131 results about "Aminopropanols" patented technology

The invention provides a preparation method of a high-flux and anti-pollution reverse osmosis membrane. The preparation method of the high-flux and anti-pollution reverse osmosis membrane comprises the following steps: soaking a support layer in an aqueous solution with multifunctional aromatic amine compounds, taking the support layer out, drying the support layer, then soaking the support layer in a multifunctional acyl chloride oil phase solution, volatilizing and drying the support layer, then soaking the support layer in a modifier for 10-600 seconds, taking the support layer out and poaching the support layer in pure water to obtain the high-flux and anti-pollution reverse osmosis membrane, wherein the modifier is selected from any one of monoethanolamine, diethanol amine, triethanolamine, dimethylaminoethanol, diethylaminoethanol, 2-amino-propanol, dimethyl amine isopropyl alcohol, 3-amino-isopropyl alcohol and the like. According to the high-flux and anti-pollution reverse osmosis membrane prepared by the method, the hydrophilcity of the membrane can be improved; the salt removing rate remains at the level before modification; the charge performance of the membrane surface is reduced; the effect of shielding pollution of the charge substances in the running water is reduced; the high-flux and anti-pollution reverse osmosis membrane is suitable for industrial production and capable of meeting the requirements for long-term operation under the ultra-low voltage condition.

The invention discloses a method for preparing aminopropanol by bipolar membrane electrodialysis. The method comprises the steps that: aminopropanol sulphate water solution is used as a raw material and enters a material liquid chamber of a bipolar membrane electrodialysis device after being treated by a microporous filter, meanwhile, sulphuric acid water solution with the mass concentration being 0.1 percent is added into an acid chamber, sulphuric acid water solution with the mass concentration being 0.4 percent is added into a pole liquid chamber, the current density of the bipolar membrane electrodialysis device is controlled to be 50 to 800 A/m<2>, the voltage is 20 to 200V, the temperature is 5 to 40 DEG C, an electrodialysis separation chamber carries out circulation cooling through frozen brine in a circulation coil pipe in the operation process, when the electrical conductivity of the material liquid chamber is reduced to 2000mus/cm, the operation is stopped, the material liquid chamber and the acid chamber respectively obtain aminopropanol water solution and sulphuric acid water solution, and the aminopropanol water solution is concentrated to obtain aminopropanol. When the bipolar membrane electrodialysis technology is adopted for preparing the aminopropanol, the production period is short, the aminopropanol recovery rate is high, the energy consumption is obviously reduced, and the sulphuric acid quality is high.

The present invention is concerned with pseudopolymorphic forms of 1-(4-carbazolyloxy)-3-[2-(2-methoxyphenoxy)ethylamino]-2-propanole (carvedilol) or of optically active forms or pharmaceutically acceptable salts thereof, processes for the preparation thereof and pharmaceutical compositions containing them.

A method for preparing aminopropanol by electrolysis comprises two steps, namely preparation of aminopropanol by electrolysis reduction of an amino acid cathode and purification; the method for preparing aminopropanol by electrolysis is characterized in that an ion exchange membrane is adopted to divide an electrolyzer into a negative chamber and a positive chamber; the concentration of the aminopropanol in catholyte is 0.3mol/L to 2.0mol/L; the pH of the catholyte is 1 to 4; the anolyte is sulfuric acid with mass percentage concentration of 2 percent to 20 percent; the temperature of the electrolyte is controlled to be from 30 DEG C to 60 DEG C; the current density is 200 A/m<2> to 2000 A/m<2>; and when electrolyte balance is reached, the aminopropanol is obtained after the catholyte experiences filtration, neutralization, re-filtration and distillation. The method for preparing aminopropanol by electrolysis has low production cost and no pollution in the production process.

The invention discloses a loaded heterogeneous catalyst. The loaded heterogeneous catalyst is prepared from main active components, an assistant and a carrier or prepared from main active components and a carrier, wherein the assistant is prepared from one or two or more of elementary substances or oxides of Fe, Cu, Ru, Re, K, Zn and B, the carrier is prepared from one or two or more of graphite,activated carbon, a carbon nano tube, graphene, silicon dioxide, aluminum oxide, a molecular sieve, titanium dioxide and zirconium dioxide, and the loaded heterogeneous catalyst is prepared through anultrasonic loading method. By adopting the loaded heterogeneous catalyst for preparing 3-aminopropanol, (1) the mass space-time yield of the 3-aminopropanol is increased; (2) selectivity of the 3-aminopropanol is improved; (3) a reaction can be implemented under the low reaction pressure; (4) stability of a catalytic system is improved; and (5) process operation is easy, convenient and feasible,the one-time investment and production costs of production and subsequent separating devices are lowered, and large-scale continuous industrial production is easy to achieve.

