DD250042A5 - Fluessige pestizide zusammensetzung - Google Patents

Fluessige pestizide zusammensetzung Download PDF

Info

Publication number: DD250042A5
Authority: DD; German Democratic Republic
Prior art keywords: volume; amitraz; aluminum; mass; composition according
Prior art date: 1985-10-16

Application number

DD86295261A

Other languages

German (de)

English (en)

Inventor

Michael A Webb

Original Assignee

��@��@��k��

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.)

1985-10-16

Filing date

1986-10-14

Publication date

1987-09-30

Family has litigation

First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10586716&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DD250042(A5) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.

1986-10-14 Application filed by ��@��@��k�� filed Critical ��@��@��k��

1987-09-30 Publication of DD250042A5 publication Critical patent/DD250042A5/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 36
239000007788 liquid Substances 0.000 title claims abstract description 8
239000000575 pesticide Substances 0.000 title description 2
QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 claims abstract description 22
229960002587 amitraz Drugs 0.000 claims abstract description 22
-1 aluminum alkoxide Chemical class 0.000 claims abstract description 19
229910052782 aluminium Inorganic materials 0.000 claims abstract description 15
RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical compound C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 claims abstract description 6
230000000361 pesticidal effect Effects 0.000 claims abstract description 6
SMZOGRDCAXLAAR-UHFFFAOYSA-N aluminium isopropoxide Chemical compound [Al+3].CC(C)[O-].CC(C)[O-].CC(C)[O-] SMZOGRDCAXLAAR-UHFFFAOYSA-N 0.000 claims abstract description 3
239000003960 organic solvent Substances 0.000 claims abstract 2
230000000087 stabilizing effect Effects 0.000 claims abstract 2
WOZZOSDBXABUFO-UHFFFAOYSA-N tri(butan-2-yloxy)alumane Chemical compound [Al+3].CCC(C)[O-].CCC(C)[O-].CCC(C)[O-] WOZZOSDBXABUFO-UHFFFAOYSA-N 0.000 claims abstract 2
239000004094 surface-active agent Substances 0.000 abstract description 3
238000009472 formulation Methods 0.000 description 10
239000003381 stabilizer Substances 0.000 description 6
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
238000000354 decomposition reaction Methods 0.000 description 4
239000004495 emulsifiable concentrate Substances 0.000 description 4
QPUYECUOLPXSFR-UHFFFAOYSA-N 1-methylnaphthalene Chemical class C1=CC=C2C(C)=CC=CC2=C1 QPUYECUOLPXSFR-UHFFFAOYSA-N 0.000 description 3
241000158500 Platanus racemosa Species 0.000 description 3
150000004703 alkoxides Chemical class 0.000 description 3
239000002736 nonionic surfactant Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
FYGHSUNMUKGBRK-UHFFFAOYSA-N 1,2,3-trimethylbenzene Chemical compound CC1=CC=CC(C)=C1C FYGHSUNMUKGBRK-UHFFFAOYSA-N 0.000 description 2
KVNYFPKFSJIPBJ-UHFFFAOYSA-N 1,2-diethylbenzene Chemical compound CCC1=CC=CC=C1CC KVNYFPKFSJIPBJ-UHFFFAOYSA-N 0.000 description 2
FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 2
UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
150000004996 alkyl benzenes Chemical class 0.000 description 2
239000003945 anionic surfactant Substances 0.000 description 2
230000000052 comparative effect Effects 0.000 description 2
150000001875 compounds Chemical class 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 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
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
229960005235 piperonyl butoxide Drugs 0.000 description 2
