WO2019240266A1 - 殺虫剤組成物 - Google Patents
殺虫剤組成物 Download PDFInfo
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- WO2019240266A1 WO2019240266A1 PCT/JP2019/023683 JP2019023683W WO2019240266A1 WO 2019240266 A1 WO2019240266 A1 WO 2019240266A1 JP 2019023683 W JP2019023683 W JP 2019023683W WO 2019240266 A1 WO2019240266 A1 WO 2019240266A1
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- WIPO (PCT)
- Prior art keywords
- insecticide composition
- solubilizer
- present
- compound
- insecticidal
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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
- 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
- A01N37/18—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
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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
- 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
- A01N37/44—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/46—N-acyl derivatives
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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
- A01N25/02—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
- A01N25/06—Aerosols
Definitions
- the present invention relates to an insecticidal composition, and more particularly to the insecticidal component 2-fluoro-3- (N-methylbenzamide) -N- (2-bromo-6-trifluoromethyl-4- (heptafluoropropan-2-yl).
- the present invention relates to an insecticide composition having excellent solubility of phenyl) benzamide and a high insecticidal effect.
- Patent Document 1 discloses an aerosol agent containing a kerosene sparingly soluble pyrethroid compound as an insecticidal component and N, N-diethyl-m-toluamide which is an aromatic amide compound as a solubilizer.
- insecticidal component exhibiting the insecticidal effect as described above is 2-fluoro-3- (N-methylbenzamide) -N- (2-bromo-6-trifluoromethyl-4- (heptafluoropropane-2). -Yl) phenyl) benzamide. It has been confirmed that this insecticidal component is an insecticidal component that exhibits a high lethal effect and persistence even against pests that have acquired resistance to insecticidal components such as pyrethroid compounds. However, although the insecticidal component is sparingly soluble and inconvenient to form various dosage forms, no investigation has been made regarding solubility.
- the present invention provides 2-fluoro-3- (N-methylbenzamide) -N- (2-bromo-6-trifluoromethyl-4- (heptafluoropropan-2-yl) phenyl) benzamide in the composition. It is an object of the present invention to provide an insecticide composition having a high insecticidal effect.
- the present invention is as follows.
- 2-fluoro-3- (N-methylbenzamide) -N- (2-bromo-6-trifluoromethyl-4- (heptafluoropropan-2-yl) phenyl) benzamide, and clogP is 0.1
- An insecticide composition comprising a solubilizer which is ⁇ 2.1.
- the above (1) contains at least one of benzyl alcohol, N-methyl-2-pyrrolidone, 3-methoxy-N, N-dimethylpropionamide, isopropanol and propylene glycol diacetate as the solubilizer.
- the described insecticide composition (3)
- An insecticidal method comprising administering the insecticide composition according to any one of (1) to (3) to a pest.
- the insecticide composition of one embodiment of the present invention uses a solubilizer having a specific range of clogP, 2-fluoro-3- (N-methylbenzamide) -N- (2-bromo-6-trifluoromethyl) -4- (Heptafluoropropan-2-yl) phenyl) benzamide can be sufficiently dissolved in the composition to provide an insecticide composition having a high insecticidal effect.
- the insecticidal composition of one embodiment of the present invention is 2-fluoro-3- (N-methylbenzamide) -N- (2-bromo-6-trifluoromethyl-4- (heptafluoropropan-2-yl).
- Phenyl) benzamide hereinafter also referred to as “compound A”.
- compound A brofuranilide (Mitsui Chemicals Agro Co., Ltd.) etc. can be used.
- the content of Compound A with respect to the insecticide composition of one embodiment of the present invention is 0.1 to 90% by mass, preferably 0.5 to 80% by mass, and 1.0 to 70% by mass. It is more preferable that
- the insecticide composition of one embodiment of the present invention contains a solubilizer having clogP of 0.1 to 2.1 together with compound A.
- Compound A can be efficiently dissolved in an insecticide composition by a solubilizer in the above range, and is suitable for, for example, a liquid agent, an aerosol agent, a spray agent, and the like.