The invention discloses a flame-retardant anti-wrinkle finishing agent for fabrics and a preparation method and application thereof. The flame-retardant anti-wrinkle finishing agent for fabrics comprises the following components in parts by weight: 8-15 parts of trimethyl phosphite, 4-9 parts of tri-isopropyl phosphite, 4-7 parts of triisopropyl borate, 3-7 parts of amino propanol ascorbyl phosphate, 8-15 parts of polyglycerol polyricinoleate, 14-20 parts of dimethyl silicone, 5-13 parts of dimethiconol stearate, 4-8 parts of secondary alcohol ethoxylate, 12-20 parts of propylene glycol and 300-400 parts of water. The preparation method comprises the following steps: mixing, heating, performing magnetic stirring, and the like. The anti-wrinkle property and the flame retardancy of a fabric treated by using the finishing agent are remarkably improved.

The invention relates to a process for synthesizing a medicinal intermediate and particularly relates to a process for synthesizing an aminopropanol, which has the advantages of safe raw materials, high yield and mild reaction condition. According to the technical scheme of the invention, ring opening is carried out on 1,4-butyrolactone, serving as a raw material, under the action of hydrazine hydrate, the aqueous solution of sodium nitrite is added to generate acyl azide, and finally the rearranging is carried out to generate 3-aminopropanol.

A process for preparing 3-aminopropanesulfonic acid includes introducing hydrogen chloride gas into 3-aminopropanol, diluting with ethanol, cooling to educe out crystal as intermediate, preparing itsaqueous solution, sulfonating reaction with the aqueous solution of alkali-metal sulfite by reflux, acidifying by hydrochloric acid, filtering, and cooling to educe out the crystal of product.

The present invention relates to a novel compound S-(−)-1-{4-[2-(allyloxy)-ethyl] phenoxy}-3-isopropylamino propan-2-ol of formula 1 and to a process for the preparation thereof. More particularly the present invention relates to a process for preparing S-(−)-1-{4-[2-(allyloxy)-ethyl]phenoxy}-3-isopropylamino propan-2-ol of formula 1 by selective allylation of p-hydroxy phenyl ethanol. The present invention also relates to a process for conversion thereof to S-(−)-betaxolol of formula 2

The invention provides a preparation method of ofloxacin. The preparation method comprises the following steps of: reacting (N,N)-dimethylamino ethyl acrylate with aminopropanols in methylbenzene; directly adding lewis base serving as a catalyst and trimethylchlorosilane to protect hydroxyl and amido; after reaction is completely finished, dropwise adding (2,3,4,5)-tetrafluorobenzoyl chloride; preserving heat; performing acid washing; removing protecting groups; concentrating an organic layer to obtain an oil layer; adding a proper amount of dimethyl formamide (DMF); diluting and dropwise adding backflow DMF having anhydrous potassium fluoride; recovering DMF and adding water to centrifuge; adding acid water into a solid to hydrolyze to obtain difluorocarboxylic acid; and completely reacting difluorocarboxylic acid and N-methyl piperazine in dimethylsulfoxide (DMSO) by using triethylamine as an acid-binding agent at 90-100 DEG C to obtain ofloxacin. According to the process, hydroxyl and amido are protected by using trimethylchlorosilane, so that the utilization degree of (2,3,4,5)-tetrafluorobenzoyl chloride is effectively increased, and the generation of impurities is reduced to ensure that the reaction yield of intermediate difluorocarboxylic acid is increased by 10 percent.

An aqueous CO2 absorbent comprising a combination of 2-amino-2-methyl-1-propanol (AMP) and 3-aminopropanol (AP), or AMP and 4-aminobutanol (AB), is described. A method for capturing CO2 from a CO2 containing gas using the mentioned absorbent, and the use of a combination of AMP and AP, or a combination of AMP and AB are also described.

The invention relates to the technical field of preparation methods of superfine fiber synthetic leather, and discloses a base fabric post-processing technology of superfine fiber synthetic leather. Adecreased base fabric is treated by the technology comprising the following steps: S1, expanding and drying; S2, oiling, wherein the base fabric which is expanded and dried in step S1 is repeatedly soaked in an oiling agent. The oiling agent comprises the following chemical components in parts by weight: 40-60 parts of amino silicone oil, 30-50 parts of aminopropanol kojic acid phosphate, 6-9 parts of diatomite, 3-7 parts of talcum powder and 10-14 parts of a surfactant; S3, shaping and drying; and S4, carrying out puffing treatment. By using the oiling agent mentioned above, the tearing strength of the base fabric is improved.

The invention discloses a method for the synthesis of L-2-aminopropanol. L-alanine is taken as starting material, and L-alanine is esterified, and then is reduced for 0.5-2h in organic solvent with tetramethylammonium borohydride as reducing agent; subsequently, is separated after reduction for 2-6h under 35-55 DEG C. The tetramethylammonium borohydride is prepared by the reaction of potassium borohydride with tetramethylammonium chloride, sodium chloride is added during reaction, the reacted product is separated by removing part of water crystallization. The yield of one crystallization separation is greater than or equal to 98 percent, and purification is not required and the product can be used to reduction directly. Since the method adopts the novel reducing agent, the original 2 tons of potassium borohydride required by each ton of L-2- aminopropanol is reduced to 1.25 tons, and as a result, the cost of levofloxacin is largely reduced.

