JP4507661B2 - Agricultural emulsion - Google Patents
Agricultural emulsion Download PDFInfo
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- JP4507661B2 JP4507661B2 JP2004094587A JP2004094587A JP4507661B2 JP 4507661 B2 JP4507661 B2 JP 4507661B2 JP 2004094587 A JP2004094587 A JP 2004094587A JP 2004094587 A JP2004094587 A JP 2004094587A JP 4507661 B2 JP4507661 B2 JP 4507661B2
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- pyriproxyfen
- phenyl ether
- agrochemical emulsion
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- 239000000839 emulsion Substances 0.000 title claims description 42
- -1 polyoxyethylene Polymers 0.000 claims description 36
- 239000003905 agrochemical Substances 0.000 claims description 35
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 22
- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 claims description 22
- 239000005927 Pyriproxyfen Substances 0.000 claims description 21
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 claims description 13
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 claims description 11
- 150000004996 alkyl benzenes Chemical class 0.000 claims description 6
- 229940077388 benzenesulfonate Drugs 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 11
- QNLZIZAQLLYXTC-UHFFFAOYSA-N 1,2-dimethylnaphthalene Chemical compound C1=CC=CC2=C(C)C(C)=CC=C21 QNLZIZAQLLYXTC-UHFFFAOYSA-N 0.000 description 10
- QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical compound C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 10
- 238000004519 manufacturing process Methods 0.000 description 10
- 239000002904 solvent Substances 0.000 description 10
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 241000219357 Cactaceae Species 0.000 description 8
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 7
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 7
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- 239000008233 hard water Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 5
- 241000607479 Yersinia pestis Species 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 125000000217 alkyl group Chemical group 0.000 description 3
- 238000004945 emulsification Methods 0.000 description 3
- 230000000361 pesticidal effect Effects 0.000 description 3
- VLODCNGYDDGPFG-UHFFFAOYSA-N 2,3-dimethyl-1-propan-2-ylnaphthalene Chemical compound C1=CC=C2C(C(C)C)=C(C)C(C)=CC2=C1 VLODCNGYDDGPFG-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- GNPWYHFXSMINJQ-UHFFFAOYSA-N 1,2-dimethyl-3-(1-phenylethyl)benzene Chemical compound C=1C=CC(C)=C(C)C=1C(C)C1=CC=CC=C1 GNPWYHFXSMINJQ-UHFFFAOYSA-N 0.000 description 1
- OHVLMTFVQDZYHP-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CN1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O OHVLMTFVQDZYHP-UHFFFAOYSA-N 0.000 description 1
- KZEVSDGEBAJOTK-UHFFFAOYSA-N 1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-2-[5-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]ethanone Chemical compound N1N=NC=2CN(CCC=21)C(CC=1OC(=NN=1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)=O KZEVSDGEBAJOTK-UHFFFAOYSA-N 0.000 description 1
- LDXJRKWFNNFDSA-UHFFFAOYSA-N 2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]ethanone Chemical compound C1CN(CC2=NNN=C21)CC(=O)N3CCN(CC3)C4=CN=C(N=C4)NCC5=CC(=CC=C5)OC(F)(F)F LDXJRKWFNNFDSA-UHFFFAOYSA-N 0.000 description 1
- JQMFQLVAJGZSQS-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-N-(2-oxo-3H-1,3-benzoxazol-6-yl)acetamide Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)CC(=O)NC1=CC2=C(NC(O2)=O)C=C1 JQMFQLVAJGZSQS-UHFFFAOYSA-N 0.000 description 1
- YLZOPXRUQYQQID-UHFFFAOYSA-N 3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)-1-[4-[2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidin-5-yl]piperazin-1-yl]propan-1-one Chemical compound N1N=NC=2CN(CCC=21)CCC(=O)N1CCN(CC1)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F YLZOPXRUQYQQID-UHFFFAOYSA-N 0.000 description 1
- PLLCCSYEGQDAIW-UHFFFAOYSA-N 5-ethyl-1,6-dimethyl-5-phenylcyclohexa-1,3-diene Chemical compound C=1C=CC=CC=1C1(CC)C=CC=C(C)C1C PLLCCSYEGQDAIW-UHFFFAOYSA-N 0.000 description 1
- BHPQYMZQTOCNFJ-UHFFFAOYSA-N Calcium cation Chemical compound [Ca+2] BHPQYMZQTOCNFJ-UHFFFAOYSA-N 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- 101150108558 PAD1 gene Proteins 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 125000005228 aryl sulfonate group Chemical group 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 229910001424 calcium ion Inorganic materials 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229940050906 magnesium chloride hexahydrate Drugs 0.000 description 1
- DHRRIBDTHFBPNG-UHFFFAOYSA-L magnesium dichloride hexahydrate Chemical compound O.O.O.O.O.O.[Mg+2].[Cl-].[Cl-] DHRRIBDTHFBPNG-UHFFFAOYSA-L 0.000 description 1
- 229910001425 magnesium ion Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- ZJMWRROPUADPEA-UHFFFAOYSA-N sec-butylbenzene Chemical compound CCC(C)C1=CC=CC=C1 ZJMWRROPUADPEA-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
Classifications
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- 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
- A01N25/30—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 characterised by the surfactants
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
本発明は農薬乳剤、詳しくはピリプロキシフェンを有効成分として含有する農薬乳剤に関する。 The present invention relates to an agrochemical emulsion, and more particularly to an agrochemical emulsion containing pyriproxyfen as an active ingredient.
