CH505540A - Herbizide Mischung - Google Patents

Herbizide Mischung

Info

Publication number: CH505540A
Authority: CH; Switzerland
Prior art keywords: sep; phenyl; carbamate; carbamoyloxy; cyclohexyl
Prior art date: 1967-09-20

Application number

CH1134068A

Other languages

German (de)

English (en)

Inventor

Friedrich Dr Arndt

Gerhard Dr Boroschewski

Original Assignee

Schering 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.)

1967-09-20

Filing date

1968-07-29

Publication date

1971-04-15

1968-07-29 Application filed by Schering Ag filed Critical Schering Ag

1971-04-15 Publication of CH505540A publication Critical patent/CH505540A/de

Links

239000000203 mixture Substances 0.000 title claims abstract description 32
230000002363 herbicidal effect Effects 0.000 title claims abstract description 15
125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 4
239000004215 Carbon black (E152) Substances 0.000 claims abstract description 3
125000001931 aliphatic group Chemical group 0.000 claims abstract description 3
125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 3
125000000623 heterocyclic group Chemical group 0.000 claims abstract description 3
229930195733 hydrocarbon Natural products 0.000 claims abstract description 3
KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 62
241000196324 Embryophyta Species 0.000 claims description 17
ZTMKADLOSYKWCA-UHFFFAOYSA-N lenacil Chemical compound O=C1NC=2CCCC=2C(=O)N1C1CCCCC1 ZTMKADLOSYKWCA-UHFFFAOYSA-N 0.000 claims description 12
239000004480 active ingredient Substances 0.000 claims description 8
229910052739 hydrogen Inorganic materials 0.000 claims description 6
239000001257 hydrogen Substances 0.000 claims description 6
238000000034 method Methods 0.000 claims description 6
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
125000000217 alkyl group Chemical group 0.000 claims description 5
150000001875 compounds Chemical class 0.000 claims description 5
230000001419 dependent effect Effects 0.000 claims description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 3
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 3
239000007788 liquid Substances 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
239000007787 solid Substances 0.000 claims description 3
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
125000003342 alkenyl group Chemical group 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
125000004414 alkyl thio group Chemical group 0.000 claims description 2
125000003277 amino group Chemical group 0.000 claims description 2
125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims description 2
125000004432 carbon atom Chemical group C* 0.000 claims description 2
125000004093 cyano group Chemical group *C#N 0.000 claims description 2
239000003085 diluting agent Substances 0.000 claims description 2
125000001188 haloalkyl group Chemical group 0.000 claims description 2
229910052736 halogen Inorganic materials 0.000 claims description 2
125000005843 halogen group Chemical group 0.000 claims description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
125000001424 substituent group Chemical group 0.000 claims description 2
125000004429 atom Chemical group 0.000 claims 1
239000000463 material Substances 0.000 claims 1
244000045561 useful plants Species 0.000 claims 1
230000000694 effects Effects 0.000 abstract description 8
125000004430 oxygen atom Chemical group O* 0.000 abstract description 2
150000001338 aliphatic hydrocarbons Chemical group 0.000 abstract 3
125000003118 aryl group Chemical group 0.000 abstract 1
229940054025 carbamate anxiolytics Drugs 0.000 abstract 1
150000002430 hydrocarbons Chemical class 0.000 abstract 1
-1 aralkyl radical Chemical class 0.000 description 34
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 32
239000003795 chemical substances by application Substances 0.000 description 6
241000335053 Beta vulgaris Species 0.000 description 3
JOYRKODLDBILNP-UHFFFAOYSA-N Ethyl urethane Chemical group CCOC(N)=O JOYRKODLDBILNP-UHFFFAOYSA-N 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
239000000969 carrier Substances 0.000 description 3
235000016068 Berberis vulgaris Nutrition 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
239000013543 active substance Substances 0.000 description 2
230000004071 biological effect Effects 0.000 description 2
150000004657 carbamic acid derivatives Chemical class 0.000 description 2
NXNKURIKNWLWKB-UHFFFAOYSA-N carbamoyloxy(phenyl)carbamic acid Chemical class NC(=O)ON(C(O)=O)C1=CC=CC=C1 NXNKURIKNWLWKB-UHFFFAOYSA-N 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
239000004009 herbicide Substances 0.000 description 2
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
FKKAGFLIPSSCHT-UHFFFAOYSA-N 1-dodecoxydodecane;sulfuric acid Chemical compound OS(O)(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC FKKAGFLIPSSCHT-UHFFFAOYSA-N 0.000 description 1
XUJLWPFSUCHPQL-UHFFFAOYSA-N 11-methyldodecan-1-ol Chemical compound CC(C)CCCCCCCCCCO XUJLWPFSUCHPQL-UHFFFAOYSA-N 0.000 description 1
