GB990111A - Fungicidal compositions - Google Patents
Fungicidal compositionsInfo
- Publication number
- GB990111A GB990111A GB1622260A GB1622260A GB990111A GB 990111 A GB990111 A GB 990111A GB 1622260 A GB1622260 A GB 1622260A GB 1622260 A GB1622260 A GB 1622260A GB 990111 A GB990111 A GB 990111A
- Authority
- GB
- United Kingdom
- Prior art keywords
- tetrachlorobenzotriazole
- methyl
- sodium salt
- group
- cor6
- 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
- 239000000203 mixture Substances 0.000 title abstract 5
- 230000000855 fungicidal effect Effects 0.000 title abstract 2
- -1 4,5,6,7-tetrachlorobenzotriazole sodium salt Chemical compound 0.000 abstract 11
- 239000004480 active ingredient Substances 0.000 abstract 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 4
- 101100134925 Gallus gallus COR6 gene Proteins 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- ZNJPBNVCQVDOJX-UHFFFAOYSA-N 4,5,6,7-tetrachloro-2h-benzotriazole Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C2=NNN=C21 ZNJPBNVCQVDOJX-UHFFFAOYSA-N 0.000 abstract 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 2
- 229910021529 ammonia Inorganic materials 0.000 abstract 2
- 239000007795 chemical reaction product Substances 0.000 abstract 2
- 230000002538 fungal effect Effects 0.000 abstract 2
- 229910052736 halogen Inorganic materials 0.000 abstract 2
- 150000002367 halogens Chemical class 0.000 abstract 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 2
- 239000011976 maleic acid Substances 0.000 abstract 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 abstract 2
- 229910052751 metal Inorganic materials 0.000 abstract 2
- 239000002184 metal Substances 0.000 abstract 2
- 150000002739 metals Chemical class 0.000 abstract 2
- 239000003973 paint Substances 0.000 abstract 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
- 125000000547 substituted alkyl group Chemical group 0.000 abstract 2
- 239000004094 surface-active agent Substances 0.000 abstract 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 2
- VSEROABGEVRIRY-UHFFFAOYSA-N 1-(chloromethyl)benzotriazole Chemical compound C1=CC=C2N(CCl)N=NC2=C1 VSEROABGEVRIRY-UHFFFAOYSA-N 0.000 abstract 1
- CQQUWTMMFMJEFE-UHFFFAOYSA-N 2-chloro-n,n-diethylacetamide Chemical compound CCN(CC)C(=O)CCl CQQUWTMMFMJEFE-UHFFFAOYSA-N 0.000 abstract 1
- HOZLOOPIXHWKCI-UHFFFAOYSA-N 2-chloro-n-methylacetamide Chemical compound CNC(=O)CCl HOZLOOPIXHWKCI-UHFFFAOYSA-N 0.000 abstract 1
- XZASMRJDZQLRMV-UHFFFAOYSA-N 3,4,6-trichlorobenzene-1,2-diamine Chemical compound NC1=C(N)C(Cl)=C(Cl)C=C1Cl XZASMRJDZQLRMV-UHFFFAOYSA-N 0.000 abstract 1
- KYCCJMLIWVYOJN-UHFFFAOYSA-N 4,5,6,7-tetrachloro-3-methoxy-2-methyl-1H-benzotriazole Chemical compound CON1N(NC2=C1C(=C(C(=C2Cl)Cl)Cl)Cl)C KYCCJMLIWVYOJN-UHFFFAOYSA-N 0.000 abstract 1
- UPOHHKQFJSIPBW-UHFFFAOYSA-N 4,5,6-trichloro-2h-benzotriazole Chemical compound ClC1=C(Cl)C(Cl)=CC2=NNN=C21 UPOHHKQFJSIPBW-UHFFFAOYSA-N 0.000 abstract 1
- AMZMJQJXYYNIEO-UHFFFAOYSA-N 4,5,7-trichloro-2h-benzotriazole Chemical compound ClC1=CC(Cl)=C2NN=NC2=C1Cl AMZMJQJXYYNIEO-UHFFFAOYSA-N 0.000 abstract 1
- IFVFXSNVYLJHDF-UHFFFAOYSA-N 5-chloro-6-methoxy-2h-benzotriazole Chemical compound C1=C(Cl)C(OC)=CC2=NNN=C21 IFVFXSNVYLJHDF-UHFFFAOYSA-N 0.000 abstract 1
- SUPSFAUIWDRKKZ-UHFFFAOYSA-N 5-methoxy-2h-benzotriazole Chemical compound C1=C(OC)C=CC2=NNN=C21 SUPSFAUIWDRKKZ-UHFFFAOYSA-N 0.000 abstract 1
