US1981123A - Composition of matter and process of preparing the same - Google Patents

Composition of matter and process of preparing the same Download PDF

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US1981123A
US1981123A US518496A US51849631A US1981123A US 1981123 A US1981123 A US 1981123A US 518496 A US518496 A US 518496A US 51849631 A US51849631 A US 51849631A US 1981123 A US1981123 A US 1981123A
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oil
tar
neutral
water
disinfectant
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US518496A
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James N Roche
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AMERICAN TAR PRODUCTS Co Inc
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AMERICAN TAR PRODUCTS CO Inc
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C39/00Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a six-membered aromatic ring
    • C07C39/24Halogenated derivatives
    • C07C39/26Halogenated derivatives monocyclic monohydroxylic containing halogen bound to ring carbon atoms
    • C07C39/27Halogenated derivatives monocyclic monohydroxylic containing halogen bound to ring carbon atoms all halogen atoms being bound to ring carbon atoms

Definitions

  • This invention relates to a composition of matter and a process of preparing the same and more particularly to compositions for use as antiseptics or disinfectants.
  • tar-acid oil fraction of tar contains various tar acids including benzophenol, cresols and xylenols and various hydrocarbons.
  • the tar-acid oil is made up in the form of an emulsion by mixing it with a soap solution.
  • Disinfectants of the type described have certain disadvantages.
  • One of the most serious disadvantages is that they have a high content of benzophenol which is highly caustic and very poisonous.
  • Another disadvantage is that due to the high benzophenol content, the germicidal effect is relatively weak.
  • the germicidal activity ofthe homologues of phenol increases in the order of phenol, cresols, xylenols, and that their harmful action to tissues decreases in the same order.
  • the benzophenol content of tar-acid oils may be decreased by distilling the tar-acid oil up to a temperature at which the benzophenol is vaporized. In so doing, however, a large proportion of the lower boiling oils which boil in the range of the boiling point of phenol are also removed. A residue is left which has a low benzophenol content, but which is relatively difiicult to emulsify. Furthermore, this procedure is expensive and wasteful.
  • a disinfectant of the above type free from benzophenol may also be prepared in the following manner: Tar-acid oil is treated with caustic soda solutions. The tar acids are separated from the hydrocarbon oil portion of the tar-acid oil in the form of sodium salts. These sodium salts are treated with carbon dioxide to produce free tar acids. The free tar acids are fractionally distilled to remove phenol, and the higher boiling tar acids including cresols and xylenols are returned to the aforementioned hydrocarbon oil portion or so-called neutral oil. A disinfectant is then prepared from the resulting reconstructed oil.
  • composition D which contains both chlorinated xylenols and neutral oil
  • the phenol coefficient is surprisingly greater than the phenol coeflicient of the compositions A or C, the latter containing chloroxylenols and no neutral oil, while the composition A contains neutral oil and no chloroxyle- 11015.
  • the composition B shows the effect of chloroxylenols combined with glycerine instead of neutral oil.
  • hydrocarbon oil either steps up the toxicity of the halogenated phenolic compound or in some way breaks down the resistance of the microbe with which it comes into contact.
  • halogenated phenolic compounds which may be used in the present invention are the chlorine, bromine, iodine, or fluorinecompounds of phenols or of carbocyclic compounds having an hydroxyl group or groups directly attached to 110 the benzene nucleus; the halogen being likewise directly attached to a benzene nucleus.
  • Such compounds are the nuclear halogenated produ ts of benzophenol (such as orthoor parachlorop enols and the 2,4- and 2,4,6- trichlorophenols), isomeric cresols (such as parachlorometa cresol, tetrachlorocresol), isomeric xylenols (such as monochloroparaxylenol, trichlorometaxylenol), higher substituted homologues of phenol (such as butyl, amyl or hexylchlorophenol, chlorothymol, chlorocarvacrol), naphthols (such as mono-diand tetrachloronaphthols) .phenylphenols (such as orthoand parahydroxychlorodiphenyl) polyhydroxyphenols (such as 2,4,6- trichlororesorcinol, chlorobutylor chlorohexylresorcinol), phenols of the structure RCR' where
  • Mixtures of the foregoing compounds which have been halogenated or which contain halogen as part of their aryl nucleus may be used.
  • the chlorine compounds are preferred, and of these, mixed chloroxylenols are preferably used. These compounds are used in the present invention to the extent of 2% to substantially 60%.
  • the oil which is preferred is a neutral coal tar oil which is produced in large quantities as a byproduct in the manufacture of tar acids and naphthalene in coal tar distilleries and which is substantially free from tar acids, and free from crystalline matter when at 20C. or when cooled below substantially 20 (7., preferably at or between 10 C. and +5 C.
