CS197266B2 - Insecticide and acaricide means - Google Patents

Insecticide and acaricide means Download PDF

Info

Publication number: CS197266B2
Authority: CS; Czechoslovakia
Prior art keywords: align; insecticidal; ppm; compound; carboxylic acid
Prior art date: 1975-02-13

Application number

CS76965A

Other languages

Czech (cs)

English (en)

Inventor

Roger W Addor

Michael S Schrider

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.)

1975-02-13

Filing date

1976-02-13

Publication date

1980-04-30

1976-02-13 Application filed by American Cyanamid Co filed Critical American Cyanamid Co

1980-04-30 Publication of CS197266B2 publication Critical patent/CS197266B2/cs

Links

230000000895 acaricidal effect Effects 0.000 title claims abstract description 10
239000002917 insecticide Substances 0.000 title abstract description 10
239000000642 acaricide Substances 0.000 title 1
230000000749 insecticidal effect Effects 0.000 claims abstract description 54
239000002253 acid Substances 0.000 claims abstract description 16
150000001875 compounds Chemical class 0.000 claims description 100
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238000002360 preparation method Methods 0.000 claims description 22
238000000034 method Methods 0.000 claims description 13
239000004480 active ingredient Substances 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 10
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238000006243 chemical reaction Methods 0.000 claims description 7
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SHCRDCOTRILILT-WOBDGSLYSA-N cinerin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C)C(=O)C1 SHCRDCOTRILILT-WOBDGSLYSA-N 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
235000005687 corn oil Nutrition 0.000 description 1
239000002285 corn oil Substances 0.000 description 1
YMGUBTXCNDTFJI-UHFFFAOYSA-N cyclopropanecarboxylic acid Chemical compound OC(=O)C1CC1 YMGUBTXCNDTFJI-UHFFFAOYSA-N 0.000 description 1
125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
230000007812 deficiency Effects 0.000 description 1
210000003298 dental enamel Anatomy 0.000 description 1
238000001514 detection method Methods 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
238000007865 diluting Methods 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
239000003937 drug carrier Substances 0.000 description 1
230000009977 dual effect Effects 0.000 description 1
239000003480 eluent Substances 0.000 description 1
238000010828 elution Methods 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000003628 erosive effect Effects 0.000 description 1
230000001747 exhibiting effect Effects 0.000 description 1
239000004744 fabric Substances 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
230000002496 gastric effect Effects 0.000 description 1
238000000227 grinding Methods 0.000 description 1
DMEGYFMYUHOHGS-UHFFFAOYSA-N heptamethylene Natural products C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
238000007918 intramuscular administration Methods 0.000 description 1
239000007927 intramuscular injection Substances 0.000 description 1
239000007928 intraperitoneal injection Substances 0.000 description 1
235000021374 legumes Nutrition 0.000 description 1
230000000670 limiting effect Effects 0.000 description 1
239000012669 liquid formulation Substances 0.000 description 1
231100000053 low toxicity Toxicity 0.000 description 1
229910052943 magnesium sulfate Inorganic materials 0.000 description 1
235000019341 magnesium sulphate Nutrition 0.000 description 1
235000009973 maize Nutrition 0.000 description 1
ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 1
235000019713 millet Nutrition 0.000 description 1
239000004570 mortar (masonry) Substances 0.000 description 1
239000006199 nebulizer Substances 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
238000006864 oxidative decomposition reaction Methods 0.000 description 1
125000004430 oxygen atom Chemical group O* 0.000 description 1
230000035515 penetration Effects 0.000 description 1
RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
FAIAAWCVCHQXDN-UHFFFAOYSA-N phosphorus trichloride Chemical compound ClP(Cl)Cl FAIAAWCVCHQXDN-UHFFFAOYSA-N 0.000 description 1
229960005235 piperonyl butoxide Drugs 0.000 description 1
231100000614 poison Toxicity 0.000 description 1
239000002574 poison Substances 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
238000004321 preservation Methods 0.000 description 1
230000002035 prolonged effect Effects 0.000 description 1
229940059835 pyrethrines Drugs 0.000 description 1
NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000000926 separation method Methods 0.000 description 1
235000011803 sesame oil Nutrition 0.000 description 1
239000008159 sesame oil Substances 0.000 description 1
125000003003 spiro group Chemical group 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
239000011550 stock solution Substances 0.000 description 1
238000007920 subcutaneous administration Methods 0.000 description 1
239000007929 subcutaneous injection Substances 0.000 description 1
239000008400 supply water Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
230000009897 systematic effect Effects 0.000 description 1
239000003826 tablet Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
HFRXJVQOXRXOPP-UHFFFAOYSA-N thionyl bromide Chemical compound BrS(Br)=O HFRXJVQOXRXOPP-UHFFFAOYSA-N 0.000 description 1
LSJNBGSOIVSBBR-UHFFFAOYSA-N thionyl fluoride Chemical compound FS(F)=O LSJNBGSOIVSBBR-UHFFFAOYSA-N 0.000 description 1
238000012546 transfer Methods 0.000 description 1
210000004291 uterus Anatomy 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000013585 weight reducing agent Substances 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/31—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing rings other than six-membered aromatic rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/74—Esters of carboxylic acids having an esterified carboxyl group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/76—Esters of carboxylic acids having a carboxyl group bound to a carbon atom of a six-membered aromatic ring

