CA1098726A - Herbicide selectif - Google Patents

Herbicide selectif

Info

Publication number: CA1098726A
Authority: CA; Canada
Prior art keywords: component; weeds; composition; herbicidal; chlorophenyl
Prior art date: 1975-12-04
Legal status (The legal status 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 status listed.): Expired

Application number

CA267,089A

Other languages

English (en)

Inventor

Hanskarl Kirfel

Helmut Hack

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bayer AG

Original Assignee

Bayer 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.)

1975-12-04

Filing date

1976-12-03

Publication date

1981-04-07

1975-12-04 Priority claimed from DE19752554532 external-priority patent/DE2554532A1/de

1976-10-21 Priority claimed from DE19762647484 external-priority patent/DE2647484A1/de

1976-12-03 Application filed by Bayer AG filed Critical Bayer AG

1981-04-07 Application granted granted Critical

1981-04-07 Publication of CA1098726A publication Critical patent/CA1098726A/fr

Status Expired legal-status Critical Current

Links

239000004009 herbicide Substances 0.000 title abstract description 6
239000000203 mixture Substances 0.000 claims abstract description 37
230000002363 herbicidal effect Effects 0.000 claims abstract description 23
239000004094 surface-active agent Substances 0.000 claims abstract description 23
239000002480 mineral oil Substances 0.000 claims abstract description 17
235000010446 mineral oil Nutrition 0.000 claims abstract description 14
YJKIALIXRCSISK-UHFFFAOYSA-N Chlorfenprop-methyl Chemical compound COC(=O)C(Cl)CC1=CC=C(Cl)C=C1 YJKIALIXRCSISK-UHFFFAOYSA-N 0.000 claims abstract description 11
239000003921 oil Substances 0.000 claims abstract description 8
239000003085 diluting agent Substances 0.000 claims abstract description 6
150000001875 compounds Chemical class 0.000 claims description 32
241000196324 Embryophyta Species 0.000 claims description 18
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 16
235000007320 Avena fatua Nutrition 0.000 claims description 15
241000209764 Avena fatua Species 0.000 claims description 14
238000000034 method Methods 0.000 claims description 10
239000004480 active ingredient Substances 0.000 claims description 7
235000013339 cereals Nutrition 0.000 claims description 7
229920000151 polyglycol Polymers 0.000 claims description 7
239000010695 polyglycol Substances 0.000 claims description 7
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 5
238000009835 boiling Methods 0.000 claims description 4
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 claims description 3
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 3
239000000306 component Substances 0.000 claims 20
-1 sorbitol fatty acid esters Chemical class 0.000 abstract description 8
239000007788 liquid Substances 0.000 abstract description 5
150000002170 ethers Chemical class 0.000 abstract description 3
239000000194 fatty acid Substances 0.000 abstract description 3
239000007787 solid Substances 0.000 abstract description 3
125000000217 alkyl group Chemical group 0.000 abstract description 2
FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 abstract 2
229920003171 Poly (ethylene oxide) Polymers 0.000 abstract 2
235000014113 dietary fatty acids Nutrition 0.000 abstract 2
229930195729 fatty acid Natural products 0.000 abstract 2
239000000600 sorbitol Substances 0.000 abstract 2
125000003710 aryl alkyl group Chemical group 0.000 abstract 1
229920001296 polysiloxane Polymers 0.000 abstract 1
230000002195 synergetic effect Effects 0.000 abstract 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
238000009472 formulation Methods 0.000 description 9
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 8
239000003995 emulsifying agent Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
239000007921 spray Substances 0.000 description 6
230000006378 damage Effects 0.000 description 5
125000002877 alkyl aryl group Chemical group 0.000 description 4
239000000969 carrier Substances 0.000 description 4
239000000243 solution Substances 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
229940000425 combination drug Drugs 0.000 description 3
230000000694 effects Effects 0.000 description 3
241000209761 Avena Species 0.000 description 2
235000005781 Avena Nutrition 0.000 description 2
244000075850 Avena orientalis Species 0.000 description 2
SLCGUGMPSUYJAY-UHFFFAOYSA-N Benzoylprop-ethyl Chemical compound C=1C=C(Cl)C(Cl)=CC=1N(C(C)C(=O)OCC)C(=O)C1=CC=CC=C1 SLCGUGMPSUYJAY-UHFFFAOYSA-N 0.000 description 2
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 2
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 2
239000005977 Ethylene Substances 0.000 description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
239000004606 Fillers/Extenders Substances 0.000 description 2
235000005373 Uvularia sessilifolia Nutrition 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
239000011575 calcium Substances 0.000 description 2
229910052791 calcium Inorganic materials 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
244000038559 crop plants Species 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
230000001804 emulsifying effect Effects 0.000 description 2
238000003306 harvesting Methods 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
239000011707 mineral Substances 0.000 description 2
238000002360 preparation method Methods 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
239000002689 soil Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
239000000725 suspension Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
DXBQEHHOGRVYFF-UHFFFAOYSA-N 3-pyridin-4-ylpentane-2,4-dione Chemical group CC(=O)C(C(C)=O)C1=CC=NC=C1 DXBQEHHOGRVYFF-UHFFFAOYSA-N 0.000 description 1
102000009027 Albumins Human genes 0.000 description 1
108010088751 Albumins Proteins 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
235000004535 Avena sterilis Nutrition 0.000 description 1
240000005979 Hordeum vulgare Species 0.000 description 1
235000007340 Hordeum vulgare Nutrition 0.000 description 1
239000005909 Kieselgur Substances 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
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000209140 Triticum Species 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical class ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
239000013543 active substance Substances 0.000 description 1
238000007792 addition Methods 0.000 description 1
230000002730 additional effect Effects 0.000 description 1
239000000654 additive Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
125000005228 aryl sulfonate group Chemical group 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
HCWYXKWQOMTBKY-UHFFFAOYSA-N calcium;dodecyl benzenesulfonate Chemical compound [Ca].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 HCWYXKWQOMTBKY-UHFFFAOYSA-N 0.000 description 1
150000008422 chlorobenzenes Chemical class 0.000 description 1
GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000006260 foam Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 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
150000002576 ketones Chemical class 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
229940043265 methyl isobutyl ketone Drugs 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
229910052901 montmorillonite Inorganic materials 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000010690 paraffinic oil Substances 0.000 description 1
239000006072 paste Substances 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000003223 protective agent Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000002699 waste material Substances 0.000 description 1
150000003738 xylenes Chemical class 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)

