EA016582B1 - Производные лактамида, способ их получения и применение - Google Patents
Производные лактамида, способ их получения и применение Download PDFInfo
- Publication number
- EA016582B1 EA016582B1 EA200870362A EA200870362A EA016582B1 EA 016582 B1 EA016582 B1 EA 016582B1 EA 200870362 A EA200870362 A EA 200870362A EA 200870362 A EA200870362 A EA 200870362A EA 016582 B1 EA016582 B1 EA 016582B1
- Authority
- EA
- Eurasian Patent Office
- Prior art keywords
- ethyl
- ris
- butyl
- formula
- lactamide
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 10
- SXQFCVDSOLSHOQ-UHFFFAOYSA-N lactamide Chemical class CC(O)C(N)=O SXQFCVDSOLSHOQ-UHFFFAOYSA-N 0.000 title abstract description 20
- 230000008569 process Effects 0.000 title abstract description 4
- 239000002904 solvent Substances 0.000 claims abstract description 33
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims abstract description 31
- 238000002360 preparation method Methods 0.000 claims abstract description 20
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims abstract description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
- 239000001257 hydrogen Substances 0.000 claims abstract description 12
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 11
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims abstract description 10
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims abstract description 9
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims abstract description 9
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims abstract description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 7
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims abstract description 4
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims abstract description 4
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 44
- 231100000419 toxicity Toxicity 0.000 claims description 9
- 230000001988 toxicity Effects 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 6
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical group [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 claims description 6
- 239000003905 agrochemical Substances 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 6
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 5
- 235000019333 sodium laurylsulphate Nutrition 0.000 claims description 5
- 241000124008 Mammalia Species 0.000 claims description 4
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 claims description 2
- 230000008520 organization Effects 0.000 claims 1
- -1 1-3-dimethylbutyl Chemical group 0.000 abstract description 19
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 abstract 1
- 101150065749 Churc1 gene Proteins 0.000 abstract 1
- 102100038239 Protein Churchill Human genes 0.000 abstract 1
- 125000005468 isobutylenyl group Chemical group 0.000 abstract 1
- JJTUDXZGHPGLLC-UHFFFAOYSA-N lactide Chemical compound CC1OC(=O)C(C)OC1=O JJTUDXZGHPGLLC-UHFFFAOYSA-N 0.000 description 20
- 239000000243 solution Substances 0.000 description 20
- 241000196324 Embryophyta Species 0.000 description 16
- 230000006378 damage Effects 0.000 description 16
- LZCLXQDLBQLTDK-UHFFFAOYSA-N ethyl 2-hydroxypropanoate Chemical compound CCOC(=O)C(C)O LZCLXQDLBQLTDK-UHFFFAOYSA-N 0.000 description 13
- 239000003814 drug Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 10
- 241000238578 Daphnia Species 0.000 description 8
- 230000003993 interaction Effects 0.000 description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M Lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 7
- 238000004519 manufacturing process Methods 0.000 description 7
- 229940079593 drug Drugs 0.000 description 6
