AT149170B - Seed dressing. - Google Patents

Seed dressing.

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Publication number
AT149170B
AT149170B AT149170DA AT149170B AT 149170 B AT149170 B AT 149170B AT 149170D A AT149170D A AT 149170DA AT 149170 B AT149170 B AT 149170B
Authority
AT
Austria
Prior art keywords
sep
content
seed dressing
hydrogen
ethane
Prior art date
Application number
Other languages
German (de)
Original Assignee
Schering Kahlbaum Ag
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.)
Filing date
Publication date
Application filed by Schering Kahlbaum Ag filed Critical Schering Kahlbaum Ag
Application granted granted Critical
Publication of AT149170B publication Critical patent/AT149170B/en

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Description

  

   <Desc/Clms Page number 1> 
 



  Saatgutbeize. 



   Es ist bekannt, dass gewisse organische   Queeksilberverbindungen   geeignete Saatgutbeizen bilden. Es hat sich nun gezeigt, dass organische   Quecksilberverbindungen   von der Strukturformel 
 EMI1.1 
 
 EMI1.2 
 

 <Desc/Clms Page number 2> 

 
 EMI2.1 
 
<tb> 
<tb> 



  Mit <SEP> einer <SEP> Mischung <SEP> behandelt, <SEP> die <SEP> enthielt <SEP> # <SEP> Stark <SEP> # <SEP> Mässig <SEP> # <SEP> Insgesamt
<tb> infiziert <SEP> infiziert <SEP> Prozent
<tb> Unbehandelt <SEP> 41 <SEP> 34 <SEP> 75
<tb> &alpha;-Trichlor-ss-acetomercuriäthoxy-äthan <SEP> ............... <SEP> 2 <SEP> 18 <SEP> 20
<tb> 1-25% <SEP> Hg-Gehalt
<tb> &alpha;-Trichlor-ss-methoxy-ss-acetomercuriäthoxy-äthan <SEP> ........... <SEP> 2 <SEP> 12 <SEP> 14
<tb> 1-25% <SEP> Hg-Gehalt
<tb> &alpha;-Trichlor-ss-isopropyloxy-ss-acetomercuriäthoxy-äthan <SEP> .......... <SEP> 1 <SEP> 18 <SEP> 19
<tb> 1-5% <SEP> Hg-Gehalt
<tb> &alpha;-Trichlor-ss-butoxy-ss-acetomercuriäthoxy-äthan <SEP> ............... <SEP> 1 <SEP> 20 <SEP> 21
<tb> 1. <SEP> 5% <SEP> Hg-Gehalt
<tb> &alpha;

  -Trichlor-ss-isoamyloxy-ss-acetomercuriäthoxy-äthan <SEP> ........... <SEP> 2 <SEP> 14 <SEP> 16
<tb> 1'5% <SEP> Hg-Gehalt
<tb> &alpha;-Trichlor-ss-methoxy-ss-acetomercuricyclohexyloxy-äthan........ <SEP> 2 <SEP> 20 <SEP> 22
<tb> 1-5% <SEP> Hg-Gehalt
<tb> &alpha;-Trichlor-ss-äthoxy-ss-acetomercuriisopropyloxy-äthan <SEP> .......... <SEP> 2 <SEP> 14 <SEP> 16
<tb> 1'5% <SEP> Hg-Gehalt
<tb> x-Tribrom-3-äthoxy-S-aeetomereuriäthoxy-äthan............... <SEP> 1 <SEP> 14 <SEP> 15
<tb> 2% <SEP> Hg-Gehalt
<tb> &alpha;-Trichlor-ss-äthoxy-ss-chlormercuriisopropyloxy-äthan........... <SEP> 2 <SEP> 16 <SEP> 18
<tb> 2% <SEP> Hg-Gehalt
<tb> Vergleich <SEP> mit <SEP> bekannten <SEP> Quecksilberverbindungen <SEP> :

