NO781517L - Herbicid preparat. - Google Patents

Herbicid preparat.

Info

Publication number: NO781517L
Authority: NO; Norway
Prior art keywords: group; stated; compound; formula; ethylamino
Prior art date: 1977-05-03

Application number

NO781517A

Other languages

English (en)

Norwegian (no)

Inventor

Clive Alan Raven

Alan John Sampson

Original Assignee

Shell Int Research

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.)

1977-05-03

Filing date

1978-04-28

Publication date

1978-11-06

1978-04-28 Application filed by Shell Int Research filed Critical Shell Int Research

1978-11-06 Publication of NO781517L publication Critical patent/NO781517L/no

Links

238000002360 preparation method Methods 0.000 title claims description 37
230000002363 herbicidal effect Effects 0.000 claims description 25
-1 polymethylene group Polymers 0.000 claims description 19
150000001294 alanine derivatives Chemical class 0.000 claims description 16
150000001875 compounds Chemical class 0.000 claims description 15
125000004432 carbon atom Chemical group C* 0.000 claims description 13
239000002253 acid Substances 0.000 claims description 12
MZZBPDKVEFVLFF-UHFFFAOYSA-N cyanazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C#N)=N1 MZZBPDKVEFVLFF-UHFFFAOYSA-N 0.000 claims description 11
125000000217 alkyl group Chemical group 0.000 claims description 10
229910052801 chlorine Inorganic materials 0.000 claims description 10
125000003118 aryl group Chemical group 0.000 claims description 9
229910052731 fluorine Inorganic materials 0.000 claims description 9
125000001153 fluoro group Chemical group F* 0.000 claims description 9
239000004480 active ingredient Substances 0.000 claims description 8
125000003342 alkenyl group Chemical group 0.000 claims description 8
125000000547 substituted alkyl group Chemical group 0.000 claims description 8
125000002877 alkyl aryl group Chemical group 0.000 claims description 7
125000001309 chloro group Chemical group Cl* 0.000 claims description 7
125000000753 cycloalkyl group Chemical group 0.000 claims description 7
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
239000004094 surface-active agent Substances 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 claims description 4
OFADGFSRMKSMPB-UHFFFAOYSA-N 2-[[4-(ethylamino)-6-methylsulfanyl-1,3,5-triazin-2-yl]amino]-2-methylpropanenitrile Chemical compound CCNC1=NC(NC(C)(C)C#N)=NC(SC)=N1 OFADGFSRMKSMPB-UHFFFAOYSA-N 0.000 claims description 4
125000003545 alkoxy group Chemical group 0.000 claims description 4
239000000460 chlorine Substances 0.000 claims description 4
125000000623 heterocyclic group Chemical group 0.000 claims description 4
229910052760 oxygen Inorganic materials 0.000 claims description 4
239000001301 oxygen Substances 0.000 claims description 4
125000004414 alkyl thio group Chemical group 0.000 claims description 3
125000005842 heteroatom Chemical group 0.000 claims description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 3
125000004434 sulfur atom Chemical group 0.000 claims description 3
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical class [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical compound ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims description 2
MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 2
125000003277 amino group Chemical group 0.000 claims description 2
125000003710 aryl alkyl group Chemical group 0.000 claims description 2
239000002184 metal Substances 0.000 claims description 2
229910052717 sulfur Inorganic materials 0.000 claims description 2
125000004430 oxygen atom Chemical group O* 0.000 claims 2
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims 2
125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
235000007319 Avena orientalis Nutrition 0.000 description 30
239000000203 mixture Substances 0.000 description 26
241000196324 Embryophyta Species 0.000 description 17
241000209761 Avena Species 0.000 description 15
244000075850 Avena orientalis Species 0.000 description 15
241000209219 Hordeum Species 0.000 description 12
230000000694 effects Effects 0.000 description 12
235000007340 Hordeum vulgare Nutrition 0.000 description 10
235000013339 cereals Nutrition 0.000 description 9
239000004009 herbicide Substances 0.000 description 9
230000012010 growth Effects 0.000 description 7
WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 5
230000002195 synergetic effect Effects 0.000 description 5
244000036975 Ambrosia artemisiifolia Species 0.000 description 4
235000003129 Ambrosia artemisiifolia var elatior Nutrition 0.000 description 4
235000003484 annual ragweed Nutrition 0.000 description 4
235000006263 bur ragweed Nutrition 0.000 description 4
235000003488 common ragweed Nutrition 0.000 description 4
238000002474 experimental method Methods 0.000 description 4
235000009736 ragweed Nutrition 0.000 description 4
230000000996 additive effect Effects 0.000 description 3
235000004279 alanine Nutrition 0.000 description 3
238000010586 diagram Methods 0.000 description 3
239000000428 dust Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
238000005259 measurement Methods 0.000 description 3
238000005507 spraying Methods 0.000 description 3
YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
235000007320 Avena fatua Nutrition 0.000 description 2
241000209764 Avena fatua Species 0.000 description 2
241000209082 Lolium Species 0.000 description 2
241000209140 Triticum Species 0.000 description 2
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
235000013305 food Nutrition 0.000 description 2
230000009036 growth inhibition Effects 0.000 description 2
230000008635 plant growth Effects 0.000 description 2
239000004071 soot Substances 0.000 description 2
238000003892 spreading Methods 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
VCZPLKWFZCIVCR-YFKPBYRVSA-N (2s)-2-(3-chloro-4-fluoroanilino)propanoic acid Chemical class OC(=O)[C@H](C)NC1=CC=C(F)C(Cl)=C1 VCZPLKWFZCIVCR-YFKPBYRVSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
235000021307 Triticum Nutrition 0.000 description 1
239000013543 active substance Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
KTYVHLCLTPLSGC-UHFFFAOYSA-N amino propanoate Chemical compound CCC(=O)ON KTYVHLCLTPLSGC-UHFFFAOYSA-N 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000002361 compost Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000011161 development Methods 0.000 description 1
230000018109 developmental process Effects 0.000 description 1
238000007865 diluting Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000006185 dispersion Substances 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
230000035784 germination Effects 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
238000011835 investigation Methods 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000011344 liquid material Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
238000000034 method Methods 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
125000004433 nitrogen atom Chemical group N* 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
LVZPYQMBOPESIL-UHFFFAOYSA-N propan-2-yl 2-(3-chloro-4-fluoroanilino)propanoate Chemical compound CC(C)OC(=O)C(C)NC1=CC=C(F)C(Cl)=C1 LVZPYQMBOPESIL-UHFFFAOYSA-N 0.000 description 1
IKVXBIIHQGXQRQ-UHFFFAOYSA-N propan-2-yl 2-(n-benzoyl-3-chloro-4-fluoroanilino)propanoate Chemical compound C=1C=C(F)C(Cl)=CC=1N(C(C)C(=O)OC(C)C)C(=O)C1=CC=CC=C1 IKVXBIIHQGXQRQ-UHFFFAOYSA-N 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000011343 solid material Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
241000894007 species Species 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
238000001308 synthesis method Methods 0.000 description 1
150000003918 triazines Chemical class 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000000080 wetting agent 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
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
- A01N43/70—Diamino—1,3,5—triazines with only one oxygen, sulfur or halogen atom or only one cyano, thiocyano (—SCN), cyanato (—OCN) or azido (—N3) group directly attached to a ring carbon atom

