EP4384007A1 - Emulsifiable concentrated composition comprising carvacrol - Google Patents
Emulsifiable concentrated composition comprising carvacrolInfo
- Publication number
- EP4384007A1 EP4384007A1 EP22764851.6A EP22764851A EP4384007A1 EP 4384007 A1 EP4384007 A1 EP 4384007A1 EP 22764851 A EP22764851 A EP 22764851A EP 4384007 A1 EP4384007 A1 EP 4384007A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- esters
- oil
- amount
- composition according
- ethoxylated
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 74
- RECUKUPTGUEGMW-UHFFFAOYSA-N carvacrol Chemical compound CC(C)C1=CC=C(C)C(O)=C1 RECUKUPTGUEGMW-UHFFFAOYSA-N 0.000 title claims abstract description 40
- HHTWOMMSBMNRKP-UHFFFAOYSA-N carvacrol Natural products CC(=C)C1=CC=C(C)C(O)=C1 HHTWOMMSBMNRKP-UHFFFAOYSA-N 0.000 title claims abstract description 40
- 235000007746 carvacrol Nutrition 0.000 title claims abstract description 39
- WYXXLXHHWYNKJF-UHFFFAOYSA-N isocarvacrol Natural products CC(C)C1=CC=C(O)C(C)=C1 WYXXLXHHWYNKJF-UHFFFAOYSA-N 0.000 title claims abstract description 39
- 150000002148 esters Chemical class 0.000 claims description 30
- 239000002736 nonionic surfactant Substances 0.000 claims description 30
- 239000002904 solvent Substances 0.000 claims description 29
- 241000196324 Embryophyta Species 0.000 claims description 20
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 claims description 18
- 239000000839 emulsion Substances 0.000 claims description 16
- 239000003945 anionic surfactant Substances 0.000 claims description 14
- 239000004359 castor oil Substances 0.000 claims description 14
- 235000019438 castor oil Nutrition 0.000 claims description 14
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 claims description 14
- TVFWYUWNQVRQRG-UHFFFAOYSA-N 2,3,4-tris(2-phenylethenyl)phenol Chemical class C=1C=CC=CC=1C=CC1=C(C=CC=2C=CC=CC=2)C(O)=CC=C1C=CC1=CC=CC=C1 TVFWYUWNQVRQRG-UHFFFAOYSA-N 0.000 claims description 13
- 235000019484 Rapeseed oil Nutrition 0.000 claims description 13
- 150000004702 methyl esters Chemical class 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 11
- 239000008158 vegetable oil Substances 0.000 claims description 11
- 229940092714 benzenesulfonic acid Drugs 0.000 claims description 9
- 239000003921 oil Substances 0.000 claims description 7
- 235000019198 oils Nutrition 0.000 claims description 7
- 208000015181 infectious disease Diseases 0.000 claims description 6
- 125000000129 anionic group Chemical group 0.000 claims description 5
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 5
- 229930195729 fatty acid Natural products 0.000 claims description 5
- 239000000194 fatty acid Substances 0.000 claims description 5
- 150000004665 fatty acids Chemical class 0.000 claims description 5
- 150000002790 naphthalenes Chemical class 0.000 claims description 4
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 3
- 150000001298 alcohols Chemical class 0.000 claims description 3
- 229920001400 block copolymer Polymers 0.000 claims description 3
- 150000003961 organosilicon compounds Chemical class 0.000 claims description 3
- BCFOOQRXUXKJCL-UHFFFAOYSA-N 4-amino-4-oxo-2-sulfobutanoic acid Chemical class NC(=O)CC(C(O)=O)S(O)(=O)=O BCFOOQRXUXKJCL-UHFFFAOYSA-N 0.000 claims description 2
- 229920001732 Lignosulfonate Polymers 0.000 claims description 2
- 240000007594 Oryza sativa Species 0.000 claims description 2
- 235000007164 Oryza sativa Nutrition 0.000 claims description 2
- 235000019482 Palm oil Nutrition 0.000 claims description 2
- 235000019483 Peanut oil Nutrition 0.000 claims description 2
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 claims description 2
- 235000019486 Sunflower oil Nutrition 0.000 claims description 2
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 claims description 2
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 claims description 2
- 150000008052 alkyl sulfonates Chemical group 0.000 claims description 2
- 239000002385 cottonseed oil Substances 0.000 claims description 2
- 235000012343 cottonseed oil Nutrition 0.000 claims description 2
- 239000010460 hemp oil Substances 0.000 claims description 2
- 239000000944 linseed oil Substances 0.000 claims description 2
- 235000021388 linseed oil Nutrition 0.000 claims description 2
- 239000003346 palm kernel oil Substances 0.000 claims description 2
- 235000019865 palm kernel oil Nutrition 0.000 claims description 2
- 239000002540 palm oil Substances 0.000 claims description 2
- 239000000312 peanut oil Substances 0.000 claims description 2
- 235000009566 rice Nutrition 0.000 claims description 2
- 239000003549 soybean oil Substances 0.000 claims description 2
- 235000012424 soybean oil Nutrition 0.000 claims description 2
- 239000002600 sunflower oil Substances 0.000 claims description 2
- MCVUKOYZUCWLQQ-UHFFFAOYSA-N tridecylbenzene Chemical class CCCCCCCCCCCCCC1=CC=CC=C1 MCVUKOYZUCWLQQ-UHFFFAOYSA-N 0.000 claims description 2
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 claims 7
- 206010017533 Fungal infection Diseases 0.000 claims 2
- 208000031888 Mycoses Diseases 0.000 claims 2
- 239000004711 α-olefin Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 abstract description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 239000004480 active ingredient Substances 0.000 description 15
- 239000004476 plant protection product Substances 0.000 description 7
- 159000000007 calcium salts Chemical class 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 6
- 238000005191 phase separation Methods 0.000 description 6
- 150000003871 sulfonates Chemical class 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- 239000004495 emulsifiable concentrate Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000047 product Substances 0.000 description 4
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 238000010348 incorporation Methods 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 241000221198 Basidiomycota Species 0.000 description 2
- 241001291118 Dubautia plantaginea Species 0.000 description 2
- 241000258937 Hemiptera Species 0.000 description 2
- 241000255777 Lepidoptera Species 0.000 description 2
- 241000233654 Oomycetes Species 0.000 description 2
- 241000233622 Phytophthora infestans Species 0.000 description 2
- 241001123569 Puccinia recondita Species 0.000 description 2
- 241000233639 Pythium Species 0.000 description 2
- 241000246354 Satureja Species 0.000 description 2
- 241000228452 Venturia inaequalis Species 0.000 description 2
- 241000269425 Xanthomonas campestris pv. viticola Species 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 230000000843 anti-fungal effect Effects 0.000 description 2
- 229940121375 antifungal agent Drugs 0.000 description 2
- 239000012736 aqueous medium Substances 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 239000000284 extract Substances 0.000 description 2
- 230000002538 fungal effect Effects 0.000 description 2
- 230000000749 insecticidal effect Effects 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 241000162400 Dicladispa armigera Species 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 235000013628 Lantana involucrata Nutrition 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 235000006677 Monarda citriodora ssp. austromontana Nutrition 0.000 description 1
- 241001529744 Origanum Species 0.000 description 1
- 235000011203 Origanum Nutrition 0.000 description 1
- 240000007673 Origanum vulgare Species 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 230000000590 parasiticidal effect Effects 0.000 description 1
- 239000002297 parasiticide Substances 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000004083 survival effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- -1 that is Substances 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 239000000341 volatile oil Substances 0.000 description 1
Classifications
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- 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
- A01N65/00—Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
- A01N65/08—Magnoliopsida [dicotyledons]
- A01N65/22—Lamiaceae or Labiatae [Mint family], e.g. thyme, rosemary, skullcap, selfheal, lavender, perilla, pennyroyal, peppermint or spearmint
-
- 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
- A01P13/00—Herbicides; Algicides
Definitions
- the present invention refers to compositions for the phytosanitary use.
