CH442862A - Verfahren und Mittel zur Regelung des Pflanzenwachstums - Google Patents
Verfahren und Mittel zur Regelung des PflanzenwachstumsInfo
- Publication number
- CH442862A CH442862A CH210963A CH210963A CH442862A CH 442862 A CH442862 A CH 442862A CH 210963 A CH210963 A CH 210963A CH 210963 A CH210963 A CH 210963A CH 442862 A CH442862 A CH 442862A
- Authority
- CH
- Switzerland
- Prior art keywords
- sep
- dichlorophenyl
- denotes
- methyl
- lower alkyl
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 23
- 230000008635 plant growth Effects 0.000 title claims description 8
- 230000001105 regulatory effect Effects 0.000 title claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 19
- -1 N- (2-chloro-6-methylphenyl) maleamic acid propyl ester Chemical compound 0.000 claims description 17
- 239000002253 acid Substances 0.000 claims description 16
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 229910052757 nitrogen Inorganic materials 0.000 claims description 5
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 5
- 125000005907 alkyl ester group Chemical group 0.000 claims description 4
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 150000004702 methyl esters Chemical class 0.000 claims description 3
- DIZAIWRTXVZYTM-PLNGDYQASA-N (z)-4-(4-chloro-2-methylanilino)-4-oxobut-2-enoic acid Chemical compound CC1=CC(Cl)=CC=C1NC(=O)\C=C/C(O)=O DIZAIWRTXVZYTM-PLNGDYQASA-N 0.000 claims description 2
- BSSNZUFKXJJCBG-UPHRSURJSA-N (z)-but-2-enediamide Chemical compound NC(=O)\C=C/C(N)=O BSSNZUFKXJJCBG-UPHRSURJSA-N 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- WFWKZRKAECLVSE-ARJAWSKDSA-N (z)-4-(2,4-dichloroanilino)-4-oxobut-2-enoic acid Chemical compound OC(=O)\C=C/C(=O)NC1=CC=C(Cl)C=C1Cl WFWKZRKAECLVSE-ARJAWSKDSA-N 0.000 claims 2
- YMYKNYVBUCMJOG-ONEGZZNKSA-N (e)-4-(3,4-dichloroanilino)-4-oxobut-2-enoic acid Chemical compound OC(=O)\C=C\C(=O)NC1=CC=C(Cl)C(Cl)=C1 YMYKNYVBUCMJOG-ONEGZZNKSA-N 0.000 claims 1
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 1
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims 1
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims 1
- 229960003887 dichlorophen Drugs 0.000 claims 1
- 239000000839 emulsion Substances 0.000 description 12
- 150000002148 esters Chemical class 0.000 description 12
- 241000196324 Embryophyta Species 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 240000007019 Oxalis corniculata Species 0.000 description 9
- 235000016499 Oxalis corniculata Nutrition 0.000 description 9
- 229920000742 Cotton Polymers 0.000 description 7
- 241000219146 Gossypium Species 0.000 description 7
- 230000012010 growth Effects 0.000 description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 7
- 244000075850 Avena orientalis Species 0.000 description 6
- 231100000674 Phytotoxicity Toxicity 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 235000007320 Avena fatua Nutrition 0.000 description 5
- 235000016068 Berberis vulgaris Nutrition 0.000 description 5
- 241000335053 Beta vulgaris Species 0.000 description 5
- 241000209140 Triticum Species 0.000 description 5
- 230000002363 herbicidal effect Effects 0.000 description 5
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 5
- 240000003768 Solanum lycopersicum Species 0.000 description 4
- 235000021307 Triticum Nutrition 0.000 description 4
- 235000005373 Uvularia sessilifolia Nutrition 0.000 description 4
- 240000002024 Gossypium herbaceum Species 0.000 description 3
- 235000004341 Gossypium herbaceum Nutrition 0.000 description 3
- 235000004431 Linum usitatissimum Nutrition 0.000 description 3
- 240000006240 Linum usitatissimum Species 0.000 description 3
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 3
- 125000005843 halogen group Chemical group 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- 239000003350 kerosene Substances 0.000 description 3
