CN114190386A - Compound composition of propamidine and sabinenol, bactericide and application - Google Patents
Compound composition of propamidine and sabinenol, bactericide and application Download PDFInfo
- Publication number
- CN114190386A CN114190386A CN202111451130.3A CN202111451130A CN114190386A CN 114190386 A CN114190386 A CN 114190386A CN 202111451130 A CN202111451130 A CN 202111451130A CN 114190386 A CN114190386 A CN 114190386A
- Authority
- CN
- China
- Prior art keywords
- propamidine
- juniperol
- hinokitiol
- propaneamidine
- alcohol
- 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.)
- Granted
Links
- 230000000844 anti-bacterial effect Effects 0.000 title claims abstract description 34
- 239000003899 bactericide agent Substances 0.000 title claims abstract description 33
- 239000000203 mixture Substances 0.000 title claims abstract description 33
- 150000001875 compounds Chemical class 0.000 title claims abstract description 26
- WTFXJFJYEJZMFO-UHFFFAOYSA-N propamidine Chemical group C1=CC(C(=N)N)=CC=C1OCCCOC1=CC=C(C(N)=N)C=C1 WTFXJFJYEJZMFO-UHFFFAOYSA-N 0.000 title abstract description 73
- 229960003761 propamidine Drugs 0.000 title abstract description 73
- FUWUEFKEXZQKKA-UHFFFAOYSA-N beta-thujaplicin Chemical compound CC(C)C=1C=CC=C(O)C(=O)C=1 FUWUEFKEXZQKKA-UHFFFAOYSA-N 0.000 claims abstract description 129
- TUFYVOCKVJOUIR-UHFFFAOYSA-N alpha-Thujaplicin Natural products CC(C)C=1C=CC=CC(=O)C=1O TUFYVOCKVJOUIR-UHFFFAOYSA-N 0.000 claims abstract description 66
- 229930007845 β-thujaplicin Natural products 0.000 claims abstract description 66
- 241000221662 Sclerotinia Species 0.000 claims abstract description 16
- 238000002360 preparation method Methods 0.000 claims abstract description 6
- -1 alcohol compound Chemical class 0.000 claims description 26
- 239000003795 chemical substances by application Substances 0.000 claims description 23
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 21
- 239000002270 dispersing agent Substances 0.000 claims description 21
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 18
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 18
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 14
- 229920000056 polyoxyethylene ether Polymers 0.000 claims description 13
- 229940051841 polyoxyethylene ether Drugs 0.000 claims description 13
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 12
- 241000196324 Embryophyta Species 0.000 claims description 12
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims description 12
- 239000004562 water dispersible granule Substances 0.000 claims description 12
- 241000123650 Botrytis cinerea Species 0.000 claims description 11
- 238000002156 mixing Methods 0.000 claims description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 238000009736 wetting Methods 0.000 claims description 10
- 239000003995 emulsifying agent Substances 0.000 claims description 9
- 239000002994 raw material Substances 0.000 claims description 9
- 239000000080 wetting agent Substances 0.000 claims description 9
- 239000000230 xanthan gum Substances 0.000 claims description 9
- 235000010493 xanthan gum Nutrition 0.000 claims description 9
- 229920001285 xanthan gum Polymers 0.000 claims description 9
- 229940082509 xanthan gum Drugs 0.000 claims description 9
- 239000000839 emulsion Substances 0.000 claims description 8
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 7
- 239000004202 carbamide Substances 0.000 claims description 7
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 7
- 239000002562 thickening agent Substances 0.000 claims description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Natural products CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 235000010323 ascorbic acid Nutrition 0.000 claims description 6
- 229960005070 ascorbic acid Drugs 0.000 claims description 6
- 239000011668 ascorbic acid Substances 0.000 claims description 6
- HUMNYLRZRPPJDN-UHFFFAOYSA-N benzaldehyde Chemical compound O=CC1=CC=CC=C1 HUMNYLRZRPPJDN-UHFFFAOYSA-N 0.000 claims description 6
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 6
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 6
- 239000000417 fungicide Substances 0.000 claims description 6
- 235000019422 polyvinyl alcohol Nutrition 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- 239000000375 suspending agent Substances 0.000 claims description 6
- 230000002528 anti-freeze Effects 0.000 claims description 5
- 239000003963 antioxidant agent Substances 0.000 claims description 5
- 230000003078 antioxidant effect Effects 0.000 claims description 5
- 235000006708 antioxidants Nutrition 0.000 claims description 5
- 239000003755 preservative agent Substances 0.000 claims description 5
- 230000002335 preservative effect Effects 0.000 claims description 5
- 239000004563 wettable powder Substances 0.000 claims description 5
