CA1318495C - Evaporation inhibitor - Google Patents
Evaporation inhibitorInfo
- Publication number
- CA1318495C CA1318495C CA000494746A CA494746A CA1318495C CA 1318495 C CA1318495 C CA 1318495C CA 000494746 A CA000494746 A CA 000494746A CA 494746 A CA494746 A CA 494746A CA 1318495 C CA1318495 C CA 1318495C
- Authority
- CA
- Canada
- Prior art keywords
- weight
- wax
- composition
- mixture
- accordance
- 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 - Fee Related
Links
- 238000001704 evaporation Methods 0.000 title claims abstract description 61
- 230000008020 evaporation Effects 0.000 title claims abstract description 61
- 239000003112 inhibitor Substances 0.000 title claims abstract description 55
- 239000000203 mixture Substances 0.000 claims abstract description 171
- 239000001993 wax Substances 0.000 claims abstract description 88
- 239000012188 paraffin wax Substances 0.000 claims abstract description 74
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 64
- 239000007921 spray Substances 0.000 claims abstract description 45
- 150000002148 esters Chemical class 0.000 claims abstract description 24
- 238000000034 method Methods 0.000 claims abstract description 22
- 239000003960 organic solvent Substances 0.000 claims abstract description 19
- 238000009835 boiling Methods 0.000 claims abstract description 18
- 229930195733 hydrocarbon Natural products 0.000 claims abstract description 15
- 150000002430 hydrocarbons Chemical class 0.000 claims abstract description 15
- 239000012875 nonionic emulsifier Substances 0.000 claims abstract description 15
- 239000012874 anionic emulsifier Substances 0.000 claims abstract description 12
- 150000002576 ketones Chemical class 0.000 claims abstract description 12
- 239000003905 agrochemical Substances 0.000 claims abstract description 11
- 150000001412 amines Chemical class 0.000 claims abstract description 8
- 150000008044 alkali metal hydroxides Chemical class 0.000 claims abstract description 6
- 235000019271 petrolatum Nutrition 0.000 claims description 66
- 235000019809 paraffin wax Nutrition 0.000 claims description 62
- -1 olefin sulfonate Chemical class 0.000 claims description 46
- 150000002191 fatty alcohols Chemical class 0.000 claims description 37
- 239000002253 acid Substances 0.000 claims description 28
- 239000003995 emulsifying agent Substances 0.000 claims description 27
- 125000004432 carbon atom Chemical group C* 0.000 claims description 26
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 22
- 150000003839 salts Chemical class 0.000 claims description 21
- 125000000217 alkyl group Chemical group 0.000 claims description 15
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 14
- 239000008096 xylene Substances 0.000 claims description 14
- 239000002736 nonionic surfactant Substances 0.000 claims description 12
- 239000010695 polyglycol Substances 0.000 claims description 12
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 11
- 239000000194 fatty acid Substances 0.000 claims description 11
- 229930195729 fatty acid Natural products 0.000 claims description 11
- 239000003752 hydrotrope Substances 0.000 claims description 11
- 229920000151 polyglycol Polymers 0.000 claims description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 10
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 10
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 10
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 claims description 10
