SU673140A3 - Инсектоакарицидное средство - Google Patents

Инсектоакарицидное средство

Info

Publication number: SU673140A3
Authority: SU; USSR - Soviet Union
Prior art keywords: insecto; agent; cariocide; phosphorus acids; activity
Prior art date: 1971-12-10

Application number

SU721855798A

Other languages

English (en)

Russian (ru)

Inventor

Бенер Бит

Доз Даг

Мейер Вилли

Original Assignee

Циба -Гейги Аг (Фирма)

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.)

1971-12-10

Filing date

1972-12-08

Publication date

1979-07-05

1972-12-08 Application filed by Циба -Гейги Аг (Фирма) filed Critical Циба -Гейги Аг (Фирма)

1979-07-05 Application granted granted Critical

1979-07-05 Publication of SU673140A3 publication Critical patent/SU673140A3/ru

Links

239000002253 acid Substances 0.000 claims description 6
150000007513 acids Chemical class 0.000 claims description 6
150000001875 compounds Chemical class 0.000 claims description 6
239000003795 chemical substances by application Substances 0.000 claims description 5
229910052698 phosphorus Inorganic materials 0.000 claims description 4
239000011574 phosphorus Substances 0.000 claims description 4
125000001425 triazolyl group Chemical group 0.000 claims description 4
239000003085 diluting agent Substances 0.000 claims description 3
230000000694 effects Effects 0.000 claims description 3
239000000654 additive Substances 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims description 2
125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 claims description 2
125000004706 n-propylthio group Chemical group C(CC)S* 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
230000000996 additive effect Effects 0.000 claims 1
125000004414 alkyl thio group Chemical group 0.000 claims 1
239000000945 filler Substances 0.000 claims 1
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
230000000749 insecticidal effect Effects 0.000 description 3
229920000742 Cotton Polymers 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
241000196324 Embryophyta Species 0.000 description 2
244000061176 Nicotiana tabacum Species 0.000 description 2
235000002637 Nicotiana tabacum Nutrition 0.000 description 2
244000061456 Solanum tuberosum Species 0.000 description 2
241000607479 Yersinia pestis Species 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
QARVLSVVCXYDNA-UHFFFAOYSA-N bromobenzene Chemical compound BrC1=CC=CC=C1 QARVLSVVCXYDNA-UHFFFAOYSA-N 0.000 description 2
238000006243 chemical reaction Methods 0.000 description 2
238000001816 cooling Methods 0.000 description 2
239000008187 granular material Substances 0.000 description 2
239000000203 mixture Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
230000009885 systemic effect Effects 0.000 description 2
241000238876 Acari Species 0.000 description 1
241001124076 Aphididae Species 0.000 description 1
241000238631 Hexapoda Species 0.000 description 1
241000258916 Leptinotarsa decemlineata Species 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
241000256248 Spodoptera Species 0.000 description 1
241000219873 Vicia Species 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
150000001335 aliphatic alkanes Chemical class 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
239000007864 aqueous solution Substances 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
239000002585 base Substances 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000013043 chemical agent Substances 0.000 description 1
KMJJJTCKNZYTEY-UHFFFAOYSA-N chloro-diethoxy-sulfanylidene-$l^{5}-phosphane Chemical compound CCOP(Cl)(=S)OCC KMJJJTCKNZYTEY-UHFFFAOYSA-N 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
150000002012 dioxanes Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
125000004494 ethyl ester group Chemical group 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
235000003599 food sweetener Nutrition 0.000 description 1
238000009472 formulation Methods 0.000 description 1
230000002496 gastric effect Effects 0.000 description 1
239000011521 glass Substances 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
RUNIEFCRNHEYJO-UHFFFAOYSA-N oxolane;sodium Chemical compound [Na].C1CCOC1 RUNIEFCRNHEYJO-UHFFFAOYSA-N 0.000 description 1
150000003017 phosphorus Chemical class 0.000 description 1
239000004033 plastic Substances 0.000 description 1
-1 polychlorobenzene Chemical compound 0.000 description 1
229940072033 potash Drugs 0.000 description 1
BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
235000015320 potassium carbonate Nutrition 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-N pyridine Substances C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000003765 sweetening agent Substances 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
RYYWUUFWQRZTIU-UHFFFAOYSA-K thiophosphate Chemical compound [O-]P([O-])([O-])=S RYYWUUFWQRZTIU-UHFFFAOYSA-K 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D249/12—Oxygen or sulfur atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6515—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having three nitrogen atoms as the only ring hetero atoms
- C07F9/6518—Five-membered rings

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Biochemistry (AREA)
General Health & Medical Sciences (AREA)
Molecular Biology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)

SU721855798A 1971-12-10 1972-12-08 Инсектоакарицидное средство SU673140A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH1806471A CH563117A5 (en)	1971-12-10	1971-12-10	Biocidal triazolylphosphorus cpds - by reaction of hydroxytriazoles and organophosphorus cpds

Publications (1)