- 230000007613 environmental effect Effects 0.000 description 6
- 229940116333 ethyl lactate Drugs 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 150000001412 amines Chemical class 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 4
- FXHOOIRPVKKKFG-UHFFFAOYSA-N N,N-Dimethylacetamide Chemical compound CN(C)C(C)=O FXHOOIRPVKKKFG-UHFFFAOYSA-N 0.000 description 4
- 206010040880 Skin irritation Diseases 0.000 description 4
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 4
- 238000009472 formulation Methods 0.000 description 4
- 231100000053 low toxicity Toxicity 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 238000012545 processing Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 231100000475 skin irritation Toxicity 0.000 description 4
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 description 3
- 239000005757 Cyproconazole Substances 0.000 description 3
- 229920001213 Polysorbate 20 Polymers 0.000 description 3
- RWRDLPDLKQPQOW-UHFFFAOYSA-N Pyrrolidine Chemical compound C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 239000012298 atmosphere Substances 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000007794 irritation Effects 0.000 description 3
- 239000000575 pesticide Substances 0.000 description 3
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 3
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 3
- 239000002453 shampoo Substances 0.000 description 3
- 230000036556 skin irritation Effects 0.000 description 3
- 239000012855 volatile organic compound Substances 0.000 description 3
- UUFQTNFCRMXOAE-UHFFFAOYSA-N 1-methylmethylene Chemical compound C[CH] UUFQTNFCRMXOAE-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 2
- KDSNLYIMUZNERS-UHFFFAOYSA-N 2-methylpropanamine Chemical compound CC(C)CN KDSNLYIMUZNERS-UHFFFAOYSA-N 0.000 description 2
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 2
- 240000001592 Amaranthus caudatus Species 0.000 description 2
- 235000009328 Amaranthus caudatus Nutrition 0.000 description 2
- 101100480738 Arabidopsis thaliana TFCC gene Proteins 0.000 description 2
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 2
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- 206010059516 Skin toxicity Diseases 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- WEHWNAOGRSTTBQ-UHFFFAOYSA-N dipropylamine Chemical compound CCCNCCC WEHWNAOGRSTTBQ-UHFFFAOYSA-N 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 239000012634 fragment Substances 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000000622 irritating effect Effects 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- PQPFFKCJENSZKL-UHFFFAOYSA-N pentan-3-amine Chemical compound CCC(N)CC PQPFFKCJENSZKL-UHFFFAOYSA-N 0.000 description 2
- 239000002884 skin cream Substances 0.000 description 2
- 231100000438 skin toxicity Toxicity 0.000 description 2
- 239000002689 soil Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000000829 suppository Substances 0.000 description 2
- 239000001993 wax Substances 0.000 description 2
- MTIRIKBRVALRPJ-NTMALXAHSA-N (Z)-[3-aminopropyl(propan-2-yl)amino]-hydroxyimino-oxidoazanium Chemical compound CC(C)N(CCCN)[N+](\[O-])=N\O MTIRIKBRVALRPJ-NTMALXAHSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- XNIOWJUQPMKCIJ-UHFFFAOYSA-N 2-(benzylamino)ethanol Chemical compound OCCNCC1=CC=CC=C1 XNIOWJUQPMKCIJ-UHFFFAOYSA-N 0.000 description 1
- MIJDSYMOBYNHOT-UHFFFAOYSA-N 2-(ethylamino)ethanol Chemical compound CCNCCO MIJDSYMOBYNHOT-UHFFFAOYSA-N 0.000 description 1
- JCBPETKZIGVZRE-UHFFFAOYSA-N 2-aminobutan-1-ol Chemical compound CCC(N)CO JCBPETKZIGVZRE-UHFFFAOYSA-N 0.000 description 1
