505 results about "Morpholine" patented technology

The invention discloses an easy-to-apply single-component polyurethane waterproof coating and a preparation method thereof, and belongs to the technical field of waterproof coatings. The easy-to-apply single-component polyurethane waterproof coating disclosed by the invention is prepared from the following raw materials: polyol, a plasticizer, a solid filler, isocyanate, a catalyst and a solvent, the polyol comprises polyether glycol and polyether triol; the plasticizer comprises acetyl tributyl citrate; the catalyst comprises a bismuth neodecanoate catalyst and a dimorpholine diethyl ether catalyst. According to the easy-to-apply single-component polyurethane waterproof coating disclosed by the invention, acetyl tributyl citrate is used for replacing traditional plasticizer chlorinated paraffin, and a bismuth neodecanoate catalyst and a dimorpholine diethyl ether (DMDEE) catalyst are compounded, so that the viscosity of the waterproof coating is effectively reduced, and construction is facilitated; meanwhile, the drying speed of the waterproof coating is increased.

The invention discloses a cellulose coated diaphragm and a preparation method thereof in the field of lithium ion batteries, the diaphragm comprises alpha-cellulose pulp, a cellulose grafted phenylboronic acid-co-oligomeric ethylene oxide copolymer, a thermal response star zwitterionic polymer and nano aluminum oxide, and an N-methylmorpholine-N-oxide aqueous solution is adopted as a solvent system. The preparation method comprises the following steps: firstly synthesizing a cellulose grafted copolymer with dynamic borate bonds through atom transfer radical polymerization, then preparing a star polymer with thermal response arms and zwitter-ion terminals by taking cyclodextrin as a core, and finally mixing all the components to prepare coating slurry. And the composite diaphragm is prepared through the processes of coating, phase conversion, ultraviolet curing and drying. The diaphragm combines the thermal stability and lyophilic property of cellulose, forms a dynamic self-adaptive interface layer through the synergistic effect of two functional compounds, has the advantages of active safety protection, dendritic crystal inhibition, long cycle life and the like, and remarkably improves the comprehensive performance of the lithium ion battery.

The invention relates to a corrosion and scale inhibitor for TRT and a preparation method of the corrosion and scale inhibitor, and relates to the technical field of chemical reagents. The corrosion and scale inhibitor is prepared from the following components in percentage by mass: 15 to 20 percent of morpholine, 25 to 30 percent of aminoethyl ethanolamine, 15 to 20 percent of 1-hydroxyethyl-2-undecylimidazoline onium salt, 12 to 18 percent of sodium polyaspartate, 8 to 12 percent of itaconic acid-allylsulfonic acid copolymer, 1 to 3 percent of alkyl glycoside and the balance of a mixture of water and glycerol in a mass ratio of 1 to (1 to 3). The corrosion and scale inhibitor disclosed by the invention can synchronously inhibit corrosion of an acid medium and scale deposition of salts such as NH4Cl and the like, and the corrosion inhibition rate and the scale inhibition rate are effectively improved.

The invention relates to the technical field of thickening agents for fracturing fluids, and particularly discloses a composite fracturing fluid thickening agent for an oil and gas well and a preparation process of the composite fracturing fluid thickening agent. The invention relates to a composite fracturing fluid densifier for oil and gas wells. The composite fracturing fluid densifier comprises 30-50 parts of acrylamide; 20 to 35 parts of 2-acrylamide-2-methyl propane sulfonic acid; 10 to 25 parts of acryloyl morpholine; 3-8 parts of a polyether amine modified organic zirconium cross-linking agent; 2-6 parts of sulfonated konjac gum; 1-5 parts of a salt-tolerant synergistic aid; 0.5-2 parts of a composite initiator; 0.1 to 0.8 part of an inhibitor; and 150 to 180 parts of deionized water. The fracturing fluid thickening agent provided by the invention has the advantages of high viscosity, high temperature resistance and high salt resistance.

