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80 results about "Isopropyl methyl ketone" patented technology

3-Methyl-2-butanone (methyl isopropyl ketone, MIPK) is a ketone and solvent of minor importance. It is comparable to MEK (Methyl ethyl ketone), but has a lower solvency and is more expensive. "NIOSH Pocket Guide to Chemical Hazards #0424". National Institute for Occupational Safety and Health (NIOSH).

Room temperature vulcanizable polymers

A room-temperature vulanizable (RTV) polymeric composition comprising organosiloxane or polyurethane units having at least one terminal methyl isopropyl ketoximino or methyl propyl ketoximino moiety, as well as methods of making the same.
Owner:NITROCHEM ASCHAU

Method for synthesizing methyl isopropyl ketone

The invention relates to a method for synthesizing methyl isopropyl ketone, which is characterized in that rare earth oxides are loaded on an aluminum oxide, titanium oxide or titanium-aluminum compound carrier to be used as a synthesis catalyst, wherein rare earth elements in the rare earth oxides are lanthanum, cerium, praseodymium and neodymium, the loading capacity of the rare earth metals is 3-20%, and the molar ratio of titanium to aluminum in the carrier is 0.2-0.5. A preparation method of the catalyst comprises the following steps of: weighing a certain amount of nitrates of rare earth metal oxides to prepare a uniform solution; then, adding a certain amount aluminum oxide, titanium oxide or titanium-aluminum compound carrier into the solution, and impregnating for 5-10h at 25 DEG C; vacuumizing and drying for 3-6h at 120 DEG C, and roasting for 4-8h at 450-700 DEG C in a muffle furnace to obtain the catalyst. Methyl isopropyl ketone is synthesized by using isobutyric acid and acetic acid as synthesis raw materials under the conditions that the reaction temperature is 420-440 DEG C and the liquid hourly space velocity is 0.5-0.8 g.g<-1>.h<-1>, and the molar ratio of isobutyric acid to acetic acid is 0.8-1.2:1. The reaction process is as follows: a raw material mixture is pumped into a fixed bed reactor through a charging pump, and the content of the products is analyzed by using gas chromatography after the raw material mixture reacts in a catalyst bed.
Owner:CHINA NAT OFFSHORE OIL CORP +1

Method for synthesizing (E,E) Geranyl linalool

This invention relates to synthetic method of a ( E, E) - geranyl linalool. The invention takes (E) - nerolidol as raw material. The hydroxyl is shield by dihydropyrane, gain ( E) - nerolidol tetrahydropyrane aether; selenium dioxide and teri-butyl hydroperoxide selectively oxidize the anti-form methyl of ( E) - nerolidol tetrahydropyrane aether to gain anti-form allyl position hydroxylated oxidative product ( E, E) - 12 - hydroxy nerolidol tetrahydropyrane aether, transit halogenating reaction to gain ( E, E) - 12 - halogeno- nerolidol tetrahydropyrane aether, then take reaction with isopropyl methyl ketone that is selectively divested one proton by diisopropyl amido lithium, generate ( 6E, 10E) - 2, 6, 10, 14 - tetramethyl - 14 - ( tetrahydropyrane - 2 - oxygen) -16 - 6, 10, 15 - triene - 3 - ketone, use sodium borohydride to reduce to gain ( 6E, 10E) - 2, 6, 10, 14 - tetramethyl - 14 - ( tetrahydropyrane - 2 - oxygen) -16 - 6, 10, 15 - triene - 3 - alcohol, takes reaction with sulfonyl chloride or sulphonic acid ester with alkali presence to gain ( 6E, 10E) - 2, 6, 10, 14 - tetramethyl - 14 - ( tetrahydropyrane - 2 oxygen) -16 - 6, 10, 15 - triene - 3 - alcoholic sulphonic acid ester, then divide sulphonic acid ester group under base catalysis to gain ( E, E) - geranyl linalool tetrahydropyrane aether, and by deprotection to gain ( E, E) - geranyl linalool. ˕For the configuration of ( E) - nerolidol 3 position tertiary carbon is not influenced in the course of reaction, if use ( E) - nerolidol that has optical activity as raw material, should gain optical active ( E, E) - geranyl linalool. ((E, E)-geranyl linalool can replace Teprenone and such type medicament intermediate, natural product intermediate, insect pheromone and spice etc.
Owner:CHENGDU UNIVERSITY OF TECHNOLOGY

New synthetic method for (earth)4-fluor-alpha-(2-methyl-1-oxypropyl )-gamma-oxo-N, beta-diphenyl benzene butanamide

The invention discloses a method for preparing an intermediate product of an Atorvastatin medicine. The isobutyrylacetanilide utilized in the prior method has low yield coefficient, expensive raw materials and high industrial cost. The method comprises the following steps that: 4- fluorophenyl benzyl ketone is obtained by performing the Friedel-Crafts reaction on phenylacetyl chloride and fluorobenzene which are catalyzed by aluminium chloride; methyl isopropyl ketone reacts with dimethyl carbonate or diethyl carbonate in an inert solvent with sodium hydrosulfate as catalyst to produce methyl 4-methyl-3-Oxopentanoate or ethyl isobutyrylacetate; next, the methyl 4-methyl-3-Oxopentanoate or the ethyl isobutyrylacetate reacts with aniline to produce isobutyrylacetanilide; carbon-based alpha position of the 4-fluorophenyl benzyl ketone is chloridized in the solvent to produce alpha-chlorine-4-fluorophenyl benzyl ketone; afterwards, the alpha-chlorine-4-fluorophenyl benzyl ketone reacts with the isobutyrylacetanilide in the action of alkali. The process for synthesizing isobutyrylacetanilide has short flow, the yield coefficient is high, and the cost is low, thereby improving the total yield of reaction directly.
Owner:ZHEJIANG JINGXIN PHARMA

