US2354334A - Germicide and method of producing same - Google Patents

Germicide and method of producing same Download PDF

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Publication number
US2354334A
US2354334A US463543A US46354342A US2354334A US 2354334 A US2354334 A US 2354334A US 463543 A US463543 A US 463543A US 46354342 A US46354342 A US 46354342A US 2354334 A US2354334 A US 2354334A
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US
United States
Prior art keywords
molecular weight
manganous
reducing agent
chlorophenol
chloride
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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 - Lifetime
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US463543A
Inventor
Anthony J Salle
Howard L Guest
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LEO A GUNTHER
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LEO A GUNTHER
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Priority to US463543A priority Critical patent/US2354334A/en
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Publication of US2354334A publication Critical patent/US2354334A/en
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Expired - Lifetime legal-status Critical Current

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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

Definitions

  • This invention relates to g'ermicides of the phenol group that are in oxidized form, such as chlorophenol and sulfophenol.
  • the object of the invention is to greatly increase the germicidal properties of chlorophenol, sulfophenol, or-any of the solutions of phenol generally in which the phenol is in the oxidized form, thus tion, one gram molecular weight of a reducing agent, such as ferrous chloride, ferrous sulphate, manganous chloride or manganous sulphate.
  • a reducing agent such as ferrous chloride, ferrous sulphate, manganous chloride or manganous sulphate.
  • the killing power of the solution as applied to micro-organisms is substantially increased so that the per cent concentration of the resultant solution may be from one-third to one-half of the concentration required, before the addition, for accomplishing the same results.
  • the objectionable causticity to tissue of the phenol is correspondingly reduced and the resultant product is less caustic to tissue.
  • the concentration is such that it is caustic to tissue if it has the requisite killing power to be effective as a germicide, as demonstrated by the following; the least lethal dilution of chlorophenol is 1:500; the effective dilution is -l:100.
  • the least lethal dilution of improved chlorophenol is 1:1400; the effective dilution is 1:460.
  • the method of increasing the germicidal properties of phenols that are in oxidized form that comprises adding to each gram.
  • molecular weight of the phenol one gram molecular weight of a reducing agent from the group; ferrous chloride, ferrous sulfate, "manganous chloride, manganous sulfate.
  • a germicidal product comprising one of the phenols that is in oxidized form and areducing agent from one of the group; ferrous chloride, ferrous sulfate, manganous chloride, manganous sulfate, in the proportion of one gram molecular weight of the phenol to one gram molecular weight of the reducing agent.
  • a germicidal product comprising one of the phenol in the group; chlorophenol, sulfophenol, and a reducing agent from one of the group; ferrous chloride, ferrous sulfate, manganous chloride, manganous sulfate, in the proportion of one gram molecular weight of the reducing agent to. each gram molecular weight of the phenol.
  • a germicidal solution comprising one of the phenols in the group; chlorophenol, sulfophenol and a reducing agent from one of the group; ferrous chloride, ferrous sulfate, manganous chloride, manganous sulfate, in the proportion of onev gram molecular weight of the reducing agent to each gram molecular weight of the phenol.

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  • 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

Patented July 25, 1944 I v 2,354,334 onmvncma AND MElHOD or PRODUCING Anthony J. Salle, West Los Angeles, as Howard L. Guest, Ocean Park, hall to Leo A. Gunther, Robbins, Calif.
No Drawing. Application October 27, 1942, Serial No. 463,543
7 Claims. (Cl. 167-31) This invention relates to g'ermicides of the phenol group that are in oxidized form, such as chlorophenol and sulfophenol.
The object of the invention is to greatly increase the germicidal properties of chlorophenol, sulfophenol, or-any of the solutions of phenol generally in which the phenol is in the oxidized form, thus tion, one gram molecular weight of a reducing agent, such as ferrous chloride, ferrous sulphate, manganous chloride or manganous sulphate.
By the above addition of the reducing agent, the killing power of the solution as applied to micro-organisms, such as Staphylococcus aureus, is substantially increased so that the per cent concentration of the resultant solution may be from one-third to one-half of the concentration required, before the addition, for accomplishing the same results.
By thi addition, the objectionable causticity to tissue of the phenol is correspondingly reduced and the resultant product is less caustic to tissue.
It is pertinent to note that in a conventional solution of chlorophenol, without the addition of a reducing agent, the concentration is such that it is caustic to tissue if it has the requisite killing power to be effective as a germicide, as demonstrated by the following; the least lethal dilution of chlorophenol is 1:500; the effective dilution is -l:100. The least lethal dilution of improved chlorophenol is 1:1400; the effective dilution is 1:460.
The advantages of the invention are therefore,
., assignors of one- 2. The method of increasing the germicidal properties of phenols that are in oxidized form that comprises adding to each gram. molecular weight of the phenol one gram molecular weight of a reducing agent from the group; ferrous chloride, ferrous sulfate, "manganous chloride, manganous sulfate.
3. The method of increasing the germicidal property of one of the group; chlorophenol, sulfophenol, that comprises adding to each gram molecular weight thereof one gram molecular weight of one ofthe group; ferrous chloride, ferrous sulfate, manganous chloride, manganous sulfate.
4. A germicidal product comprising one of the phenols that is in oxidized form and areducing agent from one of the group; ferrous chloride, ferrous sulfate, manganous chloride, manganous sulfate, in the proportion of one gram molecular weight of the phenol to one gram molecular weight of the reducing agent.
5. A germicidal product comprising one of the phenol in the group; chlorophenol, sulfophenol, and a reducing agent from one of the group; ferrous chloride, ferrous sulfate, manganous chloride, manganous sulfate, in the proportion of one gram molecular weight of the reducing agent to. each gram molecular weight of the phenol.
6. A germicidal solution comprising one of the phenols in the group; chlorophenol, sulfophenol and a reducing agent from one of the group; ferrous chloride, ferrous sulfate, manganous chloride, manganous sulfate, in the proportion of onev gram molecular weight of the reducing agent to each gram molecular weight of the phenol.
7. A germicidal solution having substantially the same killing power to Staphylococcus aureus -of a 1:100 solution of chlorophenol that comprises substantially a 1:1400 solution of chlorophenol and a reducing agent from one of the group; ferrous chloride, ferrous sulphate, manganous chloride, manganous sulfate, in the proportion of one gram molecular weight of the reducing agent to each-gram molecular weight of .45 the chlorophnol.
ANTHONY J. SALLE. HOWARD L. GUEST.
US463543A 1942-10-27 1942-10-27 Germicide and method of producing same Expired - Lifetime US2354334A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2585965A (en) * 1946-03-01 1952-02-19 Anthony J Salle Iodine solution comprising an oxidation-reduction system

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2585965A (en) * 1946-03-01 1952-02-19 Anthony J Salle Iodine solution comprising an oxidation-reduction system

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