- clogP is a scale representing the distribution of substances between the octanol phase and the aqueous phase. Specifically, it is obtained by decomposing the chemical structure of the compound into its structural elements and integrating the hydrophobic fragment constants (f values) possessed by the fragments.
- the clogP can be calculated using, for example, the MedChem 1.01 software program (Medical Chemistry Project, Pona Collage, Pomona California).
- clogP of the solubilizing agent in the present invention can be obtained from the ChemExper website (https://www.chemexper.com/) or the like.
- the clogP of the solubilizer in the present invention is 0.1 to 2.1, preferably 0.15 to 1.4.
- the solubilizer in the present invention is not particularly limited as long as clogP is in the above range and can dissolve compound A.
- a solvent a solid carrier, a liquid carrier, or a diluent
- it mainly plays a role as a carrier for holding the active ingredient, or a role as a diluent for mainly diluting the compound A. Those responsible for are excluded.
- benzyl alcohol N-methyl-2-pyrrolidone, 3-methoxy-N, N-dimethylpropionamide, propylene glycol diacetate, methyl acetate, ethyl acetate, butyl acetate, benzyl acetate, 1.2-dimethoxy
- examples include ethane, 1-propanol, isopropanol, 1-butanol, 4-methoxybenzyl alcohol, cinnamyl alcohol, phenol, and tetrahydrofuran.
- benzyl alcohol N-methyl-2-pyrrolidone, 3-methoxy-N, N-dimethylpropionamide, 1.2-dimethoxyethane, isopropanol, phenol, and tetrahydrofuran are more preferable.
- benzyl alcohol N-methyl-2-pyrrolidone
- phenol tetrahydrofuran
- the insecticidal composition of one embodiment of the present invention is a benzyl alcohol, N-methyl-2-pyrrolidone from the above-mentioned solubilizers because of its high flash point, excellent safety, low toxicity, and low odor. , 3-methoxy-N, N-dimethylpropionamide, isopropanol and propylene glycol diacetate.
- the dissolving agent in the present invention is preferably a dissolving agent capable of dissolving 2.5% by mass or more of Compound A, more preferably a dissolving agent capable of dissolving 5% by mass or more, and further preferably a dissolving agent capable of dissolving 10% by mass or more.
- a solubilizer capable of dissolving at least mass% is particularly preferred.
- the above-mentioned solubilizer can be used alone or in combination of two or more.
- the content of the solubilizer is 0.1 to 90% by mass, preferably 1.0 to 60% by mass, more preferably 2.0 to 50% by mass. preferable.
- the content of the dissolving agent may be 3.0% by mass or more and 4.0% by mass or more, and is 40% by mass or less, 30% by mass or less, 20% by mass or less, and 10% by mass or less. May be.
- the content ratio of Compound A and the above-mentioned solubilizer is 900: 1 to 1: 900 in terms of mass ratio, and 200: 1 to 1: 200.
- a ratio of 50: 1 to 1:50 is more preferable.
- the insecticide composition of one embodiment of the present invention includes, for example, various solvents, insecticide components such as pyrethroid compounds and carbamate compounds, repellents, synergists, antioxidants in addition to compound A and the above-described solubilizer. , Emulsifiers and the like may be contained.
- Solvent is distinguished from the above-mentioned solubilizer and means a solid carrier, a liquid carrier, or a diluent used. In other words, it means a role mainly serving as a carrier for holding the active ingredient and a role as a diluent for diluting the compound A. Excludes those that play a role in dissolution. Examples thereof include saturated hydrocarbon solvents such as ethanol, normal paraffin, isoparaffin and naphthene, ethers such as dipropylene glycol monomethyl ether and 3-methoxy-3-methyl-1-butanol, and water. These can be used alone or in admixture of two or more. Of these, ethanol is preferably used.
