AT126151B - Pesticides. - Google Patents
Pesticides.Info
- Publication number
- AT126151B AT126151B AT126151DA AT126151B AT 126151 B AT126151 B AT 126151B AT 126151D A AT126151D A AT 126151DA AT 126151 B AT126151 B AT 126151B
- Authority
- AT
- Austria
- Prior art keywords
- parts
- weight
- pesticides
- water
- sodium
- Prior art date
Links
- 239000000575 pesticide Substances 0.000 title description 3
- -1 alkali metal salts Chemical class 0.000 claims description 5
- 150000001491 aromatic compounds Chemical class 0.000 claims description 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 150000001875 compounds Chemical class 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- LYIIBVSRGJSHAV-UHFFFAOYSA-N 2-aminoacetaldehyde Chemical compound NCC=O LYIIBVSRGJSHAV-UHFFFAOYSA-N 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- HSQFVBWFPBKHEB-UHFFFAOYSA-N 2,3,4-trichlorophenol Chemical compound OC1=CC=C(Cl)C(Cl)=C1Cl HSQFVBWFPBKHEB-UHFFFAOYSA-N 0.000 description 2
- PCXDJQZLDDHMGX-UHFFFAOYSA-N 3-aminopropanal Chemical compound NCCC=O PCXDJQZLDDHMGX-UHFFFAOYSA-N 0.000 description 2
- VGVRPFIJEJYOFN-UHFFFAOYSA-N 2,3,4,6-tetrachlorophenol Chemical compound OC1=C(Cl)C=C(Cl)C(Cl)=C1Cl VGVRPFIJEJYOFN-UHFFFAOYSA-N 0.000 description 1
- LLOUHNPGOGFIMX-UHFFFAOYSA-N 2,3-dichlorophenol;sodium Chemical compound [Na].OC1=CC=CC(Cl)=C1Cl LLOUHNPGOGFIMX-UHFFFAOYSA-N 0.000 description 1
- OLXZIGFHNNMHOE-UHFFFAOYSA-N 2-(trichloromethyl)phenol Chemical compound OC1=CC=CC=C1C(Cl)(Cl)Cl OLXZIGFHNNMHOE-UHFFFAOYSA-N 0.000 description 1
- SCWBSTVOWDDYHH-UHFFFAOYSA-N 4-amino-2,6-dichlorophenol;4-aminophenol Chemical compound NC1=CC=C(O)C=C1.NC1=CC(Cl)=C(O)C(Cl)=C1 SCWBSTVOWDDYHH-UHFFFAOYSA-N 0.000 description 1
- CMSOZKWEPIDRMC-UHFFFAOYSA-N [Na].Oc1cc(Cl)c(Cl)c(Cl)c1Cl Chemical compound [Na].Oc1cc(Cl)c(Cl)c(Cl)c1Cl CMSOZKWEPIDRMC-UHFFFAOYSA-N 0.000 description 1
- 150000001447 alkali salts Chemical class 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- FZJHJGOSQIGJJX-UHFFFAOYSA-N sodium;2,3,4-trichlorophenol Chemical compound [Na].OC1=CC=C(Cl)C(Cl)=C1Cl FZJHJGOSQIGJJX-UHFFFAOYSA-N 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
<Desc/Clms Page number 1>
Schädlingsbekämpfungsmittel.
Die vorligende Anmeldung betrifft Mittel mit insektiziden. fungiziden und bakteriziden Eigenschaften zum Pflanzenschutz, beispielsweise als Saatgutbeize, bestehend aus Molekülverbindungen von halogenierten hydroxylhaltigen aromatischen Verbindungen, ihren Derivaten.
Alkalisalzen und Substitutionsprodukten mit aliphatischen Aminoalkoholen.
Beispiel 1 : 50 Gewichtsteile Trichlorphenol und 50 Gewichtsteile Aminoisopropylalkohol werden zusammen gemischt. Diese Mischung ist mit Wasser in jedem Verhältnis mischbar.