  • Other oils, such as petroleum or its fractions, water gas tar, shale tar may be used in place of or combined with neutral coal tar oil.
  • the emulsifying or dispersing agents may be any of those commonly employed such as rosin soap, a castor oil soap, cocoanut oil soap, animal fat soaps, or mixtures of these soaps or meta silicates mixed with soap. Such agents may, if desired, be mixed with other dispersing or stabilizing agents, such as gelatin, casein, saponins and the like.
  • a disinfectant having a phenol coefllcient of 11 may be prepared as follows:
  • a xylenol fraction, 50% of which distills off up to 225 C. is chlorinated in the usual manner employed in obtaining the monochlor compound.
  • An emulsion is prepared containing 10% of chloroxylenol, 63% of neutral oil free from tar acids and 27% of a rosin soap solution in water. It is noted that a disinfectant containing 10% xylenols in place 'of 10% chloroxylenols and similar proportions of the other ingredients, has a coeflicient of only between 3 and 4.
  • a mixture of 20 parts by weight of rosin and 60' parts by weight of oil such as neutral coal tar oil having a boiling range between substantially 160 C. and 250 C. are placed in a vat and heated to about 70 'C.
  • the rosin melts and is thoroughly mixed with the oil.
  • To this mixture are added about 10 parts by weight of chloroxylenol and 6 parts by weightof a 50% solution of sodium hydroxide in water. Additional water is added to make up parts.
  • the resulting product has I a phenol coeflicient of about 14.
  • Products now on the market including disinfectants and insecticides, may be rendered-more germicidal by the addition of either halogenated phenolic compounds or oils, or both, depending on whether they contain one or the other or neither of these substances.
  • a product which is now being sold contains chlorinated xylenols, chlorinated cresols, soap and water.
  • a hydrocarbon oil such as neutral coal tar oil
  • the phenol coeflicient thereof may he stepped up from about 3 to a coefllcient greater than 10.
  • Another product which is generally sold as a disinfectant is one which contains a coal tar hydrocarbon oil, tar acids to the extent of 15 to 30% by weight of the said oil, soap, and water.
  • a halogenated phenolic substance such as chlorinated xylenol, the phenol coefllcient may be increased considerably.
  • mixtures of halogenated phenolic compounds such as chloroxylenols, and oil such as neutral oil, may be prepared in any desired proportion and sold as such, to be later emulsi'fled with soap solutions or other dispersing agents.
  • Mixtures of tar acid oil and halogenated phenolic compounds may also be prepared for similar distribution.
  • the higher tar phenols are of small commercial value and therefore relatiyely inexpensive.
  • The'process of chlorination is simple and likewise inexpensive.
  • a disinfectant substance is isodurene, methyl naphthalene. Its distillation range has been described as 5% off at 160 C. and dry at300 C.
  • any hydrocarbon oils may be used that are adapted to function in a manner similar to the manner in which the hydrocarbon oils mentioned above function with respect to increasing the phenol coefiicient of an emulsion of a chlorophenolic material.
  • dispersion in the appending claims, denotes a mixture of all of the ingredients mentioned therein, either as a suspension of the oily material in the water or of the water in the oily material. It is intended that this term shall includecases in which the dispersion of all of the ingredients forms, insofar as it is possible to determine definitely, a solution or an emulsion.
  • a disinfectant consisting of a dispersion containing a dispersing agent, water, chlorophenolic material to the extent of 2% to substantially 60%, and neutral tar oil to the extent of greater than 10% and up to substantially 63%.
  • a disinfectant consisting of a dispersion containing a dispersing agent, water, chloroxylenol material to the extent of 2 to substantially 60%, and neutral tar oil to the extent of greater than 10% and up to substantially 63%.
  • a disinfectant consisting of a dispersion containing substantially 27% to 44% soap solution, 2% to substantially 60% chloroxylenols, and greater than 10% neutral tar oil.
  • a disinfectant consisting of a dispersion containing a dispersing agent, water, chlorophenolic material to the extent of 2% to substantially 60%, and neutral tar oil to the extent of greater than 10% and up to substantially 63%, the said oil being substantially free from tar acids and free from crystalline matter at 20 C. or below.
  • a disinfectant consisting of a dispersion containing substantially 10% chloroxylenol, substantially 60% neutral tar oil, and substantially 30% of an aqueous soap solution.