NFAOATPOYUWEHM-UHFFFAOYSA-N 2-(6-methylheptyl)phenol Chemical class CC(C)CCCCCC1=CC=CC=C1O NFAOATPOYUWEHM-UHFFFAOYSA-N 0.000 description 1
241000743985 Alopecurus Species 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
235000013479 Amaranthus retroflexus Nutrition 0.000 description 1
244000237956 Amaranthus retroflexus Species 0.000 description 1
241000208479 Anagallis arvensis Species 0.000 description 1
241000681416 Anchusa arvensis Species 0.000 description 1
235000009066 Atriplex patula Nutrition 0.000 description 1
244000022181 Atriplex patula Species 0.000 description 1
235000007320 Avena fatua Nutrition 0.000 description 1
241000209764 Avena fatua Species 0.000 description 1
235000021537 Beetroot Nutrition 0.000 description 1
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
235000011305 Capsella bursa pastoris Nutrition 0.000 description 1
240000008867 Capsella bursa-pastoris Species 0.000 description 1
235000005940 Centaurea cyanus Nutrition 0.000 description 1
240000004385 Centaurea cyanus Species 0.000 description 1
240000006122 Chenopodium album Species 0.000 description 1
235000009344 Chenopodium album Nutrition 0.000 description 1
235000008733 Citrus aurantifolia Nutrition 0.000 description 1
FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical class OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
241000309579 Erysimum cheiranthoides Species 0.000 description 1
241001539473 Euphoria Species 0.000 description 1
206010015535 Euphoric mood Diseases 0.000 description 1
241001289540 Fallopia convolvulus Species 0.000 description 1
240000009088 Fragaria x ananassa Species 0.000 description 1
244000044980 Fumaria officinalis Species 0.000 description 1
235000006961 Fumaria officinalis Nutrition 0.000 description 1
241001508646 Galeopsis tetrahit Species 0.000 description 1
235000018914 Galinsoga parviflora Nutrition 0.000 description 1
244000214240 Galinsoga parviflora Species 0.000 description 1
241000288105 Grus Species 0.000 description 1
235000009198 Lamium amplexicaule Nutrition 0.000 description 1
244000303225 Lamium amplexicaule Species 0.000 description 1
235000009193 Lamium purpureum Nutrition 0.000 description 1
240000006503 Lamium purpureum Species 0.000 description 1
244000042664 Matricaria chamomilla Species 0.000 description 1
235000007232 Matricaria chamomilla Nutrition 0.000 description 1
IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000209117 Panicum Species 0.000 description 1
235000006443 Panicum miliaceum subsp. miliaceum Nutrition 0.000 description 1
235000009037 Panicum miliaceum subsp. ruderale Nutrition 0.000 description 1
235000007846 Papaver rhoeas Nutrition 0.000 description 1
240000004674 Papaver rhoeas Species 0.000 description 1
240000006928 Persicaria lapathifolia Species 0.000 description 1
244000037751 Persicaria maculosa Species 0.000 description 1
244000292693 Poa annua Species 0.000 description 1
241000209504 Poaceae Species 0.000 description 1
235000006386 Polygonum aviculare Nutrition 0.000 description 1
244000292697 Polygonum aviculare Species 0.000 description 1
235000004442 Polygonum persicaria Nutrition 0.000 description 1
241000218206 Ranunculus Species 0.000 description 1
241000220259 Raphanus Species 0.000 description 1
240000003461 Setaria viridis Species 0.000 description 1
235000002248 Setaria viridis Nutrition 0.000 description 1
241000488874 Sonchus Species 0.000 description 1
244000113423 Sonchus asper Species 0.000 description 1
235000006744 Sonchus asper Nutrition 0.000 description 1
240000003728 Spergula arvensis Species 0.000 description 1
235000009337 Spinacia oleracea Nutrition 0.000 description 1
244000300264 Spinacia oleracea Species 0.000 description 1
240000006694 Stellaria media Species 0.000 description 1
235000021536 Sugar beet Nutrition 0.000 description 1
235000008214 Thlaspi arvense Nutrition 0.000 description 1
240000008488 Thlaspi arvense Species 0.000 description 1
235000011941 Tilia x europaea Nutrition 0.000 description 1
235000009108 Urtica dioica Nutrition 0.000 description 1
240000001261 Urtica urens Species 0.000 description 1
241000990144 Veronica persica Species 0.000 description 1
240000002895 Vicia hirsuta Species 0.000 description 1
231100000136 action limit Toxicity 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
150000008051 alkyl sulfates Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
244000038559 crop plants Species 0.000 description 1
HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
239000008187 granular material Substances 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 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
239000004571 lime Substances 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
238000003801 milling Methods 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
239000000126 substance Substances 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000008096 xylene 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
- 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
- A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48