  
<tb> Äthanolquecksilberchlorid <SEP> .................................. <SEP> 5 <SEP> 14 <SEP> 19
<tb> 6% <SEP> Hg-Gehalt
<tb> Terpinolenmercuriaeetat..................................... <SEP> 12 <SEP> 31 <SEP> 43
<tb> 2% <SEP> Hg-Gehalt
<tb> Cumarinmercurichlorid...................................... <SEP> 4 <SEP> 22 <SEP> 26
<tb> 2-5% <SEP> Hg-Gehalt
<tb> Acetoxyeyelohexylmereurichlorid <SEP> 6 <SEP> 18 <SEP> 24
<tb> 3% <SEP> Hg-Gehalt
<tb> Standard <SEP> Saatgutbeize, <SEP> wie <SEP> auf <SEP> dem <SEP> Markte <SEP> erhältlich........ <SEP> 2 <SEP> 25 <SEP> 27
<tb> 2% <SEP> Hg-Gehalt
<tb> 
 
Hieraus ergibt sich, dass die erfindungsgemässe Saatgutbeize den bekannten   Quecksilbersaat-   gutbeizen überlegen ist. 



   Die bei diesen Versuchen benützten Gemenge wurden z. B. dadurch erzeugt, dass man   1#25   bis 2 Teile der Quecksilberverbindung mit 98-98'75 Teilen von Kaolin als Verdünnungsmittel mischte. 



   Es können natürlich viele Änderungen in der Zusammensetzung der erwähnten Saatgutbeizen gemacht werden, ohne den Rahmen der Erfindung zu verlassen. 

**WARNUNG** Ende DESC Feld kannt Anfang CLMS uberlappen**.



   <Desc / Clms Page number 1>
 



  Seed dressing.



   It is known that certain organic queek silver compounds form suitable seed dressings. It has now been shown that organic mercury compounds of the structural formula
 EMI1.1
 
 EMI1.2
 

 <Desc / Clms Page number 2>

 
 EMI2.1
 
<tb>
<tb>



  Treated with <SEP> a <SEP> mixture <SEP>, <SEP> containing <SEP> <SEP> # <SEP> Strong <SEP> # <SEP> Moderately <SEP> # <SEP> Overall
<tb> infected <SEP> infected <SEP> percent
<tb> Untreated <SEP> 41 <SEP> 34 <SEP> 75
<tb> α-trichloro-ss-acetomercuriethoxy-ethane <SEP> ............... <SEP> 2 <SEP> 18 <SEP> 20
<tb> 1-25% <SEP> Hg content
<tb>? -Trichlor-ss-methoxy-ss-acetomercuriethoxy-ethane <SEP> ........... <SEP> 2 <SEP> 12 <SEP> 14
<tb> 1-25% <SEP> Hg content
<tb> α-trichloro-ss-isopropyloxy-ss-acetomercuriethoxy-ethane <SEP> .......... <SEP> 1 <SEP> 18 <SEP> 19
<tb> 1-5% <SEP> Hg content
<tb> α-Trichlor-ss-butoxy-ss-acetomercuriethoxy-ethane <SEP> ............... <SEP> 1 <SEP> 20 <SEP> 21
<tb> 1. <SEP> 5% <SEP> Hg content
<tb>?

  -Trichlor-ss-isoamyloxy-ss-acetomercuriethoxy-ethane <SEP> ........... <SEP> 2 <SEP> 14 <SEP> 16
<tb> 1'5% <SEP> Hg content
<tb> α-Trichlor-ss-methoxy-ss-acetomercuricyclohexyloxy-ethane ........ <SEP> 2 <SEP> 20 <SEP> 22
<tb> 1-5% <SEP> Hg content
<tb> α-trichloro-ss-ethoxy-ss-acetomercuriisopropyloxy-ethane <SEP> .......... <SEP> 2 <SEP> 14 <SEP> 16
<tb> 1'5% <SEP> Hg content
<tb> x-tribromo-3-ethoxy-S-aeetomereuriethoxy-ethane ............... <SEP> 1 <SEP> 14 <SEP> 15
<tb> 2% <SEP> Hg content
<tb> α-trichloro-ss-ethoxy-ss-chlormercuriisopropyloxy-ethane ........... <SEP> 2 <SEP> 16 <SEP> 18
<tb> 2% <SEP> Hg content
<tb> Comparison <SEP> with <SEP> known <SEP> mercury compounds <SEP>:

