CA1207792A - Herbicidal use of trimethylamine and triethylamine salts of 3,5-dibromo-4-hydroxybenzonitrile - Google Patents

Herbicidal use of trimethylamine and triethylamine salts of 3,5-dibromo-4-hydroxybenzonitrile

Info

Publication number: CA1207792A
Authority: CA; Canada
Prior art keywords: bromoxynil; dibromo; triethylamine; salt; hydroxybenzonitrile
Prior art date: 1982-10-05
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

CA000438209A

Other languages

English (en)

French (fr)

Inventor

Leslie V. Hunt

Ponnan Veerasekaran

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.)

May and Baker Ltd

Original Assignee

May and Baker Ltd

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.)

1982-10-05

Filing date

1983-10-03

Publication date

1986-07-15

1983-10-03 Application filed by May and Baker Ltd filed Critical May and Baker Ltd

1986-07-15 Application granted granted Critical

1986-07-15 Publication of CA1207792A publication Critical patent/CA1207792A/en

Status Expired legal-status Critical Current

Links

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GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 title claims abstract description 97
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RDJTWDKSYLLHRW-UHFFFAOYSA-N Dinoseb acetate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(C)=O RDJTWDKSYLLHRW-UHFFFAOYSA-N 0.000 description 1
239000004150 EU approved colour Substances 0.000 description 1
241001193601 Funneliformis xanthium Species 0.000 description 1
241000748465 Galinsoga Species 0.000 description 1
241000125413 Lapsana Species 0.000 description 1
CPLXHLVBOLITMK-UHFFFAOYSA-N Magnesium oxide Chemical compound [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
240000004658 Medicago sativa Species 0.000 description 1
101100305983 Mus musculus Rom1 gene Proteins 0.000 description 1
241000881225 Persicaria Species 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
241001310793 Podium Species 0.000 description 1
241000220261 Sinapis Species 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical class OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
244000098338 Triticum aestivum Species 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
241000209149 Zea Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
239000003463 adsorbent Substances 0.000 description 1
150000003973 alkyl amines Chemical class 0.000 description 1
PZZYQPZGQPZBDN-UHFFFAOYSA-N aluminium silicate Chemical compound O=[Al]O[Si](=O)O[Al]=O PZZYQPZGQPZBDN-UHFFFAOYSA-N 0.000 description 1
229910000323 aluminium silicate Inorganic materials 0.000 description 1
238000013459 approach Methods 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
239000002152 aqueous-organic solution Substances 0.000 description 1
238000009835 boiling Methods 0.000 description 1
HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
229920005551 calcium lignosulfonate Polymers 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
239000006229 carbon black Substances 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
229940125898 compound 5 Drugs 0.000 description 1
238000009833 condensation Methods 0.000 description 1
230000005494 condensation Effects 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
239000007799 cork Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
LAWOZCWGWDVVSG-UHFFFAOYSA-N dioctylamine Chemical compound CCCCCCCCNCCCCCCCC LAWOZCWGWDVVSG-UHFFFAOYSA-N 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
JCYWCSGERIELPG-UHFFFAOYSA-N imes Chemical class CC1=CC(C)=CC(C)=C1N1C=CN(C=2C(=CC(C)=CC=2C)C)[C]1 JCYWCSGERIELPG-UHFFFAOYSA-N 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
238000002955 isolation Methods 0.000 description 1
JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-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
125000001400 nonyl group Chemical group [H]C([*])([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])[H] 0.000 description 1
125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
239000002245 particle Substances 0.000 description 1
239000003415 peat Substances 0.000 description 1
230000000149 penetrating effect Effects 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-M phenolate Chemical compound [O-]C1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-M 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
238000004382 potting Methods 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
238000011160 research Methods 0.000 description 1
IOVGROKTTNBUGK-SJCJKPOMSA-N ritodrine Chemical compound N([C@@H](C)[C@H](O)C=1C=CC(O)=CC=1)CCC1=CC=C(O)C=C1 IOVGROKTTNBUGK-SJCJKPOMSA-N 0.000 description 1
238000005096 rolling process Methods 0.000 description 1
229920005552 sodium lignosulfonate Polymers 0.000 description 1
239000008247 solid mixture Substances 0.000 description 1
239000004550 soluble concentrate Substances 0.000 description 1
238000009331 sowing Methods 0.000 description 1
125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical class OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
239000004546 suspension concentrate Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
230000001052 transient effect Effects 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
229940078499 tricalcium phosphate Drugs 0.000 description 1
229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
235000019731 tricalcium phosphate Nutrition 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
- 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
- A01N37/36—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system

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)

CA000438209A 1982-10-05 1983-10-03 Herbicidal use of trimethylamine and triethylamine salts of 3,5-dibromo-4-hydroxybenzonitrile Expired CA1207792A (en)

Applications Claiming Priority (4)

Application Number	Priority Date	Filing Date	Title
GB8228343		1982-10-05
GB8228343		1982-10-05
GB8232767		1982-11-17
GB8232767		1982-11-17

Publications (1)