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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CH1134068A 1967-09-20 1968-07-29 Herbizide Mischung CH505540A (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE1642346		1967-09-20

Publications (1)

Publication Number	Publication Date
CH505540A true CH505540A (de)	1971-04-15

Family

ID=5684180

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH1134068A CH505540A (de)	1967-09-20	1968-07-29	Herbizide Mischung

Country Status (5)

Country	Link
CH (1)	CH505540A (cs)
CS (1)	CS157645B2 (cs)
ES (1)	ES357597A1 (cs)
IE (1)	IE32330B1 (cs)
PL (1)	PL72582B1 (cs)

1968
- 1968-07-29 CH CH1134068A patent/CH505540A/de not_active IP Right Cessation
- 1968-08-23 CS CS606068A patent/CS157645B2/cs unknown
- 1968-08-27 ES ES357597A patent/ES357597A1/es not_active Expired
- 1968-09-11 IE IE1098/68A patent/IE32330B1/xx unknown
- 1968-09-19 PL PL1968129135A patent/PL72582B1/pl unknown

Also Published As

Publication number	Publication date
IE32330L (en)	1969-03-20
ES357597A1 (es)	1970-03-16
CS157645B2 (cs)	1974-09-16
IE32330B1 (en)	1973-06-27
PL72582B1 (cs)	1974-08-30

Legal Events

Date	Code	Title	Description
1988-09-30	PL	Patent ceased

Publication	Publication Date	Title
EP1104232B2 (de)	2010-03-17	Herbizide mittel
DE1905599A1 (de)	1970-08-13	Verwendung von Harnstoffen als selektive Herbizide
DE1567164C2 (de)	1985-03-07	Herbizide Mittel auf Basis von N-Carbamoyloxyphenyl-Carbamaten
DE1284151B (de)	1968-11-28	Selektive herbicide Mittel
DE2341079C2 (de)	1982-05-06	m-Diurethane und selektive herbizide Mittel enthaltend diese Verbindungen als Wirkstoffe
DE2108975B2 (de)	1979-04-19	N-Acyl-Diurethane sowie diese enthaltendes herbizides Mittel
DE1642346C3 (de)	1978-04-27	Herbizide Mittel
DE1542711C3 (de)	1973-11-29	N Phenyl N5 oxyalkyl NP alkylharnstof fe, ihre Verwendung als Herbizide und diese enthaltende herbizide Mittel
CH505540A (de)	1971-04-15	Herbizide Mischung
DE2121957C3 (de)	1979-11-29	Diurethane sowie diese enthaltende herbizide Mittel
DE2020729C2 (de)	1983-04-21	Herbizide Mittel auf Basis von N-(3-(N'-Aryl-carbamoyloxy)-phenyl)-carbamaten
DD250253A5 (de)	1987-10-08	Herbizide mittel und seine verwendung
DE2528302A1 (de)	1977-01-13	Mittel zur selektiven unkrautbekaempfung in rueben und sojabohnen
DE2210540A1 (de)	1973-09-06	Cyanphenylcarbonate
DE2310649C3 (de)	1982-05-06	Diurethane sowie diese enthaltende selektive herbizide Mittel
DE2527394A1 (de)	1976-12-30	Mittel zur selektiven unkrautbekaempfung in getreide
DE1793755C3 (de)	1977-09-29	Diurethane sowie diese enthaltende herbizide Mittel
DE1567165C3 (de)	1978-08-17	Algizide Mittel auf Carbamat-Basis
DE2121958C3 (de)	1981-05-27	Herbizide Mittel auf Basis von Carbamoyloxyphenylcarbamat-Gemischen
DE1809838C3 (de)	1978-01-05	N-(3-Brom-4-chlorphenyl)-N'methoxy-N'-methylharnstoff und seine Verwendung als Herbizid
DE2404659C2 (de)	1983-02-17	Selektiv herbizides Wirkstoffgemisch für die Nachlaufbehandlung von Getreide-Kulturen
DE1913850A1 (de)	1970-10-01	Herbizid
AT275961B (de)	1969-11-10	Herbizide Mittel mit verstärkter Wirksamkeit
EP0052825A1 (de)	1982-06-02	Selektiv-herbizide Mittel auf Triazindion-Basis
DE2217698A1 (de)	1973-10-18	Herbizid