ピリプロキシフェン［４−フェノキシフェニル （ＲＳ）−２−（２−ピリジルオキシ）プロピル エーテル；下式で示される化合物］
一方、硬水で希釈した場合にも乳化安定性が優れる農薬乳剤を得ることは困難な場合があることが知られている。
Pyriproxyfen [4-phenoxyphenyl (RS) -2- (2-pyridyloxy) propyl ether; compound represented by the following formula]
On the other hand, it is known that it may be difficult to obtain an agrochemical emulsion having excellent emulsification stability even when diluted with hard water.
本発明は、ピリプロキシフェンを有効成分として含有する農薬乳剤であって、カルシウムイオン又はマグネシウムイオンを多量に含む硬水で希釈した場合でも、乳化安定性に優れる農薬乳剤を提供することを目的とするものである。 An object of the present invention is to provide a pesticidal emulsion containing pyriproxyfen as an active ingredient, which is excellent in emulsion stability even when diluted with hard water containing a large amount of calcium ions or magnesium ions. Is.
本発明者等は、ピリプロキシフェンを有効成分として含有する農薬乳剤であって、硬水で希釈した場合でも乳化安定性に優れる農薬乳剤を提供するために種々検討した結果、芳香族炭化水素を溶剤とし、ＨＬＢが特定範囲のポリオキシエチレンスチリルフェニルエーテル、及びアルキルアリールスルホン酸塩を含有する農薬乳剤が目的を達することを見出し本発明を完成したものである。 The present inventors have made various studies to provide an agrochemical emulsion containing pyriproxyfen as an active ingredient and having excellent emulsification stability even when diluted with hard water. The present invention has been completed by finding that an agrochemical emulsion containing polyoxyethylene styryl phenyl ether having an HLB in a specific range and an alkylaryl sulfonate achieves the object.
即ち、本発明は以下のものである。
１．ピリプロキシフェン、ＨＬＢが１０．０〜１５．０であるポリオキシエチレンスチリルフェニルエーテル、アルキルアリールスルホン酸塩、及び芳香族炭化水素を含有する農薬乳剤。
２．ピリプロキシフェン１〜１５重量％、ＨＬＢが１０．０〜１５．０であるポリオキシエチレンスチリルフェニルエーテル５〜２５重量％、アルキルアリールスルホン酸塩１〜１０重量％、及び芳香族炭化水素６５〜９０重量％を含有する農薬乳剤。
３．ポリオキシエチレンスチリルフェニルエーテルがポリオキシエチレントリスチリルフェニルエーテルである１．又は２．記載の農薬乳剤。
４．アルキルアリールスルホン酸塩が、アルキルベンゼンスルホン酸塩である１．〜３．いずれか１項記載の農薬乳剤。
That is, the present invention is as follows.
1. An agrochemical emulsion containing pyriproxyfen, polyoxyethylene styryl phenyl ether having an HLB of 10.0 to 15.0, an alkylaryl sulfonate, and an aromatic hydrocarbon.
2. 1 to 15% by weight of pyriproxyfen, 5 to 25% by weight of polyoxyethylene styryl phenyl ether having an HLB of 10.0 to 15.0, 1 to 10% by weight of alkylaryl sulfonate, and 65 to 65% of aromatic hydrocarbons Agrochemical emulsion containing 90% by weight.
