CH635303A5 - Mittel zur erhoehung von wurzelausbeute und zuckergehalt von zuckerrueben. - Google Patents

Mittel zur erhoehung von wurzelausbeute und zuckergehalt von zuckerrueben. Download PDF

Info

Publication number: CH635303A5
Authority: CH; Switzerland
Prior art keywords: reference sample; triazine; sugar; sugar content; given
Prior art date: 1977-08-01

Application number

CH817178A

Other languages

German (de)

English (en)

Inventor

Jan Kralovi

Emanuel Beska

Pavel Rapos

Stefan Truchlik

Original Assignee

Urad Predsednictva Slovenskej

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1977-08-01

Filing date

1978-07-28

Publication date

1983-03-31

1978-07-28 Application filed by Urad Predsednictva Slovenskej filed Critical Urad Predsednictva Slovenskej

1983-03-31 Publication of CH635303A5 publication Critical patent/CH635303A5/de

Links

235000016068 Berberis vulgaris Nutrition 0.000 title description 2
241000335053 Beta vulgaris Species 0.000 title description 2
239000013074 reference sample Substances 0.000 description 72
238000010998 test method Methods 0.000 description 46
150000001875 compounds Chemical class 0.000 description 40
125000004432 carbon atom Chemical group C* 0.000 description 30
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical compound C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 description 10
241000196324 Embryophyta Species 0.000 description 10
241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 8
235000021536 Sugar beet Nutrition 0.000 description 8
JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 description 7
239000003795 chemical substances by application Substances 0.000 description 7
239000000203 mixture Substances 0.000 description 7
WOPHAXVWACNHPM-UHFFFAOYSA-N 2-(methylthio)-1,3,5-triazine Chemical compound CSC1=NC=NC=N1 WOPHAXVWACNHPM-UHFFFAOYSA-N 0.000 description 6
239000013543 active substance Substances 0.000 description 6
125000003282 alkyl amino group Chemical group 0.000 description 6
239000003995 emulsifying agent Substances 0.000 description 6
HTSVYUUXJSMGQC-UHFFFAOYSA-N 2-chloro-1,3,5-triazine Chemical compound ClC1=NC=NC=N1 HTSVYUUXJSMGQC-UHFFFAOYSA-N 0.000 description 5
239000002904 solvent Substances 0.000 description 5
NCMONXLWVRSCBP-UHFFFAOYSA-N 2-methoxy-1,3,5-triazine Chemical compound COC1=NC=NC=N1 NCMONXLWVRSCBP-UHFFFAOYSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
125000003545 alkoxy group Chemical group 0.000 description 4
-1 methoxyamino Chemical group 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
239000002270 dispersing agent Substances 0.000 description 3
239000006185 dispersion Substances 0.000 description 3
230000000694 effects Effects 0.000 description 3
239000004009 herbicide Substances 0.000 description 3
239000007788 liquid Substances 0.000 description 3
239000000126 substance Substances 0.000 description 3
QPFMBZIOSGYJDE-UHFFFAOYSA-N 1,1,2,2-tetrachloroethane Chemical compound ClC(Cl)C(Cl)Cl QPFMBZIOSGYJDE-UHFFFAOYSA-N 0.000 description 2
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 2
SQROAKSRUALIEJ-UHFFFAOYSA-N 4-methylsulfanyl-1,3,5-triazin-2-amine Chemical compound CSC1=NC=NC(N)=N1 SQROAKSRUALIEJ-UHFFFAOYSA-N 0.000 description 2
VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
125000006323 alkenyl amino group Chemical group 0.000 description 2
125000005083 alkoxyalkoxy group Chemical group 0.000 description 2
125000004414 alkyl thio group Chemical group 0.000 description 2
IVRMZWNICZWHMI-UHFFFAOYSA-N azide group Chemical group [N-]=[N+]=[N-] IVRMZWNICZWHMI-UHFFFAOYSA-N 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
125000006310 cycloalkyl amino group Chemical group 0.000 description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
125000004663 dialkyl amino group Chemical group 0.000 description 2
239000000839 emulsion Substances 0.000 description 2
125000005191 hydroxyalkylamino group Chemical group 0.000 description 2
238000004519 manufacturing process Methods 0.000 description 2
239000000843 powder Substances 0.000 description 2
230000001105 regulatory effect Effects 0.000 description 2
239000000344 soap Substances 0.000 description 2
238000005507 spraying Methods 0.000 description 2
235000013311 vegetables Nutrition 0.000 description 2
WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
JEJKTJKRRRARGT-UHFFFAOYSA-N 1h-diazet-4-one Chemical compound O=C1NN=C1 JEJKTJKRRRARGT-UHFFFAOYSA-N 0.000 description 1
ZLKYBXDNXFQYDL-UHFFFAOYSA-N 2,4,6-triethoxy-1,3,5-triazine Chemical compound CCOC1=NC(OCC)=NC(OCC)=N1 ZLKYBXDNXFQYDL-UHFFFAOYSA-N 0.000 description 1
ULVNIJSKNRGBHX-UHFFFAOYSA-N 4-chloro-1,3,5-triazin-2-amine Chemical compound NC1=NC=NC(Cl)=N1 ULVNIJSKNRGBHX-UHFFFAOYSA-N 0.000 description 1
NROXQTDIDGVYHK-UHFFFAOYSA-N 4-methoxy-1,3,5-triazin-2-amine Chemical compound COC1=NC=NC(N)=N1 NROXQTDIDGVYHK-UHFFFAOYSA-N 0.000 description 1
QHXDTLYEHWXDSO-UHFFFAOYSA-N 6-chloro-2-n,2-n,4-n,4-n-tetraethyl-1,3,5-triazine-2,4-diamine Chemical compound CCN(CC)C1=NC(Cl)=NC(N(CC)CC)=N1 QHXDTLYEHWXDSO-UHFFFAOYSA-N 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