Multi-purpose paint diluting agent and preparation technology thereof

The invention discloses a multi-purpose paint diluting agent and a preparation technology thereof. The multi-purpose paint diluting agent is prepared from the following raw materials: ethylene glycolmonoethyl ether acetate, dichloropropane, pentaerythritol, cyclohexanone, tetrabutyl orthosilicate, ethyl cellosolve, diethoxymethane, methyl isopropyl ketone, turpentine and isophoron. The paint diluting agent prepared by the preparation technology does not contain benzene toxic substances, is safe and has no toxin, and has good stability and strong dissolubility; various types of paint can be dissolved through the multi-purpose paint diluting agent; the production flow is simple, the production cost is low and no three wastes are discharged, so that the multi-purpose paint diluting agent hasa good application prospect.
Owner:韩立志

Synthesis method of 2-[2-(4-fluorophenyl)-2-oxa-1-phenylethyl]-4-methyl-3-oxa-N-phenylpentanamide

The invention discloses a synthesis method of 2-[2-(4-fluorophenyl)-2-oxa-1-phenylethyl]-4-methyl-3-oxa-N-phenylpentanamide. The method is characterized by comprising the following steps: firstly preparing methyl isobutyryl acetate from toluene, sodium hydride, dimethyl cabonate, methyl isopropyl ketone and the like as raw materials; then preparing isobutyryl acetanilide from toluene, methyl isobutyl acetate, HCl, sodium bicarbonate and the like as raw materials; preparing 4-fluorophenylacetophenone from aluminium choride, phenylacetyl chloride and the like as raw materials; preparing 2-chloro-1-(4-fluorophenyl)-acetophenone from 4-fluorophenylacetophenone, dichloromethane, chlorine and the like as raw materials; and finally preparing the finished product from isobutyryl acetanilide, potassium carbonate and 2-chloro-1-(4-fluorophenyl)-acetophenone. The raw materials of the synthesis method are inexpensive and easily available, the reaction has five steps and the yield of each step is high, thus the production cost can be greatly reduced; and the reaction conditions are mild, the method can be controlled easily, the process is simple, the pollution is low and the method is suitable for industrial production.
Owner:LIANYUNGANG HONGYE CHEM

Preparation method of safinamide mesilate A1 crystal form

The invention relates to a preparation method of safinamide mesilate A1 crystal form. The preparation method comprises following steps: methane sulfonic acid is reacted with safinamide at a certain temperature, cooling is carried out, and an obtained reaction liquid is subjected to crystallization at 10 to 30 DEG C, wherein one ingredient selected from acetone, butanone, methyl isobutyl ketone, methyl isopropyl ketone, cyclohexanone, and acetic acid isopropyl ester is taken as a reaction and crystallization solvent, and unexpected crystallization effect is achieved. The maximum yield of the prepared safinamide mesilate A1 crystal form can be higher than 99%, purity is 99.9% or higher in HPLC, impurity content is less than 0.01%, and optical isomer content is less than 0.05%.
Owner:ZHEJIANG MENOVO PHARMA

Method for continuously synthesizing methyl isopropyl ketone

ActiveCN112159317APrecise control of input ratioInput ratio controlOrganic compound preparationCarbonyl compound preparationIsopropylEngineering
The invention provides a method for continuously synthesizing methyl isopropyl ketone. The methyl isopropyl ketone is continuously synthesized in n stages of reaction kettles which are sequentially connected in series. According to the method disclosed by the invention, the purity of the prepared methyl isopropyl ketone reaches 99% or above, and the yield is 73-78%. According to the method, continuous industrial production of methyl isopropyl ketone can be achieved, manual participation operation is reduced, the operation cost is reduced, the raw material input proportion, the raw material input amount and the reaction time can be accurately controlled, automatic control can be achieved, and the industrial production process is safer, more environmentally friendly and more reliable.
Owner:山东智永化工产业技术研究院有限公司

Preparation method of underwater LED lamp pouring sealant

The invention discloses a preparation method of an underwater LED lamp pouring sealant. The method includes: firstly carrying out stiring hydrolysis condensation polymerization on multifunctional epoxy alkyl alkoxy silane, alkoxy silane, methyl isopropyl ketone and triethylamine, then performing pressure reduced distillation to obtain a component A; stirring phenyl trimethyloxysilane and trifluoromethanesulfonic acid at room temperature to obtain a methyl phenyl siloxane oligomer containing an Si-OH group, and mixing the oligomer with an Al catalyst and an azo compound to obtain a component B; and finally mixing the component A with the component B according to a weight ratio of 3:1-5:1 and stirring them evenly, carrying out decompression and bubble removal, and performing curing, thus obtaining the underwater LED lamp pouring sealant. The sealant for LED lamp packaging obtained by the method provided by the invention has good water proofness and high light transmittance, good adhesive power, toughness and plasticity, and can effectively improve the service life of LED lamps.
Owner:GOLOHO TECH CHANGZHOU CO LTD

Method for preparing 3,4-dimethylpyrazole and phosphate and metal organic complex thereof

The invention discloses a method for preparing 3,4-dimethylpyrazole and phosphate and metal organic complex thereof. The method for preparing the 3,4-dimethylpyrazole comprises the steps that (1) isoprene is in contact with water under the action of a catalyst to obtain methyl isopropyl ketone; (2) the methyl isopropyl ketone is in contact with hydrazine hydrate under the action of sulfuric acid and iodide to obtain the 3,4-dimethylpyrazole. The method for preparing the 3,4-dimethylpyrazole has the advantages that the isoprene is taken as a raw material, the preparation method is simple, and the yield and purity of the product are high.
Owner:SINOCHEM AGRI LINYI R&D CENT CO LTD
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