- insecticidal component examples include allethrin, tetramethrin, praretrin, phenothrin, resmethrin, ciphenothrin, permethrin, cypermethrin, deltamethrin, tralomethrin, cyfluthrin, flamethrin, imiprothrin, etofenprox, fenvalerate, fenpropathrin, silafluofen, Mepafluthrin, dimeflutrin, transfluthrin, 2-methyl-4-oxo-3- (2-propynyl) -cyclopent-2-enyl-3- (2,2-dichlorovinyl) -2,2-dimethylcyclopropanecarboxylate Pyrethroid compounds such as dichlorvos, fenitrothion, tetrachlorobinphos, fenthion, chlorpyrifos, diazinon and other organic phosphorus compounds,
- repellents examples include N, N-diethyl-m-toluamide, limonene, linalool, citronellal, menthol, menthone, hinokitiol, geraniol, eucalyptol, indoxacarb, caran-3,4-diol, 2- ( 2-hydroxyethyl) -1-piperidinecarboxylic acid 1-methylpropyl ester, 3- (Nn-butyl-N-acetyl) aminopropionic acid ethyl ester, P-menthane-3,8-diol, and the like.
- synergist examples include piperonyl butoxide, MGK264, S421, IBTA, and cinepirin 500.
- antioxidant examples include BHT and BHA
- emulsifier examples include surfactants such as polyoxyethylene fatty acid ester, glycerin fatty acid ester, and sorbitan fatty acid ester.
- the insecticide composition of one embodiment of the present invention can be obtained by mixing Compound A, the above-described solubilizer, and other desired components as necessary at room temperature or under heating.
- the insecticide composition of one embodiment of the present invention can be used as an aerosol agent, a pump agent, a liquid agent, a powder agent, a heat transpiration agent, and the like.
- a dosage form in which droplets such as aerosols, pumps, and liquids adhere to pests. By setting it as such a dosage form, an insecticidal effect is exhibited efficiently.
- a propellant such as liquefied petroleum gas, dimethyl ether, 1,3,3,3-tetrafluoropropene, nitrogen gas, carbon dioxide gas or the like can be used.
- the insecticide composition of one embodiment of the present invention includes, for example, cockroaches such as German cockroaches, black cockroaches, American cockroaches, Japanese cockroaches, giant cockroaches; fleas such as dog fleas and cat fleas; bees such as bees and wasps; Flies such as Drosophila, Drosophila, etc .; multipods such as Dung beetle, Paramecium, Tobismkade; spiders such as red spider spider, spider spider, jumping spider; Stink bugs such as stink bugs, blue stink bugs, whitefly, whitefly, etc .; moths such as leafhopper, hornworm, etc .; mosquitoes such as oyster mite, Aedes albopictus; It can be administered to pests mites etc. mites.
- cockroaches such as German cockroaches, black cockroaches, American cockroaches, Japanese cockroaches, giant
- Test Example 1 Solubility test (Examples 1 to 19, Comparative Examples 1 to 8) As 2-fluoro-3- (N-methylbenzamide) -N- (2-bromo-6-trifluoromethyl-4- (heptafluoropropan-2-yl) phenyl) benzamide (Compound A), brofuranilide (Mitsui Chemicals) Agro Co., Ltd.) was used for the test.
- the solubilizers shown in Table 1 were stirred and dissolved so that the concentration of Compound A was 2.5, 5, 10, 20, 30, and 40% by weight.
- the test results are shown in Table 1.
- the evaluation criteria in Table 1 are as follows. (Evaluation criteria) ⁇ : Dissolved sufficiently, no residual solids ⁇ : Not completely dissolved, with residual solids
- Test Example 2 Insecticidal efficacy test (Examples 20 to 24, Comparative Example 9, Control Examples 1 to 5) (Sample preparation) Each component described in Table 2 was dissolved by stirring at room temperature (about 25 ° C.). Specifically, an ethanol solution containing 1.0 mass / volume% of Compound A and 5.0 mass / volume% of the solubilizer described in Table 2 was prepared. The ethanol solution 105 mL was filled with 345 mL of liquefied petroleum gas to obtain an aerosol agent.
- test insect black wagtail: 10 female adults
- a plastic cup ⁇ 130 mm, height 100 mm.
- the cup containing the test insect was placed obliquely (at an angle of 45 °) at the corner of the floor, and the specimen was sprayed for 1 second from a position 50 cm away from the cup using a quantitative spray device.
- the test insect was transferred to a clean container, and absorbent cotton soaked with water was added.