- 235000013873 oxidized polyethylene wax Nutrition 0.000 claims description 10
- 150000001346 alkyl aryl ethers Chemical class 0.000 claims description 9
- 150000004665 fatty acids Chemical class 0.000 claims description 8
- 239000004209 oxidized polyethylene wax Substances 0.000 claims description 8
- 238000005507 spraying Methods 0.000 claims description 8
- 229910017053 inorganic salt Inorganic materials 0.000 claims description 7
- 239000004200 microcrystalline wax Substances 0.000 claims description 7
- 230000036961 partial effect Effects 0.000 claims description 7
- 239000003208 petroleum Substances 0.000 claims description 7
- QUCDWLYKDRVKMI-UHFFFAOYSA-M sodium;3,4-dimethylbenzenesulfonate Chemical compound [Na+].CC1=CC=C(S([O-])(=O)=O)C=C1C QUCDWLYKDRVKMI-UHFFFAOYSA-M 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 claims description 7
- 235000019808 microcrystalline wax Nutrition 0.000 claims description 6
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims description 5
- 239000006260 foam Substances 0.000 claims description 5
- 229930182470 glycoside Natural products 0.000 claims description 5
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 claims description 4
- 150000001298 alcohols Chemical class 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 4
- 239000003755 preservative agent Substances 0.000 claims description 4
- 230000002335 preservative effect Effects 0.000 claims description 4
- 238000011282 treatment Methods 0.000 claims description 4
- 239000004480 active ingredient Substances 0.000 claims description 3
- 150000003138 primary alcohols Chemical class 0.000 claims description 3
- 238000002156 mixing Methods 0.000 claims description 2
- 150000003871 sulfonates Chemical class 0.000 claims description 2
- 239000003945 anionic surfactant Substances 0.000 claims 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 6
- 229910052799 carbon Inorganic materials 0.000 claims 5
- 150000001735 carboxylic acids Chemical class 0.000 claims 5
- 239000004215 Carbon black (E152) Substances 0.000 claims 3
- RZXLPPRPEOUENN-UHFFFAOYSA-N Chlorfenson Chemical compound C1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=C(Cl)C=C1 RZXLPPRPEOUENN-UHFFFAOYSA-N 0.000 claims 3
- 239000000375 suspending agent Substances 0.000 claims 3
- 239000006185 dispersion Substances 0.000 abstract description 21
- 238000012360 testing method Methods 0.000 description 24
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 21
- 239000003760 tallow Substances 0.000 description 21
- 239000012141 concentrate Substances 0.000 description 17
- 235000008504 concentrate Nutrition 0.000 description 15
- 241000196324 Embryophyta Species 0.000 description 11
- 229940056211 paraffin Drugs 0.000 description 11
- 239000002917 insecticide Substances 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 8
- 239000000470 constituent Substances 0.000 description 8
- 239000000047 product Substances 0.000 description 7
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 6
- 229940043237 diethanolamine Drugs 0.000 description 6
- 239000000843 powder Substances 0.000 description 6
- 239000011814 protection agent Substances 0.000 description 6
- 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 5
- 125000000129 anionic group Chemical group 0.000 description 5
- 239000011734 sodium Substances 0.000 description 5
- 239000004264 Petrolatum Substances 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 description 4