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 abstract 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- XJUZRXYOEPSWMB-UHFFFAOYSA-N Chloromethyl methyl ether Chemical compound COCCl XJUZRXYOEPSWMB-UHFFFAOYSA-N 0.000 abstract 1
- QPLDLSVMHZLSFG-UHFFFAOYSA-N Copper oxide Chemical compound [Cu]=O QPLDLSVMHZLSFG-UHFFFAOYSA-N 0.000 abstract 1
- 239000005751 Copper oxide Substances 0.000 abstract 1
- 239000005752 Copper oxychloride Substances 0.000 abstract 1
- 240000000491 Corchorus aestuans Species 0.000 abstract 1
- 235000011777 Corchorus aestuans Nutrition 0.000 abstract 1
- 235000010862 Corchorus capsularis Nutrition 0.000 abstract 1
- 229920000742 Cotton Polymers 0.000 abstract 1
- YXHKONLOYHBTNS-UHFFFAOYSA-N Diazomethane Chemical compound C=[N+]=[N-] YXHKONLOYHBTNS-UHFFFAOYSA-N 0.000 abstract 1
- 101100440695 Dictyostelium discoideum corB gene Proteins 0.000 abstract 1
- YIIMEMSDCNDGTB-UHFFFAOYSA-N Dimethylcarbamoyl chloride Chemical compound CN(C)C(Cl)=O YIIMEMSDCNDGTB-UHFFFAOYSA-N 0.000 abstract 1
- 241000196324 Embryophyta Species 0.000 abstract 1
- 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 abstract 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 abstract 1
- 244000082204 Phyllostachys viridis Species 0.000 abstract 1
- 229910000004 White lead Inorganic materials 0.000 abstract 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000000129 anionic group Chemical group 0.000 abstract 1
- 125000004104 aryloxy group Chemical group 0.000 abstract 1
- 239000011575 calcium Substances 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 1
- 125000002091 cationic group Chemical group 0.000 abstract 1
- 150000001768 cations Chemical class 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 abstract 1
- VXIVSQZSERGHQP-UHFFFAOYSA-N chloroacetamide Chemical compound NC(=O)CCl VXIVSQZSERGHQP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 150000001879 copper Chemical class 0.000 abstract 1
- 229910000431 copper oxide Inorganic materials 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 238000006193 diazotization reaction Methods 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
- PVZKKBSJLLDFQD-UHFFFAOYSA-N ethyl 4,5,6,7-tetrachlorobenzotriazole-1-carboxylate Chemical compound C(=O)(OCC)N1N=NC2=C1C(=C(C(=C2Cl)Cl)Cl)Cl PVZKKBSJLLDFQD-UHFFFAOYSA-N 0.000 abstract 1
- RIFGWPKJUGCATF-UHFFFAOYSA-N ethyl chloroformate Chemical compound CCOC(Cl)=O RIFGWPKJUGCATF-UHFFFAOYSA-N 0.000 abstract 1
- 239000004744 fabric Substances 0.000 abstract 1
- 239000003337 fertilizer Substances 0.000 abstract 1
- 239000000417 fungicide Substances 0.000 abstract 1
- 239000003292 glue Substances 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229910052744 lithium Inorganic materials 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 239000000463 material Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- QABLOFMHHSOFRJ-UHFFFAOYSA-N methyl 2-chloroacetate Chemical compound COC(=O)CCl QABLOFMHHSOFRJ-UHFFFAOYSA-N 0.000 abstract 1
- XZNPPQNECRHHJP-UHFFFAOYSA-N methyl 4,5,6,7-tetrachloro-2-methyl-3H-benzotriazole-1-carboxylate Chemical compound COC(=O)N1N(NC2=C1C(=C(C(=C2Cl)Cl)Cl)Cl)C XZNPPQNECRHHJP-UHFFFAOYSA-N 0.000 abstract 1
- BFDHFSHZJLFAMC-UHFFFAOYSA-L nickel(ii) hydroxide Chemical compound [OH-].[OH-].[Ni+2] BFDHFSHZJLFAMC-UHFFFAOYSA-L 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 239000000123 paper Substances 0.000 abstract 1
- 239000011505 plaster Substances 0.000 abstract 1
