HUE034014T2 - Alkohol-alkoxilátok mint agrokémiai készítmények adjuvánsai - Google Patents
Alkohol-alkoxilátok mint agrokémiai készítmények adjuvánsai Download PDFInfo
- Publication number
- HUE034014T2 HUE034014T2 HUE10718253A HUE10718253A HUE034014T2 HU E034014 T2 HUE034014 T2 HU E034014T2 HU E10718253 A HUE10718253 A HU E10718253A HU E10718253 A HUE10718253 A HU E10718253A HU E034014 T2 HUE034014 T2 HU E034014T2
- Authority
- HU
- Hungary
- Prior art keywords
- adjuvant
- rate
- butylene oxide
- adjuvants
- compared
- Prior art date
Links
- 239000002671 adjuvant Substances 0.000 title claims abstract description 211
- 239000000203 mixture Substances 0.000 title claims description 27
- 239000003905 agrochemical Substances 0.000 title claims description 18
- 238000009472 formulation Methods 0.000 title description 17
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 17
- 239000001257 hydrogen Substances 0.000 claims abstract description 17
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 15
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 10
- 239000000575 pesticide Substances 0.000 claims description 45
- 150000001875 compounds Chemical class 0.000 claims description 16
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 125000003700 epoxy group Chemical group 0.000 claims description 3
- -1 ethylene- Chemical class 0.000 claims 1
- 239000003090 pesticide formulation Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 claims 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 abstract description 82
- 230000002708 enhancing effect Effects 0.000 abstract description 7
- 125000003342 alkenyl group Chemical group 0.000 abstract description 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 description 87
- 235000002248 Setaria viridis Nutrition 0.000 description 28
- 244000304962 green bristle grass Species 0.000 description 28
- 240000006995 Abutilon theophrasti Species 0.000 description 26
- 240000006122 Chenopodium album Species 0.000 description 24
- 235000009344 Chenopodium album Nutrition 0.000 description 24
- 244000152970 Digitaria sanguinalis Species 0.000 description 24
- 235000010823 Digitaria sanguinalis Nutrition 0.000 description 24
- 239000004009 herbicide Substances 0.000 description 23
- 239000007921 spray Substances 0.000 description 23
- 230000002363 herbicidal effect Effects 0.000 description 22
- 238000012066 statistical methodology Methods 0.000 description 22
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 17
- 239000005578 Mesotrione Substances 0.000 description 12
- KPUREKXXPHOJQT-UHFFFAOYSA-N mesotrione Chemical compound [O-][N+](=O)C1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O KPUREKXXPHOJQT-UHFFFAOYSA-N 0.000 description 12
- YLQLIQIAXYRMDL-UHFFFAOYSA-N propylheptyl alcohol Chemical compound CCCCCC(CO)CCC YLQLIQIAXYRMDL-UHFFFAOYSA-N 0.000 description 12
- 244000067505 Xanthium strumarium Species 0.000 description 11
- BGZZWXTVIYUUEY-UHFFFAOYSA-N fomesafen Chemical compound C1=C([N+]([O-])=O)C(C(=O)NS(=O)(=O)C)=CC(OC=2C(=CC(=CC=2)C(F)(F)F)Cl)=C1 BGZZWXTVIYUUEY-UHFFFAOYSA-N 0.000 description 11
- 235000007320 Avena fatua Nutrition 0.000 description 10
- 241000209764 Avena fatua Species 0.000 description 10
- 241001289540 Fallopia convolvulus Species 0.000 description 10
- 240000004296 Lolium perenne Species 0.000 description 10
- 239000005597 Pinoxaden Substances 0.000 description 10
- MGOHCFMYLBAPRN-UHFFFAOYSA-N pinoxaden Chemical compound CCC1=CC(C)=CC(CC)=C1C(C1=O)=C(OC(=O)C(C)(C)C)N2N1CCOCC2 MGOHCFMYLBAPRN-UHFFFAOYSA-N 0.000 description 10
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 9
- LJKDOMVGKKPJBH-UHFFFAOYSA-N 2-ethylhexyl dihydrogen phosphate Chemical compound CCCCC(CC)COP(O)(O)=O LJKDOMVGKKPJBH-UHFFFAOYSA-N 0.000 description 8
- 241000482638 Amaranthus tuberculatus Species 0.000 description 8
- 239000005586 Nicosulfuron Substances 0.000 description 8
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 8
- 239000007983 Tris buffer Substances 0.000 description 8
- RTCOGUMHFFWOJV-UHFFFAOYSA-N nicosulfuron Chemical compound COC1=CC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CN=2)C(=O)N(C)C)=N1 RTCOGUMHFFWOJV-UHFFFAOYSA-N 0.000 description 8
