DE800877C - Disinfectants and preservatives - Google Patents

Disinfectants and preservatives

Info

Publication number
DE800877C
DE800877C DEP13038A DEP0013038A DE800877C DE 800877 C DE800877 C DE 800877C DE P13038 A DEP13038 A DE P13038A DE P0013038 A DEP0013038 A DE P0013038A DE 800877 C DE800877 C DE 800877C
Authority
DE
Germany
Prior art keywords
dioxy
dimethyldiphenyl
cresol
disinfectants
preservatives
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
Application number
DEP13038A
Other languages
German (de)
Inventor
Kurt Dr Kraft
Leonhard Dr Schuler
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Abbott GmbH and Co KG
Original Assignee
Knoll GmbH
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 Knoll GmbH filed Critical Knoll GmbH
Priority to DEP13038A priority Critical patent/DE800877C/en
Application granted granted Critical
Publication of DE800877C publication Critical patent/DE800877C/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N31/00Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
    • A01N31/08Oxygen or sulfur directly attached to an aromatic ring system
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D1/00Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Agronomy & Crop Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

(WiGBl. S. 175)(WiGBl. P. 175)

AUSGEGEBEN AM 11. DEZEMBER 1950ISSUED DECEMBER 11, 1950

ρ τ3038 II' a j 30 i Dρ τ3038 II 'a j 30 i D

Es wurde gefunden, daß 4, 4'-Dioxy-3, 3'-dimethvldiphenyl eine überraschend starke Wirkung als Konservierung*- und Desinfektionsmittel aufweist. Vergleichende Versuche zur Gärungshemmung hei Traubenzuckerbouillon und Hefe enthaltenden Gärlösungen ergaben z. H. gegenüber den vielfach als Konservierungsmittel gebrauchten p-Oxybenzoesäureestern die folgenden Konzentrationen, bei welchen innerhalb von 14 Tagen noch Hemmung eintritt:It has been found that 4,4'-dioxy-3, 3'-dimethyl diphenyl has a surprisingly strong effect as a preservative * and disinfectant. Comparative attempts to inhibit fermentation in dextrose bouillon and yeast containing Fermentation solutions resulted in z. H. compared to the often used as a preservative p-Oxybenzoic acid esters the following concentrations, at which within 14 days Inhibition occurs:

Ph 3. 5 Ph 4. 5~6 Neutralpunkt p-Oxybenzoesäureester 1:5 000 1:1000 >als 1:1000 4,4'-Dioxy-3,3'-Ph 3.5 Ph 4.5 ~ 6 neutral point p-oxybenzoic acid ester 1: 5,000 1: 1000 > as 1: 1000 4,4'-dioxy-3,3'-

dimethyldiphenyl 1:20000 1:5000 1:2000dimethyldiphenyl 1: 20000 1: 5000 1: 2000

Ähnliche Ergebnisse wurden bei Versuchen zur Hemmung des Schimnielpilzwachstums auf Apfelsaft erhaltenSimilar results were obtained from attempts to inhibit mold growth on apple juice obtain

bei p-Oxybenzoesäureestern 1 : 2000,for p-oxybenzoic acid esters 1: 2000,

bei 4. 4'-Dioxy-3, 3'-dimethyldiphenyl 1:10000.at 4. 4'-dioxy-3,3'-dimethyldiphenyl 1: 10000.

Hei Vergleichsversuchen mit Benzoesäure und Salicylsäure, die bei einem pn von 4 nur bei ι : rooo bis ι : 2000, bei Pij(i sogar unter 1 : τ000 hemmten, wurden für 4, 4'-Dioxy-3, 3'-dimethyldiphenyl dieselben günstigen Konzentrationen wie oben gefunden.Hei comparison tests with benzoic acid and salicylic acid, which with a pn of 4 only with ι: rooo up to ι: 2000, at Pij (i even inhibited below 1: τ000, became the same for 4,4'-dioxy-3, 3'-dimethyldiphenyl favorable concentrations as found above.

Eine besonders hohe Wirksamkeit besitzt 4. 4'-Dioxy-3, 3'-ditnethyldiphenvl gegenüber pathogenen Bakterien. So wurde das Wachstum von Staphylococcus aureus Stamm FT im Verdünnungsreihentest bei Oberflächenbeimpfung in einer Verdünnung von ι : 50000 bis 1 : 100 000 gehemmt, gegenüber Kresol 1 : 2000 und p-Oxybenzoesäureester 1 : 1000 bis ι : 2000.4. 4'-Dioxy-3,3'-diethyldiphenyl is particularly effective against pathogens Bacteria. Thus, the growth of Staphylococcus aureus strain FT in the dilution series test with surface inoculation in a dilution of ι: 50,000 to 1: 100,000 inhibited, compared to Cresol 1: 2000 and p-oxybenzoic acid ester 1: 1000 until ι: 2000.

Der Vergleich mit o-Kresol ergab folgende Hemmungsgrenzen im Gärungsversuch (20°/oige Traubenzuckerbouillon mit Bäckerhefe):The comparison with o-cresol showed the following inhibition limits in the fermentation test (20% dextrose bouillon with baker's yeast):

o-Kresol 1 : 2000,o-cresol 1: 2000,

4, 4'-I)ioxy-3, 3'-dimethyldiphenyl 1 : 10 000; gegenüber Schimmelpilz:4, 4'-I) ioxy-3, 3'-dimethyldiphenyl 1: 10,000; against mold:

o-Kresol 1 : 2000,o-cresol 1: 2000,

4, 4'-Dioxy-3,3'-dimethyldiphenyl r: iobis2oooo; gegenüber Staphylococcus aureus:4,4'-Dioxy-3,3'-dimethyldiphenyl r: iobis2oooo; against Staphylococcus aureus:

o-Kresol 1 : 2000,o-cresol 1: 2000,

4, 4'"Di°xy~3> 3'-dimethyldiphenyl ι : 50 bis
ι oo ooo.
4, 4 '"Di ° x y ~ 3>3'-dimethyldiphenyl ι: 50 to
ι oo ooo.

