GB818925A - Compositions for controlling plant growth - Google Patents
Compositions for controlling plant growthInfo
- Publication number
- GB818925A GB818925A GB1407055A GB1407055A GB818925A GB 818925 A GB818925 A GB 818925A GB 1407055 A GB1407055 A GB 1407055A GB 1407055 A GB1407055 A GB 1407055A GB 818925 A GB818925 A GB 818925A
- Authority
- GB
- United Kingdom
- Prior art keywords
- acid
- esters
- chlorophenyl
- boronic
- carrier
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title abstract 2
- 230000008635 plant growth Effects 0.000 title abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 abstract 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 4
- 150000001875 compounds Chemical class 0.000 abstract 4
- -1 methyl- Chemical group 0.000 abstract 4
- HXITXNWTGFUOAU-UHFFFAOYSA-N phenylboronic acid Chemical class OB(O)C1=CC=CC=C1 HXITXNWTGFUOAU-UHFFFAOYSA-N 0.000 abstract 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract 3
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 abstract 3
- VIGVRXYWWFPORY-UHFFFAOYSA-N diphenylborinic acid Chemical class C=1C=CC=CC=1B(O)C1=CC=CC=C1 VIGVRXYWWFPORY-UHFFFAOYSA-N 0.000 abstract 3
- 150000002148 esters Chemical class 0.000 abstract 3
- 239000007788 liquid Substances 0.000 abstract 3
- 239000007787 solid Substances 0.000 abstract 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 abstract 2
- 150000008064 anhydrides Chemical class 0.000 abstract 2
- YCIMNLLNPGFGHC-UHFFFAOYSA-N catechol Chemical compound OC1=CC=CC=C1O YCIMNLLNPGFGHC-UHFFFAOYSA-N 0.000 abstract 2
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 abstract 2
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 abstract 2
- 239000002904 solvent Substances 0.000 abstract 2
- 239000004094 surface-active agent Substances 0.000 abstract 2
- RRCMGJCFMJBHQC-UHFFFAOYSA-N (2-chlorophenyl)boronic acid Chemical compound OB(O)C1=CC=CC=C1Cl RRCMGJCFMJBHQC-UHFFFAOYSA-N 0.000 abstract 1
- ROEQGIFOWRQYHD-UHFFFAOYSA-N (2-methoxyphenyl)boronic acid Chemical compound COC1=CC=CC=C1B(O)O ROEQGIFOWRQYHD-UHFFFAOYSA-N 0.000 abstract 1
- SDEAGACSNFSZCU-UHFFFAOYSA-N (3-chlorophenyl)boronic acid Chemical compound OB(O)C1=CC=CC(Cl)=C1 SDEAGACSNFSZCU-UHFFFAOYSA-N 0.000 abstract 1
- CAYQIZIAYYNFCS-UHFFFAOYSA-N (4-chlorophenyl)boronic acid Chemical compound OB(O)C1=CC=C(Cl)C=C1 CAYQIZIAYYNFCS-UHFFFAOYSA-N 0.000 abstract 1
- VOAAEKKFGLPLLU-UHFFFAOYSA-N (4-methoxyphenyl)boronic acid Chemical compound COC1=CC=C(B(O)O)C=C1 VOAAEKKFGLPLLU-UHFFFAOYSA-N 0.000 abstract 1
- BLZVCIGGICSWIG-UHFFFAOYSA-N 2-aminoethoxydiphenylborane Chemical compound C=1C=CC=CC=1B(OCCN)C1=CC=CC=C1 BLZVCIGGICSWIG-UHFFFAOYSA-N 0.000 abstract 1
- 125000000022 2-aminoethyl group Chemical group [H]C([*])([H])C([H])([H])N([H])[H] 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 abstract 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- UYANAUSDHIFLFQ-UHFFFAOYSA-N borinic acid Chemical class OB UYANAUSDHIFLFQ-UHFFFAOYSA-N 0.000 abstract 1
- HQABUPZFAYXKJW-UHFFFAOYSA-N butan-1-amine Chemical compound CCCCN HQABUPZFAYXKJW-UHFFFAOYSA-N 0.000 abstract 1
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 239000004927 clay Substances 0.000 abstract 1
- 229910052570 clay Inorganic materials 0.000 abstract 1
- 229940062233 di-isopropylammonium Drugs 0.000 abstract 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 abstract 1
- HRHHBUOORHRASE-UHFFFAOYSA-N diphenoxyboron Chemical compound C=1C=CC=CC=1O[B]OC1=CC=CC=C1 HRHHBUOORHRASE-UHFFFAOYSA-N 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 229940083124 ganglion-blocking antiadrenergic secondary and tertiary amines Drugs 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine group Chemical group N1=CCC2=CC=CC=C12 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 abstract 1
- LPAGFVYQRIESJQ-UHFFFAOYSA-N indoline Chemical compound C1=CC=C2NCCC2=C1 LPAGFVYQRIESJQ-UHFFFAOYSA-N 0.000 abstract 1
- 229910017464 nitrogen compound Inorganic materials 0.000 abstract 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 1
- 230000000361 pesticidal effect Effects 0.000 abstract 1
- 239000003208 petroleum Substances 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000000377 silicon dioxide Substances 0.000 abstract 1
- 239000007921 spray Substances 0.000 abstract 1
- 150000005846 sugar alcohols Polymers 0.000 abstract 1
- 239000000454 talc Substances 0.000 abstract 1
