公开(公告)号：WO2010010005A3

公开(公告)日：2011-02-24

申请号：PCT/EP2009058983

申请日：2009-07-14

Applicant: BASF SE ,  SOWA CHRISTIAN ,  LEVY TATJANA ,  VOGEL RALF ,  MEIER WOLFGANG ,  KRAPP MICHAEL ,  MONTAG JURITH ,  TARANTA CLAUDE

Inventor： SOWA CHRISTIAN ,  LEVY TATJANA ,  VOGEL RALF ,  MEIER WOLFGANG ,  KRAPP MICHAEL ,  MONTAG JURITH ,  TARANTA CLAUDE

IPC: A01N25/02 ,  A01N25/04 ,  A01N43/653 ,  A01N47/24 ,  A01N53/00 ,  A01P3/00 ,  A01P7/02 ,  A01P7/04 ,  A01P13/00 ,  A01P21/00

CPC classification number: A01N25/04 ,  A01N43/653 ,  A01N47/24 ,  A01N53/00 ,  A01N25/02 ,  A01N2300/00

Abstract: The object of the present invention is an oil-in-water emulsion comprising solvent (A), water (B), surfactant (C) and at least 2 wt.% pesticide (D) based on the emulsion, wherein the solvent contains an aromatic hydrocarbon (a), and a ketone (b). The invention further relates to a method for producing an oil-in-water emulsion in that solvent (A), water (B), surfactant (C) and at least 2 wt.% pesticide (D), based on the emulsion, are mixed together. Other objects include an agrochemical formulation comprising the emulsion according to the invention and other auxiliary materials; a method for combating phytopathogenic fungi and/or undesirable plant growth and/or undesirable insect or mite infestations and/or for regulating the growth of plants; a method for combating undesirable insect or mite infestations on plants and/or for combating phytopathogenic fungi and/or for combating undesirable plant growth; also, seeds treated with an agrochemical formulation according to the invention.

Abstract translation: 本发明是一种油包水乳液，其包含基于乳液，其中该溶剂是芳族烃溶剂（A），水（B），表面活性剂（C）和至少2％（重量）的杀虫剂（D）（一 ）和酮（b）中。 本发明进一步涉及一种用于制备油包水乳状液，通过溶剂（A），水（B），表面活性剂（C）和基于乳液的至少2重量％的杀虫剂（D），混合在一起 ， 进一步的目的是提供包含本发明和进一步的赋形剂的乳剂的农化配制剂; 防治植物病原性真菌和/或不希望的植物生长和/或不希望的昆虫或螨虫侵染的方法和/或调节植物的生长; 用于控制植物上不希望的昆虫或螨虫侵染和/或用于控制植物致病真菌和/或用于控制不需要的植物生长的方法; 与根据本发明的农化配制剂处理的种子。

公开(公告)号：WO2009013247A3

公开(公告)日：2009-11-19

申请号：PCT/EP2008059476

申请日：2008-07-18

Applicant: BASF SE ,  STOESSER MICHAEL ,  BERGHAUS RAINER ,  KRENNRICH GERHARD ,  KUMMETER MARKUS ,  OETTER GUENTER ,  MONTAG JURITH

Inventor： STOESSER MICHAEL ,  BERGHAUS RAINER ,  KRENNRICH GERHARD ,  KUMMETER MARKUS ,  OETTER GUENTER ,  MONTAG JURITH

IPC: A01N25/30 ,  A01N37/46 ,  A01N37/50 ,  A01N43/32 ,  A01N43/653 ,  A01N43/76 ,  A01N43/88 ,  A01N43/90 ,  A01P3/00

CPC classification number: A01N25/30 ,  A01N37/46 ,  A01N37/50 ,  A01N43/32 ,  A01N43/40 ,  A01N43/54 ,  A01N43/653 ,  A01N43/76 ,  A01N43/88 ,  A01N43/90 ,  A01N2300/00

Abstract: The present invention relates to agrochemical compositions which comprise certain alcohol alkoxylates of the amphiphilic type and to the use of the alcohol alkoxylates as potentiating adjuvant in the agrochemical sector and in particular in the crop protection sector. The alcohol alkoxylates are alkoxylated alcohols of the formula (I) R-O-[(CnH2nO)x-(PhC2H3O)y-(CmH2mO)z]co-H in which R represents a hydrocarbon radical having 1 to 30 carbon atoms; n, m independently of one another represent a value of from 2 to 16; x represents a value of from 0 to 100; y represents a value of from 0.5 to 100; z represents a value of from 0 to 100; and x+y+z corresponds to a value of from 2 to 100, with at least one of x or z being greater than 0.