Beim vergleichenden Desinfektionsversuch (Konzentration/Zeitmethode) wurden folgende Werte gefunden: In a comparative disinfection attempt (concentration / time method) the following values were found:

4, 4'-Dioxy-3, 3'-dimethyldiphenyl 1 : 1000 nach4,4'-Dioxy-3, 3'-dimethyldiphenyl 1: 1000 according to

6 Minuten Sterilisierung,
Phenol 1 : 100 Abtötung nach 3 Stunden,
o-Kresol 1 : 100 nach 1A Stunde keine Sterilisierung.
6 minutes sterilization,
Phenol 1: 100 kill after 3 hours,
o-cresol 1: 100 after 1 ½ hour no sterilization.

Die Toxizität von 4, 4'-Dioxy-3, 3'-dimethyldiphenyl ist sehr günstig: Die Dosis letalis med. beträgt an der weißen Maus etwa 1,5 g pro Kilogramm per os. Im Dauerversuch wurden sechs Mäusen täglich 200 mg/kg 30 Tage lang verabreicht. Dabei traten keine toxischen Erscheinungen auf. Nachomaliger Verabreichung von je 200 mg/kg per os an drei Kaninchen ergab sich weder eine Beeinflussung des Hämoglobins noch eine Veränderung des Blutbildes.The toxicity of 4,4'-dioxy-3, 3'-dimethyldiphenyl is very cheap: the dose letalis med. is about 1.5 g per kilogram on the white mouse per os. In the long-term experiment, six mice were administered 200 mg / kg daily for 30 days. No toxic phenomena occurred. Subsequent administration of 200 mg / kg each Per os on three rabbits there was neither an influence on the hemoglobin nor a change the blood count.

4, 4'-Dioxy-3, 3'-dimethyldiphenyl als Desinfektionsmittel besitzt ferner besondere Vorzüge in seiner Kochbeständigkeit, seiner Geruch- und Geschmacklosigkeit und in seiner guten \rerträglich- ; keit. Die Substanz kann als solche oder in Form ihrer Salze, ζ. B. in Form ihrer Alkalisalze allein oder zusammen mit anderen Stoffen verwendet werden, wobei sie dem zu konservierenden Material trocken oder in Lösung zugesetzt wird. Sie kann aber auch als Desinfektions- und Konservierungsmittel Emulsionen, Pudern und Pasten beigemischt werden.4, 4'-Dioxy-3, 3'-dimethyldiphenyl as a disinfectant also has particular advantages in its resistance to cooking, its odorless and tastelessness and its good \ r tolerable; speed. The substance can be used as such or in the form of its salts, ζ. B. can be used in the form of their alkali salts alone or together with other substances, being added to the material to be preserved dry or in solution. However, it can also be added to emulsions, powders and pastes as a disinfectant and preservative.

Beispielexample

Zur Anwendung des 4, 4'-Dioxy-3, 3'dimethyldiphenyls als Konservierungsmittel löst man die erforderliche Menge des Stoffes entweder direkt in dem zu konservierenden Material, gegebenenfalls unter Erhitzen, oder man stellt eine alkoholische Lösung des Stoffes her und gießt dieselbe in das zu konservierende Gut. Man kann 4, 4'-Dioxy-3, 3'-dimethyldiphenyl aber auch in einem Unterschuß von Lauge lösen und diese Lösung dem zu konservierenden Material zusetzen.To use the 4,4'-dioxy-3, 3'dimethyldiphenyls as a preservative, dissolve the required amount of the substance either directly in the material to be preserved, if necessary with heating, or one puts an alcoholic Solution of the substance and pour the same into the goods to be preserved. You can use 4,4'-dioxy-3, 3'-dimethyldiphenyl but also dissolve in a deficit of lye and add this solution to the one to be preserved Add material.

Claims (1)

Patentanspruch:Claim: Desinfektions- und Konservierungsmittel, gekennzeichnet durch die Verwendung von 4, 4'-Dioxy-3, 3'-dimethyldiphenyl bzw. seiner Salze.Disinfectants and preservatives, characterized by the use of 4, 4'-Dioxy-3, 3'-dimethyldiphenyl or its salts. 2900 12.502900 12.50
DEP13038A 1948-10-02 1948-10-02 Disinfectants and preservatives Expired DE800877C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DEP13038A DE800877C (en) 1948-10-02 1948-10-02 Disinfectants and preservatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEP13038A DE800877C (en) 1948-10-02 1948-10-02 Disinfectants and preservatives

Publications (1)

Publication Number Publication Date
DE800877C true DE800877C (en) 1950-12-11

Family

ID=7364403

Family Applications (1)

Application Number Title Priority Date Filing Date
DEP13038A Expired DE800877C (en) 1948-10-02 1948-10-02 Disinfectants and preservatives

Country Status (1)

Country Link
DE (1) DE800877C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE945950C (en) * 1952-06-21 1956-07-19 Bayer Ag Protective agent with a fungicidal and bactericidal effect

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE945950C (en) * 1952-06-21 1956-07-19 Bayer Ag Protective agent with a fungicidal and bactericidal effect

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