ZA200602099B - Surfactant/solvent mixtures - Google Patents
Surfactant/solvent mixtures Download PDFInfo
- Publication number
- ZA200602099B ZA200602099B ZA200602099A ZA200602099A ZA200602099B ZA 200602099 B ZA200602099 B ZA 200602099B ZA 200602099 A ZA200602099 A ZA 200602099A ZA 200602099 A ZA200602099 A ZA 200602099A ZA 200602099 B ZA200602099 B ZA 200602099B
- Authority
- ZA
- South Africa
- Prior art keywords
- surfactant
- active ingredient
- solvent mixture
- oil
- concentrate
- Prior art date
Links
- 239000004094 surface-active agent Substances 0.000 title claims description 20
- 239000011877 solvent mixture Substances 0.000 title claims description 8
- 239000002904 solvent Substances 0.000 claims description 13
- 239000000203 mixture Substances 0.000 claims description 12
- -1 suspoemulssion Substances 0.000 claims description 12
- 239000004480 active ingredient Substances 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 8
- 238000009472 formulation Methods 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 239000003921 oil Substances 0.000 claims description 5
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 5
- 150000001875 compounds Chemical class 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 3
- 239000007921 spray Substances 0.000 claims description 3
- 239000012868 active agrochemical ingredient Substances 0.000 claims description 2
- 125000000129 anionic group Chemical group 0.000 claims description 2
- 150000002989 phenols Chemical class 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 239000012141 concentrate Substances 0.000 claims 7
- 239000000839 emulsion Substances 0.000 claims 4
- 241000607479 Yersinia pestis Species 0.000 claims 3
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims 2
- 239000004530 micro-emulsion Substances 0.000 claims 2
- 239000000654 additive Substances 0.000 claims 1
- 239000003905 agrochemical Substances 0.000 claims 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims 1
- 239000007795 chemical reaction product Substances 0.000 claims 1
- 239000000417 fungicide Substances 0.000 claims 1
- 239000002917 insecticide Substances 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 239000012053 oil suspension Substances 0.000 claims 1
- 239000004576 sand Substances 0.000 claims 1
- 239000000725 suspension Substances 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 4
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 4
- 241000640882 Condea Species 0.000 description 3
- 235000019484 Rapeseed oil Nutrition 0.000 description 3
- 125000005529 alkyleneoxy group Chemical group 0.000 description 3
- 235000014113 dietary fatty acids Nutrition 0.000 description 3
- 239000000194 fatty acid Substances 0.000 description 3
- 229930195729 fatty acid Natural products 0.000 description 3
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- QFMDFTQOJHFVNR-UHFFFAOYSA-N 1-[2,2-dichloro-1-(4-ethylphenyl)ethyl]-4-ethylbenzene Chemical compound C1=CC(CC)=CC=C1C(C(Cl)Cl)C1=CC=C(CC)C=C1 QFMDFTQOJHFVNR-UHFFFAOYSA-N 0.000 description 2
- 244000303965 Cyamopsis psoralioides Species 0.000 description 2
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N Furan Chemical compound C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 2
- 229920004482 WACKER® Polymers 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- IOJUPLGTWVMSFF-UHFFFAOYSA-N benzothiazole Chemical compound C1=CC=C2SC=NC2=C1 IOJUPLGTWVMSFF-UHFFFAOYSA-N 0.000 description 2