- 230000000361 pesticidal effect Effects 0.000 description 8
- 239000000243 solution Substances 0.000 description 7
- 241000611157 Brachiaria Species 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 230000036515 potency Effects 0.000 description 6
- 229920001213 Polysorbate 20 Polymers 0.000 description 5
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 5
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 5
- ONJQDTZCDSESIW-UHFFFAOYSA-N polidocanol Chemical compound CCCCCCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO ONJQDTZCDSESIW-UHFFFAOYSA-N 0.000 description 4
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 description 2
- 244000237956 Amaranthus retroflexus Species 0.000 description 2
- 235000013479 Amaranthus retroflexus Nutrition 0.000 description 2
- 239000005757 Cyproconazole Substances 0.000 description 2
- 239000005760 Difenoconazole Substances 0.000 description 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 1
- QYOVMAREBTZLBT-KTKRTIGZSA-N CCCCCCCC\C=C/CCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO Chemical compound CCCCCCCC\C=C/CCCCCCCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO QYOVMAREBTZLBT-KTKRTIGZSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
- 241001123569 Puccinia recondita Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 239000003139 biocide Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 238000012417 linear regression Methods 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- GAGSAAHZRBTRGD-UHFFFAOYSA-N oxirane;oxolane Chemical compound C1CO1.C1CCOC1 GAGSAAHZRBTRGD-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/04—Saturated ethers
- C07C43/10—Saturated ethers of polyhydroxy compounds
- C07C43/11—Polyethers containing —O—(C—C—O—)n units with ≤ 2 n≤ 10
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/178—Unsaturated ethers containing hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
- C08G65/2609—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aliphatic hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/66—Non-ionic compounds
- C11D1/722—Ethers of polyoxyalkylene glycols having mixed oxyalkylene groups; Polyalkoxylated fatty alcohols or polyalkoxylated alkylaryl alcohols with mixed oxyalkylele groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Zoology (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Toxicology (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Steroid Compounds (AREA)
- Peptides Or Proteins (AREA)
- Cephalosporin Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Catching Or Destruction (AREA)
- Polyethers (AREA)
Claims (2)
- SZABADALMI IGÉNY PONTOK h Agrokémiai peszticid készítmény, amely (i) képleîû, biológiai teljesítményt javító adjuváns vegyit-letet tartalmazff) aboi BO jelentése CH(R4)€H(R$)Q és, minden egyes BO egységre egymástól .függetleníti, üt jelemé-se inetil és R$ jelentése melií; vagy Rj jelentése etil és R< jelentése hidrogén; vagy Rt jelentése hidrogén és R5 jelentése etil; valamennyi AO jelentése egymástól vágy;fíÜfi* Oxid; n értéke 1 * 12; m értéke 5 -15; Rí jelentése C!0->6 á!ki| amely adott esetben szubszfclit hidroxi vagy epoxi csoportokkal; és Kijelentése hidrogén vigy €j.3 áikil; azzal a mepzorMssa!, hogy az (I) képleté vegyüíet nem 2>propílheptanoB-3BC>-H2EO, 2-propiiheptanoK?BOH2EO, 2-pröpiíheptanoH9BO+l 2EO vagy 2*pfOpilheptanol+12B(>i-9EO,2. Az 1. igény pont szerinti agrokémiai peszticid készítmény, ahol R2 jelentése hidrogén vagy Ci,2 alkil.3. Az; 1. vagy 2. igénypont szerinti agrokémiai peszticid készítmény, »hol az ti) képleté vegyüíet (1¾ kepietü vegyüíet:{Ihj ahol (m' T m" ~ m).4. Az 1-3/ igénypontok bármelyike szerinti agrokémiai peszticid készítmény, ahol. n értéke 2 8.5. Az 1-4. igénypontok bármelyike szerinti agrokémiai peszticid készítmény, ahol m értéke 8 - 12.6. Az 1. igénypont szerinti agrokémiai peszticid készítmény, ahol A<) jelentése etiÍén->oxíd,
- 2, Az előző· igénypontok bármelyike szerinti (!) képietü vegyüíet àikâlmgléàt:.^Âï^'-p«$3«tey bio-iógiai teljesítményének javításira.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0907003.8A GB0907003D0 (en) | 2009-04-23 | 2009-04-23 | Formulation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HUE034014T2 true HUE034014T2 (hu) | 2018-01-29 |
