DE289220C - - Google Patents
Info
- Publication number
- DE289220C DE289220C DENDAT289220D DE289220DA DE289220C DE 289220 C DE289220 C DE 289220C DE NDAT289220 D DENDAT289220 D DE NDAT289220D DE 289220D A DE289220D A DE 289220DA DE 289220 C DE289220 C DE 289220C
- Authority
- DE
- Germany
- Prior art keywords
- dinitrophenol
- mold
- agent according
- dissolved
- oil
- 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.)
- Active
Links
- 201000010099 disease Diseases 0.000 claims description 4
- 230000003071 parasitic Effects 0.000 claims description 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 150000007524 organic acids Chemical class 0.000 claims description 2
- 238000002360 preparation method Methods 0.000 claims description 2
- 238000004321 preservation Methods 0.000 claims description 2
- 239000002023 wood Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 239000000126 substance Substances 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 229910052739 hydrogen Inorganic materials 0.000 claims 1
- 239000001257 hydrogen Substances 0.000 claims 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 1
- 241000196324 Embryophyta Species 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- IQUPABOKLQSFBK-UHFFFAOYSA-N 2-nitrophenol Chemical class OC1=CC=CC=C1[N+]([O-])=O IQUPABOKLQSFBK-UHFFFAOYSA-N 0.000 description 3
- 239000002360 explosive Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- KCQORPKRJCTRID-UHFFFAOYSA-N 2,3-dinitronaphthalen-1-ol Chemical class C1=CC=C2C(O)=C([N+]([O-])=O)C([N+]([O-])=O)=CC2=C1 KCQORPKRJCTRID-UHFFFAOYSA-N 0.000 description 2
- MHKBMNACOMRIAW-UHFFFAOYSA-N 2,3-dinitrophenol Chemical compound OC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O MHKBMNACOMRIAW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 230000002421 anti-septic Effects 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 235000021388 linseed oil Nutrition 0.000 description 2
- 239000000944 linseed oil Substances 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 150000003460 sulfonic acids Chemical class 0.000 description 2
- LDEDNODNBRFNNS-UHFFFAOYSA-N C1=CC=CC=C1.[N+](=O)([O-])C=1C(=C(C=CC1)O)[N+](=O)[O-] Chemical compound C1=CC=CC=C1.[N+](=O)([O-])C=1C(=C(C=CC1)O)[N+](=O)[O-] LDEDNODNBRFNNS-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 229920001353 Dextrin Polymers 0.000 description 1
- 239000004375 Dextrin Substances 0.000 description 1
- SUSXNXXFQXUGBJ-UHFFFAOYSA-N OC1=CC=C(C=O)C(=C1[N+]([O-])=O)[N+]([O-])=O Chemical compound OC1=CC=C(C=O)C(=C1[N+]([O-])=O)[N+]([O-])=O SUSXNXXFQXUGBJ-UHFFFAOYSA-N 0.000 description 1
- 208000006551 Parasitic Disease Diseases 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000003433 contraceptive agent Substances 0.000 description 1
- 230000000249 desinfective Effects 0.000 description 1
- 235000019425 dextrin Nutrition 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000008149 soap solution Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/18—Nitro compounds
- A01N33/20—Nitro compounds containing oxygen or sulfur attached to the carbon skeleton containing the nitro group
- A01N33/22—Nitro compounds containing oxygen or sulfur attached to the carbon skeleton containing the nitro group having at least one oxygen or sulfur atom and at least one nitro group directly attached to the same aromatic ring system
-
- 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
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)
Description
KAISERLICHESIMPERIAL
PATENTAMT.PATENT OFFICE.
PATENTSCHRIFTPATENT LETTERING
JVi 289220 KLASSE 30«. GRUPPEJVi 289220 CLASS 30 «. GROUP
Dr. FR. PFENNING in BERLIN-WILMERSDORF.Dr. FR. PFENNING in BERLIN-WILMERSDORF.
Mittel zur Verhütung von Fäulnis und Schimmel und zur Bekämpfung parasitärer Pflanzenkrankheiten mit Ausnahme der Holzkonservierung.Preparations for preventing rot and mold and for combating parasitic plant diseases with the exception of wood preservation.
Patentiert im Deutschen Reiche vom 30. Oktober 1913 ab.Patented in the German Empire on October 30, 1913.
Die desinfizierende Wirkung von Nitrophenolen und Derivaten derselben, welche freie Hydroxylgruppen enthalten, ist bekannt. Die Verbindungen haben den Übelstand, stark gefärbt, explosiv und leicht brennbar zu sein. Letzterer Eigenschaften wegen können sie nur mit großer Vorsicht angewendet werden. Die vorliegende Erfindung betrifft Mittel zur Verhütung von Fäulnis und Schimmel, sowie zurThe disinfecting effect of nitrophenols and derivatives thereof, which free Containing hydroxyl groups is known. The connections have the evil, strongly colored, to be explosive and highly flammable. Because of the latter properties, they can only be used with great caution. The present invention relates to contraceptive agents of rot and mold, as well as for
ίο Bekämpfung parasitärer Pflanzenkrankheiten, aus Verbindungen der Nitrophenole, die weder explosiv sind, noch die Färbung der freien Nitrophenole besitzen. Es hat sich gezeigt, daß durch Einführung der Alkylreste oder der Reste von organischen Säuren in Mono- und Polynitrophenole Körper entstehen, welche große antiseptische Wirkung besitzen, die wenigstens ebenso hoch ist wie diejenige der Ausgangsstoffe, welche aber nicht explosiv sind.ίο combating parasitic plant diseases, from compounds of nitrophenols, which are neither explosive nor the coloring of the free ones Possess nitrophenols. It has been shown that by introducing the alkyl radicals or the Residues of organic acids in mono- and polynitrophenols are formed which bodies have a great antiseptic effect, which is at least as high as that of the starting materials, but which are not explosive.
