AR124874A1 - Derivados de soforolípidos mejorados - Google Patents
Derivados de soforolípidos mejoradosInfo
- Publication number
- AR124874A1 AR124874A1 ARP220100295A ARP220100295A AR124874A1 AR 124874 A1 AR124874 A1 AR 124874A1 AR P220100295 A ARP220100295 A AR P220100295A AR P220100295 A ARP220100295 A AR P220100295A AR 124874 A1 AR124874 A1 AR 124874A1
- Authority
- AR
- Argentina
- Prior art keywords
- slp
- linear
- aldehyde
- cationic
- derivative
- Prior art date
Links
- ZTOKUMPYMPKCFX-CZNUEWPDSA-N (E)-17-[(2R,3R,4S,5S,6R)-6-(acetyloxymethyl)-3-[(2S,3R,4S,5S,6R)-6-(acetyloxymethyl)-3,4,5-trihydroxyoxan-2-yl]oxy-4,5-dihydroxyoxan-2-yl]oxyoctadec-9-enoic acid Chemical class OC(=O)CCCCCCC/C=C/CCCCCCC(C)O[C@@H]1O[C@H](COC(C)=O)[C@@H](O)[C@H](O)[C@H]1O[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](COC(C)=O)O1 ZTOKUMPYMPKCFX-CZNUEWPDSA-N 0.000 title abstract 23
- -1 SLP aldehyde Chemical class 0.000 abstract 15
- 238000000034 method Methods 0.000 abstract 9
- 125000002091 cationic group Chemical group 0.000 abstract 7
- 239000000203 mixture Substances 0.000 abstract 7
- 239000000645 desinfectant Substances 0.000 abstract 5
- 150000001299 aldehydes Chemical class 0.000 abstract 4
- 150000001408 amides Chemical class 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 4
- 238000006268 reductive amination reaction Methods 0.000 abstract 4
- 150000001735 carboxylic acids Chemical class 0.000 abstract 3
- 238000004140 cleaning Methods 0.000 abstract 3
- 244000005700 microbiome Species 0.000 abstract 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 2
- 125000003275 alpha amino acid group Chemical group 0.000 abstract 2
- 239000003638 chemical reducing agent Substances 0.000 abstract 2
- 239000007822 coupling agent Substances 0.000 abstract 2
- 150000002009 diols Chemical group 0.000 abstract 2
- HTCGTPMYJVLOJV-UHFFFAOYSA-N lithium;(2-methylpropan-2-yl)oxy-bis(2-methylpropyl)aluminum(1-) Chemical compound [Li+].CC(C)(C)[O-].CC(C)C[Al]CC(C)C HTCGTPMYJVLOJV-UHFFFAOYSA-N 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 239000000463 material Substances 0.000 abstract 2
- 150000004702 methyl esters Chemical class 0.000 abstract 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 abstract 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 abstract 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 abstract 1
- 102000004190 Enzymes Human genes 0.000 abstract 1
- 108090000790 Enzymes Proteins 0.000 abstract 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 abstract 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000005642 Oleic acid Substances 0.000 abstract 1
- 241001278026 Starmerella bombicola Species 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 238000005904 alkaline hydrolysis reaction Methods 0.000 abstract 1
- 125000002009 alkene group Chemical group 0.000 abstract 1
- 230000000845 anti-microbial effect Effects 0.000 abstract 1
- 239000003876 biosurfactant Substances 0.000 abstract 1
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 abstract 1
- 239000007844 bleaching agent Substances 0.000 abstract 1
- 125000002843 carboxylic acid group Chemical group 0.000 abstract 1
- 239000002738 chelating agent Substances 0.000 abstract 1
- 230000000249 desinfective effect Effects 0.000 abstract 1
- 239000008121 dextrose Substances 0.000 abstract 1
- 150000002118 epoxides Chemical class 0.000 abstract 1
- 150000004665 fatty acids Chemical group 0.000 abstract 1
- 238000000855 fermentation Methods 0.000 abstract 1
- 230000004151 fermentation Effects 0.000 abstract 1
- 239000004088 foaming agent Substances 0.000 abstract 1
- 238000009472 formulation Methods 0.000 abstract 1
- 239000003205 fragrance Substances 0.000 abstract 1
- 125000000524 functional group Chemical group 0.000 abstract 1
- 239000003456 ion exchange resin Substances 0.000 abstract 1
- 229920003303 ion-exchange polymer Polymers 0.000 abstract 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 abstract 1
- MZRVEZGGRBJDDB-UHFFFAOYSA-N n-Butyllithium Substances [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 abstract 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 abstract 1