3. 1. Polyoxyethylene styryl phenyl ether is polyoxyethylene tristyryl phenyl ether Or 2. The agrochemical emulsion as described.
4). 1. The alkyl aryl sulfonate is an alkyl benzene sulfonate ~ 3. The agrochemical emulsion according to any one of the above.
本発明の農薬乳剤は、硬水で希釈した場合にも乳化安定性に優れるものであり、希釈する水の硬度に関わらず安定した乳化状態の希釈液を得ることができる。 The agrochemical emulsion of the present invention has excellent emulsification stability even when diluted with hard water, and a stable diluted solution in an emulsified state can be obtained regardless of the hardness of the water to be diluted.
本発明の農薬乳剤は、ピリプロキシフェン、ＨＬＢが１０．０〜１５．０であるポリオキシエチレンスチリルフェニルエーテル、アルキルアリールスルホン酸塩、及び芳香族炭化水素を含有する農薬乳剤である。
本発明の農薬乳剤を構成する各成分の割合は、通常ピリプロキシフェンが１〜１５重量％、ＨＬＢが１０．０〜１５．０であるポリオキシエチレンスチリルフェニルエーテルが５〜２５重量％、アルキルアリールスルホン酸塩が１〜１０重量％、芳香族炭化水素が６５〜９０重量％である。
The agricultural chemical emulsion of the present invention is an agricultural chemical emulsion containing pyriproxyfen, polyoxyethylene styryl phenyl ether having an HLB of 10.0 to 15.0, an alkyl aryl sulfonate, and an aromatic hydrocarbon.
The proportion of each component constituting the agricultural chemical emulsion of the present invention is usually 1 to 15% by weight of pyriproxyfen, 5 to 25% by weight of polyoxyethylene styryl phenyl ether having an HLB of 10.0 to 15.0, and alkyl. The aryl sulfonate is 1 to 10% by weight, and the aromatic hydrocarbon is 65 to 90% by weight.
本発明に用いられるピリプロキシフェンは、例えば特許文献１（特開昭６０−２１５６７１号公報）に記載された方法で製造することができる。本発明の農薬乳剤には上述の通り、ピリプロキシフェンが通常１〜１５重量％含有される。 The pyriproxyfen used in the present invention can be produced, for example, by the method described in Patent Document 1 (Japanese Patent Laid-Open No. 60-215671). As described above, the agrochemical emulsion of the present invention usually contains 1 to 15% by weight of pyriproxyfen.
本発明には、ＨＬＢが１０．０〜１５．０であるポリオキシエチレンスチリルフェニルエーテルが用いられる。
本発明の農薬乳剤には、ポリオキシエチレンスチリルフェニルエーテルが通常５〜２５重量％含有される。
本発明の農薬乳剤に用いられるポリオキシエチレンスチリルフェニルエーテルとしては、例えばポリオキシエチレンジスチリルフェニルエーテル、及びポリオキシエチレントリスチリルフェニルエーテルが挙げられ、入手性の点からポリオキシエチレントリスチリルフェニルエーテルが好適に用いられる。
In the present invention, polyoxyethylene styryl phenyl ether having an HLB of 10.0 to 15.0 is used.
The agrochemical emulsion of the present invention usually contains 5 to 25% by weight of polyoxyethylene styryl phenyl ether.
Examples of the polyoxyethylene styryl phenyl ether used in the agrochemical emulsion of the present invention include polyoxyethylene distyryl phenyl ether and polyoxyethylene tristyryl phenyl ether, and polyoxyethylene tristyryl phenyl ether from the viewpoint of availability. Are preferably used.
本発明に用いられるアルキルアリールスルホン酸塩のアルキル基は通常炭素数が８〜１５個のアルキル基である。また、アルキルアリールスルホン酸塩の塩としては、例えばナトリウム塩、カリウム塩等のアルカリ金属塩、カルシウム塩、マグネシウム塩等のアルカリ土類金属塩、及びアミン塩が挙げられる。
本発明に用いられるアルキルアリールスルホン酸塩としては、例えばアルキルベンゼンスルホン酸塩が挙げられ、具体的には例えばドデシルベンゼンスルホン酸ナトリウム塩、ドデシルベンゼンスルホン酸カルシウム塩が挙げられる。
本発明の農薬乳剤においては、アルキルアリールスルホン酸塩の量がピリプロキシフェン１重量部に対して０．１〜１重量部重量部の範囲内である。また、アルキルアリールスルホン酸塩は、本発明の農薬乳剤に通常１〜１０重量％含有される。
The alkyl group of the alkylaryl sulfonate used in the present invention is usually an alkyl group having 8 to 15 carbon atoms. Examples of the salt of alkylaryl sulfonate include alkali metal salts such as sodium salt and potassium salt, alkaline earth metal salts such as calcium salt and magnesium salt, and amine salt.