- the present invention refers to emulsifiable concentrated formulations comprising carvacrol.
- plant protection product means compounds or compositions used in agriculture to at least partially kill the parasites damaging cultivated plants, such as for example fungi, pathogenic insects and the like, in order to protect the health of said plants and to guarantee their survival.
- plant protection products or phytodrugs are also named, sometimes inappropriately, parasiticides, fungicides, pesticides and biocides.
- Carvacrol or 2-methyl-5 -isopropylphenol, having the following formula (I) is present for example in the essential oil of oregano (Origanum spp.) and Satureja (Satureja spp.) and has very good antifungal and antibacterial properties, showing at the same time little toxicity to higher species of animals.
- Carvacrol is poorly soluble in water.
- the poor water solubility of such compound makes its administration to the plants difficult. Indeed, typically, the plant protection products are administered to the plants through an aqueous medium.
- emulsifiable concentrates also known as "EC"
- EC emulsifiable concentrates
- the resulting emulsions are generally scarcely stable, quickly undergoing phase separation, that is, the separation of the oil phase from the aqueous one.
- phase separation makes the product unusable.
- a further problem of the known emulsifiable concentrates is the difficult to obtain homogeneous emulsions, that is, emulsions where the active ingredients, for example carvacrol, are uniformly distributed in the aqueous medium and do not form concentration gradients which could compromise the effectiveness of the treatment on the plants. Therefore, there is a need of having available formulations which allow to obtain homogeneous and stable emulsions of poorly water-soluble active ingredients, in particular of carvacrol.
- Subject-matter of the invention is a composition comprising, and alternatively consists of: a) carvacrol in an amount from 10 to 45 wt%, for example from 10 wt% to 40 wt% or from 10 to 30 wt%; b) at least one water-immiscible solvent selected from vegetable oils and esters of the vegetable oils, preferably the esters of the vegetable oils, in an amount from 20 wt% to 40 wt%; c) at least one first non-ionic surfactant selected from ethoxylated vegetable oils, in an amount from 25 wt% to 40 wt%; d) at least one sulfonated anionic surfactant; e) at least one second non-ionic surfactant selected from ethoxylated polyarylphenols, for example ethoxylated tristyrylphenol, ethoxylated alcohols, ethoxylated fatty acids, sorbitan esters and eth
- composition of the invention allows to obtain particularly stable emulsions in water that comprise carvacrol, that is, which do not undergo a substantial phase separation once diluted in water, making their application, that is, administration to plants, impossible.
- composition of the invention allows to obtain particularly homogeneous emulsions in water.
- composition is an emulsifiable concentrate (EC).
- carvacrol it is meant herein the compound of formula (I) above indicated, whether of natural origin, i.e. obtained by extraction from the plants containing it, or produced by synthesis.
- carvacrol also includes the extracts of the plants containing carvacrol, for example the oils extracted from said plants; in this case, the amounts of carvacrol set forth herein are always referred to carvacrol and not to the amounts of extract.
- component a) can be in an amount in the range from 10 to 45 wt%, for example from 10 wt% to 40 wt% or from 10 wt% to 30 wt%, for example from 28 wt% to 32 wt%.
- carvacrol is in an amount from 30 wt% to 30,8 wt%.
- carvacrol is in an amount of 30 wt%.
- carvacrol is in an amount of 30.8 wt%.
- the water-immiscible solvent is in an amount in the range from 20 wt% to 36 wt%, preferably from 21 wt% to 30 wt%. In embodiments, the water-immiscible solvent can be in an amount of 21 wt%, in an amount of 28 wt%, in an amount of 29 wt%, in an amount of 29.2 wt%, in an amount of 30 wt%.
- the weight ratio between said carvacrol a) and said water-immiscible solvent b) is 1 : 0.60 - 1.30, preferably 1 : 0.70 - 1.20, for example 1 : 0.70 - 1.
- the weight ratio between said carvacrol and said water-immiscible solvent can be 1 : 0.7, can be 1 : 0.93, can be 1 : 0.95, can be 1 : 0.967, can be 1:1, can be 1 : 1.167, can be 1:1.2.
- the water-immiscible solvent is selected from the esters of vegetable oils.
- Such compounds can be used as water-immiscible solvents and are preferably selected from esters of rapeseed oil (CAS n. 85586-25-0), the esters of soybean oil, the esters of palm oil, the esters of palm kernel oil, the esters of hemp oil, the esters of linseed oil, the esters of rice oil, the esters of com oil, the esters of sunflower oil, the esters of peanut oil, the esters of cotton-seed oil and mixtures thereof, preferably said esters being methyl esters.