  • a disinfectant consisting of a dispersion containing a dispersing agent, water, chlorophenolic material to the extent of 2% to substantially 60%; and substantially 10% up to substantially 63% of hydrocarbon oil selected from at least one of a group consisting of neutral coal tar oil, hydrocarbon oils of neutral coal tar oil, petroleum, its fractions, water gas tar, and shale tar.
  • a disinfectant consisting of a dispersion containing a dispersing agent, water, chlorophenolic material to the extent of 2% to substantially 60%; and greater than 10% and up to substantially 63% of neutral coal tar oil containing 15% to 30% tar acids by weight of the said oil.
  • a disinfectant consisting of a dispersion containing a dispersing agent, water, chlorophenolic material to the extent of 2% to substantially 60% and hydrocarbon oil containing tar acids, the said hydrocarbon oil being present in the dispersion to the extent of from substantially 10% up to substantially 63%, and said hydrocarbon oil being at least one of a group consisting of neutral coal tar oil, hydrocarbon oils of neutral coal tar oil, petroleum, its fractions, water gas tar, and shale tar.

Description

Patented Nov. 20, 1934 COMPOSITION OF MATTER AND PROCESS OF PREPARING THE SAME James N. Roche, Pittsburgh, Pa., assignor to American Tar Products 00., Inc., a corporation of Delaware No Drawing. Application February 26, 1931, Serial No. 518,496
8 Claims.
This invention relates to a composition of matter and a process of preparing the same and more particularly to compositions for use as antiseptics or disinfectants.
In the preparation of disinfectants containing tar acids, it is customary to employ a tar-acid oil fraction of tar. Such a fraction contains various tar acids including benzophenol, cresols and xylenols and various hydrocarbons. For disin- 10 feetant purposes, the tar-acid oil is made up in the form of an emulsion by mixing it with a soap solution.
Disinfectants of the type described have certain disadvantages. One of the most serious disadvantages is that they have a high content of benzophenol which is highly caustic and very poisonous. Another disadvantage is that due to the high benzophenol content, the germicidal effect is relatively weak.
It is well known that the germicidal activity ofthe homologues of phenol increases in the order of phenol, cresols, xylenols, and that their harmful action to tissues decreases in the same order. Ordinarily, the benzophenol content of tar-acid oils may be decreased by distilling the tar-acid oil up to a temperature at which the benzophenol is vaporized. In so doing, however, a large proportion of the lower boiling oils which boil in the range of the boiling point of phenol are also removed. A residue is left which has a low benzophenol content, but which is relatively difiicult to emulsify. Furthermore, this procedure is expensive and wasteful.
A disinfectant of the above type free from benzophenol may also be prepared in the following manner: Tar-acid oil is treated with caustic soda solutions. The tar acids are separated from the hydrocarbon oil portion of the tar-acid oil in the form of sodium salts. These sodium salts are treated with carbon dioxide to produce free tar acids. The free tar acids are fractionally distilled to remove phenol, and the higher boiling tar acids including cresols and xylenols are returned to the aforementioned hydrocarbon oil portion or so-called neutral oil. A disinfectant is then prepared from the resulting reconstructed oil.
I have found that when the cresols or xylenols separatedin the manner described, are halogehated and then returned to the neutral oil, a remarkable increase in the germicidal strength of the disinfectant is obtained, particularly whenthese materials are embodied in an emulsion. I have discovered that disinfectants comprising emulsions containing both a nuclear halogenated 5 phenolic substance and an oil, such as neutral coal according to the 1921 modification of the Ridealtar oil, exhibit greater germicidal activity than similar disinfectants comprising emulsions containing nuclear chlorinated phenolic substances or neutral coal tar oil separately. This phenomenon may be readily illustrated by means of the 00 following table:
Percent Percent Percent Mixed chloroxylenols Neutral coal tar nil Glycerine- Scap.-.-
Water- Phenol coeificient -non:
Walker method. so
It is readily seen that in the case of the composition D which contains both chlorinated xylenols and neutral oil, the phenol coefficient is surprisingly greater than the phenol coeflicient of the compositions A or C, the latter containing chloroxylenols and no neutral oil, while the composition A contains neutral oil and no chloroxyle- 11015. The composition B shows the effect of chloroxylenols combined with glycerine instead of neutral oil.
The reason for the above phenomenon is not known, but I have found that by preparingan emulsion in which both nuclear halogenated phenolic compounds and oils, such as neutral tar oil are present, disinfectants of unusually high strength are produced. In fact, my disinfectants have a phenol coefficient considerably higher than most disinfectants on the market considering the percentage of active ingredient present.