Examples of the alkyl aryl sulfonate used in the present invention include alkyl benzene sulfonate, and specific examples include sodium dodecyl benzene sulfonate and calcium dodecyl benzene sulfonate.
In the pesticidal emulsion of the present invention, the amount of alkylaryl sulfonate is in the range of 0.1 to 1 part by weight with respect to 1 part by weight of pyriproxyfen. The alkylaryl sulfonate is usually contained in the agricultural chemical emulsion of the present invention in an amount of 1 to 10% by weight.
本発明に用いられる芳香族炭化水素としては、例えばトルエン等のアルキルベンゼン、キシレン等のジアルキルベンゼン、メチルナフタレン等のアルキルナフタレン、ジメチルナフタレン等のジアルキルナフタレン、ジメチルモノイソプロピルナフタレン等のトリアルキルナフタレン、及びフェニルキシリルエタンが挙げられる。
本発明には、芳香族炭化水素として市販の溶剤をそのまま用いることもでき、そのような市販の溶剤としては、例えば、ハイゾールＳＡＳ−２９６（１−フェニル−１−キシリルエタンと１−フェニル−１−エチルフェニルエタンの混合物、日本石油株式会社の商品名）、カクタスソルベントＨＰ−ＭＮ（メチルナフタレン８０％、日鉱石油化学株式会社の商品名）、カクタスソルベントＨＰ−ＤＭＮ（ジメチルナフタレン８０％、日鉱石油化学株式会社の商品名）、カクタスソルベントＰ−１００（炭素数９〜１０のアルキルベンゼン、日鉱石油化学株式会社の商品名）、カクタスソルベントＰ−１５０（アルキルベンゼン、日鉱石油化学株式会社の商品名）、カクタスソルベントＰ−１８０（メチルナフタレンとジメチルナフタレンの混合物、日鉱石油化学株式会社の商品名）、カクタスソルベントＰ−２００（メチルナフタレンとジメチルナフタレンの混合物、日鉱石油化学株式会社の商品名）、カクタスソルベントＰ−２２０（メチルナフタレンとジメチルナフタレンの混合物、日鉱石油化学株式会社の商品名）、カクタスソルベントＰＡＤ−１（ジメチルモノイソプロピルナフタレン、日鉱石油化学株式会社の商品名）、ソルベッソ１００（芳香族炭化水素、エクソン化学株式会社の商品名）、ソルベッソ１５０（芳香族炭化水素、エクソン化学株式会社の商品名）、ソルベッソ２００（芳香族炭化水素、エクソン化学株式会社の商品名）、ＵＬＴＲＡ ＬＯＷ ＨＡＰＨＴＨＡＬＥＮＥ ＡＲＯＭＡＴＩＣ １５０（ＥｘｘｏｎＭｏｂｉｌ Ｃｈｅｍｉｃａｌ Ｃｏｍｐａｎｙ）、ＵＬＴＲＡ ＬＯＷ ＮＡＰＨＴＨＡＬＥＮＥ ＡＲＯＭＡＴＩＣ ２００（ＥｘｘｏｎＭｏｂｉｌ Ｃｈｅｍｉｃａｌ Ｃｏｍｐａｎｙ）、スワゾール１００（トルエン、丸善石油株式会社の商品名）、及びスワゾール２００（キシレン、丸善石油株式会社の商品名）が挙げられる。
芳香族炭化水素は、本発明の農薬乳剤に通常６５〜９０重量％含有される。
Examples of the aromatic hydrocarbon used in the present invention include alkylbenzene such as toluene, dialkylbenzene such as xylene, alkylnaphthalene such as methylnaphthalene, dialkylnaphthalene such as dimethylnaphthalene, trialkylnaphthalene such as dimethylmonoisopropylnaphthalene, and phenyl. Xylylethane.
