DE898664C - Disinfectants - Google Patents

Disinfectants

Info

Publication number
DE898664C
DE898664C DESCH2029D DESC002029D DE898664C DE 898664 C DE898664 C DE 898664C DE SCH2029 D DESCH2029 D DE SCH2029D DE SC002029 D DESC002029 D DE SC002029D DE 898664 C DE898664 C DE 898664C
Authority
DE
Germany
Prior art keywords
cyclohexylphenol
chloroxylenol
chlorocresol
chloro
preparation
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
DESCH2029D
Other languages
German (de)
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.)
Schuelke and Mayr GmbH
Original Assignee
Schuelke and Mayr 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 Schuelke and Mayr GmbH filed Critical Schuelke and Mayr GmbH
Priority to DESCH2029D priority Critical patent/DE898664C/en
Application granted granted Critical
Publication of DE898664C publication Critical patent/DE898664C/en
Expired legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09GPOLISHING COMPOSITIONS; SKI WAXES
    • C09G1/00Polishing compositions
    • C09G1/06Other polishing compositions
    • C09G1/08Other polishing compositions based on wax
    • 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)
  • Chemical & Material Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Engineering & Computer Science (AREA)
  • Organic Chemistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Oil, Petroleum & Natural Gas (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)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Description

Desinfektionsmittel Die Erfindung betrifft ein Desinfektionsmittel, das durch ein Gemisch von 4-Chlor-2-cyclohexylphenol mit Chlorkresol und/oder Chlorxylenol gekennzeichnet ist.Disinfectant The invention relates to a disinfectant, that by a mixture of 4-chloro-2-cyclohexylphenol with chlorocresol and / or chloroxylenol is marked.

Die bakterizide Wirkung von 4-Chlor-2-cyclohexylphenol ist bekannt und beschrieben. Die Verbindung zeichnet sich durch eine sehr gute Wirkung gegenüber Staph. aureus, Streptokokkus und andere grampositive Keime aus, während die bakterizide Kraft gegenüber Bact. Coli und Bact. Pyoc. sehr gering ist. Dieses unterschiedliche Verhalten setzt ihren technischen Wert stark herab und läßt diese Verbindung für die Praxis ungeeignet erscheinen.The bactericidal effect of 4-chloro-2-cyclohexylphenol is known and described. The compound is characterized by a very good effect against Staph. aureus, streptococcus and other gram-positive germs, while the bactericidal Force versus Bact. Coli and Bact. Pyoc. is very low. This different Behavior greatly reduces their technical merit and leaves this connection for the practice appear unsuitable.

Es wurde nun die Beobachtung gemacht, daß sich Chlor-cyclohexylphenol mit besonderem Vorteil zur Herstellung von Desinfektionsmitteln verwenden läßt, wenn man erfindungsgemäß diese Verbindung in Kombination mit Chlorkresol und/oder Chlorxylenol zur Anwendung bringt. Man erhält auf diese Weise Präparate, deren bakterizide Wirkung gegenüber grampositiven Keimen um ein Vielfaches größer ist, als es auf Grund der Wirkung der Komponenten erwartet werden konnte. Dies zeigen die folgenden Versuchsergebnisse, die mit Bact. Coli erhalten wurden I 1I (Ricinus- (Leinöl- ölseife) seife) 1. 5 % 4-Chlor- 2-cyclohexylphenol = : io i : io IL 50/, Chlorkresol ....... i : 6o i : 2o III. 51)/o Chlorxylenol ...... 1 : 150 1 : 6o IV. 2,50/, 4-Chlor- 2-cyclohexylphenol i : ioo i : 6o 2,50/, Chlorkresol ... . . . . V. 2,5 0/0 4-Chlor- 2-cyclohexylphenol 1:15o 1:125 2,5 0/0 Chlorxylenol ...... Die Zahlen der Tabelle geben diejenigen Grenzverdünnungen an, bei denen noch Abtötung aller Keime erzielt werden konnte.It has now been observed that chlorocyclohexylphenol can be used with particular advantage for the production of disinfectants if, according to the invention, this compound is used in combination with chlorocresol and / or chloroxylenol. In this way, preparations are obtained whose bactericidal action against gram-positive germs is many times greater than could be expected on the basis of the action of the components. This is shown by the following test results obtained with Bact. Coli were obtained I 1I (Castor (linseed oil) oil soap) soap) 1.5% 4-chlorine 2-cyclohexylphenol =: io i: io IL 50 /, chlorocresol ....... i: 6o i: 2o III. 51) / o chloroxylenol ...... 1: 150 1: 6o IV. 2.50 /, 4-chloro 2-cyclohexylphenol i: 100 i: 6o 2.50 /, chlorocresol .... . . . V. 2.5 0/0 4-chlorine- 2-cyclohexylphenol 1:15 o 1: 125 2.5 0/0 chloroxylenol ...... The figures in the table indicate the limit dilutions at which all germs could still be killed.