The invention provides dust-free antibacterial deodorant bentonite cat litter and a preparation method thereof, and belongs to the technical field of cat litter. Firstly, a certain amount of sodium bentonite, baking soda and calcium carbonate are used for preparing bentonite cat litter, then polyvinyl alcohol and sodium carboxymethyl cellulose which have the film forming property, polyhexamethylene guanidine hydrochloride which has the bactericidal property and soybean ethyl sulfate morpholine which has the deodorization function are used for preparing the bentonite cat litter; the components are compounded to obtain a functional dust suppressant with antibacterial, deodorant and film-forming effects, the functional dust suppressant is sprayed and coated on the surface layer of the bentonite cat litter, so that the prepared dust-free antibacterial and deodorant bentonite cat litter is remarkable in deodorant and antibacterial effects and good in wear resistance, and a layer of water-soluble film is formed on the surface of the dust suppressant after the functional dust suppressant is sprayed for dust suppression treatment, so that the dust suppression effect is good. The bentonite cat litter has the advantages that the structure and the film-forming property of the surface layer of the bentonite cat litter are improved, the hardness and the wear resistance of the surface are improved, the dust suppression effect of the cat litter is obviously improved, dust is extremely low under simulated falling and transportation conditions, and the cat litter has excellent water absorption and caking performance.

The invention discloses a preserving fluid for stably preserving sample DNA at normal temperature and a preparation method thereof, and belongs to the technical field of biological sample preservation. The preserving fluid comprises a lysis system, a nucleic acid protection system and a buffering and stabilizing system, the cracking system comprises a composite surfactant and an enzymolysis auxiliary agent; the composite surface active agent is prepared from polyether polyol fatty acid ester and cocamidopropyl hydroxy sulfobetaine; the enzymolysis auxiliary agent comprises lysozyme Lyso-V and protease K; the nucleic acid protection system comprises a nitrogen heterocyclic polyamine-carboxylic acid derivative and dextran sulfate; the nitrogen heterocyclic polyamine-carboxylic acid derivative comprises 1, 4, 7, 10-tetraazacyclododecane-N, N ', N' ', N ''tetraacetic acid, 1, 4, 7-triazacyclononane-N, N', N''-triacetic acid, disodium ethylene diamine tetraacetate-nitrogen heterocyclic derivative, and diethylenetriamine pentaacetic acid-piperazine derivative, and the nitrogen heterocyclic polyamine-carboxylic acid derivative comprises 1, 4, 7, 10-tetraazacyclododecane-N, N ', N '', N'' tetraacetic acid, 1, 4, 7-triazacyclononane-N, N', N ''-triacetic acid. The buffering and stabilizing system comprises an amphoteric buffering agent and a polymer stabilizer; the amphoteric buffering agent comprises 2-(N-morpholino) ethanesulfonic acid and N-tri (hydroxymethyl) methylglycine.

The invention discloses a functional hydrogel microsphere and a preparation method and application thereof, and relates to the technical field of medicines.The preparation method comprises the steps that a hyaluronic acid methacrylic acid precursor solution and an IL-1beta shRNA adenovirus stock solution are mixed to obtain an Ad-atHAMA precursor solution; preparing the Ad (at) HAMA precursor solution through an oil-in-water micro-fluidic technology to obtain an Ad (at) HAMA microsphere; and sequentially adding the Ad (at) HAMA microspheres, 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and N-hydroxysuccinimide into a 2-morpholinoethanesulfonic acid buffer solution, carrying out activating treatment, adding E selectin, and incubating to obtain the functionalized hydrogel microspheres. The functionalized hydrogel microspheres can inhibit a related mechanism of acute spinal cord injury pathological progress and promote neural function repair by targeting adsorption of neutrophil to regulate Nets-triggered innate immune inflammation cascade.

