SK105197A3 - Stabile arylpyrrole particles, method for their preparation and compositions created by suspension concenrate containing such particles - Google Patents

Stabile arylpyrrole particles, method for their preparation and compositions created by suspension concenrate containing such particles Download PDF

Info

Publication number: SK105197A3
Authority: SK; Slovakia
Prior art keywords: weight; carbon atoms; arylpyrrole; particles; group
Prior art date: 1996-08-02

Application number

SK1051-97A

Other languages

English (en)

Slovak (sk)

Inventor

Mimi Yih-Pei Chou Schaaf

Steven Brunt

Jian James Xu

Andrew E Goldsmith

Anthony F Walker

Patrick C Mowery

Edward S Donoghue

Srinivasan Rajan

Original Assignee

American Cyanamid Co

Priority date (The priority date 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 date listed.)

1996-08-02

Filing date

1997-08-01

Publication date

1998-02-04

1997-08-01 Application filed by American Cyanamid Co filed Critical American Cyanamid Co

1998-02-04 Publication of SK105197A3 publication Critical patent/SK105197A3/sk

Links

239000002245 particle Substances 0.000 title claims abstract description 117
239000000203 mixture Substances 0.000 title claims abstract description 99
238000000034 method Methods 0.000 title claims abstract description 42
239000000725 suspension Substances 0.000 title claims description 6
238000002360 preparation method Methods 0.000 title claims description 5
239000004546 suspension concentrate Substances 0.000 claims abstract description 25
230000008569 process Effects 0.000 claims abstract description 18
125000004432 carbon atom Chemical group C* 0.000 claims description 34
CWFOCCVIPCEQCK-UHFFFAOYSA-N chlorfenapyr Chemical compound BrC1=C(C(F)(F)F)N(COCC)C(C=2C=CC(Cl)=CC=2)=C1C#N CWFOCCVIPCEQCK-UHFFFAOYSA-N 0.000 claims description 31
239000000460 chlorine Substances 0.000 claims description 24
229910052801 chlorine Inorganic materials 0.000 claims description 22
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 19
125000000217 alkyl group Chemical group 0.000 claims description 17
229910052739 hydrogen Inorganic materials 0.000 claims description 17
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 16
229910052731 fluorine Inorganic materials 0.000 claims description 16
239000001257 hydrogen Substances 0.000 claims description 16
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 14
239000007798 antifreeze agent Substances 0.000 claims description 14
239000002270 dispersing agent Substances 0.000 claims description 14
239000002562 thickening agent Substances 0.000 claims description 14
229910052794 bromium Inorganic materials 0.000 claims description 13
239000011737 fluorine Chemical group 0.000 claims description 13
WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 claims description 12
239000000375 suspending agent Substances 0.000 claims description 12
-1 alkylsulfonyl carbon Chemical compound 0.000 claims description 10
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 10
239000003381 stabilizer Substances 0.000 claims description 10
YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical group [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 9
DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 9
229910052736 halogen Inorganic materials 0.000 claims description 9
125000005843 halogen group Chemical group 0.000 claims description 9
150000002431 hydrogen Chemical class 0.000 claims description 9
239000003755 preservative agent Substances 0.000 claims description 9
125000004429 atom Chemical group 0.000 claims description 8
125000004093 cyano group Chemical group *C#N 0.000 claims description 8
230000002335 preservative effect Effects 0.000 claims description 8
239000000047 product Substances 0.000 claims description 8
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 7
125000003545 alkoxy group Chemical group 0.000 claims description 7
239000002518 antifoaming agent Substances 0.000 claims description 7
