Virtual Titration Laboratory

The software is designed to emulate potentiometric titration in the Online mode. Virtual Titration allows to conduct laboratory work on analytical chemistry in virtual mode via the Internet. This allows to learn more about different types of titration in a relatively short time and reduce spending on equipment and reagents. The complex software simulates real laboratory work – students drop by drop add a standardized solution of alkali to a solution of acid of unknown concentration. At the same time, a graph on the dependence of pH of the titrated solution on the volume of the added titrant appears on the screen. Analyzing the graph, students should determine the concentration of titrated acid, then the software checks the accuracy of the calculation and informs the students on the mistake in their calculation.

Anna Marakhova A.Kuznetsov

Chemistry Nanotechnologies and Nanomaterials

№2018612682 Registered 21 Feb 2018

  • Priority08 Nov 2017
  • Class of ICPI000
  • Application number2017661415
  • PublicationBul. of Russian Federal Service for Intellectual Property (Rospatent) No. 3

Calculation of the Solubility of Slightly Soluble Salts of Weak Acids Depending on the Solution pH Level

The software is used to calculate the solubility of slightly soluble residuals of salts of weak acids in solutions of a strong acid. The software comprises two software packages: the first is responsible for the software- user interaction, and the second – for the actual calculation. The software contains two auxiliary user functions that provide solubility calculations depending on the experimental conditions. The software provides convenient input of initial data and output of results.

Anna Marakhova A.Kuznetsov

Chemistry Nanotechnologies and Nanomaterials

№2018610297 Registered 09 Jan 2018

  • Priority08 Nov 2017
  • Class of ICPI000
  • Application number2017661413
  • PublicationBul. of Russian Federal Service for Intellectual Property (Rospatent) No. 1

Methane Tank

The utility model refers to agriculture, namely to installations for processing organic sewage sludge and manure and can be used in the production of biogas and organic fertilizers.

A.P.Svintsov N.A. Stashevskaya S.L. Shambina

Chemistry Organic chemistry

№178698 Registered 17 Apr 2018

  • Priority13 Apr 2017
  • Class of ICPIC12
  • Application number2017112754
  • PublicationBul. of Russian Federal Service for Intellectual Property (Rospatent) No. 11

Method for Producing Pyrrol[2,1-a] isoquinoline derivatives

The invention relates to organic chemistry, namely the method for producing pyrro[2,1-a]isoquinoline 3-6 derivatives, where 3: R1=OCH3, R2=H, R3=Cl, R4=H; 4: R1=OCH3, R2=H, R3=Cl, R4=CH3; 5: R1=R2=R3=OC2H5, R4=H; 6: R1=R2=R3=OC2H5, R4=CH3, comprising dissolution of 6,7-dimethoxy-3,4-dihydro-1-(4-benzoyl chloride)isoquinoline or 6,7-diethoxy-3,4-dihydro-1-(3,4-diethoxybenzoyl)isoquinoline in acetonitrile and addition of 1,5-diphenyl-1-peptene-4-in-3-ona 1-(4-methylphenyl)-5-phenyl-1-peptene-4-in-3-ona and 30 mole percent of cuprous bromide, and subjecting to microwave irradiation (300 W) for 30 min at +200 °C, wherein the residue received after the end of the reaction and removal of the solvent, is crystallized from ether. Technical Result: The method for producing pyrrol[2,1-a]isoquinoline derivatives, which may have useful biological properties, was developed. 4 ex.

T.N.Borisova A.V.Varlamov Leonid Voskresenskiy Matveeva Maria Dmitrievna

Chemistry Organic chemistry

№2656225 Registered 04 Jun 2018

  • Priority22 Jun 2017
  • Class of ICPIC07
  • Application number2017122018
  • PublicationBul. of Russian Federal Service for Intellectual Property (Rospatent) No. 16

Process for the preparation of 5,6-dihydropyrrolo [2,1-a] isoquinoline derivatives containing functional group in position 2

The invention pertains to a novel method for the synthesis of 5,6-dihydropyrrolo [2,1-a] isoquinoline derivatives containing a functional group in position 2. The method consists of dissolving 6,7-diethoxy-3,4-dihydro-1- (3,4-diethoxybenzoyl) isoquinoline in trifluoroethanol and adding acrolein or crotonaldehyde or cinnamaldehyde or acrylonitrile and stirring at a temperature of + 70 ° C. The residue obtained after completion of the reaction and removal of the reagents is crystallized in a mixture of ether and hexane. The proposed process allows the preparation of 2-functionally substituted 5,6-dihydropyrrolo derivatives by acrolein or crotonaldehyde or cinnamic aldehyde or acrylonitrile to 6,7-diethoxy-3,4-dihydro-1- (3,4-diethoxybenzoyl) isoquinoline in trifluoroethanol [2,1-a] isoquinolines.

T.N.Borisova L.G.Voskresenskii T.M.Chervyakova A.N.Varlamov

Chemistry Organic chemistry

№2575174 Registered 20 Jan 2016

  • Priority12 Mar 2015
  • Class of ICPIC07
  • Application number2015108637
  • PublicationRospatent Bul. No. 5

Process for the preparation of 5,6-dihydropyrrolo [2,1-a] isoquinoline derivatives

The invention pertains to the field of organic chemistry, more specifically to a process of the preparation of 5,6-dihydropyrrolo [2,1-a] isoquinoline 1-4 derivatives with the same structural formula. The synthesis of 5,6-dihydropyrrolo [2,1-a] isoquinoline derivatives method with a three-component reaction is proposed.

T.N.Borisova M.V.Moiseeva A.V.Varlamov L.G.Voskresenskii A.A.Titov R.S.Borisov

Chemistry Organic chemistry

№2550366 Registered 09 Apr 2015

  • Priority22 May 2014
  • Class of ICPIC07
  • Application number2014120644
  • PublicationRospatent Bul. No. 13

Nanocrystalline catalyst for cracking propane for producing olefins and the method of its production

The invention pertains to the field of petrochemistry. The nanocrystalline catalyst for the cracking of propane for the production of olefins is a nanocrystalline form of an airgel of aluminum oxide.

Yu.M.Serov O.K.Krasilnikova T.F.Sheshko E.B.Markova

Chemistry Catalysis

№2604882 Registered 23 Nov 2016

  • Priority14 Aug 2015
  • Class of ICPIB01
  • Application number2015134198
  • PublicationRospatent Bul. No. 35