2-ones from urea. It can undergo ruthenium-hydride catalyzed dehydrative coupling with anilines to form substituted indole and quinoline products. General Description 1,2-Hexanediol acts as cosurfactant, used for modifying the sodium dodecyl sulfate micelles. Solubility of 1,2-hexanediol in supercritical CO2 has been reported. It has a tendency of self-association to form micelle-like aggregates. Purification Methods Fractionally distil it, preferably in a vacuum. Alternatively, dissolve it in Et2O, dry with K2CO3 then Na2SO4, filter, evaporate and distil it in a vacuum. The bis-4-nitrobenzoyl derivative has m 101.5-102.5o. [Rudloff Can J Chem 36 486 1958, Beilstein 1 I 251, 1 III 2200, 1 IV 2554.]   DL-1,2-Hexanediol Preparation Products And Raw materials