Abstract translation: 本发明涉及含有所述类型的某些两亲醇烷氧基化的农药组合物，以及使用作为有效地提高在农业化学领域的佐剂的醇，特别是在植物保护领域。 在醇烷氧基化的情况下，烷氧基化的式（I）R-O的醇 - [（CN H 2 N O）X（PhC2H3O）Y-（C mH2mO）Z] CO-H，其中R是基团的碳原子数1〜30的烃; N，M分别独立地为2至16的值; x表示0〜100的值; y具有从0.5到100的一个值; 为Z表示0至100的值; 并且x + y + z表示2〜100的值，其中，X或Z中的至少一个大于零更大

公开(公告)号：WO2009133166A3

公开(公告)日：2010-05-14

申请号：PCT/EP2009055249

申请日：2009-04-30

Applicant: BASF SE ,  TARANTA CLAUDE ,  MEIER WOLFGANG ,  BORK THOMAS ,  STRAUSS KARL ,  LEVY TATJANA ,  MONTAG JURITH

Inventor： TARANTA CLAUDE ,  MEIER WOLFGANG ,  BORK THOMAS ,  STRAUSS KARL ,  LEVY TATJANA ,  MONTAG JURITH

IPC: A01N25/04

CPC classification number: A01N25/04 ,  A01N43/653 ,  A01N47/02 ,  A01N2300/00

Abstract: The present invention relates to a microemulsion, comprising (A) 0.1 to 50 wt.% of at least one active agent as component A, (B) 0.5 to 40 wt.% of at least one solvent that can be completely mixed with water and selected from the group consisting of esters from acetic acid, lactic acid, benzoic acid, dicarboxylic acids, cyclic esters, cyclic amides, carbonates, sulfurous solvents, phosphates, ethers and mixtures thereof, as component B, (C) 10 to 40 wt.% of at least one non-ionic surfactant as component C, (D) 0 to 10 wt.% further additives as component D, (E) 10 to 90 wt.% water as component E, and (F) 0.1 to 60 wt.% of at least one solvent that can be partially mixed with water as component F, each in relation to the entire microemulsion, wherein the sum of the amounts of components, A, B, C, D, E, and F is 100 wt.%, and the microemulsion does not comprise any anionic surfactants. The invention further relates to a method for the production of said microemulsion and to the use of said microemulsion for treating plants.

Abstract translation: 本发明涉及包含0.1微乳液（A）至50重量％的活性剂作为组分A，（B）0.5〜40重量的组中选择的至少一个完全与水混溶的溶剂中的至少一个的％ 自由乙酸，乳酸，苯甲酸，二羧酸的酯，环状酯，环状酰胺，碳酸酯，含硫溶剂，磷酸盐，醚和它们的混合物的酯的酯，作为组分B，（C）10〜40重量％的至少一种非离子型的％ 表面活性剂作为组分C，（D）0至10重量％的其它添加剂作为组分D，（E）为10至90重量的水作为组分e％，和（F）0.1〜60重量％的至少一种％ 部分地包含水可混溶的溶剂作为组分F，在基于总微滴乳状液每一种情况下，其中组分A的量的总和，B，C，D，E和F是100重量％，和微乳液没有阴离子表面活性剂，和 用于制备这些Mik的一个方法 roemulsion和用于治疗植物中的用途，这些微乳化的。

公开(公告)号：WO2010040834A2

公开(公告)日：2010-04-15

申请号：PCT/EP2009063196

申请日：2009-10-09

Applicant: BASF SE ,  SCHLOTTERBECK ULF ,  TARANTA CLAUDE ,  LURTZ RALF ,  MONTAG JURITH

Inventor： SCHLOTTERBECK ULF ,  TARANTA CLAUDE ,  LURTZ RALF ,  MONTAG JURITH

CPC classification number: A01N25/04 ,  A01N25/00 ,  A01N43/653 ,  A01N47/24 ,  A01N47/38 ,  A01N25/30 ,  A01N2300/00

