HU180831B - Fungicide compositions containing synergetic combination of manganege-ethylene-bis/dithiocarbamate/ and of a pyrmidine-methanol derivative - Google Patents
Fungicide compositions containing synergetic combination of manganege-ethylene-bis/dithiocarbamate/ and of a pyrmidine-methanol derivative Download PDFInfo
- Publication number
- HU180831B HU180831B HU78LI332A HULI000332A HU180831B HU 180831 B HU180831 B HU 180831B HU 78LI332 A HU78LI332 A HU 78LI332A HU LI000332 A HULI000332 A HU LI000332A HU 180831 B HU180831 B HU 180831B
- Authority
- HU
- Hungary
- Prior art keywords
- weight
- dithiocarbamate
- maneb
- ethylene
- bis
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 38
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 7
- 230000002195 synergetic effect Effects 0.000 title description 6
- 239000012990 dithiocarbamate Substances 0.000 title description 2
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 title 1
- 239000000417 fungicide Substances 0.000 title 1
- KCDACWMWSAEJNW-UHFFFAOYSA-N methanol;pyrimidine Chemical compound OC.C1=CN=CN=C1 KCDACWMWSAEJNW-UHFFFAOYSA-N 0.000 claims abstract description 8
- 231100001184 nonphytotoxic Toxicity 0.000 claims abstract description 3
- 239000004480 active ingredient Substances 0.000 claims description 7
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 6
- 239000000969 carrier Substances 0.000 claims description 3
- 229910052731 fluorine Inorganic materials 0.000 claims description 3
- 239000011737 fluorine Substances 0.000 claims description 3
- YAUCKEPYKXHCFF-UHFFFAOYSA-N 2-carbamothioylsulfanylethyl carbamodithioate;manganese Chemical compound [Mn].NC(=S)SCCSC(N)=S YAUCKEPYKXHCFF-UHFFFAOYSA-N 0.000 claims description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 125000001309 chloro group Chemical group Cl* 0.000 claims 1
- 235000012054 meals Nutrition 0.000 claims 1
- 239000004575 stone Substances 0.000 claims 1
- 239000011885 synergistic combination Substances 0.000 claims 1
- 241000209140 Triticum Species 0.000 abstract description 6
- 235000021307 Triticum Nutrition 0.000 abstract description 6
- 244000075850 Avena orientalis Species 0.000 abstract description 3
- 235000007319 Avena orientalis Nutrition 0.000 abstract description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 abstract description 3
- 240000005979 Hordeum vulgare Species 0.000 abstract description 3
- 238000000034 method Methods 0.000 abstract description 3
- 235000013339 cereals Nutrition 0.000 abstract description 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 229910052748 manganese Inorganic materials 0.000 abstract 1
- 239000011572 manganese Substances 0.000 abstract 1
- 239000000546 pharmaceutical excipient Substances 0.000 abstract 1
- 239000003981 vehicle Substances 0.000 abstract 1
- YKSNLCVSTHTHJA-UHFFFAOYSA-L maneb Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S YKSNLCVSTHTHJA-UHFFFAOYSA-L 0.000 description 19
- 229920000940 maneb Polymers 0.000 description 19
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 13
- HVFLCNVBZFFHBT-ZKDACBOMSA-N cefepime Chemical compound S([C@@H]1[C@@H](C(N1C=1C([O-])=O)=O)NC(=O)\C(=N/OC)C=2N=C(N)SC=2)CC=1C[N+]1(C)CCCC1 HVFLCNVBZFFHBT-ZKDACBOMSA-N 0.000 description 12
- 239000004615 ingredient Substances 0.000 description 11
- 238000009472 formulation Methods 0.000 description 9
- 238000002360 preparation method Methods 0.000 description 8
- 239000005995 Aluminium silicate Substances 0.000 description 7
- 241000196324 Embryophyta Species 0.000 description 7
- 235000012211 aluminium silicate Nutrition 0.000 description 7
- 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 7
- 239000000463 material Substances 0.000 description 7
- 239000000843 powder Substances 0.000 description 6
- 239000000377 silicon dioxide Substances 0.000 description 6
- 239000011734 sodium Substances 0.000 description 6
- 229910052708 sodium Inorganic materials 0.000 description 5
- 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
- JLYXXMFPNIAWKQ-GNIYUCBRSA-N gamma-hexachlorocyclohexane Chemical compound Cl[C@H]1[C@H](Cl)[C@@H](Cl)[C@@H](Cl)[C@H](Cl)[C@H]1Cl JLYXXMFPNIAWKQ-GNIYUCBRSA-N 0.000 description 4
- 239000000454 talc Substances 0.000 description 4
- 229910052623 talc Inorganic materials 0.000 description 4
- 239000004711 α-olefin Substances 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
- -1 alkyl succinates Chemical class 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 239000002917 insecticide Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 2
- 208000031888 Mycoses Diseases 0.000 description 2
- 241000736122 Parastagonospora nodorum Species 0.000 description 2
- ONTQJDKFANPPKK-UHFFFAOYSA-L chembl3185981 Chemical compound [Na+].[Na+].CC1=CC(C)=C(S([O-])(=O)=O)C=C1N=NC1=CC(S([O-])(=O)=O)=C(C=CC=C2)C2=C1O ONTQJDKFANPPKK-UHFFFAOYSA-L 0.000 description 2
- 238000004040 coloring Methods 0.000 description 2
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N gamma-hexachlorocyclohexane Natural products ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 229960002809 lindane Drugs 0.000 description 2
- 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 2
