NO812901L - Nye fosforsyremonoestersalter og fungicide preparater inneholdende samme. - Google Patents

Nye fosforsyremonoestersalter og fungicide preparater inneholdende samme.

Info

Publication number: NO812901L
Authority: NO; Norway
Prior art keywords: alkyl; carbon atoms; phosphoric acid; group; alkoxyalkyl
Prior art date: 1980-08-27

Application number

NO812901A

Other languages

English (en)

Norwegian (no)

Inventor

Katalin Goeroeg

Erzsebet Dudar

Maria Kocsis

Marta Tasnadi

Eva Egyhazi

Valeria M Varga

Istvan Kajati

Janos Molnar

Bertalan Toth

Laszlo Bodnar

Sandor Gaal

Gyoergy Kis

Original Assignee

Borsodi Vegyi Komb

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.)

1980-08-27

Filing date

1981-08-26

Publication date

1982-03-01

1981-08-26 Application filed by Borsodi Vegyi Komb filed Critical Borsodi Vegyi Komb

1982-03-01 Publication of NO812901L publication Critical patent/NO812901L/no

Links

NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 title claims abstract description 18
230000000855 fungicidal effect Effects 0.000 title claims abstract description 12
238000002360 preparation method Methods 0.000 title claims abstract description 11
229910000147 aluminium phosphate Inorganic materials 0.000 title claims abstract description 9
239000000417 fungicide Substances 0.000 title description 2
125000004432 carbon atom Chemical group C* 0.000 claims abstract description 34
229910052739 hydrogen Inorganic materials 0.000 claims abstract description 32
125000000217 alkyl group Chemical group 0.000 claims abstract description 30
-1 picolyl Chemical group 0.000 claims abstract description 25
239000004480 active ingredient Substances 0.000 claims abstract description 19
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 13
125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 11
150000003839 salts Chemical class 0.000 claims abstract description 10
125000003545 alkoxy group Chemical group 0.000 claims abstract description 9
125000003342 alkenyl group Chemical group 0.000 claims abstract description 8
239000000460 chlorine Substances 0.000 claims abstract description 7
229910052801 chlorine Inorganic materials 0.000 claims abstract description 7
239000001257 hydrogen Substances 0.000 claims abstract description 7
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims abstract description 7
125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims abstract description 6
125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 6
229910052736 halogen Inorganic materials 0.000 claims abstract description 4
125000005843 halogen group Chemical group 0.000 claims abstract description 4
150000002431 hydrogen Chemical group 0.000 claims abstract description 4
125000001113 thiadiazolyl group Chemical group 0.000 claims abstract description 4
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
125000000278 alkyl amino alkyl group Chemical group 0.000 claims abstract description 3
125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 3
125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 3
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims abstract description 3
125000004985 dialkyl amino alkyl group Chemical group 0.000 claims abstract description 3
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 3
125000005359 phenoxyalkyl group Chemical group 0.000 claims abstract description 3
229960005235 piperonyl butoxide Drugs 0.000 claims abstract description 3
125000004591 piperonyl group Chemical group C(C1=CC=2OCOC2C=C1)* 0.000 claims abstract description 3
125000004076 pyridyl group Chemical group 0.000 claims abstract description 3
125000000714 pyrimidinyl group Chemical group 0.000 claims abstract description 3
125000002769 thiazolinyl group Chemical group 0.000 claims abstract description 3
125000000335 thiazolyl group Chemical group 0.000 claims abstract description 3
125000001425 triazolyl group Chemical group 0.000 claims abstract description 3
125000000304 alkynyl group Chemical group 0.000 claims description 3
125000004103 aminoalkyl group Chemical group 0.000 claims description 3
125000003277 amino group Chemical group 0.000 claims 1
