GB1037761A - Fungicides - Google Patents
FungicidesInfo
- Publication number
- GB1037761A GB1037761A GB531663A GB531663A GB1037761A GB 1037761 A GB1037761 A GB 1037761A GB 531663 A GB531663 A GB 531663A GB 531663 A GB531663 A GB 531663A GB 1037761 A GB1037761 A GB 1037761A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- mercury
- methyl
- radical
- tri
- Prior art date
- 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
Links
- 239000000417 fungicide Substances 0.000 title abstract 2
- -1 seeds Substances 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 4
- 229910052742 iron Inorganic materials 0.000 abstract 4
- 229910052725 zinc Inorganic materials 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 3
- 229910052748 manganese Inorganic materials 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 229910052708 sodium Inorganic materials 0.000 abstract 3
- 239000011734 sodium Substances 0.000 abstract 3
- AZQWKYJCGOJGHM-UHFFFAOYSA-N 1,4-benzoquinone Chemical compound O=C1C=CC(=O)C=C1 AZQWKYJCGOJGHM-UHFFFAOYSA-N 0.000 abstract 2
- UVCFFGYNJOPUSF-UHFFFAOYSA-M acetyloxy(ethyl)mercury Chemical compound CC[Hg+].CC([O-])=O UVCFFGYNJOPUSF-UHFFFAOYSA-M 0.000 abstract 2
- 229910052793 cadmium Inorganic materials 0.000 abstract 2
- 229910052802 copper Inorganic materials 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 abstract 2
- 229910052759 nickel Inorganic materials 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical class C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 abstract 1
- IAKOZHOLGAGEJT-UHFFFAOYSA-N 1,1,1-trichloro-2,2-bis(p-methoxyphenyl)-Ethane Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1 IAKOZHOLGAGEJT-UHFFFAOYSA-N 0.000 abstract 1
- BGPPUXMKKQMWLV-UHFFFAOYSA-N 1,2,4,5-tetrachloro-3-methoxy-6-nitrobenzene Chemical compound COC1=C(Cl)C(Cl)=C([N+]([O-])=O)C(Cl)=C1Cl BGPPUXMKKQMWLV-UHFFFAOYSA-N 0.000 abstract 1
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical class CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 abstract 1
- KVJOLVBEUYUHLD-UHFFFAOYSA-M 2,3-dihydroxypropylsulfanyl(ethyl)mercury Chemical compound CC[Hg]SCC(O)CO KVJOLVBEUYUHLD-UHFFFAOYSA-M 0.000 abstract 1
- ISPYQTSUDJAMAB-UHFFFAOYSA-N 2-chlorophenol Chemical compound OC1=CC=CC=C1Cl ISPYQTSUDJAMAB-UHFFFAOYSA-N 0.000 abstract 1
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical compound OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 abstract 1
- DFLYENJSQHCMKL-UHFFFAOYSA-N 4,6-dimethyl-1,3,5-thiadiazinane-2-thione Chemical compound CC1NC(C)SC(=S)N1 DFLYENJSQHCMKL-UHFFFAOYSA-N 0.000 abstract 1
- CDIJOYCNNFLOAX-UHFFFAOYSA-N 4-(trichloromethylsulfanyl)isoindole-1,3-dione Chemical compound ClC(Cl)(Cl)SC1=CC=CC2=C1C(=O)NC2=O CDIJOYCNNFLOAX-UHFFFAOYSA-N 0.000 abstract 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 1
- 239000005745 Captan Chemical class 0.000 abstract 1
- WMUWVSVEPKAKCJ-UHFFFAOYSA-N ClC1=NN(Cl)NC(NC=2C(=CC=CC=2)Cl)=C1 Chemical class ClC1=NN(Cl)NC(NC=2C(=CC=CC=2)Cl)=C1 WMUWVSVEPKAKCJ-UHFFFAOYSA-N 0.000 abstract 1
- YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 abstract 1
- 239000005766 Dodine Chemical class 0.000 abstract 1
- 239000005977 Ethylene Substances 0.000 abstract 1
- IWDQPCIQCXRBQP-UHFFFAOYSA-M Fenaminosulf Chemical compound [Na+].CN(C)C1=CC=C(N=NS([O-])(=O)=O)C=C1 IWDQPCIQCXRBQP-UHFFFAOYSA-M 0.000 abstract 1
- 229910003202 NH4 Inorganic materials 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 239000003945 anionic surfactant Substances 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- 229940117949 captan Drugs 0.000 abstract 1
- 125000002091 cationic group Chemical group 0.000 abstract 1
- 239000003093 cationic surfactant Substances 0.000 abstract 1
- BIWJNBZANLAXMG-YQELWRJZSA-N chloordaan Chemical compound ClC1=C(Cl)[C@@]2(Cl)C3CC(Cl)C(Cl)C3[C@]1(Cl)C2(Cl)Cl BIWJNBZANLAXMG-YQELWRJZSA-N 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 239000010730 cutting oil Substances 0.000 abstract 1
