BE547413A - Fongicides et leur procédé de fabrication - Google Patents

Fongicides et leur procédé de fabrication

Info

Publication number: BE547413A
Authority: BE; Belgium
Prior art keywords: desc; clms page; page number; product; solution
Prior art date: 1955-05-06

Application number

BE547413A

Other languages

English (en)

French (fr)

Inventor

Lothar Martin

Harold Randolph Chipman

Charles William Gates

Original Assignee

Us Rubber Co

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.)

1955-05-06

Filing date

1956-04-28

Publication date

1959-11-06

1956-04-28 Application filed by Us Rubber Co filed Critical Us Rubber Co

1959-11-06 Publication of BE547413A publication Critical patent/BE547413A/fr

Links

239000000417 fungicide Substances 0.000 title description 10
238000004519 manufacturing process Methods 0.000 title description 3
239000000047 product Substances 0.000 description 26
239000000243 solution Substances 0.000 description 24
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 20
239000000126 substance Substances 0.000 description 17
241000196324 Embryophyta Species 0.000 description 16
238000006243 chemical reaction Methods 0.000 description 12
230000000855 fungicidal effect Effects 0.000 description 11
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 10
239000000203 mixture Substances 0.000 description 10
KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 description 9
238000000034 method Methods 0.000 description 9
150000002500 ions Chemical class 0.000 description 8
239000000463 material Substances 0.000 description 8
230000003647 oxidation Effects 0.000 description 8
238000007254 oxidation reaction Methods 0.000 description 8
229920000642 polymer Polymers 0.000 description 8
238000001228 spectrum Methods 0.000 description 8
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 7
238000003756 stirring Methods 0.000 description 7
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 6
QGJOPFRUJISHPQ-UHFFFAOYSA-N Carbon disulfide Chemical compound S=C=S QGJOPFRUJISHPQ-UHFFFAOYSA-N 0.000 description 5
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 5
238000002441 X-ray diffraction Methods 0.000 description 5
239000007864 aqueous solution Substances 0.000 description 5
230000000694 effects Effects 0.000 description 5
238000002844 melting Methods 0.000 description 5
230000008018 melting Effects 0.000 description 5
239000011541 reaction mixture Substances 0.000 description 5
229910052717 sulfur Inorganic materials 0.000 description 5
239000011593 sulfur Substances 0.000 description 5
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 4
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
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 4
150000001875 compounds Chemical class 0.000 description 4
239000012065 filter cake Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000007800 oxidant agent Substances 0.000 description 4
229910052708 sodium Inorganic materials 0.000 description 4
239000011734 sodium Substances 0.000 description 4
XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 3
239000002253 acid Substances 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 3
230000006378 damage Effects 0.000 description 3
238000000354 decomposition reaction Methods 0.000 description 3
238000006477 desulfuration reaction Methods 0.000 description 3
230000023556 desulfurization Effects 0.000 description 3
-1 diethylcne trianc Chemical class 0.000 description 3
230000003902 lesion Effects 0.000 description 3
230000001590 oxidative effect Effects 0.000 description 3
150000003839 salts Chemical class 0.000 description 3
239000002002 slurry Substances 0.000 description 3
239000011780 sodium chloride Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
238000012360 testing method Methods 0.000 description 3
229960002447 thiram Drugs 0.000 description 3
QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
244000046052 Phaseolus vulgaris Species 0.000 description 2
238000013019 agitation Methods 0.000 description 2
239000003513 alkali Substances 0.000 description 2
FPIPGXGPPPQFEQ-OVSJKPMPSA-N all-trans-retinol Chemical compound OC\C=C(/C)\C=C\C=C(/C)\C=C\C1=C(C)CCCC1(C)C FPIPGXGPPPQFEQ-OVSJKPMPSA-N 0.000 description 2
239000002585 base Substances 0.000 description 2
238000009412 basement excavation Methods 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
238000001816 cooling Methods 0.000 description 2
150000002019 disulfides Chemical class 0.000 description 2
239000011521 glass Substances 0.000 description 2
239000001257 hydrogen Substances 0.000 description 2
229910052739 hydrogen Inorganic materials 0.000 description 2
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
239000000155 melt Substances 0.000 description 2
229910052751 metal Inorganic materials 0.000 description 2
239000002184 metal Substances 0.000 description 2
229910052757 nitrogen Inorganic materials 0.000 description 2
235000015097 nutrients Nutrition 0.000 description 2
150000002978 peroxides Chemical class 0.000 description 2
235000021395 porridge Nutrition 0.000 description 2
239000002244 precipitate Substances 0.000 description 2
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
239000004094 surface-active agent Substances 0.000 description 2
238000012546 transfer Methods 0.000 description 2
SVPKNMBRVBMTLB-UHFFFAOYSA-N 2,3-dichloronaphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(Cl)=C(Cl)C(=O)C2=C1 SVPKNMBRVBMTLB-UHFFFAOYSA-N 0.000 description 1
241000238876 Acari Species 0.000 description 1
239000004160 Ammonium persulphate Substances 0.000 description 1
101100125371 Caenorhabditis elegans cil-1 gene Proteins 0.000 description 1
