HU181414B - Növekedésszabályozó készítmények - Google Patents

Növekedésszabályozó készítmények Download PDF

Info

Publication number: HU181414B
Authority: HU; Hungary
Prior art keywords: growth; compound; formula; plant growth; growth regulating
Prior art date: 1978-05-03

Application number

Other languages

English (en)

Hungarian (hu)

Inventor

Georg Dd Kleiner Ralf Hoh

Werner Kochmann

Dd Lang Sieghard Wilfried

Kurt Naumann

Guenther Sembdner

Klaus Schreiber

Horst R Schuette

Walter Steinke

Original Assignee

Bitterfeld Chemie

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.)

1978-05-03

Filing date

1979-05-03

Publication date

1983-07-28

1979-05-03 Application filed by Bitterfeld Chemie filed Critical Bitterfeld Chemie

1983-07-28 Publication of HU181414B publication Critical patent/HU181414B/hu

Links

239000000203 mixture Substances 0.000 title claims description 12
230000008635 plant growth Effects 0.000 title description 2
230000001105 regulatory effect Effects 0.000 title description 2
UDPGUMQDCGORJQ-UHFFFAOYSA-N (2-chloroethyl)phosphonic acid Chemical compound OP(O)(=O)CCCl UDPGUMQDCGORJQ-UHFFFAOYSA-N 0.000 claims description 11
239000004480 active ingredient Substances 0.000 claims description 9
239000003630 growth substance Substances 0.000 claims description 8
150000001875 compounds Chemical class 0.000 claims description 7
125000000217 alkyl group Chemical group 0.000 claims description 4
239000000969 carrier Substances 0.000 claims description 4
UHZZMRAGKVHANO-UHFFFAOYSA-M chlormequat chloride Chemical compound [Cl-].C[N+](C)(C)CCCl UHZZMRAGKVHANO-UHFFFAOYSA-M 0.000 claims description 3
229910052736 halogen Inorganic materials 0.000 claims description 3
150000002367 halogens Chemical class 0.000 claims description 3
229910001413 alkali metal ion Inorganic materials 0.000 claims description 2
229910052799 carbon Inorganic materials 0.000 claims description 2
125000000753 cycloalkyl group Chemical group 0.000 claims description 2
229910052739 hydrogen Inorganic materials 0.000 claims description 2
239000001257 hydrogen Substances 0.000 claims description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
239000007788 liquid Substances 0.000 claims 2
239000007787 solid Substances 0.000 claims 2
239000013543 active substance Substances 0.000 claims 1
125000000129 anionic group Chemical group 0.000 claims 1
239000003945 anionic surfactant Substances 0.000 claims 1
150000001721 carbon Chemical group 0.000 claims 1
150000002431 hydrogen Chemical class 0.000 claims 1
239000002736 nonionic surfactant Substances 0.000 claims 1
230000012010 growth Effects 0.000 description 12
241000196324 Embryophyta Species 0.000 description 11
238000012360 testing method Methods 0.000 description 10
125000001424 substituent group Chemical group 0.000 description 9
230000000694 effects Effects 0.000 description 8
238000004690 coupled electron pair approximation Methods 0.000 description 7
239000000126 substance Substances 0.000 description 6
229940126062 Compound A Drugs 0.000 description 5
NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 description 5
241000209140 Triticum Species 0.000 description 5
235000021307 Triticum Nutrition 0.000 description 5
238000000034 method Methods 0.000 description 4
230000015572 biosynthetic process Effects 0.000 description 3
235000013339 cereals Nutrition 0.000 description 3
125000002887 hydroxy group Chemical group [H]O* 0.000 description 3
230000004060 metabolic process Effects 0.000 description 3
239000000243 solution Substances 0.000 description 3
239000012085 test solution Substances 0.000 description 3
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
244000046052 Phaseolus vulgaris Species 0.000 description 2
235000010627 Phaseolus vulgaris Nutrition 0.000 description 2
238000011161 development Methods 0.000 description 2
230000018109 developmental process Effects 0.000 description 2
239000012153 distilled water Substances 0.000 description 2
238000009472 formulation Methods 0.000 description 2
230000035784 germination Effects 0.000 description 2
239000004615 ingredient Substances 0.000 description 2
238000011835 investigation Methods 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 2
230000002195 synergetic effect Effects 0.000 description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
VYPKFHFVKFKHMK-UHFFFAOYSA-N 2-(1h-indol-2-yl)butanoic acid Chemical compound C1=CC=C2NC(C(C(O)=O)CC)=CC2=C1 VYPKFHFVKFKHMK-UHFFFAOYSA-N 0.000 description 1
229930192334 Auxin Natural products 0.000 description 1
239000005982 Indolylbutyric acid Substances 0.000 description 1
-1 Indolyloxy Chemical group 0.000 description 1
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
239000002253 acid Substances 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
239000002363 auxin Substances 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
229940125890 compound Ia Drugs 0.000 description 1
238000013270 controlled release Methods 0.000 description 1
125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
238000011156 evaluation Methods 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
230000004720 fertilization Effects 0.000 description 1
239000012634 fragment Substances 0.000 description 1
239000008187 granular material Substances 0.000 description 1
238000003898 horticulture Methods 0.000 description 1
125000004435 hydrogen atom Chemical class [H]* 0.000 description 1
SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 description 1
230000001939 inductive effect Effects 0.000 description 1
230000000968 intestinal effect Effects 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
230000004660 morphological change Effects 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
239000006072 paste Substances 0.000 description 1
239000000546 pharmaceutical excipient Substances 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
QIIPQYDSKRYMFG-UHFFFAOYSA-N phenyl hydrogen carbonate Chemical class OC(=O)OC1=CC=CC=C1 QIIPQYDSKRYMFG-UHFFFAOYSA-N 0.000 description 1
239000000843 powder Substances 0.000 description 1
LVTJOONKWUXEFR-FZRMHRINSA-N protoneodioscin Natural products O(C[C@@H](CC[C@]1(O)[C@H](C)[C@@H]2[C@]3(C)[C@H]([C@H]4[C@@H]([C@]5(C)C(=CC4)C[C@@H](O[C@@H]4[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@@H](O)[C@H](O[C@H]6[C@@H](O)[C@@H](O)[C@@H](O)[C@H](C)O6)[C@H](CO)O4)CC5)CC3)C[C@@H]2O1)C)[C@H]1[C@H](O)[C@H](O)[C@H](O)[C@@H](CO)O1 LVTJOONKWUXEFR-FZRMHRINSA-N 0.000 description 1
230000011514 reflex Effects 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
230000036301 sexual development Effects 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000012086 standard solution Substances 0.000 description 1
238000005728 strengthening Methods 0.000 description 1
239000001384 succinic acid Substances 0.000 description 1
239000000725 suspension Substances 0.000 description 1
230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1