- 229910052623 talc Inorganic materials 0.000 abstract 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
- A01N55/00—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur
- A01N55/08—Biocides, pest repellants or attractants, or plant growth regulators, containing organic compounds containing elements other than carbon, hydrogen, halogen, oxygen, nitrogen and sulfur containing boron
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)
Abstract
A plant growth controlling composition comprises an organoboron compound and a surface-active agent, or an inert solid or liquid non-solvent carrier, or a surface-active agent and an inert solid or liquid (including solvent) carrier, the organoboron compound being selected from a group consisting of halogen-, methyl-, halogenomethyl- or methoxy-substituted phenyl-boronic and diphenylborinic acids, the unsubstituted diphenylborinic acids, the anhydrides, esters such as those with monohydric or polyhydric alcohols and phenols, for example, ethanol, isopropanol, cyclohexanol, ethylene glycol and catechol, the esters with the alkanolamines, particularly ethanolamine and diethanolamine, salts and nitrogenous base, such as aliphatic primary, secondary and tertiary amines, for example n-butylamine, di-isopropylamine and triethylamine, and heterocyclic nitrogen compounds, preferably those containing aromatic type unsaturation such as pyridine and indolenine complexes of the boronic and borinic acids and the anhydride, esters and nitrogenous base complexes of the unsubstituted phenylboronic acid. The carrier may be solid, e.g. finely powdered talc, silica, carbon, clay, fuller's earth or kieselguhr which may be oil treated to improve adhesivity, or an organic liquid, which may contain an emulsifier, e.g. methanol, ethanol, isopropanol, secondary butanol, cyclohexanol, acetone, methyl isobutyl ketone, pyridine or a petroleum spray oil. Other pesticidal compounds and stickers may also be included. Specified compounds are 2-, 3- or 4-chlorophenyl boronic acid, 2- or 4-methoxyphenylboronic acid, di - (4 - chlorophenyl borinic acid, 3-azapentamethylene diphenyl boronate, 2-aminoethyl diphenylborinate, 2 - aminoethyl di (4 - chlorophenyl borinate, the di-isopropylammonium, pyridinium or indolinium complex of a phenylboronic acid or of a diphenylborinic acid. Specification 814,647,[Group IV (b)], is referred to.
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1407055A GB818925A (en) | 1955-05-16 | 1955-05-16 | Compositions for controlling plant growth |
| MY6000015A MY6000015A (en) | 1955-05-16 | 1960-12-31 | Compositions for controlling plant growth |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB1407055A GB818925A (en) | 1955-05-16 | 1955-05-16 | Compositions for controlling plant growth |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB818925A true GB818925A (en) | 1959-08-26 |
Family
ID=10034436
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1407055A Expired GB818925A (en) | 1955-05-16 | 1955-05-16 | Compositions for controlling plant growth |
Country Status (2)
| Country | Link |
|---|---|
| GB (1) | GB818925A (en) |
| MY (1) | MY6000015A (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4110426A (en) * | 1973-07-24 | 1978-08-29 | Colgate-Palmolive Company | Method of treating skin and hair with a self-heated cosmetic |
| WO2017207358A1 (en) * | 2016-06-03 | 2017-12-07 | Basf Se | Benzoxaborole compounds |
| WO2019101560A1 (en) * | 2017-11-22 | 2019-05-31 | Basf Se | Benzoxaborole compounds |
-
1955
- 1955-05-16 GB GB1407055A patent/GB818925A/en not_active Expired
-
1960
- 1960-12-31 MY MY6000015A patent/MY6000015A/en unknown
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4110426A (en) * | 1973-07-24 | 1978-08-29 | Colgate-Palmolive Company | Method of treating skin and hair with a self-heated cosmetic |
| WO2017207358A1 (en) * | 2016-06-03 | 2017-12-07 | Basf Se | Benzoxaborole compounds |
| US11064701B2 (en) | 2016-06-03 | 2021-07-20 | Basf Se | Benzoxaborole compounds |
| WO2019101560A1 (en) * | 2017-11-22 | 2019-05-31 | Basf Se | Benzoxaborole compounds |
| US11058117B2 (en) | 2017-11-22 | 2021-07-13 | Basf Se | Benzoxaborole compounds |
Also Published As
| Publication number | Publication date |
|---|---|
| MY6000015A (en) | 1960-12-31 |
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