- GELMWIVBBPAMIO-UHFFFAOYSA-N 2-methylbutan-2-amine Chemical compound CCC(C)(C)N GELMWIVBBPAMIO-UHFFFAOYSA-N 0.000 description 1
- LPUBRQWGZPPVBS-UHFFFAOYSA-N 3-butoxypropan-1-amine Chemical compound CCCCOCCCN LPUBRQWGZPPVBS-UHFFFAOYSA-N 0.000 description 1
- UNBMPKNTYKDYCG-UHFFFAOYSA-N 4-methylpentan-2-amine Chemical compound CC(C)CC(C)N UNBMPKNTYKDYCG-UHFFFAOYSA-N 0.000 description 1
- 241000251468 Actinopterygii Species 0.000 description 1
- 241000271566 Aves Species 0.000 description 1
- 241000581650 Ivesia Species 0.000 description 1
- 206010058667 Oral toxicity Diseases 0.000 description 1
- 241001274961 Rubus repens Species 0.000 description 1
- 230000000895 acaricidal effect Effects 0.000 description 1
- 239000000642 acaricide Substances 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 210000000577 adipose tissue Anatomy 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 235000012735 amaranth Nutrition 0.000 description 1
- 239000004178 amaranth Substances 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000012459 cleaning agent Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000013270 controlled release Methods 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 230000000254 damaging effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- HPNMFZURTQLUMO-UHFFFAOYSA-N diethylamine Chemical compound CCNCC HPNMFZURTQLUMO-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000003912 environmental pollution Methods 0.000 description 1
- 231100000584 environmental toxicity Toxicity 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LZCLXQDLBQLTDK-BYPYZUCNSA-N ethyl (2S)-lactate Chemical compound CCOC(=O)[C@H](C)O LZCLXQDLBQLTDK-BYPYZUCNSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 230000007684 eye toxicity Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 238000005246 galvanizing Methods 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- 239000000499 gel Substances 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 208000006278 hypochromic anemia Diseases 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- QOHMWDJIBGVPIF-UHFFFAOYSA-N n',n'-diethylpropane-1,3-diamine Chemical compound CCN(CC)CCCN QOHMWDJIBGVPIF-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 230000001338 necrotic effect Effects 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- 231100000327 ocular toxicity Toxicity 0.000 description 1
- 231100000418 oral toxicity Toxicity 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
- 229940100684 pentylamine Drugs 0.000 description 1
- 230000000885 phytotoxic effect Effects 0.000 description 1
- 230000000485 pigmenting effect Effects 0.000 description 1
- 230000008654 plant damage Effects 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000002953 preparative HPLC Methods 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000011253 protective coating Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 239000012047 saturated solution Substances 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000037380 skin damage Effects 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- YBRBMKDOPFTVDT-UHFFFAOYSA-N tert-butylamine Chemical compound CC(C)(C)N YBRBMKDOPFTVDT-UHFFFAOYSA-N 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 229940034610 toothpaste Drugs 0.000 description 1
- 239000000606 toothpaste Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000012808 vapor phase Substances 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/02—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
- C07C233/04—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
- C07C233/05—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals with carbon atoms of carboxamide groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C235/06—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