Abstract: The present invention relates to a novel liquid aqueous crop protection formulation which comprises a) at least one organic active crop protection ingredient with a water solubility of less than 5 g/l at 20°C; b) at least one organic solvent with a water solubility of more than 100 g/l at 20°C; c) at least one organic solvent with a water solubility of 2 to 100 g/l at 20°C; d) at least one organic solvent with a water solubility of less than 2 g/l at 20°C; e) at least one nonionic surfactant; f) at least one anionic surfactant; and g) water. The invention also relates to the use of the crop protection formulation for treatment of plants and seed, to corresponding methods and to treated seed.

Abstract translation: 本发明涉及一种新颖的液态水性作物保护制剂，其包含：a）至少一种有机作物保护剂，其在20℃下的水溶解度小于5g / l; b）至少一种在20℃下水溶解度超过100g / l的有机溶剂; c）至少一种在20℃下具有2至100g / l的水溶解度的有机溶剂; d）至少一种在20℃下水溶性小于2g / l的有机溶剂; e）至少一种非离子表面活性剂; f）至少一种阴离子表面活性剂; 和g）水。 本发明还涉及作物保护制剂用于处理植物和种子，相关方法和处理的种子的用途。

公开(公告)号：WO2012172064A3

公开(公告)日：2013-02-07

申请号：PCT/EP2012061473

申请日：2012-06-15

Applicant: BASF SE ,  BOUDET NADEGE ,  GRAMMENOS WASSILIOS ,  DIETZ JOCHEN ,  HADEN EGON ,  RIGGS RICHARD ,  MUELLER BERND ,  LOHMANN JAN KLAAS ,  MONTAG JURITH ,  CRAIG IAN ROBERT

Inventor： BOUDET NADEGE ,  GRAMMENOS WASSILIOS ,  DIETZ JOCHEN ,  HADEN EGON ,  RIGGS RICHARD ,  MUELLER BERND ,  LOHMANN JAN KLAAS ,  MONTAG JURITH ,  CRAIG IAN ROBERT

IPC: A01N43/32 ,  A01P3/00 ,  C07D339/08

CPC classification number: A01N43/32

Abstract: The present invention relates to the use of 2,3,5,6-tetracyano-[1,4]dithiine and the N-oxides and the salts thereof for combating phytopathogenic fungi on cultivated plants, and to seeds coated with 2,3,5,6-tetracyano-[1,4]dithiine. The invention also relates to methods for combating harmful fungi, comprising treating the plants or seeds to be protected against fungal attack.

Abstract translation: 本发明涉及2,3,5,6-四氰基 - [1,4]二噻吩及其N-氧化物及其盐对抗栽培植物上的植物病原性真菌的用途，以及用2,3， 5,6-四氰基[1,4] dithiine。 本发明还涉及用于防治有害真菌的方法，包括处理待保护的植物或种子免受真菌侵袭。

公开(公告)号：WO2008053044A3

公开(公告)日：2008-09-12

申请号：PCT/EP2007061834

申请日：2007-11-02

Applicant: BASF SE ,  DIETZ JOCHEN ,  GROTE THOMAS ,  GRAMMENOS WASSILIOS ,  MUELLER BERND ,  LOHMANN JAN KLAAS ,  RENNER JENS ,  ULMSCHNEIDER SARAH ,  STRATHMANN SIEGFRIED ,  STIERL REINHARD ,  SCHERER MARIA ,  MONTAG JURITH

Inventor： DIETZ JOCHEN ,  GROTE THOMAS ,  GRAMMENOS WASSILIOS ,  MUELLER BERND ,  LOHMANN JAN KLAAS ,  RENNER JENS ,  ULMSCHNEIDER SARAH ,  STRATHMANN SIEGFRIED ,  STIERL REINHARD ,  SCHERER MARIA ,  MONTAG JURITH