- the water-immiscible solvent is made of methyl esters of rapeseed oil (CAS n.
- the water-immiscible solvent can be the product currently available in the market under the name “Radia 7961” (methyl esters of rapeseed oil, CAS n. 85586-25-0), distributed by Oleon N.V.
- the first non-ionic surfactant is in an amount in the range from 28 wt% to 40 wt%, preferably from 28 wt% to 39 wt%.
- the first non-ionic surfactant is selected from ethoxylated vegetable oils.
- the first non-ionic surfactant is the ethoxylated castor oil (CAS. n. 61791-12-6).
- the first non-ionic surfactant is ethoxylated castor oil (CAS. n. 61791-12-6), for example ethoxylated castor oil comprising from 30 to 40 units of ethylene oxide, preferably comprising from 34 to 38 units of ethylene oxide, more preferably comprising 36 units of ethylene oxide per molecule.
- the first non- ionic surfactant can be the product currently available on the market under the name “Emulson CO/36” (Ethoxylated castor oil), distributed by Lamberti S.p.A.
- the weight ratio between said carvacrol a) and said first non-ionic surfactant c) can be 1 : 0.60 - 1.50, preferably 1 : 0.90 - 1.30, preferably 1 : 0.93 - 1.30.
- the weight ratio between said carvacrol and said water-immiscible solvent can be, for example, 1 : 0.93, can be 1:1, can be 1 : 1.167, can be 1 : 1.168, can be 1 : 1.30.
- the weight ratio between said water-immiscible solvent b) and said first non-ionic surfactant c) is 1 : 0.75 - 1.75, preferably 1 : 1 - 1.75, for example 1 : 1.2 - 1.75.
- the weight ratio between said water-immiscible solvent and said first non-ionic surfactant can be 1 : 0.75 - 1.75, preferably 1 : 1 - 1.75, for example 1 : 1.2 - 1.75.
- the weight ratio between said water-immiscible solvent and said first non-ionic surfactant can
- 4 be, for example, 1 : 0.8, can be 1 : 0.83, can be 1 : 1, can be 1 : 1.23, can be 1 : 1.34, can be 1 : 1.67.
- the anionic surfactant is in an amount in the range from 0.4 wt% to 7.5 wt%; preferably from 0.5 wt% to 7 wt%, for example from 0.8 wt% to 7 wt%.
- the anionic surfactant is selected from the sulfonated surfactants.
- the anionic surfactant can be selected from alkylsulfonates, alkylarylsulfonates, diphenylsulfonates, alpha-olefmsulfonates, lignosulfonates, sulfonates of fatty acids, sulfonates of alkylphenols, sulfonates of alkoxylated arylphenols, sulfonates of condensed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes, sulfonates of naphthalenes and alkylnaphthalenes, sulfosuccinates and sulfosuccinamates.
- the anionic surfactant can be selected from the alkyl derivatives of benzenesulfonic acid.
- the anionic surfactant is the calcium salt of linear C10-C13 alkyl derivatives of benzenesulfonic acid (CAS n. 1335202-81-7).
- the second non-ionic surfactant is in an amount in the range from 0.15 wt% to 3 wt%, preferably from 0.2 wt% to 2.8 wt%, for example from 0.3 wt% to 2.8 wt%.
- the second non-ionic surfactant is selected from ethoxylated polyarylphenols, preferably ethoxylated tristyrylphenol (CAS n. 99734-09-5), ethoxylated alcohols, ethoxylated fatty acids, sorbitan esters and ethoxylated derivatives thereof, ethoxylated and/or propoxylated block copolymers, alkyl polyglycosides, organosilicon compounds and mixtures thereof.
- the second non-ionic surfactant is the ethoxylated tristyrylphenol (CAS. n. 99734-09-5).
- the composition comprises the product currently available on the market under the name “Geronol FF 4 E” (mixture of calcium salt of linear C10-C13 alkyl derivatives of benzenesulfonic acid (CAS n. 1335202-81-7) and ethoxylated tristyrylphenol (CAS n. 99734-09-5) in 2-ethylhexanol), distributed by Solvay Solutions Italia S.p.A.
- the composition can include a second solvent f), preferably 2- ethylhexanol.
- a second solvent f preferably 2- ethylhexanol.
- such second solvent, preferably 2-ethylhexanol is in an amount from 0.3 wt% to 6 %wt, preferably from 0.4 wt% to 5.6 wt%, and for example from 0.6 wt% to 4.5 wt%.
- the composition does not include esters of lactic acid.
- carvacrol a) is preferably in an amount in the range from 28 wt% to 32 wt%, more preferably from 29 wt% to 31 wt%, still more preferably from 30 wt% to 30.8 wt%.
- the water-immiscible solvent b) is preferably in an amount in the range from 21 wt% to 30 wt%.
- the first non-ionic surfactant c) is preferably in an amount in the range from 28 wt% to 39 wt%.
- the second non-ionic surfactant e) is preferably in an amount in the range from 0.2 wt% to 2.8 wt%, for example from 0.3 wt% to 2.8 wt% or from 0.3 to 2.3 %.
- the composition comprises: a) carvacrol in an amount in the range from 29 wt% to 31 wt%; b) at least one ester of a vegetable oil in an amount in the range from 21 wt% to 30 wt%; c) at least one ethoxylated vegetable oil in an amount in the range from 28 wt% to 39 wt%; d) at least one sulfonated surfactant in an amount in the range from 0.5 wt% to 7 wt%, for example from 0.8 wt% to 7 wt%; e) ethoxylated tristyrylphenol in an amount in the range from 0.2 wt% to 2.8 wt%, for example from 0.3 wt% to 2.8 wt%.
- the composition comprises: a) carvacrol in an amount in the range from 29 wt% to 31 wt%; b) methyl esters of rapeseed oil in an amount in the range from 21 wt% to 30 wt%; c) ethoxylated castor oil in an amount in the range from 28 wt% to 39 wt%;
- the composition can further comprise a second solvent f), preferably 2-ethylhexanol, in an amount from 0.3 wt% to 6 %wt, preferably from 0.4 wt% to 5.6 wt%, for example from 0.6 wt% to 4.5 wt%.
