DD148288A1 - Verfahren zur selektiven behandlung von nutzpflanzenkulturen - Google Patents
Verfahren zur selektiven behandlung von nutzpflanzenkulturen Download PDFInfo
- Publication number
- DD148288A1 DD148288A1 DD79218168A DD21816879A DD148288A1 DD 148288 A1 DD148288 A1 DD 148288A1 DD 79218168 A DD79218168 A DD 79218168A DD 21816879 A DD21816879 A DD 21816879A DD 148288 A1 DD148288 A1 DD 148288A1
- Authority
- DD
- German Democratic Republic
- Prior art keywords
- formula
- acetamide
- cocl
- mixtures
- weight
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims abstract description 13
- 239000000460 chlorine Substances 0.000 claims abstract description 36
- 239000000203 mixture Substances 0.000 claims abstract description 27
- 150000001875 compounds Chemical class 0.000 claims abstract description 20
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229910052801 chlorine Inorganic materials 0.000 claims abstract description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 10
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 10
- 239000003995 emulsifying agent Substances 0.000 claims abstract description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 6
- 239000001257 hydrogen Substances 0.000 claims abstract description 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims abstract description 5
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910052794 bromium Inorganic materials 0.000 claims abstract description 5
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 4
- 239000002270 dispersing agent Substances 0.000 claims abstract description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 125000001424 substituent group Chemical group 0.000 claims abstract description 3
- 150000002431 hydrogen Chemical class 0.000 claims abstract 2
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- 239000004480 active ingredient Substances 0.000 claims description 12
- 150000003869 acetamides Chemical class 0.000 claims description 7
- RMRFFCXPLWYOOY-UHFFFAOYSA-N allyl radical Chemical compound [CH2]C=C RMRFFCXPLWYOOY-UHFFFAOYSA-N 0.000 claims description 2
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims 18
- 238000010790 dilution Methods 0.000 claims 1
- 239000012895 dilution Substances 0.000 claims 1
- 239000000080 wetting agent Substances 0.000 abstract description 4
- 238000009736 wetting Methods 0.000 abstract description 3
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- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 abstract 1
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- 239000000428 dust Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 230000012010 growth Effects 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 239000012442 inert solvent Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 238000002955 isolation Methods 0.000 description 1
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 1
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 1
- 150000002540 isothiocyanates Chemical class 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
- 235000012054 meals Nutrition 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- VYQNWZOUAUKGHI-UHFFFAOYSA-N monobenzone Chemical compound C1=CC(O)=CC=C1OCC1=CC=CC=C1 VYQNWZOUAUKGHI-UHFFFAOYSA-N 0.000 description 1
- HCVKQZHVTQDNKN-UHFFFAOYSA-N n-(2-methylpropyl)-n-(2,3,3-trimethylcyclopenten-1-yl)acetamide Chemical compound CC(C)CN(C(C)=O)C1=C(C)C(C)(C)CC1 HCVKQZHVTQDNKN-UHFFFAOYSA-N 0.000 description 1
- SYSQUGFVNFXIIT-UHFFFAOYSA-N n-[4-(1,3-benzoxazol-2-yl)phenyl]-4-nitrobenzenesulfonamide Chemical class C1=CC([N+](=O)[O-])=CC=C1S(=O)(=O)NC1=CC=C(C=2OC3=CC=CC=C3N=2)C=C1 SYSQUGFVNFXIIT-UHFFFAOYSA-N 0.000 description 1
- IYVZDZVSRPDIPH-UHFFFAOYSA-N n-methyl-n-(2,3,3-trimethylcyclopenten-1-yl)acetamide Chemical compound CC(=O)N(C)C1=C(C)C(C)(C)CC1 IYVZDZVSRPDIPH-UHFFFAOYSA-N 0.000 description 1
- PDUSWJORWQPNRP-UHFFFAOYSA-N n-propan-2-ylacetamide Chemical compound CC(C)NC(C)=O PDUSWJORWQPNRP-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 235000019198 oils Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000011837 pasties Nutrition 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 230000029553 photosynthesis Effects 0.000 description 1
- 238000010672 photosynthesis Methods 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 1