- DHKAICYEDDOCRO-UHFFFAOYSA-N cyano(methyl)mercury Chemical compound C[Hg]C#N DHKAICYEDDOCRO-UHFFFAOYSA-N 0.000 abstract 1
- DFBKLUNHFCTMDC-PICURKEMSA-N dieldrin Chemical compound C([C@H]1[C@H]2[C@@]3(Cl)C(Cl)=C([C@]([C@H]22)(Cl)C3(Cl)Cl)Cl)[C@H]2[C@@H]2[C@H]1O2 DFBKLUNHFCTMDC-PICURKEMSA-N 0.000 abstract 1
- 229950006824 dieldrin Drugs 0.000 abstract 1
- NGPMUTDCEIKKFM-UHFFFAOYSA-N dieldrin Natural products CC1=C(Cl)C2(Cl)C3C4CC(C5OC45)C3C1(Cl)C2(Cl)Cl NGPMUTDCEIKKFM-UHFFFAOYSA-N 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 239000004495 emulsifiable concentrate Substances 0.000 abstract 1
- 239000000839 emulsion Substances 0.000 abstract 1
- AWYFNIZYMPNGAI-UHFFFAOYSA-N ethylenebis(dithiocarbamic acid) Chemical class SC(=S)NCCNC(S)=S AWYFNIZYMPNGAI-UHFFFAOYSA-N 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 239000008187 granular material Substances 0.000 abstract 1
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 239000002917 insecticide Substances 0.000 abstract 1
- 239000010985 leather Substances 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229910052749 magnesium Inorganic materials 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- JVJUWCMBRUMDDQ-UHFFFAOYSA-N methylmercuric dicyanamide Chemical compound C[Hg]N=C(N)NC#N JVJUWCMBRUMDDQ-UHFFFAOYSA-N 0.000 abstract 1
- 239000002736 nonionic surfactant Substances 0.000 abstract 1
- 239000011368 organic material Substances 0.000 abstract 1
- 239000003973 paint Substances 0.000 abstract 1
- 239000008188 pellet Substances 0.000 abstract 1
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical class [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 abstract 1
- XEBWQGVWTUSTLN-UHFFFAOYSA-M phenylmercury acetate Chemical class CC(=O)O[Hg]C1=CC=CC=C1 XEBWQGVWTUSTLN-UHFFFAOYSA-M 0.000 abstract 1
- 229910052700 potassium Inorganic materials 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 239000002689 soil Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- UGNWTBMOAKPKBL-UHFFFAOYSA-N tetrachloro-1,4-benzoquinone Chemical compound ClC1=C(Cl)C(=O)C(Cl)=C(Cl)C1=O UGNWTBMOAKPKBL-UHFFFAOYSA-N 0.000 abstract 1
- 239000004753 textile Substances 0.000 abstract 1
- 229960002447 thiram Drugs 0.000 abstract 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 abstract 1
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 abstract 1
- 239000001993 wax Substances 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
Classifications
-
- H—ELECTRICITY
- H03—ELECTRONIC CIRCUITRY
- H03F—AMPLIFIERS
- H03F1/00—Details of amplifiers with only discharge tubes, only semiconductor devices or only unspecified devices as amplifying elements
- H03F1/02—Modifications of amplifiers to raise the efficiency, e.g. gliding Class A stages, use of an auxiliary oscillation
- H03F1/0205—Modifications of amplifiers to raise the efficiency, e.g. gliding Class A stages, use of an auxiliary oscillation in transistor amplifiers
- H03F1/0294—Modifications of amplifiers to raise the efficiency, e.g. gliding Class A stages, use of an auxiliary oscillation in transistor amplifiers using vector summing of two or more constant amplitude phase-modulated signals
-
- H—ELECTRICITY
- H03—ELECTRONIC CIRCUITRY
- H03C—MODULATION
- H03C1/00—Amplitude modulation
- H03C1/52—Modulators in which carrier or one sideband is wholly or partially suppressed
- H03C1/60—Modulators in which carrier or one sideband is wholly or partially suppressed with one sideband wholly or partially suppressed
Landscapes
- Engineering & Computer Science (AREA)
- Power Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Amplitude Modulation (AREA)
Abstract
