DD141407A5 - Schaedlingsbekaempfungsmittel - Google Patents

Schaedlingsbekaempfungsmittel Download PDF

Info

Publication number: DD141407A5
Authority: DD; German Democratic Republic
Prior art keywords: binapacryl; triazophos; pesticides; berlin; weight ratio
Prior art date: 1978-01-17

Application number

DD79210478A

Other languages

German (de)

English (en)

Inventor

Ludwig Emmel

Anna Waltersdorfer

Original Assignee

Hoechst 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.)

1978-01-17

Filing date

1979-01-15

Publication date

1980-04-30

1979-01-15 Application filed by Hoechst Ag filed Critical Hoechst Ag

1980-04-30 Publication of DD141407A5 publication Critical patent/DD141407A5/de

Links

239000000575 pesticide Substances 0.000 claims abstract description 9
ZRDUSMYWDRPZRM-UHFFFAOYSA-N 2-sec-butyl-4,6-dinitrophenyl 3-methylbut-2-enoate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)C=C(C)C ZRDUSMYWDRPZRM-UHFFFAOYSA-N 0.000 description 16
AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 15
239000000203 mixture Substances 0.000 description 10
241000607479 Yersinia pestis Species 0.000 description 6
239000013543 active substance Substances 0.000 description 6
239000012141 concentrate Substances 0.000 description 5
239000000839 emulsion Substances 0.000 description 5
238000009472 formulation Methods 0.000 description 5
230000000895 acaricidal effect Effects 0.000 description 4
239000004480 active ingredient Substances 0.000 description 4
239000000126 substance Substances 0.000 description 4
241000239290 Araneae Species 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
238000009835 boiling Methods 0.000 description 3
150000003014 phosphoric acid esters Chemical class 0.000 description 3
239000000843 powder Substances 0.000 description 3
238000002360 preparation method Methods 0.000 description 3
238000005507 spraying Methods 0.000 description 3
239000008096 xylene Substances 0.000 description 3
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
241000238631 Hexapoda Species 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
244000046052 Phaseolus vulgaris Species 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
241001454293 Tetranychus urticae Species 0.000 description 2
239000000853 adhesive Substances 0.000 description 2
230000001070 adhesive effect Effects 0.000 description 2
SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical compound [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
235000013601 eggs Nutrition 0.000 description 2
239000008187 granular material Substances 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
239000011707 mineral Substances 0.000 description 2
239000002904 solvent Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
YYPNJNDODFVZLE-UHFFFAOYSA-N 3-methylbut-2-enoic acid Chemical compound CC(C)=CC(O)=O YYPNJNDODFVZLE-UHFFFAOYSA-N 0.000 description 1
241000196324 Embryophyta Species 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
241000118205 Ovicides Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
241001454294 Tetranychus Species 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
125000000217 alkyl group Chemical group 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical class [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229940124558 contraceptive agent Drugs 0.000 description 1
239000003433 contraceptive agent Substances 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000000945 filler Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
-1 kieselguhr Chemical class 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000019198 oils Nutrition 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
230000003151 ovacidal effect Effects 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
230000002195 synergetic effect Effects 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
150000003738 xylenes Chemical class 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic radicals

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)

DD79210478A 1978-01-17 1979-01-15 Schaedlingsbekaempfungsmittel DD141407A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19782801787 DE2801787A1 (de)	1978-01-17	1978-01-17	Schaedlingsbekaempfungsmittel

Publications (1)

Publication Number	Publication Date
DD141407A5 true DD141407A5 (de)	1980-04-30

Family

ID=6029650

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79210478A DD141407A5 (de)	1978-01-17	1979-01-15	Schaedlingsbekaempfungsmittel

Country Status (27)

Country	Link
JP (1)	JPS54101429A (cs)
AR (1)	AR219961Q (cs)
AT (1)	ATA26479A (cs)
AU (1)	AU516996B2 (cs)
BE (1)	BE873536A (cs)
BG (1)	BG28696A3 (cs)
BR (1)	BR7900268A (cs)
CS (1)	CS203030B2 (cs)
DD (1)	DD141407A5 (cs)
DE (1)	DE2801787A1 (cs)
DK (1)	DK18279A (cs)
EG (1)	EG13763A (cs)
FR (1)	FR2414300A1 (cs)
GB (1)	GB2012587B (cs)
IL (1)	IL56432A0 (cs)
IT (1)	IT1110014B (cs)
MW (1)	MW279A1 (cs)
MX (1)	MX6664E (cs)
NL (1)	NL7900349A (cs)
NZ (1)	NZ189371A (cs)
OA (1)	OA06152A (cs)
PH (1)	PH14337A (cs)
PL (1)	PL212821A1 (cs)
PT (1)	PT69082A (cs)
SU (1)	SU717989A3 (cs)
ZA (1)	ZA79171B (cs)
ZM (1)	ZM479A1 (cs)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2200436A1 (de) *	1971-01-19	1972-08-10	Agripat Sa	Neue Ester