Publication Number	Publication Date
SU673140A3 true SU673140A3 (ru)	1979-07-05

Family

ID=4430171

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
SU721855798A SU673140A3 (ru)	1971-12-10	1972-12-08	Инсектоакарицидное средство
SU721855102A SU603318A3 (ru)	1971-12-10	1972-12-08	Средство борьбы с насекомыми,клещами и нематодами

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
SU721855102A SU603318A3 (ru)	1971-12-10	1972-12-08	Средство борьбы с насекомыми,клещами и нематодами

Country Status (9)

Country	Link
AT (1)	AT314904B (th)
BG (1)	BG22785A3 (th)
CH (1)	CH563117A5 (th)
CS (3)	CS169831B2 (th)
ES (1)	ES409487A1 (th)
HU (2)	HU167245B (th)
SU (2)	SU673140A3 (th)
TR (1)	TR17149A (th)
ZA (1)	ZA728704B (th)

1971
- 1971-12-10 CH CH1806471A patent/CH563117A5/de not_active IP Right Cessation
1972
- 1972-12-06 BG BG022051A patent/BG22785A3/xx unknown
- 1972-12-07 TR TR17149A patent/TR17149A/xx unknown
- 1972-12-07 AT AT1042372A patent/AT314904B/de not_active IP Right Cessation
- 1972-12-08 ZA ZA728704A patent/ZA728704B/xx unknown
- 1972-12-08 CS CS8438A patent/CS169831B2/cs unknown
- 1972-12-08 HU HUCI1314A patent/HU167245B/hu unknown
- 1972-12-08 CS CS8439A patent/CS169832B2/cs unknown
- 1972-12-08 SU SU721855798A patent/SU673140A3/ru active
- 1972-12-08 CS CS8440A patent/CS172962B2/cs unknown
- 1972-12-08 SU SU721855102A patent/SU603318A3/ru active
- 1972-12-08 HU HUCI1316A patent/HU165795B/hu unknown
- 1972-12-09 ES ES409487A patent/ES409487A1/es not_active Expired

Also Published As

Publication number	Publication date
ZA728704B (en)	1973-07-25
CS169832B2 (th)	1976-07-29
CS172962B2 (th)	1977-01-28
AT314904B (de)	1974-04-25
HU165795B (th)	1974-11-28
CS169831B2 (th)	1976-07-29
TR17149A (tr)	1974-04-25
HU167245B (th)	1975-09-27
SU603318A3 (ru)	1978-04-15
BG22785A3 (bg)	1977-04-20
ES409487A1 (es)	1976-04-01
CH563117A5 (en)	1975-06-30

Publication	Publication Date	Title
CA1130308A (en)	1982-08-24	Preparation of cyclopropane carboxylic acids and esters
SU673140A3 (ru)	1979-07-05	Инсектоакарицидное средство
US3371132A (en)	1968-02-27	O-alkyl o(s)-(n-alkoxy-n-alkyl-carbamyl methyl) phenyl (thiolo) (thiono)phosphonates
IL45780A (en)	1977-12-30	Urea thiolphosphonates their preparation and their use in pest control
SU701518A3 (ru)	1979-11-30	Пестицидна композици
US3632621A (en)	1972-01-04	Novel oximecarbamates
US3726973A (en)	1973-04-10	1-alkoxy(-alk enyloxy,-phenoxy)-1-thiono-3-chloro(3-alkyl) phospholines compositions and their use
US4137308A (en)	1979-01-30	1,3-Oxazole phosphates and phosphonates as insecticides and miticides
US3723625A (en)	1973-03-27	Process for killing plant pests using cyanoalkyl-nitrophenyl carbonates
US3364230A (en)	1968-01-16	Novel phosphorylated 2-imino-1, 3-dithioles
US3714176A (en)	1973-01-30	Pesticidal phosphorous-containing imino oxazolidines
US3911122A (en)	1975-10-07	Insecticidal and acarididal substituted phenyl thiophosphoric acid esters
US4537901A (en)	1985-08-27	Insecticidal carbamates
US3803312A (en)	1974-04-09	Certain phosphorus containing imino oxazolidines,and their utility
US4015974A (en)	1977-04-05	Amido phosphorothiolates
US2729668A (en)	1956-01-03	Process for making diethoxyphosphoryl tetramethyldiamidothiophosphate
CA1234823A (en)	1988-04-05	Oximinophosphoric acid derivatives, their preparation and their use for controlling pests
US3925517A (en)	1975-12-09	Phosphorylformamidines
SU847895A3 (ru)	1981-07-15	Инсектоакарицидное средство
US3920671A (en)	1975-11-18	Certain phosphorus acid esters
US3681505A (en)	1972-08-01	Method of controlling insects and acarina with cyanoalkylaldoxime carbamates
US2893910A (en)	1959-07-07	Toxic reaction products of organosulfinylamines with dialkyl phosphites
US4670425A (en)	1987-06-02	Oximinophosphoric acid derivatives and their use for controlling pests
US3891728A (en)	1975-06-24	O-alkyl-S-alkyl-O-substituted phenyl-thiophosphoric acid esters
IL43144A (en)	1977-02-28	Thiophosphoric acid amide esters their preparation and their use in insecticidal acaricidal and nematicidal compositions