In the present invention, a commercially available solvent can be used as it is as an aromatic hydrocarbon. Examples of such a commercially available solvent include Hysol SAS-296 (1-phenyl-1-xylylethane and 1-phenyl-1- Mixture of ethyl phenyl ethane, Nippon Oil Co., Ltd., Cactus Solvent HP-MN (Methylnaphthalene 80%, Nikko Petrochemical Co., Ltd.), Cactus Solvent HP-DMN (Dimethylnaphthalene 80%, Nikko Petrochemical) Cactus Solvent P-100 (alkylbenzene having 9 to 10 carbon atoms, trade name of Nikko Petrochemical Co., Ltd.), Cactus Solvent P-150 (alkylbenzene, trade name of Nikko Petrochemical Co., Ltd.), Cactus Solvent P-180 (Mixture of methylnaphthalene and dimethylnaphthalene Product, trade name of Nikko Petrochemical Co., Ltd.), cactus solvent P-200 (mixture of methylnaphthalene and dimethylnaphthalene, trade name of Nikko Petrochemical Co., Ltd.), cactus solvent P-220 (mixture of methylnaphthalene and dimethylnaphthalene), Product name of Nikko Petrochemical Co., Ltd.), Cactus Solvent PAD-1 (Dimethylmonoisopropylnaphthalene, product name of Nikko Petrochemical Co., Ltd.), Solvesso 100 (Product name of aromatic hydrocarbon, Exxon Chemical Co., Ltd.), Solvesso 150 (Aromatic hydrocarbon, trade name of Exxon Chemical Co., Ltd.), Solvesso 200 (Product name of aromatic hydrocarbon, Exxon Chemical Co., Ltd.), ULTRA LOW HAPHTHALENE AROMATIC 150 (ExxonMobil Chemical Company) , ULTRA LOW NAPHTHALENE AROMATIC 200 (ExxonMobil Chemical Company), Swasol 100 (toluene, Maruzen trade name Oil Corporation), and Swasol 200 (xylene, product name of Maruzen Petrochemical Co., Ltd.) and the like.
Aromatic hydrocarbons are usually contained in the agricultural chemical emulsion of the present invention in an amount of 65 to 90% by weight.
本発明の農薬乳剤は、例えばピリプロキシフェン、ＨＬＢが１０．０〜１５．０であるポリオキシエチレンスチリルフェニルエーテル、アルキルアリールスルホン酸塩、及び芳香族炭化水素を必要に応じて加熱しながら（８０℃以下）均一になるまで攪拌することにより製造することができる。 The agrochemical emulsion of the present invention is prepared by heating, for example, pyriproxyfen, polyoxyethylene styryl phenyl ether having an HLB of 10.0 to 15.0, an alkylaryl sulfonate, and an aromatic hydrocarbon as necessary ( 80 ° C. or lower) It can be produced by stirring until uniform.
本発明の農薬乳剤は、通常水で希釈して害虫又は害虫が生息する場所に施用される。即ち例えば、本発明の農薬乳剤を１０〜５０００倍程度に水で希釈して、害虫が生息する植物及び／又は土壌に散布することにより施用される。また、１０〜１０００倍程度に水で希釈した本発明の農薬乳剤をヘリコプター等で空中散布してもよい。
本発明の農薬乳剤の施用量は、ピリプロキシフェンの量として通常０．１〜１０００ｇ／１０ａ、好ましくは１〜１００ｇ／１０ａの割合である。
The agricultural chemical emulsion of the present invention is usually diluted with water and applied to a pest or a place where a pest lives. That is, for example, it is applied by diluting the agrochemical emulsion of the present invention with water about 10 to 5000 times and spraying it on plants and / or soil inhabiting pests. Alternatively, the agrochemical emulsion of the present invention diluted with water to about 10 to 1000 times may be sprayed in the air with a helicopter or the like.
The application amount of the agrochemical emulsion of the present invention is usually 0.1 to 1000 g / 10a, preferably 1 to 100 g / 10a as the amount of pyriproxyfen.
以下、製造例、試験例を挙げて本発明を更に詳しく説明するが、本発明はこれらの例に限定されるものではない。 Hereinafter, the present invention will be described in more detail with reference to production examples and test examples, but the present invention is not limited to these examples.