- YMGJBCGPNTUNSL-UHFFFAOYSA-N methyl 4-(2,4-dichloroanilino)-4-oxobutanoate Chemical compound COC(=O)CCC(=O)NC1=CC=C(Cl)C=C1Cl YMGJBCGPNTUNSL-UHFFFAOYSA-N 0.000 description 3
- 230000006911 nucleation Effects 0.000 description 3
- 238000010899 nucleation Methods 0.000 description 3
- 231100000208 phytotoxic Toxicity 0.000 description 3
- 230000000885 phytotoxic effect Effects 0.000 description 3
- 235000015277 pork Nutrition 0.000 description 3
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 3
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 description 2
- HXKWSTRRCHTUEC-UHFFFAOYSA-N 2,4-Dichlorophenoxyaceticacid Chemical compound OC(=O)C(Cl)OC1=CC=C(Cl)C=C1 HXKWSTRRCHTUEC-UHFFFAOYSA-N 0.000 description 2
- OMSLSFZIEVFEIH-UHFFFAOYSA-N 4-methoxy-4-methylpentan-2-ol Chemical compound COC(C)(C)CC(C)O OMSLSFZIEVFEIH-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 235000007319 Avena orientalis Nutrition 0.000 description 2
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 2
- 241000132536 Cirsium Species 0.000 description 2
- 241000209082 Lolium Species 0.000 description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
- 244000046052 Phaseolus vulgaris Species 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- 244000088415 Raphanus sativus Species 0.000 description 2
- 235000006140 Raphanus sativus var sativus Nutrition 0.000 description 2
- 235000021536 Sugar beet Nutrition 0.000 description 2
- 125000003368 amide group Chemical group 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 244000013123 dwarf bean Species 0.000 description 2
- 244000037666 field crops Species 0.000 description 2
- 230000000855 fungicidal effect Effects 0.000 description 2
- 235000021331 green beans Nutrition 0.000 description 2
- FSQQTNAZHBEJLS-UPHRSURJSA-N maleamic acid Chemical class NC(=O)\C=C/C(O)=O FSQQTNAZHBEJLS-UPHRSURJSA-N 0.000 description 2
- 239000011976 maleic acid Substances 0.000 description 2
- 231100000252 nontoxic Toxicity 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 239000008096 xylene Substances 0.000 description 2
- 150000003738 xylenes Chemical class 0.000 description 2
- FBTQVXSNFILAQY-WAYWQWQTSA-N (z)-4-(4-chloroanilino)-4-oxobut-2-enoic acid Chemical compound OC(=O)\C=C/C(=O)NC1=CC=C(Cl)C=C1 FBTQVXSNFILAQY-WAYWQWQTSA-N 0.000 description 1
- HTHHBTMNLHMBHQ-UHFFFAOYSA-N 10-(1-azabicyclo[2.2.2]octan-3-yl)-n,n-dimethylphenothiazine-2-sulfonamide Chemical compound C1N(CC2)CCC2C1N1C2=CC=CC=C2SC2=CC=C(S(=O)(=O)N(C)C)C=C21 HTHHBTMNLHMBHQ-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-DOMIDYPGSA-N 2-(2,4-dichlorophenoxy)acetic acid Chemical compound OC(=O)[14CH2]OC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-DOMIDYPGSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- PJDNXAOTRKBXCC-HJWRWDBZSA-N C1(=CC=CC2=CC=CC=C12)NC(\C=C/C(=O)N)=O Chemical compound C1(=CC=CC2=CC=CC=C12)NC(\C=C/C(=O)N)=O PJDNXAOTRKBXCC-HJWRWDBZSA-N 0.000 description 1
- 244000025254 Cannabis sativa Species 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- 241001164397 Maireana aphylla Species 0.000 description 1
- 206010067482 No adverse event Diseases 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 240000004713 Pisum sativum Species 0.000 description 1
- 235000010582 Pisum sativum Nutrition 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- SNCZNSNPXMPCGN-UHFFFAOYSA-N butanediamide Chemical compound NC(=O)CCC(N)=O SNCZNSNPXMPCGN-UHFFFAOYSA-N 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 125000004093 cyano group Chemical group *C#N 0.000 description 1
- 239000012024 dehydrating agents Substances 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- LRCFXGAMWKDGLA-UHFFFAOYSA-N dioxosilane;hydrate Chemical compound O.O=[Si]=O LRCFXGAMWKDGLA-UHFFFAOYSA-N 0.000 description 1