- 239000008262 pumice Substances 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000011403 purification operation Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 125000005624 silicic acid group Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000004455 soybean meal Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 238000010626 work up procedure Methods 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 239000011592 zinc chloride Substances 0.000 description 1
- 235000005074 zinc chloride Nutrition 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
- A01N37/20—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 group, wherein Cn means a carbon skeleton not containing a ring; Thio analogues thereof
-
- 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
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19782856651 DE2856651A1 (de) | 1978-12-29 | 1978-12-29 | Alpha -substituierte n-(trimethyl- cycloalkenyl)-n-alkyl-acetamide und deren verwendung in phytotoxischen zubereitungen |
| DE19792940231 DE2940231A1 (de) | 1979-10-04 | 1979-10-04 | (alpha)-substituierte n-(trimethylcycloalkenyl)-n-alkyl-acetamide und deren verwendung in phytotoxischen zubereitungen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DD148288A1 true DD148288A1 (de) | 1981-05-20 |
Family
ID=25777109
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DD79218168A DD148288A1 (de) | 1978-12-29 | 1979-12-27 | Verfahren zur selektiven behandlung von nutzpflanzenkulturen |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US4319918A (en, 2012) |
| EP (1) | EP0013429B1 (en, 2012) |
| BG (1) | BG33881A3 (en, 2012) |
| BR (1) | BR7908491A (en, 2012) |
| CA (1) | CA1135720A (en, 2012) |
| DD (1) | DD148288A1 (en, 2012) |
| DE (1) | DE2965973D1 (en, 2012) |
| EG (1) | EG14212A (en, 2012) |
| IL (1) | IL59050A (en, 2012) |
| IN (1) | IN151526B (en, 2012) |
| TR (1) | TR20508A (en, 2012) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3245020A1 (de) * | 1982-12-06 | 1984-06-07 | Celamerck Gmbh & Co Kg, 6507 Ingelheim | Cycloalkenylderivate, ihre herstellung und verwendung |
| DE3315601A1 (de) * | 1983-04-29 | 1984-10-31 | Bayer Ag, 5090 Leverkusen | N-cyclohexadienyl-chloracetamide |
| DE3319187A1 (de) * | 1983-05-27 | 1984-11-29 | Chemische Werke Hüls AG, 4370 Marl | (alpha)-alkoxylierte n-(3,3,5- bzw. 3,5,5-trimethylcyclohexen-1-yl)-n-alkyl- oder -n-allyl-acetamide und deren verwendung in phytotoxischen zubereitungen |
| US4608082A (en) * | 1985-02-19 | 1986-08-26 | Union Carbide Corporation | Herbicidal cycloalkenyl acetamides |
| EP0281521B1 (de) * | 1987-03-06 | 1992-07-08 | Ciba-Geigy Ag | Herbizide Zusammensetzungen |
| DE58908525D1 (de) * | 1988-09-02 | 1994-11-24 | Hoechst Ag | Wässrige Formulierungen und deren Verwendung. |
| KR101258137B1 (ko) * | 2011-05-26 | 2013-04-25 | 고등기술연구원연구조합 | 하이브리드 집진장치 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES336244A1 (es) * | 1966-02-01 | 1967-12-16 | Monsanto Co | Procedimiento para preparar una composicion fitotoxica. |
| US3574746A (en) * | 1967-06-05 | 1971-04-13 | Monsanto Co | N-(cycloalken-1-yl) alpha-haloacetamides |
| BE756119R (fr) * | 1969-09-15 | 1971-03-15 | Monsanto Co | Procedes de preparation d'alpha-chloroacetamides, nouveaux produits et compositions phytotoxiques ainsi |
-
1979
- 1979-12-08 TR TR20508A patent/TR20508A/xx unknown
- 1979-12-21 CA CA000342460A patent/CA1135720A/en not_active Expired
- 1979-12-26 BR BR7908491A patent/BR7908491A/pt unknown
- 1979-12-27 EP EP79105383A patent/EP0013429B1/de not_active Expired
- 1979-12-27 BG BG046084A patent/BG33881A3/xx unknown
- 1979-12-27 DD DD79218168A patent/DD148288A1/de not_active IP Right Cessation
- 1979-12-27 DE DE7979105383T patent/DE2965973D1/de not_active Expired
- 1979-12-28 IL IL59050A patent/IL59050A/xx unknown
- 1979-12-28 US US06/108,226 patent/US4319918A/en not_active Expired - Lifetime
- 1979-12-29 IN IN1361/CAL/79A patent/IN151526B/en unknown
- 1979-12-29 EG EG778/78A patent/EG14212A/xx active
Also Published As
| Publication number | Publication date |
|---|---|
| US4319918A (en) | 1982-03-16 |
| IL59050A0 (en) | 1980-03-31 |
| TR20508A (tr) | 1981-09-03 |
| EP0013429A1 (de) | 1980-07-23 |
| IN151526B (en, 2012) | 1983-05-14 |
| EP0013429B1 (de) | 1983-07-20 |
| BR7908491A (pt) | 1980-09-23 |
| DE2965973D1 (en) | 1983-08-25 |
| CA1135720A (en) | 1982-11-16 |
| EG14212A (en) | 1983-12-31 |
| IL59050A (en) | 1983-09-30 |
| BG33881A3 (en) | 1983-05-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| ENJ | Ceased due to non-payment of renewal fee |