UOHMMEJUHBCKEE-UHFFFAOYSA-N prehnitene Chemical compound CC1=CC=C(C)C(C)=C1C UOHMMEJUHBCKEE-UHFFFAOYSA-N 0.000 description 2
150000003871 sulfonates Chemical class 0.000 description 2
150000003467 sulfuric acid derivatives Chemical class 0.000 description 2
YTZKOQUCBOVLHL-UHFFFAOYSA-N tert-butylbenzene Chemical compound CC(C)(C)C1=CC=CC=C1 YTZKOQUCBOVLHL-UHFFFAOYSA-N 0.000 description 2
LRJOXARIJKBUFE-UHFFFAOYSA-N 1,2-diethyl-3-methylbenzene Chemical compound CCC1=CC=CC(C)=C1CC LRJOXARIJKBUFE-UHFFFAOYSA-N 0.000 description 1
QFMDFTQOJHFVNR-UHFFFAOYSA-N 1-[2,2-dichloro-1-(4-ethylphenyl)ethyl]-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1C(C(Cl)Cl)C1=CC=C(CC)C=C1 QFMDFTQOJHFVNR-UHFFFAOYSA-N 0.000 description 1
BAMWORSGQSUNSC-UHFFFAOYSA-N 1-ethyl-2,3,4-trimethylbenzene Chemical compound CCC1=CC=C(C)C(C)=C1C BAMWORSGQSUNSC-UHFFFAOYSA-N 0.000 description 1
HYFLWBNQFMXCPA-UHFFFAOYSA-N 1-ethyl-2-methylbenzene Chemical compound CCC1=CC=CC=C1C HYFLWBNQFMXCPA-UHFFFAOYSA-N 0.000 description 1
IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical compound CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 1
CDOUZKKFHVEKRI-UHFFFAOYSA-N 3-bromo-n-[(prop-2-enoylamino)methyl]propanamide Chemical compound BrCCC(=O)NCNC(=O)C=C CDOUZKKFHVEKRI-UHFFFAOYSA-N 0.000 description 1
JYCQQPHGFMYQCF-UHFFFAOYSA-N 4-tert-Octylphenol monoethoxylate Chemical compound CC(C)(C)CC(C)(C)C1=CC=C(OCCO)C=C1 JYCQQPHGFMYQCF-UHFFFAOYSA-N 0.000 description 1
239000004215 Carbon black (E152) Substances 0.000 description 1
BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
239000004606 Fillers/Extenders Substances 0.000 description 1
241001465754 Metazoa Species 0.000 description 1
NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
229920013802 TRITON CF-10 Polymers 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000004480 active ingredient Substances 0.000 description 1
150000001335 aliphatic alkanes Chemical class 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
QXAITBQSYVNQDR-UHFFFAOYSA-N amitraz Chemical group C=1C=C(C)C=C(C)C=1N=CN(C)C=NC1=CC=C(C)C=C1C QXAITBQSYVNQDR-UHFFFAOYSA-N 0.000 description 1
150000001449 anionic compounds Chemical class 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
150000001555 benzenes Chemical class 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
229920001577 copolymer Polymers 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
238000001030 gas--liquid chromatography Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
239000005453 ketone based solvent Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
XLDBGFGREOMWSL-UHFFFAOYSA-N n,n'-bis[2,6-di(propan-2-yl)phenyl]methanediimine Chemical compound CC(C)C1=CC=CC(C(C)C)=C1N=C=NC1=C(C(C)C)C=CC=C1C(C)C XLDBGFGREOMWSL-UHFFFAOYSA-N 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
229920002113 octoxynol Polymers 0.000 description 1
BEZDDPMMPIDMGJ-UHFFFAOYSA-N pentamethylbenzene Chemical compound CC1=CC(C)=C(C)C(C)=C1C BEZDDPMMPIDMGJ-UHFFFAOYSA-N 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
OGHBATFHNDZKSO-UHFFFAOYSA-N propan-2-olate Chemical compound CC(C)[O-] OGHBATFHNDZKSO-UHFFFAOYSA-N 0.000 description 1
239000000243 solution Substances 0.000 description 1
238000005507 spraying Methods 0.000 description 1
230000006641 stabilisation Effects 0.000 description 1
238000011105 stabilization Methods 0.000 description 1
239000000126 substance Substances 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/22—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/52—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing groups, e.g. carboxylic acid amidines