- 235000010489 acacia gum Nutrition 0.000 claims description 4
- 235000010199 sorbic acid Nutrition 0.000 claims description 4
- 239000004334 sorbic acid Substances 0.000 claims description 4
- 229940075582 sorbic acid Drugs 0.000 claims description 4
- 238000003756 stirring Methods 0.000 claims description 4
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 claims description 3
- DMAXMXPDVWTIRV-UHFFFAOYSA-N 2-(2-phenylethyl)phenol Chemical compound OC1=CC=CC=C1CCC1=CC=CC=C1 DMAXMXPDVWTIRV-UHFFFAOYSA-N 0.000 claims description 3
- 239000005711 Benzoic acid Substances 0.000 claims description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- HSFWRNGVRCDJHI-UHFFFAOYSA-N alpha-acetylene Natural products C#C HSFWRNGVRCDJHI-UHFFFAOYSA-N 0.000 claims description 3
- SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 claims description 3
- 235000010233 benzoic acid Nutrition 0.000 claims description 3
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 3
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- 239000000194 fatty acid Substances 0.000 claims description 3
- 229930195729 fatty acid Natural products 0.000 claims description 3
- 150000002191 fatty alcohols Chemical class 0.000 claims description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 3
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 claims description 3
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 claims description 3
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 claims description 3
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 claims description 3
- QNGNSVIICDLXHT-UHFFFAOYSA-N para-ethylbenzaldehyde Natural products CCC1=CC=C(C=O)C=C1 QNGNSVIICDLXHT-UHFFFAOYSA-N 0.000 claims description 3
- IIOADSXXVWNOSC-UHFFFAOYSA-N pentyl 3,4,5-trihydroxybenzoate Chemical compound CCCCCOC(=O)C1=CC(O)=C(O)C(O)=C1 IIOADSXXVWNOSC-UHFFFAOYSA-N 0.000 claims description 3
- 229940068984 polyvinyl alcohol Drugs 0.000 claims description 3
- 229920001289 polyvinyl ether Polymers 0.000 claims description 3
- 239000011347 resin Substances 0.000 claims description 3
- 229920005989 resin Polymers 0.000 claims description 3
- 235000010413 sodium alginate Nutrition 0.000 claims description 3
- 239000000661 sodium alginate Substances 0.000 claims description 3
- 229940005550 sodium alginate Drugs 0.000 claims description 3
- 125000003944 tolyl group Chemical group 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- 238000005469 granulation Methods 0.000 claims description 2
- 230000003179 granulation Effects 0.000 claims description 2
- WSWCOQWTEOXDQX-MQQKCMAXSA-N sorbic acid group Chemical group C(\C=C\C=C\C)(=O)O WSWCOQWTEOXDQX-MQQKCMAXSA-N 0.000 claims description 2
- GNFWGDKKNWGGJY-UHFFFAOYSA-N propanimidamide Chemical group CCC(N)=N GNFWGDKKNWGGJY-UHFFFAOYSA-N 0.000 claims 19
- MNNFKQAYXGEKFA-UHFFFAOYSA-N (+)-Juniperol Natural products CC1(C)CCCC2(C)C3(C)C(O)C1C2CC3 MNNFKQAYXGEKFA-UHFFFAOYSA-N 0.000 claims 11
- MNNFKQAYXGEKFA-MJBFILCRSA-N longiborneol Chemical compound CC1(C)CCCC2(C)C3(C)[C@@H](O)C1C2CC3 MNNFKQAYXGEKFA-MJBFILCRSA-N 0.000 claims 10
- 235000019441 ethanol Nutrition 0.000 claims 7
- 241000721662 Juniperus Species 0.000 claims 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 4
- 239000013530 defoamer Substances 0.000 claims 4
- 230000000855 fungicidal effect Effects 0.000 claims 3
- 239000002131 composite material Substances 0.000 claims 2
- 244000215068 Acacia senegal Species 0.000 claims 1
- 241000218691 Cupressaceae Species 0.000 claims 1
- 229920000084 Gum arabic Polymers 0.000 claims 1
- 239000000205 acacia gum Substances 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 239000007798 antifreeze agent Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 241000894007 species Species 0.000 claims 1
- 239000013589 supplement Substances 0.000 claims 1
- 235000012055 fruits and vegetables Nutrition 0.000 abstract description 15
- 239000003814 drug Substances 0.000 abstract description 12
- 235000006008 Brassica napus var napus Nutrition 0.000 abstract description 8
- 206010059866 Drug resistance Diseases 0.000 abstract description 6
- 229940079593 drug Drugs 0.000 abstract description 6
- HYZJCKYKOHLVJF-UHFFFAOYSA-N 1H-benzimidazole Chemical compound C1=CC=C2NC=NC2=C1 HYZJCKYKOHLVJF-UHFFFAOYSA-N 0.000 abstract description 4
- WLLGXSLBOPFWQV-UHFFFAOYSA-N MGK 264 Chemical compound C1=CC2CC1C1C2C(=O)N(CC(CC)CCCC)C1=O WLLGXSLBOPFWQV-UHFFFAOYSA-N 0.000 abstract description 4
- 229930014626 natural product Natural products 0.000 abstract description 3
- 244000060924 Brassica campestris Species 0.000 abstract 2
- TWFZGCMQGLPBSX-UHFFFAOYSA-N Carbendazim Natural products C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 18
- 239000006013 carbendazim Substances 0.000 description 18
- JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 description 18
- 230000002195 synergetic effect Effects 0.000 description 15
- 201000010099 disease Diseases 0.000 description 12
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 12
- 241000221696 Sclerotinia sclerotiorum Species 0.000 description 11
- 230000000694 effects Effects 0.000 description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- 239000002518 antifoaming agent Substances 0.000 description 9
- 244000052616 bacterial pathogen Species 0.000 description 9
- 240000002791 Brassica napus Species 0.000 description 7
- 239000000575 pesticide Substances 0.000 description 7
- 230000003902 lesion Effects 0.000 description 6
- 238000002474 experimental method Methods 0.000 description 5
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- 230000005764 inhibitory process Effects 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- 230000002265 prevention Effects 0.000 description 4
- 239000012747 synergistic agent Substances 0.000 description 4
- 230000001988 toxicity Effects 0.000 description 4
- 231100000419 toxicity Toxicity 0.000 description 4
- GJJYQFPADNKBDY-UHFFFAOYSA-N Sabinol Natural products C=C1CCC2(C(C)C)C1(O)C2 GJJYQFPADNKBDY-UHFFFAOYSA-N 0.000 description 3
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 3
- 239000001785 acacia senegal l. willd gum Substances 0.000 description 3
- 238000001125 extrusion Methods 0.000 description 3
- 239000002609 medium Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000011160 research Methods 0.000 description 3
- MDFQXBNVOAKNAY-HWOCKDDLSA-N sabinol Chemical compound C([C@@H](O)C1=C)C2(C(C)C)C1C2 MDFQXBNVOAKNAY-HWOCKDDLSA-N 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 239000010703 silicon Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- MDYOLVRUBBJPFM-UHFFFAOYSA-N tropolone Chemical compound OC1=CC=CC=CC1=O MDYOLVRUBBJPFM-UHFFFAOYSA-N 0.000 description 3
- 206010034133 Pathogen resistance Diseases 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 238000012271 agricultural production Methods 0.000 description 2
- 230000003385 bacteriostatic effect Effects 0.000 description 2
- 238000012258 culturing Methods 0.000 description 2
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- 239000001963 growth medium Substances 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 239000003960 organic solvent Substances 0.000 description 2
- 230000002829 reductive effect Effects 0.000 description 2
- 230000001018 virulence Effects 0.000 description 2
- 235000011293 Brassica napus Nutrition 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 239000005867 Iprodione Substances 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- CFZLNRGUBAVQNO-UHFFFAOYSA-N N-(3,5-Dichlorophenyl)succinimide Chemical compound ClC1=CC(Cl)=CC(N2C(CCC2=O)=O)=C1 CFZLNRGUBAVQNO-UHFFFAOYSA-N 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 description 1
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 230000002452 interceptive effect Effects 0.000 description 1
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229930003658 monoterpene Natural products 0.000 description 1
- 239000010413 mother solution Substances 0.000 description 1
- 239000000447 pesticide residue Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000013641 positive control Substances 0.000 description 1
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- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005303 weighing Methods 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/52—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing groups, e.g. carboxylic acid amidines
-
- 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
- A01N25/12—Powders or granules
- A01N25/14—Powders or granules wettable
-
- 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing keto or thioketo groups as part of a ring, e.g. cyclohexanone, quinone; Derivatives thereof, e.g. ketals
-
- 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
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
The invention provides a compound composition of propamidine and hinokitiol, a bactericide and application; the ratio by mass of propamidine: hinokitiol (1-8): 2-1). The propamidine and the natural product sabinenol are compounded to prevent and treat sclerotinia rot of colza and gray mold of fruits and vegetables, and can be used for treating sclerotinia rot of colza and gray mold of fruits and vegetables which have drug resistance to benzimidazole and dicarboximide bactericides. The binary compound preparation has obvious synergy and can obviously reduce the use amount of the preparation for preventing and treating drug-resistant rape sclerotinia rot and fruit and vegetable gray mold, and the compound preparation is expected to be developed into a new generation of green agricultural bactericide.