Fungicidal compositions comprise a compound of formula <FORM:1037761/A5-A6/1> wherein R1-R3, are alkyl radicals of 1-10C or alkenyl radicals of 2-10C, with the proviso that R1-R3 together do not contain less than 6C or more than 12C; and Q is chlorine or a radical of the formula OR4, wherein R4 is H, an alkyl radical of 1-6C, Na, K, Ca, Mg, Zn, Mn, Cu, Fe, Ni or Cd, an ammonium radical, a mono, di or tri-(alkyl) ammonium radical where each alkyl contains 1-4C, a mono-, di-, or tri- (alkoxy alkyl) ammonium radical where the alkoxy and alkyl groups each have 1-4C, or a monodi-, or tri- (hydroxy alkyl) ammonium radical where each alkyl contains 1-4C; or a basic Zn, Mn, Cd, Cu, Fe or Ni salt of a compound of the above formula in which Q is OH, and a solid or liquid diluent. The compounds or the active ingredients, thereof may be applied to or incorporated in organic materials e.g. paints, seeds, soil, greases, waxes, cutting oils, leather textile goods and fibres, paper and wood. The compositions may be formulated as solutions, emulsions, emulsifiable concentrates, dispersions, dusts, granules, pellets and wettable powders. The compositions may contain non-ionic, cationic or anionic surfactants and other fungicides e.g. p-dimethyl amino benzene diazo sodium sulphonate, quinone oxyamino benzo-oxohydrazone, tetraalkyl thiuram mono and disulphides, Mn, Zn, Fe or Na salts of ethylene bis dithio carbamic acid, PCNB, Dodine, Captan, phenyl mercury acetate, 2, 4-dichloro-6-(o-chloroanilino) triazine, N-methyl mercury-p-toluene sulphonanilide, chlorophenol mercuri hydroxide, nitrophenol mercuri hydroxide, ethyl mercury acetate, ethyl mercury 2, 3-dihydroxy propyl mercaptide, methyl and ethyl mercury acetate, 3, 31-ethylene bis (tetrahydro-4, 6-dimethyl-2H-1, 3, 5-thiadiazine-2-thione), methyl mercury dicyandiamide, N-ethyl mercury p-toluene sulphonanilide, Fe, Na, Zn, NH4 + and amine salts of alkyl and dialkyl dithio carbamic acids, tetrachloronitroanisole, hexachlorobenzene, methyl mercury cyanide, tetrachloro quinone and N-trichloro methyl thio-phthalimide; or insecticides e.g. chlordane, DDT, dieldrin and methoxychlor.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17208262A | 1962-02-09 | 1962-02-09 | |
| US25257363A | 1963-01-21 | 1963-01-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1037761A true GB1037761A (en) | 1966-08-03 |
Family
ID=26867732
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB531663A Expired GB1037761A (en) | 1962-02-09 | 1963-02-08 | Fungicides |
Country Status (4)
| Country | Link |
|---|---|
| DE (1) | DE1285020B (en) |
| FR (1) | FR1356995A (en) |
| GB (1) | GB1037761A (en) |
| NL (2) | NL279632A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2801646A1 (en) * | 1977-01-17 | 1978-07-20 | Block Drug Co | LICE DISTRIBUTORS |
| US4380561A (en) | 1980-04-28 | 1983-04-19 | Kenogard A.B. | Treatment of wood using branched-chain aliphatic carboxylic acids |
| EP0843964A4 (en) * | 1996-06-07 | 2000-05-24 | Nippon Soda Co | Granular hydrating agent |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2371190A1 (en) * | 1976-11-22 | 1978-06-16 | Sertog | INSECTIVE COMPLEXES |
| DE2965346D1 (en) * | 1978-05-05 | 1983-06-16 | Cuprinol Ltd | Anti-fungal compositions and method of preserving materials therewith |
| DE3229097A1 (en) * | 1982-08-04 | 1984-02-09 | Schülke & Mayr GmbH, 2000 Hamburg | Microbicidal agents |
-
1962
- 1962-06-13 NL NL279632D patent/NL279632A/xx unknown
- 1962-06-14 DE DE1962K0046982 patent/DE1285020B/en active Pending
-
1963
- 1963-02-07 NL NL288677D patent/NL288677A/xx unknown
- 1963-02-08 FR FR924231A patent/FR1356995A/en not_active Expired
- 1963-02-08 GB GB531663A patent/GB1037761A/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2801646A1 (en) * | 1977-01-17 | 1978-07-20 | Block Drug Co | LICE DISTRIBUTORS |
| US4380561A (en) | 1980-04-28 | 1983-04-19 | Kenogard A.B. | Treatment of wood using branched-chain aliphatic carboxylic acids |
| EP0843964A4 (en) * | 1996-06-07 | 2000-05-24 | Nippon Soda Co | Granular hydrating agent |
Also Published As
| Publication number | Publication date |
|---|---|
| FR1356995A (en) | 1964-04-03 |
| DE1285020B (en) | 1968-12-12 |
| NL288677A (en) | 1965-03-10 |
| NL279632A (en) | 1964-11-25 |
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