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33 results about "Pentylamine" patented technology

1-Aminopentane is a organic compound with the formula CH₃(CH₂)₄NH₂. It is used as a solvent, as a raw material in the manufacture of a variety of other compounds, including dyes, emulsifiers, and pharmaceutical products, and as a flavoring agent.

Preservative composition

The invention relates to a preservative composition. The preservative composition comprises the following substances: a) one or multiple cell protective agents; b) one or multiple inhibitors; c) one or multiple chelate stabilizers; and d) one or multiple acid-base buffer solutions, wherein the cell protective agent is one or more than one of allantoin, 5,5-dimethyl hydantoin and oxazolidine, the inhibitor is one or more than one of N-acetic acid methylenimine and N-(3-acetic acid-amylamine), the chelate stabilizer is one or more than one of ethylenediaminotetraacetate, oxalate, heparinate and citrate, and the acid-base buffer agent can be glycine-sodium hydroxide-hydrochloride buffer solution. The preservative composition provided by the invention can be used for preserving a product preparation or a biological sample for a long time at normal temperature, the preservative system does not contain free aldehydes, is safer and more reliable and is beneficial to maintaining of nucleic acid completeness in the product preparation and the biological sample, and aldehyde detection accuracy is guaranteed.
Owner:广州维帝医疗技术有限公司

Synthetic method of 5-(N-ethyl-N-2-ethylol amine)-2-amylamine

The invention discloses a synthetic method of 5-(N-ethyl-N-2-ethylol amine)-2-amylamine. The method comprises the following steps: (1) the preparation of a catalyst, to be specific, dispersing and dissolving nitrate into an organic solvent, adding oxide or nanopowder of carbonate into the organic solvent, after ultrasonic stirring, evaporating the organic solvent to dryness, carrying out vacuum drying and grinding the dried solvent into fine powder to obtain the catalyst; (2) adding xylene, 5-chlorine-2-pentanone and N-ethylethanolamine in a reaction flask in sequence, stirring the materials, adding the prepared catalyst, heating the flask to increase the temperature till reflux occurs, cooling the heated materials to room temperature, filtering the materials to obtain a filtrate, fractionating the filtrate to obtain 5-(N-ethyl-N-2-ethylol amine)-2-pentanone; (3) putting 5-(N-ethyl-N-2-ethylol amine)-2-pentanone in a hydrogenation flask, adding aminomethanol and raney nickel to perform reaction under hydrogen pressure; after the reaction, displacing the hydrogen and ammonia in the system with nitrogen, filtering the reaction liquid to obtain a filtrate, fractionating the filtrate to obtain 5-(N-ethyl-N-2-ethylol amine)-2-amylamine. The method is high in conversion rate, simple and convenient to operate, high in yield, low in cost, easy for industrial production, safe and environment-friendly.
Owner:WUHAN RUIKAIXING SCI & TECH

Method for preparing pendimethalin by aminating dimethyl dinitroanisole

The invention relates to a method for preparing pendimethalin by aminating dimethyl-dinitro anisole. The method comprises the following concrete steps of: firstly, mixing, heating and refluxing 3,4-dimethyl-2,6-dinitroanisole, catalyst and excessive 3-pentyl amine for carrying out aminating reaction to generate N-(1-ethyl propyl)-3,4-dimethyl-2,6-dinitraniline; and secondly, distilling and reclaiming the unreacted 3-pentyl amine, cooling residues, and dissolving the cooled residuces with absolute ethanol, filtering to remove the catalyst and other insoluble substances, then removing ethanol to obtain 98 percent pendimethalin raw drug with the yield over 92 percent. Compared with the traditional synthetic production process of the pendimethalin raw drug, the preparation method not only has high yield, favorable quality and less wastewater, but also more importantly puts an end to the generation of N-nitrosamine substances in the pendimethalin raw drug.
Owner:乐斯化学有限公司