Description
Technical Field
The invention belongs to the field of agricultural bactericides, and particularly relates to a compound composition of propamidine and hinokitiol, a bactericide and application. The two compounds are compounded to prevent and treat sclerotinia rot of colza, gray mold of fruits and vegetables and the method for treating sclerotinia rot of colza and gray mold of fruits and vegetables which have generated drug resistance to benzimidazole and dicarboximide bactericides, belonging to the invention of new application and application technology of the bactericides.
Background
Crop diseases cause enormous economic losses to agricultural production each year. At the present stage, chemical control is still an important means for controlling plant diseases. However, as chemical pesticides are repeatedly used for a long time, the problems of pathogenic bacteria resistance and pesticide residue are increasingly prominent. At present, people pay close attention to green food and environmental safety, and development of new environment-friendly green pesticides for preventing and treating crop diseases and insect pests is urgently needed. The pesticide can make up for the deficiencies of the pesticides, improve the control effect, reduce the cost and more importantly delay the occurrence of drug resistance. Propamidine (Propamidine) is an alkyl amidine environment-friendly compound, and is a novel bactericide variety developed and researched by Shanxi province biological pesticide engineering technical research center. Early researches show that propamidine has broad-spectrum antibacterial activity, has good inhibition effect on botrytis cinerea and sclerotinia sclerotiorum, does not have interactive drug resistance with the existing bactericide, and has wide application prospect.
Hinokitiol (hinokitiol) is a plant-derived natural product of tropolone family extracted from hinoki, and is a monoterpenoid compound having tropolone skeleton. Earlier researches find that the hinokitiol has wide biological activity, can be used as a natural plant source bactericide, and has excellent control effect on soil-borne diseases. The hinokitiol has simple structure, easy synthesis, environment friendship and high safety to non-target organism, is a natural, safe and efficient matter and has great potential for being developed into plant source bactericide.
Sclerotinia sclerotiorum (sclerotiniose rot) caused by saprophytic fungi Sclerotinia sclerotiorum (Lib.) de bark is a worldwide crop disease and can infect more than 400 plants of 278 genus of 75 families. The disease is generated in various rape planting areas in China, particularly serious in middle and lower reaches watershed of the south east coast and the Yangtze river, the annual disease area is nearly 5000 ten thousand mu, the annual average yield loss is about 20%, and even the annual average yield loss is up to 80% when serious, even the disease is completely harvested. After the rape is infected with the disease, the yield and the quality of the rapeseeds are seriously reduced, and the economic loss is hundreds of millions of yuan. Crop gray mold caused by Botrytis cinerea (Botrytis cinerea) is one of ten major fungal diseases in the world. The pathogenic bacteria has wide host range, can infect more than 500 kinds of plants including various fruits, vegetables and flowers, and causes huge economic loss for agricultural production. The host of botrytis cinerea will be attacked in each period from seedling stage to adult stage, and the pathogenic bacteria produce conidiophores and conidia on the surface of the diseased part and form a grey mould layer on the surface of the diseased part after gradually accumulating. Benzimidazole fungicides such as carbendazim and benomyl, and dicarboximide fungicides such as dimethachlon and iprodione have been common agents for controlling the above two diseases for many years. However, the frequency and level of resistance of pathogenic bacteria to these agents has gradually increased due to the repeated use of these agents in large quantities. Such as Botrytis cinerea, have developed different levels of resistance to most agents registered on manufacture for the control of gray mold, and the problem of multiple resistance has become increasingly serious. Therefore, screening of novel efficient green alternative agents and compound agents is one of the important ways for preventing and treating the diseases.
Disclosure of Invention
The invention aims to provide binary compounding of propamidine and a natural product, namely hinokitiol, and can be simultaneously used for treating drug-resistant sclerotinia rot of colza and gray mold of fruits and vegetables.
The specific technical scheme is as follows:
a compound composition of propamidine and hinokitiol comprises the following components in percentage by mass: hinokitiol (1-8): 2-1).
A compound composition of propamidine and hinokitiol comprises the following components in percentage by mass: hinokitiol 2: 1.
A compound composition of propamidine and hinokitiol comprises the following components in percentage by mass: hinokitiol 4: 1.
A compound composition of propamidine and hinokitiol comprises the following components in percentage by mass: hinokitiol is 6: 1.
The invention relates to application of a compound composition of propamidine and hinokitiol in preparation of a plant bactericide.
The invention discloses a propamidine and hinokitiol compound bactericide, which comprises the effective components of the propamidine and hinokitiol compound composition.