239000000203 mixture Substances 0.000 abstract description 40
125000003785 benzimidazolyl group Chemical group N1=C(NC2=C1C=CC=C2)* 0.000 abstract description 2
150000001875 compounds Chemical class 0.000 description 55
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 40
229910052757 nitrogen Inorganic materials 0.000 description 36
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 33
229910052698 phosphorus Inorganic materials 0.000 description 24
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 21
238000004458 analytical method Methods 0.000 description 18
239000000047 product Substances 0.000 description 17
238000004809 thin layer chromatography Methods 0.000 description 15
LXCYSACZTOKNNS-UHFFFAOYSA-N diethoxy(oxo)phosphanium Chemical compound CCO[P+](=O)OCC LXCYSACZTOKNNS-UHFFFAOYSA-N 0.000 description 14
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
239000003795 chemical substances by application Substances 0.000 description 9
238000002844 melting Methods 0.000 description 8
230000008018 melting Effects 0.000 description 8
238000000034 method Methods 0.000 description 8
239000000243 solution Substances 0.000 description 8
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
239000011541 reaction mixture Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
239000000969 carrier Substances 0.000 description 5
CZHYKKAKFWLGJO-UHFFFAOYSA-N dimethyl phosphite Chemical compound COP([O-])OC CZHYKKAKFWLGJO-UHFFFAOYSA-N 0.000 description 5
238000010410 dusting Methods 0.000 description 5
239000004495 emulsifiable concentrate Substances 0.000 description 4
239000000839 emulsion Substances 0.000 description 4
239000000843 powder Substances 0.000 description 4
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
241000233866 Fungi Species 0.000 description 3
239000000654 additive Substances 0.000 description 3
238000006243 chemical reaction Methods 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
238000002329 infrared spectrum Methods 0.000 description 3
239000003960 organic solvent Substances 0.000 description 3
239000004094 surface-active agent Substances 0.000 description 3
HYEOYFUOERFWIX-UHFFFAOYSA-N 3-(7-methyloctoxy)propan-1-amine Chemical compound CC(C)CCCCCCOCCCN HYEOYFUOERFWIX-UHFFFAOYSA-N 0.000 description 2
LPUBRQWGZPPVBS-UHFFFAOYSA-N 3-butoxypropan-1-amine Chemical compound CCCCOCCCN LPUBRQWGZPPVBS-UHFFFAOYSA-N 0.000 description 2
YIBAAOIJLRPJMA-UHFFFAOYSA-N 3-butoxypropylazanium;methyl-dioxido-oxo-$l^{5}-phosphane Chemical compound CP([O-])([O-])=O.CCCCOCCC[NH3+].CCCCOCCC[NH3+] YIBAAOIJLRPJMA-UHFFFAOYSA-N 0.000 description 2
SOYBEXQHNURCGE-UHFFFAOYSA-N 3-ethoxypropan-1-amine Chemical compound CCOCCCN SOYBEXQHNURCGE-UHFFFAOYSA-N 0.000 description 2
FAXDZWQIWUSWJH-UHFFFAOYSA-N 3-methoxypropan-1-amine Chemical compound COCCCN FAXDZWQIWUSWJH-UHFFFAOYSA-N 0.000 description 2
SPMGVKMIRAGRFM-UHFFFAOYSA-N 3-methoxypropylazanium;methyl-dioxido-oxo-$l^{5}-phosphane Chemical compound CP([O-])([O-])=O.COCCC[NH3+].COCCC[NH3+] SPMGVKMIRAGRFM-UHFFFAOYSA-N 0.000 description 2
241000123650 Botrytis cinerea Species 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
241000196324 Embryophyta Species 0.000 description 2
241000223221 Fusarium oxysporum Species 0.000 description 2
XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 2
NISGSNTVMOOSJQ-UHFFFAOYSA-N cyclopentanamine Chemical compound NC1CCCC1 NISGSNTVMOOSJQ-UHFFFAOYSA-N 0.000 description 2
239000006185 dispersion Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
SCJQAOKATBDLSS-UHFFFAOYSA-N ethyl-dioxido-oxo-$l^{5}-phosphane;3-methoxypropylazanium Chemical compound CCP([O-])([O-])=O.COCCC[NH3+].COCCC[NH3+] SCJQAOKATBDLSS-UHFFFAOYSA-N 0.000 description 2
ZQPIYLASEDWLQU-UHFFFAOYSA-N ethyl-dioxido-oxo-$l^{5}-phosphane;octadecylazanium Chemical compound CCP([O-])([O-])=O.CCCCCCCCCCCCCCCCCC[NH3+].CCCCCCCCCCCCCCCCCC[NH3+] ZQPIYLASEDWLQU-UHFFFAOYSA-N 0.000 description 2
239000001963 growth medium Substances 0.000 description 2
239000007788 liquid Substances 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
238000002156 mixing Methods 0.000 description 2
UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 2
239000000376 reactant Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
239000007921 spray Substances 0.000 description 2
239000003381 stabilizer Substances 0.000 description 2
239000000725 suspension Substances 0.000 description 2
239000001993 wax Substances 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 description 1
FJLUATLTXUNBOT-UHFFFAOYSA-N 1-Hexadecylamine Chemical compound CCCCCCCCCCCCCCCCN FJLUATLTXUNBOT-UHFFFAOYSA-N 0.000 description 1
IKYFHRVPKIFGMH-UHFFFAOYSA-N 1-phenoxypropan-2-amine Chemical compound CC(N)COC1=CC=CC=C1 IKYFHRVPKIFGMH-UHFFFAOYSA-N 0.000 description 1
XSBBUUWRWUJLAZ-UHFFFAOYSA-N 1h-benzimidazol-2-ylazanium;ethyl-dioxido-oxo-$l^{5}-phosphane Chemical compound CCP([O-])([O-])=O.C1=CC=C2NC([NH3+])=NC2=C1.C1=CC=C2NC([NH3+])=NC2=C1 XSBBUUWRWUJLAZ-UHFFFAOYSA-N 0.000 description 1
JWYUFVNJZUSCSM-UHFFFAOYSA-N 2-aminobenzimidazole Chemical compound C1=CC=C2NC(N)=NC2=C1 JWYUFVNJZUSCSM-UHFFFAOYSA-N 0.000 description 1
SDYWXFYBZPNOFX-UHFFFAOYSA-N 3,4-dichloroaniline Chemical compound NC1=CC=C(Cl)C(Cl)=C1 SDYWXFYBZPNOFX-UHFFFAOYSA-N 0.000 description 1
NRRSAAQRPDGNPF-UHFFFAOYSA-N 3,4-dichloroaniline;hydrobromide Chemical compound Br.NC1=CC=C(Cl)C(Cl)=C1 NRRSAAQRPDGNPF-UHFFFAOYSA-N 0.000 description 1
VAUOTPOMXGBOAL-UHFFFAOYSA-N 3-butoxypropylazanium;ethyl-dioxido-oxo-$l^{5}-phosphane Chemical compound CCP([O-])([O-])=O.CCCCOCCC[NH3+].CCCCOCCC[NH3+] VAUOTPOMXGBOAL-UHFFFAOYSA-N 0.000 description 1
YGZASYADRSPBDS-UHFFFAOYSA-N 3-ethoxypropylazanium;methyl-dioxido-oxo-$l^{5}-phosphane Chemical compound CP([O-])([O-])=O.CCOCCC[NH3+].CCOCCC[NH3+] YGZASYADRSPBDS-UHFFFAOYSA-N 0.000 description 1
229920001817 Agar Polymers 0.000 description 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
KPCSDOJEZUFIOH-UHFFFAOYSA-N COP([O-])=O.CC(C)CCCCCCOCCC[NH3+] Chemical compound COP([O-])=O.CC(C)CCCCCCOCCC[NH3+] KPCSDOJEZUFIOH-UHFFFAOYSA-N 0.000 description 1
RIMFKAPKOXCQLB-UHFFFAOYSA-N CP([O-])([O-])=O.C(CCCCCC(C)C)OCCC[NH3+].C(CCCCCC(C)C)OCCC[NH3+] Chemical compound CP([O-])([O-])=O.C(CCCCCC(C)C)OCCC[NH3+].C(CCCCCC(C)C)OCCC[NH3+] RIMFKAPKOXCQLB-UHFFFAOYSA-N 0.000 description 1
OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical compound [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 description 1
JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
239000005977 Ethylene Substances 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 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 description 1
FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
MKYBYDHXWVHEJW-UHFFFAOYSA-N N-[1-oxo-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propan-2-yl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(C(C)NC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 MKYBYDHXWVHEJW-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
REYJJPSVUYRZGE-UHFFFAOYSA-N Octadecylamine Chemical compound CCCCCCCCCCCCCCCCCCN REYJJPSVUYRZGE-UHFFFAOYSA-N 0.000 description 1
BPQQTUXANYXVAA-UHFFFAOYSA-N Orthosilicate Chemical compound [O-][Si]([O-])([O-])[O-] BPQQTUXANYXVAA-UHFFFAOYSA-N 0.000 description 1
BYPQCJNFGBCJKT-UHFFFAOYSA-N P(OCC)([O-])=O.C(CCCCCCCCCCCCC)[NH3+] Chemical compound P(OCC)([O-])=O.C(CCCCCCCCCCCCC)[NH3+] BYPQCJNFGBCJKT-UHFFFAOYSA-N 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
PLZVEHJLHYMBBY-UHFFFAOYSA-N Tetradecylamine Chemical compound CCCCCCCCCCCCCCN PLZVEHJLHYMBBY-UHFFFAOYSA-N 0.000 description 1
XSTXAVWGXDQKEL-UHFFFAOYSA-N Trichloroethylene Chemical group ClC=C(Cl)Cl XSTXAVWGXDQKEL-UHFFFAOYSA-N 0.000 description 1
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
DDBLMSMQONIGCJ-UHFFFAOYSA-L [Ca+2].P(OCCCCCCCC)([O-])=O.C(CCCCCCC)OP([O-])=O Chemical compound [Ca+2].P(OCCCCCCCC)([O-])=O.C(CCCCCCC)OP([O-])=O DDBLMSMQONIGCJ-UHFFFAOYSA-L 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
239000008272 agar Substances 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
229910052784 alkaline earth metal Inorganic materials 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
239000004411 aluminium Substances 0.000 description 1
