CS265219B2 - Insecticide - Google Patents

Insecticide Download PDF

Info

Publication number: CS265219B2
Authority: CS; Czechoslovakia
Prior art keywords: hydroprene; cockroaches; compositions; cockroach; enantiomer
Prior art date: 1985-05-13

Application number

CS863397A

Other languages

Czech (cs)

English (en)

Other versions

CS339786A2 (en

Inventor

Gustave K Kohn

David L Grant

Robin R Rudolph

Gerardus B Staal

Original Assignee

Sandoz Ag

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.)

1985-05-13

Filing date

1986-05-12

Publication date

1989-10-13

1986-05-12 Application filed by Sandoz Ag filed Critical Sandoz Ag

1987-07-16 Publication of CS339786A2 publication Critical patent/CS339786A2/cs

1989-10-13 Publication of CS265219B2 publication Critical patent/CS265219B2/cs

Links

239000002917 insecticide Substances 0.000 title description 2
241001674044 Blattodea Species 0.000 claims description 29
FYQGBXGJFWXIPP-UHFFFAOYSA-N hydroprene Chemical compound CCOC(=O)C=C(C)C=CCC(C)CCCC(C)C FYQGBXGJFWXIPP-UHFFFAOYSA-N 0.000 claims description 13
239000004480 active ingredient Substances 0.000 claims description 6
FYQGBXGJFWXIPP-OJROSNHMSA-N (S)-hydroprene Chemical compound CCOC(=O)\C=C(/C)\C=C\C[C@@H](C)CCCC(C)C FYQGBXGJFWXIPP-OJROSNHMSA-N 0.000 description 33
239000000203 mixture Substances 0.000 description 29
229930000073 hydroprene Natural products 0.000 description 11
-1 polyvinyl chloride Chemical compound 0.000 description 11
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
235000013305 food Nutrition 0.000 description 8
239000002904 solvent Substances 0.000 description 8
239000000758 substrate Substances 0.000 description 7
241000238631 Hexapoda Species 0.000 description 6
230000000694 effects Effects 0.000 description 6
239000007921 spray Substances 0.000 description 6
239000000443 aerosol Substances 0.000 description 5
238000009472 formulation Methods 0.000 description 5
239000002949 juvenile hormone Substances 0.000 description 5
229930014550 juvenile hormone Natural products 0.000 description 5
150000003633 juvenile hormone derivatives Chemical class 0.000 description 5
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 4
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
239000003963 antioxidant agent Substances 0.000 description 4
230000001276 controlling effect Effects 0.000 description 4
239000003085 diluting agent Substances 0.000 description 4
239000004495 emulsifiable concentrate Substances 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
239000003595 mist Substances 0.000 description 4
239000003380 propellant Substances 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 3
239000004322 Butylated hydroxytoluene Substances 0.000 description 3
NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 3
OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
240000008042 Zea mays Species 0.000 description 3
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 3
235000002017 Zea mays subsp mays Nutrition 0.000 description 3
230000003078 antioxidant effect Effects 0.000 description 3
229940095259 butylated hydroxytoluene Drugs 0.000 description 3
235000010354 butylated hydroxytoluene Nutrition 0.000 description 3
KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
235000005822 corn Nutrition 0.000 description 3
230000000875 corresponding effect Effects 0.000 description 3
239000011521 glass Substances 0.000 description 3
230000005764 inhibitory process Effects 0.000 description 3
239000000463 material Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
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229920000915 polyvinyl chloride Polymers 0.000 description 3
239000004800 polyvinyl chloride Substances 0.000 description 3
239000007787 solid Substances 0.000 description 3
239000008247 solid mixture Substances 0.000 description 3
239000002562 thickening agent Substances 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
241000238657 Blattella germanica Species 0.000 description 2
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
239000005909 Kieselgur Substances 0.000 description 2
241001465754 Metazoa Species 0.000 description 2
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CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
241000238675 Periplaneta americana Species 0.000 description 2
239000004698 Polyethylene Substances 0.000 description 2
239000004743 Polypropylene Substances 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
239000013543 active substance Substances 0.000 description 2
150000001335 aliphatic alkanes Chemical class 0.000 description 2
229910000019 calcium carbonate Inorganic materials 0.000 description 2
239000000969 carrier Substances 0.000 description 2
235000019504 cigarettes Nutrition 0.000 description 2
239000004927 clay Substances 0.000 description 2
235000014113 dietary fatty acids Nutrition 0.000 description 2
239000000194 fatty acid Substances 0.000 description 2
229930195729 fatty acid Natural products 0.000 description 2
230000003054 hormonal effect Effects 0.000 description 2
NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000000034 method Methods 0.000 description 2
239000003094 microcapsule Substances 0.000 description 2
229920001778 nylon Polymers 0.000 description 2
229920000573 polyethylene Polymers 0.000 description 2
229920000642 polymer Polymers 0.000 description 2
229920001155 polypropylene Polymers 0.000 description 2
239000001294 propane Substances 0.000 description 2
230000001850 reproductive effect Effects 0.000 description 2
229920005989 resin Polymers 0.000 description 2
239000011347 resin Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
FYQGBXGJFWXIPP-HNNXBMFYSA-N (7S)-hydroprene Chemical compound CCOC(=O)C=C(C)C=CC[C@@H](C)CCCC(C)C FYQGBXGJFWXIPP-HNNXBMFYSA-N 0.000 description 1
FYQGBXGJFWXIPP-RCSINJDYSA-N (R)-hydroprene Chemical compound CCOC(=O)\C=C(/C)\C=C\C[C@H](C)CCCC(C)C FYQGBXGJFWXIPP-RCSINJDYSA-N 0.000 description 1
229930009625 (S)-hydroprene Natural products 0.000 description 1
GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
241000256118 Aedes aegypti Species 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
241000238662 Blatta orientalis Species 0.000 description 1
241000238658 Blattella Species 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
241000255925 Diptera Species 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
241000255896 Galleria mellonella Species 0.000 description 1
108010010803 Gelatin Proteins 0.000 description 1
241000256244 Heliothis virescens Species 0.000 description 1
241000257159 Musca domestica Species 0.000 description 1
241000819999 Nymphes Species 0.000 description 1
FBPFZTCFMRRESA-NQAPHZHOSA-N Sorbitol Polymers OCC(O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-NQAPHZHOSA-N 0.000 description 1
241000254109 Tenebrio molitor Species 0.000 description 1
239000012963 UV stabilizer Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
238000003556 assay Methods 0.000 description 1
VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
238000009835 boiling Methods 0.000 description 1
DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 description 1
239000001273 butane Substances 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
239000002738 chelating agent Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
230000000052 comparative effect Effects 0.000 description 1
238000011109 contamination Methods 0.000 description 1
230000003111 delayed effect Effects 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
238000009826 distribution Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000005038 ethylene vinyl acetate Substances 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
239000000284 extract Substances 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
239000008273 gelatin Substances 0.000 description 1
229920000159 gelatin Polymers 0.000 description 1
235000019322 gelatine Nutrition 0.000 description 1
235000011852 gelatine desserts Nutrition 0.000 description 1
239000012760 heat stabilizer Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
230000036512 infertility Effects 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
238000007689 inspection Methods 0.000 description 1
239000001282 iso-butane Substances 0.000 description 1
230000000366 juvenile effect Effects 0.000 description 1
239000002950 juvenile hormone derivative Substances 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
238000012986 modification Methods 0.000 description 1
230000004048 modification Effects 0.000 description 1
230000000877 morphologic effect Effects 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
239000000049 pigment Substances 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 1
229920000058 polyacrylate Polymers 0.000 description 1
229920002635 polyurethane Polymers 0.000 description 1
239000004814 polyurethane Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
HLWRUJAIJJEZDL-UHFFFAOYSA-M sodium;2-[2-[bis(carboxymethyl)amino]ethyl-(carboxymethyl)amino]acetate Chemical compound [Na+].OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC([O-])=O HLWRUJAIJJEZDL-UHFFFAOYSA-M 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
241000894007 species Species 0.000 description 1
238000005507 spraying Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
239000006188 syrup Substances 0.000 description 1
235000020357 syrup Nutrition 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
230000035899 viability Effects 0.000 description 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
229920001285 xanthan gum Polymers 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)
Catching Or Destruction (AREA)

CS863397A 1985-05-13 1986-05-12 Insecticide CS265219B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US73344485A	1985-05-13	1985-05-13

Publications (2)

Publication Number	Publication Date
CS339786A2 CS339786A2 (en)	1987-07-16
CS265219B2 true CS265219B2 (en)	1989-10-13

Family

ID=24947626

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS863397A CS265219B2 (en)	1985-05-13	1986-05-12	Insecticide

Country Status (14)