Optionally, the bactericide is an aqueous emulsion, and the weight percentage content is as follows:
1 to 40 percent of propamidine, 1 to 40 percent of hinokitiol, 5 to 10 percent of emulsifier, 0.5 to 2 percent of dispersant, 0.5 to 2 percent of antifreeze, 0.5 to 1 percent of preservative and 100 percent of solvent;
the dispersing agent is polyvinyl alcohol, Arabic gum, xanthan gum or magnesium aluminum silicate;
the solvent is toluene, xylene, ethyl acetate or cyclohexanone;
the antifreezing agent is ethylene glycol, propylene glycol, glycerol or urea;
the preservative is sorbic acid, benzoic acid or benzaldehyde;
the emulsifier is one or a mixture of more than two of alkyl polyoxyethylene ether, polyoxyethylene fatty acid ester, phenethyl phenol polyoxyethylene ether, 7780, 7781T, 4103, OP-10, Well201, No. 500, No. 602, Well205 and M30.
Optionally, the bactericide is a suspending agent, and the weight percentage content is as follows:
1 to 50 percent of propamidine, 1 to 30 percent of hinokitiol, 1 to 5 percent of wetting dispersant, 0.2 to 5 percent of defoaming agent, 0.5 to 5 percent of thickening agent, 0.5 to 5 percent of antioxidant, 0.5 to 2 percent of antifreezing agent and water to be supplemented to 100 percent;
the wetting dispersant is one or a mixture of more than two of alkylphenol resin polyvinyl ether, alkylbenzene sulfonate, long-chain fatty alcohol polyoxyethylene ether, alkylphenol polyoxyethylene ether and fatty alcohol sulfate;
the defoaming agent is an acetylene glycol wetting defoaming agent or an organic silicon defoaming agent;
the thickening agent is polyvinyl alcohol, xanthan gum, sodium alginate, xanthan gum or hydroxypropyl methyl cellulose;
the antioxidant is ascorbic acid or amyl gallate;
the antifreezing agent is ethylene glycol, propylene glycol, glycerol or urea.
Optionally, the bactericide is water dispersible granules, and the weight percentage content is as follows:
1 to 40 percent of propamidine, 1 to 40 percent of hinokitiol, 1 to 5 percent of wetting agent, 1 to 5 percent of dispersing agent and 0.15 to 3 percent of disintegrating agent;
the raw materials of propamidine, sabinenol, wetting agent, dispersant and disintegrant are mixed uniformly, and then pulverized by a jet mill to prepare superfine wettable powder, then a certain amount of water is added and stirred uniformly, and the mixture is granulated by an extrusion granulator, dried by a jet dryer and sieved to obtain the water dispersible granule.
The propamidine and hinokitiol compound bactericide is applied to prevention and treatment of plant sclerotinia rot and/or gray mold.
Compared with the prior art, the invention has the advantages that:
(1) according to a series of proportioning researches, the propamidine and the hinokitiol are proportioned according to the mass ratio of (1-8) to (2-1), the synergistic coefficient is larger than 1.5, and the propamidine and the hinokitiol have obvious synergistic effects.
(2) Greenhouse pot control experiments show that the bactericide prepared from propamidine and juniperitol has good control effects on sclerotinia rot and gray mold of carbendazim.
Detailed Description
In order to make the objects, technical solutions and advantages of the present invention clearer, the present invention will be described in further detail with reference to embodiments, and it is obvious that the described embodiments are only a part of the embodiments of the present invention, not all of the embodiments. All other embodiments, which can be derived by a person skilled in the art from the embodiments given herein without making any creative effort, shall fall within the protection scope of the present invention.
The compound bactericide of the propamidine and the hinokitiol is a preparation compounded by the propamidine and the hinokitiol according to the mass ratio of (1-8) to (2-1), so that the compound bactericide can be used for preventing and treating wild sensitive strains of sclerotinia sclerotiorum and botrytis cinerea of fruits and vegetables, and can be used for preventing and treating sclerotinia sclerotiorum and botrytis cinerea strains of fruits and vegetables which have drug resistance to benzimidazole and dicarboximide bactericides, and more importantly, the two bactericides have an obvious synergistic effect under the above proportion, and the dosage of chemical bactericides can be reduced.
Dosage forms such as bactericides include aqueous emulsions, suspending agents and water dispersible granules;
the aqueous emulsion comprises the following components in percentage by weight: 1 to 40 percent of propamidine, 1 to 40 percent of hinokitiol, 5 to 10 percent of emulsifier, 0.5 to 2 percent of dispersant, 0.5 to 2 percent of antifreeze, 0.5 to 1 percent of preservative and 100 percent of solvent; the dispersant is polyvinyl alcohol, Arabic gum, xanthan gum or magnesium aluminum silicate; the solvent is toluene, xylene, ethyl acetate or cyclohexanone; the antifreezing agent is ethylene glycol, propylene glycol, glycerol or urea; the antiseptic is sorbic acid, benzoic acid or benzaldehyde; the emulsifier is one or more of alkyl polyoxyethylene ether, polyoxyethylene fatty acid ester, phenethyl phenol polyoxyethylene ether, 7780, 7781T, 4103, OP-10, Well201, No. 500, No. 602, Well205 or M30.