229910052782 aluminium Inorganic materials 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
239000012736 aqueous medium Substances 0.000 description 1
239000012431 aqueous reaction media Substances 0.000 description 1
229910052788 barium Inorganic materials 0.000 description 1
DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 description 1
239000011575 calcium Substances 0.000 description 1
229910052791 calcium Inorganic materials 0.000 description 1
OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
239000004927 clay Substances 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
239000013078 crystal Substances 0.000 description 1
239000002178 crystalline material Substances 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
239000008121 dextrose Substances 0.000 description 1
125000004663 dialkyl amino group Chemical group 0.000 description 1
HCSGFPOIAYPFIU-UHFFFAOYSA-N diazanium ethyl-dioxido-oxo-lambda5-phosphane Chemical compound [NH4+].C(C)P([O-])([O-])=O.[NH4+] HCSGFPOIAYPFIU-UHFFFAOYSA-N 0.000 description 1
DTOMFYCTRINWHW-UHFFFAOYSA-N diazanium;methyl phosphate Chemical compound [NH4+].[NH4+].COP([O-])([O-])=O DTOMFYCTRINWHW-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
HPWDQZDPFDFAHA-UHFFFAOYSA-N ethyl-dioxido-oxo-$l^{5}-phosphane;1-phenoxypropan-2-ylazanium Chemical compound CCP([O-])([O-])=O.CC([NH3+])COC1=CC=CC=C1.CC([NH3+])COC1=CC=CC=C1 HPWDQZDPFDFAHA-UHFFFAOYSA-N 0.000 description 1
DKUDFVUOATZKQO-UHFFFAOYSA-N ethyl-dioxido-oxo-$l^{5}-phosphane;3-(7-methyloctoxy)propylazanium Chemical compound CCP([O-])([O-])=O.CC(C)CCCCCCOCCC[NH3+].CC(C)CCCCCCOCCC[NH3+] DKUDFVUOATZKQO-UHFFFAOYSA-N 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
150000002222 fluorine compounds Chemical class 0.000 description 1
DDRPCXLAQZKBJP-UHFFFAOYSA-N furfurylamine Chemical compound NCC1=CC=CO1 DDRPCXLAQZKBJP-UHFFFAOYSA-N 0.000 description 1
239000007789 gas Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
125000002768 hydroxyalkyl group Chemical group 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
239000011777 magnesium Substances 0.000 description 1
229910052749 magnesium Inorganic materials 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
239000000463 material Substances 0.000 description 1
239000008268 mayonnaise Substances 0.000 description 1
235000010746 mayonnaise Nutrition 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
229910052759 nickel Inorganic materials 0.000 description 1
239000002736 nonionic surfactant Substances 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000012430 organic reaction media Substances 0.000 description 1
DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
230000001737 promoting effect Effects 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000002689 soil Substances 0.000 description 1
238000001179 sorption measurement Methods 0.000 description 1
239000000126 substance Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-N sulfonic acid Chemical class OS(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-N 0.000 description 1
229920002994 synthetic fiber Polymers 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
239000013008 thixotropic agent Substances 0.000 description 1
UBOXGVDOUJQMTN-UHFFFAOYSA-N trichloroethylene Natural products ClCC(Cl)Cl UBOXGVDOUJQMTN-UHFFFAOYSA-N 0.000 description 1
238000005292 vacuum distillation Methods 0.000 description 1
239000004552 water soluble powder Substances 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000008096 xylene Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/141—Esters of phosphorous acids
- C07F9/142—Esters of phosphorous acids with hydroxyalkyl compounds without further substituents on alkyl
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/12—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing acyclic or cycloaliphatic radicals
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/10—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
- A01N57/14—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing aromatic radicals
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/08—Esters of oxyacids of phosphorus
- C07F9/141—Esters of phosphorous acids