- a second solvent f preferably 2-ethylhexanol
- the composition comprises: a) carvacrol in an amount in the range from 30 wt% to 31 wt%; b) methyl esters of rapeseed oil in an amount in the range from 28 wt% to 30 wt%; c) ethoxylated castor oil in an amount in the range from 35 wt% to 38 wt%; d) calcium salt of linear C10-C13 alkyl derivatives of benzenesulfonic acid, preferably in an amount in the range from 1.6 wt% to 2 wt%; e) ethoxylated tristyrylphenol, preferably in an amount in the range from 0.6 wt% to 0.8 wt%, and optionally, f) 2-ethylhexanol, preferably in an amount in the range from 1.2 wt% to 1.6 wt%.
- the weight ratio between methyl esters of rapeseed oil b) and ethoxylated castor oil c) e 1 1.60 - 1.80.
- the weight ratio between carvacrol a) and methyl esters of rapeseed oil b) is 1 : 0.9 - 1.
- the emulsifiable concentrated compositions are typically diluted with water to form an emulsion.
- dilution can, for example, occur in suitable containers, such as barrels, where usually the plant protection products are diluted before the administration to plants; the dilution is carried out until obtaining a suitable concentration of the active ingredients, for example of carvacrol.
- the emulsion is then administered to the plants by means of known methods such as, for example, foliar spray, administrations by fertigation to the soil and in the seed furrow and treatment by seed incorporation.
- the composition of the invention is diluted with water at a concentration from 0.1 wt% to 3.0 wt% for foliar applications and soil fertigation, preferably from 0.5 wt% to 2.0 wt%, while it is used as it is for the incorporation in seed.
- the present invention refers to an aqueous composition
- an aqueous composition comprising the composition of the invention in an amount from 0.1 wt% to 3.0 wt%, for example from 0.5 wt% to 2.0 wt%.
- tackifiers and/or colorants can for example be added, during the seed dressing.
- composition of the invention can be used in combination with other plant protection products added for example in the aqueous composition described above.
- subject-matter of the invention is the use of the concentrated composition and/or the aqueous composition to prevent or treat a variety of plant infections, in particular fungal such as, for examples but not limited to, infections by Oomycetes, Aschomycota, Basidiomycota, e.g. Pythium, V. inaequalis, P. recondita, P. viticola, P. infestans.
- fungal such as, for examples but not limited to, infections by Oomycetes, Aschomycota, Basidiomycota, e.g. Pythium, V. inaequalis, P. recondita, P. viticola, P. infestans.
- subject-matter of the invention is the use of the concentrated composition and/or the aqueous composition as an insecticide to kill a variety of plant pests included, but not limited to, Hemiptera, Lepidoptera, e,g, the D. plantaginea and H. armigera.
- subject-matter of the invention is a method to prevent or treat a variety of plant infections, in particular fungal such as, for examples but not limited to, infections by Oomycetes, Aschomycota, Basidiomycota, e.g. Pythium, V. inaequalis, P. recondita, P. viticola, P. infestans, which comprises administering to the plant or crop concerned the concentrated composition and/or the aqueous composition of the invention.
- fungal such as, for examples but not limited to, infections by Oomycetes, Aschomycota, Basidiomycota, e.g. Pythium, V. inaequalis, P. recondita, P. viticola, P. infestans
- subject-matter of the invention is a method to provide insecticidal activity to kill a variety of plant pests included, but not limited to, Hemiptera, Lepidoptera, e,g, the D. plantaginea and H armigera. which comprises administering to the plant or crop concerned the concentrated composition and/or the aqueous composition of the invention.
- composition of the invention allows to obtain homogeneous and particularly stable emulsions in water, that is, which do not undergo phase separation, or which do not substantially undergo a phase separation once diluted in water.
- present "experimental section” reports experiments which demonstrate such technical effect.
- Emmulson CO/36 Ethoxylated castor oil, distributed by Lamberti S.p.A., (amount of active ingredient: 100%)
- Soprophor BSU ethoxylated tristyrylphenol (CAS n. 99734-09-5; amount of active ingredient >99% - ⁇ 100%), distributed by Solvay Solutions Italia S.p.A.
- Rhodacal 60 BE mixture of calcium salt of linear C10-C13 alkyl derivatives of benzenesulfonic acid (CAS n. 1335202-81-7; amount of active ingredient >60% - ⁇ 70%) and 2-ethylhexanol CAS n. 104-76-7; amount of active ingredient >30% - ⁇ 40%).
- amount of active ingredient it is meant the concentration of the compound specified within the commercial product.
- the stability of the compositions has been measured by diluting each composition at 5% in CIPAC D water (water with hardness of 342 ppm), in a graduated cylinder, and by evaluating the amount of cream or oil or phase separation after 2 hours.
- Table 1 reports the data of the compositions according to the present invention, and the respective results.
- Table 2 reports the data of comparative compositions, and the respective results. particular, a sulfonated anionic surfactant) and do not comprise the second non-ionic surfactant (in particular, ethoxylated tristyrylphenol).
- the comparative composition 10 shows a weight ratio between the water-immiscible solvent (methyl esters of rapeseed oil) and the first non-ionic surfactant (ethoxylated castor oil) of 1 : 0.47; and a weight ratio between carvacrol and said solvent of 1 : 1.50.
- the comparative composition 11 shows a weight ratio between the water-immiscible solvent (methyl esters of rapeseed oil) and the first non-ionic surfactant (ethoxylated castor oil) of 1 : 2.14.
- the comparative composition 13 does not comprise the second non-ionic surfactant (in particular, ethoxylated tristyrylphenol).
- the comparative composition 14 does not comprise the first non-ionic surfactant, i.e. the ethoxylated castor oil.
- compositions of the invention are particularly stable and result to be particularly useful in the use as phytosanitary agent, in particular as antifungal and/or insecticidal agricultural agent.
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Abstract
The present invention refers to compositions for the phytosanitary use. In particular, the present invention refers to emulsifiable concentrated formulations comprising carvacrol.
Description
"Emulsifiable concentrated composition comprising carvacrol"
****
Summary
The present invention refers to compositions for the phytosanitary use. In particular, the present invention refers to emulsifiable concentrated formulations comprising carvacrol.
Technical background
Several chemicals, of natural or synthetic origin, are used as plant protection products, where plant protection product means compounds or compositions used in agriculture to at least partially kill the parasites damaging cultivated plants, such as for example fungi, pathogenic insects and the like, in order to protect the health of said plants and to guarantee their survival. Said plant protection products or phytodrugs are also named, sometimes inappropriately, parasiticides, fungicides, pesticides and biocides.