CA267,089A 1975-12-04 1976-12-03 Herbicide selectif Expired CA1098726A (fr)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
DE19752554532 DE2554532A1 (de)	1975-12-04	1975-12-04	Selektive herbizide mittel
DEP2554532.8		1976-05-11
DEP2647484.0		1976-10-21
DE19762647484 DE2647484A1 (de)	1976-10-21	1976-10-21	Selektive herbizide mittel

Publications (1)

Publication Number	Publication Date
CA1098726A true CA1098726A (fr)	1981-04-07

Family

ID=25769697

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA267,089A Expired CA1098726A (fr)	1975-12-04	1976-12-03	Herbicide selectif

Country Status (11)

Country	Link
AT (1)	AT354799B (fr)
AU (1)	AU2024376A (fr)
CA (1)	CA1098726A (fr)
DD (1)	DD128790A5 (fr)
DK (1)	DK545776A (fr)
ES (1)	ES453906A1 (fr)
FI (1)	FI763472A7 (fr)
FR (1)	FR2333442A1 (fr)
GB (1)	GB1521007A (fr)
NL (1)	NL7613453A (fr)
PT (1)	PT65912B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5658851A (en) *	1993-10-13	1997-08-19	Osi Specialties, Inc.	Lipophilic siloxanes as adjuvants for agriculture
US5561099A (en) *	1993-10-13	1996-10-01	Osi Specialties, Inc.	Alkylsiloxanes as adjuvants for agriculture

