CN1385069A - N-(4,6-二甲基嘧啶-2-基)苯胺杀菌组合物 - Google Patents
N-(4,6-二甲基嘧啶-2-基)苯胺杀菌组合物 Download PDFInfo
- Publication number
- CN1385069A CN1385069A CN 01118007 CN01118007A CN1385069A CN 1385069 A CN1385069 A CN 1385069A CN 01118007 CN01118007 CN 01118007 CN 01118007 A CN01118007 A CN 01118007A CN 1385069 A CN1385069 A CN 1385069A
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- Prior art keywords
- methyl
- acid
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- composition
- dimethyl
- Prior art date
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- Granted
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- 239000000203 mixture Substances 0.000 title claims abstract description 36
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 title abstract description 6
- 239000005828 Pyrimethanil Substances 0.000 title abstract 2
- 238000004659 sterilization and disinfection Methods 0.000 title 1
- 230000000844 anti-bacterial effect Effects 0.000 claims abstract description 14
- 239000003899 bactericide agent Substances 0.000 claims abstract description 7
- 230000009885 systemic effect Effects 0.000 claims abstract description 5
- -1 formamido Chemical group 0.000 claims description 21
- 239000000417 fungicide Substances 0.000 claims description 13
- 239000002689 soil Substances 0.000 claims description 9
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
- 238000010521 absorption reaction Methods 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 230000000855 fungicidal effect Effects 0.000 claims description 5
- 239000000843 powder Substances 0.000 claims description 5
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 4
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- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 4
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- PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 claims description 3
- HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims description 3
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- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 claims description 3
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 claims description 3
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 claims description 3
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- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 claims description 2
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- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 2
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- 240000008067 Cucumis sativus Species 0.000 claims description 2
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- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 claims 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 claims description 2
- JLTDJTHDQAWBAV-UHFFFAOYSA-N N,N-dimethylaniline Chemical compound CN(C)C1=CC=CC=C1 JLTDJTHDQAWBAV-UHFFFAOYSA-N 0.000 claims description 2
- KUASNEOESQHXSJ-UHFFFAOYSA-N N1=C(NC2=C1C=CC=C2)NC(=O)OCC=O Chemical compound N1=C(NC2=C1C=CC=C2)NC(=O)OCC=O KUASNEOESQHXSJ-UHFFFAOYSA-N 0.000 claims description 2
- LXVTVZIGIVHKHK-UHFFFAOYSA-P N[S+]=C(CCC(S)=[S+]N)S.[Zn] Chemical compound N[S+]=C(CCC(S)=[S+]N)S.[Zn] LXVTVZIGIVHKHK-UHFFFAOYSA-P 0.000 claims description 2
- 240000007594 Oryza sativa Species 0.000 claims description 2
- 235000007164 Oryza sativa Nutrition 0.000 claims description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 claims description 2
- 241000220324 Pyrus Species 0.000 claims description 2
- 208000032825 Ring chromosome 2 syndrome Diseases 0.000 claims description 2
- 206010039509 Scab Diseases 0.000 claims description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 2
- 235000009754 Vitis X bourquina Nutrition 0.000 claims description 2
- 235000012333 Vitis X labruscana Nutrition 0.000 claims description 2
- 240000006365 Vitis vinifera Species 0.000 claims description 2
- 235000014787 Vitis vinifera Nutrition 0.000 claims description 2
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 claims description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 claims description 2