製造例１
ピリプロキシフェン２ｇ、ポリオキシエチレントリスチリルフェニルエーテル（ＨＬＢ：１２．５、商品名：Ｓｏｐｒｏｐｈｏｒ ＢＳＵ（Ｒｈｏｄｉａ社製））１．２ｇ、ドデシルベンゼンスルホン酸カルシウム塩０．４ｇ、及びソルベッソ１５０ １６．４ｇを室温で混合して、本発明の農薬乳剤を得た。
Production Example 1
2 g of pyriproxyfen, 1.2 g of polyoxyethylene tristyryl phenyl ether (HLB: 12.5, trade name: Soprophor BSU (manufactured by Rhodia)), 0.4 g of calcium dodecylbenzenesulfonate, and 16.4 g of Solvesso 150 Were mixed at room temperature to obtain the agrochemical emulsion of the present invention.
製造例２
ピリプロキシフェン２ｇ、ポリオキシエチレントリスチリルフェニルエーテル（ＨＬＢ：１０．４、商品名Ｓｏｐｒｏｐｈｏｒ ＴＳ １０（Ｒｈｏｄｉａ社製））４ｇ、ドデシルベンゼンスルホン酸カルシウム塩０．４ｇ、ソルベッソ１５０ １３．６ｇを室温で混合して、本発明の農薬乳剤を得た。
Production Example 2
2 g of pyriproxyfen, 4 g of polyoxyethylene tristyryl phenyl ether (HLB: 10.4, trade name Soprophor TS 10 (manufactured by Rhodia)), 0.4 g of calcium dodecylbenzenesulfonate, 13.6 g of Solvesso 150 at room temperature By mixing, the agrochemical emulsion of the present invention was obtained.
製造例３
ピリプロキシフェン２ｇ、ポリオキシエチレントリスチリルフェニルエーテル（ＨＬＢ：１２．５、商品名：Ｓｏｐｒｏｐｈｏｒ ＢＳＵ（Ｒｈｏｄｉａ社製））４ｇ、ドデシルベンゼンスルホン酸カルシウム塩０．４ｇ、及びソルベッソ１５０ １３．６ｇを室温で混合して、本発明の農薬乳剤を得た。
Production Example 3
2 g of pyriproxyfen, 4 g of polyoxyethylene tristyryl phenyl ether (HLB: 12.5, trade name: Soprophor BSU (manufactured by Rhodia)), 0.4 g of calcium dodecylbenzenesulfonate, and 13.6 g of Solvesso 150 at room temperature To obtain an agrochemical emulsion of the present invention.
製造例４
ピリプロキシフェン２ｇ、ポリオキシエチレントリスチリルフェニルエーテル（ＨＬＢ：１４．５、商品名：Ｓｏｐｒｏｐｈｏｒ Ｓ ２５（Ｒｈｏｄｉａ社製））１．２ｇ、ドデシルベンゼンスルホン酸カルシウム塩１ｇ、及びソルベッソ１５０ １５．８ｇを室温で混合して、本発明の農薬乳剤を得た。
Production Example 4
2 g of pyriproxyfen, 1.2 g of polyoxyethylene tristyryl phenyl ether (HLB: 14.5, trade name: Soprophor S 25 (manufactured by Rhodia)), 1 g of calcium salt of dodecylbenzene sulfonate, and 15.8 g of Solvesso 150 By mixing at room temperature, the agrochemical emulsion of the present invention was obtained.
製造例５
ピリプロキシフェン２ｇ、ポリオキシエチレントリスチリルフェニルエーテル（ＨＬＢ：１２．５、商品名：Ｓｏｐｒｏｐｈｏｒ ＢＳＵ（Ｒｈｏｄｉａ社製））２．４ｇ、ドデシルベンゼンスルホン酸カルシウム塩１ｇ、及びソルベッソ１５０ １４．６ｇを室温で混合して、本発明の農薬乳剤を得た。
Production Example 5
2 g of pyriproxyfen, 2.4 g of polyoxyethylene tristyryl phenyl ether (HLB: 12.5, trade name: Soprophor BSU (manufactured by Rhodia)), 1 g of calcium dodecylbenzenesulfonate and 14.6 g of Solvesso 150 at room temperature To obtain an agrochemical emulsion of the present invention.
製造例６
ピリプロキシフェン２ｇ、ポリオキシエチレントリスチリルフェニルエーテル（ＨＬＢ：１２．５、商品名：Ｓｏｐｒｏｐｈｏｒ ＢＳＵ（Ｒｈｏｄｉａ社製））２．４ｇ、ドデシルベンゼンスルホン酸カルシウム塩１ｇ、及びソルベッソ１００ １４．６ｇを室温で混合して、本発明の農薬乳剤を得た。
Production Example 6
2 g of pyriproxyfen, 2.4 g of polyoxyethylene tristyryl phenyl ether (HLB: 12.5, trade name: Soprophor BSU (manufactured by Rhodia)), 1 g of calcium dodecylbenzenesulfonate, and 14.6 g of Solvesso 100 at room temperature To obtain an agrochemical emulsion of the present invention.