The suspending agent comprises the following components in percentage by weight: 1 to 50 percent of propamidine, 1 to 30 percent of hinokitiol, 1 to 5 percent of wetting dispersant, 0.2 to 5 percent of defoaming agent, 0.5 to 5 percent of thickening agent, 0.5 to 5 percent of ascorbic acid, 0.5 to 2 percent of antifreezing agent and water to be supplemented to 100 percent. The antioxidant is ascorbic acid or amyl gallate, and the wetting dispersant is one or more of alkylphenol resin polyvinyl ether, alkylbenzene sulfonate, long-chain fatty alcohol polyoxyethylene ether, alkylphenol polyoxyethylene ether and fatty alcohol sulfate; the thickener is polyvinyl alcohol, xanthan gum, sodium alginate, xanthan gum or hydroxypropyl methyl cellulose; the defoaming agent is an acetylene glycol wetting defoaming agent and an organic silicon defoaming agent; the antifreezing agent is ethylene glycol, propylene glycol, glycerol or urea, etc.
The water dispersible granule comprises the following components in percentage by weight: 1-40% of propamidine, 1-40% of hinokitiol, 1-5% of wetting agent, 1-5% of dispersing agent and 0.15-3% of disintegrating agent, wherein the raw materials of propamidine, hinokitiol, wetting agent, dispersing agent and disintegrating agent are uniformly mixed, then crushed by a jet mill to prepare superfine wettable powder, then a certain amount of water is added and uniformly stirred, and the superfine wettable powder is granulated by an extrusion granulator, dried by a gas flow dryer and screened to obtain the water dispersible granule.
The propamidine and hinokitiol compounded synergistic bactericide is applied to the prevention and treatment of plant sclerotinia rot and gray mold, and is a substitute medicament for the drug resistance treatment of the sclerotinia rot and the gray mold.
Example 1: indoor in vitro determination of toxicity of propamidine and hinokitiol
The toxicity of propamidine and hinokitiol to pathogenic bacteria is determined by hypha growth rate method. Dissolving propamidine with methanol to 5000, 2500, 1250, 625, 312.5, 156.2 and 78.125 ug/ml; dissolving hinokitiol with methanol to 25000, 12500, 6250, 3125, 1562.5, 781.25 and 390.625 ug/ml; carbendazim was dissolved with 0.2M hydrochloric acid to 500, 250, 125, 62.5 and 31.25 ug/ml. Sucking 0.2mL of the mother solution by using a pipette gun respectively, adding 100mL of PDA culture medium to prepare drug-containing culture medium with final concentrations of 10, 5, 2.5, 1.25, 0.625 and 0.3125ug/mL propamidine respectively; medicated medium with final concentration of 50, 25, 12.5, 6.25, 3.125, 1.5625 and 0.78125ug/ml hinokitiol respectively; drug-containing media with final concentrations of 1, 0.5, 0.25, 0.125, and 0.0625ug/ml carbendazim, respectively. The cake of pathogenic bacteria with the diameter of 0.5cm at the edge of the colony was placed in the center of the dish (hypha facing down) and 0.2mL of methanol or 0.2M hydrochloric acid was added as a control. Culturing the inoculated culture dish at 25 deg.C for 3d, respectively measuring colony diameter by cross method, calculating bacteriostasis rate by using blank control as standard, and calculating effective inhibitory concentration (EC) by DPS software50). The Sclerotinia sclerotiorum and Botrytis cinerea strains used in the experiment are both preserved in the laboratory. All adopt the conventional strain separation method to separate the strain from the diseased residues of the susceptible plants and adopt the conventional strain identification methodThe specific pathogenic bacteria number is the strain obtained by different isolates at different time, and has no special meaning.
TABLE 1 determination of the sensitivity of carbendazim, propamidine, and sabinenol to Sclerotinia sclerotiorum
S is a multi-bacterium sensitive strain; r is carbendazim resistant strain.
As can be seen from Table 1, there is no cross-resistance between propamidine, hinokitiol and carbendazim, and propamidine and hinokitiol have good bacteriostatic activity against Sclerotinia sclerotiorum.
TABLE 2 determination of susceptibility of carbendazim, propamidine, and sabinenol to Botrytis cinerea
S is a multi-bacterium sensitive strain; r is carbendazim resistant strain.
As can be seen from Table 2, there is no cross-resistance between propamidine, hinokitiol and carbendazim, and propamidine and hinokitiol have good bacteriostatic activity against gray mold of fruits and vegetables.