Die Präparate I bis V wurden hergestellt, indem die halogenierten Phenole in Ricinus- bzw. Leinölseife unter Zusatz von Alkohol gelöst wurden. Der Phenolgehalt betrug stets 5 °/o, der Seifen- und Alkoholgehalt jeweils io °/a. Die bakteriologische Prüfung erfolgte in der üblichen Weise mit Hilfe der Suspensionsmethode. Zu g ccm der Verdünnungen von den Präparaten I bis V (aqua dest.) wurde i ccm einer dichten Keimaufschwemmung einer einen Tag alten Kultur gegeben und nach einer Einwirkungszeit von 5 Minuten in Traubenzuckerbouillon übergeimpft. Abgelesen wurde nach 6tägiger Bebrütung.The preparations I to V were made by the halogenated Phenols were dissolved in castor or linseed oil soap with the addition of alcohol. Of the The phenol content was always 5%, the soap and alcohol content each 10%. the bacteriological testing was carried out in the usual way using the suspension method. For g ccm of the dilutions of preparations I to V (distilled water), 1 ccm was added dense germ suspension of a one-day-old culture and after an exposure time inoculated in glucose bouillon for 5 minutes. The reading was taken after 6 days Incubation.

Das Präparat I, das eine 5°/oige Lösung von 4-Chlor-2-cyclohexylphenol darstellt, ist nur in einer Verdünnung i : io gegenüber Bact. Coli wirksam. Mischt man jedoch dieses Präparat mit Präparat II, das 5 °/o Chlorkresol enthält, im Verhältnis i : i, wodurch Präparat IV entsteht, so steigt die Wirksamkeit weit über den additiven Wert an. Der Summenwert entspräche einer noch wirksamen Grenzverdünnung von i : 35. Die tatsächliche Wirkungssteigerung ist jedoch viel größer, da eine Verdünnung des Präparates IV von x : ioo noch voll wirksam gefunden wurde. Die gleiche über den Summenwert hinausgehende Wirkungssteigerung zeigt ein Vergleich der Ergebnisse von Präparat V mit I und III (Chlorxylenol). Ähnliche Resultate wurden auch bei Verwendung von Leinölseife, wie die Tabelle zeigt, erhalten.The preparation I, which is a 5% solution of 4-chloro-2-cyclohexylphenol represents is only in a dilution i: io compared to Bact. Coli effective. Mixes However, this preparation is compared with preparation II, which contains 5% chlorocresol i: i, whereby preparation IV is created, the effectiveness increases far above the additive Value. The total value would correspond to an effective limiting dilution of i: 35. The actual increase in effectiveness, however, is much greater because of a dilution of preparation IV of x: ioo was still found to be fully effective. The same about A comparison of the results shows an increase in effectiveness beyond the total value of preparation V with I and III (chloroxylenol). Similar results were also obtained for Use linseed oil soap as the table shows.

Mit ähnlichem Erfolg läßt sich auch eine Mischung von 4-Chlor-2-cyclohexylphenol und 2-Chlor-4-cyclohexylphenol in Kombination mit Chlorkresol und,loder Chlorxylenol verwenden.A mixture of 4-chloro-2-cyclohexylphenol can also be used with similar success and 2-chloro-4-cyclohexylphenol in combination with chlorocresol and, l or chloroxylenol use.

Claims (1)

PATENTANSPRUCH: Desinfektionsmittel, bestehend aus einem Gemisch von Chlor-cyclohexylphenol und Chlorkresol und/oder Chlorxylenol.PATENT CLAIM: Disinfectant, consisting of a mixture of Chlorocyclohexylphenol and chlorocresol and / or chloroxylenol.
DESCH2029D 1945-01-03 1945-01-03 Disinfectants Expired DE898664C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
DESCH2029D DE898664C (en) 1945-01-03 1945-01-03 Disinfectants

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DESCH2029D DE898664C (en) 1945-01-03 1945-01-03 Disinfectants

Publications (1)

Publication Number Publication Date
DE898664C true DE898664C (en) 1953-12-03

Family

ID=7423123

Family Applications (1)

Application Number Title Priority Date Filing Date
DESCH2029D Expired DE898664C (en) 1945-01-03 1945-01-03 Disinfectants

Country Status (1)

Country Link
DE (1) DE898664C (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3323988A (en) * 1964-11-25 1967-06-06 Dow Chemical Co Bactericidal 4-chloro-2-cyclopentylphenol

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3323988A (en) * 1964-11-25 1967-06-06 Dow Chemical Co Bactericidal 4-chloro-2-cyclopentylphenol

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