150000002367 halogens Chemical class 0.000 claims description 7
229910052799 carbon Inorganic materials 0.000 claims description 6
239000003795 chemical substances by application Substances 0.000 claims description 6
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
229920001285 xanthan gum Polymers 0.000 claims description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 5
239000007859 condensation product Substances 0.000 claims description 5
239000000230 xanthan gum Substances 0.000 claims description 5
235000010493 xanthan gum Nutrition 0.000 claims description 5
229940082509 xanthan gum Drugs 0.000 claims description 5
125000006273 (C1-C3) alkyl group Chemical group 0.000 claims description 4
ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 claims description 4
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 4
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical group C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 4
229920001400 block copolymer Polymers 0.000 claims description 4
125000001188 haloalkyl group Chemical group 0.000 claims description 4
229910052740 iodine Inorganic materials 0.000 claims description 4
150000003839 salts Chemical group 0.000 claims description 4
229910052708 sodium Inorganic materials 0.000 claims description 4
239000011734 sodium Substances 0.000 claims description 4
125000004455 (C1-C3) alkylthio group Chemical group 0.000 claims description 3
125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 3
SQAINHDHICKHLX-UHFFFAOYSA-N 1-naphthaldehyde Chemical compound C1=CC=C2C(C=O)=CC=CC2=C1 SQAINHDHICKHLX-UHFFFAOYSA-N 0.000 claims description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 3
125000004414 alkyl thio group Chemical group 0.000 claims description 3
125000000304 alkynyl group Chemical group 0.000 claims description 3
125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 3
CPPKAGUPTKIMNP-UHFFFAOYSA-N cyanogen fluoride Chemical compound FC#N CPPKAGUPTKIMNP-UHFFFAOYSA-N 0.000 claims description 3
125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims description 3
238000000227 grinding Methods 0.000 claims description 3
240000007472 Leucaena leucocephala Species 0.000 claims description 2
235000010643 Leucaena leucocephala Nutrition 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
HZVVJJIYJKGMFL-UHFFFAOYSA-N almasilate Chemical compound O.[Mg+2].[Al+3].[Al+3].O[Si](O)=O.O[Si](O)=O HZVVJJIYJKGMFL-UHFFFAOYSA-N 0.000 claims description 2
229910000323 aluminium silicate Inorganic materials 0.000 claims description 2
125000001153 fluoro group Chemical group F* 0.000 claims description 2
YUCFVHQCAFKDQG-UHFFFAOYSA-N fluoromethane Chemical compound F[CH] YUCFVHQCAFKDQG-UHFFFAOYSA-N 0.000 claims description 2
238000007710 freezing Methods 0.000 claims description 2
239000001814 pectin Substances 0.000 claims description 2
235000010987 pectin Nutrition 0.000 claims description 2
229920001277 pectin Polymers 0.000 claims description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 2
238000006277 sulfonation reaction Methods 0.000 claims description 2
125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 1
244000007835 Cyamopsis tetragonoloba Species 0.000 claims 1
SNAAJJQQZSMGQD-UHFFFAOYSA-N aluminum magnesium Chemical compound [Mg].[Al] SNAAJJQQZSMGQD-UHFFFAOYSA-N 0.000 claims 1
239000008199 coating composition Substances 0.000 claims 1
238000012937 correction Methods 0.000 claims 1
HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 claims 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 1
238000005187 foaming Methods 0.000 claims 1
125000003827 glycol group Chemical group 0.000 claims 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
229910052919 magnesium silicate Inorganic materials 0.000 claims 1
235000019792 magnesium silicate Nutrition 0.000 claims 1
239000000391 magnesium silicate Substances 0.000 claims 1
ZADYMNAVLSWLEQ-UHFFFAOYSA-N magnesium;oxygen(2-);silicon(4+) Chemical compound [O-2].[O-2].[O-2].[Mg+2].[Si+4] ZADYMNAVLSWLEQ-UHFFFAOYSA-N 0.000 claims 1
