JPWO2019046921A5 - - Google Patents
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- JPWO2019046921A5 JPWO2019046921A5 JP2020514610A JP2020514610A JPWO2019046921A5 JP WO2019046921 A5 JPWO2019046921 A5 JP WO2019046921A5 JP 2020514610 A JP2020514610 A JP 2020514610A JP 2020514610 A JP2020514610 A JP 2020514610A JP WO2019046921 A5 JPWO2019046921 A5 JP WO2019046921A5
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- JP
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- Prior art keywords
- acetate
- blend
- cypermethrin
- methyl
- thiamethoxam
- 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.)
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Description
－フォルシステイン（FOLCISTEINE）：非生物学的要因及び生物学的要因によって引き起こされるストレスを予防又は軽減するのに役立つ生化学反応を促進する特性を有するアミノ酸誘導体である。植物の生長も促進する。 - FOLCISTEINE : an amino acid derivative with properties that promote biochemical reactions that help prevent or reduce stress caused by non-biological and biological factors. It also promotes plant growth.
したがって、液体ブレンド製剤形態は、以下の式によって表すことができる：
Ｂｌ＝（（（Ｗ１）＋（Ｗ２）＋（Ｗ３）＋（Ｗ４）＋（Ｗ５）＋（（Ｘ）＋（Ｙ）））
式中、
Ｂｌは、フォルシステイン系生物刺激剤及び少なくとも１つの対象の毒性農薬から得られたブレンドであり、
Ｘは、０．５０～２，０００ｇ ａｉ／ｈａの濃度範囲のフォルシステインであり、
Ｙは対象の毒性農薬であり、
Ｗ１は安定化剤であり、
Ｗ２は、水と混和しない非極性溶媒（Ｗ２１）、非プロトン性溶媒（Ｗ２２）、非プロトン性水と混合した極性有機溶媒などの希釈剤であり、
Ｗ２１は非極性溶媒であり、例えば、置換又は非置換脂肪族又は芳香族炭化水素及びアルキルエステルを含み、キャノーラ（Ｂ．ｎａｐｕｓ）、亜麻仁、サフラン（Ｃａｒｔｈａｍｕｓ ｔｉｎｃｔｏｒｉｕｓ Ｌ）、大豆及びヒマワリ油由来のメチルエステル、エチルエステル及びブチルエステルを含むが、これらに限定されない。メチルエステルの非限定的な一例は、Ｓｔｅｐａｎ Ｃｏｍｐａｎｙ（イリノイ州、ノースフィールド、フロンテージロード ２２ Ｗ．）製のＡｇｅｎｔ２４１６－２１である。
Thus, a liquid blend dosage form can be represented by the following formula:
Bl=(((W1)+(W2)+(W3)+(W4)+(W5)+((X)+(Y)))
During the ceremony,
Bl is a blend obtained from a forcysteine biostimulant and at least one target toxic pesticide;
X is forcysteine at concentrations ranging from 0.50 to 2,000 g ai/ha;
Y is the toxic pesticide of interest;
W1 is a stabilizer,
W2 is a diluent such as a non-polar solvent immiscible with water (W21), an aprotic solvent (W22), a polar organic solvent mixed with aprotic water,
W21 is a non-polar solvent containing, for example, substituted or unsubstituted aliphatic or aromatic hydrocarbons and alkyl esters, methyl sulfides from canola (B. napus), linseed, saffron (Carthamus tinctorius L), soybean and sunflower oil. Including, but not limited to, esters, ethyl esters and butyl esters. A non-limiting example of a methyl ester is Agent 2416-21 from Stepan Company (22 W. Frontage Road, Northfield, IL).