Example 2: synergistic effect of propamidine and sabinenol in different proportions
Respectively measuring the toxicity of propamidine and hinokitiol to pathogenic bacteria at different ratios by using a hypha growth rate reference method
The fungus cake is transferred to a PDA plate containing a series of compound medicines with concentration, and is cultured at 25 ℃ for 2 constant temperature culture. Measuring the diameters of all colonies when the diameters of the colonies in the blank control group exceed 2/3, repeating the treatment for 3 times, and calculating the inhibition rate of hypha growth and effective inhibition medium concentration (EC)50) The synergistic system of the mixed drug is calculated according to the following formulaAnd (4) counting. When the synergistic coefficient is more than 1.5, the synergistic effect is achieved; the additive effect is between 0.5 and 1.5; less than 0.5 is antagonistic (a and b are the ratio of propamidine and hinokitiol in the composition, EC50(A) And EC50(B) Is an effective medium concentration of propamidine and hinokitiol, EC50(Exp) is the theoretical inhibitory median concentration, EC50(Obs) is the actual concentration in inhibition measured).
TABLE 3 virulence determination of the Propamidine and Hinokitiol at different ratios against the Sclerotinia sclerotiorum carbendazim resistant Strain JK16R
The data in Table 3 show that the toxicity of the propamidine and the hinokitiol to sclerotinia sclerotiorum is different, the synergy coefficient value is 0.9558-2.0774, the synergy coefficients of the proportions are larger than 0.5, the synergistic effects are shown under the proportions, particularly when the mass ratio of the propamidine to the hinokitiol is 1: 2-8: 1, the synergy coefficients are larger than 1.5, and the propamidine and the hinokitiol have obvious synergy to the sclerotinia sclerotiorum under the proportions.
TABLE 4 virulence of Propamidine and Hinokitiol against Botrytis cinerea carbendazim resistant strain NJ4-1R in different ratios
The data in table 4 show that the ratio of propamidine to hinokitiol is 1: when the ratio of the synergistic agent to the organic solvent is 10-10: 1, the synergistic coefficients are 0.6317-2.3037 and are all larger than 0.5, so that the synergistic agent has an additive effect under the mixture ratio, and particularly when the ratio of the synergistic agent to the organic solvent is 1: 1-8: 1, the synergistic coefficients are all larger than 1.5, so that the synergistic agent has a remarkable synergistic effect. The propamidine and the hinokitiol in the proportion have obvious synergistic effect on preventing and treating gray mold of fruits and vegetables under the combined action.
Example 3: production of 15% propamidine and 15% hinokitiol composition emulsion in water A
167 kg of 90% propamidine raw material and 160 kg of 94% hinokitiol raw material are weighed accurately and quantitatively. Mixing the two active components in 2M3Mixing in blending tank. Accurately weighing 10 kg of ascorbic acid, putting into a blending tank, and fully and uniformly mixing again. Then 80 kg of emulsifier Well201, 10 kg of Arabic gum, 10 kg of urea, 10 kg of sorbic acid and 500 kg of ethyl acetate are accurately put into a blending tank, and the mixture is added until the mixture is completely filled to 1000 kg, and is fully and uniformly mixed in the blending tank. Stirring was continued for 1 hour. 1 ton of propamidine and hinokitiol composition in an aqueous emulsion is prepared.
The content of propamidine and hinokitiol was 15% by sampling analysis. And (3) subpackaging the product into aluminum cans coated with barrier materials, wherein each can contains 5 kg of the product, and the total amount of the product is 200 cans. Sealing the opening of the tank, and sticking a label to obtain the composition product A aqueous emulsion product with the content of 30 percent.
Example 4: production of 30% propamidine and 15% hinokitiol composition as suspending agent B
333 kilograms of 90 percent propamidine raw material, 160 kilograms of 94 percent hinokitiol raw material, 10 kilograms of ascorbic acid, 20590 kilograms of emulsifier Well, 40 kilograms of wetting dispersant long-chain fatty alcohol-polyoxyethylene ether, 30 kilograms of thickening agent polyvinyl alcohol and 25 kilograms of defoaming agent organic silicon are weighed accurately and quantitatively, and are put into a blending tank and are fully and uniformly stirred in the blending tank. Then quantitatively adding agricultural emulsifier TX-10100 kg into the blending tank, adding the mixture to 1000 kg, stirring while adding, and after all the materials are added, continuing stirring for 1 hour by using the stirrer.
The content of propamidine in the sampled test product is 30 percent, the content of hinokitiol in the sampled test product is 15 percent, and 1 ton of the product with the total content of effective components of 45 percent is finally obtained, and the bottle mouth of the product is sealed by a 500mL brown plastic bottle.
