107 results about "4-Hydroxybenzoic acid" patented technology

A wholly aromatic polyester amide liquid crystal resin including repeating units of: (I) a 6-hydroxy-2-naphthoic acid residue: 1 to 15 mol %, (II) a 4-hydroxybenzoic acid residue: 40 to 70 mol %, (III) an aromatic diol residue: 5 to 28.5 mol %, (IV) a 4-aminophenol residue: 1 to 20 mol %, and (V) an aromatic dicarboxylic acid residue: 6 to 29.5 mol %, and having a melting point of 270° C. to 370° C., and having a melt viscosity of 60 Pa.s to 200 Pa.s at a shear rate of 1000 / sec at a temperature higher by 10° C. to 20° C. than this melting point is molten at a temperature of the melting point +40° C., and extruded at a rate of 0.3 kg / min or more and less than 5 kg / min to form a parison. A pair of molds arranged with the parison interposed there between are closed under a prescribed mold closing pressure, so that air is blown into the interior of the parison.

New polymers and new anti-reflective compositions containing such polymers are provided. The compositions comprise a polymer (e.g., epoxy cresol novolac resins) bonded with a chromophore (4-hydroxybenzoic acid, trimellitic anhydride). The inventive compositions can be applied to substrates (e.g., silicon wafers) to form anti-reflective coating layers having high etch rates which minimize or prevent reflection during subsequent photoresist exposure and developing.

The invention relates to a new method for synthesizing 3-cyclopropyl methoxy-4-(difluoromethoxy) benzoic acid. The method is characterized by taking 3-nitro-4-hydroxybenzoic acid ester as the raw material to obtain the 3-cyclopropyl methoxy-4-(difluoromethoxy) benzoic acid through alkylation, reduction, diazotization, hydrolysis, alkylation, deprotection and the like. The 3-cyclopropyl methoxy-4-(difluoromethoxy) benzoic acid is a key intermediate for synthesizing the drug roflumilast.

A thermal sensitive recording medium which has a feature to change the color of recorded pattern slowly and spontaneously after development, and the recorded pattern which has several days passed can be easily distinguished from that of just after development. Said thermal sensitive recording medium contains 4-hydroxybenzoic acid ester represented by general formula (I) as a color developer and uses triphenylmethane-based leuco dye and reddish color developing leuco dye whose maximum absorption wave length is 450 DIFFERENCE 560 nm as a dye precursor. In this formula, R represents unsubstituted or substituted lower alkyl group of carbon number 1-7 or benzyl group.

The present invention is to provide an amorphous wholly aromatic polyester amide composition which has an excellent stretching property and a good adhesion to a heterogeneous polymer and thereby can be in particular suitably used for a multilayer film, or a multilayer sheet, a multilayer blow formed product and the like. That is, (the first invention) an amorphous wholly aromatic polyester amide composition obtained by blending 1 to 30% by weight of a modified polyolefin resin or a polyamide resin having a melting point of 230° C. or lower or being amorphous with an amorphous wholly aromatic polyester amide exhibiting an optical anisotropy at softening and flowing and being a wholly aromatic polyester amide obtained by copolymerizing (A) 4-hydroxybenzoic acid, (B) 2-hydroxy-6-naphthoic acid, (C) an aromatic aminophenol and (D) an aromatic dicarboxylic acid, wherein (1) the ratio of (C) the aromatic aminophenol is from 7 to 35% by mol, (2) the ratio of the bending monomer(s) among the starting monomers is from 7 to 35% by mol, (3) the ratio ((A) / (B)) between (A) 4-hydroxybenzoic acid and (B) 2-hydroxy-6-naphthoic acid is from 0.15 to 4.0, (4) the ratio of isophthalic acid is at least 35% by mol in (D) the aromatic dicarboxylic acid, (5) any melting point is not found by DSC measurement at a temperature rising rate of 20° C. / min and (6) the glass transition temperature is from 100 to 180° C., and (the second invention) an amorphous wholly aromatic polyester amide composition obtained by blending 1 to 30% by weight of a modified polyolefin resin or a polyamide resin having a melting point of 230° C. or lower or being amorphous with an amorphous wholly aromatic polyester amide exhibiting optical anisotropy at softening and flowing and being a wholly aromatic polyester amide obtained by copolymerizing (A) 4-hydroxybenzoic acid, (B) 2-hydroxy-6-naphthoic acid, (C)′ an aromatic diamine and (D) an aromatic dicarboxylic acid, wherein (1) the ratio of (C)′ the aromatic diamine is from 3 to 15% by mol, (2) the ratio of the bending monomer(s) is from 7 to 35% by mol in the starting monomers, (3) the ratio ((A) / (B)) between (A) 4-hydroxybenzoic acid and (B) 2-hydroxy-4-naphthoic acid is from 0.15 to 4.0, (4) any melting point is not found by DSC measurement at a temperature rising rate of 20° C. / min and (5) the glass transition temperature is from 100 to 180° C.

