BE666973A - - Google Patents

Info

Publication number: BE666973A
Authority: BE; Belgium
Prior art keywords: products; fungicidal; weight; formula; compound
Prior art date: 1964-07-16

Application number

BE666973A

Other languages

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.)

1964-07-16

Filing date

1965-07-15

Publication date

1966-01-17

1965-07-15 Application filed filed Critical

1966-01-17 Publication of BE666973A publication Critical patent/BE666973A/fr

Links

230000000855 fungicidal effect Effects 0.000 claims description 14
239000013543 active substance Substances 0.000 claims description 12
239000007788 liquid Substances 0.000 claims description 9
150000001875 compounds Chemical class 0.000 claims description 8
150000003839 salts Chemical class 0.000 claims description 7
241000233866 Fungi Species 0.000 claims description 6
239000007787 solid Substances 0.000 claims description 6
230000003071 parasitic effect Effects 0.000 claims description 5
125000000217 alkyl group Chemical group 0.000 claims description 3
238000000034 method Methods 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 2
239000000047 product Substances 0.000 description 16
239000000203 mixture Substances 0.000 description 9
239000000843 powder Substances 0.000 description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
239000000126 substance Substances 0.000 description 6
241000196324 Embryophyta Species 0.000 description 5
241000221785 Erysiphales Species 0.000 description 5
239000002904 solvent Substances 0.000 description 5
239000000725 suspension Substances 0.000 description 5
239000000080 wetting agent Substances 0.000 description 5
239000002270 dispersing agent Substances 0.000 description 4
-1 fungal pots Substances 0.000 description 4
239000003921 oil Substances 0.000 description 4
239000000779 smoke Substances 0.000 description 4
238000005507 spraying Methods 0.000 description 4
239000004563 wettable powder Substances 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
239000005995 Aluminium silicate Substances 0.000 description 3
102000011632 Caseins Human genes 0.000 description 3
108010076119 Caseins Proteins 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
235000012211 aluminium silicate Nutrition 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
150000004665 fatty acids Chemical class 0.000 description 3
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 3
238000002156 mixing Methods 0.000 description 3
239000000243 solution Substances 0.000 description 3
PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 2
240000008067 Cucumis sativus Species 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 2
241000228452 Venturia inaequalis Species 0.000 description 2
239000002253 acid Substances 0.000 description 2
239000000443 aerosol Substances 0.000 description 2
150000004982 aromatic amines Chemical class 0.000 description 2
239000000440 bentonite Substances 0.000 description 2
229910000278 bentonite Inorganic materials 0.000 description 2
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
235000010233 benzoic acid Nutrition 0.000 description 2
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
238000011109 contamination Methods 0.000 description 2
238000010410 dusting Methods 0.000 description 2
230000000694 effects Effects 0.000 description 2
239000003995 emulsifying agent Substances 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
238000000227 grinding Methods 0.000 description 2
HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
239000011734 sodium Substances 0.000 description 2
229910052708 sodium Inorganic materials 0.000 description 2
229940080237 sodium caseinate Drugs 0.000 description 2
239000007921 spray Substances 0.000 description 2
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
239000002023 wood Substances 0.000 description 2
239000008096 xylene Substances 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
239000005711 Benzoic acid Substances 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
240000007049 Juglans regia Species 0.000 description 1
235000009496 Juglans regia Nutrition 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
206010034972 Photosensitivity reaction Diseases 0.000 description 1
241000317981 Podosphaera fuliginea Species 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
206010039509 Scab Diseases 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
HXELGNKCCDGMMN-UHFFFAOYSA-N [F].[Cl] Chemical class [F].[Cl] HXELGNKCCDGMMN-UHFFFAOYSA-N 0.000 description 1
230000000895 acaricidal effect Effects 0.000 description 1
239000000642 acaricide Substances 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
230000004523 agglutinating effect Effects 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
159000000032 aromatic acids Chemical class 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
150000001559 benzoic acids Chemical class 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
239000008116 calcium stearate Substances 0.000 description 1
235000013539 calcium stearate Nutrition 0.000 description 1
239000001175 calcium sulphate Substances 0.000 description 1
235000011132 calcium sulphate Nutrition 0.000 description 1
239000012159 carrier gas Substances 0.000 description 1
239000005018 casein Substances 0.000 description 1
BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
235000021240 caseins Nutrition 0.000 description 1
239000001913 cellulose Substances 0.000 description 1
229920002678 cellulose Polymers 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000004927 clay Substances 0.000 description 1
238000002485 combustion reaction Methods 0.000 description 1
239000002131 composite material Substances 0.000 description 1
239000007859 condensation product Substances 0.000 description 1
230000035613 defoliation Effects 0.000 description 1
239000012895 dilution Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
239000000446 fuel Substances 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
230000035784 germination Effects 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
239000004615 ingredient Substances 0.000 description 1
230000005764 inhibitory process Effects 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
235000019359 magnesium stearate Nutrition 0.000 description 1
239000000463 material Substances 0.000 description 1
VNWKTOKETHGBQD-UHFFFAOYSA-N methane Natural products C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
239000007800 oxidant agent Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000003209 petroleum derivative Substances 0.000 description 1
208000007578 phototoxic dermatitis Diseases 0.000 description 1
231100000018 phototoxicity Toxicity 0.000 description 1
229920000136 polysorbate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000011148 porous material Substances 0.000 description 1
VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
239000002002 slurry Substances 0.000 description 1
230000004763 spore germination Effects 0.000 description 1
239000001117 sulphuric acid Substances 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
239000002641 tar oil Substances 0.000 description 1
238000009834 vaporization Methods 0.000 description 1
230000008016 vaporization Effects 0.000 description 1
235000020234 walnut Nutrition 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides
- A01N47/48—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having a double or triple bond to nitrogen, e.g. cyanates, cyanamides containing —S—C≡N groups