Preparation method of 1, 4-dimethyl pentylamine hydrochloride

The invention discloses a preparation method of 1, 4-dimethyl pentylamine hydrochloride, and relates to the field of organic synthesis preparation chemistry. The preparation method comprises the following steps: by taking 5-methyl-2-hexanone as a raw material, adding a reducing agent formic acid and ammonium formate or formamide while stirring, mixing, heating to 110-115 DEG C, reacting for 3 hours, heating to 130-135 DEG C, reacting for 3 hours, finally heating to 150-160 DEG C, keeping the temperature for 3 hours, cooling, standing for layering, washing, drying, and performing suction filtration to obtain the 1, 4-dimethyl formyl amyl amine; and adding 1, 4-dimethyl formyl pentylamine into hydrochloric acid with the mass concentration of 36%, carrying out heating reflux reaction under stirring, carrying out reduced pressure distillation, performing standing for layering, collecting a lower-layer material, carrying out suction filtration, and carrying out crystallization and drying, thereby obtaining the 1, 4-dimethyl formyl pentylamine. The preparation method of the 1, 4-dimethyl pentylamine hydrochloride provided by the invention is simple, the raw materials are easy to obtain, the process is easy to control, the cost is low, and the preparation method has the characteristics of high yield, clean production, environmental protection and the like, and is suitable for mass production.
Owner:HUNAN PROVINCE HONGJIANG HUAGUANG BIOTECH

Process for the preparation of tapentadol

Disclosed herein is an improved process for the preparation of 3-[(2R,3R)-1-(dimethylamino)-2-methylpentan-3-yl]phenol of Formula-I and its pharmaceutically acceptable salt which comprises the reaction of (S)-1-(dimethylamino)-2-methylpentan-3-one of formula VIII with 3-bromo anisole of formula II under Grignard conditions to get the compound (2S, 3R)-1-(dimethylamino)-3-(3-methoxyphenyl)-2-methyl pentan-3-ol of formula V followed by activation of the —OH group of the formula V to convert into sulfonate esters of formula IX, which are on reductive deoxygenation to yield (2R,3R)-3-(3-methoxyphenyl)-N,N,2-trimethylpentan-1-amine of formula VII and demethylation of formula VII to obtain the compound 3-[(2R,3R)-1-(dimethylamino)-2-methylpentan-3-yl]phenol of Formula-1.
Owner:INDOCO REMEDIES

Preparation method of large-size and high-quality two-dimensional halide perovskite single crystal

The invention relates to a preparation method of a large-size and high-quality two-dimensional halide perovskite single crystal, the molecular formula of the two-dimensional halide perovskite is A2PbX4 or BPbX4, A represents one or more of PEA (phenylethylamine), BI (benzimidazole), propylamine, BA (butylamine) and PA (pentylamine), B represents one or more of propane diamine, BDA (butanediamine), PDA (pentamethylene diamine) and p-xylylenediamine, and X represents one or more of F, Cl, Br and I. A seed crystal induced volatile solvent method is utilized, and the two-dimensional perovskite single crystal with large size and high quality can be obtained under room-temperature or constant-temperature volatilization by heating and dissolving at the initial stage of seed crystal addition. According to the method, the solution can be recycled, the requirements on equipment and energy consumption are low, and the large-size and high-quality two-dimensional perovskite single crystal can be obtained at low cost.
Owner:WENZHOU ADVANCED MFG TECH INST OF HUAZHONG UNIV OF SCI & TECH

Benzoxazine resin monomer based on magnolia cortex derivative and preparation method and application thereof

The invention discloses a benzoxazine resin monomer based on a magnolia cortex derivative. A preparation method comprises the following steps: under heating effect, magnolol or honokiol and monoamineand paraformaldehyde are subjected to a polymerization to obtain the benzoxazine resin monomer; and the amine monomer is selected from at least one of furfuryl amine, ethylamine, propylanmine, butyl amine, pentylamine, hexylamine and phenylamine. The preparation is simple, the operation is simple, controllability is good, implementation is easy, and the method is adapted to large scale industrialproduction.
Owner:NINGBO INST OF MATERIALS TECH & ENG CHINESE ACADEMY OF SCI

Preparation method of N-methyl-pentylamine

The invention discloses a preparation method of N-methyl-pentylamine, which comprises the following steps of: adding anhydrous methylbenzene, n-pentylamine and benzaldehyde in a reactor, heating to reflux for 30-40minutes; evaporating to remove a solvent, cooling a residue to 0-5 DEG C, adding an anhydrous methylbenzene solution of dimethyl sulfate under the condition that the temperature is preserved, heating to reflux for 20-25minutes, decompressing and removing methylbenzene and benzaldehyde; and cooling the left solution to -5-0 DEG C, adding solid KOH, regulating pH to be 8.0-9.0, separating out an amine layer, and distilling at reduced pressure to obtain N-methyl-pentylamine. The preparation method disclosed by the invention is simple, low in requirement of equipment, stable in process, simple in route, high in yield, easy to post-process in a preparation process, and easy to industrialize.
Owner:张家港市大伟助剂有限公司
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