The invention provides a preparing method for 3,5-bis(tertiary butyl)-4-hydroxybenzoic acid hexadecane alkyl ester. The preparing method comprises the steps that 3,5-bis(tertiary butyl)-4-hydroxybenzoic acid, cetyl alcohol and a catalyst are added into a reaction vessel, flow of inert gas is introduced, a heat-preserving reaction is carried out at the temperature of 80 DEG C-160 DEG C, TLC tracks and monitors the reaction till the reaction endpoint, and reaction liquid is subjected to after-treatment to obtain 3,5-bis(tertiary butyl)-4-hydroxybenzoic acid hexadecane alkyl ester. By means of the preparing method, it is unnecessary to adopt other solvent, production cost is saved, and waste gas exhaustion of organic solvent is avoided in the synthesis process; the inert gas serves as a water-carrying agent and a protective agent, operation and control are simple, production safety is good, the color of products is improved, and the method has remarkable economic benefits and has remarkable environmental protection significance.

The present invention relates to new substance combinations as vapor phase corrosion inhibitors for protecting a broad range of customary utility metals, including iron, chromium, nickel, tin, zinc, aluminum, copper, magnesium and their alloys, against corrosion in humid climates. Said substance combinations comprise (1) at least one C6 to C10 aliphatic monocarboxylic acid, (2) at least one C6 to C10 aliphatic dicarboxylic acid, and (3) a primary aromatic amide. Preferably they further comprise (4) an aliphatic ester of hydroxybenzoic acid, in particular of 4-hydroxybenzoic acid, and / or (5) a bemzimidazole, in particular a benzimidazole substituted on the benzene ring.

The invention relates to the field of drug synthesis and in particular relates to a method for preparing benzbromarone. The method for preparing benzbromarone is characterized by comprising the steps of carrying out an acetylation reaction, a Friedel-Craft reaction, a hydrolysis reaction and the like to prepare the benzbromarone by using 3,5-dibromo-4-hydroxybenzoic acid and 2-ethyl benzofuran as raw materials. The preparation method disclosed by the invention has the advantages of being simple and safe to operate, convenient for post-treatment, high in product purity, low in economic cost, small in environment pollution, easier to realize industrialization and the like.

The present invention provides a fully aromatic polyester that can be produced in a normal polymerization device and that has superior heat resistance and ductility. The fully aromatic polyester comprises: a constituent unit (I) derived from 4-hydroxybenzoic acid; a constituent unit (II) derived from 6-hydroxy-2-naphthoic acid; a constituent unit (III) derived from 1,4-phenylene dicarboxylic acid; a constituent unit (IV) derived from 1,3-phenylene dicarboxylic acid; and a constituent unit (V) derived from 4,4'-dihydroxybiphenyl. The fully aromatic polyester exhibits optical anisotropy when melted and, with respect to all the constituent units, there are 35-75 mol% of constituent unit (I), 2-8 mol% of constituent unit (II), 4.5-30.5 mol% of constituent unit (III), 2-8 mol% of constituent unit (IV), 12.5-32.5 mol% of constituent unit (V), and 4-10 mol% of constituent units (II)+(IV).

PCT No. PCT / US97 / 00068 Sec. 371 Date Jun. 25, 1998 Sec. 102(e) Date Jun. 25, 1998 PCT Filed Jan. 2, 1997 PCT Pub. No. WO97 / 25363 PCT Pub. Date Jul. 17, 1997A thermotropic liquid crystalline polymer constituted of repeat units derived from hydroquinone, terephthalic acid, isophthalic acid, 2,6-naphthalene dicarboxylic acid, and 4-hydroxybenzoic acid, all present in defined amounts. Such polymer has excellent physical properties and high temperature stability. It is suitable as a molding resin.