- 239000003240 coconut oil Substances 0.000 description 4
- 235000019864 coconut oil Nutrition 0.000 description 4
- 239000008367 deionised water Substances 0.000 description 4
- 229910021641 deionized water Inorganic materials 0.000 description 4
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 description 4
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 description 4
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- RDYMFSUJUZBWLH-UHFFFAOYSA-N endosulfan Chemical compound C12COS(=O)OCC2C2(Cl)C(Cl)=C(Cl)C1(Cl)C2(Cl)Cl RDYMFSUJUZBWLH-UHFFFAOYSA-N 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- BACHBFVBHLGWSL-UHFFFAOYSA-N methyl 2-[4-(2,4-dichlorophenoxy)phenoxy]propanoate Chemical group C1=CC(OC(C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-UHFFFAOYSA-N 0.000 description 4
- 229940055577 oleyl alcohol Drugs 0.000 description 4
- XMLQWXUVTXCDDL-UHFFFAOYSA-N oleyl alcohol Natural products CCCCCCC=CCCCCCCCCCCO XMLQWXUVTXCDDL-UHFFFAOYSA-N 0.000 description 4
- 229940066842 petrolatum Drugs 0.000 description 4
- JOOMJVFZQRQWKR-UHFFFAOYSA-N pyrazophos Chemical compound N1=C(C)C(C(=O)OCC)=CN2N=C(OP(=S)(OCC)OCC)C=C21 JOOMJVFZQRQWKR-UHFFFAOYSA-N 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 4
- ALSTYHKOOCGGFT-KTKRTIGZSA-N (9Z)-octadecen-1-ol Chemical compound CCCCCCCC\C=C/CCCCCCCCO ALSTYHKOOCGGFT-KTKRTIGZSA-N 0.000 description 3
- 239000004698 Polyethylene Substances 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 239000000417 fungicide Substances 0.000 description 3
- GBAWQJNHVWMTLU-UHFFFAOYSA-N heptenophos Chemical compound C1=CCC2C(OP(=O)(OC)OC)=C(Cl)C21 GBAWQJNHVWMTLU-UHFFFAOYSA-N 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 229920000573 polyethylene Polymers 0.000 description 3
- 229940079842 sodium cumenesulfonate Drugs 0.000 description 3
- RPACBEVZENYWOL-XFULWGLBSA-M sodium;(2r)-2-[6-(4-chlorophenoxy)hexyl]oxirane-2-carboxylate Chemical compound [Na+].C=1C=C(Cl)C=CC=1OCCCCCC[C@]1(C(=O)[O-])CO1 RPACBEVZENYWOL-XFULWGLBSA-M 0.000 description 3
- QEKATQBVVAZOAY-UHFFFAOYSA-M sodium;4-propan-2-ylbenzenesulfonate Chemical compound [Na+].CC(C)C1=CC=C(S([O-])(=O)=O)C=C1 QEKATQBVVAZOAY-UHFFFAOYSA-M 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 2
- 229920000742 Cotton Polymers 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 241000219146 Gossypium Species 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- GBAWQJNHVWMTLU-RQJHMYQMSA-N [(1R,5S)-7-chloro-6-bicyclo[3.2.0]hepta-2,6-dienyl] dimethyl phosphate Chemical compound C1=CC[C@@H]2C(OP(=O)(OC)OC)=C(Cl)[C@@H]21 GBAWQJNHVWMTLU-RQJHMYQMSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical compound C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 2
- 230000005764 inhibitory process Effects 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 239000003595 mist Substances 0.000 description 2
- 239000002674 ointment Substances 0.000 description 2
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
- 239000010452 phosphate Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- BACHBFVBHLGWSL-JTQLQIEISA-N rac-diclofop methyl Natural products C1=CC(O[C@@H](C)C(=O)OC)=CC=C1OC1=CC=C(Cl)C=C1Cl BACHBFVBHLGWSL-JTQLQIEISA-N 0.000 description 2
- HEMHJVSKTPXQMS-UHFFFAOYSA-M sodium hydroxide Inorganic materials [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- SMYMJHWAQXWPDB-UHFFFAOYSA-N (2,4,5-trichlorophenoxy)acetic acid Chemical compound OC(=O)COC1=CC(Cl)=C(Cl)C=C1Cl SMYMJHWAQXWPDB-UHFFFAOYSA-N 0.000 description 1
- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 1
- WURBVZBTWMNKQT-UHFFFAOYSA-N 1-(4-chlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=NC=NN1C(C(=O)C(C)(C)C)OC1=CC=C(Cl)C=C1 WURBVZBTWMNKQT-UHFFFAOYSA-N 0.000 description 1
- YNEKMCSWRMRXIR-UHFFFAOYSA-N 2,3,5,5-tetrachloro-4,7-bis(chloromethyl)-7-(dichloromethyl)bicyclo[2.2.1]heptane Chemical compound C1C(Cl)(Cl)C2(CCl)C(Cl)C(Cl)C1C2(C(Cl)Cl)CCl YNEKMCSWRMRXIR-UHFFFAOYSA-N 0.000 description 1
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 1
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 1
- MZHCENGPTKEIGP-UHFFFAOYSA-N 2-(2,4-dichlorophenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1Cl MZHCENGPTKEIGP-UHFFFAOYSA-N 0.000 description 1
- WNTGYJSOUMFZEP-UHFFFAOYSA-N 2-(4-chloro-2-methylphenoxy)propanoic acid Chemical compound OC(=O)C(C)OC1=CC=C(Cl)C=C1C WNTGYJSOUMFZEP-UHFFFAOYSA-N 0.000 description 1
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 1
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 description 1
- MIJLZGZLQLAQCM-UHFFFAOYSA-N 2-ethoxyethyl 2-(4-{[3-chloro-5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoate Chemical group C1=CC(OC(C)C(=O)OCCOCC)=CC=C1OC1=NC=C(C(F)(F)F)C=C1Cl MIJLZGZLQLAQCM-UHFFFAOYSA-N 0.000 description 1
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical class OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 description 1
- ZRDUSMYWDRPZRM-UHFFFAOYSA-N 2-sec-butyl-4,6-dinitrophenyl 3-methylbut-2-enoate Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1OC(=O)C=C(C)C ZRDUSMYWDRPZRM-UHFFFAOYSA-N 0.000 description 1
- UPMXNNIRAGDFEH-UHFFFAOYSA-N 3,5-dibromo-4-hydroxybenzonitrile Chemical compound OC1=C(Br)C=C(C#N)C=C1Br UPMXNNIRAGDFEH-UHFFFAOYSA-N 0.000 description 1
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 1
- DXBQEHHOGRVYFF-UHFFFAOYSA-N 3-pyridin-4-ylpentane-2,4-dione Chemical group CC(=O)C(C(C)=O)C1=CC=NC=C1 DXBQEHHOGRVYFF-UHFFFAOYSA-N 0.000 description 1
- DEXFNLNNUZKHNO-UHFFFAOYSA-N 6-[3-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperidin-1-yl]-3-oxopropyl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1CCN(CC1)C(CCC1=CC2=C(NC(O2)=O)C=C1)=O DEXFNLNNUZKHNO-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- XKJMBINCVNINCA-UHFFFAOYSA-N Alfalone Chemical compound CON(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XKJMBINCVNINCA-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- NXQDBZGWYSEGFL-UHFFFAOYSA-N Anilofos Chemical compound COP(=S)(OC)SCC(=O)N(C(C)C)C1=CC=C(Cl)C=C1 NXQDBZGWYSEGFL-UHFFFAOYSA-N 0.000 description 1
- 241000254177 Anthonomus Species 0.000 description 1
- 239000005476 Bentazone Substances 0.000 description 1
- 239000005489 Bromoxynil Substances 0.000 description 1
- 229920002101 Chitin Polymers 0.000 description 1
- 239000005944 Chlorpyrifos Substances 0.000 description 1
- 239000005496 Chlorsulfuron Substances 0.000 description 1
- 239000005654 Clofentezine Substances 0.000 description 1
- 244000180278 Copernicia prunifera Species 0.000 description 1
- 239000005752 Copper oxychloride Substances 0.000 description 1
- 239000005946 Cypermethrin Substances 0.000 description 1
- 239000005892 Deltamethrin Substances 0.000 description 1
- 239000005503 Desmedipham Substances 0.000 description 1
- MUMQYXACQUZOFP-UHFFFAOYSA-N Dialifor Chemical compound C1=CC=C2C(=O)N(C(CCl)SP(=S)(OCC)OCC)C(=O)C2=C1 MUMQYXACQUZOFP-UHFFFAOYSA-N 0.000 description 1
