China Largest Manufacturer factory sales Butyl 4-aminobenzoate CAS 94-25-7 CAS NO.94-25-7

                                PRODUCT DETAILS                           

Butyl 4-aminobenzoate Basic information Product Name: Butyl 4-aminobenzoate Synonyms: 4-(Butoxycarbonyl)aniline;4-amino-benzoicacibutylester;Scuroforme;P-AMINOBENZOIC ACID BUTYL ESTER;PLANOFORM;N-BUTYL P-AMINOBENZOATE;N-BUTYL 4-AMINOBENZOATE;BUTYL-P-AMINOBENZOATE CAS: 94-25-7 MF: C11H15NO2 MW: 193.24 EINECS: 202-317-1 Product Categories: CECLOR;Building Blocks;C10 to C11;Carbonyl Compounds;Chemical Synthesis;Esters;Aromatic Esters;Organic Building Blocks Mol File: 94-25-7.mol   Butyl 4-aminobenzoate Chemical Properties Melting point  57-58 °C(lit.) Boiling point  174 °C8 mm Hg(lit.) density  1.0945 (rough estimate) refractive index  1.5480 (estimate) storage temp.  Keep in dark place,Inert atmosphere,Room temperature solubility  Chloroform (Slightly), Methanol (Slightly) pka pKa 5.38 (Uncertain) form  Solid color  White Water Solubility  Very slightly soluble in water. Sensitive  Light Sensitive Merck  14,1512 BRN  1211465 CAS DataBase Reference 94-25-7(CAS DataBase Reference) NIST Chemistry Reference Butamben(94-25-7) EPA Substance Registry System Butyl p-aminobenzoate (94-25-7)   Safety Information Hazard Codes  Xi Risk Statements  36/37/38-43 Safety Statements  26-36/37-36 WGK Germany  3 RTECS  DG1530000 TSCA  Yes HS Code  29224995 Hazardous Substances Data 94-25-7(Hazardous Substances Data) MSDS Information Provider Language Butyl 4-aminobenzoate English SigmaAldrich English   Butyl 4-aminobenzoate Usage And Synthesis Chemical Properties It is a solid at room temperature, with a melting point of 58°C and a boiling point of 173.4°C (at 8mmHg). Butyl p-aminobenzoate is insoluble in water. Uses n-Butyl 4-aminobenzoate is used as pharmaceutical intermediate. Uses antibacterial Definition ChEBI: An amino acid ester resulting from the formal condensation of the carboxy group of 4-aminobenzoic acid with the hydroxy group of butan-1-ol. Its local anaesthetic properties have been used for surface anaesthesia of the skin and mucous membranes, and for r lief of pain and itching associated with some anorectal disorders. Production Methods Butyl p-aminobenzoate is manufactured via esterification of p-nitrobenzoic acid with n-butyl alcohol, followed by the reduction of the nitro group to an amino group. Brand name Butesin (Abbott). General Description Yellow powder. Insoluble in water. Air & Water Reactions May be sensitive to light and air. Insoluble in water. Slowly hydrolyzed when boiled in water. Also will hydrolyze under high and low pH conditions . Reactivity Profile Butyl 4-aminobenzoate is an aminophenyl ester derivative. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Fire Hazard Flash point data for Butyl 4-aminobenzoate are not available. Butyl 4-aminobenzoate is probably combustible. Purification Methods Crystallise Butamben from EtOH. [Beilstein 14 IV 1130.]   Butyl 4-aminobenzoate Preparation Products And Raw materials Raw materials 1-Butanol-->4-Aminobenzoic acid

                                                                       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

Butyl 4-aminobenzoate Basic information Product Name: Butyl 4-aminobenzoate Synonyms: 4-(Butoxycarbonyl)aniline;4-amino-benzoicacibutylester;Scuroforme;P-AMINOBENZOIC ACID BUTYL ESTER;PLANOFORM;N-BUTYL P-AMINOBENZOATE;N-BUTYL 4-AMINOBENZOATE;BUTYL-P-AMINOBENZOATE CAS: 94-25-7 MF: C11H15NO2 MW: 193.24 EINECS: 202-317-1 Product Categories: CECLOR;Building Blocks;C10 to C11;Carbonyl Compounds;Chemical Synthesis;Esters;Aromatic Esters;Organic Building Blocks Mol File: 94-25-7.mol   Butyl 4-aminobenzoate Chemical Properties Melting point  57-58 °C(lit.) Boiling point  174 °C8 mm Hg(lit.) density  1.0945 (rough estimate) refractive index  1.5480 (estimate) storage temp.  Keep in dark place,Inert atmosphere,Room temperature solubility  Chloroform (Slightly), Methanol (Slightly) pka pKa 5.38 (Uncertain) form  Solid color  White Water Solubility  Very slightly soluble in water. Sensitive  Light Sensitive Merck  14,1512 BRN  1211465 CAS DataBase Reference 94-25-7(CAS DataBase Reference) NIST Chemistry Reference Butamben(94-25-7) EPA Substance Registry System Butyl p-aminobenzoate (94-25-7)   Safety Information Hazard Codes  Xi Risk Statements  36/37/38-43 Safety Statements  26-36/37-36 WGK Germany  3 RTECS  DG1530000 TSCA  Yes HS Code  29224995 Hazardous Substances Data 94-25-7(Hazardous Substances Data) MSDS Information Provider Language Butyl 4-aminobenzoate English SigmaAldrich English   Butyl 4-aminobenzoate Usage And Synthesis Chemical Properties It is a solid at room temperature, with a melting point of 58°C and a boiling point of 173.4°C (at 8mmHg). Butyl p-aminobenzoate is insoluble in water. Uses n-Butyl 4-aminobenzoate is used as pharmaceutical intermediate. Uses antibacterial Definition ChEBI: An amino acid ester resulting from the formal condensation of the carboxy group of 4-aminobenzoic acid with the hydroxy group of butan-1-ol. Its local anaesthetic properties have been used for surface anaesthesia of the skin and mucous membranes, and for r lief of pain and itching associated with some anorectal disorders. Production Methods Butyl p-aminobenzoate is manufactured via esterification of p-nitrobenzoic acid with n-butyl alcohol, followed by the reduction of the nitro group to an amino group. Brand name Butesin (Abbott). General Description Yellow powder. Insoluble in water. Air & Water Reactions May be sensitive to light and air. Insoluble in water. Slowly hydrolyzed when boiled in water. Also will hydrolyze under high and low pH conditions . Reactivity Profile Butyl 4-aminobenzoate is an aminophenyl ester derivative. Amines are chemical bases. They neutralize acids to form salts plus water. These acid-base reactions are exothermic. The amount of heat that is evolved per mole of amine in a neutralization is largely independent of the strength of the amine as a base. Amines may be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated by amines in combination with strong reducing agents, such as hydrides. Esters react with acids to liberate heat along with alcohols and acids. Strong oxidizing acids may cause a vigorous reaction that is sufficiently exothermic to ignite the reaction products. Heat is also generated by the interaction of esters with caustic solutions. Flammable hydrogen is generated by mixing esters with alkali metals and hydrides. Fire Hazard Flash point data for Butyl 4-aminobenzoate are not available. Butyl 4-aminobenzoate is probably combustible. Purification Methods Crystallise Butamben from EtOH. [Beilstein 14 IV 1130.]   Butyl 4-aminobenzoate Preparation Products And Raw materials Raw materials 1-Butanol-->4-Aminobenzoic acid