To provide an easily-manufactured liquid-crystalline polymer having high thermal conductivity, as well as a molded article that is formed of the liquid crystalline polymer and has a property of being highly mechanical. A liquid-crystalline polymer is used that is formed by polymerizing monomers having an asymmetrical molecular structure, in which the enthalpy of fusion ΔH measured by way of DSC (Differential Scanning calorimetry) is greater than or equal to 2.5 J / g (joules per gram) and less than or equal to 10 J / g, and the inherent viscosity (I.V.) is greater than or equal to 5 dl / g and less than or equal to 7 dl / g. It is preferable for the monomer having asymmetrical molecular structure to be at least one selected from a group consisting of 4-hydroxybenzoic acid (HBA), 6-hydroxy-2-naphthoic acid (HNA), N-acetyl-p-aminophenol (APAP), and 4-hydroxy-4′-biphenylcarboxylic acid (HBCA).

Provided is a method for efficiently producing a 3-amino-4-hydroxybenzoic acid-type compound by culturing a coryneform bacterium that has a gene encoding a mutated aspartokinase not subject to feedback inhibition, and that is transformed with a recombinant vector containing a DNA encoding a protein having an activity to form 3-amino-4-hydroxybenzoic acid from dihydroxyacetone phosphate and aspartate semialdehyde.

The invention discloses a production method of 3,5-di-tert-butyl-4-hydroxybenzoic acid. The production method sequentially comprises the steps as follows: 2,6-di-tert-butylphenol, a potassium hydroxide aqueous solution and toluene are added to a reactor under protection of nitrogen to be subjected to a reflux reaction under a water distribution condition; CO2 is introduced into the reactor until the pressure is 0.1-3.0 MPa, a Kolbe-Schmitt reaction is conducted under a pressure holding condition, after the reaction, corresponding aftertreatment is carried out, and a crude product of 3,5-di-tert-butyl-4-hydroxybenzoic acid is obtained. The method has short reaction time and high conversion rate, has obvious advantages as compared with traditional gas-solid processes and existing solvent-process synthesis processes and is suitable for further industrialization.

The invention discloses a halogenated benzoic acid degradation strain, an inoculant produced by the strain and an application. The halogenated benzoic acid degradation strain H8 is preserved in ChinaCenter for Type Culture Collection on April 28, 2017 with preservation number of CCTCC NO.M2017222. The invention provides the halogenated benzoic acid degradation inoculant which is produced by the halogenated benzoic acid degradation strain H8. The bacterium H8 provided by the invention can be used for effectively and rapidly degrading halogenated benzoic acid. The degradation strain H8 has a relatively wide degradation spectrum and is capable of degrading such halogenated aromatic hydrocarbon as 3,5-dibromo-4-hydroxybenzoic acid, 3-bromo-4-hydroxybenzoic acid, 3,5-dichloro-4-hydroxybenzoicacid, 3-chloro-4-hydroxybenzoic acid and the like. The halogenated benzoic acid degradation strain can be used for conditioning halogenated benzoic acid pollution.

The liquid crystal polymer (LCP) material contains in its chain structure repeated units introducing by p-hydroxybenzoic acid, hydroquinol, mixed aromatic acid, terephthalic acid and 4, 4'-diphenyl diformic acid. Adding small amount of 4, 4'-diphenyl diformic acid in certain range can lower the smelting point of LCP to expand its processing temperature window; lower the rate and melt viscosity of its late sage polymerization for easy control; and raise its toughness. In some composition range, the processing temperature window has its width increased with the increasing molar content of p-hydroxybenzoic acid and terephthalic acid.

Liquid crystalline polymer having repeat units derived from 4,4'-biphenol, terephthalic acid, 2,6-naphthalenedicarboxylic acid, and 4-hydroxybenzoic acid in a limited compositional range have melting points of 400° C. or more, and are useful for molded articles and for films, particularly for uses where good high temperature resistance is needed.

The invention discloses high-temperature-resistant polyester lubricating oil base oil and a preparation method thereof, and belongs to the field of fine chemical engineering. The base oil is preparedfrom 1,3,5-cyclohexane trimethyl alcohol, diethyl fluoromalonate, 12-benzoyl stearic acid, 2,2-difluoropropionic acid, 3-fluoro-4-hydroxybenzoic acid, perfluoroheptanoic acid and tris(trimethylsilyl)phosphate; fluorine-contained carboxylic acid and the 1,3,5-cyclohexane trimethyl alcohol with high heat resistance are used as main raw materials, the 12-benzoyl stearic acid and the 3-fluoro-4-hydroxybenzoic acid are introduced to adjust the viscosity index of the base oil, and the tris(trimethylsilyl) phosphate is used as a high-temperature-resistant antioxidant; through fluorinated compounds in the raw materials, the high temperature resistance and the carbon deposition resistance of the product are guaranteed. The preparation method has the advantages that the raw materials are easy to obtain, and the method is simple and convenient to operate; the prepared lubricating oil base oil has good high-temperature resistance, a moderate viscosity index, good lubricating performance and wearresistance, can be applied to lubrication of most automotive engines, and is especially applicable to high temperature environments.