- 238000007248 oxidative elimination reaction Methods 0.000 abstract 1
- WURFKUQACINBSI-UHFFFAOYSA-M ozonide Chemical compound [O]O[O-] WURFKUQACINBSI-UHFFFAOYSA-M 0.000 abstract 1
- 238000005949 ozonolysis reaction Methods 0.000 abstract 1
- 239000003755 preservative agent Substances 0.000 abstract 1
- 230000002335 preservative effect Effects 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 238000011012 sanitization Methods 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000000758 substrate Substances 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- 239000002562 thickening agent Substances 0.000 abstract 1
- 239000000341 volatile oil Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
- C07H15/10—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical containing unsaturated carbon-to-carbon bonds
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/14—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings
- A01N43/16—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom six-membered rings with oxygen as the ring hetero atom
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P1/00—Disinfectants; Antimicrobial compounds or mixtures thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
- A61L2/18—Liquid substances or solutions comprising solids or dissolved gases
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/16—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using chemical substances
- A61L2/22—Phase substances, e.g. smokes, aerosols or sprayed or atomised substances
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L9/00—Disinfection, sterilisation or deodorisation of air
- A61L9/01—Deodorant compositions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/02—Acyclic radicals, not substituted by cyclic structures
- C07H15/04—Acyclic radicals, not substituted by cyclic structures attached to an oxygen atom of the saccharide radical
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07H—SUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
- C07H15/00—Compounds containing hydrocarbon or substituted hydrocarbon radicals directly attached to hetero atoms of saccharide radicals
- C07H15/26—Acyclic or carbocyclic radicals, substituted by hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/06—Dipeptides
- C07K5/06008—Dipeptides with the first amino acid being neutral
- C07K5/06017—Dipeptides with the first amino acid being neutral and aliphatic
- C07K5/06026—Dipeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atom, i.e. Gly or Ala
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/08—Tripeptides
- C07K5/0802—Tripeptides with the first amino acid being neutral
- C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
- C07K5/0806—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
- C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
- C07K5/10—Tetrapeptides
- C07K5/1002—Tetrapeptides with the first amino acid being neutral
- C07K5/1005—Tetrapeptides with the first amino acid being neutral and aliphatic
- C07K5/1008—Tetrapeptides with the first amino acid being neutral and aliphatic the side chain containing 0 or 1 carbon atoms, i.e. Gly, Ala
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/20—Organic compounds containing oxygen
- C11D3/22—Carbohydrates or derivatives thereof
- C11D3/221—Mono, di- or trisaccharides or derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/44—Preparation of O-glycosides, e.g. glucosides
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2101/00—Chemical composition of materials used in disinfecting, sterilising or deodorising
- A61L2101/32—Organic compounds
- A61L2101/34—Hydroxy compounds
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2101/00—Chemical composition of materials used in disinfecting, sterilising or deodorising
- A61L2101/32—Organic compounds
- A61L2101/44—Heterocyclic compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/10—Apparatus features
- A61L2202/17—Combination with washing or cleaning means