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CS76965A 1975-02-13 1976-02-13 Insecticide and acaricide means CS197266B2 (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US05/550,105 US3966959A (en)	1975-02-13	1975-02-13	Insecticidal and acaricidal, pyrethroid compounds

Publications (1)

Publication Number	Publication Date
CS197266B2 true CS197266B2 (en)	1980-04-30

Family

ID=24195771

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CS76965A CS197266B2 (en)	1975-02-13	1976-02-13	Insecticide and acaricide means

Country Status (6)

Country	Link
US (1)	US3966959A (fr)
BE (1)	BE838500A (fr)
CA (1)	CA1084943A (fr)
CS (1)	CS197266B2 (fr)
PH (1)	PH11929A (fr)
ZA (1)	ZA76861B (fr)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4060632A (en) *	1975-02-13	1977-11-29	American Cyanamid Company	Method for controlling acarina
US4454127A (en) *	1975-10-20	1984-06-12	American Cyanamid Co.	Insecticidal pyrethroid compositions
US4340608A (en) *	1975-10-20	1982-07-20	American Cyanamid Company	Insecticidal pyrethroid compositions
US4087523A (en) *	1975-10-20	1978-05-02	American Cyanamid Company	Insecticidal pyrethroid compositions
US4292322A (en) *	1976-06-16	1981-09-29	Fumakilla Limited	Method for killing insects with electro-mechanical ultrasonic nebulizer
US4078080A (en) *	1976-12-13	1978-03-07	American Cyanamid Company	Oral administration of pyrethroids to warm-blooded animals to prevent fly development in their droppings
DE2730515A1 (de) *	1977-07-06	1979-01-18	Bayer Ag	Substituierte phenoxybenzyloxycarbonylderivate, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
AU526817B2 (en) *	1978-06-21	1983-02-03	Ici Australia Limited	Pesticides
US4203918A (en) *	1978-07-21	1980-05-20	American Cyanamid Company	Halo-substituted benzospiro cyclopropane carboxylates as insecticides and ixodicides
US4189598A (en) *	1978-07-24	1980-02-19	Zoecon Corporation	Phenoxybenzyl 2-[2-(2-hydroxy)indanyl]-3-methyl-butanoates
US4217302A (en) *	1978-07-24	1980-08-12	Zoecon Corporation	Phenoxybenzyl 2-indenyl-3-methylbutanoates
DE2947209A1 (de) *	1979-11-23	1981-06-11	Bayer Ag, 5090 Leverkusen	Fluor-substituierte spirocarbonsaeure-benzylester, verfahren zu ihrer herstellung und ihre verendung in schaedlingsbekaempfungsmitteln
HU182802B (en) *	1980-02-26	1984-03-28	Biogal Gyogyszergyar	Fotostabil delousing (insecticide) composition containing synthetic piretroides
US4617318A (en) *	1981-09-25	1986-10-14	American Cyanamid Company	Non-irritating pyrethroid formulations in vegetable oils and tall oils
EP1355895B1 (fr) *	2000-12-08	2008-07-23	The Government of the United States of America, as represented by the Secretary, Department of Health & Human Services	Composes pour intervention phytosanitaire

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3647857A (en) *	1970-03-16	1972-03-07	Procter & Gamble	Novel esters of chrysanthemic acid and alcohols related to 2-indanol
US3823177A (en) *	1971-06-25	1974-07-09	Procter & Gamble	Insecticidal esters of spiro carboxylic acids
JPS515450B1 (fr) *	1971-06-29	1976-02-20
GB1437987A (fr)	1973-10-08	1976-06-03