Claims (8)
式Ｂ＝（Ｘ）＋（Ｙ３）
式中、
Ｂは前記ブレンドを表し、
Ｘは０．５０～２，０００ｇ ａｉ／ｈａの濃度範囲内のフォルシステインを表し、
Ｙ３は殺虫剤を表す。 A blend comprising folcisteine and an insecticide characterized by the formula:
Formula B = (X) + (Y3)
During the ceremony,
B represents said blend,
X represents forcysteine in the concentration range of 0.50-2,000 g ai/ha;
Y3 represents an insecticide.
Ｂｓ＝（（Ｘ＋Ｙ３＋Ｚ１＋Ｚ２）＋Ｚ３）
式中、
Ｂｓは固体ブレンドを表し、
Ｘは０．５０～２，０００ｇ ａｉ／ｈａの濃度範囲内のフォルシステインを表し、
Ｙ３は殺虫剤を表し、
Ｚ１は、酸化鉄、酸化チタン、プルシアンブルーから選ばれる無機の顔料又は色素、あるいはアリザリン色素、アゾ色素及び金属フタロシアニン色素から選ばれる有機色素を表し、
Ｚ２は、鉄、マンガン、ホウ素、銅、コバルト、モリブデン及び亜鉛塩から選ばれるスクリーニング栄養素を表し、
Ｚ３は、カルボキシメチルセルロース、天然又は合成のポリマー、ラテックス、アラビアゴム、ポリビニルアルコール、ポリ酢酸ビニル、リン脂質及から選ばれる粘着コーティングを表す。 2. The blend of claim 1, wherein said blend is a solid blend characterized by the formula:
Bs=((X+Y3+Z1+Z2)+Z3)
During the ceremony,
Bs represents a solid blend,
X represents forcysteine in the concentration range of 0.50-2,000 g ai/ha;
Y3 represents an insecticide,
Z1 represents an inorganic pigment or dye selected from iron oxide, titanium oxide, and Prussian blue, or an organic dye selected from alizarin dyes, azo dyes, and metal phthalocyanine dyes;
Z2 represents a screening nutrient selected from iron, manganese, boron, copper, cobalt, molybdenum and zinc salts;
Z3 represents an adhesive coating selected from carboxymethylcellulose, natural or synthetic polymers, latex, gum arabic, polyvinyl alcohol, polyvinyl acetate, phospholipids and.
Ｂｌ＝（（（Ｗ１）＋（Ｗ２）＋（Ｗ３）＋（Ｗ４））＋（（Ｘ）＋（Ｙ３）））
式中、
Ｂｌは液体ブレンドを表し、
Ｘは０．５０～２，０００ｇ ａｉ／ｈａの濃度範囲内の活性成分であるフォルシステインを表し、
Ｙ３は殺虫剤を表し、
Ｗ１は安定化剤を表し、
Ｗ２は、水混和性でない非極性溶媒（Ｗ２１）、非プロトン性溶媒（Ｗ２２）、又は非プロトン性の水と混合した極性有機溶媒から選ばれる希釈剤を表し、
Ｗ３は、界面活性剤、乳化剤、作物油、肥料、分散剤、相溶性剤、発泡剤、消泡剤、修正剤及び噴霧色素から選ばれるアジュバントを表し、
Ｗ４は、酸化鉄、酸化チタン及びプルシアンブルーから選ばれる無機の顔料又は色素、アリザリン色素、アゾ色素及び金属フタロシアニン色素から選ばれる有機色素、あるいは鉄、マンガン、ホウ素、銅、コバルト、モリブデン及び亜鉛塩から選ばれるスクリーニング栄養素を表す。 2. The blend of claim 1, wherein said blend is a liquid blend characterized by the formula:
Bl=(((W1)+(W2)+(W3)+(W4))+((X)+(Y3)))
During the ceremony,
Bl stands for liquid blend,
X represents forcysteine, the active ingredient in the concentration range of 0.50-2,000 g ai/ha;
Y3 represents an insecticide,
W1 represents a stabilizer,
W2 represents a diluent selected from non-polar solvents that are not water-miscible (W21), aprotic solvents (W22), or polar organic solvents mixed with aprotic water;
W3 represents an adjuvant selected from surfactants, emulsifiers, crop oils, fertilizers, dispersants, compatibilizers, blowing agents, defoamers, modifiers and spray pigments;
W4 is an inorganic pigment or dye selected from iron oxide, titanium oxide and Prussian blue, an organic dye selected from alizarin dyes, azo dyes and metal phthalocyanine dyes, or iron, manganese, boron, copper, cobalt, molybdenum and zinc salts represents a screening nutrient selected from.