239000004471 Glycine Substances 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
BGRDGMRNKXEXQD-UHFFFAOYSA-N Maleic hydrazide Chemical compound OC1=CC=C(O)N=N1 BGRDGMRNKXEXQD-UHFFFAOYSA-N 0.000 description 1
239000005983 Maleic hydrazide Substances 0.000 description 1
YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical group C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
239000002202 Polyethylene glycol Substances 0.000 description 1
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
HFBWPRKWDIRYNX-UHFFFAOYSA-N Trietazine Chemical compound CCNC1=NC(Cl)=NC(N(CC)CC)=N1 HFBWPRKWDIRYNX-UHFFFAOYSA-N 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical class 0.000 description 1
150000001447 alkali salts Chemical class 0.000 description 1
125000006524 alkoxy alkyl amino group Chemical group 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000010775 animal oil Substances 0.000 description 1
125000000129 anionic group Chemical group 0.000 description 1
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 1
125000000852 azido group Chemical group *N=[N+]=[N-] 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
235000012216 bentonite Nutrition 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
229910000019 calcium carbonate Inorganic materials 0.000 description 1
235000010216 calcium carbonate Nutrition 0.000 description 1
239000001506 calcium phosphate Substances 0.000 description 1
229910000389 calcium phosphate Inorganic materials 0.000 description 1
235000011010 calcium phosphates Nutrition 0.000 description 1
125000002091 cationic group Chemical class 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
125000001309 chloro group Chemical group Cl* 0.000 description 1
239000011280 coal tar Substances 0.000 description 1
239000000084 colloidal system Substances 0.000 description 1
239000012141 concentrate Substances 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
235000013312 flour Nutrition 0.000 description 1
235000011389 fruit/vegetable juice Nutrition 0.000 description 1
238000000227 grinding Methods 0.000 description 1
238000003306 harvesting Methods 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000000463 material Substances 0.000 description 1
230000004060 metabolic process Effects 0.000 description 1
238000000034 method Methods 0.000 description 1
125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
239000011707 mineral Substances 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
235000010446 mineral oil Nutrition 0.000 description 1
125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
239000003921 oil Substances 0.000 description 1
235000011837 pasties Nutrition 0.000 description 1
230000035515 penetration Effects 0.000 description 1
230000035790 physiological processes and functions Effects 0.000 description 1
238000006068 polycondensation reaction Methods 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
239000004576 sand Substances 0.000 description 1
ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
239000007787 solid Substances 0.000 description 1
239000000243 solution Substances 0.000 description 1
239000007921 spray Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
239000000725 suspension Substances 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000002699 waste material Substances 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
239000002023 wood Substances 0.000 description 1
239000008096 xylene 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
- 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
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring 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
- 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
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen 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
- 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
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
- A01N43/68—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms with two or three nitrogen atoms directly attached to ring carbon atoms
- A01N43/70—Diamino—1,3,5—triazines with only one oxygen, sulfur or halogen atom or only one cyano, thiocyano (—SCN), cyanato (—OCN) or azido (—N3) group directly attached to a ring carbon atom

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)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

CH817178A 1977-08-01 1978-07-28 Mittel zur erhoehung von wurzelausbeute und zuckergehalt von zuckerrueben. CH635303A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CS506577A CS197620B1 (en)	1977-08-01	1977-08-01	Agent for enhancement of root yield and sugar content of sugar beet

Publications (1)

Publication Number	Publication Date
CH635303A5 true CH635303A5 (de)	1983-03-31

Family

ID=5394796

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH817178A CH635303A5 (de)	1977-08-01	1978-07-28	Mittel zur erhoehung von wurzelausbeute und zuckergehalt von zuckerrueben.