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2202/00—Aspects relating to methods or apparatus for disinfecting or sterilising materials or objects
- A61L2202/20—Targets to be treated
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Genetics & Genomics (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Biotechnology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- General Chemical & Material Sciences (AREA)
- Zoology (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Crystallography & Structural Chemistry (AREA)
- Biophysics (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- General Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Microbiology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Dentistry (AREA)
- Emergency Medicine (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Saccharide Compounds (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Confectionery (AREA)
- General Preparation And Processing Of Foods (AREA)
Abstract
Se identificó a los nuevos derivados de soforolípidos con actividad antimicrobiana mejorada como ingredientes activos desinfectantes. Estos derivados se producen a partir de la fermentación de Starmerella bombicola utilizando dextrosa y una materia prima oleoquímica que es alta en ácido oleico. Se utiliza un esquema sintético de dos pasos para generar un grupo de aldehidos reactivos y luego instalar grupos funcionales catiónicos biodegradables naturales. Estos derivados catiónicos de soforolípidos se purifican utilizando resinas de intercambio iónico para obtener sales de alta pureza derivadas de soforolípidos para la formulación en productos desinfectantes. Reivindicación 1: Un método para producir un derivativo de soforolípido (SLP) catiónico, el método caracterizado porque comprende a) producir una molécula de SLP lineal purificado que tiene una porción de ácido graso de 18 carbonos con un solo enlace insaturado en el noveno carbono y uno de b), c) o d): b) someter la molécula de SLP lineal de a) una ozonólisis para oxidar la porción de ácido graso a una ozonido y reducir el SLP-ozonido con un agente reductor para producir un aldehído de SLP lineal crudo acuoso; c) someter la molécula de SLP lineal de a) a un proceso que comprende: 1) epoxidizar el grupo alqueno del SLP; 2) abrir el epóxido para formar un diol vecinal; y 3) escindir de manera oxidativa el diol vecinal para producir un aldehído de SLP lineal crudo acuoso; o d) convertir el grupo de ácido carboxílico libre de la molécula de SLP línea de a) en un éster de metilo usando hidrólisis alcalina y aplicar DIBAL-H como un agente reductor para convertir el éster de metilo en un grupo funcional de aldehído, por lo tanto, producir un aldehído de SLP lineal crudo; y e) después de uno de b), c) o d), extraer el SLP lineal aldehído a partir del aldehído de SLP lineal crudo acuoso y someter el aldehído de SLP lineal extraído a aminación reductora, por lo tanto, producir un andamiaje de SLP covalentemente ligado a una amina primaria en una mezcla de reacción de aminación reductora, dicho andamiaje de SLP ligado y amina primaria que comprende el derivativo de SLP catiónico y purificar el derivativo de SLP catiónico a partir de la mezcla de aminación reductora. Reivindicación 25: Un método para producir un derivativo de soforolípido (SLP) catiónico, el método caracterizado porque comprende a) obtener una molécula de SLP lactónico; b) reducir el enlace de lactona en un aldehído al aplicar un complejo ato, hidruro de tri-tert-butoxialuminio de litio (LTBA), hidruro de diisobutil-tert-butoxialuminio de litio (LDBBA) o hidruro de diisobutilaluminio y complejo ato de n-butilitio, por lo tanto, produce un aldehído acuoso de SLP lineal crudo; y e) extraer el aldehído de SLP lineal del aldehído de SLP lineal crudo acuoso y someter el aldehído de SLP lineal a aminación reductora, por lo tanto, producir un andamiaje de SLP covalentemente ligado a una amina primaria, dicho andamiaje de SLP ligado y amina primaria que comprende el derivativo de SLP y purificar el derivativo de