- 239000003921 oil Substances 0.000 description 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 1
- 241000190150 Bipolaris sorokiniana Species 0.000 description 1
- 241001480061 Blumeria graminis Species 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 241001459558 Monographella nivalis Species 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- 241000520647 Pyrenophora avenae Species 0.000 description 1
- 241000228454 Pyrenophora graminea Species 0.000 description 1
- 241001533598 Septoria Species 0.000 description 1
- 241000722133 Tilletia Species 0.000 description 1
- 241000959260 Typhula Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000004996 alkyl benzenes Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000002519 antifouling agent Substances 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000003795 chemical substances by application Substances 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
- 239000002270 dispersing agent Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- ZQURKOAMICBVAW-UHFFFAOYSA-N ethene;manganese Chemical group [Mn].C=C ZQURKOAMICBVAW-UHFFFAOYSA-N 0.000 description 1
- YXOGSLZKOVPUMH-UHFFFAOYSA-N ethene;phenol Chemical group C=C.OC1=CC=CC=C1 YXOGSLZKOVPUMH-UHFFFAOYSA-N 0.000 description 1
- 230000003631 expected effect Effects 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 235000019357 lignosulphonate Nutrition 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000010705 motor oil Substances 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 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
- 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
- A01N47/08—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 one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
- A01N47/14—Di-thio analogues thereof
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)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB37251/77A GB1597363A (en) | 1977-09-07 | 1977-09-07 | Fungicidal combinations |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU180831B true HU180831B (en) | 1983-04-29 |
Family
ID=10394975
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU78LI332A HU180831B (en) | 1977-09-07 | 1978-09-06 | Fungicide compositions containing synergetic combination of manganege-ethylene-bis/dithiocarbamate/ and of a pyrmidine-methanol derivative |
Country Status (35)
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1143721B (it) * | 1977-12-01 | 1986-10-22 | Sipcam Spa | Composizione fungicida per la lotta contro le malattie delle piante |
| DE4304172A1 (de) * | 1993-02-12 | 1994-08-25 | Bayer Ag | Fungizide Wirkstoffkombinationen |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1561634A (en) * | 1975-10-29 | 1980-02-27 | Lilly Industries Ltd | Fungicidal compositions |
-
1977
- 1977-09-07 GB GB37251/77A patent/GB1597363A/en not_active Expired
-
1978
- 1978-08-21 IE IE1685/78A patent/IE47245B1/en not_active IP Right Cessation
- 1978-08-22 CA CA309,834A patent/CA1090247A/en not_active Expired
- 1978-08-23 NZ NZ188229A patent/NZ188229A/xx unknown
- 1978-08-25 IL IL7855441A patent/IL55441A0/xx not_active IP Right Cessation
- 1978-08-28 ZA ZA00784883A patent/ZA784883B/xx unknown
- 1978-08-28 GR GR57104A patent/GR63167B/el unknown
- 1978-08-29 TR TR20300A patent/TR20300A/xx unknown
- 1978-09-01 FI FI782685A patent/FI61608C/fi not_active IP Right Cessation
- 1978-09-01 IN IN961/CAL/78A patent/IN149680B/en unknown
- 1978-09-01 FR FR7825298A patent/FR2402409A1/fr active Granted
- 1978-09-01 AR AR273534A patent/AR218330A1/es active
- 1978-09-04 IT IT50962/78A patent/IT1106132B/it active
- 1978-09-04 BG BG040814A patent/BG32111A3/xx unknown
- 1978-09-05 CS CS785753A patent/CS207667B2/cs unknown
- 1978-09-05 BR BR7805811A patent/BR7805811A/pt unknown
- 1978-09-05 DK DK391378A patent/DK156753C/da not_active IP Right Cessation
- 1978-09-05 DE DE19782838575 patent/DE2838575A1/de active Granted
- 1978-09-05 BE BE6046599A patent/BE870237A/xx not_active IP Right Cessation
- 1978-09-05 CH CH933078A patent/CH634462A5/fr not_active IP Right Cessation
- 1978-09-06 NL NL7809096A patent/NL7809096A/xx active Search and Examination
- 1978-09-06 SE SE7809387A patent/SE447441B/sv not_active IP Right Cessation
- 1978-09-06 PH PH21574A patent/PH14333A/en unknown
- 1978-09-06 HU HU78LI332A patent/HU180831B/hu not_active IP Right Cessation
- 1978-09-06 JP JP10954378A patent/JPS5452727A/ja active Pending
- 1978-09-06 SU SU782658657A patent/SU816390A3/ru active
- 1978-09-06 AU AU39616/78A patent/AU526357B2/en not_active Expired
- 1978-09-06 UA UA2658657A patent/UA6333A1/uk unknown
- 1978-09-06 NO NO783044A patent/NO147091C/no unknown
- 1978-09-07 AT AT647578A patent/AT361248B/de not_active IP Right Cessation
- 1978-09-07 JO JO1978983A patent/JO983B1/en active
- 1978-09-07 ES ES473293A patent/ES473293A1/es not_active Expired
- 1978-09-07 PL PL1978209466A patent/PL111723B1/pl unknown
- 1978-09-07 MX MX787381U patent/MX5503E/es unknown
- 1978-09-07 DD DD78207689A patent/DD138593A5/xx not_active IP Right Cessation
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| HU90 | Patent valid on 900628 | ||
| HMM4 | Cancellation of final prot. due to non-payment of fee |