IPC: A01N43/40 ,  A01N43/56 ,  A01N43/78 ,  C07D213/82 ,  C07D231/14 ,  C07D277/56

CPC classification number: C07D213/82 ,  A01N43/40 ,  A01N43/56 ,  A01N43/78 ,  C07D231/14 ,  C07D277/56

Abstract: The present invention relates to hetaryl carbon acid-N-(biphen-2-yl) compounds, the use thereof for controlling harmful fungi, fungicidal substances comprising said compounds, and method for controlling harmful fungi, wherein m stands for 0, 1, 2, 3 or 4, n for 0, 1 or 2, R for C 1 -C 4 -alkyl or C 1 -C 4 -halogen alkyl or n = 2 can also stand for NH 2; Hal for halogen, particularly for fluoride or chlorine, and A for a heteroaromatic remainder, chosen from the remainders of the common formula A.1, A.2, and A.3, wherein R 1 stands for methyl or halogen methyl, R 2 for carbon, fluoride or chlorine, R 3 for carbon, chlorine, methyl or trifluormethyl, R 4 for carbon, fluoride, chlorine, methyl or trifluormethyl; and R 5 for fluoride, chlorine, methyl, difluourmethyl, trifluormethyl or methoxy; and the salts thereof, except compounds, wherein the group S(O) n -R stands for a thio-C 1 -C 4 -alkyl group, that is bound in the 4'-position of the biphenyl unit, when A stands for a remainder A.2 or a remainder A.3.

Abstract translation: 本发明涉及Hetarylcarbonsäure-N-（联苯-2-基）酰胺化合物，它们在防治有害真菌的，含有这些化合物的杀真菌组合物，和方法，用于防治有害真菌，其中m为0，1，2，3使用 或4; n为0，1或2; R表示ç _{1 -C 4 烷基或C 1 -C 4 是卤代烷基或对于n = 2和NH 2 经得起; Hal表示卤素，特别是氟或氯; A是杂芳基从通式A.1，A.2和A.3其中R ^{1 为甲基或卤代甲基的基团中选择; [R 2 代表氢，氟或氯; [R 3 代表氢，氯，甲基或三氟甲基; [R 4 代表氢，氟，氯，甲基或三氟甲基; 且R 5 代表氟，氯，甲基，二氟甲基，三氟甲基或甲氧基; 和它们的盐，比其它的化合物，其中基团S（O）名词 -Ra·奥-C 1 -C 4 是烷基 这是在联苯基部分的4'位键合，当A为基团A.2或A.3的残基。}}

公开(公告)号：WO2013135671A1

公开(公告)日：2013-09-19

申请号：PCT/EP2013054966

申请日：2013-03-12

Applicant: BASF SE ,  BASF SCHWEIZ AG

Inventor： GRAMMENOS WASSILIOS ,  CRAIG IAN ROBERT ,  BOUDET NADEGE ,  MUELLER BERND ,  DIETZ JOCHEN ,  LAUTERWASSER ERICA MAY WILSON ,  LOHMANN JAN KLAAS ,  MONTAG JURITH

IPC: C07D403/12 ,  A01N43/54 ,  A01N43/90 ,  C07D401/12 ,  C07D471/04 ,  C07D487/04 ,  C07D513/04

CPC classification number: A01N43/90 ,  A01N43/54 ,  C07D401/12 ,  C07D403/12 ,  C07D471/04 ,  C07D487/04 ,  C07D513/04 ,  A01N2300/00

Abstract: The present invention relates to fungicidal pyrimidine compounds, to their use and to methods for combating phytopathogenic fungi. The present invention also relates to seeds treated with at least one such compound. Furthermore the invention relates to processes for preparing compounds of formula I.