-
- 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
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/16—Amides, e.g. hydroxamic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/42—Amides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P39/00—General protective or antinoxious agents
- A61P39/02—Antidotes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/02—Preparations for cleaning the hair
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C235/08—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by singly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C235/00—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
- C07C235/02—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
- C07C235/04—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C235/16—Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/12—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms
- C07D295/125—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/13—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly or doubly bound nitrogen atoms with the ring nitrogen atoms and the substituent nitrogen atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/74—Biological properties of particular ingredients
- A61K2800/75—Anti-irritant
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Medicinal Chemistry (AREA)
- Wood Science & Technology (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Agronomy & Crop Science (AREA)
- Dermatology (AREA)
- Toxicology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Birds (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Hydrogenated Pyridines (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Detergent Compositions (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
- Medicinal Preparation (AREA)
- Cosmetics (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0605780.6A GB0605780D0 (en) | 2006-03-22 | 2006-03-22 | Formulations |
| PCT/GB2007/000986 WO2007107745A2 (en) | 2006-03-22 | 2007-03-21 | Process for producing lactamide compounds, new lactamide compounds and formulations containing lactamide compounds |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA200870362A1 EA200870362A1 (ru) | 2009-02-27 |
| EA016582B1 true EA016582B1 (ru) | 2012-06-29 |
Family
ID=36383990
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201000413A EA017866B1 (ru) | 2006-03-22 | 2007-03-21 | Применение производных лактамида в составе препаратов для снижения токсичности |
| EA200870362A EA016582B1 (ru) | 2006-03-22 | 2007-03-21 | Производные лактамида, способ их получения и применение |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201000413A EA017866B1 (ru) | 2006-03-22 | 2007-03-21 | Применение производных лактамида в составе препаратов для снижения токсичности |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US8420859B2 (enExample) |
| EP (1) | EP2001288B1 (enExample) |
| JP (1) | JP2009534302A (enExample) |
| KR (1) | KR101384748B1 (enExample) |
| CN (2) | CN101404879A (enExample) |
| AR (1) | AR059925A1 (enExample) |
| AU (1) | AU2007228629B2 (enExample) |
| BR (1) | BRPI0708097A2 (enExample) |
| CA (1) | CA2637630C (enExample) |
| DK (1) | DK2001288T3 (enExample) |
| EA (2) | EA017866B1 (enExample) |
| ES (1) | ES2545102T3 (enExample) |
| GB (1) | GB0605780D0 (enExample) |
| HU (1) | HUE025333T2 (enExample) |
| IL (1) | IL193060A0 (enExample) |
| MX (1) | MX2008011771A (enExample) |
| NO (1) | NO20083435L (enExample) |
| NZ (1) | NZ569751A (enExample) |
| PL (1) | PL2001288T3 (enExample) |
| PT (1) | PT2001288E (enExample) |
| TW (1) | TW200800016A (enExample) |
| UA (1) | UA95105C2 (enExample) |