The invention provides synthesis of a T-2 toxin antigen and preparation and application of a monoclonal antibody. Relates to the technical field of biotoxin detection. The preparation method of the T-2 toxin antigen comprises the following steps: step 1, synthesizing an immunogen T-2-BSA by adopting a carbodiimide method, dissolving 2mg of T-2 adipic acid with 0.5 mL of dimethylformamide, and recording as a solution A; 5 mg of bovine serum albumin and 3 mg of EDC are dissolved with a 2-morpholine ethanesulfonic acid buffer solution with the pH being 5.5, and the solution is marked as a solution B; step 2, under the condition of stirring, dropwise adding the solution A into the solution B, stirring for 18 hours in a dark place at 4 DEG C, then dialyzing for 3 days by using a phosphate buffer solution, changing the solution once a day, centrifuging the dialysate for 10 minutes at 3,500 r / min, and discarding the precipitate; the adipic acid is coupled with the T-2 toxin through a chemical method, and the unique step enriches the structural characteristics of the hapten, so that the prepared T-2 toxin complete antigen is excellent in immune effect, can efficiently excite immune response of an organism, and shows high specificity and sensitivity.

The invention relates to a structure, synthesis and application of morpholine ring oligonucleotide. A morpholine ring oligonucleotide structure is named Mo-CEBPA, can induce intracellular redox imbalance and trigger ferroptosis by inhibiting expression of CEBPA in hepatoma carcinoma cells, can assist sorafenib in killing hepatoma carcinoma cells, and overcomes the defect that existing drugs cannot efficiently induce hepatoma carcinoma cell ferroptosis.

Methods featuring phosphoryl guanidinium based backbone and morpholino with phosphoramidite chemistry result in neutral antisense oligonucleotides. The PGMO is composed of a morpholino backbone linked to a phosphoryl guanidinium internucleotide (PG) linkage. These oligonucleotides can be used to treat cancer, autoimmune diseases, and other rare diseases.

The invention discloses a piezoelectric dissimilar metal co-doped titanium-oxygen cluster compound as well as a preparation method and application thereof, and relates to the field of materials. The molecular formula of the piezoelectric dissimilar metal co-doped titanium-oxygen cluster compound is H2Ti26Pb10 (mu4-O) 4 (mu3-O) 34 (mu2-O) 6Bz38. 6MeCN. 2 (C4H9ON), and the molecular formula of the piezoelectric dissimilar metal co-doped titanium-oxygen cluster compound is Ti26Pb10, and the molecular formula of the piezoelectric dissimilar metal co-doped titanium-oxygen cluster compound is Ti26Pb10. Wherein mu3-O represents a three-bridged O atom, mu2-O represents a two-bridged O atom, mu4-O represents a four-bridged O atom, Bz represents a benzoic acid ligand, MeCN represents an acetonitrile solvent molecule, and C4H9ON represents a morpholine solvent molecule. The adopted preparation method is simple, raw materials are easy to obtain, aftertreatment is simple, pollution is little, and the green and environment-friendly requirements are met. The piezoelectric dissimilar metal co-doped titanium-oxygen cluster compound prepared by the preparation method disclosed by the invention is relatively high in stability, has piezoelectric activity and has a relatively high degradation rate on antibiotics.

The invention discloses a perovskite photovoltaic device and a preparation method and application thereof, and the preparation method of the perovskite photovoltaic device comprises the following steps: dissolving heterocyclic molecules in a solvent, stirring and dissolving to prepare an interface dipole material, spin-coating the interface dipole material on a hole transport layer, and annealing to form an interface dipole layer, a perovskite material is spin-coated through an anti-solvent method and annealed to form a perovskite film, and then an electron transport layer and a metal electrode are subjected to vacuum evaporation to obtain the perovskite photovoltaic device. Wherein the heterocyclic molecules are one or two of pyridine hydriodate, morpholine hydriodate or pyrrole hydriodate. The perovskite photovoltaic device prepared by the invention has high energy conversion efficiency.