Family
ID=40774862
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HUE10718253A HUE034014T2 (hu) | 2009-04-23 | 2010-04-23 | Alkohol-alkoxilátok mint agrokémiai készítmények adjuvánsai |
| HUE17161850A HUE049891T2 (hu) | 2009-04-23 | 2010-04-23 | Alkohol-alkoxilátok adjuvánsként agrokémiai készítményekhez |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HUE17161850A HUE049891T2 (hu) | 2009-04-23 | 2010-04-23 | Alkohol-alkoxilátok adjuvánsként agrokémiai készítményekhez |
Country Status (23)
| Country | Link |
|---|---|
| US (1) | US20120172228A1 (hu) |
| EP (2) | EP2421362B1 (hu) |
| JP (2) | JP2012524768A (hu) |
| KR (2) | KR101748740B1 (hu) |
| CN (2) | CN102438446B (hu) |
| AR (3) | AR076398A1 (hu) |
| AU (1) | AU2010240690B2 (hu) |
| BR (2) | BRPI1013416B1 (hu) |
| CA (2) | CA2758627C (hu) |
| DK (2) | DK3251508T3 (hu) |
| EA (2) | EA029868B1 (hu) |
| ES (2) | ES2802539T3 (hu) |
| GB (1) | GB0907003D0 (hu) |
| HU (2) | HUE034014T2 (hu) |
| IL (2) | IL215170A (hu) |
| MX (1) | MX2011010123A (hu) |
| PH (1) | PH12015500425A1 (hu) |
| PL (2) | PL3251508T3 (hu) |
| PT (2) | PT2421362T (hu) |
| SG (1) | SG174399A1 (hu) |
| UA (2) | UA105661C2 (hu) |
| WO (1) | WO2010122313A1 (hu) |
| ZA (1) | ZA201107375B (hu) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0907003D0 (en) * | 2009-04-23 | 2009-06-03 | Syngenta Ltd | Formulation |
| EP2811828B1 (en) * | 2012-01-23 | 2021-09-01 | Syngenta Participations AG | Adjuvant compositions |
| WO2014046990A1 (en) * | 2012-09-18 | 2014-03-27 | Dow Global Technologies Llc | Microbicidal composition |
| WO2014149160A1 (en) | 2013-03-20 | 2014-09-25 | Dow Global Technologies Llc | Polyalkoxylated alcohols as excipients for pharmaceutical compositions |
| CN105592698B (zh) * | 2013-10-03 | 2018-08-21 | 陶氏环球技术有限责任公司 | 包含2-甲基异噻唑啉-3-酮的杀微生物组合物 |
| PL3636691T3 (pl) | 2015-10-07 | 2021-09-27 | Elementis Specialties, Inc. | Środek zwilżający i przeciwpieniący |
| GB201621396D0 (en) * | 2016-12-15 | 2017-02-01 | Syngenta Participations Ag | Adjuvants |
| UA128582C2 (uk) * | 2018-07-30 | 2024-08-21 | Байєр Акцієнгезелльшафт | Гербіцидні композиції з поліпшеними властивостями |
| US20220015356A1 (en) * | 2018-12-11 | 2022-01-20 | Dow Global Technologies Llc | Aqueous solutions of poorly soluble pesticides using polyalkyoxylated alcohols |
| EP4255188A1 (en) * | 2020-12-01 | 2023-10-11 | Bayer Aktiengesellschaft | Compositions comprising mesosulfuron-methyl and tehp |
| WO2022117515A1 (en) | 2020-12-01 | 2022-06-09 | Bayer Aktiengesellschaft | Compositions comprising iodosulfuron-methyl and tehp |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3420785A (en) * | 1964-02-12 | 1969-01-07 | Union Carbide Corp | Curable and cured compositions of diepoxide ethers such as bis(3,4-epoxybutyl)ether with active organic hardeners |
| US3843706A (en) * | 1969-05-23 | 1974-10-22 | Us Agriculture | Long chain ether alcohol sulfates from propylene oxide and 1,2-butylene oxide |
| US4448697A (en) * | 1982-01-22 | 1984-05-15 | Texaco Inc. | Secondary recovery process |
| US4966728A (en) * | 1988-08-26 | 1990-10-30 | Basf Corporation | Adjuvants for use with postemergent herbicides |
| DE3943562C2 (de) * | 1989-08-24 | 1994-07-14 | Schuelke & Mayr Gmbh | Desinfektions- und Konservierungsmittel |
| JPH0597749A (ja) * | 1991-10-14 | 1993-04-20 | Kao Corp | α−（２，４，４−トリメチルヘプチル又はヘプテニル−３−オキシ）−β−アルカノール及び該化合物を含有する香料組成物 |
| GB9322806D0 (en) * | 1993-11-05 | 1993-12-22 | Dow Europ Sa | Aqueous alkaline composition |
| DE4416303A1 (de) * | 1994-05-09 | 1995-11-16 | Bayer Ag | Schaumarmes Netzmittel und seine Verwendung |
| TW519535B (en) * | 1996-12-06 | 2003-02-01 | Nippon Catalytic Chem Ind | Higher secondary alcohol alkoxylate compound composition, method for production thereof, and detergent and emulsifier using the composition |
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| DE10129855A1 (de) * | 2001-06-21 | 2003-01-02 | Bayer Ag | Suspensionskonzentrate auf Ölbasis |
| GB0121580D0 (en) * | 2001-09-06 | 2001-10-24 | Syngenta Ltd | Novel compounds |
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