Die neuen Körper bieten auch den Vorteil, einen niedrigen Schmelzpunkt zu besitzen und dementsprechend für die angeführten Zwecke leicht verwendet werden zu können. Die Körper sind außerdem in· ölen u. dgl. löslich undThe new bodies also offer the advantage of having a low melting point and Accordingly, it can be easily used for the stated purposes. The body are also soluble in oils and the like and
z5 können auch in dieser Form benutzt werden. Durch einen geringen Zusatz der neuen Verbindungen läßt sich das Schimmeln von Ölfarben, Dextrinmassen, Appreturen, appretierten Stoffen und sonstigen unter der Einwirkung von Luft und Feuchtigkeit leicht schimmelnden oder faulenden Massen verhindern. In öl gelöst und mit Seife emulgiert eignen sich die Verbindungen vorzüglich zur Bekämpfung parasitärer Pflanzenkrankheiten. z5 can also be used in this form. By adding a small amount of the new compounds, the mold of oil paints, Dextrin masses, finishes, finished fabrics and others under the influence Prevent molds from mold or putrefaction from air and moisture. Dissolved in oil and emulsified with soap the compounds are particularly suitable for combating parasitic plant diseases.
i. Herstellung einer antiseptischen
Gaze.i. Making an antiseptic
Gauze.
a) io'o g Acetyl-2 · 4-dinitrophenol werden in 700 g Äther gelöst und mit 700 g Weingeist von 90 Prozent vermischt. Mit dieser Lösung werden 900 g hydrophyler Gaze getränkt. Man schlägt in Papier ein, beschwert mit Gewichten und trocknet auf Haspeln o. dgl.a) 100 g of acetyl-2 · 4-dinitrophenol Dissolved in 700 g of ether and mixed with 700 g of 90 percent alcohol. With this 900 g of hydrophylic gauze are soaked in the solution. You wrap paper, complain with weights and dries on reels or the like.
b) 200 g Acetyl-2 · 4-dinitrophenol werden in 200 g Aceton gelöst und mit dieser Lösung 800 g hydrophyler Gaze wie vorher behandelt.b) 200 g of acetyl-2 · 4-dinitrophenol are dissolved in 200 g of acetone and mixed with this solution 800 g of hydrophylic gauze treated as before.
In gleicher Weise kann man auch Watte behandeln. You can also treat cotton wool in the same way.
An Stelle von Acetyl-2 · 4-dinitrophenol kann man auch Formyldinitrophenol oder Benzoldinitrophenol anwenden. Ebenso kann man andere Säurederivate oder Alkylverbindungen sowohl des Mono- und Dinitrophenols, sowie der Mono- und Dinitronaphtole, ihrer Sulfosäuren u. dgl. benutzen.Instead of acetyl-2 · 4-dinitrophenol, formyl dinitrophenol or benzene dinitrophenol can also be used use. You can also use other acid derivatives or alkyl compounds of both mono- and dinitrophenol, as well the mono- and dinitronaphthols, their sulfonic acids and the like.
2. Herstellung von Ölfarben.2. Manufacture of oil paints.
100 g Ultramarin werden mit Leinölfirnis zu einer leicht auftragbaren Masse verrieben. Man setzt ι Prozent der Alkylverbindungen oder Säurederivate des Mono- oder Dinitrophenols, der Mono- und Dinitronaphtole oder ihrer Sulfosäuren hinzu.100 g of ultramarine are rubbed with linseed oil varnish to form an easily applied mass. Man sets ι percent of the alkyl compounds or acid derivatives of mono- or dinitrophenol, the mono- and dinitronaphthols or their sulfonic acids.
gegen parasitäre
krankheiten.against parasitic
Diseases.
Pflanzen-Plants-
Man löst 3 g Acetyl-2 ■ 4-dinitrophenol (oder eine andere der angeführten Verbindungen) in 10 g Leinöl und gibt die Mischung in 1 1 einer 10 prozentigen Seifenlösung. Man rührt, bis eine Emulsion entsteht. Die erhaltene Lösung wird eventuell mit Wasser verdünnt auf Pflanzen aufgespritzt und in den Erdboden gegossen. Dissolve 3 g of acetyl-2 ■ 4-dinitrophenol (or another of the listed compounds) in 10 g of linseed oil and gives the mixture in 1 1 of a 10 percent soap solution. Stir until an emulsion is formed. The solution obtained may be diluted with water and sprayed onto plants and poured into the ground.
Claims (3)
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE289220C true DE289220C (en) |
Family
ID=544268
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DENDAT289220D Active DE289220C (en) |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE289220C (en) |
-
0
- DE DENDAT289220D patent/DE289220C/de active Active
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