- 239000004033 plastic Substances 0.000 abstract 1
- 229920003023 plastic Polymers 0.000 abstract 1
- 239000000843 powder Substances 0.000 abstract 1
- 238000006798 ring closing metathesis reaction Methods 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000011734 sodium Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- 229920002994 synthetic fiber Polymers 0.000 abstract 1
- 239000002966 varnish Substances 0.000 abstract 1
- 239000002023 wood Substances 0.000 abstract 1
- 210000002268 wool Anatomy 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/35—Heterocyclic compounds
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M16/00—Biochemical treatment of fibres, threads, yarns, fabrics, or fibrous goods made from such materials, e.g. enzymatic
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Microbiology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| NL264236D NL264236A (enrdf_load_stackoverflow) | 1960-05-07 | ||
| GB1622260A GB990111A (en) | 1960-05-07 | 1960-05-07 | Fungicidal compositions |
| CH513861A CH372499A (fr) | 1960-05-07 | 1961-05-02 | Procédé pour rendre les fibres textiles, brutes ou déjà travaillées, résistantes à la moisissure, bain pour la mise en oeuvre de ce procédé et fibres textiles traitées par ce procédé |
| FR860846A FR1296048A (fr) | 1960-05-07 | 1961-05-05 | Composés chimiques et compositions ayant un effet fongicide à usage industriel |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1622260A GB990111A (en) | 1960-05-07 | 1960-05-07 | Fungicidal compositions |
| GB3340760 | 1960-09-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB990111A true GB990111A (en) | 1965-04-28 |
Family
ID=26251905
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1622260A Expired GB990111A (en) | 1960-05-07 | 1960-05-07 | Fungicidal compositions |
Country Status (3)
| Country | Link |
|---|---|
| CH (1) | CH372499A (enrdf_load_stackoverflow) |
| GB (1) | GB990111A (enrdf_load_stackoverflow) |
| NL (1) | NL264236A (enrdf_load_stackoverflow) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4038403A (en) | 1975-10-17 | 1977-07-26 | American Cyanamid Company | Benzotriazole ovicides and larvicides |
| US4086242A (en) * | 1974-07-22 | 1978-04-25 | American Cyanamid Company | 1H- and 2H-Benzotriazoles |
| US4240822A (en) * | 1978-12-04 | 1980-12-23 | American Cyanamid Company | Method for controlling undesirable plants using 1H-benzotriazole and 2H-benzotriazole compounds |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CS151135B1 (enrdf_load_stackoverflow) * | 1970-04-30 | 1973-09-17 |
-
0
- NL NL264236D patent/NL264236A/xx unknown
-
1960
- 1960-05-07 GB GB1622260A patent/GB990111A/en not_active Expired
-
1961
- 1961-05-02 CH CH513861A patent/CH372499A/fr unknown
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4086242A (en) * | 1974-07-22 | 1978-04-25 | American Cyanamid Company | 1H- and 2H-Benzotriazoles |
| US4038403A (en) | 1975-10-17 | 1977-07-26 | American Cyanamid Company | Benzotriazole ovicides and larvicides |
| US4240822A (en) * | 1978-12-04 | 1980-12-23 | American Cyanamid Company | Method for controlling undesirable plants using 1H-benzotriazole and 2H-benzotriazole compounds |
Also Published As
| Publication number | Publication date |
|---|---|
| NL264236A (enrdf_load_stackoverflow) | 1900-01-01 |
| CH513861A4 (enrdf_load_stackoverflow) | 1963-06-15 |
| CH372499A (fr) | 1963-11-30 |
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