- IJFPVINAQGWBRJ-UHFFFAOYSA-N Diisooctyl phthalate Chemical compound CC(C)CCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCC(C)C IJFPVINAQGWBRJ-UHFFFAOYSA-N 0.000 description 1
- KKUKTXOBAWVSHC-UHFFFAOYSA-N Dimethylphosphate Chemical compound COP(O)(=O)OC KKUKTXOBAWVSHC-UHFFFAOYSA-N 0.000 description 1
- 239000005510 Diuron Substances 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
- 241001292274 Eumenes Species 0.000 description 1
- PQKBPHSEKWERTG-UHFFFAOYSA-N Fenoxaprop ethyl Chemical group C1=CC(OC(C)C(=O)OCC)=CC=C1OC1=NC2=CC=C(Cl)C=C2O1 PQKBPHSEKWERTG-UHFFFAOYSA-N 0.000 description 1
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- RLBIQVVOMOPOHC-UHFFFAOYSA-N parathion-methyl Chemical group COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C=C1 RLBIQVVOMOPOHC-UHFFFAOYSA-N 0.000 description 1
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 description 1
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- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 description 1
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- 239000003016 pheromone Substances 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
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- LFULEKSKNZEWOE-UHFFFAOYSA-N propanil Chemical compound CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 LFULEKSKNZEWOE-UHFFFAOYSA-N 0.000 description 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
- 150000005599 propionic acid derivatives Chemical class 0.000 description 1
- 230000004224 protection Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 239000012176 shellac wax Substances 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- FZMKKCQHDROFNI-UHFFFAOYSA-N sulfometuron Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 FZMKKCQHDROFNI-UHFFFAOYSA-N 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- JXHJNEJVUNHLKO-UHFFFAOYSA-N sulprofos Chemical compound CCCSP(=S)(OCC)OC1=CC=C(SC)C=C1 JXHJNEJVUNHLKO-UHFFFAOYSA-N 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229940042055 systemic antimycotics triazole derivative Drugs 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
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- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
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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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S47/00—Plant husbandry
- Y10S47/11—The application of protective coatings to plants
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Pest Control & Pesticides (AREA)
- Environmental Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Cosmetics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DEP3441587.4 | 1984-11-14 | ||
DE19843441587 DE3441587A1 (de) | 1984-11-14 | 1984-11-14 | Verdunstungshemmendes zusatzmittel fuer pflanzenschutzmittel-spritzbruehen |
DE19853507380 DE3507380A1 (de) | 1985-03-02 | 1985-03-02 | Verdunstungshemmende mittel |
DEP3507380.2 | 1985-03-02 |
Publications (1)
Publication Number | Publication Date |
---|---|
CA1318495C true CA1318495C (en) | 1993-06-01 |
Family
ID=25826534
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA000494746A Expired - Fee Related CA1318495C (en) | 1984-11-14 | 1985-11-06 | Evaporation inhibitor |
Country Status (24)
Country | Link |
---|---|
EP (1) | EP0185185B1 (OSRAM) |
KR (1) | KR860003776A (OSRAM) |
CN (1) | CN85108159A (OSRAM) |
AR (1) | AR242334A1 (OSRAM) |
AU (1) | AU580811B2 (OSRAM) |
BR (1) | BR8505708A (OSRAM) |
CA (1) | CA1318495C (OSRAM) |