101100042788 Caenorhabditis elegans him-1 gene Proteins 0.000 description 1
101100398835 Caenorhabditis elegans leo-1 gene Proteins 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
241000587717 Chlorurus Species 0.000 description 1
MFYSYFVPBJMHGN-UHFFFAOYSA-N Cortisone Natural products O=C1CCC2(C)C3C(=O)CC(C)(C(CC4)(O)C(=O)CO)C4C3CCC2=C1 MFYSYFVPBJMHGN-UHFFFAOYSA-N 0.000 description 1
101100421144 Danio rerio selenoo1 gene Proteins 0.000 description 1
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
241000282326 Felis catus Species 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
241000102542 Kara Species 0.000 description 1
241000269777 Mugilidae Species 0.000 description 1
101100202896 Mus musculus Selenoo gene Proteins 0.000 description 1
MMOXZBCLCQITDF-UHFFFAOYSA-N N,N-diethyl-m-toluamide Chemical compound CCN(CC)C(=O)C1=CC=CC(C)=C1 MMOXZBCLCQITDF-UHFFFAOYSA-N 0.000 description 1
IOVCWXUNBOPUCH-UHFFFAOYSA-N Nitrous acid Chemical compound ON=O IOVCWXUNBOPUCH-UHFFFAOYSA-N 0.000 description 1
241000282320 Panthera leo Species 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
239000004698 Polyethylene Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241000282330 Procyon lotor Species 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
239000011717 all-trans-retinol Substances 0.000 description 1
235000019169 all-trans-retinol Nutrition 0.000 description 1
230000004075 alteration Effects 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
229910001870 ammonium persulfate Inorganic materials 0.000 description 1
235000019395 ammonium persulphate Nutrition 0.000 description 1
238000013459 approach Methods 0.000 description 1
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
150000001540 azides Chemical class 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
238000011109 contamination Methods 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
239000013078 crystal Substances 0.000 description 1
230000001066 destructive effect Effects 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
238000009826 distribution Methods 0.000 description 1
239000012990 dithiocarbamate Substances 0.000 description 1
238000001035 drying Methods 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000012530 fluid Substances 0.000 description 1
ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical compound C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
230000004927 fusion Effects 0.000 description 1
230000005021 gait Effects 0.000 description 1
230000035784 germination Effects 0.000 description 1
PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
239000010931 gold Substances 0.000 description 1
229910052737 gold Inorganic materials 0.000 description 1
230000009931 harmful effect Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
150000002431 hydrogen Chemical class 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000010985 leather Substances 0.000 description 1
ONCZDRURRATYFI-QTCHDTBASA-N methyl (2z)-2-methoxyimino-2-[2-[[(e)-1-[3-(trifluoromethyl)phenyl]ethylideneamino]oxymethyl]phenyl]acetate Chemical compound CO\N=C(/C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-QTCHDTBASA-N 0.000 description 1
239000010445 mica Substances 0.000 description 1
229910052618 mica group Inorganic materials 0.000 description 1
239000011707 mineral Substances 0.000 description 1
208000001491 myopia Diseases 0.000 description 1
230000004379 myopia Effects 0.000 description 1
231100000252 nontoxic Toxicity 0.000 description 1
230000003000 nontoxic effect Effects 0.000 description 1
150000002894 organic compounds Chemical class 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229910052760 oxygen Inorganic materials 0.000 description 1
239000001301 oxygen Substances 0.000 description 1
230000001717 pathogenic effect Effects 0.000 description 1
JRKICGRDRMAZLK-UHFFFAOYSA-L peroxydisulfate Chemical compound [O-]S(=O)(=O)OOS([O-])(=O)=O JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
229920000573 polyethylene Polymers 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000011591 potassium Substances 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000002265 prevention Effects 0.000 description 1
238000012545 processing Methods 0.000 description 1
238000010791 quenching Methods 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
230000001105 regulatory effect Effects 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
235000010288 sodium nitrite Nutrition 0.000 description 1
239000002689 soil Substances 0.000 description 1
230000004763 spore germination Effects 0.000 description 1
238000003860 storage Methods 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
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
238000005406 washing Methods 0.000 description 1
238000009736 wetting Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G73/00—Macromolecular compounds obtained by reactions forming a linkage containing nitrogen with or without oxygen or carbon in the main chain of the macromolecule, not provided for in groups C08G12/00 - C08G71/00
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/14—Dithiocarbamic acids; Derivatives thereof
- C07C333/16—Salts of dithiocarbamic acids
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C333/00—Derivatives of thiocarbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
- C07C333/14—Dithiocarbamic acids; Derivatives thereof
- C07C333/30—Dithiocarbamic acids; Derivatives thereof having sulfur atoms of dithiocarbamic groups bound to other sulfur atoms
- C07C333/32—Thiuramsulfides; Thiurampolysulfides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
Polymerisation Methods In General (AREA)