- 125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- YIGDAUZSYXKBHT-UHFFFAOYSA-N n,n-dibutylbutanamide Chemical compound CCCCN(CCCC)C(=O)CCC YIGDAUZSYXKBHT-UHFFFAOYSA-N 0.000 description 2
- XAROAZKXMDRYAF-UHFFFAOYSA-N n,n-dibutylpropanamide Chemical compound CCCCN(C(=O)CC)CCCC XAROAZKXMDRYAF-UHFFFAOYSA-N 0.000 description 2
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 2
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- 125000001400 nonyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 235000019198 oils Nutrition 0.000 description 2
- 235000021317 phosphate Nutrition 0.000 description 2
- 239000010773 plant oil Substances 0.000 description 2
- 229920001983 poloxamer Polymers 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 2
- 125000002948 undecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 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 description 1
- JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 1
- BCMCBBGGLRIHSE-UHFFFAOYSA-N 1,3-benzoxazole Chemical compound C1=CC=C2OC=NC2=C1 BCMCBBGGLRIHSE-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- GXJQMKFJQFGQKV-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS(O)(=O)=O GXJQMKFJQFGQKV-KHPPLWFESA-N 0.000 description 1
- BJAXAJXLQZSAMF-UHFFFAOYSA-N 2-methyl-n,n-dioctylpropanamide Chemical compound CCCCCCCCN(C(=O)C(C)C)CCCCCCCC BJAXAJXLQZSAMF-UHFFFAOYSA-N 0.000 description 1
- MDOXVKPJBKXAFA-UHFFFAOYSA-N 2-methyl-n,n-dipentylpropanamide Chemical compound CCCCCN(C(=O)C(C)C)CCCCC MDOXVKPJBKXAFA-UHFFFAOYSA-N 0.000 description 1
- NECRQCBKTGZNMH-UHFFFAOYSA-N 3,5-dimethylhex-1-yn-3-ol Chemical compound CC(C)CC(C)(O)C#C NECRQCBKTGZNMH-UHFFFAOYSA-N 0.000 description 1
- BCFOOQRXUXKJCL-UHFFFAOYSA-N 4-amino-4-oxo-2-sulfobutanoic acid Chemical class NC(=O)CC(C(O)=O)S(O)(=O)=O BCFOOQRXUXKJCL-UHFFFAOYSA-N 0.000 description 1
- 235000017060 Arachis glabrata Nutrition 0.000 description 1
- 244000105624 Arachis hypogaea Species 0.000 description 1
- 235000010777 Arachis hypogaea Nutrition 0.000 description 1
- 235000018262 Arachis monticola Nutrition 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 235000019482 Palm oil Nutrition 0.000 description 1
- 229920002257 Plurafac® Polymers 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical group CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 235000019498 Walnut oil Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 239000002585 base Substances 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 235000005687 corn oil Nutrition 0.000 description 1
- 239000002285 corn oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
- 239000010931 gold Substances 0.000 description 1
- 229910052737 gold Inorganic materials 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- YLGXILFCIXHCMC-JHGZEJCSSA-N methyl cellulose Chemical compound COC1C(OC)C(OC)C(COC)O[C@H]1O[C@H]1C(OC)C(OC)C(OC)OC1COC YLGXILFCIXHCMC-JHGZEJCSSA-N 0.000 description 1
- 150000004702 methyl esters Chemical class 0.000 description 1
- ZLDDRTXRHCTWQB-UHFFFAOYSA-N n,n-bis(2-methylpropyl)butanamide Chemical compound CCCC(=O)N(CC(C)C)CC(C)C ZLDDRTXRHCTWQB-UHFFFAOYSA-N 0.000 description 1
- PKCDVUYGEAUYRP-UHFFFAOYSA-N n,n-bis(2-methylpropyl)propanamide Chemical compound CCC(=O)N(CC(C)C)CC(C)C PKCDVUYGEAUYRP-UHFFFAOYSA-N 0.000 description 1
- YMVURTUZGBUDBC-UHFFFAOYSA-N n,n-bis(hydroxymethyl)formamide Chemical compound OCN(CO)C=O YMVURTUZGBUDBC-UHFFFAOYSA-N 0.000 description 1