Abstract translation: 本发明涉及杀真菌嘧啶化合物，它们的用途以及用于防治植物病原性真菌的方法。 本发明还涉及用至少一种这样的化合物处理的种子。 此外，本发明涉及制备式I化合物的方法。

公开(公告)号：WO2010040835A3

公开(公告)日：2011-01-06

申请号：PCT/EP2009063197

申请日：2009-10-09

Applicant: BASF SE ,  TROPPMANN ULRIKE ,  MEIER WOLFGANG ,  OETTER GUENTER ,  STEINBRENNER ULRICH ,  LEVY TATJANA ,  MONTAG JURITH ,  BRUNNER TANJA ,  WEILER REINER

Inventor： TROPPMANN ULRIKE ,  MEIER WOLFGANG ,  OETTER GUENTER ,  STEINBRENNER ULRICH ,  LEVY TATJANA ,  MONTAG JURITH ,  BRUNNER TANJA ,  WEILER REINER

IPC: A01N25/02 ,  A01N25/04 ,  A01N25/30 ,  A01N47/24 ,  A01P3/00

CPC classification number: A01N47/24 ,  A01N25/04 ,  A01N2300/00

Abstract: The present invention relates to a novel liquid formulation for crop protection which comprises a) pyraclostrobin; b) at least one organic solvent S1 with a water solubility of less than 2 g/l at 20°C; c) at least one organic solvent S2 with a water solubility of at least 2 g/l at 20°C, where S2 comprises at least one solvent S2.1 with a water solubility of more than 200 g/l at 20°C and optionally at least one solvent S2.2 with a water solubility of 2 to 200 g/l at 20°C; d) at least one anionic surface-active substance SA1; e) at least one nonionic surface-active substance SA2; and f) water. The invention also relates to the use of the crop protection formulation for treatment of plants and seed, and to corresponding methods.

Abstract translation: 本发明涉及一种用于作物保护的新颖的液体制剂，其包含a）唑菌胺酯; b）具有在20℃下小于2克/升的水溶解度的至少一种有机溶剂LM1; c）具有在20℃至少为2克/升的水溶解度，至少一种有机溶剂LM2，其中至少一种溶剂LM2 LM2.1约200克/升的水溶解度在20℃下，和任选地至少一种溶剂LM2.2 包括具有在20℃下的2至200克/升的水溶解度; d）至少一种阴离子表面活性OS1; e）至少一种非离子表面活性剂OS2; 和f）水。 本发明还涉及使用所述植物保护配制剂用于治疗植物或种子，以及相应的方法。

公开(公告)号：ES2604152T3

公开(公告)日：2017-03-03

申请号：ES14171588

申请日：2014-06-06

Applicant: BASF SE

Inventor： GRAMMENOS WASSILIOS ,  ROHRER SEBASTIAN GEORGIOS ,  RHEINHEIMER JOACHIM ,  WINTER CHRISTIAN ,  ESCRIBANO CUESTA ANA ,  HADEN EGON ,  MONTAG JURITH