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)

BE666973A 1964-07-16 1965-07-15 BE666973A (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
NL6408088A NL6408088A (de)	1964-07-16	1964-07-16

Publications (1)

Publication Number	Publication Date
BE666973A true BE666973A (de)	1966-01-17

Family

ID=19790536

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BE666973A BE666973A (de)	1964-07-16	1965-07-15

Country Status (2)

Country	Link
BE (1)	BE666973A (de)
NL (1)	NL6408088A (de)

1964
- 1964-07-16 NL NL6408088A patent/NL6408088A/xx unknown
1965
- 1965-07-15 BE BE666973A patent/BE666973A/fr unknown

Also Published As

Publication number	Publication date
NL6408088A (de)	1966-01-17

Publication	Publication Date	Title
BE529063A (de)
CH427400A (fr)	1966-12-31	Composition fongicide
US3098001A (en)	1963-07-16	Acaricide agent
BE666973A (de)	1966-01-17
BE898428A (fr)	1984-06-12	Compositions fongicides et leur utilisation.
US3697589A (en)	1972-10-10	N-(4-carboxy-benzylidene)amines
IL26594A (en)	1971-11-29	Molluscicidal preparations containing aliphatic nitrile compounds and certain novel aliphatic nitriles
US3958977A (en)	1976-05-25	Herbicidal composition
US3819609A (en)	1974-06-25	Fungicidal-2-alkoxy-5-halogeno-benzene diazonium cyanides
US3504091A (en)	1970-03-31	Method of combatting fungi with n,n dialkyl substituted dithiocyanoanilines
EP0231714A1 (de)	1987-08-12	Heterocyclische Verbindungen enthaltende Nematizid- und Insektizid-Mittel
US3751466A (en)	1973-08-07	N-benzylidene alkylamines
US2936262A (en)	1960-05-10	Diels-alder adduct of tetrachloro cyclopentadiene with quinone as a fungicide
US3785799A (en)	1974-01-15	Herbicidal compositions containing 2-(2',6'-dichlorophenyl)-1,3-thiazine-4-one and methods of employing the same
EP0249567A2 (de)	1987-12-16	Propargyloxybenzolderivate, ihre Herstellung und sie enthaltende fungizide Zusammensetzungen
EP0246171A2 (de)	1987-11-19	Fungizide Zusammensetzungen, die Nikotinsäurederivate enthalten, Nikotinsäurederivate und ihre Herstellung
BE767244A (fr)	1971-11-17	Derives d'aminothiophenes.
BE891210A (fr)	1982-05-21	Nouveaux derives organophosphonothioiques
US2624665A (en)	1953-01-06	Herbicidal composition
EP0041298A2 (de)	1981-12-09	Zusammensetzung zum Hemmen oder Vorbeugen der Entwickelung von Seitentrieben bei Tabakpflanzen
FR2617844A1 (fr)	1989-01-13	Compositions fongicides a base de derives nicotiniques. nouveaux derives nicotiniques et leur preparation
US3501455A (en)	1970-03-17	Phenylazothioformamide-s-oxides
EP0033265B1 (de)	1983-02-09	Herbizide Zusammensetzungen auf der Basis von 2,4-Diamino-6-chlor-5-methylthio-pyrimidin und Diclofop-methyl und Verfahren zur Behandlung von Kulturen mit den genannten Zusammensetzungen
EP0080917B1 (de)	1985-01-23	Herbizide Zusammensetzungen auf der Basis von 4-Amino-6-chlor-5-methylthiopyrimidinderivaten und Pyridate und Verfahren zur Behandlung von Kulturen mit den genannten Zusammensetzungen
FR2623190A1 (fr)	1989-05-19	Nicotinates d'oximes fongicides