製造例７
ピリプロキシフェン２ｇ、ポリオキシエチレントリスチリルフェニルエーテル（ＨＬＢ：１２．５、商品名：Ｓｏｐｒｏｐｈｏｒ ＢＳＵ（Ｒｈｏｄｉａ社製））２．４ｇ、ドデシルベンゼンスルホン酸カルシウム塩１ｇ、及びソルベッソ２００ １４．６ｇを室温で混合して、本発明の農薬乳剤を得た。
Production Example 7
2 g of pyriproxyfen, 2.4 g of polyoxyethylene tristyryl phenyl ether (HLB: 12.5, trade name: Soprophor BSU (manufactured by Rhodia)), 1 g of calcium dodecylbenzenesulfonate and 14.6 g of Solvesso 200 at room temperature To obtain an agrochemical emulsion of the present invention.
次に、本発明の農薬乳剤の乳化安定性につき、試験例を示す。
試験例
塩化カルシウム３．０４ｇ及び塩化マグネシウム６水和物１．３９ｇを水に溶解し、全量を５００ｍｌとして試験用の硬水を調製した。
１００ｍｌの栓付きメスシリンダーに前記試験用の硬水９５ｍｌを入れ、２０℃の恒温水槽にしばらく放置し、水温を２０℃に調節した。次いで、上記製造例で得られた本発明の農薬乳剤５ｍｌを該メスシリンダーに加え、２秒間に１回の割合で３０回転倒させた後、再び２０℃の恒温水槽に１時間放置した。その後、メスシリンダー内の乳化液の状態を観察したところ、本発明の農薬乳剤１〜７について、いずれも均一な乳化状態が保持されているか、クリーム状の分離が３容量％以下であった。
Next, a test example is shown about the emulsion stability of the agrochemical emulsion of this invention.
Test Example Hard water for testing was prepared by dissolving 3.04 g of calcium chloride and 1.39 g of magnesium chloride hexahydrate in water to make the total amount 500 ml.
95 ml of the test hard water was placed in a 100 ml stoppered graduated cylinder and left in a constant temperature water bath at 20 ° C. for a while to adjust the water temperature to 20 ° C. Next, 5 ml of the pesticidal emulsion of the present invention obtained in the above production example was added to the graduated cylinder, tilted 30 times at a rate of once every 2 seconds, and then left again in a constant temperature water bath at 20 ° C. for 1 hour. Thereafter, the state of the emulsified liquid in the graduated cylinder was observed. As for the agricultural chemical emulsions 1 to 7 of the present invention, a uniform emulsified state was maintained or the cream-like separation was 3% by volume or less.
本発明の農薬乳剤は、希釈する水の硬度によらず安定な乳化状態の希釈液を得ることができる。
The agrochemical emulsion of the present invention can provide a stable emulsion in an emulsified state regardless of the hardness of the water to be diluted.
Claims (2)
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| JP2004094587A JP4507661B2 (en) | 2004-03-29 | 2004-03-29 | Agricultural emulsion |
| ZA2004/08239A ZA200408239B (en) | 2004-03-29 | 2004-10-12 | Pesticidal emulsifiable concentrate |
| ES200402543A ES2254016B1 (en) | 2004-03-29 | 2004-10-25 | EMULSIONABLE PESTICID CONCENTRATE. |
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| JPS60215671A (en) * | 1984-04-10 | 1985-10-29 | Sumitomo Chem Co Ltd | Nitrogen-containing heterocyclic compound, its preparation, and noxious life controlling agent containing said compound as active component |
| JPH10120502A (en) * | 1996-10-22 | 1998-05-12 | Sumitomo Chem Co Ltd | Agrochemical composition |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS60215671A (en) * | 1984-04-10 | 1985-10-29 | Sumitomo Chem Co Ltd | Nitrogen-containing heterocyclic compound, its preparation, and noxious life controlling agent containing said compound as active component |
| JPH10120502A (en) * | 1996-10-22 | 1998-05-12 | Sumitomo Chem Co Ltd | Agrochemical composition |
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| ZA200408239B (en) | 2005-09-28 |
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