Carvacrol, or 2-methyl-5 -isopropylphenol, having the following formula (I)
is present for example in the essential oil of oregano (Origanum spp.) and Satureja (Satureja spp.) and has very good antifungal and antibacterial properties, showing at the same time little toxicity to higher species of animals.
Carvacrol is poorly soluble in water. The poor water solubility of such compound makes its administration to the plants difficult. Indeed, typically, the plant protection products are administered to the plants through an aqueous medium.
It is known that, in order to use poorly water-soluble active ingredients as plant protection products (or phytodrugs), such active ingredients can be formulated in emulsifiable concentrates (also known as "EC"), that is, in formulations based on one or more solvents capable of forming homogeneous emulsions, when diluted with water.
However, after the water dilution, the resulting emulsions are generally scarcely stable, quickly undergoing phase separation, that is, the separation of the oil phase from the aqueous one. Such phase separation makes the product unusable.
A further problem of the known emulsifiable concentrates is the difficult to obtain homogeneous emulsions, that is, emulsions where the active ingredients, for example carvacrol, are uniformly distributed in the aqueous medium and do not form concentration gradients which could compromise the effectiveness of the treatment on the plants. Therefore, there is a need of having available formulations which allow to obtain homogeneous and stable emulsions of poorly water-soluble active ingredients, in particular of carvacrol.
Objects of the invention
It is an object of the invention to provide a composition comprising carvacrol which allows to obtain stable emulsions in water.
It is a further object of the invention to provide a composition comprising carvacrol which allows to obtain homogeneous emulsions in water.
It is a further object of the invention to provide a composition comprising carvacrol which allows to obtain emulsions in water in a simple, fast and safe way.
It is still an object of the invention to provide a composition comprising carvacrol which allows to obtain emulsions in water which are suitable to treat the plants in a simple and effective way.
Description of the invention
Subject-matter of the invention, according to one of the aspects thereof, is a composition comprising, and alternatively consists of: a) carvacrol in an amount from 10 to 45 wt%, for example from 10 wt% to 40 wt% or from 10 to 30 wt%; b) at least one water-immiscible solvent selected from vegetable oils and esters of the vegetable oils, preferably the esters of the vegetable oils, in an amount from 20 wt% to 40 wt%; c) at least one first non-ionic surfactant selected from ethoxylated vegetable oils, in an amount from 25 wt% to 40 wt%; d) at least one sulfonated anionic surfactant; e) at least one second non-ionic surfactant selected from ethoxylated polyarylphenols, for example ethoxylated tristyrylphenol, ethoxylated alcohols, ethoxylated fatty acids, sorbitan esters and ethoxylated derivatives thereof,
ethoxylated and/or propoxylated block copolymers, alkyl polyglycosides, organosilicon compounds and mixtures thereof; wherein the weight ratio between said water-immiscible solvent b) and said first nonionic surfactant c) is 1 : 0.75 - 1.75; and wherein the weight ratio between said carvacrol a) and said water-immiscible solvent b) is 1 : 0.60 - 1.30.
Unless otherwise stated, the percentages set forth herein are referred to weight percentages with respect to the total weight of the composition.
It has been observed that the composition of the invention allows to obtain particularly stable emulsions in water that comprise carvacrol, that is, which do not undergo a substantial phase separation once diluted in water, making their application, that is, administration to plants, impossible.
It has been also observed that the composition of the invention allows to obtain particularly homogeneous emulsions in water.
The composition, according to one of the aspects thereof, is an emulsifiable concentrate (EC).
With "carvacrol" it is meant herein the compound of formula (I) above indicated, whether of natural origin, i.e. obtained by extraction from the plants containing it, or produced by synthesis. The term "carvacrol" also includes the extracts of the plants containing carvacrol, for example the oils extracted from said plants; in this case, the amounts of carvacrol set forth herein are always referred to carvacrol and not to the amounts of extract.
In embodiments, component a) can be in an amount in the range from 10 to 45 wt%, for example from 10 wt% to 40 wt% or from 10 wt% to 30 wt%, for example from 28 wt% to 32 wt%. In preferred embodiments, carvacrol is in an amount from 30 wt% to 30,8 wt%. In embodiments, carvacrol is in an amount of 30 wt%. In embodiments, carvacrol is in an amount of 30.8 wt%.
In embodiments, the water-immiscible solvent is in an amount in the range from 20 wt% to 36 wt%, preferably from 21 wt% to 30 wt%. In embodiments, the water-immiscible solvent can be in an amount of 21 wt%, in an amount of 28 wt%, in an amount of 29 wt%, in an amount of 29.2 wt%, in an amount of 30 wt%.
As mentioned above, according to one of the aspects of the present invention, the weight ratio between said carvacrol a) and said water-immiscible solvent b) is 1 : 0.60 - 1.30,
preferably 1 : 0.70 - 1.20, for example 1 : 0.70 - 1. In embodiments, the weight ratio between said carvacrol and said water-immiscible solvent can be 1 : 0.7, can be 1 : 0.93, can be 1 : 0.95, can be 1 : 0.967, can be 1:1, can be 1 : 1.167, can be 1:1.2.
In one aspect, the water-immiscible solvent is selected from the esters of vegetable oils. Such compounds can be used as water-immiscible solvents and are preferably selected from esters of rapeseed oil (CAS n. 85586-25-0), the esters of soybean oil, the esters of palm oil, the esters of palm kernel oil, the esters of hemp oil, the esters of linseed oil, the esters of rice oil, the esters of com oil, the esters of sunflower oil, the esters of peanut oil, the esters of cotton-seed oil and mixtures thereof, preferably said esters being methyl esters. Preferably, the water-immiscible solvent is made of methyl esters of rapeseed oil (CAS n. 85586-25-0). For example, the water-immiscible solvent can be the product currently available in the market under the name “Radia 7961” (methyl esters of rapeseed oil, CAS n. 85586-25-0), distributed by Oleon N.V.
In embodiments, the first non-ionic surfactant is in an amount in the range from 28 wt% to 40 wt%, preferably from 28 wt% to 39 wt%.