Country Status (5)

Country	Link
CH (1)	CH635303A5 (cs)
CS (1)	CS197620B1 (cs)
DE (1)	DE2833582C2 (cs)
FR (1)	FR2399206A1 (cs)
GB (1)	GB2002339B (cs)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3222147A1 (de) *	1982-06-11	1983-12-15	Chemische Werke Hüls AG, 4370 Marl	Verwendung gegebenenfalls substituierter thiomethylcycloalkylamino-s-triazine als selektive mittel gegen unkraeuter und schadgraeser
WO2002036578A2 (en)	2000-10-31	2002-05-10	Lynn Bonham	Triazine derivatives as lpaat-b inhibitors and uses thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE793112A (fr) *	1971-12-22	1973-06-21	Ciba Geigy	Pyridinium-s-triazines agissant sur la croissance des plantes

1977
- 1977-08-01 CS CS506577A patent/CS197620B1/cs unknown
1978
- 1978-07-27 GB GB7831360A patent/GB2002339B/en not_active Expired
- 1978-07-28 CH CH817178A patent/CH635303A5/de not_active IP Right Cessation
- 1978-07-31 DE DE19782833582 patent/DE2833582C2/de not_active Expired
- 1978-07-31 FR FR7822594A patent/FR2399206A1/fr active Granted

Also Published As

Publication number	Publication date
GB2002339B (en)	1982-04-28
FR2399206B1 (cs)	1983-04-01
CS197620B1 (en)	1980-05-30
DE2833582A1 (de)	1979-02-15
GB2002339A (en)	1979-02-21
DE2833582C2 (de)	1986-07-10
FR2399206A1 (fr)	1979-03-02

Legal Events

Date	Code	Title	Description
1990-03-30	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DE2646712C2 (cs)	1988-02-04
DE1213665B (de)	1966-03-31	Selektive Herbicide
DE2017497A1 (cs)	1970-11-05
DE1135238B (de)	1962-08-23	Mittel zur Hemmung des Pflanzenwachstums, insbesondere Unkrautvertilgungsmittel
DE1695251A1 (de)	1971-03-25	Herbicide
CH337019A (de)	1959-03-15	Verfahren und Mittel zur Beeinflussung des Pflanzenwachstums, insbesondere zur Bekämpfung von Unkraut
DE2833582C2 (de)	1986-07-10	Verfahren zur Steigerung der Wurzelausbeute und des Zuckergehalts von Zuckerrüben
DE2512641A1 (de)	1976-03-18	Acetylenische 2,6-dichlorbenzoate und ihre verwendung als wachstumsregulatoren fuer pflanzen
DE1906050C3 (de)	1979-01-25	S-Alkyi-dnethyl-hexahydro-lHazepin)-1 -carbothiolate
DE1301819B (de)	1969-08-28	Substituierte 2, 4-Diamino-6-chlor-s-triazine
DE951181C (de)	1956-10-25	Unkrautvertilgungsmittel
DE1545755C (cs)
DE2922270A1 (de)	1979-12-06	N-(chloracetyl)-1,4oxaza-spirokohlenwasserstoffderivate, verfahren zu ihrer herstellung und solche enthaltende pflanzenschutzmittel
DE1567006C3 (de)	1974-08-08	Unkrautbekämpfungsmittel
CH373919A (de)	1963-12-15	Verfahren zum Bekämpfen von Unkräutern
CH337020A (de)	1959-03-15	Verfahren und Mittel zur Beeinflussung des Pflanzenwachstums, insbesondere zur Bekämpfung von Unkraut
CH409516A (de)	1966-03-15	Verfahren und Mittel zur Hemmung des Pflanzenwachstums, insbesondere zur Unkrautvertilgung
DE2558385A1 (de)	1977-07-07	Ertragssteigernde mittel
CH335570A (de)	1959-01-15	Verfahren und Mittel zur Beeinflussung des Pflanzenwachstums, insbesondere zur Bekämpfung von Unkraut
CH340378A (de)	1959-08-15	Mittel zur Beeinflussung des Pflanzenwachstums, insbesondere zur Bekämpfung von Unkraut
DE3116012A1 (de)	1982-10-28	Mittel, insbesondere zur entblaetterung von pflanzen
DE1138978B (de)	1962-10-31	Mittel zur Beeinflussung des Pflanzenwachstums
DE3116008A1 (de)	1982-10-28	Mittel insbesondere zur entblaetterung von pflanzen
DE1545755B1 (de)	1970-01-29	Sulfinyl- oder Sulfonylpyridine sowie Verfahren zu ihrer Herstellung
DE3116016A1 (de)	1982-11-04	Mittel insbesondere zur entblaetterung von pflanzen