The invention discloses a folic acid modified active oxygen response type sodium alginate nano-carrier and application thereof, and the preparation method comprises the following steps: firstly synthesizing-Se-Se-FA: stirring dicyclohexylcarbodiimide, 4-dimethylaminopyridine, dimethyl sulfoxide / pyridine, a double-selenium fragment and folic acid at room temperature for 18-22 hours in an argon environment; and carrying out acetone precipitation, centrifugation, washing, rotary evaporation concentration and freeze-drying. The preparation method comprises the following steps: preparing an ALG-Se-FA carrier, stirring sodium alginate, 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide hydrochloride and hydroxysuccinimide in a 2-morpholinoethanesulfonic acid buffer solution, adding DMSO, dissolving a double-selenium fragment and a-Se-Se-FA fragment in DMSO and deionized water, adding the dissolved double-selenium fragment and-Se-Se-FA fragment into a system, stirring, dialyzing, and freeze-drying to obtain the product. According to the carrier, a double-selenium bond ROS response unit and folic acid targeting molecules are introduced through covalent bonds, astaxanthin can be efficiently entrapped and protected, and after the carrier is stable in gastrointestinal environment and reaches a colitis disease part, high ROS level can be responded, and intelligent drug slow release is achieved through folic acid receptor targeting.

The present invention relates to 5′-morpholino amidite monomers as 5′-CE / 5′-tBu phosphoramidite morpholino monomers (2) and process chemistry for the efficient synthesis of N-Trityl or monomethoxytrityl (MMTr)-protected 5′-morpholino amidite monomers and their use in the synthesis of phosphorodiamidate morpholino oligonucleotides (PMO), thiophosphoramidate morpholino oligonucleotides (TMO) and their chimeras which can be used for antisense technology or in general oligonucleotides related research.

The invention discloses a high-temperature-resistant environment-friendly drilling fluid filtrate reducer based on humic acid and sodium alginate and a preparation method of the high-temperature-resistant environment-friendly drilling fluid filtrate reducer, and belongs to the technical field of petroleum drilling engineering oil fields. On the premise that a sulfonic acid group is not introduced, humic acid and sodium alginate are selected as main raw materials of the filtrate reducer, and a stable polymer structure is constructed by grafting acrylamide and N-vinyl pyrrolidone 4-acryloylmorpholine, so that the filtrate loss control capability at high temperature is effectively improved, the filtrate reducer does not contain sulfonic acid groups, and the filtrate reducer is environment-friendly and pollution-free. The environment-friendly property and the degradability are excellent. Compared with the existing filtrate reducer, the filtrate reducer provided by the invention has obvious advantages in the aspects of raw material source, synthesis cost, thermal stability, environmental protection performance and the like, is particularly suitable for high-temperature and high-salt complex working conditions of a green drilling fluid system, and has good popularization and application prospects.

The application discloses an impact-resistant mine protective clothing and belongs to the technical field of mine protective clothing. The mine protective clothing is provided with an impact-resistant protective layer, and the impact-resistant protective layer comprises alternately stacked and connected first and second functional layers. The outermost layer of the impact-resistant protective layer towards the outside of a wearer of the protective clothing is the first functional layer, the first functional layer is a composite material layer composed of aramid woven fabric and a second resin, the second resin is filled in the fiber gap of the aramid woven fabric as a continuous matrix and covers the fiber surface, the weaving raw material of the aramid woven fabric is aramid monofilament subjected to first resin impregnation pretreatment, the first and second resins are both thermosetting resins, the first resin comprises a first compound, the first compound contains a morpholine ring and is bonded in a crosslinking network of the first resin, and the second functional layer is a dynamic crosslinking polymer layer. Compared with the prior art, the application can not only resist impact and be hard, but also absorb impact force and reduce the risk of blunt injury of personnel.

The application relates to a method for continuously preparing imidacloprid intermediate 3-methyl-2-(4-morpholinyl)cyclobutyl acid methyl ester, and the specific steps are as follows: raw material morpholinyl propylene and methyl acrylate are respectively introduced into a preheater, then the preheated raw materials are pumped into a micro-channel reactor for reaction, after the reaction is completed, the materials are discharged from the micro-channel reactor outlet into a reaction kettle, reaction is carried out, then the cyclization liquid obtained in the reaction kettle is subjected to light removal in a light removal tower, 3-methyl-2-(4-morpholinyl)cyclobutyl acid methyl ester after light removal is collected from the tower kettle of the light removal tower, the 3-methyl-2-(4-morpholinyl)cyclobutyl acid methyl ester is introduced into a pentyl ester synthesis process, and the recovered methyl acrylate collected from the top of the light removal tower is reused in the reaction kettle to participate in the ripening reaction. The application has the advantages of high product purity, low raw material unit consumption, good safety, low labor cost and the like.