1975
- 1975-02-13 US US05/550,105 patent/US3966959A/en not_active Expired - Lifetime
1976
- 1976-01-23 PH PH18010A patent/PH11929A/en unknown
- 1976-02-12 BE BE164274A patent/BE838500A/fr not_active IP Right Cessation
- 1976-02-13 CS CS76965A patent/CS197266B2/cs unknown
- 1976-02-13 ZA ZA861A patent/ZA76861B/xx unknown
- 1976-02-13 CA CA245,677A patent/CA1084943A/fr not_active Expired

Also Published As

Publication number	Publication date
US3966959A (en)	1976-06-29
BE838500A (fr)	1976-08-12
CA1084943A (fr)	1980-09-02
PH11929A (en)	1978-09-13
ZA76861B (en)	1977-01-26

Publication	Publication Date	Title
US4503071A (en)	1985-03-05	Insecticidal composition containing optically active α-cyano-3-phenoxybenzyl 2-(4-chlorophenyl)isovalerate
US4889872A (en)	1989-12-26	2,3,5,6-Tetrafluorobenzyl (+) 1r-trans-2,2-dimethyl-3-(2,2-dichlorovinyl)-cyclopropanecarboxylate
HU185369B (en)	1985-01-28	Compositions containing alpha,beta-unsaturated carboxylic acid esters as active substances with insecticide activity and process for preparing the active substance
HU176713B (en)	1981-04-28	Insecticide and acaricide preparations containing hydantoin-n-methyl esters and process for preparing the hydantoin-n-methyl esters
JPS5813522B2 (ja)	1983-03-14	新しいシクロプロパンカルボン酸エステルを含有する殺虫、殺ダニ剤
US3934023A (en)	1976-01-20	Insecticidal d-cis, trans-chrysanthemates
CS197266B2 (en)	1980-04-30	Insecticide and acaricide means
JPH02233644A (ja)	1990-09-17	新規の２，２―ジメチル―３―（２―モノハロエテニル）シクロプロパンカルボン酸誘導体、それらの製造方法及び害虫駆除剤としてのそれらの使用
JPH05112519A (ja)	1993-05-07	３−［２−シアノ−２−ハロゲノエテニル−２，２−ジメチルシクロプロパンカルボン酸の新エステル誘導体、それらの製造法及び殺生物としての使用
US3795696A (en)	1974-03-05	Alkynylbenzyl cyclopropane-carboxylates
US4309439A (en)	1982-01-05	Substituted-acetic acid ester
JPH0124779B2 (fr)	1989-05-15
JPH02225442A (ja)	1990-09-07	３―エテニル―２，２―ジメチルシクロプロパンカルボン酸の新規な弗素化誘導体、その製造方法、害虫駆除剤としてのその使用及びそれを含有する組成物
US3932459A (en)	1976-01-13	Novel cyclopropanecarboxylic acid esters
AU595796B2 (en)	1990-04-12	Novel carboxylic acid esters, methods for production thereof and insecticides containing them as the active ingredient
JPS61243049A (ja)	1986-10-29	ビニルシクロプロパンカルボン酸エステル類
PL95735B1 (pl)	1977-11-30	Srodek owadobojczy i roztoczobojczy
JPH07149693A (ja)	1995-06-13	２，２−ジメチル−３−（３，３，３−トリフルオル−１−プロペニル）シクロプロパンカルボン酸から誘導される新規のエステル、その製造方法及び害虫駆除剤としてのその使用
JP3320453B2 (ja)	2002-09-03	４−アミノ−２，３，５，６−テトラフルオルフェニルメチルアルコールの新規なピレスリノイドエステル、それらの製造法及びそれらのペスチサイドとしての用途
IE43348B1 (en)	1981-02-11	Pyrethroids as insecticides
EP0037851A2 (fr)	1981-10-21	Carboxylates, procédé pour leur préparation, composition insecticide et/ou acaricide et utilisation des composés comme insecticides et/ou acaricides
JPH04352746A (ja)	1992-12-07	新規の３−（３，３，３−トリフルオル−２−クロルプロペニル）−２，２−ジメチルシクロプロパンカルボン酸エステル、その製造方法及び害虫駆除剤としてのその使用
JPS5928526B2 (ja)	1984-07-13	新しい害虫防除組成物およびその製造法
EP0061713B1 (fr)	1984-11-07	Ester d'acides cyclopropancarboxyliques, leurs préparations et compositions insecticides et acaricides
JPS6030301B2 (ja)	1985-07-16	シクロプロパンカルボン酸３−（２，２−ジクロロビニルオキシ）ベンジルエステル、その製造方法及び該化合物を含有する殺虫、殺ダニ剤