IPC: A01N37/50 ,  A01N43/56 ,  A01P3/00

Abstract: Mezcla, que comprende como componentes activos 1) al menos un compuesto de fórmula I**Fórmula** en la que n es un número entero y es 0, 1, 2, 3, 4 ó 5; y R, que puede ser el mismo o diferente de cualquier otro R, es halógeno, hidroxilo, carboxilo, alquilo C1-C4, alquenilo C2-C4, alquinilo C2-C8, haloalquilo C1-C4, alcoxilo C1-C4, haloalcoxilo C1-C4, alquilsulfanilo C1-C4, haloalquilsulfanilo C1-C4, alcoxiimino C1-C6-alquilo C1-C4, alqueniloxiimino C2-C6-alquilo C1-C4, alquiniloxiimino C2-C6-alquilo C1-C4, alcoxiimino C1-C4-alquilo C1-C4, alcoxiimino C1-C6, alqueniloxiimino C2-C6, alquiniloxiimino C2-C6, haloalqueniloxiimino C2-C6, cicloalquilo C3-C6, cicloalquenilo C3-C6, fenilo o un heterociclilo saturado, insaturado o aromático de 5 miembros que, además de átomos de carbono, contiene de uno a tres heteroátomos del grupo que consiste en N, O y S como miembros de anillo; en el que los grupos cíclicos R mencionados anteriormente se unen mediante un enlace directo, un átomo de oxígeno o azufre y donde los grupos alifáticos o cíclicos Rc por su parte pueden llevar 1, 2, 3 o hasta el número máximo posible de grupos Ra 15 idénticos o diferentes: Ra, que puede ser el mismo o diferente de cualquier otro Ra, es halógeno, alquilo C1-C4 o haloalquilo C1-C4; y 2) al menos un compuesto activo o biopesticida II seleccionado de los grupos A) a O): A) Inhibidores de la respiración seleccionados de - inhibidores del complejo III en el sitio Qo: azoxistrobina (II-1), coumetoxistrobina, coumoxistrobina, dimoxistrobina (II-2), enestroburina, fenaminstrobina, fenoxistrobina/flufenoxistrobina, fluoxastrobina (II-3), kresoxim-metilo (II-4), metominostrobina, orisastrobina (II-5), picoxistrobina (II-6), piraclostrobina (II-7), pirametostrobina, piraoxistrobina, trifloxistrobina (II-8), éster metílico del ácido 2-[2-(2,5-dimetil-fenoximetil)- fenil]-3-metoxi-acrílico y 2-(2-(3-(2,6-diclorofenil)-1-metil-alilidenaminooximetil)-fenil)2-metoxiimino-N-metil25 acetamida, piribencarb, triclopiricarb/clorodincarb, famoxadona, fenamidona; - inhibidores del complejo III en el sitio Qi: ciazofamida, amisulbrom, 2-metilpropanoato de [(3S,6S,7R,8R)-8- bencil-3-[(3-acetoxi4-metoxi-piridin-2-carbonil)amino]-6-metil-4,9-dioxo-1,5-dioxonan-7-ilo], 2-metil-propanoato de [(3S,6S,7R,8R)-8-bencil-3-[[3-(acetoximetoxi)-4-metoxi-piridin-2-carbonil]amino]-6-metil4,9-dioxo-1,5- dioxonan-7-ilo], 2-metilpropanoato de [(3S,6S,7R,8R)-8-bencil-3-[(3-isobutoxicarboniloxi4-metoxi-piridin-2- carbonil)amino]-6-metil-4,9-dioxo-1,5-dioxonan-7-il], 2-metilpropanoato de [(3S,6S,7R,8R)-8-bencil-3-[[3-(1,3- benzodioxol-5-ilmetoxi)-4-metoxi-piridin-2-carbonil]amino]-6-metil-4,9-dioxo-1,5-dioxonan-7-ilo]; 2- metilpropanoato de (3S,6S,7R,8R)-3-[[(3-hidroxi-4-metoxi-2-piridinil)carbonil]amino]-6-metil-4,9-dioxo-8- (fenilmetil)-1,5-dioxonan-7-ilo; - inhibidores del complejo II: benodanil, benzovindiflupir (II-9), bixafeno (II-10), boscalid (II-11), carboxina, fenfuram, fluopiram (II-12), flutolanil, fluxapyroxad (II-13), furametpir, isofetamid, isopirazam (II-14), mepronil, oxicarboxina, penflufeno (II-15), pentiopirad (II-16), sedaxano (II-17), tecloftalam, tifluzamida, N-(4'- trifluorometiltiobifenil-2-il)-3-difluorometil-1-metil-1H-pirazol-4-carboxamida, N-(-2-(1,3,3-trimetilbutil)-fenil)-1,3- dimetil-5-fluoro-1H-pirazol-4-carboxamida, 3-(difluorometil)-1-metil-N-(1,1,3-trimetilindan-4-il)pirazol-4- carboxamida, 