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 2
- 229910052785 arsenic Inorganic materials 0.000 claims description 2
- RQNWIZPPADIBDY-UHFFFAOYSA-N arsenic atom Chemical compound [As] RQNWIZPPADIBDY-UHFFFAOYSA-N 0.000 claims description 2
- 239000012752 auxiliary agent Substances 0.000 claims description 2
- 239000004202 carbamide Substances 0.000 claims description 2
- 235000013877 carbamide Nutrition 0.000 claims description 2
- WCBCMSHWSDPDBE-UHFFFAOYSA-N carbamodithioic acid;zinc Chemical compound [Zn].NC(S)=S WCBCMSHWSDPDBE-UHFFFAOYSA-N 0.000 claims description 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 2
- HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical compound [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 claims description 2
- TZRSCXSDYYMKQN-UHFFFAOYSA-N dimethylcarbamodithioic acid;zinc Chemical compound [Zn].CN(C)C(S)=S TZRSCXSDYYMKQN-UHFFFAOYSA-N 0.000 claims description 2
- 235000013399 edible fruits Nutrition 0.000 claims description 2
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 claims description 2
- 239000000945 filler Substances 0.000 claims description 2
- 229910052731 fluorine Inorganic materials 0.000 claims description 2
- 239000011737 fluorine Substances 0.000 claims description 2
- 125000001160 methoxycarbonyl group Chemical group [H]C([H])([H])OC(*)=O 0.000 claims description 2
- 239000004530 micro-emulsion Substances 0.000 claims description 2
- 235000021017 pears Nutrition 0.000 claims description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims description 2
- XQZYPMVTSDWCCE-UHFFFAOYSA-N phthalonitrile Chemical compound N#CC1=CC=CC=C1C#N XQZYPMVTSDWCCE-UHFFFAOYSA-N 0.000 claims description 2
- 229920006391 phthalonitrile polymer Polymers 0.000 claims description 2
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- 239000003910 polypeptide antibiotic agent Substances 0.000 claims description 2
- YRRBXJLFCBCKNW-UHFFFAOYSA-N prothiocarb Chemical compound CCSC(=O)NCCCN(C)C YRRBXJLFCBCKNW-UHFFFAOYSA-N 0.000 claims description 2
- 239000002718 pyrimidine nucleoside Substances 0.000 claims description 2
- 235000009566 rice Nutrition 0.000 claims description 2
- 229910052708 sodium Inorganic materials 0.000 claims description 2
- 239000011734 sodium Substances 0.000 claims description 2
- 239000000375 suspending agent Substances 0.000 claims description 2
- 238000013268 sustained release Methods 0.000 claims description 2
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- 150000003751 zinc Chemical class 0.000 claims description 2
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- BOENADKAGHBIFT-UHFFFAOYSA-N 4-chloro-n-(2-chlorophenyl)-1,3,5-triazin-2-amine Chemical compound ClC1=CC=CC=C1NC1=NC=NC(Cl)=N1 BOENADKAGHBIFT-UHFFFAOYSA-N 0.000 claims 1
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
处理 | 药前指数 | 药前指数 | 平均防效 | 差异 | |
0.05 | 0.01 | ||||
40%(I+福美双)WP1000倍 | 2.66 | 1.44 | 83.40 | a | A |
40%(I)SC1000倍 | 3.29 | 1.69 | 80.20 | a | A |
50%福美双WP1000倍 | 2.36 | 1.65 | 73.00 | b | B |
清水对照(CK) | 2.26 | 5.85 | - | c | C |
处理 | 药前指数 | 药前指数 | 平均防效 | 差异 | |
0.05 | 0.01 | ||||
30%(I+腈菌唑)EC2000倍 | 2.12 | 0.74 | 86.34 | a | A |
40%(I)SC1000倍 | 3.09 | 1.77 | 77.59 | b | B |
12.5%腈菌唑EC3000倍 | 2.44 | 1.45 | 76.75 | b | B |
清水对照(CK) | 2.68 | 6.85 | - | c | C |
处理 | 药前指数 | 药前指数 | 平均防效 | 差异 | |
0.05 | 0.01 | ||||
30%(I+三唑酮)EC1250倍 | 3.14 | 0.66 | 88.66 | a | A |
20%三唑酮EC1500倍 | 3.21 | 1.26 | 78.82 | b | B |
40%(I)SC1200倍 | 4.26 | 1.91 | 75.80 | b | B |
清水对照(CK) | 4.08 | 7.56 | - | c | C |
Claims (10)
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CNA031558305A Division CN1524415A (zh) | 2001-05-15 | 2001-05-15 | N-(4,6-二甲基嘧啶-2-基)苯胺杀菌组合物 |
CNA031558313A Division CN1524416A (zh) | 2001-05-15 | 2001-05-15 | N-(4,6-二甲基嘧啶-2-基)苯胺杀菌组合物 |
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CN1385069A true CN1385069A (zh) | 2002-12-18 |
CN100387128C CN100387128C (zh) | 2008-05-14 |
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- 2001-05-15 CN CNB011180072A patent/CN100387128C/zh not_active Expired - Fee Related
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