The invention provides a preparation method of 3-aminopropanol, which is high in conversion rate. The invention adopts the following technical scheme: adding 3-hydroxypropionitrile into a reactor witha nickel catalyst and silver nitrate, and then adding an amine reagent under nitrogen; then introducing hydrogen into the reactor, stirring for reducing reaction, and performing precipitation and distillation to prepare the 3-aminopropanol. The raw materials are high in utilization rate; the separation process is simple and clear; the energy consumption is low; the production cost of a product islow; and the solvent and the catalyst can be recycled for use.

The invention relates to an impurity analysis method for multiple vitamin preparations. The method comprises the following steps of preparing a test solution of the vitamin preparations; dissolving o-phthalaldehyde and 2-mercaptoethanol based on a mass ratio of 1 to (2-5) in methanol, adding a boric acid buffer solution, and adjusting the pH value to 3-5 to obtain a derivatization reagent; and taking the test solution, adding the derivatization reagent to carry out online derivatization reaction, and injecting the derivatized test solution into a high performance liquid chromatograph, therebydetecting impurities in the test solution. According to the method, folic acid impurity A, folic acid impurity D, p-aminobenzoic acid and 3-aminopropanol in the vitamin preparations can be effectivelydetected; and the method is high in sensitivity and good in specificity.

The invention discloses a metal pressure casting releasing agent. The releasing agent comprises, by mass percent, 8 to 15% of epoxy soybean oil modified amino silicone oil, 20 to 30% of Tween 80-ricinoleic acid n-hexadecyl ester-oxprenolol glucosiduronide copolymer, 2 to 5% of 1-hexadecanaminium,2-hydroxy-N-(2-hydroxyethyl)-N,N-dimethyl-,chloride, 1 to 4% of aminopropanol ascorbic acid phosphate,2 to 4% of an emulsifying agent, 0.5 to 1.2% of a defoaming agent and the balance water. The invention further discloses a preparing method of the metal pressure casting releasing agent. The metal pressure casting releasing agent has the good lubricating and mold releasing performance under the high temperature environment, stability is good, when a casting after pressure casting is separated froma mold, mold releasing is easy, smoothness on the surface of the casting after mold releasing is high, and the mold protection effect is good.

The invention discloses a salt (I) of a 3-amino-2-propanol acetamide compound, and also discloses a preparation method of the salt, and use of the salt as a reference substance or a standard substance of related substance in quality control of a linezolid preparation. In a formula, A represents boric acid, phosphoric acid, C1-8 fatty acid, trifluoroacetic acid, benzoic acid, salicylic acid, phthalic acid, mandelic acid, oxalic acid, maleic acid, fumaric acid, succinic acid, tartaric acid, citric acid, methanesulfonic acid, ethanesulfonic acid, benzenesulfonic acid, and p-toluenesulfonic acid; n represents 1/2 or 1; the compound is a racemate, an (S)-optical isomer or an (R)-optical isomer.

The invention discloses a metal surface zinc-nickel alloy electroplating solution. The formula of the electroplating solution comprises 20-50 g/L of zinc oxide, 10-20 g/L of nickel sulfate, 120-160 g/L of sodium hydroxide, 10-30 g/L of a complexing agent, 0.5-5 g/L of an additive and 1-5 g/L of a brightening agent, wherein the complexing agent is composed of ammonium citrate, triethanolamine and 1, 3-diamino-2-propanol according to the mass ratio of 1: (1-3): (3-5), the additive is composed of sodium phytate and hexadecyl trimethyl ammonium bromide according to the mass ratio of 1: (3-5), thebrightening agent is composed of saccharin, vanillin, 2-butyne-1, 4-diol and sodium allysulfonate according to the mass ratio of (5-10): (1-3): (3-5): 1. The electroplating solution can provide a bright zinc-nickel alloy coating with refined grains, improves the deep plating capability and dispersion performance of the coating, and is particularly suitable for electroplating of long-tube-shaped workpieces.

The invention relates to the technical field of medicines, and relates to a preparation method and new application of a compound. In particular to a preparation method of a compound 1-(2-ethoxyphenoxy)-3-((3-methoxy-4-(2-(4-methylpiperidin-1-yl)ethyoxyl)benzyl)(methyl)amino)propan-2-ol and application of the compound in preparation of drugs for preventing and/or treating diseases related to SphK1 dysfunction. The invention finds that 1-(2-ethoxyphenoxy)-3-((3-methoxy-4-(2-(4-methylpiperidin-1-yl)ethyoxyl)benzyl)(methyl)amino)propan-2-ol has the effect of selectively inhibiting SphK1 for the first time, and can be used for preventing and/or treating diseases related to SphK1 dysfunction.

The invention discloses a synthesis method of 2-aminopropanol. According to the method, epoxypropane and liquid ammonia are taken as raw materials, epoxypropane and liquid ammonia are introduced intoa fixed bed reactor, the molar ratio of epoxypropane to liquid ammonia is 1: (5-20), and under the action of a rare earth modified catalyst, reaction is carried out for 10-60s at the temperature of 100-200 DEG C, so that 2-aminopropanol is obtained. The method is reasonable in process, simple and convenient to operate, high in atom economy and low in emission of three wastes, and meets the requirements of industrial production.