PL431315A1 - Alkyl(2-hydroxyethyl)dimethylammonium indole-3-butyrates, method of their preparation and use as rooting hormones - Google Patents
Alkyl(2-hydroxyethyl)dimethylammonium indole-3-butyrates, method of their preparation and use as rooting hormonesInfo
- Publication number
- PL431315A1 PL431315A1 PL431315A PL43131519A PL431315A1 PL 431315 A1 PL431315 A1 PL 431315A1 PL 431315 A PL431315 A PL 431315A PL 43131519 A PL43131519 A PL 43131519A PL 431315 A1 PL431315 A1 PL 431315A1
- Authority
- PL
- Poland
- Prior art keywords
- hydroxyethyl
- alkyl
- dimethylammonium
- general formula
- butyrates
- Prior art date
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P60/00—Technologies relating to agriculture, livestock or agroalimentary industries
- Y02P60/20—Reduction of greenhouse gas [GHG] emissions in agriculture, e.g. CO2
- Y02P60/21—Dinitrogen oxide [N2O], e.g. using aquaponics, hydroponics or efficiency measures
Landscapes
- Indole Compounds (AREA)
Abstract
Przedmiotem wynalazku są ciecze jonowe z kationem alkilo(2-hydroksyetylo)dimetyloamoniowym i anionem indolilo-3-maślanowym o wzorze ogólnym 1, w którym R oznacza nierozgałęziony łańcuch alkilowy zawierający od 2 do 18 atomów węgla. Zgłoszenie obejmuje też ich sposób otrzymywania który polega na tym, że bromek alkilo(2-hydroksyetylo)dimetyloamoniowy o wzorze ogólnym 2, w którym R oznacza nierozgałęziony łańcuch alkilowy zawierający od 2 do 18 atomów węgla rozpuszcza się w rozpuszczalnikach organicznych takich jak: metanol, albo etanol, albo 2-propanol, następnie dodaje się soli alkalicznej kwasu indolilo-3-masłowego o wzorze ogólnym 3, w którym K+ oznacza kation litowy, albo sodowy, albo potasowy, w stosunku molowym od 1:1 do 1:1,1, korzystnie 1:1 i poddaje mieszaniu w temperaturze od 15 do 45°C, korzystnie 25°C i czasie od 10 do 50 minut, korzystnie 20 minut, dalej odsącza się wytrąconą sól nieorganiczną i odparowuje się rozpuszczalnik, a uzyskany produkt suszy. Zgłoszenie obejmuje też zastosowanie przedmiotowych związków jako ukorzeniaczy.The invention relates to ionic liquids with an alkyl (2-hydroxyethyl) dimethylammonium cation and an indolyl-3-butyrate anion of the general formula I, in which R is an unbranched alkyl chain containing from 2 to 18 carbon atoms. The application also covers their preparation process, which consists in the fact that the alkyl (2-hydroxyethyl) dimethylammonium bromide of the general formula 2, in which R is an unbranched alkyl chain containing from 2 to 18 carbon atoms, is dissolved in organic solvents such as: methanol or ethanol or 2-propanol, then the indolyl-3-butyric acid alkali salt of general formula 3, wherein K + is lithium, or sodium or potassium, is added in a molar ratio of 1: 1 to 1: 1.1, preferably 1: 1 and subjected to stirring at a temperature of 15 to 45 ° C, preferably 25 ° C, and for 10 to 50 minutes, preferably 20 minutes, the precipitated inorganic salt is further filtered off and the solvent is evaporated, and the obtained product is dried. The application also covers the use of the compounds in question as rooting agents.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL431315A PL240767B1 (en) | 2019-09-30 | 2019-09-30 | Alkyl(2-hydroxyethyl)dimethylammonium indole-3-butyrates, method of their preparation and use as rooting hormones |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL431315A PL240767B1 (en) | 2019-09-30 | 2019-09-30 | Alkyl(2-hydroxyethyl)dimethylammonium indole-3-butyrates, method of their preparation and use as rooting hormones |
Publications (2)
Publication Number | Publication Date |
---|---|
PL431315A1 true PL431315A1 (en) | 2021-04-06 |
PL240767B1 PL240767B1 (en) | 2022-05-30 |
Family
ID=75297894
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PL431315A PL240767B1 (en) | 2019-09-30 | 2019-09-30 | Alkyl(2-hydroxyethyl)dimethylammonium indole-3-butyrates, method of their preparation and use as rooting hormones |
Country Status (1)
Country | Link |
---|---|
PL (1) | PL240767B1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
PL245149B1 (en) * | 2022-07-12 | 2024-05-20 | Politechnika Poznanska | Composition of a rooting agent for monocotyledonous plants and use of bis-ammonium salts as rooting agents for monocotyledonous plants |
PL245148B1 (en) * | 2022-07-12 | 2024-05-20 | Politechnika Poznanska | Composition of a rooting agent for monocotyledonous plants and use of alkyl betaine bromides as rooting agents for monocotyledonous plants |