- Example 20 12.52 g / 10 seconds
- Example 21 12.24 g / 10 seconds
- Example 22 12.62 g / 10 seconds
- Example 23 13.40 g / 10 seconds
- Example 24 12 .52 g / 10 secondsComparative Example 9: 12.14 g / 10 seconds
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- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
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Abstract
Description
(1)2-フルオロ-3-(N-メチルベンズアミド)-N-(2-ブロモ-6-トリフルオロメチル-4-(ヘプタフルオロプロパン-2-イル)フェニル)ベンズアミド、及びclogPが0.1~2.1である溶解剤を含有する殺虫剤組成物。
(2)前記溶解剤として、ベンジルアルコール、N-メチル-2-ピロリドン、3-メトキシ-N,N-ジメチルプロピオンアミド、イソプロパノール及びプロピレングリコールジアセテートの少なくとも1つを含有する、前記(1)に記載の殺虫剤組成物。
(3)さらに、溶剤としてエタノールを含有する前記(1)または(2)に記載の殺虫剤組成物。
(4)前記(1)~(3)のいずれか1に記載の殺虫剤組成物と噴射剤を含有するエアゾール剤。
(5)前記(1)~(3)のいずれか1に記載の殺虫剤組成物を害虫に投与する、殺虫方法。
(実施例1~19、比較例1~8)
2-フルオロ-3-(N-メチルベンズアミド)-N-(2-ブロモ-6-トリフルオロメチル-4-(ヘプタフルオロプロパン-2-イル)フェニル)ベンズアミド(化合物A)として、ブロフラニリド(三井化学アグロ株式会社製)を試験に用いた。
化合物Aの濃度が2.5、5、10、20、30、40重量%になるように、表1に記載の溶解剤を撹拌して溶解させた。試験の結果を表1に示した。なお表1の評価基準は次のとおりである。
(評価基準)
○:十分溶解し、残存固形分なし
×:完全に溶解せず、残存固形分あり
一方、cLogPが0.1~2.1ではない溶解剤を用いた比較例では、2.5重量%の化合物Aを組成物中に溶解させることができなかった。
(実施例20~24、比較例9、対照例1~5)
(検体の調製)
表2に記載した各成分を室温下(約25℃)で撹拌して溶解した。具体的には、1.0質量/容量%の化合物A、及び表2に記載の5.0質量/容量%の溶解剤を含むエタノール溶液を作製した。上記エタノール溶液105mLに液化石油ガス345mLを充填し、エアゾール剤とした。
下記(i)~(iv)の手順で試験を実施した。
(i)プラスチック製カップ(φ130mm、高さ100mm)に供試虫(クロゴキブリ:雌成虫10頭)を入れた。
(ii)供試虫を入れたカップを床面隅に斜め(角度45°)に設置し、カップから50cm離れた位置から、定量噴霧装置を用いて検体を1秒間噴射した。
(iii)噴射終了後、供試虫を清潔な容器に移し、水を含ませた脱脂綿を入れた。
(iv)25℃の試験室に静置し、24時間後に供試虫の致死数を調べ、下記式により致死率(%)を求めた。
致死率(%)=(24時間後の供試虫の致死数/供試虫数)×100
上記試験を計3回行い、致死率(%)の平均値を下記表2に示した。
なお実施例および比較例の検体の噴射量は以下の通りであった。
・実施例20:12.52g/10秒
・実施例21:12.24g/10秒
・実施例22:12.62g/10秒
・実施例23:13.40g/10秒
・実施例24:12.52g/10秒
・比較例9:12.14g/10秒
Claims (5)
- 2-フルオロ-3-(N-メチルベンズアミド)-N-(2-ブロモ-6-トリフルオロメチル-4-(ヘプタフルオロプロパン-2-イル)フェニル)ベンズアミド、及びclogPが0.1~2.1である溶解剤を含有する殺虫剤組成物。
- 前記溶解剤として、ベンジルアルコール、N-メチル-2-ピロリドン、3-メトキシ-N,N-ジメチルプロピオンアミド、イソプロパノール及びプロピレングリコールジアセテートの少なくとも1つを含有する、請求項1に記載の殺虫剤組成物。
- さらに、溶剤としてエタノールを含有する請求項1または2に記載の殺虫剤組成物。
- 請求項1~3のいずれか1項に記載の殺虫剤組成物と噴射剤を含有するエアゾール剤。
- 請求項1~3のいずれか1項に記載の殺虫剤組成物を害虫に投与する、殺虫方法。
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BR112020025559-9A BR112020025559A2 (pt) | 2018-06-14 | 2019-06-14 | Composição inseticida |
US16/973,966 US11382329B2 (en) | 2018-06-14 | 2019-06-14 | Insecticide composition |
CN201980039630.0A CN112292034B (zh) | 2018-06-14 | 2019-06-14 | 杀虫剂组合物 |
AU2019285877A AU2019285877B2 (en) | 2018-06-14 | 2019-06-14 | Insecticide composition |