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2022194319A JP2023025196A (en) | 2017-09-06 | 2022-12-05 | Blend of folcysteine-based biostimulant and target agrotoxic substance exerting enhancing actions for quantitatively, qualitatively and time-related effects as observed in agricultural crop of target plant |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| BR102017019120-6A BR102017019120B1 (en) | 2017-09-06 | 2017-09-06 | MIXTURE COMPRISING A FOLCYSTEIN-BASED BIO-STIMULANT AND AN INSECTICIDE OBTAINING POTENTIALIZING ACTION FROM THE RESULTS OF QUALITATIVE, QUANTITATIVE AND TEMPORAL ORDER OBSERVED IN AN AGRICULTURAL CULTURE OF A PLANT OF INTEREST |
| BRBR1020170191206 | 2017-09-06 | ||
| PCT/BR2018/050323 WO2019046921A1 (en) | 2017-09-06 | 2018-09-05 | Mixture of a folcysteine-based biostimulant and an agrotoxic substance of interest resulting in a quantitatively, qualitatively and time-related result-potentiating action as observed in an agricultural crop of a plant of interest |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2022194319A Division JP2023025196A (en) | 2017-09-06 | 2022-12-05 | Blend of folcysteine-based biostimulant and target agrotoxic substance exerting enhancing actions for quantitatively, qualitatively and time-related effects as observed in agricultural crop of target plant |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2020532577A JP2020532577A (en) | 2020-11-12 |
| JPWO2019046921A5 true JPWO2019046921A5 (en) | 2023-06-28 |
| JP7365333B2 JP7365333B2 (en) | 2023-10-19 |
Family
ID=65633443
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2020514610A Active JP7365333B2 (en) | 2017-09-06 | 2018-09-05 | Blends of forcysteine biostimulants with target toxic pesticides to provide potentiation of quantitative, qualitative and temporal effects observed in target plant crops. |
| JP2022194319A Pending JP2023025196A (en) | 2017-09-06 | 2022-12-05 | Blend of folcysteine-based biostimulant and target agrotoxic substance exerting enhancing actions for quantitatively, qualitatively and time-related effects as observed in agricultural crop of target plant |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2022194319A Pending JP2023025196A (en) | 2017-09-06 | 2022-12-05 | Blend of folcysteine-based biostimulant and target agrotoxic substance exerting enhancing actions for quantitatively, qualitatively and time-related effects as observed in agricultural crop of target plant |
Country Status (19)
| Country | Link |
|---|---|
| US (2) | US11388900B2 (en) |
| EP (2) | EP4059348A1 (en) |
| JP (2) | JP7365333B2 (en) |
| KR (1) | KR102646452B1 (en) |
| CN (2) | CN111436187B (en) |
| AR (2) | AR113106A1 (en) |
| BR (1) | BR102017019120B1 (en) |
| CA (1) | CA3075123A1 (en) |
| CL (1) | CL2020000564A1 (en) |
| CO (1) | CO2020003263A2 (en) |
| CR (1) | CR20200153A (en) |
| EA (1) | EA202090911A1 (en) |
| EC (1) | ECSP20021393A (en) |
| MX (1) | MX2020002603A (en) |
| NI (1) | NI202000020A (en) |
| PH (1) | PH12020500447A1 (en) |
| UA (1) | UA125977C2 (en) |
| WO (1) | WO2019046921A1 (en) |