Landscapes

Life Sciences & Earth Sciences (AREA)
Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Pest Control & Pesticides (AREA)
Molecular Biology (AREA)
Agronomy & Crop Science (AREA)
Biochemistry (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

NO812901A 1980-08-27 1981-08-26 Nye fosforsyremonoestersalter og fungicide preparater inneholdende samme. NO812901L (no)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
HU802119A HU184319B (en)	1980-08-27	1980-08-27	Fungicide compositions salts of phosphonoic acid-monoesters and process for producing the active agents

Publications (1)

Publication Number	Publication Date
NO812901L true NO812901L (no)	1982-03-01

Family

ID=10957849

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO812901A NO812901L (no)	1980-08-27	1981-08-26	Nye fosforsyremonoestersalter og fungicide preparater inneholdende samme.

Country Status (29)

Country	Link
US (2)	US4661477A (it)
JP (1)	JPS5772994A (it)
AR (1)	AR230065A1 (it)
AT (1)	AT377161B (it)
AU (1)	AU541337B2 (it)
BE (1)	BE890114A (it)
BG (3)	BG36787A3 (it)
BR (1)	BR8105490A (it)
CA (1)	CA1255323A (it)
CH (1)	CH649076A5 (it)
CS (1)	CS232717B2 (it)
DD (2)	DD210692A5 (it)
DE (1)	DE3133190C2 (it)
DK (1)	DK379481A (it)
ES (2)	ES505472A0 (it)
FI (1)	FI812637L (it)
FR (1)	FR2489332B1 (it)
GR (1)	GR75320B (it)
HU (1)	HU184319B (it)
IT (1)	IT1200581B (it)
LU (1)	LU83584A1 (it)
NL (1)	NL8103968A (it)
NO (1)	NO812901L (it)
NZ (1)	NZ198178A (it)
PT (1)	PT73578B (it)
RO (2)	RO92074B (it)
SE (1)	SE447533B (it)
SU (2)	SU1524799A3 (it)
YU (1)	YU48450B (it)