| UY (1) | UY30233A1 (enExample) |
| WO (1) | WO2007107745A2 (enExample) |
| ZA (1) | ZA200806323B (enExample) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE202007018967U1 (de) | 2007-02-22 | 2009-12-31 | Cognis Ip Management Gmbh | Agrochemische Zusammensetzungen mit Milchsäureverbindungen (III) |
| DE202007018968U1 (de) | 2007-02-22 | 2009-12-31 | Cognis Ip Management Gmbh | Agrochemische Zusammensetzungen mit Milchsäureverbindungen (II) |
| EP1961301A1 (en) * | 2007-02-22 | 2008-08-27 | Cognis IP Management GmbH | Biocide compositions comprising a dialkylamide of a hydroxycarboxylic acid |
| DE202007018969U1 (de) | 2007-02-22 | 2009-12-31 | Cognis Ip Management Gmbh | Agrochemische Zusammensetzungen mit Milchsäureverbindungen (I) |
| GB0716593D0 (en) * | 2007-08-24 | 2007-10-03 | Syngenta Ltd | Improvements in or relating to organic compounds |
| GB0716592D0 (en) * | 2007-08-24 | 2007-10-03 | Syngenta Ltd | Improvements in or relating to organic compounds |
| CN102209706B (zh) * | 2008-10-01 | 2014-07-23 | 普拉克生化公司 | 制造n,n-二烷基乳酰胺的方法 |
| WO2010108817A1 (de) | 2009-03-26 | 2010-09-30 | Basf Se | Verfahren zur herstellung von n,n`-milchsäuredialkylamid über ionische flüssigkeiten |
| WO2010108814A1 (de) | 2009-03-26 | 2010-09-30 | Basf Se | Verfahren zur herstellung von n,n`-milchsäuredialkylamid unter druck |
| CA2769186C (en) * | 2009-08-11 | 2016-10-04 | Novartis Ag | The ring opening of lactones and lactams |
| FR2951447B1 (fr) | 2009-10-19 | 2012-10-19 | Rhodia Operations | Composes de type ether-amide et utilisattions |
| EP2387886B1 (en) | 2010-05-18 | 2016-01-06 | Cognis IP Management GmbH | Biocide compositions comprising isoamyl lactate |
| GB201012585D0 (en) * | 2010-07-27 | 2010-09-08 | Syngenta Ltd | Cleaning methods |
| GB2482299A (en) * | 2010-07-27 | 2012-02-01 | Syngenta Ltd | Use of a dialkylamide to reduce the phytotoxicity of an agrochemical |
| EP2430919B1 (en) | 2010-09-20 | 2013-06-05 | Cognis IP Management GmbH | Biocide compositions comprising amides based on 2-furoic acid and its derivatives |
| KR20120054387A (ko) * | 2010-11-19 | 2012-05-30 | 삼성정밀화학 주식회사 | 디알킬락타미드류의 제조방법 |
| EP2832735A1 (de) * | 2013-07-30 | 2015-02-04 | Sika Technology AG | Hydroxymethylcarboxamido-substituiertes Silanol für härtbare, silanterminierte Polymere. |
| EP3104699B1 (en) * | 2014-02-14 | 2018-08-29 | BASF Agro B.V. | Emulsifiable concentrate comprising pesticide, alkyl lactate, and lactamide |
| CA2938771C (en) * | 2014-02-14 | 2022-11-29 | BASF Agro B.V. | Emulsifiable concentrate comprising pesticide, fatty amide and lactamide |
| EP3201172A1 (en) * | 2014-10-03 | 2017-08-09 | PURAC Biochem BV | Method for the manufacture of n, n-dialkyllactamide |
| KR102626465B1 (ko) * | 2015-09-17 | 2024-01-17 | 바스프 에스이 | 락타미드 기재 용매를 사용하는 멤브레인의 제조 방법 |
| WO2018162554A1 (en) * | 2017-03-09 | 2018-09-13 | Basf Se | Biodegradable solvent |
| CN114847295B (zh) * | 2017-06-16 | 2024-04-12 | 百奥泰利加控股有限公司 | 包含生物碱的组合物及其用途 |
| US20220369630A1 (en) * | 2021-05-06 | 2022-11-24 | Stoller Enterprises, Inc. | Stable S-(+)-Abscisic Acid Nonaqueous Liquid Solutions |
| WO2025104168A1 (en) * | 2023-11-15 | 2025-05-22 | Syngenta Crop Protection Ag | Pesticidal compositions |
Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2990331A (en) * | 1956-11-23 | 1961-06-27 | Pfizer & Co C | Stable solutions of salts of tetracyclines for parenteral administration |
| FR2564288A1 (fr) * | 1984-05-16 | 1985-11-22 | Bayer Ag | Utilisation d'amides pour ameliorer la tolerance par des plantes cultivees d'heteroaryloxyacetamides doues d'activite herbicide |