Landscapes

Life Sciences & Earth Sciences (AREA)
General Health & Medical Sciences (AREA)
Health & Medical Sciences (AREA)
Dentistry (AREA)
Zoology (AREA)
Plant Pathology (AREA)
Environmental Sciences (AREA)
Engineering & Computer Science (AREA)
Agronomy & Crop Science (AREA)
Wood Science & Technology (AREA)
Pest Control & Pesticides (AREA)
Toxicology (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Prostheses (AREA)
Superconductors And Manufacturing Methods Therefor (AREA)
Compounds Of Unknown Constitution (AREA)

DD86295261A 1985-10-16 1986-10-14 Fluessige pestizide zusammensetzung DD250042A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB858525447A GB8525447D0 (en)	1985-10-16	1985-10-16	Pesticidal compositions

Publications (1)

Publication Number	Publication Date
DD250042A5 true DD250042A5 (de)	1987-09-30

Family

ID=10586716

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD86295261A DD250042A5 (de)	1985-10-16	1986-10-14	Fluessige pestizide zusammensetzung

Country Status (30)

Country	Link
US (1)	US4710512A (cs)
EP (1)	EP0226285B1 (cs)
JP (1)	JPH0751483B2 (cs)
KR (1)	KR950009174B1 (cs)
CN (1)	CN1017957B (cs)
AT (1)	ATE59528T1 (cs)
AU (1)	AU570596B2 (cs)
BR (1)	BR8605037A (cs)
CA (1)	CA1266229A (cs)
CS (1)	CS258491B2 (cs)
DD (1)	DD250042A5 (cs)
DE (1)	DE3676466D1 (cs)
DK (1)	DK165434C (cs)
EG (1)	EG18048A (cs)
FI (1)	FI83470C (cs)
GB (1)	GB8525447D0 (cs)
GR (1)	GR3001672T3 (cs)
HU (1)	HU203830B (cs)
IE (1)	IE58898B1 (cs)
IL (1)	IL80306A (cs)
MW (1)	MW7086A1 (cs)
NZ (1)	NZ217919A (cs)
OA (1)	OA08428A (cs)
PH (1)	PH21782A (cs)
PT (1)	PT83545B (cs)
RU (1)	RU1812944C (cs)
TR (1)	TR22547A (cs)
ZA (1)	ZA867811B (cs)
ZM (1)	ZM9586A1 (cs)
ZW (1)	ZW20786A1 (cs)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US7906128B2 (en) *	2002-10-21	2011-03-15	Wyeth Llc	Use of neuronal sodium channel antagonists for the control of ectoparasites in homeothermic animals
TWI350728B (en) *	2004-10-08	2011-10-21	Wyeth Corp	Amitraz compositions
TWI368505B (en) *	2005-05-24	2012-07-21	Wyeth Corp	Versatile high load concentrate compositions for control of ecto-parasites
US20080112993A1 (en) *	2005-05-24	2008-05-15	Wyeth	High-dose, long-lasting ectoparasiticide for extended control
TW200846029A (en) *	2007-02-09	2008-12-01	Wyeth Corp	High dose, long-acting ectoparasiticide for extended control

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB1488906A (en) *	1974-11-09	1977-10-19	Boots Co Ltd	Pesticidal compositions
ZA804985B (en) *	1979-09-20	1981-08-26	Boots Co Ltd	Pesticidal compositions
GB2058570B (en) *	1979-09-20	1983-02-23	Boots Co Ltd	Pesticidal compositions
US4479968A (en) *	1980-10-17	1984-10-30	The Wellcome Foundation Ltd.	Control of ectoparasitic infestations of pigs

1985
- 1985-10-16 GB GB858525447A patent/GB8525447D0/en active Pending
1986
- 1986-10-02 EP EP86307591A patent/EP0226285B1/en not_active Expired - Lifetime
- 1986-10-02 AT AT86307591T patent/ATE59528T1/de not_active IP Right Cessation
- 1986-10-02 DE DE8686307591T patent/DE3676466D1/de not_active Expired - Lifetime
- 1986-10-10 MW MW70/86A patent/MW7086A1/xx unknown
- 1986-10-13 ZM ZM95/86A patent/ZM9586A1/xx unknown
- 1986-10-13 FI FI864116A patent/FI83470C/fi not_active IP Right Cessation
- 1986-10-13 OA OA58976A patent/OA08428A/xx unknown
- 1986-10-13 ZW ZW207/86A patent/ZW20786A1/xx unknown
- 1986-10-13 EG EG644/86A patent/EG18048A/xx active
- 1986-10-14 DD DD86295261A patent/DD250042A5/de not_active IP Right Cessation
- 1986-10-14 DK DK490686A patent/DK165434C/da not_active IP Right Cessation
- 1986-10-14 CA CA000520358A patent/CA1266229A/en not_active Expired - Lifetime
- 1986-10-14 NZ NZ217919A patent/NZ217919A/xx unknown
- 1986-10-14 US US06/918,342 patent/US4710512A/en not_active Expired - Lifetime
- 1986-10-14 CS CS867418A patent/CS258491B2/cs not_active IP Right Cessation
- 1986-10-15 AU AU64125/86A patent/AU570596B2/en not_active Expired
- 1986-10-15 RU SU864028366A patent/RU1812944C/ru active
- 1986-10-15 ZA ZA867811A patent/ZA867811B/xx unknown
- 1986-10-15 IE IE272386A patent/IE58898B1/en not_active IP Right Cessation
- 1986-10-15 JP JP61243306A patent/JPH0751483B2/ja not_active Expired - Fee Related
- 1986-10-15 BR BR8605037A patent/BR8605037A/pt not_active IP Right Cessation
- 1986-10-15 HU HU864298A patent/HU203830B/hu unknown
- 1986-10-15 PH PH34372A patent/PH21782A/en unknown
- 1986-10-15 PT PT83545A patent/PT83545B/pt not_active IP Right Cessation
- 1986-10-15 IL IL80306A patent/IL80306A/xx not_active IP Right Cessation
- 1986-10-16 CN CN86106596A patent/CN1017957B/zh not_active Expired
- 1986-10-16 KR KR1019860008667A patent/KR950009174B1/ko not_active Expired - Lifetime
- 1986-10-16 TR TR38953/86A patent/TR22547A/xx unknown
1991
- 1991-03-27 GR GR91400385T patent/GR3001672T3/el unknown