| ZA (1) | ZA202001421B (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111978293B (en) * | 2020-08-24 | 2023-10-27 | 天津大学 | Nicosulfuron-urea eutectic and preparation method thereof |
| AR123383A1 (en) * | 2020-09-01 | 2022-11-23 | Upl Ltd | FORMULATIONS AND METHODS TO REGULATE AND STIMULATE PLANT GROWTH |
| CN112400903A (en) * | 2020-12-01 | 2021-02-26 | 重庆谷百奥生物研究院有限公司 | Beauveria bassiana and cyenopyrafen compound insecticidal composition |
| CN112535152A (en) * | 2020-12-17 | 2021-03-23 | 扬州大学 | Indoor propagation method of Aphidius gifuensis |
| KR102524963B1 (en) * | 2022-09-15 | 2023-04-25 | 산천초목조경(주) | Eco-friendly composition for grass growth and soil improvement using microorganism |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1150707B (en) * | 1982-03-19 | 1986-12-17 | Montedison Spa | METHOD FOR THE DEFENSE OF CROPS OF AGRICULTURAL INTEREST BY THE ACTION OF NON-SELECTIVE HERBICIDES |
| JPS61100504A (en) * | 1984-10-22 | 1986-05-19 | Hokko Chem Ind Co Ltd | Agent for increasing yield |
| DE102008037629A1 (en) * | 2008-08-14 | 2010-02-18 | Bayer Cropscience Ag | Herbicide combination with dimethoxytriazinyl-substituted difluoromethanesulfonylanilides |
| UY36405A (en) * | 2014-11-21 | 2016-06-30 | Arysta Lifescience North America Llc | REGULATORY FORMULATIONS / BiosTIMULANTS OF GROWTH OF PLANTS AND CROPS AND METHODS FOR USE |
-
2017
- 2017-09-06 BR BR102017019120-6A patent/BR102017019120B1/en active IP Right Grant
-
2018
- 2018-09-04 AR ARP180102504A patent/AR113106A1/en active IP Right Grant
- 2018-09-05 JP JP2020514610A patent/JP7365333B2/en active Active
- 2018-09-05 EP EP22157259.7A patent/EP4059348A1/en active Pending
- 2018-09-05 CN CN201880068441.1A patent/CN111436187B/en active Active
- 2018-09-05 KR KR1020207009638A patent/KR102646452B1/en active IP Right Grant
- 2018-09-05 MX MX2020002603A patent/MX2020002603A/en unknown
- 2018-09-05 UA UAA202002732A patent/UA125977C2/en unknown
- 2018-09-05 EA EA202090911A patent/EA202090911A1/en unknown
- 2018-09-05 CR CR20200153A patent/CR20200153A/en unknown
- 2018-09-05 WO PCT/BR2018/050323 patent/WO2019046921A1/en unknown
- 2018-09-05 CA CA3075123A patent/CA3075123A1/en active Pending
- 2018-09-05 CN CN202210069347.6A patent/CN114568442A/en active Pending
- 2018-09-05 US US16/643,998 patent/US11388900B2/en active Active
- 2018-09-05 EP EP18852950.7A patent/EP3679796A4/en active Pending
-
2020
- 2020-03-05 ZA ZA2020/01421A patent/ZA202001421B/en unknown
- 2020-03-05 PH PH12020500447A patent/PH12020500447A1/en unknown
- 2020-03-06 CL CL2020000564A patent/CL2020000564A1/en unknown
- 2020-03-06 NI NI202000020A patent/NI202000020A/en unknown
- 2020-03-20 CO CONC2020/0003263A patent/CO2020003263A2/en unknown
- 2020-04-07 EC ECSENADI202021393A patent/ECSP20021393A/en unknown
-
2022
- 2022-05-23 US US17/750,623 patent/US20220279784A1/en active Pending
- 2022-05-27 AR ARP220101409A patent/AR126341A2/en unknown
- 2022-12-05 JP JP2022194319A patent/JP2023025196A/en active Pending
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