In one aspect of the invention, the first non-ionic surfactant is selected from ethoxylated vegetable oils. In embodiments, the first non-ionic surfactant is the ethoxylated castor oil (CAS. n. 61791-12-6). Preferably, the first non-ionic surfactant is ethoxylated castor oil (CAS. n. 61791-12-6), for example ethoxylated castor oil comprising from 30 to 40 units of ethylene oxide, preferably comprising from 34 to 38 units of ethylene oxide, more preferably comprising 36 units of ethylene oxide per molecule. For example, the first non- ionic surfactant can be the product currently available on the market under the name “Emulson CO/36” (Ethoxylated castor oil), distributed by Lamberti S.p.A.
In embodiments, the weight ratio between said carvacrol a) and said first non-ionic surfactant c) can be 1 : 0.60 - 1.50, preferably 1 : 0.90 - 1.30, preferably 1 : 0.93 - 1.30. In embodiments, the weight ratio between said carvacrol and said water-immiscible solvent can be, for example, 1 : 0.93, can be 1:1, can be 1 : 1.167, can be 1 : 1.168, can be 1 : 1.30.
As mentioned above, according to one of the aspects of the present invention, the weight ratio between said water-immiscible solvent b) and said first non-ionic surfactant c) is 1 : 0.75 - 1.75, preferably 1 : 1 - 1.75, for example 1 : 1.2 - 1.75. In embodiments, the weight ratio between said water-immiscible solvent and said first non-ionic surfactant can
4
be, for example, 1 : 0.8, can be 1 : 0.83, can be 1 : 1, can be 1 : 1.23, can be 1 : 1.34, can be 1 : 1.67.
In embodiments, the anionic surfactant is in an amount in the range from 0.4 wt% to 7.5 wt%; preferably from 0.5 wt% to 7 wt%, for example from 0.8 wt% to 7 wt%.
In embodiments, the anionic surfactant is selected from the sulfonated surfactants. In embodiments, the anionic surfactant can be selected from alkylsulfonates, alkylarylsulfonates, diphenylsulfonates, alpha-olefmsulfonates, lignosulfonates, sulfonates of fatty acids, sulfonates of alkylphenols, sulfonates of alkoxylated arylphenols, sulfonates of condensed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes, sulfonates of naphthalenes and alkylnaphthalenes, sulfosuccinates and sulfosuccinamates. Preferably, the anionic surfactant can be selected from the alkyl derivatives of benzenesulfonic acid. For example, in particularly preferred embodiments, the anionic surfactant is the calcium salt of linear C10-C13 alkyl derivatives of benzenesulfonic acid (CAS n. 1335202-81-7).
In embodiments, the second non-ionic surfactant is in an amount in the range from 0.15 wt% to 3 wt%, preferably from 0.2 wt% to 2.8 wt%, for example from 0.3 wt% to 2.8 wt%.
In embodiments, the second non-ionic surfactant is selected from ethoxylated polyarylphenols, preferably ethoxylated tristyrylphenol (CAS n. 99734-09-5), ethoxylated alcohols, ethoxylated fatty acids, sorbitan esters and ethoxylated derivatives thereof, ethoxylated and/or propoxylated block copolymers, alkyl polyglycosides, organosilicon compounds and mixtures thereof. Preferably, the second non-ionic surfactant is the ethoxylated tristyrylphenol (CAS. n. 99734-09-5).
In embodiments, two or more surfactants of the composition can be used in pre-mixed form. In embodiments, the anionic surfactant and at least one of the two non-ionic surfactants can be used in pre-mixed form. For example, the anionic surfactant can be used in pre-mixed form with the second non-ionic surfactant. In embodiments, the anionic surfactant, preferably linear C10-C13 alkyl derivatives of benzenesulfonic acid, and the second non-ionic surfactant, preferably ethoxylated tristyrylphenol, can be used in premixed form. For example, in embodiments, the composition comprises the product currently available on the market under the name “Geronol FF 4 E” (mixture of calcium salt of linear C10-C13 alkyl derivatives of benzenesulfonic acid (CAS n. 1335202-81-7)
and ethoxylated tristyrylphenol (CAS n. 99734-09-5) in 2-ethylhexanol), distributed by Solvay Solutions Italia S.p.A.
In embodiments, the composition can include a second solvent f), preferably 2- ethylhexanol. In embodiments, such second solvent, preferably 2-ethylhexanol, is in an amount from 0.3 wt% to 6 %wt, preferably from 0.4 wt% to 5.6 wt%, and for example from 0.6 wt% to 4.5 wt%.
In embodiments, preferably, the composition does not include esters of lactic acid.
In embodiments, carvacrol a) is preferably in an amount in the range from 28 wt% to 32 wt%, more preferably from 29 wt% to 31 wt%, still more preferably from 30 wt% to 30.8 wt%.
In embodiments, the water-immiscible solvent b) is preferably in an amount in the range from 21 wt% to 30 wt%.
In embodiments, the first non-ionic surfactant c) is preferably in an amount in the range from 28 wt% to 39 wt%.
In embodiments, the anionic surfactant d) in preferably in an amount in the range from 0.5% to 7%, for example from 0.8% to 7% or from 0.8 to 6%.
In embodiments, the second non-ionic surfactant e) is preferably in an amount in the range from 0.2 wt% to 2.8 wt%, for example from 0.3 wt% to 2.8 wt% or from 0.3 to 2.3 %.
In embodiments, the composition comprises: a) carvacrol in an amount in the range from 29 wt% to 31 wt%; b) at least one ester of a vegetable oil in an amount in the range from 21 wt% to 30 wt%; c) at least one ethoxylated vegetable oil in an amount in the range from 28 wt% to 39 wt%; d) at least one sulfonated surfactant in an amount in the range from 0.5 wt% to 7 wt%, for example from 0.8 wt% to 7 wt%; e) ethoxylated tristyrylphenol in an amount in the range from 0.2 wt% to 2.8 wt%, for example from 0.3 wt% to 2.8 wt%.
In embodiments, the composition comprises: a) carvacrol in an amount in the range from 29 wt% to 31 wt%; b) methyl esters of rapeseed oil in an amount in the range from 21 wt% to 30 wt%; c) ethoxylated castor oil in an amount in the range from 28 wt% to 39 wt%;
6
d) calcium salt of linear C10-C13 alkyl derivatives of benzenesulfonic acid in an amount in the range from 0.5 wt% to 7 wt%, for example from 0.8 wt% to 6 wt%; e) ethoxylated tristyrylphenol in an amount in the range from 0.2 wt% to 2.8 wt%, for example from 0.3 wt% to 2.3 wt%.