Families Citing this family (23)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4935232A (en) *	1983-08-16	1990-06-19	Interface Research Corporation	Microbiocidal composition and method of preparation thereof
US5474739A (en) *	1978-02-04	1995-12-12	Interface, Inc.	Microbiocidal composition
US5133933A (en) *	1983-08-16	1992-07-28	Interface Research Corporation	Microbiocidal preservative
SE446595B (sv) *	1982-11-19	1986-09-29	Chemmar Associates Inc	Sjelvdesinfekterande matta med ett alkylfosfat inforlivat i baksidesbeleggningen
US5032310A (en) *	1983-08-16	1991-07-16	Interface, Inc.	Microbiocidal cleansing and disinfecting formulations and preparation thereof
US4908209A (en) *	1983-08-16	1990-03-13	Interface, Inc.	Biocidal delivery system of phosphate ester and method of preparation thereof
HU193701B (en) *	1984-09-21	1987-11-30	Borsodi Vegyi Komb	Seed dressing compound containing as active substance 3-isononil-oxi-propil-ammonium-methil-phosphonate
HU192890B (en) *	1984-09-21	1987-07-28	Borsodi Vegyi Komb	Plant growth regulating composition containing 3-iso-nonyl-oxy-propyl-ammonium-methyl-phosphonate as active ingredient
HU197492B (en) *	1985-12-28	1989-04-28	Borsodi Vegyi Komb	Process for production of composition regulating the growth of plants
KR910005713B1 (ko) *	1987-08-03	1991-08-02	인터페이스 리서취 코포레이션	살균성 세척 또는 소독제제 및 그의 제법
US5453275A (en)	1988-05-05	1995-09-26	Interface, Inc.	Biocidal polymeric coating for heat exchanger coils
US4957948A (en) *	1988-05-05	1990-09-18	Interface, Inc.	Biocidal protective coating for heat exchanger coils
AU733912B2 (en) *	1997-05-30	2001-05-31	Monsanto Company	Process and compositions promoting biological effectiveness of exogenous chemical substances in plants
CN1267189A (zh) *	1997-06-27	2000-09-20	孟山都公司	促进外源化学物质在植物中生物有效性的方法和组合物
DE69904444T2 (de) *	1998-02-20	2003-07-10	Aventis Cropscience Uk Ltd., Hauxton	Fungizide
BR9915788A (pt) *	1998-11-30	2001-08-21	Monsanto Co	Processo e composições que promovem eficiência biológica de subst ncias quìmicas exógenas em plantas
US6838186B2 (en)	2002-04-22	2005-01-04	Polinas Plastic Of America, Inc.	Multilayer oriented antimicrobial and antifogging films
US8197832B2 (en) *	2002-12-04	2012-06-12	Mitsui Chemicals Agro, Inc.	Methods and compositions for inhibiting mycotoxin contamination in cereals
WO2005000021A2 (en) *	2003-06-23	2005-01-06	Quest Products Corporation	Fungicidal composition for through periderm bark application to woody plants
US8475289B2 (en) *	2004-06-07	2013-07-02	Acushnet Company	Launch monitor
US7947631B2 (en) *	2008-06-24	2011-05-24	Brine-Add Fluids Ltd.	Gelled hydrocarbons for oilfield processes and methods of use
US9474282B2 (en)	2013-12-13	2016-10-25	Tony John Hall	Acid-solubilized copper-ammonium complexes and copper-zinc-ammonium complexes, compositions, preparations, methods, and uses
RU2742057C2 (ru)	2015-06-08	2021-02-02	Мико Сайенсес Лимитед	Антимикробные и агрохимические композиции

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2824113A (en) *	1953-04-06	1958-02-18	Atlas Powder Co	Quaternary ammonium phosphites
US3354166A (en) *	1964-09-28	1967-11-21	Monsanto Res Corp	Nu-substituted ammonium salts of monoesterified phosphonic acids
GB1302894A (it) *	1969-02-09	1973-01-10
FR2254276B1 (it) *	1973-12-14	1977-03-04	Philagro Sa
FR2288463A2 (fr) *	1974-10-23	1976-05-21	Philagro Sa	Compositions fongicides a base d'esters phosphoriques
US4126678A (en) *	1974-08-10	1978-11-21	Philagro S.A.	Phosphite-based fungicide compositions
FR2380286A1 (fr) *	1977-02-14	1978-09-08	Philagro Sa	Nouveaux derives de phosphites d'hydrazinium