3-(trifluorometil)-1-metil-N-(1,1,3-trimetilindan-4-il)pirazol4-carboxamida, 1,3-dimetil-N-(1,1,3- trimetilindan-4-il)pirazol-4-carboxamida, 3-(trifluorometil)-1,5-dimetil-N-(1,1,3-trimetilindan-4-il)pirazol4- carboxamida, 1,3,5-trimetil-N-(1,1,3-trimetilindan-4-il)pirazol-4-carboxamida, N-(7-fluoro-1,1,3-trimetil-indan-4- il)-1,3-dimetil-pirazol-4-carboxamida, N-[2-(2,4-diclorofenil)-2-metoxi1-metil-etil]3-(difluorometil)-1-metil-pirazol- 4-carboxamida; - otros inhibidores de la respiración: diflumetorim, (5,8-difluoroquinazolin-4-il)-{2-[2-fluoro-4-(4- trifluorometilpiridin-2-iloxi)-fenil]-etil}-amina; binapacrilo, dinobutón, dinocap, fluazinam (II-18); ferimzona; sales de fentina tales como acetato de fentina, cloruro de fentina o hidróxido de fentina; ametoctradina (II-19); y siltiofam; B) Inhibidores de la biosíntesis de esterol (fungicidas de SBI) seleccionados de - inhibidores de C14-desmetilasa (fungicidas de DMI): azaconazol, bitertanol, bromuconazol, ciproconazol (II- 20), difenoconazol (II-21), diniconazol, diniconazol-M, epoxiconazol (II-22), fenbuconazol, fluquinconazol (II-23), flusilazol, flutriafol, hexaconazol, imibenconazol, ipconazol, metconazol (II-24), miclobutanilo, oxpoconazol, paclobutrazol, penconazol, propiconazol (II-25), protioconazol (II-26), simeconazol, tebuconazol (II-27), tetraconazol, triadimefón, triadimenol, triticonazol, uniconazol; imazalilo, pefurazoato, procloraz, triflumizol; fenarimol, nuarimol, pirifenox, triforina, [3-(4-cloro-2-fluoro-fenil)-5-(2,4-difluorofenil)isoxazol-4-il]-(3- piridil)metanol; - inhibidores de delta 14-reductasa: aldimorf, dodemorf, acetato de dodemorf, fenpropimorf, tridemorf, fenpropidina, piperalina, espiroxamina; - inhibidores de 3-ceto-reductasa: fenhexamida; C) Inhibidores de la síntesis de ácidos nucleicos seleccionados de - fungicidas de acil-aminoácido o fenilamidas: benalaxilo, benalaxilo-M, kiralaxilo, metalaxilo, metalaxilo-M (mefenoxam) (II-38), ofurace, oxadixilo; - otros: himexazol, octilinona, ácido oxolínico, bupirimato, 5-fluorocitosina, 5-fluoro-2-(p-tolilmetoxi)pirimidin-4- amina, 5-fluoro-2-(-4-fluorofenilmetoxi)pirimidin-4-amina; D) Inhibidores de la división celular y el citoesqueleto seleccionados de - inhibidores de tubulina: benomilo, carbendazim, fuberidazol, tiabendazol, tiofanato-metilo (II-39); 5-cloro-7-(4- metilpiperidin-1-il)-6-(2,4,6-trifluorofenil)-[1,2,4]tri-azolo[1,5-a]pirimidina - otros inhibidores de la división celular: dietofencarb, etaboxam, pencicurón, fluopicolida, zoxamida, metrafenona (II-40), piriofenona; E) Inhibidores de la síntesis de aminoácidos y proteínas seleccionados de - inhibidores de la síntesis de metionina (anilino-pirimidinas): ciprodinil, mepanipirim, pirimetanil (II-41); - inhibidores de la síntesis de proteínas: blasticidina-S, kasugamicina, clorhidrato-hidrato de kasugamicina, mildio-micina, estreptomicina, oxitetraciclina, polioxina, validamicina A; F) Inhibidores de transducción de señales seleccionados de - inhibidores de MAP / histidina cinasa: fluoroimid, iprodiona, procimidona, vinclozolina, fenpiclonilo, fludioxonilo; - inhibidores de proteínas G: quinoxifeno; G) Inhibidores de la síntesis de lípidos y membranas seleccionados de - inhibidores de la biosíntesis de fosfolípidos: edifenfos, iprobenfos, pirazofos, isoprotiolano; - peroxidación de lípidos: dicloran, quintoceno, tecnaceno, tolclofos-metilo, bifenilo, cloroneb, etridiazol; - biosíntesis