China Largest Manufacturer factory sales N-Acetyl-L-Glutamic Acid CAS 1188-37-0 CAS NO.1188-37-0

                                PRODUCT DETAILS                           

N-Acetyl-L-glutamic acid Basic information Product Name: N-Acetyl-L-glutamic acid Synonyms: acetylglutamicacid;L-Glutamic acid, N-acetyl-;l-glutamicaci;N-ALPHA-ACETYL-L-GLUTAMIC ACID;N-AC-L-GLU;N-ACETYL-L-GLU;N-ACETYL-L-GLUTAMIC ACID;ACETYL-L-GLUTAMIC ACID CAS: 1188-37-0 MF: C7H11NO5 MW: 189.17 EINECS: 214-708-4 Product Categories: Glutamic acid [Glu, E];Ac-Amino Acids;Amino Acid Derivatives;Amino Acids;Amino Acids (N-Protected);Biochemistry;Amino Acid Derivatives;Glutamic Acid;Peptide Synthesis;amino acid;amino;1188-37-0 Mol File: 1188-37-0.mol   N-Acetyl-L-glutamic acid Chemical Properties Melting point  194-196 °C(lit.) alpha  -16 º (c=1, water) Boiling point  324.41°C (rough estimate) density  1.4119 (rough estimate) FEMA  4752 | N-ACETYL GLUTAMATE refractive index  -15 ° (C=1, H2O) storage temp.  2-8°C solubility  36g/l (Lit.) form  Solid pka 3.45±0.10(Predicted) color  White optical activity [α]22/D 15.6°, c = 1 in H2O Water Solubility  2.7 g/100 mL (20 ºC) BRN  1727473 CAS DataBase Reference 1188-37-0(CAS DataBase Reference) NIST Chemistry Reference N-acetyl-l-glutamic acid(1188-37-0) EPA Substance Registry System L-Glutamic acid, N-acetyl- (1188-37-0)   Safety Information Safety Statements  24/25 WGK Germany  2 RTECS  LZ9725000 TSCA  Yes HS Code  29241900 MSDS Information Provider Language N-Acetyl-L-glutamic acid English ACROS English SigmaAldrich English ALFA English   N-Acetyl-L-glutamic acid Usage And Synthesis Chemical Properties white crystalline powder Uses N-Acetyl-L-glutamic Acid is the N-Acetyl analogue of the non-essential amino acid, L-glutamic acid (G596960). N-Acetyl-L-glutamic Acid activates carbamoyl phosphate synthetase in the urea cycle. Uses Substrate for acetylglutamate kinase. Inhibitor of N-acetyl-L-glutamate synthetase Uses N-Acetyl-L-glutamic acid is used as pharmaceutical intermediates. Purification Methods A likely impurity is glutamic acid. Crystallise it from boiling water. It inhibits N-acetyl-L-glutamate synthase. [Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 p 1948 1961, Shigesada & Tatibana Eur J Biochem 84 285 1978, Coude Biochem Biophys Res Commun 102 1016 1981, Beilstein 4 IV 3047.]   N-Acetyl-L-glutamic acid 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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                                                       Product information

N-Acetyl-L-glutamic acid Basic information Product Name: N-Acetyl-L-glutamic acid Synonyms: acetylglutamicacid;L-Glutamic acid, N-acetyl-;l-glutamicaci;N-ALPHA-ACETYL-L-GLUTAMIC ACID;N-AC-L-GLU;N-ACETYL-L-GLU;N-ACETYL-L-GLUTAMIC ACID;ACETYL-L-GLUTAMIC ACID CAS: 1188-37-0 MF: C7H11NO5 MW: 189.17 EINECS: 214-708-4 Product Categories: Glutamic acid [Glu, E];Ac-Amino Acids;Amino Acid Derivatives;Amino Acids;Amino Acids (N-Protected);Biochemistry;Amino Acid Derivatives;Glutamic Acid;Peptide Synthesis;amino acid;amino;1188-37-0 Mol File: 1188-37-0.mol   N-Acetyl-L-glutamic acid Chemical Properties Melting point  194-196 °C(lit.) alpha  -16 º (c=1, water) Boiling point  324.41°C (rough estimate) density  1.4119 (rough estimate) FEMA  4752 | N-ACETYL GLUTAMATE refractive index  -15 ° (C=1, H2O) storage temp.  2-8°C solubility  36g/l (Lit.) form  Solid pka 3.45±0.10(Predicted) color  White optical activity [α]22/D 15.6°, c = 1 in H2O Water Solubility  2.7 g/100 mL (20 ºC) BRN  1727473 CAS DataBase Reference 1188-37-0(CAS DataBase Reference) NIST Chemistry Reference N-acetyl-l-glutamic acid(1188-37-0) EPA Substance Registry System L-Glutamic acid, N-acetyl- (1188-37-0)   Safety Information Safety Statements  24/25 WGK Germany  2 RTECS  LZ9725000 TSCA  Yes HS Code  29241900 MSDS Information Provider Language N-Acetyl-L-glutamic acid English ACROS English SigmaAldrich English ALFA English   N-Acetyl-L-glutamic acid Usage And Synthesis Chemical Properties white crystalline powder Uses N-Acetyl-L-glutamic Acid is the N-Acetyl analogue of the non-essential amino acid, L-glutamic acid (G596960). N-Acetyl-L-glutamic Acid activates carbamoyl phosphate synthetase in the urea cycle. Uses Substrate for acetylglutamate kinase. Inhibitor of N-acetyl-L-glutamate synthetase Uses N-Acetyl-L-glutamic acid is used as pharmaceutical intermediates. Purification Methods A likely impurity is glutamic acid. Crystallise it from boiling water. It inhibits N-acetyl-L-glutamate synthase. [Greenstein & Winitz The Chemistry of the Amino Acids J. Wiley, Vol 3 p 1948 1961, Shigesada & Tatibana Eur J Biochem 84 285 1978, Coude Biochem Biophys Res Commun 102 1016 1981, Beilstein 4 IV 3047.]   N-Acetyl-L-glutamic acid Preparation Products And Raw materials