PSGAAPLEWMOORI-PEINSRQWSA-N medroxyprogesterone acetate Chemical compound C([C@@]12C)CC(=O)C=C1[C@@H](C)C[C@@H]1[C@@H]2CC[C@]2(C)[C@@](OC(C)=O)(C(C)=O)CC[C@H]21 PSGAAPLEWMOORI-PEINSRQWSA-N 0.000 claims 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 1
238000003860 storage Methods 0.000 abstract description 17
230000000361 pesticidal effect Effects 0.000 abstract description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 9
150000001875 compounds Chemical class 0.000 description 8
DMSMPAJRVJJAGA-UHFFFAOYSA-N benzo[d]isothiazol-3-one Chemical compound C1=CC=C2C(=O)NSC2=C1 DMSMPAJRVJJAGA-UHFFFAOYSA-N 0.000 description 7
230000000087 stabilizing effect Effects 0.000 description 5
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
230000006641 stabilisation Effects 0.000 description 4
238000011105 stabilization Methods 0.000 description 4
230000008859 change Effects 0.000 description 3
230000000694 effects Effects 0.000 description 3
238000002156 mixing Methods 0.000 description 3
238000003756 stirring Methods 0.000 description 3
238000001238 wet grinding Methods 0.000 description 3
241000607479 Yersinia pestis Species 0.000 description 2
239000002585 base Substances 0.000 description 2
239000003153 chemical reaction reagent Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
150000002191 fatty alcohols Chemical class 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
229920001296 polysiloxane Polymers 0.000 description 2
238000001228 spectrum Methods 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical compound OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 2
GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
241000238876 Acari Species 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
229920002907 Guar gum Polymers 0.000 description 1
206010019909 Hernia Diseases 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
229920000881 Modified starch Polymers 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 1
229930006000 Sucrose Natural products 0.000 description 1
238000000862 absorption spectrum Methods 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 1
125000000051 benzyloxy group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])O* 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
125000002843 carboxylic acid group Chemical group 0.000 description 1
239000000679 carrageenan Substances 0.000 description 1
235000010418 carrageenan Nutrition 0.000 description 1
229920001525 carrageenan Polymers 0.000 description 1
229940113118 carrageenan Drugs 0.000 description 1
239000000969 carrier Substances 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
230000002542 deteriorative effect Effects 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
125000005456 glyceride group Chemical group 0.000 description 1
239000000665 guar gum Substances 0.000 description 1
235000010417 guar gum Nutrition 0.000 description 1
229960002154 guar gum Drugs 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
230000000749 insecticidal effect Effects 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
238000005259 measurement Methods 0.000 description 1
230000011987 methylation Effects 0.000 description 1
238000007069 methylation reaction Methods 0.000 description 1
239000004530 micro-emulsion Substances 0.000 description 1
235000019426 modified starch Nutrition 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-M naphthalene-1-sulfonate Chemical compound C1=CC=C2C(S(=O)(=O)[O-])=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-M 0.000 description 1
IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 1
WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
235000019260 propionic acid Nutrition 0.000 description 1
IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
230000009467 reduction Effects 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000005720 sucrose Substances 0.000 description 1
150000003871 sulfonates Chemical class 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1