- SQNZFMOVSQYBCI-UHFFFAOYSA-N n,n-di(nonyl)acetamide Chemical compound CCCCCCCCCN(C(C)=O)CCCCCCCCC SQNZFMOVSQYBCI-UHFFFAOYSA-N 0.000 description 1
- CWTGUUDJEUIPMQ-UHFFFAOYSA-N n,n-di(nonyl)formamide Chemical compound CCCCCCCCCN(C=O)CCCCCCCCC CWTGUUDJEUIPMQ-UHFFFAOYSA-N 0.000 description 1
- CTXOTGWGRLWPSJ-UHFFFAOYSA-N n,n-di(nonyl)propanamide Chemical compound CCCCCCCCCN(C(=O)CC)CCCCCCCCC CTXOTGWGRLWPSJ-UHFFFAOYSA-N 0.000 description 1
- LHYWLJYASYXTNV-UHFFFAOYSA-N n,n-di(propan-2-yl)butanamide Chemical compound CCCC(=O)N(C(C)C)C(C)C LHYWLJYASYXTNV-UHFFFAOYSA-N 0.000 description 1
- NHAUGGGONMDVER-UHFFFAOYSA-N n,n-di(undecyl)acetamide Chemical compound CCCCCCCCCCCN(C(C)=O)CCCCCCCCCCC NHAUGGGONMDVER-UHFFFAOYSA-N 0.000 description 1
- GVJQVZUERJVFDQ-UHFFFAOYSA-N n,n-didecyl-2-methylpropanamide Chemical compound CCCCCCCCCCN(C(=O)C(C)C)CCCCCCCCCC GVJQVZUERJVFDQ-UHFFFAOYSA-N 0.000 description 1
- SLPCLGLPAYVHCG-UHFFFAOYSA-N n,n-didecylacetamide Chemical compound CCCCCCCCCCN(C(C)=O)CCCCCCCCCC SLPCLGLPAYVHCG-UHFFFAOYSA-N 0.000 description 1
- QZAKFDDSRIEOAG-UHFFFAOYSA-N n,n-didecylbutanamide Chemical compound CCCCCCCCCCN(C(=O)CCC)CCCCCCCCCC QZAKFDDSRIEOAG-UHFFFAOYSA-N 0.000 description 1
- FOSREISSDRTLCP-UHFFFAOYSA-N n,n-didecylpropanamide Chemical compound CCCCCCCCCCN(C(=O)CC)CCCCCCCCCC FOSREISSDRTLCP-UHFFFAOYSA-N 0.000 description 1
- PTQJYGXFHGWRKN-UHFFFAOYSA-N n,n-didodecylacetamide Chemical compound CCCCCCCCCCCCN(C(C)=O)CCCCCCCCCCCC PTQJYGXFHGWRKN-UHFFFAOYSA-N 0.000 description 1
- YCVBFESJLOMHSG-UHFFFAOYSA-N n,n-didodecylformamide Chemical compound CCCCCCCCCCCCN(C=O)CCCCCCCCCCCC YCVBFESJLOMHSG-UHFFFAOYSA-N 0.000 description 1
- LPQADIVTBLHUBR-UHFFFAOYSA-N n,n-didodecylpropanamide Chemical compound CCCCCCCCCCCCN(C(=O)CC)CCCCCCCCCCCC LPQADIVTBLHUBR-UHFFFAOYSA-N 0.000 description 1
- CDQSTBHGKNNPSY-UHFFFAOYSA-N n,n-diethylbutanamide Chemical compound CCCC(=O)N(CC)CC CDQSTBHGKNNPSY-UHFFFAOYSA-N 0.000 description 1
- YKOQQFDCCBKROY-UHFFFAOYSA-N n,n-diethylpropanamide Chemical compound CCN(CC)C(=O)CC YKOQQFDCCBKROY-UHFFFAOYSA-N 0.000 description 1
- RLNVEUZTQKJWMH-UHFFFAOYSA-N n,n-diheptyl-2-methylpropanamide Chemical compound CCCCCCCN(C(=O)C(C)C)CCCCCCC RLNVEUZTQKJWMH-UHFFFAOYSA-N 0.000 description 1
- DDEIZNPREOWKQM-UHFFFAOYSA-N n,n-diheptylpropanamide Chemical compound CCCCCCCN(C(=O)CC)CCCCCCC DDEIZNPREOWKQM-UHFFFAOYSA-N 0.000 description 1
- JFUCOPIALLYRGN-UHFFFAOYSA-N n,n-dihexylacetamide Chemical compound CCCCCCN(C(C)=O)CCCCCC JFUCOPIALLYRGN-UHFFFAOYSA-N 0.000 description 1
- JSQYTYFBRWYWQO-UHFFFAOYSA-N n,n-dihexylbutanamide Chemical compound CCCCCCN(C(=O)CCC)CCCCCC JSQYTYFBRWYWQO-UHFFFAOYSA-N 0.000 description 1
- BUYHCCVTCJWPNU-UHFFFAOYSA-N n,n-dihexylformamide Chemical compound CCCCCCN(C=O)CCCCCC BUYHCCVTCJWPNU-UHFFFAOYSA-N 0.000 description 1
- YULBJWXEIGVLHR-UHFFFAOYSA-N n,n-dihexylpropanamide Chemical compound CCCCCCN(C(=O)CC)CCCCCC YULBJWXEIGVLHR-UHFFFAOYSA-N 0.000 description 1
- QAPQXJJNILFLOD-UHFFFAOYSA-N n,n-dioctylacetamide Chemical compound CCCCCCCCN(C(C)=O)CCCCCCCC QAPQXJJNILFLOD-UHFFFAOYSA-N 0.000 description 1
- YTHTWWXHLQCJRN-UHFFFAOYSA-N n,n-dioctylbutanamide Chemical compound CCCCCCCCN(C(=O)CCC)CCCCCCCC YTHTWWXHLQCJRN-UHFFFAOYSA-N 0.000 description 1
- HFEMVRMEPFLOCM-UHFFFAOYSA-N n,n-ditert-butylacetamide Chemical compound CC(=O)N(C(C)(C)C)C(C)(C)C HFEMVRMEPFLOCM-UHFFFAOYSA-N 0.000 description 1