The present invention relates to novel mesylate salt of N-(5-(4-(4-((dimethylamino)methyl)-3-phenyl-1H-pyrazol-1-yl)pyrimidine-2-ylamino)-4-methoxy-2-morpholinophenyl)acrylamide, a novel crystalline form thereof, and a process for preparing the same. More specifically, the present invention relates to mesylate salt of N-(5-(4-(4-((dimethylamino)methyl)-3-phenyl-1H-pyrazol-1-yl)pyrimidine-2-ylamino)-4-methoxy-2-morpholinophenyl)acrylamide, which is excellent in stability, solubility, and bioavailability when it is administered not only alone but also in combination with other drugs and which has a high purity, a crystalline form thereof, and a process for preparing the same.

The invention discloses a high-activity BODIPY type photosensitizer targeting double organelles as well as a preparation method and application of the high-activity BODIPY type photosensitizer, and relates to the technical field of medical photosensitizers. The high-activity BODIPY type photosensitizer is prepared by the following steps: reacting 2, 4-dimethyl pyrrole with 4-bromobutyryl chloride to obtain a compound Br-BY containing carboxyl, then reacting with morpholine to obtain a morpholine substituted compound Mor-BY, and finally reacting with N-iodosuccinimide (NIS) to obtain a single atom I substituted BODIPY compound Mor-IBY, namely the target photosensitizer. The photosensitizer prepared by the invention can target mitochondria and lysosome in cancer cells at the same time, and can be excited by visible light; the compound has good water solubility, can generate a large amount of reactive oxygen species (ROS) under irradiation of green light (520 nm), shows excellent photodynamic activity to tumor cells, and has low toxicity to normal cells.

The application belongs to the technical field of compound synthesis, and particularly relates to an alpha-ketoamide derivative and a preparation method thereof, wherein the preparation method of the alpha-ketoamide derivative comprises the following steps: S1, first, a graphite carbon rod electrode and a platinum sheet electrode are respectively assembled on two sides of a 10mL three-port glass bottle; S2, then, a magnetic son is added into the three-port glass bottle, the bottle mouths on two sides are sealed, the three-port glass bottle is transferred to a glove box for feeding, and benzoylformic acid, morpholine and 10mol% of ferrocene in 4mL hexafluoroisopropanol are sequentially added; S3, after the feeding is completed, the last bottle mouth of the three-port glass bottle is sealed, and a constant current of 3mA is introduced for electrolysis. The application realizes the amination reaction of alpha-keto acid by using an electrocatalytic decarboxylation strategy, selectively synthesizes alpha-ketoamide derivatives, and the reaction is suitable for primary amine compounds, secondary amine compounds, is also suitable for aromatic and aliphatic alpha-keto acids, and excellent functional group tolerance is exhibited.

The present invention relates to compounds of formula (I) or pharmaceutically acceptable salts, solvates, adducts, polymorphs, isomers and derivatives thereof useful as orexin antagonists, their preparation, their use in pharmaceutical compositions, and methods of using orexin antagonists to treat or prevent diseases or conditions mediated by orexin receptor activity.

The invention relates to the technical field of medical chemistry and tumor treatment, in particular to application of a novel NOX4 inhibitor ZZU026 and derivatives thereof in tumor resistance and immune response change. The preparation method of the ZZU026 comprises the following steps: replacing N, N-dimethylamino on a benzene ring of GKT137831 with morpholinyl; methoxyl is introduced into the core skeleton. The ZZU026 has a remarkable inhibiting effect on NOX4, has the functions of inhibiting tumor growth, new vascularization and immune-related diseases, regulating and controlling polarization of macrophages and the like, and can inhibit phenotype transformation of macrophages from M1 to M2 and finally inhibit proliferation and immune escape of lung cancer cells; the ZZU026 and the derivatives thereof can be prepared into drugs, health care products, tablets, particles, capsules, oral liquid or injection, and can be used for treating lung cancer and other tumors.