SLP. Reivindicación 26: Un método para producir un derivativo de soforolípido (SLP) catiónico, el método caracterizado porque comprende a) obtener una molécula de SLP lineal purificado desacetilado que tiene una porción de ácido graso de 18 carbonos con un solo enlace insaturado en el noveno carbono y uno de b) o c): b) usar un agente de acoplamiento, instalar una amida que comprende uno o más de grupos funcionales de aminoácido catiónico en la cola del ácido carboxílico de la molécula de SLP lineal desacetilado para producir una amida de cadena larga; o c) usar la escisión oxidativa para producir una cola de ácido carboxílico truncada en la novena posición y, usar un agente de acoplamiento, instalar una amida que comprende uno o más de grupos funcionales de aminoácido catiónico en la cola del ácido carboxílico truncado para producir una amida de cadena corta. Reivindicación 28: Una composición de limpieza caracterizada porque comprende un derivativo de SLP catiónico producido según un método de una cualquiera de las reivindicaciones 1 a 27. Reivindicación 34: Un método para desinfectar y/o higienizar un material y/o una superficie que está infectada con un microorganismo perjudicial, el método caracterizado porque comprende producir un derivativo de SLP catiónico usando un método según una cualquiera de las reivindicaciones 1 a 33 y mezclar el derivativo de SLP catiónico con uno o más de los siguientes componentes adicionales para producir una composición desinfectante de limpieza: agua, un solvente, un biotensioactivo adicional, un tensioactivo adicional, un sindético, un agente quelante, un constructor, un conservante, una fragancia, un tinte, un aceite esencial, un sustrato, una enzima, un desinfectante, un agente espumante, un agente de decoloración y un espesante y/o viscosificante; y aplicar la composición desinfectante de limpieza al material y/o superficie de forma tal que la composición entre en contacto con el microorganismo perjudicial, donde el microorganismo perjudicial se controla en el plazo de los 10 minutos o menos de contacto con la composición.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US202163149477P | 2021-02-15 | 2021-02-15 |
Publications (1)
Publication Number | Publication Date |
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AR124874A1 true AR124874A1 (es) | 2023-05-17 |
Family
ID=82837254
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP220100295A AR124874A1 (es) | 2021-02-15 | 2022-02-15 | Derivados de soforolípidos mejorados |
Country Status (13)
Country | Link |
---|---|
US (1) | US20240182940A1 (es) |
EP (1) | EP4291672A1 (es) |
JP (1) | JP2024506903A (es) |
KR (1) | KR20230148195A (es) |
CN (1) | CN117157411A (es) |
AR (1) | AR124874A1 (es) |
AU (1) | AU2022220801A1 (es) |
CA (1) | CA3205332A1 (es) |
CR (1) | CR20230444A (es) |
IL (1) | IL304774A (es) |
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CN115678687A (zh) * | 2022-09-15 | 2023-02-03 | 河南海利未来科技集团有限公司 | 一种低泡杀菌的洗碗机清洗剂及其制备方法 |
WO2024064634A1 (en) * | 2022-09-19 | 2024-03-28 | Locus Solutions Ipco, Llc | Modified sophorolipids with enhanced dispersion properties |
WO2024118749A1 (en) * | 2022-11-29 | 2024-06-06 | Locus Solutions Ipco, Llc | Methods for producing bio-derivatized linear sophorolipids |
US20240301322A1 (en) * | 2023-03-01 | 2024-09-12 | Locus Solutions Ipco, Llc | Functionalized biodegradable surfactants and methods use |
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- 2022-02-15 CN CN202280015066.0A patent/CN117157411A/zh active Pending
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AU2022220801A1 (en) | 2023-08-10 |
EP4291672A1 (en) | 2023-12-20 |
JP2024506903A (ja) | 2024-02-15 |
WO2022174190A1 (en) | 2022-08-18 |
IL304774A (en) | 2023-09-01 |
KR20230148195A (ko) | 2023-10-24 |
CR20230444A (es) | 2024-03-19 |
AU2022220801A9 (en) | 2024-05-02 |
CA3205332A1 (en) | 2022-08-18 |
TW202302859A (zh) | 2023-01-16 |
MX2023009558A (es) | 2023-10-25 |
US20240182940A1 (en) | 2024-06-06 |
CN117157411A (zh) | 2023-12-01 |
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