- OHDORAMKRGZYBL-UHFFFAOYSA-N n,n-ditert-butylbutanamide Chemical compound CCCC(=O)N(C(C)(C)C)C(C)(C)C OHDORAMKRGZYBL-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 239000002540 palm oil Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 239000001814 pectin Substances 0.000 description 1
- 229920001277 pectin Polymers 0.000 description 1
- 235000010987 pectin Nutrition 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical class O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 1
- 239000010496 thistle oil Substances 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
- 239000008170 walnut oil Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/43—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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
-
- 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
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/26—Organic compounds containing nitrogen
- C11D3/32—Amides; Substituted amides
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Environmental Sciences (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Toxicology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Chemistry (AREA)
- Dispersion Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicinal Preparation (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10343390A DE10343390A1 (de) | 2003-09-19 | 2003-09-19 | Tensid/Lösungsmittelgemische |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200602099B true ZA200602099B (en) | 2007-06-27 |
Family
ID=34305913
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200602099A ZA200602099B (en) | 2003-09-19 | 2006-03-13 | Surfactant/solvent mixtures |
Country Status (17)
| Country | Link |
|---|---|
| US (1) | US20050064004A1 (de) |
| EP (1) | EP1667519A1 (de) |
| JP (1) | JP2007505844A (de) |
| KR (1) | KR20060092217A (de) |
| CN (1) | CN1863456A (de) |
| AP (1) | AP2006003587A0 (de) |
| AR (1) | AR045668A1 (de) |
| AU (1) | AU2004281507A1 (de) |
| BR (1) | BRPI0414524A (de) |
| CA (1) | CA2539497A1 (de) |
| DE (1) | DE10343390A1 (de) |
| EA (1) | EA200600559A1 (de) |
| EC (1) | ECSP066430A (de) |
| IL (1) | IL174239A0 (de) |
| MX (1) | MXPA06003059A (de) |
| WO (1) | WO2005036962A1 (de) |
| ZA (1) | ZA200602099B (de) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102004045371A1 (de) * | 2004-09-18 | 2006-04-13 | Bayer Cropscience Gmbh | Flüssige Pflanzenschutzformulierungen enthaltend Diflufenican |
| KR20070083657A (ko) * | 2004-10-12 | 2007-08-24 | 바이엘 크롭사이언스 게엠베하 | 계면활성제와 용매의 혼합물 |
| JP2006282528A (ja) * | 2005-03-31 | 2006-10-19 | Sumitomo Chemical Co Ltd | 農薬組成物 |
| AU2006200731B2 (en) * | 2005-03-31 | 2011-05-19 | Sumitomo Chemical Company, Limited | Emulsifiable concentrate |
| WO2006131227A2 (de) * | 2005-06-10 | 2006-12-14 | Bayer Cropscience Ag | Öl-in-wasser-suspoemulsionen, enthaltend pflanzenwirksame hydroxybenzonitrile |
| WO2007140332A2 (en) | 2006-05-26 | 2007-12-06 | Huntsman Petrochemical Corporation | Low odor, low volatility solvent for agricultural chemicals |
| PL2380954T3 (pl) * | 2010-04-22 | 2013-08-30 | Cognis Ip Man Gmbh | Kompozycje rozpuszczalnikowe |
| AU2013286010A1 (en) * | 2012-07-02 | 2015-01-29 | Basf Se | Herbicidal formulation |
| US10717919B2 (en) | 2013-03-14 | 2020-07-21 | Flotek Chemistry, Llc | Methods and compositions for use in oil and/or gas wells |
| WO2014153102A1 (en) * | 2013-03-14 | 2014-09-25 | Cesi Chemical Inc. | Methods and compositions for use in oil and/or gas wells |