de fosfolípidos y deposición de pared celular: dimetomorf (II-42), flumorf, mandipropamid (II-43), pirimorf, bentiavalicarb, iprovalicarb, valifenalato, éster (4-fluorofenílico) del ácido N-(1-(1-(4-cianofenil) etanosulfonil)-but-2-il)carbámico; - compuestos que afectan a la permeabilidad de la membrana celular y ácidos grasos: propamocarb, clorhidrato de propamocarb; - inhibidores de la amida de ácido graso hidrolasa: oxatiapiprolina; H) Inhibidores con acción en múltiples sitios seleccionados de - sustancias activas inorgánicas: Mezcla de Bordeaux, acetato de cobre, hidróxido de cobre, oxicloruro de cobre (II-44), sulfato básico de cobre, azufre; - tio- y ditiocarbamatos: ferbam, mancozeb (II-45), maneb, metam, metiram (II-46), propineb, tiram, zineb, ziram; - compuestos de organocloro: anilazina, clorotalonil (II-47), captafol, captán, folpet, diclofluanid, diclorofeno, hexaclorobenceno, pentaclorofenol y sus sales, ftalida, tolilfluanida, N-(4-cloro-2-nitrofenil)-N-etil-4-metilbencenosulfonamida; - guanidinas y otros: guanidina, dodina, base libre de dodina, guazatina, acetato de guazatina, iminoctadina, triacetato de iminoctadina, tris(albesilato) de iminoctadina, ditianona, 2,6-dimetil-1H,5H-[1,4]ditiino[2,3-c:5,6- c']dipirrol-1,3,5,7(2H,6H)-tetraona (II-48); I) Inhibidores de la síntesis de la pared celular seleccionados de - inhibidores de la síntesis de glucano: validamicina, polioxina B; - inhibidores de la síntesis de melanina: piroquilón, tricoclazol, carpropamida, diciclomet, fenoxanilo; J) Inductores de la defensa de plantas seleccionados de - acibenzolar-S-metilo, probenazol, isotianilo, tiadinilo, prohexadiona de calcio; fosetilo, fosetilo de aluminio, ácido fosforoso y sus sales (II-49); K) Modo de acción desconocido seleccionado de bronopol, quinometionat, ciflufenamida, cimoxanilo, dazomet, debacarb, diclomezina, difenzoquat, metilsulfato de difenzoquat, difenilamina, fenpirazamina, flumetover, flusulfamida, flutianilo, metasulfocarb, nitrapirina, nitrotal-isopropilo, oxatiapiprolina, tolprocarb, 2-[3,5- bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{5-[2-(prop-2-in-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2- il)piperidin-1-il]etanona, 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{5-[2-fluoro-6-(prop-2-in-1-iloxi)fenil]-4,5- dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1-il]etanona, 2-[3,5-bis(difluorometil)-1H-pirazol-1-il]-1-[4-(4-{5-[2- cloro-6-(prop-2-in-1-iloxi)fenil]-4,5-dihidro-1,2-oxazol-3-il}-1,3-tiazol-2-il)piperidin-1-il]etanona, oxina de cobre, proquinazid, tebufloquina, tecloftalam, triazoxida, 2-butoxi-6-yodo-3-propilcromen-4-ona, N-(ciclopropilmetoxiimino- (6-difluoro-metoxi-2,3-difluoro-fenil)-metil)-2-fenil-acetamida, N'-(4-(4-cloro-3-trifluorometil-fenoxi)-2,5-dimetil-fenil)- N-etil-N-metil-formamidina, N'-(4-(4-fluoro-3-trifluorometil-fenoxi)-2,5-dimetil-fenil)-N-etil-N-metil-formamidina, N'-(2- metil-5-trifluorometil-4-(3-trimetil-silanil-propoxi)-fenil)-N-etil-N-metil-formamidina, N'-(5-difluorometil-2-metil-4-(3- trimetilsilanil-propoxi)-fenil)-N-etil-N-metil-formamidina, éster 6-terc-butil-8-fluoro-2,3-dimetil-quinolin-4-í

公开(公告)号：BRPI0906673A2

公开(公告)日：2016-07-26

申请号：BRPI0906673

申请日：2009-02-04

Applicant: BASF SE

Inventor： REINOLD ANKE ,  SOWA CHRISTIAN ,  HENTZE HANS-PETER ,  MONTAG JURITH ,  JUNG MARC RUDOLF ,  BERGHAUS RAINER ,  LEVY TATJANA ,  KOPLIN TOBIAS JOACHIM

IPC: B01J13/00