BE547413A 1955-05-06 1956-04-28 Fongicides et leur procédé de fabrication BE547413A (fr)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CA90740X		1955-05-06

Publications (1)

Publication Number	Publication Date
BE547413A true BE547413A (fr)	1959-11-06

Family

ID=93012975

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BE547413A BE547413A (fr)	1955-05-06	1956-04-28	Fongicides et leur procédé de fabrication

Country Status (7)

Country	Link
BE (1)	BE547413A (da)
DE (1)	DE1058982B (da)
DK (1)	DK87288C (da)
ES (1)	ES228253A1 (da)
FR (1)	FR1149577A (da)
GB (1)	GB816341A (da)
NL (1)	NL90740C (da)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE1163792B (de) *	1962-07-24	1964-02-27	Bayer Ag	Verfahren zur Herstellung von Bisdithiocarbaminsaeurederivaten

1956
- 1956-03-29 GB GB9830/56A patent/GB816341A/en not_active Expired
- 1956-04-23 FR FR1149577D patent/FR1149577A/fr not_active Expired
- 1956-04-28 BE BE547413A patent/BE547413A/fr unknown
- 1956-04-28 NL NL206762A patent/NL90740C/nl active
- 1956-04-30 ES ES0228253A patent/ES228253A1/es not_active Expired
- 1956-05-04 DK DK365456AA patent/DK87288C/da active
- 1956-05-05 DE DEU3890A patent/DE1058982B/de active Pending

Also Published As

Publication number	Publication date
NL90740C (nl)	1959-04-15
FR1149577A (fr)	1957-12-27
GB816341A (en)	1959-07-08
ES228253A1 (es)	1957-03-01
DK87288C (da)	1959-05-11
DE1058982B (de)	1959-06-11

Publication	Publication Date	Title
DE1695968C3 (de)	1979-04-12	4-Methylthiazolyl-5-carboxanilidverbindungen, Verfahren zu ihrer Herstellung und ihre Verwendung als fungizide Mittel
CA1115727A (fr)	1982-01-05	Metaphenylenediamines et compositions tinctoriales les contenant
CA1088066A (fr)	1980-10-21	Coupleurs nitres utilisables en teintures directes, teintures d'oxydation et teintures mixtes
BE547413A (fr)	1959-11-06	Fongicides et leur procédé de fabrication
US5847190A (en)	1998-12-08	Dendritic nitrogen-containing organic compounds containing planar-chiral or axial-chiral end groups and the preparation and use thereof
EP1303631B1 (de)	2010-05-26	Biotransformation von biologisch aktiven verbindungen aus verschiedenen chemischen stoffklassen mittels der enzyme laccase und manganperoxidase
EP1174491A2 (de)	2002-01-23	Bleich- und Oxidationsmittel und ihre Verwendung
EP0387195A1 (de)	1990-09-12	Mittel zum Schutz von Pflanzen gegen Krankheiten
EP0384889A2 (de)	1990-08-29	Mittel zum Schutz von Pflanzen gegen Krankheiten
LU85259A1 (fr)	1985-10-14	Ester de l'hydroxyde de tricyclohexyletain acaricide
BE818849A (fr)	1975-02-14	Derives de cyclohexane
DE2044023B2 (de)	1979-03-01	Verwendung von macrotetroliden Verbindungen zur Bekämpfung von Milben und Insekten
CH618679A5 (da)	1980-08-15
US3836582A (en)	1974-09-17	Carbamaldoximes
BE895697A (fr)	1983-07-25	Nouveaux composes utilisables pour la teinture des cheveux, leur procede de preparation, composition de teinture les contenant
US3035073A (en)	1962-05-15	N-alkyl-n(alkyl-mercuri)aliphatyl sulfonamides
Nasriddinovich	2022	Modern Methods of Studying Chemistry and Polymer Chemistry in Technical Universities
JPS58908A (ja)	1983-01-06	殺虫および殺ダニ剤
FR2460111A2 (fr)	1981-01-23	Composition a base d'un melange aqueux de n-methyl-2-pyrrolidone et d'acide 2-halogenethylphosphonique et son application au traitement de plantes
CA2409135A1 (fr)	2001-11-22	Procede de traitement de matiere vegetale, compositions comportant des derives du type n-acylglucosamine, utilisation de ces composes en tant qu'agents bio-protecteurs, et matierevegetale traitee, notamment des semences
JPH0649007A (ja)	1994-02-22	殺菌性組成物
WO2021083997A1 (fr)	2021-05-06	Nouveaux catalyseurs micellaires
BE672362A (da)	1966-03-16
FR2471364A1 (fr)	1981-06-19	Nouveaux derives de l'aniline et compositions regulatrices de la croissance des plantes les contenant
JPS58113107A (ja)	1983-07-05	除草剤