Publication Number	Publication Date
CA1207792A true CA1207792A (en)	1986-07-15

Family

ID=26284028

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA000438209A Expired CA1207792A (en)	1982-10-05	1983-10-03	Herbicidal use of trimethylamine and triethylamine salts of 3,5-dibromo-4-hydroxybenzonitrile

Country Status (7)

Country	Link
AU (1)	AU1986083A (it)
BR (1)	BR8305485A (it)
CA (1)	CA1207792A (it)
ES (1)	ES8600223A1 (it)
FR (1)	FR2533804A1 (it)
IT (1)	IT1171712B (it)
RO (1)	RO87551B (it)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US20220112136A1 (en) *	2020-10-14	2022-04-14	Helena Agri-Enterprises, Llc	Agricultural composition containing si clay and a base

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE636416A (it) *	1962-08-30
NL298303A (it) *	1962-09-24

1983
- 1983-10-03 RO RO112251A patent/RO87551B/ro unknown
- 1983-10-03 CA CA000438209A patent/CA1207792A/en not_active Expired
- 1983-10-04 AU AU19860/83A patent/AU1986083A/en not_active Abandoned
- 1983-10-04 IT IT23131/83A patent/IT1171712B/it active
- 1983-10-04 BR BR8305485A patent/BR8305485A/pt unknown
- 1983-10-04 ES ES526214A patent/ES8600223A1/es not_active Expired
- 1983-10-05 FR FR8316052A patent/FR2533804A1/fr active Pending

Also Published As

Publication number	Publication date
ES526214A0 (es)	1985-10-01
AU1986083A (en)	1984-04-12
IT1171712B (it)	1987-06-10
IT8323131A1 (it)	1985-04-04
RO87551A (ro)	1985-08-31
BR8305485A (pt)	1984-05-15
RO87551B (ro)	1985-08-31
FR2533804A1 (fr)	1984-04-06
ES8600223A1 (es)	1985-10-01
IT8323131A0 (it)	1983-10-04

Legal Events

Date	Code	Title	Description
2003-10-03	MKEX	Expiry

Publication	Publication Date	Title
KR890002084B1 (ko)	1989-06-16	N-페닐설포닐-n'-피리미디닐-및-트리아지닐-우레아의 제조방법
DE69718027T2 (de)	2003-10-02	Verfahren zur bekämpfung von unkräutern
CZ323097A3 (cs)	1998-02-18	Herbicidní prostředek a způsob potírání nežádoucího růstu rostlin
CN108024537A (zh)	2018-05-11	作为除草剂的芳氧基嘧啶基醚
US4824475A (en)	1989-04-25	Enhanced herbicidal triazine compositions and method of use
EP0003805A1 (de)	1979-09-05	Pyridazonverbindungen und diese enthaltende herbizide Zusammensetzungen
EP0128530B1 (de)	1988-04-27	Substituierte 4,5-Dimethoxypyridazone, Verfahren zu ihrer Herstellung, diese enthaltende Herbizide und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
CA1207792A (en)	1986-07-15	Herbicidal use of trimethylamine and triethylamine salts of 3,5-dibromo-4-hydroxybenzonitrile
EP0282613B1 (en)	1991-07-03	Herbicidal composition
CA1090332A (en)	1980-11-25	Polycyclic nitrogen-containing compounds
HU189217B (en)	1986-06-30	Herbicide compositions containing 4,5-dimethoxy-pyridazone derivatives and process for producing the active agents
DE1914014A1 (de)	1969-10-02	Neue 2-Alkylthio-4,6-diamino-S-triazine
GB2128090A (en)	1984-04-26	New herbicidal method
JP3084102B2 (ja)	2000-09-04	相乗的除草剤組成物
EP0090258B1 (de)	1987-07-29	3-Chlor-8-cyano-chinoline, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
GB2103610A (en)	1983-02-23	Herbicidal compounds derived from N-sulphonyl-aryloxybenamides and the processes for their preparation and use
CA1322751C (en)	1993-10-05	N-((6-trifluoromethylpyrimidin-2-yl)-aminocarbonyl)-2- carboalkoxybenzene-sulfonamides, their preparation and their use
US4452631A (en)	1984-06-05	Urea herbicides
JPS61186394A (ja)	1986-08-20	Ｎ‐（ホスホノメチルグリシル）スルホニルアミン型除草剤
EP0098440B1 (de)	1986-12-30	3,7-Dichlor-chinolinderivate, Verfahren zu ihrer Herstellung und ihre Verwendung zur Bekämpfung unerwünschten Pflanzenwuchses
HU182929B (en)	1984-03-28	Herbicide i.e. growth controlling composition containing norbornane derivatives
CS248710B2 (cs)	1987-02-12	Herbicidní prostředek se zvýšenou selektivitou v porostech kukuřice a prosa a způsob výroby účinné látky
US4345935A (en)	1982-08-24	2,4-Imidazolidinediones, compositions and herbicidal method
DE3639563A1 (de)	1988-06-01	N-arylsulfonyl-n'-pyrimidyl(triazinyl) -harnstoffe
US3785799A (en)	1974-01-15	Herbicidal compositions containing 2-(2',6'-dichlorophenyl)-1,3-thiazine-4-one and methods of employing the same