Classifications

- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/36—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom five-membered rings

Landscapes

Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Medicinal Preparation (AREA)
Seasonings (AREA)

SK1051-97A 1996-08-02 1997-08-01 Stabile arylpyrrole particles, method for their preparation and compositions created by suspension concenrate containing such particles SK105197A3 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US69147896A	1996-08-02	1996-08-02

Publications (1)

Publication Number	Publication Date
SK105197A3 true SK105197A3 (en)	1998-02-04

Family

ID=24776693

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
SK1051-97A SK105197A3 (en)	1996-08-02	1997-08-01	Stabile arylpyrrole particles, method for their preparation and compositions created by suspension concenrate containing such particles

Country Status (26)

Country	Link
EP (1)	EP0821876B1 (cs)
JP (1)	JP4173568B2 (cs)
KR (1)	KR100470863B1 (cs)
CN (1)	CN1114477C (cs)
AR (1)	AR008278A1 (cs)
AT (1)	ATE237933T1 (cs)
AU (1)	AU737971B2 (cs)
BR (1)	BR9704253A (cs)
CA (1)	CA2212242C (cs)
CZ (1)	CZ293077B6 (cs)
DE (1)	DE69721145T2 (cs)
EE (1)	EE9700159A (cs)
ES (1)	ES2197974T3 (cs)
GE (1)	GEP19991853B (cs)
HR (1)	HRP970429B1 (cs)
HU (1)	HU224173B1 (cs)
ID (1)	ID19366A (cs)
IL (1)	IL121430A (cs)
MD (1)	MD1934B2 (cs)
NO (1)	NO973544L (cs)
NZ (1)	NZ328483A (cs)
RU (1)	RU2197087C2 (cs)
SK (1)	SK105197A3 (cs)
TR (1)	TR199700729A3 (cs)
YU (1)	YU33297A (cs)
ZA (1)	ZA976831B (cs)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
ID23331A (id) *	1998-03-31	2000-04-05	American Cyanamid Co	Komposisi insektisida semprot yang memiliki kemanjuran kuat
CN100579962C (zh) *	2005-04-05	2010-01-13	湖南化工研究院	具杀虫、杀螨、杀真菌生物活性的芳基吡咯类化合物及其制备方法
CN101323584B (zh) *	2005-04-05	2010-08-25	湖南化工研究院	具杀虫、杀螨、杀真菌生物活性的肟醚芳基吡咯类化合物及其制备方法
PE20070182A1 (es)	2005-07-29	2007-03-06	Wyeth Corp	Derivados cianopirrol-fenil amida como moduladores del receptor de progesterona
AU2016259360B1 (en) *	2016-11-16	2017-09-07	Rotam Agrochem International Company Limited	A novel crystalline form of chlorfenapyr, a process for its preparation and use of the same
CN110382462A (zh)	2017-03-13	2019-10-25	巴斯夫农业公司	在dipea碱存在下生产芳基吡咯化合物
CN108976157A (zh) *	2018-09-13	2018-12-11	天津市天地创智科技发展有限公司	溴虫腈晶型ii及其制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2547968A1 (de) *	1975-10-27	1977-05-05	Basf Ag	Herbizid
CA1289065C (en) *	1986-05-23	1991-09-17	Leonard John Morgan	Aqueous suspension concentrate compositions
US4871392A (en) *	1986-05-23	1989-10-03	American Cyanamid Company	Aqueous suspension concentrate compositions of pendimethalin
US5010098A (en) *	1987-07-29	1991-04-23	American Cyanamid Company	Arylpyrrole insecticidal acaricidal and nematicidal agents and methods for the preparation thereof
IL100110A0 (en) *	1990-12-26	1992-08-18	American Cyanamid Co	Insecticidal and synergistic miticidal compositions
US5233051A (en) *	1991-05-30	1993-08-03	Bayer Aktiengesellschaft	Substituted 2-arylpyrroles
YU8592A (sh) *	1991-08-28	1994-06-10	Flumroc Ag.	Postupak i uređaj za izradu ploča od mineralnih vlakana primenjenih kao nosač zidnog premaza
CA2093737A1 (en) *	1992-05-01	1993-11-02	Yili Guo	Fungicidal compositions and methods for production thereof
US5496845A (en) *	1994-05-25	1996-03-05	American Cyanamid Co.	Suspension concentrate compositions of arylpyrrole insecticidal and acaricidal agents