1980
- 1980-08-27 HU HU802119A patent/HU184319B/hu not_active IP Right Cessation
1981
- 1981-08-21 DE DE3133190A patent/DE3133190C2/de not_active Expired
- 1981-08-24 FR FR8116156A patent/FR2489332B1/fr not_active Expired
- 1981-08-25 AT AT0370081A patent/AT377161B/de not_active IP Right Cessation
- 1981-08-25 YU YU205981A patent/YU48450B/sh unknown
- 1981-08-25 SE SE8105046A patent/SE447533B/sv not_active IP Right Cessation
- 1981-08-26 SU SU813338954A patent/SU1524799A3/ru active
- 1981-08-26 IT IT23652/81A patent/IT1200581B/it active
- 1981-08-26 CS CS816359A patent/CS232717B2/cs unknown
- 1981-08-26 DD DD81245544A patent/DD210692A5/de unknown
- 1981-08-26 AU AU74635/81A patent/AU541337B2/en not_active Ceased
- 1981-08-26 CA CA000384640A patent/CA1255323A/en not_active Expired
- 1981-08-26 NO NO812901A patent/NO812901L/no unknown
- 1981-08-26 FI FI812637A patent/FI812637L/fi not_active Application Discontinuation
- 1981-08-26 NL NL8103968A patent/NL8103968A/nl not_active Application Discontinuation
- 1981-08-26 BG BG053394A patent/BG36787A3/xx unknown
- 1981-08-26 BG BG059257A patent/BG37521A3/xx unknown
- 1981-08-26 BG BG059258A patent/BG37528A3/xx unknown
- 1981-08-26 GR GR65873A patent/GR75320B/el unknown
- 1981-08-26 RO RO113342A patent/RO92074B/ro unknown
- 1981-08-26 DD DD81232815A patent/DD201970A5/de unknown
- 1981-08-26 CH CH5510/81A patent/CH649076A5/de not_active IP Right Cessation
- 1981-08-26 RO RO105173A patent/RO83311B/ro unknown
- 1981-08-26 LU LU83584A patent/LU83584A1/fr unknown
- 1981-08-26 DK DK379481A patent/DK379481A/da not_active Application Discontinuation
- 1981-08-26 NZ NZ198178A patent/NZ198178A/en unknown
- 1981-08-27 JP JP56133423A patent/JPS5772994A/ja active Granted
- 1981-08-27 ES ES505472A patent/ES505472A0/es active Granted
- 1981-08-27 BR BR8105490A patent/BR8105490A/pt not_active IP Right Cessation
- 1981-08-27 BE BE0/205788A patent/BE890114A/fr not_active IP Right Cessation
- 1981-08-27 PT PT73578A patent/PT73578B/pt unknown
- 1981-08-27 AR AR286571A patent/AR230065A1/es active
1982
- 1982-04-01 SU SU823440451A patent/SU1273363A1/ru active
- 1982-08-16 ES ES515019A patent/ES8401089A1/es not_active Expired
- 1982-09-29 US US06/426,949 patent/US4661477A/en not_active Expired - Fee Related
1986
- 1986-07-18 US US06/888,267 patent/US4675431A/en not_active Expired - Fee Related