PH12020552137A PH12020552137A1 (en) | 2018-06-14 | 2020-12-11 | Insecticide composition |
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JP2011157296A (ja) * | 2010-01-29 | 2011-08-18 | Mitsui Chemicals Agro Inc | 有害生物防除組成物 |
JP2016088852A (ja) * | 2014-10-31 | 2016-05-23 | 日本農薬株式会社 | 有害生物防除剤組成物及びその使用方法 |
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ES2757835T3 (es) | 2008-08-13 | 2020-04-30 | Mitsui Chemicals Agro Inc | Método para producir derivados de amida |
US8686044B2 (en) | 2008-08-13 | 2014-04-01 | Mitsui Chemicals Agro, Inc. | Amide derivative, pest control agent containing the amide derivative, and use of the amide derivative |
ES2814723T3 (es) * | 2010-01-29 | 2021-03-29 | Mitsui Chemicals Agro Inc | Composición para el control de parásitos animales y método para el control de parásitos animales |
BR112017022202B1 (pt) | 2015-04-17 | 2022-06-21 | Basf Agrochemical Products B.V. | Método para o controle ou combate de pragas, uso do composto (i), isca, composição pesticida, rede ou material têxtil, método para o controle ou combate de uma população de insetos e método para a prevenção da infestação de um locus por insetos |
US10577343B2 (en) * | 2015-10-16 | 2020-03-03 | Sumitomo Chemical Company, Limited | Pyrazine compound and arthropod pest control agent containing same |
CN109415318B (zh) | 2016-07-07 | 2022-06-28 | 住友化学株式会社 | 杂环化合物及含有其的有害节肢动物防治剂 |
US11330820B2 (en) * | 2016-07-12 | 2022-05-17 | Basf Se | Pesticidally active mixtures |
CN107306976A (zh) * | 2017-06-22 | 2017-11-03 | 北京清源保生物科技有限公司 | 一种含有苦参碱与溴虫氟苯双酰胺的杀虫组合物及其应用 |
CN108077303A (zh) * | 2018-02-07 | 2018-05-29 | 湖南泽丰农化有限公司 | 一种含溴虫氟苯双酰胺和茚虫威的杀虫组合物 |
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JP2011157296A (ja) * | 2010-01-29 | 2011-08-18 | Mitsui Chemicals Agro Inc | 有害生物防除組成物 |
JP2016533378A (ja) * | 2013-10-18 | 2016-10-27 | ビーエーエスエフ アグロケミカル プロダクツ ビー.ブイ. | 土壌及び種子施用における殺有害生物活性カルボキサミド誘導体の使用、並びに処理方法 |
JP2016088852A (ja) * | 2014-10-31 | 2016-05-23 | 日本農薬株式会社 | 有害生物防除剤組成物及びその使用方法 |
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JP2019214540A (ja) | 2019-12-19 |
BR112020025559A2 (pt) | 2021-03-16 |
JP7184545B2 (ja) | 2022-12-06 |
AU2019285877A1 (en) | 2021-01-07 |
US20210251227A1 (en) | 2021-08-19 |
AU2019285877B2 (en) | 2024-04-18 |
PH12020552137A1 (en) | 2021-06-28 |
CN112292034B (zh) | 2022-02-25 |
US11382329B2 (en) | 2022-07-12 |
CN112292034A (zh) | 2021-01-29 |
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