The invention discloses a preparation method of a microbial preparation for preventing and treating powdery mildew of melons, which comprises the following steps: firstly preparing keratin microspheres, modifying the keratin microspheres with acryloylmorpholine, and compounding the modified keratin microspheres with mesoporous silica and an ethylene-vinyl alcohol copolymer to obtain a composite carrier; and finally, immersing the carrier into a mixed bacteria solution of ceriporia lacerata, bacillus velezensis and bacillus agave for adsorption and drying. Stable immobilization of strains is achieved through multiple interactions, a protective film can be formed on the surfaces of leaves through illumination after the preparation is sprayed, pathogenic bacteria are physically prevented from being attached and infected, and the fungicide can be intelligently released along with the change of environment humidity; the three strains have a synergistic effect to efficiently prevent and control powdery mildew pathogenic bacteria of melon crops by preempting sites, degrading pathogenic bacteria structures, secreting antibacterial substances and inducing plant immunity, meanwhile, the utilization efficiency and quality of crop nutrients are improved, and the application prospect is good.

The invention discloses a CO2 phase change absorbent based on N-formylmorpholine as well as a preparation method and application thereof, and belongs to the technical field of gas separation. The CO2 phase change absorbent based on N-formylmorpholine is prepared from the following components in percentage by mass: 30 to 40 percent of hydroxyethyl ethylenediamine, 30 to 40 percent of N-formylmorpholine and 27 to 37 percent of water, or 35% of compound amine composed of hydroxyethyl ethylenediamine and N-methylethylamine, 40% of N-formylmorpholine and 25% of water are contained. The preparation method of the CO2 phase change absorbent comprises the following steps: preparing the components in proportion, and uniformly mixing to obtain the CO2 phase change absorbent. The CO2 phase change absorbent is suitable for carbon capture of mixed gas with CO2 partial pressure of 10-20 kPa. The CO2 phase change absorbent can effectively reduce the volatility of the phase change absorbent and the CO2 enrichment phase viscosity, and has a good industrial application prospect.

The name of the invention is a method for preparing derivatives of substituted morpholines. Provided herein are methods of preparing derivatives and prodrugs of substituted morpholines, or pharmaceutically acceptable salts thereof. Methods of preparing substituted morpholine derivatives and prodrugs having the following chemical structure are also provided.

This invention relates to a method for preparing a broadband absorption hydrogel. The method comprises the following steps: S1, mixing solvent A (N,N-dimethylformamide or acetonitrile) with deionized water to obtain a mixed solvent; S2, adding polyethylene glycol methyl ether acrylate-480 and acryloylmorpholine to the solvent in S1 and dissolving them to obtain a mixed solution; S3, removing dissolved oxygen from the mixed solution in S2, sealing the container, and stirring under ice bath conditions; S4, adding potassium persulfate and N,N,N',N'-tetramethylethylenediamine to the mixed solution after stirring in S3, and sealing the container again; S5, completing the polymerization reaction in the container at 60 °C to obtain the hydrogel. Compared with the prior art, the hydrogel material provided by this invention has improved reflection loss intensity and effective absorption bandwidth performance, thus providing a new perspective for developing highly flexible and efficient electromagnetic wave absorbers.

The application discloses an anticoagulant biomaterial for blood purification and a preparation method and application thereof, and comprises the following steps: providing an amphiphilic copolymer P(AA-MMA); blending polyethersulfone, P(AA-MMA) and a solvent, stirring at a set temperature to obtain a casting solution, and preparing a blending membrane from the casting solution; soaking the blending membrane in a 2-morpholine-4-yl ethanesulfonic acid buffer solution containing argatroban, 1-ethyl-(3-dimethylaminopropyl) carbonyl diimide and hydroxy succinimide, and reacting at room temperature to obtain an argatroban grafted blending membrane, namely the anticoagulant biomaterial. The method improves the hydrophilicity of the membrane, reduces the albumin adsorption of the membrane, reduces the adhesion of platelets on the membrane, prolongs the coagulation time APTT, PT and TT of the membrane, and is better in biocompatibility and enhanced in anticoagulation performance.