Also Published As

Publication number	Publication date
PT73578B (en)	1982-11-10
LU83584A1 (fr)	1981-12-01
DE3133190A1 (de)	1982-06-24
FR2489332B1 (fr)	1986-09-05
IT1200581B (it)	1989-01-27
YU205981A (en)	1983-12-31
AU7463581A (en)	1982-03-04
NL8103968A (nl)	1982-03-16
RO83311A (ro)	1984-04-02
DK379481A (da)	1982-02-28
SU1524799A3 (ru)	1989-11-23
SE8105046L (sv)	1982-02-28
RO83311B (ro)	1984-04-30
DD210692A5 (de)	1984-06-20
SE447533B (sv)	1986-11-24
CS232717B2 (en)	1985-02-14
JPS5772994A (en)	1982-05-07
NZ198178A (en)	1985-05-31
YU48450B (sh)	1998-07-10
BE890114A (fr)	1982-03-01
JPH0314040B2 (it)	1991-02-25
RO92074A (ro)	1987-07-30
AR230065A1 (es)	1984-02-29
DD201970A5 (de)	1983-08-24
SU1273363A1 (ru)	1986-11-30
ES515019A0 (es)	1983-12-16
ATA370081A (de)	1984-07-15
CH649076A5 (de)	1985-04-30
ES8302012A1 (es)	1983-01-01
BG37528A3 (en)	1985-06-14
ES505472A0 (es)	1983-01-01
CS635981A2 (en)	1984-06-18
ES8401089A1 (es)	1983-12-16
AT377161B (de)	1985-02-25
PT73578A (en)	1981-09-01
BG37521A3 (en)	1985-06-14
IT8123652A0 (it)	1981-08-26
HU184319B (en)	1984-08-28
FI812637L (fi)	1982-02-28
US4661477A (en)	1987-04-28
RO92074B (ro)	1987-07-31
GR75320B (it)	1984-07-13
DE3133190C2 (de)	1985-04-18
FR2489332A1 (fr)	1982-03-05
US4675431A (en)	1987-06-23
AU541337B2 (en)	1985-01-03
BR8105490A (pt)	1982-05-11
BG36787A3 (en)	1985-01-15
CA1255323A (en)	1989-06-06

Publication	Publication Date	Title
NO812901L (no)	1982-03-01	Nye fosforsyremonoestersalter og fungicide preparater inneholdende samme.
US4139616A (en)	1979-02-13	Fungicidal compositions based on phosphorous acid esters and salts thereof
US4542023A (en)	1985-09-17	Fungicidal salts of organophosphorus derivatives
BG98637A (en)	1995-01-31	Triasolopyrimidine derivatives
EP0013581B1 (en)	1982-11-24	Tetrahydrofuran derivatives, a process for their preparation, herbicidal compositions containing them and a method of controlling undesired plant growth using them
IL43840A (en)	1977-03-31	Derivatives of 2-substituted 1,3,4-oxadiazole-5-thiol and fungicidal compositions containing them
US4382928A (en)	1983-05-10	Fungicidal compositions
EP0300574B1 (en)	1994-02-02	Phosphonium salts
US4049801A (en)	1977-09-20	Phosphite compounds as fungicidal agents
US3968208A (en)	1976-07-06	Fungicidal compositions
CS241143B2 (en)	1986-03-13	Fungicide
US4851396A (en)	1989-07-25	Fungicidal compositions based on nicotinic acid derivatives, new nicotinic acid derivatives and preparation thereof
JPH0678332B2 (ja)	1994-10-05	ジフエニルエ−テル除草剤
EP0254364B1 (en)	1991-09-11	Imidazole derivative
EP0240047B1 (en)	1991-01-02	Fungicides
EP0264988B1 (en)	1990-06-20	Fungicidal compositions
AU612162B2 (en)	1991-07-04	Phosphonium salts
GB2095114A (en)	1982-09-29	Antifungal compositions based on phosphorous acid derivatives, and their application to the protection of plants
SU736858A3 (ru)	1980-05-25	Фунгицидное средство
EP0152131B1 (en)	1989-08-23	Carboxamide derivatives, their preparation and their use as fungicides
EP0002842A1 (en)	1979-07-11	Propanthioic acid derivatives, herbicidal and/or plant growth regulating compositions comprising these derivatives and method of destroying or preventing undesirable plant growth
US4188381A (en)	1980-02-12	Fungicides hydrazinium phosphites
US4163782A (en)	1979-08-07	Fungicidal compositions containing disubstituted phosphonates
EP0007684B1 (en)	1983-09-07	Oxazolidinone phosphonates and their use as herbicides
GB2203739A (en)	1988-10-26	Herbicidal tetrazoles