China Largest Manufacturer factory sales 2-Deoxy-D-Galactose CAS 1949-89-9 for 500MT/Year CAS NO.1949-89-9

                                PRODUCT DETAILS                           

2-Deoxy-D-galactose Basic information Product Name: 2-Deoxy-D-galactose Synonyms: 2-DEOXY-D-LYXOHEXOSE;2-DEOXY-D-GALACTOPYRANOSE;2-DEOXY-D-GALACTOSE;2-DEOXYGALACTOSE;2-DEOXY-BETA-D-GALACTOSE;2-DEOXY-BETA-D-LYXO-HEXOSE;2-Deoxy-D-galactose (1.24798);Deoxygalactose CAS: 1949-89-9 MF: C6H12O5 MW: 164.16 EINECS: 217-765-3 Product Categories: carbohydrate;Sugars, Carbohydrates & Glucosides;13C & 2H Sugars;Biochemistry;Deoxysugars;Galactose;Sugars;aldehydes;Carbohydrates & Derivatives Mol File: 1949-89-9.mol   2-Deoxy-D-galactose Chemical Properties Melting point  107-110 °C(lit.) alpha  57 º (c=3.7, H20 NH3) Boiling point  211.61°C (rough estimate) density  1.1738 (rough estimate) refractive index  1.4230 (estimate) storage temp.  Sealed in dry,2-8°C solubility  Methanol, Water pka 13.47±0.20(Predicted) form  Powder color  White to Off-white optical activity [α]20/D +59.7°, c = 2 in H2O Water Solubility  Soluble in water. BRN  1723333 CAS DataBase Reference 1949-89-9(CAS DataBase Reference) EPA Substance Registry System D-lyxo-Hexose, 2-deoxy- (1949-89-9)   Safety Information Hazard Codes  Xi,Xn Risk Statements  20/21/22-36/37/38 Safety Statements  24/25-37/39-36-26 WGK Germany  3 F  3-10 HS Code  29400090 MSDS Information Provider Language 2-Deoxy-D-galactose English ACROS English SigmaAldrich English   2-Deoxy-D-galactose Usage And Synthesis Chemical Properties White Crystalline Solid Uses 2-Deoxy-D-galactose is used as an inhibitor of fucosylation, which is a process of adding hexose deoxy sugar units to a molecule. It is used for studying galactose uptake into Escherichia coli and also for competitive elution of Anadarin P lectin (a galactosyl-binding lectin from blood clam). General Description 2-Deoxy-D-galactose is a glucose analog that shows a wide range of biological activities such as inhibition of glycolysis and thereby tumor growth, interference with the biosynthetic processing of glycoproteins, antiviral activity, and hepatotoxicity. It is being extensively studied as trapping agents for phosphate and uridylate in mammalian cells due to its ability to interfere in the phosphate and nucleotide metabolism. Purification Methods Crystallise 2-deoxy-D-galactose from MeOH or diethyl ether. The aniline derivative has m 142-143o, [ ] D 16.5 -149o (c 0.8, pyridine). [Overend et al. J Chem Soc 671, 675 1950 and 992 1951.] A 30% equilibrium solution at 31o in D2O contains 40% -pyranose, 44% pyranose, 8% -furanose and 8% -furanose forms as estimated by 1HNMR spectroscopy [Angyal & Pickles Aust J Chem 25 1711 1972]. [Beilstein 1 IV 4283.]   2-Deoxy-D-galactose Preparation Products And Raw materials

                                                                       Group profiles

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.

Our Factories production lines

                                                   Our Factories R&D ability

                        Our Factories warehouse 

                                                       Product information

2-Deoxy-D-galactose Basic information Product Name: 2-Deoxy-D-galactose Synonyms: 2-DEOXY-D-LYXOHEXOSE;2-DEOXY-D-GALACTOPYRANOSE;2-DEOXY-D-GALACTOSE;2-DEOXYGALACTOSE;2-DEOXY-BETA-D-GALACTOSE;2-DEOXY-BETA-D-LYXO-HEXOSE;2-Deoxy-D-galactose (1.24798);Deoxygalactose CAS: 1949-89-9 MF: C6H12O5 MW: 164.16 EINECS: 217-765-3 Product Categories: carbohydrate;Sugars, Carbohydrates & Glucosides;13C & 2H Sugars;Biochemistry;Deoxysugars;Galactose;Sugars;aldehydes;Carbohydrates & Derivatives Mol File: 1949-89-9.mol   2-Deoxy-D-galactose Chemical Properties Melting point  107-110 °C(lit.) alpha  57 º (c=3.7, H20 NH3) Boiling point  211.61°C (rough estimate) density  1.1738 (rough estimate) refractive index  1.4230 (estimate) storage temp.  Sealed in dry,2-8°C solubility  Methanol, Water pka 13.47±0.20(Predicted) form  Powder color  White to Off-white optical activity [α]20/D +59.7°, c = 2 in H2O Water Solubility  Soluble in water. BRN  1723333 CAS DataBase Reference 1949-89-9(CAS DataBase Reference) EPA Substance Registry System D-lyxo-Hexose, 2-deoxy- (1949-89-9)   Safety Information Hazard Codes  Xi,Xn Risk Statements  20/21/22-36/37/38 Safety Statements  24/25-37/39-36-26 WGK Germany  3 F  3-10 HS Code  29400090 MSDS Information Provider Language 2-Deoxy-D-galactose English ACROS English SigmaAldrich English   2-Deoxy-D-galactose Usage And Synthesis Chemical Properties White Crystalline Solid Uses 2-Deoxy-D-galactose is used as an inhibitor of fucosylation, which is a process of adding hexose deoxy sugar units to a molecule. It is used for studying galactose uptake into Escherichia coli and also for competitive elution of Anadarin P lectin (a galactosyl-binding lectin from blood clam). General Description 2-Deoxy-D-galactose is a glucose analog that shows a wide range of biological activities such as inhibition of glycolysis and thereby tumor growth, interference with the biosynthetic processing of glycoproteins, antiviral activity, and hepatotoxicity. It is being extensively studied as trapping agents for phosphate and uridylate in mammalian cells due to its ability to interfere in the phosphate and nucleotide metabolism. Purification Methods Crystallise 2-deoxy-D-galactose from MeOH or diethyl ether. The aniline derivative has m 142-143o, [ ] D 16.5 -149o (c 0.8, pyridine). [Overend et al. J Chem Soc 671, 675 1950 and 992 1951.] A 30% equilibrium solution at 31o in D2O contains 40% -pyranose, 44% pyranose, 8% -furanose and 8% -furanose forms as estimated by 1HNMR spectroscopy [Angyal & Pickles Aust J Chem 25 1711 1972]. [Beilstein 1 IV 4283.]   2-Deoxy-D-galactose Preparation Products And Raw materials