-
2019
- 2019-09-30 PL PL431315A patent/PL240767B1/en unknown
Also Published As
Publication number | Publication date |
---|---|
PL240767B1 (en) | 2022-05-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
PL431315A1 (en) | Alkyl(2-hydroxyethyl)dimethylammonium indole-3-butyrates, method of their preparation and use as rooting hormones | |
CZ702289A3 (en) | Process for preparing perhaloalkyl thioethers | |
PL431316A1 (en) | Herbicidal ionic liquids with alkyl[2-(2-hydroxyethoxy)ethyl]dimethylammonium cation and (R)-2-(4-chloro-2-methylphenoxy)propionate anion, method of their preparation and use as herbicides | |
PL429723A1 (en) | Ionic liquids with ammonium cation and indole-3-butyrate anion, method of their preparation and application as a cut flower preservative | |
PL433625A1 (en) | New ionic liquids with (2-hydroxyethyl) didecyldimethylammonium cation, method of preparation and use as adjuvants | |
PL423896A1 (en) | Antibacterial ionic liquids with 1-alkyl-1-methyl-4-piperidinolium cation and (S)-mandelate anion, method for obtaining them and the application as antibacterial agents | |
PL434993A1 (en) | New ionic liquids with dodecyl (carboxymethyl) dimethylammonium cation, method of their preparation and application as washing agents | |
BR112019008372B1 (en) | PROCESS FOR PREPARATION OF PESTICIDES COMPOUNDS | |
PL417806A1 (en) | Ionic liquids with bis-ammonium cation and mandelate anion - method for obtaining them and applications as bactericides | |
PL425874A1 (en) | Phosphonium ionic liquids with n-alkyltriphenylphosphonium cation and (4-chloro-2-methylphenoxy)acetate or (2,4-dichlorophenoxy)acetate anion, method for obtaining them and application as herbicides | |
PL413037A1 (en) | New (alkoxymethyl)ethyldimethylammonium 4-chloro-2-methylphenoxyacetates ionic liquids, method for obtaining them and their application as herbicides | |
PL435465A1 (en) | New ionic liquids with alkyl (carbosymethyl) dimethylammonium cation and bis (2-ethylhexyl) phosphate anion, method of preparation and use as degreasing agents for work surfaces | |
PL436415A1 (en) | Method of preparation of herbicidal imidazolium ionic liquid with 4-chlorophenoxyacetate anion | |
PL435466A1 (en) | New ionic liquids with alkyl (carboxymethyl) dimethylammonium cation and 1,4-bis (2-ethylhexoxy) -1,4-dioxobutane-2-sulfonate anion, method of preparation and use as degreasing agents for work surfaces | |
PL429390A1 (en) | Tetraalkylammonium tryptophanates, method of their preparation and their use as preparations extending the life of cut flowers | |
PL420661A1 (en) | New bis-ammonium ionic liquids with alkyl-1,X-bis(bis(2-hydroxyethyl)octadec-9-en-ammonium) cation and method for obtaining them and application as food deterrents | |
PL416323A1 (en) | Methyl alkyl betaine 3,6-dichloro-2-methoxybenzoate, method for obtaining it and application as a herbicide | |
Aizina et al. | Synthesis of 2-methyl-N-(2, 2, 2-trichloroethylidene)-and 2-methyl-N-(2, 2, 2-trichloroethyl) benzenesulfonamides from N, N-dichloro-2-methylbenzenesulfonamide and trichloroethylene | |
PL416320A1 (en) | New ionic liquids with alkyl [2(2-hydroxyethoxy)ethyl]dimethylammonium cation and formate anion and method for obtaining them | |
PL417193A1 (en) | New bis-ammonium ionic liquids with alkane-1,X-bis(decyldimethylammonium) cation and formate anion, method for obtaining them and applications as bactericides | |
PL412742A1 (en) | New di[2-(2,4-dichlorophenoxy)propionates] alkano-1,X-bis(decyl dimethylammonium) bis-ammonium ionic liquids, method for obtaining them and applications as plant protection products | |
PL399974A1 (en) | Ionic liquids with tetramethylene-1,4-bis (alkyldimethylammonium) cation and (4-chloro-2-methylphenoxy) acetate anion and the method of obtaining them | |
PL439333A1 (en) | New ionic liquids consisting of 1,4-dialkyl-1,4-diazoniabicyclo[2.2.2]octane cation and anions derived from 4-chloro-2-methylphenoxyacetic acid, method of their preparation and use as herbicides | |
PL400413A1 (en) | Methyl-imidazolium ionic liquids with the theophylline anion and a method for their preparation | |
PL417286A1 (en) | New ionic liquids with alkane-1,X-bis(decyldimethylammonium) cation and acetate anion, method for obtaining them and applications as bactericides |