Beispiel 2 : 70 Gewichtsteile Trichlorkresol werden mit 30 Gewichtsteilen Aminoäthylalkohol versetzt. Diese Mischung ist ebenfalls in jedem beliebigen Verhältnis mit Wasser streckbar.
Beispiel 3 : 40 Gewichtsteile Trichlorphenol werden in 60 Gewichtsteilen eines Gemisches
EMI1.1
teile Wasser und 142-2 Gewichtsteile Monooxyäthylamin ergeben eine Lösung der Molekülverbindung von Trichlorphenolnatrium mit Monooxyäthylamin, die unbegrenzt lange haltbar ist.
Beispiel 5 : 163 Gewichtsteile 2'6-Dichlorphenol, 40 Gewichtsteile Natriumhydroxyd,' 333 Gewichtsteile Monooxypropylamin und 204 Gewichtsteile Wasser geben eine haltbare Lösung der Molekülverbindung von Dichlorphenolnatrium mit Monooxypropylamin.
Beispiel 6 : 232 Gewichtsteile 2,3, 4. 6-Tetrachlorphenol, 40 Gewichtsteile Natriumhydrooxyd, 150 Gewichtsteile Monooxyäthylamin. 75 Gewichtsteile Dioxyäthylamin und 135 Gewichtsteile Wasser geben eine haltbare Lösung der Molekülverbindung von Tetrachlorphenolnatrium mit den Oxyaminen.
PATENT-ANSPRÜCHE :
1. Schädlingsbekämpfungsmittel, bestehend aus Molekülverbindungen von halogenierten hydroxylhaltigen aromatischen Verbindungen mit aliphatischen Aminoalkoholen.
**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.
<Desc / Clms Page number 1>
Pesticides.
The present application relates to agents with insecticides. fungicidal and bactericidal properties for crop protection, for example as a seed dressing, consisting of molecular compounds of halogenated hydroxyl-containing aromatic compounds, their derivatives.
Alkali salts and substitution products with aliphatic amino alcohols.
Example 1: 50 parts by weight of trichlorophenol and 50 parts by weight of aminoisopropyl alcohol are mixed together. This mixture can be mixed with water in any proportion.
Example 2: 70 parts by weight of trichlorocresol are mixed with 30 parts by weight of aminoethyl alcohol. This mixture can also be stretched with water in any ratio.
Example 3: 40 parts by weight of trichlorophenol are used in 60 parts by weight of a mixture
EMI1.1
parts of water and 142-2 parts by weight of monooxyethylamine result in a solution of the molecular compound of trichlorophenol sodium with monooxyethylamine, which has an unlimited shelf life.
Example 5: 163 parts by weight of 2'6-dichlorophenol, 40 parts by weight of sodium hydroxide, 333 parts by weight of monooxypropylamine and 204 parts by weight of water give a stable solution of the molecular compound of sodium dichlorophenol with monooxypropylamine.
Example 6: 232 parts by weight 2,3,4,6-tetrachlorophenol, 40 parts by weight sodium hydroxide, 150 parts by weight monooxyethylamine. 75 parts by weight of dioxyethylamine and 135 parts by weight of water give a durable solution of the molecular compound of sodium tetrachlorophenol with the oxyamines.
PATENT CLAIMS:
1. Pesticides, consisting of molecular compounds of halogenated hydroxyl-containing aromatic compounds with aliphatic amino alcohols.
** WARNING ** End of DESC field may overlap beginning of CLMS **.
Claims (1)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE126151X | 1929-05-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AT126151B true AT126151B (en) | 1932-01-11 |
Family
ID=29277447
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT126151D AT126151B (en) | 1929-05-15 | 1930-05-02 | Pesticides. |
Country Status (1)
| Country | Link |
|---|---|
| AT (1) | AT126151B (en) |
-
1930
- 1930-05-02 AT AT126151D patent/AT126151B/en active
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