Also Published As

Publication number	Publication date
PT83545A (en)	1986-11-01
DE3676466D1 (de)	1991-02-07
FI83470B (fi)	1991-04-15
GR3001672T3 (en)	1992-11-23
NZ217919A (en)	1989-03-29
EP0226285A1 (en)	1987-06-24
IL80306A (en)	1990-07-26
FI83470C (fi)	1991-07-25
FI864116L (fi)	1987-04-17
BR8605037A (pt)	1987-07-14
AU6412586A (en)	1987-05-21
ATE59528T1 (de)	1991-01-15
MW7086A1 (en)	1988-08-10
DK490686D0 (da)	1986-10-14
FI864116A0 (fi)	1986-10-13
CA1266229A (en)	1990-02-27
ZM9586A1 (en)	1991-09-27
DK165434B (da)	1992-11-30
JPH0751483B2 (ja)	1995-06-05
RU1812944C (ru)	1993-04-30
IE58898B1 (en)	1993-12-01
OA08428A (en)	1988-06-30
JPS6293202A (ja)	1987-04-28
ZA867811B (en)	1987-08-26
US4710512A (en)	1987-12-01
CN1017957B (zh)	1992-08-26
ZW20786A1 (en)	1987-05-13
EP0226285B1 (en)	1991-01-02
CN86106596A (zh)	1987-04-15
EG18048A (en)	1991-08-30
PT83545B (pt)	1989-05-31
CS741886A2 (en)	1988-01-15
HU203830B (en)	1991-10-28
IE862723L (en)	1987-04-16
HUT41595A (en)	1987-05-28
KR950009174B1 (ko)	1995-08-16
AU570596B2 (en)	1988-03-17
TR22547A (tr)	1987-10-21
DK490686A (da)	1987-04-17
DK165434C (da)	1993-04-13
PH21782A (en)	1988-02-24
KR870003689A (ko)	1987-05-04
CS258491B2 (en)	1988-08-16
GB8525447D0 (en)	1985-11-20

Legal Events

Date	Code	Title	Description
2001-06-21	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
EP0257286B1 (de)	1992-07-08	Konzentrierte wässrige Mikroemulsionen
DE69605598T2 (de)	2000-07-27	Stabile Mikroemulsionen von bestimmten 3-Isothiazolonverbindungen
DE4116516A1 (de)	1991-11-28	Herbizide loesungen auf der basis von n-phosphonomethylglycin
EP0190995B1 (de)	1993-07-28	Fliessfähiges herbizides Mittel
DD250042A5 (de)	1987-09-30	Fluessige pestizide zusammensetzung
EP0074329B1 (de)	1988-09-28	Wässrige Pestizidkonzentrate
DE3486285T2 (de)	1994-08-04	Stabilisierte, flüssige, herbizide Zusammensetzung und Verfahren zu deren Herstellung.
EP0044955A1 (de)	1982-02-03	Flüssige Herbizidmischung
DE1618985A1 (de)	1971-06-09	Benzylidenmalonsaeuredenitrilverbindungen und Verfahren zu ihrer Herstellung
DE2526455A1 (de)	1976-01-22	Herbizid
DE2909158A1 (de)	1980-09-11	Herbizide mischungen
DD281952A5 (de)	1990-08-29	Stabilisierte pestizide zusammensetzung
DE4220161C2 (de)	1996-01-11	Neue Formulierungen von Wirkstoffen zum Pflanzenschutz und deren Anwendung
DE2053356A1 (de)	1972-05-04	Zwei Komponenten Emulgatorsystem fur die Formulierung von Pflanzenschutzmitteln
DE1806119C (de)	1971-09-30	Herbizide Mittel
DE1251073B (de)	1967-09-28	Nematocides Mittel
DE2308102C2 (de)	1987-01-22	Verwendung von herbiziden Zusammensetzungen
AT200389B (de)	1958-10-25	Mittel zur Bekämpfung von Spinnmilben
DD243846A5 (de)	1987-03-18	Makroemulsionen
DE2417056A1 (de)	1974-10-31	In geringem volumen auftragbare pestizidzubereitungen
DE1806119B (de)		Herbizide Mittel
DE1290129B (de)	1969-03-06	3, 5-Di-tert.-butylphenyl-N-methylcarbamat und seine Verwendung als Insektizid
DD215227A1 (de)	1984-11-07	Stabile suspensionskonzentrate fungizider wirkstoffe
DE2311615A1 (de)	1973-09-20	Herbizide zusammensetzungen
DE3512916A1 (de)	1986-10-16	Makroemulsionen