  
<tb> Ethanol mercury chloride <SEP> .................................. <SEP> 5 <SEP> 14 < SEP> 19
<tb> 6% <SEP> Hg content
<tb> terpinolene mercury acetate ..................................... <SEP> 12 <SEP> 31 < SEP> 43
<tb> 2% <SEP> Hg content
<tb> Coumarin Mercury Chloride ...................................... <SEP> 4 <SEP> 22 <SEP> 26
<tb> 2-5% <SEP> Hg content
<tb> Acetoxyeyelohexylmereurichlorid <SEP> 6 <SEP> 18 <SEP> 24
<tb> 3% <SEP> Hg content
<tb> Standard <SEP> seed treatment, <SEP> like <SEP> available on <SEP> the <SEP> market <SEP> ........ <SEP> 2 <SEP> 25 <SEP> 27
<tb> 2% <SEP> Hg content
<tb>
 
It follows from this that the seed dressing according to the invention is superior to the known mercury seed dressing.



   The mixture used in these experiments were z. B. generated by mixing 1 # 25 to 2 parts of the mercury compound with 98-98'75 parts of kaolin as a diluent.



   Many changes can of course be made in the composition of the seed dressings mentioned without departing from the scope of the invention.

** WARNING ** End of DESC field may overlap beginning of CLMS **.

Claims (1)

PATENT-ANSPRÜCHE : 1. Saatgutbeize, dadurch gekennzeichnet, dass sie aus einer organischen Quecksilberverbindung EMI2.2 EMI2.3 <Desc/Clms Page number 3> besteht, worin Y ein negatives Radikal, R ein Kohlenwasserstoffradikal, R'entweder Wasserstoff oder ein Kohlenwasserstoffradikal, R"entweder Wasserstoff, gleiche oder verschiedene Kohlenwasserstoffradikale bedeuten, die derart angeordnet sein können, dass sie einen Kern bilden, für sich oder unter Zusatz von vorzugsweise 98-99% anderer Verbindungen, wie Verdünnungsmitteln, stimulierende Mittel, Mittel zur Verhinderung des Staubens und/oder Mittel zur Vergrösserung der Haftfähigkeit. PATENT CLAIMS: 1. Seed dressing, characterized in that it consists of an organic mercury compound EMI2.2 EMI2.3 <Desc / Clms Page number 3> where Y is a negative radical, R is a hydrocarbon radical, R 'is either hydrogen or a hydrocarbon radical, R "is either hydrogen, identical or different hydrocarbon radicals, which can be arranged in such a way that they form a nucleus, individually or with the addition of, preferably 98-99% of other compounds such as diluents, stimulants, anti-dusting agents and / or adhesives increasing agents. 2. Saatgutbeize nach Anspruch 1, dadurch gekennzeichnet, dass Y Halogen, die CHgCOO-oder die NOg-Gruppe bedeutet. EMI3.1 EMI3.2 EMI3.3 von der Formel EMI3.4 enthält, worin R'ein Alkylradikal bedeutet und N'entweder Wasserstoff oder dasselbe oder ver- schiedene Alkylradikale. 2. Seed dressing according to claim 1, characterized in that Y is halogen, the CHgCOO or the NOg group. EMI3.1 EMI3.2 EMI3.3 from the formula EMI3.4 contains where R 'denotes an alkyl radical and N' denotes either hydrogen or the same or different alkyl radicals.
AT149170D 1934-09-28 1935-09-28 Seed dressing. AT149170B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE149170X 1934-09-28

Publications (1)

Publication Number Publication Date
AT149170B true AT149170B (en) 1937-04-10

Family

ID=5673174

Family Applications (1)

Application Number Title Priority Date Filing Date
AT149170D AT149170B (en) 1934-09-28 1935-09-28 Seed dressing.

Country Status (1)

Country Link
AT (1) AT149170B (en)

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