RU2001132860A - Pymetrosine Solvates - Google Patents
Pymetrosine SolvatesInfo
- Publication number
- RU2001132860A RU2001132860A RU2001132860/04A RU2001132860A RU2001132860A RU 2001132860 A RU2001132860 A RU 2001132860A RU 2001132860/04 A RU2001132860/04 A RU 2001132860/04A RU 2001132860 A RU2001132860 A RU 2001132860A RU 2001132860 A RU2001132860 A RU 2001132860A
- Authority
- RU
- Russia
- Prior art keywords
- formula
- pesticidal
- tetra
- compound
- methyl
- Prior art date
Links
- 239000012453 solvate Substances 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 7
- 239000000203 mixture Substances 0.000 claims 6
- 230000000361 pesticidal Effects 0.000 claims 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims 4
- 241000607479 Yersinia pestis Species 0.000 claims 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N acetic acid ethyl ester Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 claims 3
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N Isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims 2
- BZLVMXJERCGZMT-UHFFFAOYSA-N MeOtBu Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 claims 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N Methyl acetate Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims 2
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims 2
- WEVYAHXRMPXWCK-UHFFFAOYSA-N acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- YMWUJEATGCHHMB-UHFFFAOYSA-N methylene dichloride Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 claims 2
- KWOLFJPFCHCOCG-UHFFFAOYSA-N methylphenylketone Chemical compound CC(=O)C1=CC=CC=C1 KWOLFJPFCHCOCG-UHFFFAOYSA-N 0.000 claims 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N n-butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims 2
- 150000003839 salts Chemical group 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N t-BuOH Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 claims 2
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-Trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 claims 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 claims 1
- XNLICIUVMPYHGG-UHFFFAOYSA-N 2-Pentanone Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 claims 1
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims 1
- JNODDICFTDYODH-UHFFFAOYSA-N 2-hydroxytetrahydrofuran Chemical compound OC1CCCO1 JNODDICFTDYODH-UHFFFAOYSA-N 0.000 claims 1
- 229960001701 Chloroform Drugs 0.000 claims 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N Cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 claims 1
- JHIVVAPYMSGYDF-UHFFFAOYSA-N Cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims 1
- LZCLXQDLBQLTDK-UHFFFAOYSA-N Ethyl lactate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 claims 1
- KMTRUDSVKNLOMY-UHFFFAOYSA-N Ethylene carbonate Chemical compound O=C1OCCO1 KMTRUDSVKNLOMY-UHFFFAOYSA-N 0.000 claims 1
- 241001436646 Evinus Species 0.000 claims 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 claims 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N Propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 230000000240 adjuvant Effects 0.000 claims 1
- HEDRZPFGACZZDS-UHFFFAOYSA-N chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 claims 1
- XTHFKEDIFFGKHM-UHFFFAOYSA-N dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 claims 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 claims 1
- -1 dimstylacetamide Chemical compound 0.000 claims 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N ethanolamine Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims 1
- 229940116333 ethyl lactate Drugs 0.000 claims 1
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 1
- 235000011187 glycerol Nutrition 0.000 claims 1
- KFZMGEQAYNKOFK-UHFFFAOYSA-N iso-propanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims 1
- SECXISVLQFMRJM-UHFFFAOYSA-N n-methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 claims 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propanol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims 1
- YEJRWHAVMIAJKC-UHFFFAOYSA-N γ-lactone 4-hydroxy-butyric acid Chemical compound O=C1CCCO1 YEJRWHAVMIAJKC-UHFFFAOYSA-N 0.000 claims 1
Claims (8)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CH90599 | 1999-05-12 | ||
CH905/99 | 1999-05-12 | ||
CH1606/99 | 1999-09-03 | ||
CH160699 | 1999-09-03 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2001132860A true RU2001132860A (en) | 2003-08-20 |
RU2238941C2 RU2238941C2 (en) | 2004-10-27 |
Family
ID=25686072
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2001132860A RU2238941C2 (en) | 1999-05-12 | 2000-05-10 | Pimetrozine dihydrate, method for its preparing, methods for preparing insecticide composition, insecticide composition |
Country Status (26)
Country | Link |
---|---|
US (1) | US6784176B2 (en) |
EP (1) | EP1177189B1 (en) |
JP (1) | JP4824172B2 (en) |
KR (1) | KR100736060B1 (en) |
CN (1) | CN1219779C (en) |
AR (1) | AR035908A1 (en) |
AT (1) | ATE312832T1 (en) |
AU (1) | AU764924B2 (en) |
BR (1) | BR0010501B1 (en) |
CA (1) | CA2372156C (en) |
CO (1) | CO5210907A1 (en) |