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)
Medicines Containing Plant Substances (AREA)

NO781517A 1977-05-03 1978-04-28 Herbicid preparat. NO781517L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
GB18435/77A GB1599293A (en)	1977-05-03	1977-05-03	Herbicide mixture

Publications (1)

Publication Number	Publication Date
NO781517L true NO781517L (no)	1978-11-06

Family

ID=10112401

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO781517A NO781517L (no)	1977-05-03	1978-04-28	Herbicid preparat.

Country Status (20)

Country	Link
US (1)	US4353733A (xx)
AR (1)	AR220532A1 (xx)
AT (1)	AT360268B (xx)
AU (1)	AU525886B2 (xx)
BE (1)	BE866604A (xx)
CA (1)	CA1111275A (xx)
CH (1)	CH637269A5 (xx)
DE (1)	DE2819156A1 (xx)
DK (1)	DK188678A (xx)
FR (1)	FR2389325B1 (xx)
GB (1)	GB1599293A (xx)
GR (1)	GR64989B (xx)
IT (1)	IT1094805B (xx)
NL (1)	NL7804680A (xx)
NO (1)	NO781517L (xx)
NZ (1)	NZ187141A (xx)
PT (1)	PT67973B (xx)
SE (1)	SE7805065L (xx)
TR (1)	TR20176A (xx)
ZA (1)	ZA782495B (xx)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4666509A (en) *	1984-12-19	1987-05-19	Union Carbide Corporation	Herbicide antidotes for cotton crops

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3505325A (en) *	1966-07-16	1970-04-07	Degussa	Cyanoalkylamino substituted triazines having plant growth regulating action
GB1164160A (en) *	1966-12-30	1969-09-17	Shell Int Research	N,N-Disubstituted Amino Acid Derivatives and their use as Herbicides