1978
- 1978-01-17 DE DE19782801787 patent/DE2801787A1/de not_active Withdrawn
1979
- 1979-01-12 BG BG042052A patent/BG28696A3/xx unknown
- 1979-01-15 NZ NZ189371A patent/NZ189371A/xx unknown
- 1979-01-15 AT AT26479A patent/ATA26479A/de not_active IP Right Cessation
- 1979-01-15 DD DD79210478A patent/DD141407A5/de unknown
- 1979-01-15 EG EG25/79A patent/EG13763A/xx active
- 1979-01-15 PH PH22064A patent/PH14337A/en unknown
- 1979-01-15 IT IT19306/79A patent/IT1110014B/it active
- 1979-01-15 AR AR275160A patent/AR219961Q/es unknown
- 1979-01-15 MW MW2/79A patent/MW279A1/xx unknown
- 1979-01-15 IL IL56432A patent/IL56432A0/xx unknown
- 1979-01-15 ZM ZM4/79A patent/ZM479A1/xx unknown
- 1979-01-16 AU AU43397/79A patent/AU516996B2/en not_active Ceased
- 1979-01-16 JP JP229579A patent/JPS54101429A/ja active Pending
- 1979-01-16 ZA ZA79171A patent/ZA79171B/xx unknown
- 1979-01-16 SU SU792712808A patent/SU717989A3/ru active
- 1979-01-16 NL NL7900349A patent/NL7900349A/xx not_active Application Discontinuation
- 1979-01-16 CS CS79346A patent/CS203030B2/cs unknown
- 1979-01-16 PT PT7969082A patent/PT69082A/pt unknown
- 1979-01-16 BR BR7900268A patent/BR7900268A/pt unknown
- 1979-01-16 GB GB791567A patent/GB2012587B/en not_active Expired
- 1979-01-16 DK DK18279A patent/DK18279A/da not_active Application Discontinuation
- 1979-01-16 PL PL21282179A patent/PL212821A1/xx unknown
- 1979-01-17 OA OA56712A patent/OA06152A/xx unknown
- 1979-01-17 BE BE0/192941A patent/BE873536A/xx unknown
- 1979-01-17 MX MX797664U patent/MX6664E/es unknown
- 1979-01-17 FR FR7901077A patent/FR2414300A1/fr active Pending

Also Published As

Publication number	Publication date
MX6664E (es)	1985-10-07
PT69082A (en)	1979-02-01
ATA26479A (de)	1981-01-15
PL212821A1 (pl)	1979-09-10
FR2414300A1 (fr)	1979-08-10
DE2801787A1 (de)	1979-07-19
ZA79171B (en)	1980-01-30
ZM479A1 (en)	1980-08-22
SU717989A3 (ru)	1980-02-25
OA06152A (fr)	1981-06-30
BE873536A (fr)	1979-07-17
GB2012587A (en)	1979-08-01
GB2012587B (en)	1982-06-16
AU4339779A (en)	1979-07-26
DK18279A (da)	1979-07-18
NL7900349A (nl)	1979-07-19
IL56432A0 (en)	1979-03-12
MW279A1 (en)	1980-03-12
JPS54101429A (en)	1979-08-10
PH14337A (en)	1981-05-29
BG28696A3 (en)	1980-06-16
AU516996B2 (en)	1981-07-02
IT7919306A0 (it)	1979-01-15
CS203030B2 (en)	1981-02-27
AR219961Q (es)	1980-09-30
NZ189371A (en)	1980-10-24
EG13763A (en)	1982-03-31
IT1110014B (it)	1985-12-23
BR7900268A (pt)	1979-08-14

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EP0012452B1 (de)	1983-02-09	Phosphorsäureester und deren Verwendung zur Herstellung von Schädlingsbekämpfungsmitteln
EP0477676B1 (de)	1995-01-04	Pyrethroid-Wirkstoffkombinationen enthaltend Benfluthrin und Prallethrin
DE2713163C3 (de)	1987-12-03	Fungizid auf Basis von Methylbenzimidazol-2-yl-carbamat
DE3721852A1 (de)	1989-01-12	Fungizide saatgutbehandlungsmittel
DD141407A5 (de)	1980-04-30	Schaedlingsbekaempfungsmittel
EP0438712A1 (de)	1991-07-31	Fungizide Wirkstoffkombinationen
EP0513567B1 (de)	1995-11-15	Fungizide Wirkstoffkombinationen
EP0026829B1 (de)	1983-05-11	Ein Triazolderivat und ein Phosphorthioat enthaltende Schädlingsbekämpfungsmittel und deren Verwendung zur Bekämpfung von Schadinsekten und Akariden
DE69709895T2 (de)	2002-08-01	Hydrazincarboxylat-mitizide und -insectizide
DE10059609A1 (de)	2002-06-06	Fungizide Wirkstoffkombinationen
DE19649459C2 (de)	2002-04-18	Fungizide Wirkstoffkombinationen
DE2223936A1 (de)	1973-12-06	Fungizide mittel
DE1210620B (de)	1966-02-10	Fungitoxische Mittel
EP0275013B1 (de)	1992-04-22	Fungizide Wirkstoffkombinationen
AT364671B (de)	1981-11-10	Insektizides mittel
EP0077300B1 (de)	1985-02-13	Triorganozinnhydantoin-Verbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung in der Schädlingsbekämpfung
AT357364B (de)	1980-07-10	Mittel zur selektiven bekaempfung von avena fatua
DE3934714A1 (de)	1991-04-25	Fungizide wirkstoffkombinationen
DE2453210B2 (de)	1979-03-29	Bekämpfung von Pilzen der Gattung Helminthosporium mit Dimethylpyrazolylbenzimidazol
DE2818497A1 (de)	1979-11-08	Akarizide und insektizide mittel
DE3715705A1 (de)	1988-11-24	Fungizide wirkstoffkombinationen
DE1668792A1 (de)	1971-04-08	Neue Alkyl-2-methylpropenyl-ketoxim-carbamate
DE1693169B2 (cs)	1974-05-09
DE1795824C2 (de)	1977-01-13	Acetylierte 4-Amino-3-methylthioe-phenyl-1,2,4-triazin-5-one
DE2012973C3 (de)	1978-09-28	Benzohydroximsäureesterverbindungen, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende acarizide Mittel