1997
- 1997-07-30 CZ CZ19972428A patent/CZ293077B6/cs not_active IP Right Cessation
- 1997-07-30 IL IL12143097A patent/IL121430A/en not_active IP Right Cessation
- 1997-07-31 CA CA002212242A patent/CA2212242C/en not_active Expired - Lifetime
- 1997-07-31 AT AT97305762T patent/ATE237933T1/de active
- 1997-07-31 EE EE9700159A patent/EE9700159A/xx unknown
- 1997-07-31 ZA ZA976831A patent/ZA976831B/xx unknown
- 1997-07-31 TR TR97/00729A patent/TR199700729A3/tr unknown
- 1997-07-31 DE DE69721145T patent/DE69721145T2/de not_active Expired - Lifetime
- 1997-07-31 ID IDP972665A patent/ID19366A/id unknown
- 1997-07-31 EP EP97305762A patent/EP0821876B1/en not_active Expired - Lifetime
- 1997-07-31 ES ES97305762T patent/ES2197974T3/es not_active Expired - Lifetime
- 1997-08-01 SK SK1051-97A patent/SK105197A3/sk unknown
- 1997-08-01 NO NO973544A patent/NO973544L/no not_active Application Discontinuation
- 1997-08-01 JP JP22101697A patent/JP4173568B2/ja not_active Expired - Lifetime
- 1997-08-01 KR KR1019970036850A patent/KR100470863B1/ko not_active Expired - Lifetime
- 1997-08-01 GE GEAP19973835A patent/GEP19991853B/en unknown
- 1997-08-01 AR ARP970103528A patent/AR008278A1/es active IP Right Grant
- 1997-08-01 AU AU32451/97A patent/AU737971B2/en not_active Ceased
- 1997-08-01 YU YU33297A patent/YU33297A/sh unknown
- 1997-08-01 NZ NZ328483A patent/NZ328483A/en unknown
- 1997-08-01 RU RU97113518/04A patent/RU2197087C2/ru not_active IP Right Cessation
- 1997-08-01 HU HU9701346A patent/HU224173B1/hu not_active IP Right Cessation
- 1997-08-01 HR HR970429A patent/HRP970429B1/xx not_active IP Right Cessation
- 1997-08-04 CN CN97117469A patent/CN1114477C/zh not_active Expired - Lifetime
- 1997-08-04 BR BR9704253A patent/BR9704253A/pt not_active IP Right Cessation
- 1997-08-04 MD MD97-0260A patent/MD1934B2/ro unknown

Also Published As

Publication number	Publication date
IL121430A (en)	2002-03-10
CA2212242A1 (en)	1998-02-02
DE69721145T2 (de)	2003-12-11
EP0821876B1 (en)	2003-04-23
EP0821876A1 (en)	1998-02-04
HRP970429B1 (en)	2003-10-31
GEP19991853B (en)	1999-12-06
HU9701346D0 (en)	1997-09-29
HUP9701346A1 (hu)	1999-03-29
JP4173568B2 (ja)	2008-10-29
NO973544D0 (no)	1997-08-01
TR199700729A2 (xx)	1998-05-21
CA2212242C (en)	2007-08-28
ID19366A (id)	1998-07-02
MX9705908A (es)	1998-08-30
KR100470863B1 (ko)	2005-07-18
YU33297A (sh)	1999-07-28
CZ293077B6 (cs)	2004-02-18
IL121430A0 (en)	1998-01-04
ES2197974T3 (es)	2004-01-16
HRP970429A2 (en)	1998-08-31
TR199700729A3 (tr)	1998-05-21
MD970260A (en)	1999-05-31
NO973544L (no)	1998-02-03
ATE237933T1 (de)	2003-05-15
AU3245197A (en)	1998-02-12
ZA976831B (en)	1999-02-01
EE9700159A (et)	1998-02-16
AR008278A1 (es)	1999-12-29
RU2197087C2 (ru)	2003-01-27
DE69721145D1 (de)	2003-05-28
AU737971B2 (en)	2001-09-06
NZ328483A (en)	1998-05-27
CN1114477C (zh)	2003-07-16
KR19980018294A (ko)	1998-06-05
BR9704253A (pt)	1998-09-01
CN1181992A (zh)	1998-05-20
MD1934B2 (ro)	2002-06-30
JPH1087412A (ja)	1998-04-07
HU224173B1 (hu)	2005-06-28
CZ242897A3 (cs)	1998-03-18

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