CY (1) | CY1105396T1 (en) |
CZ (1) | CZ303340B6 (en) |
DE (1) | DE60024807T2 (en) |
DK (1) | DK1177189T3 (en) |
DZ (1) | DZ3157A1 (en) |
EG (1) | EG22667A (en) |
ES (1) | ES2252021T3 (en) |
HU (1) | HU229398B1 (en) |
IL (1) | IL145831A0 (en) |
NZ (1) | NZ515025A (en) |
PL (1) | PL202065B1 (en) |
RU (1) | RU2238941C2 (en) |
TR (1) | TR200102931T2 (en) |
TW (1) | TW542830B (en) |
WO (1) | WO2000068222A2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EA019843B1 (en) * | 2004-07-01 | 2014-06-30 | Е. И. Дюпон Де Немур Энд Компани | Synergistic mixtures of anthranilamide invertebrate pest control agents |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TWI280128B (en) | 2002-05-22 | 2007-05-01 | Smithkline Beecham Corp | 3'-[(2Z)-[1-(3,4- dimethylphenyl)-1,5-dihydro-3-methyl-5-oxo-4H-pyrazol-4-ylidene]hydrazino]-2'-hydroxy-[1,1'-biphenyl]-3-carboxylic acid bis-(monoethanolamine) |
WO2007115967A1 (en) * | 2006-04-12 | 2007-10-18 | F. Hoffmann-La Roche Ag | Crystalline isopropanol solvate of glucokinase activator |
ECSP077628A (en) | 2007-05-03 | 2008-12-30 | Smithkline Beechman Corp | NEW PHARMACEUTICAL COMPOSITION |
EP2002722A1 (en) * | 2007-06-15 | 2008-12-17 | Syngeta Participations AG | Methods of controlling insects |
GB0811300D0 (en) * | 2008-06-19 | 2008-07-30 | Syngenta Participations Ag | Methods of controlling neonicotinoid resistant insects |
US8609693B2 (en) | 2009-05-29 | 2013-12-17 | Glaxosmithkline Llc | Methods of administration of thrombopoietin agonist compounds |
WO2011134816A1 (en) | 2010-04-27 | 2011-11-03 | Syngenta Participations Ag | Methods of controlling neonicotinoid resistant aphids |
EP2776381B1 (en) | 2011-11-07 | 2016-06-01 | 3M Innovative Properties Company | Method for selectively treating the surface of dental ceramic |
US10028809B2 (en) | 2012-10-17 | 2018-07-24 | 3M Innovative Properties Company | Multi sectional dental zirconia milling block, process of production and use thereof |
CN103098799B (en) * | 2013-02-02 | 2016-08-03 | 广东中迅农科股份有限公司 | Pymetrozine and azone suspended emulsion and preparation method thereof |
WO2015096013A1 (en) | 2013-12-23 | 2015-07-02 | Dow Global Technologies Llc | Pymetrozine formulations |
MA41827A (en) * | 2015-03-27 | 2018-01-30 | Pharmacyclics Llc | SOLVATED FORMS OF A BRUTON TYROSINE KINASE INHIBITOR |
CN107935689A (en) * | 2017-11-29 | 2018-04-20 | 章立功 | A kind of disease-resistant pear tree fertilizer |
CN112538070B (en) * | 2020-12-02 | 2023-04-07 | 天津大学 | Pymetrozine-p-hydroxybenzoic acid eutectic crystal and preparation method thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3853662D1 (en) * | 1987-10-16 | 1995-06-01 | Ciba Geigy Ag | Pesticides. |
US5384403A (en) * | 1993-03-31 | 1995-01-24 | Ciba-Geigy Corporation | Process for the preparation of aminotriazine derivatives |
-
2000
- 2000-05-09 CO CO00033208A patent/CO5210907A1/en not_active Application Discontinuation
- 2000-05-10 DK DK00943716T patent/DK1177189T3/en active
- 2000-05-10 WO PCT/EP2000/004251 patent/WO2000068222A2/en active IP Right Grant
- 2000-05-10 NZ NZ515025A patent/NZ515025A/en not_active IP Right Cessation
- 2000-05-10 CZ CZ20014046A patent/CZ303340B6/en not_active IP Right Cessation
- 2000-05-10 AT AT00943716T patent/ATE312832T1/en active
- 2000-05-10 RU RU2001132860A patent/RU2238941C2/en active
- 2000-05-10 EP EP00943716A patent/EP1177189B1/en not_active Expired - Lifetime
- 2000-05-10 AU AU58082/00A patent/AU764924B2/en not_active Expired
- 2000-05-10 ES ES00943716T patent/ES2252021T3/en not_active Expired - Lifetime
- 2000-05-10 KR KR1020017014315A patent/KR100736060B1/en active IP Right Grant
- 2000-05-10 HU HU0201105A patent/HU229398B1/en unknown
- 2000-05-10 CA CA002372156A patent/CA2372156C/en not_active Expired - Lifetime
- 2000-05-10 PL PL351394A patent/PL202065B1/en unknown
- 2000-05-10 TW TW089108896A patent/TW542830B/en not_active IP Right Cessation
- 2000-05-10 EG EG20000600A patent/EG22667A/en active
- 2000-05-10 AR ARP000102242A patent/AR035908A1/en active IP Right Grant
- 2000-05-10 DZ DZ003157A patent/DZ3157A1/en active
- 2000-05-10 TR TR2001/02931T patent/TR200102931T2/en unknown
- 2000-05-10 JP JP2000617202A patent/JP4824172B2/en not_active Expired - Lifetime
- 2000-05-10 BR BRPI0010501-5A patent/BR0010501B1/en active IP Right Grant
- 2000-05-10 IL IL14583100A patent/IL145831A0/en not_active IP Right Cessation
- 2000-05-10 CN CNB008074240A patent/CN1219779C/en not_active Expired - Lifetime
- 2000-05-10 DE DE60024807T patent/DE60024807T2/en not_active Expired - Lifetime
-
2001
- 2001-11-09 US US10/039,706 patent/US6784176B2/en not_active Expired - Lifetime
-
2006
- 2006-03-07 CY CY20061100317T patent/CY1105396T1/en unknown
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EA019843B1 (en) * | 2004-07-01 | 2014-06-30 | Е. И. Дюпон Де Немур Энд Компани | Synergistic mixtures of anthranilamide invertebrate pest control agents |
EA019922B1 (en) * | 2004-07-01 | 2014-07-30 | Е.И. Дюпон Де Немур Энд Компани | Synergistic mixtures of anthranilamide compounds for controlling invertebrate pests |
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