DE (1) | DE3575514D1 (OSRAM) |
DK (1) | DK165158B (OSRAM) |
ES (1) | ES8704706A1 (OSRAM) |
GB (1) | GB2166974B (OSRAM) |
GR (1) | GR852752B (OSRAM) |
HU (1) | HU200886B (OSRAM) |
IL (1) | IL77038A0 (OSRAM) |
KE (1) | KE3836A (OSRAM) |
MA (1) | MA20573A1 (OSRAM) |
MX (1) | MX9206187A (OSRAM) |
MY (1) | MY101422A (OSRAM) |
NZ (1) | NZ214136A (OSRAM) |
OA (1) | OA08669A (OSRAM) |
PH (1) | PH23126A (OSRAM) |
PL (1) | PL255501A1 (OSRAM) |
TR (1) | TR23456A (OSRAM) |
ZW (1) | ZW18585A1 (OSRAM) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3545908A1 (de) * | 1985-12-23 | 1987-06-25 | Henkel Kgaa | Verwendung von langkettigen ethern in pflanzenschutzmitteln |
DK191386D0 (da) * | 1986-04-24 | 1986-04-24 | Koege Kemisk Vaerk | Emulgatorsystem |
GB8804988D0 (en) * | 1988-03-02 | 1988-03-30 | Wellcome Found | Sprayable formulations |
CN1056723C (zh) * | 1995-11-22 | 2000-09-27 | 中国石油化工总公司 | 一种蜡基农药增效助剂及其制备和使用方法 |
EP1246528B1 (en) * | 2000-01-14 | 2004-01-02 | Nederlandse Organisatie voor toegepast-natuurwetenschappelijk Onderzoek TNO | Sprayable composition for insect control |
KR20030038185A (ko) * | 2001-11-09 | 2003-05-16 | 양두석 | 파라핀왁스 전착제 및 그 제조방법 |
KR101034324B1 (ko) * | 2008-04-30 | 2011-05-16 | 주식회사 한두아이펨 | 방제용 약제 살포 장치 |
WO2011043748A1 (en) * | 2009-10-07 | 2011-04-14 | Chrysamed Ki̇mya Sanayi̇ Ve Diş Ti̇caret Li̇mi̇ted Şi̇rketi̇ | Composition used in the dissolution and stabilization of pesticide active agents |
KR101034323B1 (ko) * | 2010-08-10 | 2011-05-16 | 주식회사 한두아이펨 | 방제용 약제 및 약제 살포 장치 |
KR101028660B1 (ko) * | 2010-12-28 | 2011-04-12 | 주식회사 한두아이펨 | 방제용 약제 살포 장치 |
CN103734134B (zh) * | 2014-01-26 | 2016-04-20 | 上海艳紫化工科技有限公司 | 乙基多杀菌素和杀虫单复配的油悬浮剂 |
JP2017511370A (ja) * | 2014-04-17 | 2017-04-20 | ダウ アグロサイエンシィズ エルエルシー | パラフィン油を含むタンク混合添加剤濃縮液を使用する方法 |
WO2021206165A1 (ja) * | 2020-04-10 | 2021-10-14 | 花王株式会社 | 植物処理剤用蒸発抑制剤 |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2580653A (en) * | 1946-08-23 | 1952-01-01 | Johnson & Son Inc S C | Composition for killing weeds |
US2658004A (en) * | 1950-03-11 | 1953-11-03 | United Shoe Machinery Corp | Last slip for removing shoes from lasts |
US3063852A (en) * | 1959-05-22 | 1962-11-13 | Socony Mobil Oil Co Inc | Coating composition and method of application |
NL266499A (OSRAM) * | 1960-07-08 | |||
US3265568A (en) * | 1962-03-12 | 1966-08-09 | Exxon Research Engineering Co | Wax-water emulsions containing pyrethrum in the phase |
GB1072044A (en) * | 1962-11-15 | 1967-06-14 | Rohm & Haas | Polish compositions |
FR1347905A (fr) * | 1962-11-23 | 1964-01-04 | Exxon Research Engineering Co | Compositions herbicides |
GB1062457A (en) * | 1963-07-29 | 1967-03-22 | Colgate Palmolive Co | Polish |
GB1136082A (en) * | 1965-02-22 | 1968-12-11 | Hickson S Timber Impregnation | Wood-treatment compositions |
GB1168062A (en) * | 1967-03-28 | 1969-10-22 | Mobil Oil Corp | Biocidal Composition |
DE1937634C3 (de) * | 1968-07-30 | 1980-10-30 | N.V. Philips' Gloeilampenfabrieken, Eindhoven (Niederlande) | Einphasige Pestizidfliissigkeit mit herabgesetzter Phytotoxizität |
GB1226790A (OSRAM) * | 1968-12-13 | 1971-03-31 | ||
FR2053631A5 (en) * | 1969-07-11 | 1971-04-16 | Sun Oil Co | Stabilised aqs wax emulsions for polishes,co - plant transpiration |
GB1307313A (en) * | 1970-04-06 | 1973-02-21 | Ragosine Oil Co Ltd | Wax emulsion |
DE2139751C3 (de) * | 1971-08-07 | 1979-03-01 | Hoechst Ag, 6000 Frankfurt | Metallsalzhaltige Selbstglanzemulsionen und Verfahren zu ihrer Herstellung |