As mentioned above, in embodiments, the composition can further comprise a second solvent f), preferably 2-ethylhexanol, in an amount from 0.3 wt% to 6 %wt, preferably from 0.4 wt% to 5.6 wt%, for example from 0.6 wt% to 4.5 wt%.
In an embodiment, the composition comprises: a) carvacrol in an amount in the range from 30 wt% to 31 wt%; b) methyl esters of rapeseed oil in an amount in the range from 28 wt% to 30 wt%; c) ethoxylated castor oil in an amount in the range from 35 wt% to 38 wt%; d) calcium salt of linear C10-C13 alkyl derivatives of benzenesulfonic acid, preferably in an amount in the range from 1.6 wt% to 2 wt%; e) ethoxylated tristyrylphenol, preferably in an amount in the range from 0.6 wt% to 0.8 wt%, and optionally, f) 2-ethylhexanol, preferably in an amount in the range from 1.2 wt% to 1.6 wt%. In embodiments, the weight ratio between methyl esters of rapeseed oil b) and ethoxylated castor oil c) e 1 : 1.20 - 1.25.
In embodiments, the weight ratio between methyl esters of rapeseed oil b) and ethoxylated castor oil c) e 1 : 1.60 - 1.80.
In embodiments, the weight ratio between carvacrol a) and methyl esters of rapeseed oil b) is 1 : 0.9 - 1.
In embodiments, the weight ratio between carvacrol a) and ethoxylated castor oil c) is 1 : 1.15 - 1.20.
According to one aspect of the present invention, the composition can be prepared by mixing, optionally in sequence, all the components, according to techniques known, per se, in the art.
As mentioned above, the emulsifiable concentrated compositions are typically diluted with water to form an emulsion. Such dilution can, for example, occur in suitable containers, such as barrels, where usually the plant protection products are diluted before
the administration to plants; the dilution is carried out until obtaining a suitable concentration of the active ingredients, for example of carvacrol.
The emulsion is then administered to the plants by means of known methods such as, for example, foliar spray, administrations by fertigation to the soil and in the seed furrow and treatment by seed incorporation.
In embodiments, the composition of the invention is diluted with water at a concentration from 0.1 wt% to 3.0 wt% for foliar applications and soil fertigation, preferably from 0.5 wt% to 2.0 wt%, while it is used as it is for the incorporation in seed.
According to a further aspect, the present invention refers to an aqueous composition comprising the composition of the invention in an amount from 0.1 wt% to 3.0 wt%, for example from 0.5 wt% to 2.0 wt%.
In the case of incorporation in seed, if desired or necessary, tackifiers and/or colorants can for example be added, during the seed dressing.
If desired or necessary, the composition of the invention can be used in combination with other plant protection products added for example in the aqueous composition described above.
According to a preferred embodiment, subject-matter of the invention is the use of the concentrated composition and/or the aqueous composition to prevent or treat a variety of plant infections, in particular fungal such as, for examples but not limited to, infections by Oomycetes, Aschomycota, Basidiomycota, e.g. Pythium, V. inaequalis, P. recondita, P. viticola, P. infestans.
According to a preferred embodiment, subject-matter of the invention is the use of the concentrated composition and/or the aqueous composition as an insecticide to kill a variety of plant pests included, but not limited to, Hemiptera, Lepidoptera, e,g, the D. plantaginea and H. armigera.
According to a preferred embodiment, subject-matter of the invention is a method to prevent or treat a variety of plant infections, in particular fungal such as, for examples but not limited to, infections by Oomycetes, Aschomycota, Basidiomycota, e.g. Pythium, V. inaequalis, P. recondita, P. viticola, P. infestans, which comprises administering to the plant or crop concerned the concentrated composition and/or the aqueous composition of the invention.
8
According to a preferred embodiment, subject-matter of the invention is a method to provide insecticidal activity to kill a variety of plant pests included, but not limited to, Hemiptera, Lepidoptera, e,g, the D. plantaginea and H armigera. which comprises administering to the plant or crop concerned the concentrated composition and/or the aqueous composition of the invention.
As discussed above, the composition of the invention allows to obtain homogeneous and particularly stable emulsions in water, that is, which do not undergo phase separation, or which do not substantially undergo a phase separation once diluted in water. The present "experimental section" reports experiments which demonstrate such technical effect.
Experimental section
14 concentrated emulsions have been produced by mixing, as set forth below, the following raw materials according to techniques per se known to the one skilled in the field:
- “technical ” carvacrol (amount of active ingredient: 99.9%- 100%)
- “Radia 7961”: methyl esters of rapeseed oil, CAS n. 85586-25-0, distributed by Oleon N.V., (amount of active ingredient: 100%)
- “Emulson CO/36”: Ethoxylated castor oil, distributed by Lamberti S.p.A., (amount of active ingredient: 100%)
- “Geronol FF 4 E”: mixture of calcium salt of linear C10-C13 alkyl derivatives of benzenesulfonic acid (CAS n. 1335202-81-7; amount of active ingredient >40% - <50%) and ethoxylated tristyrylphenol (CAS n. 99734-09-5; amount of active ingredient >15%
- <20%) and 2-ethylhexanol CAS n. 104-76-7; amount of active ingredient >30% - <40%), distributed by Solvay Solutions Italia S.p.A.
- “Soprophor BSU”: ethoxylated tristyrylphenol (CAS n. 99734-09-5; amount of active ingredient >99% - <100%), distributed by Solvay Solutions Italia S.p.A.
- “Rhodacal 60 BE”: mixture of calcium salt of linear C10-C13 alkyl derivatives of benzenesulfonic acid (CAS n. 1335202-81-7; amount of active ingredient >60% - <70%) and 2-ethylhexanol CAS n. 104-76-7; amount of active ingredient >30% - <40%).
By "amount of active ingredient", it is meant the concentration of the compound specified within the commercial product.
The stability of the compositions has been measured by diluting each composition at 5% in CIPAC D water (water with hardness of 342 ppm), in a graduated cylinder, and by evaluating the amount of cream or oil or phase separation after 2 hours.