1976
- 1976-11-30 PT PT6591276A patent/PT65912B/pt unknown
- 1976-12-02 NL NL7613453A patent/NL7613453A/xx not_active Application Discontinuation
- 1976-12-02 DD DD19608876A patent/DD128790A5/xx unknown
- 1976-12-02 GB GB50299/76A patent/GB1521007A/en not_active Expired
- 1976-12-02 FI FI763472A patent/FI763472A7/fi not_active Application Discontinuation
- 1976-12-02 AT AT893476A patent/AT354799B/de not_active IP Right Cessation
- 1976-12-03 CA CA267,089A patent/CA1098726A/fr not_active Expired
- 1976-12-03 FR FR7636542A patent/FR2333442A1/fr active Pending
- 1976-12-03 DK DK545776A patent/DK545776A/da unknown
- 1976-12-03 AU AU20243/76A patent/AU2024376A/en not_active Expired
- 1976-12-03 ES ES453906A patent/ES453906A1/es not_active Expired

Also Published As

Publication number	Publication date
FI763472A7 (fr)	1977-06-05
ES453906A1 (es)	1978-03-01
AT354799B (de)	1979-01-25
DD128790A5 (de)	1977-12-07
FR2333442A1 (fr)	1977-07-01
DK545776A (da)	1977-06-05
GB1521007A (en)	1978-08-09
AU2024376A (en)	1978-06-08
NL7613453A (nl)	1977-06-07
ATA893476A (de)	1979-06-15
PT65912B (en)	1978-05-23
PT65912A (en)	1976-12-01

Legal Events

Date	Code	Title	Description
1998-04-07	MKEX	Expiry

Publication	Publication Date	Title
HU180094B (en)	1983-01-28	Synergetic composition for controlling growth of plants first of all for defoliation
EP0274634A1 (fr)	1988-07-20	Compositions herbicides synergiques et procédé d'application
US4047928A (en)	1977-09-13	Wild oat herbicide mixture
EP0236273A2 (fr)	1987-09-09	Compositions synergétiques et procédés d'éradication sélective des mauvaises herbes dans les céréales
KR900004697B1 (ko)	1990-07-02	2-(3-피리딜)-1,3,4-옥사디아졸류의 제조방법
CH686210A5 (de)	1996-02-15	Herbizide Zusammensetzung mit einer verminderten Phytotoxizitot.
HU184676B (en)	1984-09-28	Pesticide preparation containing organic phosphorus compound and pyretroide derivative
SE430845B (sv)	1983-12-19	Akaricidisk komposition innefattande s-metyl-n-(metylkarbamoyloxi)tioacetamidat och en pyretroid insekticid
EP0008474B1 (fr)	1985-10-02	Compositions pesticides contenant un sulfure d'acide carbamique et un insecticide pyréthroide synthétique et leur utilisation
JP4069218B2 (ja)	2008-04-02	殺虫・殺ダニ剤
HU176584B (en)	1981-03-28	Herbicide preparation containing of active mateirals of two types
DE3101889A1 (de)	1982-08-26	"neue phenoxycarbonsaeureamide, verfahren zu ihrer herstellung und ihre verwendung als herbizide"
CS241143B2 (en)	1986-03-13	Fungicide
JPS5857404B2 (ja)	1983-12-20	除草剤組成物
WO1998047356A2 (fr)	1998-10-29	Herbicide
CA1081493A (fr)	1980-07-15	Agents utilises pour la repression selective des mauvaises herbes dans les cereales
US4308262A (en)	1981-12-29	Pyrethroid pesticidal compositions
US3505455A (en)	1970-04-07	Nematocidal method
US4906275A (en)	1990-03-06	Composition for defoliation of plants II
US3504091A (en)	1970-03-31	Method of combatting fungi with n,n dialkyl substituted dithiocyanoanilines
EP0009091B1 (fr)	1981-11-18	Procédé de lutte sélective contre la croissance de plantes indésirables au moyen d'herbicides à base d'acétanilides et de N-dichloroacétyl-2,2-diméthyl-1,3-oxazolidine
DE2724786A1 (de)	1978-12-14	Cyclopropansaeureanilide, fungizide mittel enthaltend diese verbindungen sowie verfahren zu ihrer herstellung
EP0147683B1 (fr)	1989-08-30	Procédé de lutte contre Galium Aparine
CA1094842A (fr)	1981-02-03	Herbicide contre la folle avoine
EP0149268A2 (fr)	1985-07-24	Procédé de lutte contre la croissance des plantes