Landscapes

Agricultural Chemicals And Associated Chemicals (AREA)
Crystals, And After-Treatments Of Crystals (AREA)

HUCE001212 1978-05-03 1979-05-03 Növekedésszabályozó készítmények HU181414B (hu)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DD20513078A DD136208B1 (de)	1978-05-03	1978-05-03	Wachstumsregulatoren

Publications (1)

Publication Number	Publication Date
HU181414B true HU181414B (hu)	1983-07-28

Family

ID=5512460

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
HUCE001212 HU181414B (hu)	1978-05-03	1979-05-03	Növekedésszabályozó készítmények

Country Status (7)

Country	Link
BG (1)	BG32289A1 (fr)
CS (1)	CS217441B1 (fr)
DD (1)	DD136208B1 (fr)
HU (1)	HU181414B (fr)
PL (1)	PL122379B1 (fr)
RO (1)	RO76184A (fr)
SU (1)	SU1519613A1 (fr)

1978
- 1978-05-03 DD DD20513078A patent/DD136208B1/de not_active IP Right Cessation
1979
- 1979-04-17 BG BG7943408A patent/BG32289A1/xx unknown
- 1979-04-25 SU SU797770545A patent/SU1519613A1/ru active
- 1979-04-26 CS CS290879A patent/CS217441B1/cs unknown
- 1979-05-03 RO RO7997411A patent/RO76184A/fr unknown
- 1979-05-03 PL PL21534579A patent/PL122379B1/pl unknown
- 1979-05-03 HU HUCE001212 patent/HU181414B/hu unknown

Also Published As

Publication number	Publication date
CS217441B1 (cs)	1983-01-28
DD136208B1 (de)	1981-02-25
BG32289A1 (en)	1982-07-15
PL215345A1 (fr)	1980-01-28
PL122379B1 (en)	1982-07-31
DD136208A1 (de)	1979-06-27
SU1519613A1 (ru)	1989-11-07
RO76184A (fr)	1981-02-28

Publication	Publication Date	Title
JPH0624917A (ja)	1994-02-01	除草剤組成物
Folker-Hansen et al.	1996	Effect of dimethoate on body growth of representatives of the soil living mesofauna
DE2141586C2 (de)	1983-07-21	Herbizides Saatschutzmittel auf Sulfonatbasis
JPH0472801B2 (fr)	1992-11-19
HU181414B (hu)	1983-07-28	Növekedésszabályozó készítmények
DE60132248T2 (de)	2009-01-15	Fungizide zusammensetzung auf der basis von saurem kaliumphosphit
DE2265535C3 (de)	1982-04-29	Herbizide Mittel und ihre Verwendung als Pflanzenwuchsregler
SE455259B (sv)	1988-07-04	Anvendning av vissa aminoalkanfosfonsyror for bekempning av svampsjukdomar hos vexter
SU843695A3 (ru)	1981-06-30	Гербицидна композици
KR850000222B1 (ko)	1985-03-11	제초제 조성물
DE2349970C2 (de)	1982-09-16	N-Benzoyl-N-(3-chlor-4-fluorphenyl)-alanin-methylester und -isopropylester, Verfahren zu deren Herstellung und deren Verwendung
DE2417257A1 (de)	1974-10-24	Pflanzenwuchsregler
DE2805941C2 (de)	1985-12-12	Hydraziniumphosphite, ihre Herstellung und funigzide Zusammensetzungen
JPH05221812A (ja)	1993-08-31	イネ種子用殺菌剤
JP4937647B2 (ja)	2012-05-23	銀担持ゼオライトを有効成分として含有する水稲種子消毒剤および該消毒剤による稲病害の防除方法
DE1001854C2 (de)	1957-07-04	Fungicide Mittel
US3674878A (en)	1972-07-04	Process for controlling nematodes
SU782789A1 (ru)	1980-11-30	Состав дл регулировани роста растений
SU668566A3 (ru)	1979-06-15	Гербицидный состав
CS218346B1 (cs)	1983-02-25	Stimulátor růstu rostlin
DE2200941A1 (de)	1972-08-24	Mittel zur Beeinflussung des Wasserhaushaltes und zur Steigerung des Ertrages von Pflanzen
JPH0327521B2 (fr)	1991-04-16
US4035496A (en)	1977-07-12	Methods of combatting nematodes using certain derivatives of 1,3,5-oxathiazine
RU2438311C1 (ru)	2012-01-10	3-пиперидинил-4-бензосульфамидобутиролактон, проявляющий корнеобразующую активность на семенах озимой пшеницы
SU249317A1 (ru)		Гербицидный состав