It may be said that the hydrocarbon oil either steps up the toxicity of the halogenated phenolic compound or in some way breaks down the resistance of the microbe with which it comes into contact. 1
The halogenated phenolic compounds which may be used in the present invention are the chlorine, bromine, iodine, or fluorinecompounds of phenols or of carbocyclic compounds having an hydroxyl group or groups directly attached to 110 the benzene nucleus; the halogen being likewise directly attached to a benzene nucleus.
Such compounds are the nuclear halogenated produ ts of benzophenol (such as orthoor parachlorop enols and the 2,4- and 2,4,6- trichlorophenols), isomeric cresols (such as parachlorometa cresol, tetrachlorocresol), isomeric xylenols (such as monochloroparaxylenol, trichlorometaxylenol), higher substituted homologues of phenol (such as butyl, amyl or hexylchlorophenol, chlorothymol, chlorocarvacrol), naphthols (such as mono-diand tetrachloronaphthols) .phenylphenols (such as orthoand parahydroxychlorodiphenyl) polyhydroxyphenols (such as 2,4,6- trichlororesorcinol, chlorobutylor chlorohexylresorcinol), phenols of the structure RCR' where R may be a phenyl, alkyl or substituted phenyl group and C may be carbon, sulphur or a linkage of carbon atoms (such as chlorinated 2,4- dihydroxydiphenylethane, orthochloroparahydroxy diphenylsulphide) and compounds resulting from the condensation of phenols and aldehydes (such as chlorinated 0,0 dihydroxydiphenylmethane) One or more halogen atoms may be combined with these compounds. Mixtures of the foregoing compounds which have been halogenated or which contain halogen as part of their aryl nucleus may be used. The chlorine compounds are preferred, and of these, mixed chloroxylenols are preferably used. These compounds are used in the present invention to the extent of 2% to substantially 60%.
The oil which is preferred is a neutral coal tar oil which is produced in large quantities as a byproduct in the manufacture of tar acids and naphthalene in coal tar distilleries and which is substantially free from tar acids, and free from crystalline matter when at 20C. or when cooled below substantially 20 (7., preferably at or between 10 C. and +5 C. Other oils, such as petroleum or its fractions, water gas tar, shale tar, may be used in place of or combined with neutral coal tar oil.
In the preparation of emulsions, the emulsifying or dispersing agents may be any of those commonly employed such as rosin soap, a castor oil soap, cocoanut oil soap, animal fat soaps, or mixtures of these soaps or meta silicates mixed with soap. Such agents may, if desired, be mixed with other dispersing or stabilizing agents, such as gelatin, casein, saponins and the like.
By way of example, a disinfectant having a phenol coefllcient of 11 may be prepared as follows:
A xylenol fraction, 50% of which distills off up to 225 C. is chlorinated in the usual manner employed in obtaining the monochlor compound. An emulsion is prepared containing 10% of chloroxylenol, 63% of neutral oil free from tar acids and 27% of a rosin soap solution in water. It is noted that a disinfectant containing 10% xylenols in place 'of 10% chloroxylenols and similar proportions of the other ingredients, has a coeflicient of only between 3 and 4.
In preparing a disinfectant for commercial purposes and on a large scale, the following procedure may be used:
A mixture of 20 parts by weight of rosin and 60' parts by weight of oil such as neutral coal tar oil having a boiling range between substantially 160 C. and 250 C. are placed in a vat and heated to about 70 'C. The rosin melts and is thoroughly mixed with the oil. To this mixture are added about 10 parts by weight of chloroxylenol and 6 parts by weightof a 50% solution of sodium hydroxide in water. Additional water is added to make up parts. The resulting product has I a phenol coeflicient of about 14.
Expressing this differently, about 1 cubic centimeter of this product when added to about 280 cubic centimeters of water gives an emulsion equivalent to a 5% solution of benzophenol. An emulsion containing these proportions is very satisfactory for disinfecting inanimate objects. An emulsion containing about 1 cubic centimeter of the above product in about 1400 cubic centimeters of water is satisfactory for disinfecting the hands or other skin portions of the human body.
Products now on the market, including disinfectants and insecticides, may be rendered-more germicidal by the addition of either halogenated phenolic compounds or oils, or both, depending on whether they contain one or the other or neither of these substances. For instance, a product which is now being sold contains chlorinated xylenols, chlorinated cresols, soap and water. By the addition of a hydrocarbon oil such as neutral coal tar oil, to this product, the phenol coeflicient thereof may he stepped up from about 3 to a coefllcient greater than 10.