| DE3618004A1 (de) * | 1986-05-28 | 1987-12-03 | Bayer Ag | Verwendung von amiden zur verbesserung der kulturpflanzen-vertraeglichkeit von herbizid wirksamen sulfonyliso(thio)-harnstoff-derivaten |
| DE4112873A1 (de) * | 1991-04-19 | 1992-10-22 | Richard H Dr Sehring | Fungicides pflanzenschutzmittel mit wirkung im zierpflanzen und obstbau sowie gegen echten mehltau an getreide, gurken, reben und hopfen |
| US5693126A (en) * | 1994-12-27 | 1997-12-02 | Seiko Epson Corporation | Water-base ink composition and process for producing the same |
| WO2006124899A2 (en) * | 2005-05-13 | 2006-11-23 | Cargill, Incorporated | Production of derivatives of lactide, production of lactides, and use of lactide in foods and to produce polymers |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2631284A1 (de) * | 1976-07-12 | 1978-01-26 | Henkel Kgaa | Kosmetische mittel mit einem gehalt an haut-feuchthaltemitteln |
-
2006
- 2006-03-22 GB GBGB0605780.6A patent/GB0605780D0/en not_active Ceased
-
2007
- 2007-03-09 TW TW096108244A patent/TW200800016A/zh unknown
- 2007-03-16 AR ARP070101087A patent/AR059925A1/es active IP Right Grant
- 2007-03-21 CN CNA2007800097819A patent/CN101404879A/zh active Pending
- 2007-03-21 KR KR1020087021903A patent/KR101384748B1/ko active Active
- 2007-03-21 PL PL07732078T patent/PL2001288T3/pl unknown
- 2007-03-21 NZ NZ569751A patent/NZ569751A/en unknown
- 2007-03-21 UA UAA200812396A patent/UA95105C2/ru unknown
- 2007-03-21 HU HUE07732078A patent/HUE025333T2/en unknown
- 2007-03-21 US US12/293,894 patent/US8420859B2/en active Active
- 2007-03-21 EA EA201000413A patent/EA017866B1/ru not_active IP Right Cessation
- 2007-03-21 DK DK07732078.6T patent/DK2001288T3/en active
- 2007-03-21 PT PT77320786T patent/PT2001288E/pt unknown
- 2007-03-21 EA EA200870362A patent/EA016582B1/ru not_active IP Right Cessation
- 2007-03-21 AU AU2007228629A patent/AU2007228629B2/en active Active
- 2007-03-21 CA CA2637630A patent/CA2637630C/en active Active
- 2007-03-21 ES ES07732078.6T patent/ES2545102T3/es active Active
- 2007-03-21 JP JP2009500917A patent/JP2009534302A/ja active Pending
- 2007-03-21 CN CN201510035557.3A patent/CN104782624A/zh active Pending
- 2007-03-21 BR BRPI0708097-2A patent/BRPI0708097A2/pt not_active Application Discontinuation
- 2007-03-21 MX MX2008011771A patent/MX2008011771A/es not_active Application Discontinuation
- 2007-03-21 EP EP07732078.6A patent/EP2001288B1/en active Active
- 2007-03-21 WO PCT/GB2007/000986 patent/WO2007107745A2/en not_active Ceased
- 2007-03-22 UY UY30233A patent/UY30233A1/es unknown
-
2008
- 2008-07-21 ZA ZA200806323A patent/ZA200806323B/xx unknown
- 2008-07-24 IL IL193060A patent/IL193060A0/en unknown
- 2008-08-05 NO NO20083435A patent/NO20083435L/no not_active Application Discontinuation
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2990331A (en) * | 1956-11-23 | 1961-06-27 | Pfizer & Co C | Stable solutions of salts of tetracyclines for parenteral administration |
| FR2564288A1 (fr) * | 1984-05-16 | 1985-11-22 | Bayer Ag | Utilisation d'amides pour ameliorer la tolerance par des plantes cultivees d'heteroaryloxyacetamides doues d'activite herbicide |
| DE3618004A1 (de) * | 1986-05-28 | 1987-12-03 | Bayer Ag | Verwendung von amiden zur verbesserung der kulturpflanzen-vertraeglichkeit von herbizid wirksamen sulfonyliso(thio)-harnstoff-derivaten |
| DE4112873A1 (de) * | 1991-04-19 | 1992-10-22 | Richard H Dr Sehring | Fungicides pflanzenschutzmittel mit wirkung im zierpflanzen und obstbau sowie gegen echten mehltau an getreide, gurken, reben und hopfen |
| US5693126A (en) * | 1994-12-27 | 1997-12-02 | Seiko Epson Corporation | Water-base ink composition and process for producing the same |