An amount of cream lower or equal to 2 ml results to be acceptable for the purposes of the application.
Table 1 reports the data of the compositions according to the present invention, and the respective results.
Table 2 reports the data of comparative compositions, and the respective results.
particular, a sulfonated anionic surfactant) and do not comprise the second non-ionic surfactant (in particular, ethoxylated tristyrylphenol).
The comparative composition 10 shows a weight ratio between the water-immiscible solvent (methyl esters of rapeseed oil) and the first non-ionic surfactant (ethoxylated castor oil) of 1 : 0.47; and a weight ratio between carvacrol and said solvent of 1 : 1.50.
The comparative composition 11 shows a weight ratio between the water-immiscible solvent (methyl esters of rapeseed oil) and the first non-ionic surfactant (ethoxylated castor oil) of 1 : 2.14. The comparative composition 13 does not comprise the second non-ionic surfactant (in particular, ethoxylated tristyrylphenol).
The comparative composition 14 does not comprise the first non-ionic surfactant, i.e. the ethoxylated castor oil.
As demonstrated above, contrary to the comparative compositions, the compositions of the invention are particularly stable and result to be particularly useful in the use as phytosanitary agent, in particular as antifungal and/or insecticidal agricultural agent.
Claims
1. A composition comprising: a) carvacrol in an amount from 10 to 45 wt%, for example from 10 wt% to 40 wt% or from 10 to 30 wt%; b) at least one water-immiscible solvent selected from vegetable oils and esters of vegetable oils, in an amount from 20 wt% to 40 wt%; c) at least one first non-ionic surfactant selected from ethoxylated vegetable oils, in an amount from 25 wt% to 40 wt%; d) at least one sulfonated anionic surfactant; e) at least one second non-ionic surfactant selected from ethoxylated polyarylphenols, preferably ethoxylated tristyrylphenol, ethoxylated alcohols, ethoxylated fatty acids, sorbitan esters and ethoxylated derivatives thereof, ethoxylated and/or propoxylated block copolymers, alkyl polyglycosides, organosilicon compounds and mixtures thereof; wherein the weight ratio between said water-immiscible solvent b) and said first non-ionic surfactant c) is 1 : 0.75 - 1.75 and wherein the weight ratio between said carvacrol a) and said water-immiscible solvent b) is 1 : 0.60 - 1.30.
2. The composition according to claim 1, wherein the weight ratio between said water-immiscible solvent b) and said first non-ionic surfactant c) is 1 : 1 - 1.75.
3. The composition according to claim 1 or 2, wherein the weight ratio between said carvacrol a) and said water-immiscible solvent b) is 1 : 0.70 - 1.20.
4. The composition according to any one of the preceding claims, wherein said water-immiscible solvent b) is selected from the esters of rapeseed oil, the esters of soybean oil, the esters of palm oil, the esters of palm kernel oil, the esters of hemp oil, the esters of linseed oil, the esters of rice oil, the esters of com oil, the esters of sunflower oil, the esters of peanut oil, the esters of cotton-seed oil and mixtures thereof, preferably said esters being methyl esters, more preferably being the methyl esters of rapeseed oil.
5. The composition according to any one of the preceding claims, wherein said first non-ionic surfactant c) is ethoxylated castor oil.
6. The composition according to any one of the preceding claims, wherein said sulfonated anionic surfactant d) is in an amount in the range from 0.4% to 7.5%.
7. The composition according to any one of the preceding claims, wherein said non-ionic surfactant e) is in an amount in the range from 0.2% to 2.8%.
8. The composition according to any one of the preceding claims, wherein said sulfonated anionic surfactant is selected from alkylsulfonates, alkylarylsulfonates, diphenylsulfonates, alpha-olefin sulfonates, lignosulfonates, sulfonates of fatty acids, sulfonates of alkylphenols, sulfonates of alkoxylated arylphenols, sulfonates of condensed naphthalenes, sulfonates of dodecyl- and tridecylbenzenes, sulfonates of naphthalenes and alkylnaphthalenes, sulfosuccinates, sulfosuccinamates, and preferably it is selected from the alkyl derivatives of benzenesulfonic acid.
9. The composition according to any one of the preceding claims, further comprising a second solvent f), preferably 2-ethylhexanol, in an amount from 0.3 wt% to 6 wt%.
10. An aqueous composition comprising the composition according to any one of the preceding claims, in an amount from 0.1 wt% to 3.0 wt%, preferably from 0.5 wt% to 2.0 wt%.
11. Use of the composition according to any one of claims 1 to 9 or of the aqueous composition according to claim 10, to prevent or treat a variety of plant infections, preferably fungal infections.
12. Use of the composition according to any one of claims 1 to 9 for the preparation of aqueous emulsions suitable to prevent or treat a variety of plant infections, preferably fungal infections.
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AU2016378260A1 (en) * | 2015-12-22 | 2018-05-24 | Bayer Cropscience Aktiengesellschaft | Emulsion concentrates of lipophilic compounds |
CN105613524A (en) * | 2015-12-23 | 2016-06-01 | 太仓东浔生物科技有限公司 | Environment-friendly and multi-effect biopesticide for vegetable planting |
CN110476972A (en) * | 2019-09-05 | 2019-11-22 | 湖南宇山玉月农业科技有限公司 | A kind of looper insecticide |
CN111034861A (en) * | 2020-02-10 | 2020-04-21 | 中国科学院兰州化学物理研究所盱眙凹土应用技术研发中心 | Method for preparing oil-in-water emulsion coated plant essential oil by using lauric acid monoglyceride |
CN111213679A (en) * | 2020-02-27 | 2020-06-02 | 无锡迈莱博生物科技有限公司 | Plant acarus killing bacteriostatic solution and preparation method and application thereof |
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2021
- 2021-08-10 IT IT102021000021710A patent/IT202100021710A1/en unknown
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2022
- 2022-08-08 AR ARP220102128A patent/AR126736A1/en unknown
- 2022-08-10 EP EP22764851.6A patent/EP4384007A1/en active Pending
- 2022-08-10 WO PCT/IB2022/057439 patent/WO2023017427A1/en unknown
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IT202100021710A1 (en) | 2023-02-10 |
AR126736A1 (en) | 2023-11-08 |
WO2023017427A1 (en) | 2023-02-16 |
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