Another product which is generally sold as a disinfectant is one which contains a coal tar hydrocarbon oil, tar acids to the extent of 15 to 30% by weight of the said oil, soap, and water. By mixing with this product a halogenated phenolic substance such as chlorinated xylenol, the phenol coefllcient may be increased considerably.
In the commercial distribution of the product of the present invention, mixtures of halogenated phenolic compounds such as chloroxylenols, and oil such as neutral oil, may be prepared in any desired proportion and sold as such, to be later emulsi'fled with soap solutions or other dispersing agents. Mixtures of tar acid oil and halogenated phenolic compounds may also be prepared for similar distribution.
The higher tar phenols are of small commercial value and therefore relatiyely inexpensive. The'process of chlorination is simple and likewise inexpensive. By combining the inexpensive chlorinated products with the by-product neutral oil, for instance, a disinfectant substance is isodurene, methyl naphthalene. Its distillation range has been described as 5% off at 160 C. and dry at300 C. It is further understood that any hydrocarbon oils may be used that are adapted to function in a manner similar to the manner in which the hydrocarbon oils mentioned above function with respect to increasing the phenol coefiicient of an emulsion of a chlorophenolic material. v
The term dispersion, in the appending claims, denotes a mixture of all of the ingredients mentioned therein, either as a suspension of the oily material in the water or of the water in the oily material. It is intended that this term shall includecases in which the dispersion of all of the ingredients forms, insofar as it is possible to determine definitely, a solution or an emulsion.
I claim as my invention:
1. A disinfectant consisting of a dispersion containing a dispersing agent, water, chlorophenolic material to the extent of 2% to substantially 60%, and neutral tar oil to the extent of greater than 10% and up to substantially 63%.
2. A disinfectant consisting of a dispersion containing a dispersing agent, water, chloroxylenol material to the extent of 2 to substantially 60%, and neutral tar oil to the extent of greater than 10% and up to substantially 63%.
3. A disinfectant consisting of a dispersion containing substantially 27% to 44% soap solution, 2% to substantially 60% chloroxylenols, and greater than 10% neutral tar oil.
4. A disinfectant consisting of a dispersion containing a dispersing agent, water, chlorophenolic material to the extent of 2% to substantially 60%, and neutral tar oil to the extent of greater than 10% and up to substantially 63%, the said oil being substantially free from tar acids and free from crystalline matter at 20 C. or below.
5. A disinfectant consisting of a dispersion containing substantially 10% chloroxylenol, substantially 60% neutral tar oil, and substantially 30% of an aqueous soap solution.
6. A disinfectant consisting of a dispersion containing a dispersing agent, water, chlorophenolic material to the extent of 2% to substantially 60%; and substantially 10% up to substantially 63% of hydrocarbon oil selected from at least one of a group consisting of neutral coal tar oil, hydrocarbon oils of neutral coal tar oil, petroleum, its fractions, water gas tar, and shale tar.
7. A disinfectant consisting of a dispersion containing a dispersing agent, water, chlorophenolic material to the extent of 2% to substantially 60%; and greater than 10% and up to substantially 63% of neutral coal tar oil containing 15% to 30% tar acids by weight of the said oil.
8. A disinfectant consisting of a dispersion containing a dispersing agent, water, chlorophenolic material to the extent of 2% to substantially 60% and hydrocarbon oil containing tar acids, the said hydrocarbon oil being present in the dispersion to the extent of from substantially 10% up to substantially 63%, and said hydrocarbon oil being at least one of a group consisting of neutral coal tar oil, hydrocarbon oils of neutral coal tar oil, petroleum, its fractions, water gas tar, and shale tar.
JAMES N. ROCHE.
US518496A 1931-02-26 1931-02-26 Composition of matter and process of preparing the same Expired - Lifetime US1981123A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2961375A (en) * 1957-08-27 1960-11-22 Charles G Shaw Nontoxic fungicidal preparations
US3046190A (en) * 1956-09-28 1962-07-24 Monsanto Chemicals Germicides
US3150662A (en) * 1961-12-07 1964-09-29 Haver Lockhart Lab Method of lubricating body cavities
US3291687A (en) * 1963-01-25 1966-12-13 Boots Pure Drug Co Ltd Cattle dips

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3046190A (en) * 1956-09-28 1962-07-24 Monsanto Chemicals Germicides
US2961375A (en) * 1957-08-27 1960-11-22 Charles G Shaw Nontoxic fungicidal preparations
US3150662A (en) * 1961-12-07 1964-09-29 Haver Lockhart Lab Method of lubricating body cavities
US3291687A (en) * 1963-01-25 1966-12-13 Boots Pure Drug Co Ltd Cattle dips

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