DE2205590A1 (de) * | 1972-02-07 | 1973-08-16 | Hoechst Ag | Verdunstungshemmendes zusatzmittel fuer konzentrierte pflanzenschutzmitteldispersionen |
US3791839A (en) * | 1972-05-25 | 1974-02-12 | Mobil Oil Corp | Wax emulsions for controlling transpiration in plants |
DE2556656A1 (de) * | 1975-12-16 | 1977-06-30 | Tama Flex Sansho Inc | Mittel fuer waessrige, fein zu vernebelnde wirkstoff-loesungen, -emulsionen oder -suspensionen sowie dessen verwendung zur herstellung und zum feinen vernebeln von waessrigen wirkstoff-loesungen, -emulsionen oder -suspensionen |
HU183354B (en) * | 1981-03-06 | 1984-04-28 | Magyar Asvanyolaj Es Foeldgaz | Paraffin-based emulsion of high activity containing food-materials diminishing transspiration |
DD214519A1 (de) * | 1983-04-13 | 1984-10-17 | Bitterfeld Chemie | Mineraloelfreie tankmischungen |
-
1985
- 1985-09-24 PL PL25550185A patent/PL255501A1/xx unknown
- 1985-10-01 HU HU853806A patent/HU200886B/hu not_active IP Right Cessation
- 1985-10-23 ZW ZW185/85A patent/ZW18585A1/xx unknown
- 1985-11-01 GB GB08526995A patent/GB2166974B/en not_active Expired
- 1985-11-03 AR AR85302253A patent/AR242334A1/es active
- 1985-11-06 CA CA000494746A patent/CA1318495C/en not_active Expired - Fee Related
- 1985-11-06 DE DE8585114129T patent/DE3575514D1/de not_active Expired - Fee Related
- 1985-11-06 EP EP85114129A patent/EP0185185B1/de not_active Expired - Lifetime
- 1985-11-07 CN CN198585108159A patent/CN85108159A/zh active Pending
- 1985-11-11 NZ NZ214136A patent/NZ214136A/xx unknown
- 1985-11-12 PH PH33049A patent/PH23126A/en unknown
- 1985-11-13 BR BR8505708A patent/BR8505708A/pt unknown
- 1985-11-13 DK DK523985A patent/DK165158B/da not_active Application Discontinuation
- 1985-11-13 GR GR852752A patent/GR852752B/el unknown
- 1985-11-13 IL IL77038A patent/IL77038A0/xx not_active IP Right Cessation
- 1985-11-13 AU AU49851/85A patent/AU580811B2/en not_active Ceased
- 1985-11-13 TR TR46238/85A patent/TR23456A/xx unknown
- 1985-11-14 MA MA20798A patent/MA20573A1/fr unknown
- 1985-11-14 OA OA58725A patent/OA08669A/xx unknown
- 1985-11-14 ES ES548884A patent/ES8704706A1/es not_active Expired
- 1985-11-14 KR KR1019850008539A patent/KR860003776A/ko not_active Ceased
-
1987
- 1987-04-27 MY MYPI87000545A patent/MY101422A/en unknown
-
1988
- 1988-10-10 KE KE3836A patent/KE3836A/xx unknown
-
1992
- 1992-10-27 MX MX9206187A patent/MX9206187A/es unknown
Also Published As
Publication number | Publication date |
---|---|
ZW18585A1 (en) | 1986-02-12 |
EP0185185A1 (de) | 1986-06-25 |
GR852752B (OSRAM) | 1986-03-11 |
NZ214136A (en) | 1989-01-06 |
EP0185185B1 (de) | 1990-01-24 |
GB8526995D0 (en) | 1985-12-04 |
DK523985A (da) | 1986-05-15 |
BR8505708A (pt) | 1986-08-12 |
GB2166974B (en) | 1988-06-02 |
GB2166974A (en) | 1986-05-21 |
DE3575514D1 (de) | 1990-03-01 |
AR242334A1 (es) | 1993-03-31 |
HU200886B (en) | 1990-09-28 |
OA08669A (fr) | 1989-03-31 |
KE3836A (en) | 1988-12-02 |
HUT38795A (en) | 1986-07-28 |
MX9206187A (es) | 1994-04-29 |
MA20573A1 (fr) | 1986-07-01 |
ES8704706A1 (es) | 1987-04-16 |
DK165158B (da) | 1992-10-19 |
DK523985D0 (da) | 1985-11-13 |
AU580811B2 (en) | 1989-02-02 |
AU4985185A (en) | 1986-05-22 |
PH23126A (en) | 1989-05-05 |
KR860003776A (ko) | 1986-06-13 |
PL255501A1 (en) | 1987-06-01 |
ES548884A0 (es) | 1987-04-16 |
MY101422A (en) | 1991-11-18 |
IL77038A0 (en) | 1986-04-29 |
CN85108159A (zh) | 1986-05-10 |
TR23456A (tr) | 1989-12-29 |
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MKLA | Lapsed |