- YWEUIGNSBFLMFL-UHFFFAOYSA-N diphosphonate Chemical compound O=P(=O)OP(=O)=O YWEUIGNSBFLMFL-UHFFFAOYSA-N 0.000 description 1
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 231100000162 fungitoxic Toxicity 0.000 description 1
- 230000002464 fungitoxic effect Effects 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000003966 growth inhibitor Substances 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- BOYANPPIKWSQRQ-SNAWJCMRSA-N methyl (e)-4-(3,4-dichloroanilino)-4-oxobut-2-enoate Chemical compound COC(=O)\C=C\C(=O)NC1=CC=C(Cl)C(Cl)=C1 BOYANPPIKWSQRQ-SNAWJCMRSA-N 0.000 description 1
- BOYANPPIKWSQRQ-PLNGDYQASA-N methyl (z)-4-(3,4-dichloroanilino)-4-oxobut-2-enoate Chemical compound COC(=O)\C=C/C(=O)NC1=CC=C(Cl)C(Cl)=C1 BOYANPPIKWSQRQ-PLNGDYQASA-N 0.000 description 1
- PERIEXQXFGPQDM-UHFFFAOYSA-N methyl 4-(3,4-dichloroanilino)-4-oxobutanoate Chemical compound COC(=O)CCC(=O)NC1=CC=C(Cl)C(Cl)=C1 PERIEXQXFGPQDM-UHFFFAOYSA-N 0.000 description 1
- JXTHEWSKYLZVJC-UHFFFAOYSA-N naptalam Chemical compound OC(=O)C1=CC=CC=C1C(=O)NC1=CC=CC2=CC=CC=C12 JXTHEWSKYLZVJC-UHFFFAOYSA-N 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- DLYUQMMRRRQYAE-UHFFFAOYSA-N phosphorus pentoxide Inorganic materials O1P(O2)(=O)OP3(=O)OP1(=O)OP2(=O)O3 DLYUQMMRRRQYAE-UHFFFAOYSA-N 0.000 description 1
- 230000001766 physiological effect Effects 0.000 description 1
- 230000001931 phytocidal effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000007226 seed germination Effects 0.000 description 1
- 229960004029 silicic acid Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- JDVPQXZIJDEHAN-UHFFFAOYSA-N succinamic acid Chemical class NC(=O)CCC(O)=O JDVPQXZIJDEHAN-UHFFFAOYSA-N 0.000 description 1
- 235000011044 succinic acid Nutrition 0.000 description 1
- 150000003444 succinic acids Chemical class 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-N sulfuric acid Substances OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
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
- 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
- A01N37/18—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/30—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof containing the groups —CO—N< and, both being directly attached by their carbon atoms to the same carbon skeleton, e.g. H2N—NH—CO—C6H4—COOCH3; Thio-analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Indole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US17471662A | 1962-02-21 | 1962-02-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CH442862A true CH442862A (de) | 1967-08-31 |
Family
ID=22637220
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CH210963A CH442862A (de) | 1962-02-21 | 1963-02-18 | Verfahren und Mittel zur Regelung des Pflanzenwachstums |
Country Status (4)
| Country | Link |
|---|---|
| JP (1) | JPS41579B1 (en(2012)) |
| BE (1) | BE628524A (en(2012)) |
| CH (1) | CH442862A (en(2012)) |
| GB (1) | GB1010569A (en(2012)) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991015464A1 (en) * | 1990-04-11 | 1991-10-17 | Warner-Lambert Company | Amide ester acat inhibitors |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4087942B2 (ja) * | 1998-03-11 | 2008-05-21 | 雪印種苗株式会社 | 植物成長調整剤 |
| JP4877679B2 (ja) * | 1999-09-03 | 2012-02-15 | 雪印種苗株式会社 | 植物成長調整剤 |
-
0
- BE BE628524D patent/BE628524A/xx unknown
-
1963
- 1963-02-12 GB GB570063A patent/GB1010569A/en not_active Expired
- 1963-02-14 JP JP782463A patent/JPS41579B1/ja active Pending
- 1963-02-18 CH CH210963A patent/CH442862A/de unknown
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1991015464A1 (en) * | 1990-04-11 | 1991-10-17 | Warner-Lambert Company | Amide ester acat inhibitors |
Also Published As
| Publication number | Publication date |
|---|---|
| BE628524A (en(2012)) | |
| GB1010569A (en) | 1965-11-17 |
| JPS41579B1 (en(2012)) | 1966-01-21 |
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