The invention relates to compositions and co-crystals each comprising VX-950 and a co-crystal former selected from the group consisting of 4-hydroxybenzoic acid, 4-amino salicylic acid, phenylalanine, threonline, tartaric acid, adipic acid, succinic acetate, proline, methyl 4-hydroxybenzoate, anthranilic acid, and d-Biotin. Also within the scope of this invention are methods of making and using the same.

The invention discloses a method for synthesizing 3-geranyl-4-hydroxybenzoic acid and xiamenmycin by utilizing escherichia coli. According to the method, an adopted escherichia coli strain contains xiamenmycin synthesis related genes and mevalonic acid pathway related genes which are partially or entirely subjected to codon optimization; three genes required by synthesis of the xiamenmycin are imported into the escherichia coli; the three genes are subjected to inducible expression, and GBA and the xiamenmycin are synthesized in the escherichia coli; the feed of intracellular geranyl pyrophosphate of the escherichia coli is further improved by introducing a mevalonic acid synthesis pathway, and the yield of the GBA is further increased by adding 4-hydroxybenzoic acid into a fermentation medium; the yield of the synthesized 3-geranyl-4-hydroxybenzoic acid reaches 94 mg / L, and the yield of the xiamenmycin reaches 11 mg / L; and the biosynthesis of the 3-geranyl-4-hydroxybenzoic acid and the xiamenmycin in the escherichia coli is realized for the first time.

The invention discloses a method for preparing 4-hydroxybenzoyl chloride. The method comprises the following steps: (1) adding 4-hydroxybenzoic acid, a benzene solvent and N,N-dimethyl formamide as an cosolvent into a container, heating up to 30-65 DEG C while stirring, slowly and dropwise adding thionyl chloride for 0.5 to 1 hour and reacting at 30 to 65 DEG C for 2 to 5 hour; (2) standing to demix the reaction solution; and (3) respectively recovering thionyl chloride, benzene and N,N-dimethyl formamide respectively by distilling and distilling under the reduced pressure, and concentrating the benzene layer solution to separate viscose solid (4-hydroxybenzoyl chloride). The method is simple and reliable, and by adopting the method, 4-hydroxybenzoyl chloride with high purity and high yield can be obtained without need of the reduced pressure distillation.

An immediate release formulation of an active ingredient, wherein the active ingredient is a co-crystal of VX-950 and a 4-hydroxybenzoic acid.

The invention provides application of Bacillus in degrading aromatic compounds, belonging to the technical field of microbes. The experiment proves that the Bacillus L1 strain has the capacity for degrading 3,4-dihydroxybenzoic acid, 3-methoxy-4-hydroxybenzaldehyde, catechol and other environmental pollutants; the degradation rates for para-hydroxybenzoic acid, 3,4-dihydroxybenzoic acid, 2,5-dihydroxybenzoic acid, 3-methoxy-4-hydroxybenzoic acid, 3-methoxy-4-hydroxybenzaldehyde, catechol and benzoic acid with the concentration of 500 mg / L can respectively reach 90% or above; and thus, the Bacillus L1 strain has wide application prospects in the aspect of environmental treatment.

The invention discloses a method for catalytic synthesis of 3,5-ditertbutyl-4-hydroxybenzoic acid n-hexadecyl ester by acidic ionic liquid, and belongs to the field of chemical industry. By adoption of the method, the problems of complex process flow, troublesome aftertreatment and pollution to the environment of the existing method are solved. The method comprises the following steps: by utilizing acidic dual-core functional ionic liquid as a catalyst, and adopting 3,5-ditertbutyl-4-hydroxybenzoic acid and n-hexadecyl alcohol as raw materials, utilizing vacuumization for dewatering, controlling reaction temperature to be 100-160 DEG C and reacting for 3-8 hours, after reaction is ended, cooling, and standing for layering, separating out a lower layer namely ionic liquid to repeatedly usethe same; pouring an upper layer into methanol solution to generate a large amount of crystals, and filtering to obtain filter cakes, namely a target product. The method disclosed by the invention adopts the ionic liquid as a pollution-free catalyst and shows the advantages of high efficiency, high selectivity, mild reaction condition, simple and controllable effects, environment friendliness, high catalytic efficiency, simple aftertreatment and the like in various acid catalytic reactions.