1977
- 1977-05-03 GB GB18435/77A patent/GB1599293A/en not_active Expired
1978
- 1978-04-18 CA CA301,402A patent/CA1111275A/en not_active Expired
- 1978-04-28 IT IT22869/78A patent/IT1094805B/it active
- 1978-04-28 FR FR7812732A patent/FR2389325B1/fr not_active Expired
- 1978-04-28 NO NO781517A patent/NO781517L/no unknown
- 1978-05-01 NZ NZ187141A patent/NZ187141A/xx unknown
- 1978-05-01 CH CH472278A patent/CH637269A5/de not_active IP Right Cessation
- 1978-05-01 DK DK188678A patent/DK188678A/da not_active Application Discontinuation
- 1978-05-01 AU AU35598/78A patent/AU525886B2/en not_active Expired
- 1978-05-01 ZA ZA00782495A patent/ZA782495B/xx unknown
- 1978-05-02 AT AT315778A patent/AT360268B/de not_active IP Right Cessation
- 1978-05-02 AR AR271995A patent/AR220532A1/es active
- 1978-05-02 NL NL7804680A patent/NL7804680A/xx not_active Application Discontinuation
- 1978-05-02 BE BE187304A patent/BE866604A/xx not_active IP Right Cessation
- 1978-05-02 DE DE19782819156 patent/DE2819156A1/de not_active Withdrawn
- 1978-05-02 SE SE7805065A patent/SE7805065L/xx unknown
- 1978-05-02 TR TR20176A patent/TR20176A/xx unknown
- 1978-05-02 GR GR56117A patent/GR64989B/el unknown
- 1978-05-02 PT PT67973A patent/PT67973B/pt unknown
1979
- 1979-04-10 US US06/028,766 patent/US4353733A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
BE866604A (fr)	1978-11-03
CA1111275A (en)	1981-10-27
PT67973A (en)	1978-06-01
AR220532A1 (es)	1980-11-14
AU3559878A (en)	1979-11-08
TR20176A (tr)	1980-09-29
NL7804680A (nl)	1978-11-07
NZ187141A (en)	1981-03-16
PT67973B (en)	1980-03-05
ZA782495B (en)	1979-04-25
IT7822869A0 (it)	1978-04-28
AT360268B (de)	1980-12-29
AU525886B2 (en)	1982-12-09
FR2389325A1 (xx)	1978-12-01
US4353733A (en)	1982-10-12
SE7805065L (sv)	1978-11-04
ATA315778A (de)	1980-05-15
DK188678A (da)	1978-11-04
IT1094805B (it)	1985-08-10
GR64989B (en)	1980-06-11
FR2389325B1 (xx)	1982-12-31
CH637269A5 (de)	1983-07-29
GB1599293A (en)	1981-09-30
DE2819156A1 (de)	1978-11-16

Publication	Publication Date	Title
RU2569817C2 (ru)	2015-11-27	Способ борьбы с сорными растениями, обладающими устойчивостью к гербицидам на основе феноксиалкановых кислот, с помощью 4-амино-3-хлор-6-(4-хлор-2-фтор-3-метоксифенил)пиридин-2-карбоновой кислоты и ее солей или сложных эфиров
EA019698B1 (ru)	2014-05-30	Способ борьбы с сорняками и гербицидная композиция
EP0274634A1 (en)	1988-07-20	Synergistic herbicide compositions and method of application
JP2023116747A (ja)	2023-08-22	界面活性剤で安定化されたシクロヘキサンジオキシドオキシム製剤
EP0347950B1 (en)	1993-08-04	Synergistic herbicide combinations and method of application
BG63904B1 (bg)	2003-06-30	Фунгициден състав, съдържащ 2-имидазолин-5-он
EP0256785B1 (en)	1990-12-27	Herbicide
CA2374150A1 (en)	2000-12-14	Strobilurin-based fungicide composition causing reduced chemical damage
AU2013354223B2 (en)	2017-04-20	Method of controlling resistant harmful plants
DK157285B (da)	1989-12-04	Fremgangsmaade til haemning af antagonismen mellem et pyridyloxyphenoxyalkanoat-herbicid og benzothiadiazinon-herbicider ved anvendelse efter planternes fremkomst af jorden samt herbicidt sproejtemiddel
NO781517L (no)	1978-11-06	Herbicid preparat.
US2868633A (en)	1959-01-13	Control of grass growth
JPH0725709A (ja)	1995-01-27	除草剤組成物
NO834796L (no)	1984-06-28	Tinn(iv)-n-fosfonometylglycin-forbindelser og herbicider inneholdende slike forbindelser
EP0147683B1 (en)	1989-08-30	A method for the control of galium aparine
NO161835B (no)	1989-06-26	Synergisk herbicid-blanding inneholdende n-fosfonometylglycin og aryloksyfenoksypentansyreestere.
NO772714L (no)	1978-02-03	Herbicide preparater.
NO844278L (no)	1985-04-29	Synergiske herbicide blandinger
SU530628A3 (ru)	1976-09-30	Гербицидное средство
EP0150529A2 (en)	1985-08-07	Synergistic herbicidal compositions
US4154600A (en)	1979-05-15	Thiolcarbamates as plant growth regulators
NO161719B (no)	1989-06-12	Fremgangsmaate og anlegg for fremstilling av en fortynnet slurry inneholdende sinkstoev.
WO2023233400A1 (en)	2023-12-07	Stabilized liquid herbicide formulation of high-load pyrasulfotole
CA1094842A (en)	1981-02-03	Wild oat herbicide
GB2101889A (en)	1983-01-26	Herbicide composition containing a mixture of two active thiocarbamate agents.