Country	Link
CN (1)	CN1014768B (tr)
AR (1)	AR241623A1 (tr)
CS (1)	CS265219B2 (tr)
DD (1)	DD247821A5 (tr)
DK (1)	DK174607B1 (tr)
GR (1)	GR861220B (tr)
HU (1)	HU204657B (tr)
IL (1)	IL78762A (tr)
IT (1)	IT1203787B (tr)
MX (1)	MX163537B (tr)
NZ (1)	NZ216123A (tr)
TR (1)	TR23016A (tr)
UA (1)	UA12838A (tr)
ZA (1)	ZA863531B (tr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CN108124870B (zh) *	2017-12-28	2024-01-09	常州胜杰化工有限公司	一种绿色生物蟑螂控制制剂及其使用方法
KR102377395B1 (ko) *	2021-11-05	2022-03-22	주식회사 에스비티제약	살충제 및 이를 이용한 해충 구제 방법

1986
- 1986-04-30 HU HU181786A patent/HU204657B/hu unknown
- 1986-05-12 IL IL7876286A patent/IL78762A/xx not_active IP Right Cessation
- 1986-05-12 IT IT48002/86A patent/IT1203787B/it active
- 1986-05-12 CN CN 86103267 patent/CN1014768B/zh not_active Expired
- 1986-05-12 DD DD29015986A patent/DD247821A5/de not_active IP Right Cessation
- 1986-05-12 CS CS863397A patent/CS265219B2/cs not_active IP Right Cessation
- 1986-05-12 DK DK219886A patent/DK174607B1/da not_active IP Right Cessation
- 1986-05-12 NZ NZ21612386A patent/NZ216123A/xx unknown
- 1986-05-12 GR GR861220A patent/GR861220B/el unknown
- 1986-05-12 UA UA4027510A patent/UA12838A/uk unknown
- 1986-05-13 AR AR30393186A patent/AR241623A1/es active
- 1986-05-13 MX MX247586A patent/MX163537B/es unknown
- 1986-05-13 ZA ZA863531A patent/ZA863531B/xx unknown
- 1986-05-13 TR TR24686A patent/TR23016A/tr unknown

Also Published As

Publication number	Publication date
AR241623A1 (es)	1992-10-30
ZA863531B (en)	1987-12-30
IL78762A (en)	1989-09-28
HUT41207A (en)	1987-04-28
NZ216123A (en)	1989-01-27
DK219886D0 (da)	1986-05-12
MX163537B (es)	1992-05-27
CN1014768B (zh)	1991-11-20
UA12838A (uk)	1997-02-28
HU204657B (en)	1992-02-28
CS339786A2 (en)	1987-07-16
GR861220B (en)	1986-09-05
DK219886A (da)	1986-11-14
DD247821A5 (de)	1987-07-22
CN86103267A (zh)	1986-11-12
IT8648002A0 (it)	1986-05-12
TR23016A (tr)	1989-01-16
DK174607B1 (da)	2003-07-21
IT1203787B (it)	1989-02-23

Legal Events

Date	Code	Title	Description
2000-06-30	IF00	In force as of 2000-06-30 in czech republic
2001-07-11	MK4A	Patent expired	Effective date: 20010512

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SU1743330A3 (ru)	1992-06-23	Способ борьбы с тараканами
Dobrin et al.	1985	The antifeeding activity of selected pyrethroids towards the Mexican bean beetle (Coleoptera: Coccinellidae)
Wiltz et al.	2010	Activity of bifenthrin, chlorfenapyr, fipronil, and thiamethoxam against red imported fire ants (Hymenoptera: Formicidae)
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Nelson et al.	1973	Toxicity of apple orchard pesticides to Agistemus fleschneri
US5066482A (en)	1991-11-19	Compositions and method for controlling cockroaches
Greenway et al.	1981	Attractant lures for males of the pea moth, Cydia nigricana (F.) containing (E)-10-dodecen-1-yl acetate and (E, E)-8, 10-dodecadien-1-yl acetate
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Andrews et al.	1948	Developments in the use of the newer organic insecticides of public health importance
US2639259A (en)	1953-05-19	Insecticides
Carter et al.	1978	Permethrin as a residual insecticide against cockroaches
Grayson	1966	Recent developments in the control of some arthropods of public health and veterinary importance: cockroaches
CN1036759C (zh)	1997-12-24	除虫防霉气雾剂
Lucas et al.	1993	Factors involved in the successful use of hydramethylnon baits in household and industrial pest control
EP0788306B1 (en)	2001-01-31	Method and means for controlling insect species
Strong	1969	Relative susceptibility of five stored-product moths to some organophosphorus insecticides
Nolan	1979	New acaricides to control resistant ticks.
JP2024005984A (ja)	2024-01-17	殺卵剤
JPS5785342A (en)	1982-05-28	Alpha-ethynylbenzyl 2,2-dimethyl-3-(2,2-dichlorovinyl) cyclopropane-carboxylate and insecticide containing the same as an active ingredient
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