Example 5: production of propamidine and hinokitiol 4:1 composition water dispersible granule C
The embodiment provides a formula of a propamidine and hinokitiol 4:1 compound water dispersible granule, and the prepared compound medicament water dispersible granule comprises the following raw materials in percentage by mass: 40 to 60 percent of propamidine, 10 to 15 percent of hinokitiol, 2.5 to 5 percent of dispersant, 2.5 to 5 percent of wetting agent, 2.5 to 5 percent of disintegrant and 5 to 10 percent of filler, wherein the sum of the mass percentages of the raw materials is 100 percent.
The propamidine technical, the hinokitiol technical, the wetting agent, the dispersing agent, the disintegrating agent and the filler are uniformly mixed and then crushed by a jet mill to prepare superfine wettable powder, then a certain amount of water is added, granulation is carried out by an extrusion granulator, and the granules are dried by air flow and screened to obtain the water dispersible granules.
Example 6: compound agent of propamidine and sabinenol for preventing sclerotinia rot of rape and gray mold of fruit and vegetable
The prevention and treatment effects of the compound pesticide on sclerotinia rot of colza and gray mold of fruits and vegetables are determined by adopting a greenhouse pot experiment. When the seedlings grow to 3-5 leaves, the test is carried out. The tested agents are the prepared emulsion in water A, a suspending agent B, a water dispersible granule C, propamidine and hinokitiol. Carbendazim (50% WP) was a positive control. Each treatment was repeated 3 pots. And (4) inoculating carbendazim resistant pathogenic bacteria and then applying the pesticide by using conventional spraying. The treated seedlings were cultivated in a greenhouse. After culturing for 3-5 days, measuring the diameter of the disease spot, and calculating the prevention and treatment effect according to the following formula, wherein the measurement results are shown in tables 5 and 6.
TABLE 5 propamidine and sabinenol combinations for combating sclerotinia rot of colza against carbendazim
Note: values in the same column are labeled with different letters to indicate significant differences between values (P ═ 0.05) as determined by Fisher's least significant difference. Control effect (%) - (control lesion diameter-treatment lesion diameter)/(control lesion diameter-0.5) × 100.
As shown in Table 5, greenhouse pot experiments prove that the synergistic effect of the two agents of the propamidine and the sabinol for preventing and treating the sclerotinia rot of rape is obvious. The control effect of different formulations of the propamidine and hinokitiol compound medicament on sclerotinia rot of colza is higher than that of each single agent when the single agent is used independently, and is obviously higher than that of a contrast medicament carbendazim.
TABLE 6 propamidine and hinokitiol combinations against carbendazim-resistant grey mould of fruits and vegetables
Note: values in the same column are labeled with different letters to indicate significant differences between values (P ═ 0.05) as determined by Fisher's least significant difference. Control effect (%) - (control lesion diameter-treatment lesion diameter)/(control lesion diameter-0.5) × 100.
As shown in Table 6, a greenhouse pot experiment proves that the synergistic effect of the propamidine and the sabinol on preventing and controlling the gray mold of the fruits and vegetables is obvious when the propamidine and the sabinol are compounded. The control effect of different formulations of the propamidine and hinokitiol compound medicament on the gray mold of fruits and vegetables is higher than that of a contrast medicament carbendazim and each single agent.
Although the invention has been described in detail hereinabove with respect to a general description and specific embodiments thereof, it will be apparent to those skilled in the art that modifications or improvements may be made thereto based on the invention. Accordingly, such modifications and improvements are intended to be within the scope of the invention as claimed.
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Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1613847A (en) * | 2004-09-13 | 2005-05-11 | 西北农林科技大学无公害农药研究服务中心 | Aromatic diamidine compound with bactericidal activity and application thereof |
CN102917591A (en) * | 2010-06-10 | 2013-02-06 | 詹森药业有限公司 | Combinations of pyrimethanil and monoterpenes |
CN112868653A (en) * | 2021-01-19 | 2021-06-01 | 兰州大学 | Application of bactericidal composition containing hinokitiol and plant essential oil and main components thereof in preventing and treating plant diseases and mold |
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CN1613847A (en) * | 2004-09-13 | 2005-05-11 | 西北农林科技大学无公害农药研究服务中心 | Aromatic diamidine compound with bactericidal activity and application thereof |
CN102917591A (en) * | 2010-06-10 | 2013-02-06 | 詹森药业有限公司 | Combinations of pyrimethanil and monoterpenes |
CN112868653A (en) * | 2021-01-19 | 2021-06-01 | 兰州大学 | Application of bactericidal composition containing hinokitiol and plant essential oil and main components thereof in preventing and treating plant diseases and mold |
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