| RU2665099C2 (ru) * | 2013-11-05 | 2018-08-28 | Басф Се | Композиция, содержащая пестицид и амид |
| FR3046179A1 (fr) * | 2015-12-23 | 2017-06-30 | Oleon Nv | Composition dispersante |
| CA3015260C (en) * | 2016-03-14 | 2021-02-02 | Basf Coatings Gmbh | Cleaning composition |
| US11732214B2 (en) * | 2019-11-20 | 2023-08-22 | Nissan Chemical Corporation | Cleaning agent composition comprising an alkylamide solvent and a fluorine-containing quaternary ammonium salt |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BE620135A (de) * | 1962-07-09 | |||
| DE1944568A1 (de) * | 1969-09-03 | 1971-03-11 | Henkel & Cie Gmbh | Fluessige Wasch- und Reinigungsmittel |
| DE2328192A1 (de) * | 1972-06-06 | 1974-01-03 | Procter & Gamble | Herbizide zusammensetzungen |
| DE3027959A1 (de) * | 1980-07-24 | 1982-03-04 | Basf Ag, 6700 Ludwigshafen | Fluessige herbizidmischung |
| IL79472A (en) * | 1985-07-23 | 1989-09-10 | May & Baker Ltd | Herbicidal compositions containing diflufenican and bromoxynil or ioxynil |
| US5283229A (en) * | 1989-12-11 | 1994-02-01 | Isp Investments Inc. | Delivery system for agricultural chemicals |
| DE4341986A1 (de) * | 1993-12-09 | 1995-06-14 | Bayer Ag | Verwendung von Carbonsäure-amiden als Kristallisationsinhibitoren |
| US5693129A (en) * | 1997-01-13 | 1997-12-02 | Xerox Corporation | Ink jet ink compositions comprising anti-curl hydroxyamide derivatives and printing processes |
| US6420361B1 (en) * | 1999-10-04 | 2002-07-16 | George B. Baker | Soil pesticide |
-
2003
- 2003-09-19 DE DE10343390A patent/DE10343390A1/de not_active Ceased
-
2004
- 2004-09-02 EA EA200600559A patent/EA200600559A1/ru unknown
- 2004-09-02 CN CNA2004800290884A patent/CN1863456A/zh active Pending
- 2004-09-02 BR BRPI0414524-0A patent/BRPI0414524A/pt not_active IP Right Cessation
- 2004-09-02 AU AU2004281507A patent/AU2004281507A1/en not_active Abandoned
- 2004-09-02 EP EP04764713A patent/EP1667519A1/de not_active Withdrawn
- 2004-09-02 AP AP2006003587A patent/AP2006003587A0/xx unknown
- 2004-09-02 MX MXPA06003059A patent/MXPA06003059A/es unknown
- 2004-09-02 CA CA002539497A patent/CA2539497A1/en not_active Abandoned
- 2004-09-02 JP JP2006526542A patent/JP2007505844A/ja not_active Abandoned
- 2004-09-02 WO PCT/EP2004/009753 patent/WO2005036962A1/de not_active Application Discontinuation
- 2004-09-02 KR KR1020067005461A patent/KR20060092217A/ko not_active Application Discontinuation
- 2004-09-16 AR ARP040103331A patent/AR045668A1/es unknown
- 2004-09-17 US US10/943,402 patent/US20050064004A1/en not_active Abandoned
-
2006
- 2006-03-09 IL IL174239A patent/IL174239A0/en unknown
- 2006-03-13 ZA ZA200602099A patent/ZA200602099B/en unknown
- 2006-03-17 EC EC2006006430A patent/ECSP066430A/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MXPA06003059A (es) | 2006-05-31 |
| CN1863456A (zh) | 2006-11-15 |
| AP2006003587A0 (en) | 2006-04-30 |
| EP1667519A1 (de) | 2006-06-14 |
| KR20060092217A (ko) | 2006-08-22 |
| WO2005036962A1 (de) | 2005-04-28 |
| DE10343390A1 (de) | 2005-04-14 |
| ECSP066430A (es) | 2006-11-24 |
| AR045668A1 (es) | 2005-11-02 |
| JP2007505844A (ja) | 2007-03-15 |
| AU2004281507A1 (en) | 2005-04-28 |
| CA2539497A1 (en) | 2005-04-28 |
| US20050064004A1 (en) | 2005-03-24 |
| IL174239A0 (en) | 2006-08-01 |
| BRPI0414524A (pt) | 2006-11-07 |
| EA200600559A1 (ru) | 2006-08-25 |
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