| WO2006124899A2 (en) * | 2005-05-13 | 2006-11-23 | Cargill, Incorporated | Production of derivatives of lactide, production of lactides, and use of lactide in foods and to produce polymers |
Non-Patent Citations (6)
| Title |
|---|
| BUDDEN, R. ET AL.: "Experiments on the toxic, sedative abd muscle relaxant effect of various drug solvents in mice". PHARM. THER., vol. 5, 1979, pages 467-474, XP002470081, tables 1-4 - Discussion - page 473, paragraph 43, page 474 * |
| FEIN M.L. ET AL.: "N-Substituted Lactamides". JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, AMERICAN CHEMICAL SOCIETY, WASHINGTON, DC, US, vol. 75, 5 May 1953 (1953-05-05), pages 2097-2099, XP002415482, ISSN: 0002-7863, page 2098; table 1 * |
| NIJBURG, R.E. AND GIJSEN R.M.R.: "Benefits and effectiveness of lactates as skin friendly ingredients in manual dishwashing". S?ûFW-JOURNAL, vol. 128, no. 5, 2002, pages 1-4, XP002470080, Conclusion - page 4; figures 2-5; table 1 * |
| RATCHFORD ET AL.: "Preparation and properties of N-n-alkyllactamides". 19500101; 19500000, vol. 15, 1 January 1950 (1950-01-01), pages 326-332, XP002479105, page 327 * |
| RATCHFORD W.P. ET AL.: "Preparation of N-substituted lactamides by aminolysis of methyl lactate". J. ORG. CHEM, vol. 15, 1950, pages 317-323, XP002470083, cited in the application, table 1 * |
| SHAPIRO ET AL.: "Alpha-hydroxy amides and related compounds", J. AM. CHEM. SOC., vol. 81, 5 December 1959 (1959-12-05), pages 6322-6329, XP002470082, page 6323 - page 6326; table 1, Preparation of Amides-Method S, page 6328, line R * |
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EA016582B1 (ru) | Производные лактамида, способ их получения и применение | |
| CN103547151B (zh) | 含有叔酰胺作为助剂或作为表面活性剂的农业和清洁剂组合物 | |
| JPH01503044A (ja) | 農業用乳剤組成物 | |
| US20120148514A1 (en) | N-alkyl lactam ethers, and compositions and uses thereof | |
| JPH01157971A (ja) | 安定化されたイソチアゾロン組成物 | |
| EP0156275A2 (de) | Antimikrobiell wirksame Substanzen, ihre Herstellung und ihre Verwendung | |
| Stachowiak et al. | “Sweet” ionic liquids comprising the acesulfame anion–synthesis, physicochemical properties and antifeedant activity towards stored product insects | |
| Czuryszkiewicz et al. | Herbicidal ionic liquids containing the acetylcholine cation | |
| JPH02240090A (ja) | ホスホニュウム塩およびそれからなる殺生物剤 | |
| Song et al. | Biological behaviors of guanidine-based cationic surfactants | |
| CA1210019A (en) | Insoluble polymeric contact preservatives | |
| CN105461814B (zh) | 一种醋酸纤维素衍生物及其制备方法和用途 | |
| DE69214399T2 (de) | Iod-Verbindungen enthaltende germizide Zusammensetzungen | |
| Kuruca et al. | Synthesis and antimicrobial activity testing of quaternary ammonium silane compounds | |
| KR20230012549A (ko) | 천연 생물학적 항균 및 항 바이러스제, 성분, 조제 과정 및 용도 | |
| RU2640816C2 (ru) | Применение ароматических азометинов с высшими алкильными заместителями в качестве средства, обладающего бактерицидной и фунгицидной активностью | |
| KR101746806B1 (ko) | 제형 | |
| CS229687B2 (en) | Acaricide agent and its manufacturing process | |
| RU2238268C2 (ru) | Дезинфицирующее средство | |
| JP2017210426A (ja) | 生分解性カチオン界面活性剤 | |
| UA53738C2 (uk) | Спосіб одержання бактерицидного препарату | |
| EP3262942A1 (de) | Selenodiaryle zur anwendung als mikrobizid sowie als arzneimittel | |
| FR2516748A1 (fr) | Compositions herbicides a base de derives d'amino-4 chloro-6 alkylthio-5 pyrimidine et de pyridate, et procede de traitement des cultures a l'aide desdites compositions | |
| TH53997A (th) | เฮเทอโรไซคลิกเอซิลซัลฟิไมด์, กระบวนการในการเตรียมสาร ดังกล่าว, สารผสมซึ่งประกอบรวมด้วยสารดังกล่าว และการใช้สารดังกล่าวเป็นสารฆ่าศัตรูพืชและสัตว์ |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s) |
Designated state(s): AM AZ BY KZ KG MD TJ TM |