US2236387A - Perspiration inhibiting composition - Google Patents

Perspiration inhibiting composition Download PDF

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Publication number
US2236387A
US2236387A US205702A US20570238A US2236387A US 2236387 A US2236387 A US 2236387A US 205702 A US205702 A US 205702A US 20570238 A US20570238 A US 20570238A US 2236387 A US2236387 A US 2236387A
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acid
perspiration
composition
astringent
aluminum
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US205702A
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Jr John H Wallace
Wilfred C Hand
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q15/00Anti-perspirants or body deodorants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/26Aluminium; Compounds thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/42Amides
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof

Definitions

  • This invention relates to improved perspiration retarding or inhibiting compounds.
  • the objects of the invention are carried out by providing a compound in which are combined one or more water soluble heavy metal salts of strong acids, usually mineral acids, and a normally neutral water soluble amino compound possessing one or more intact reactive amino (NHz) groups.
  • the metallic salt astringent or coagulant ingredient of our composition preferably comprises ,a water soluble strong acid salt of one or more metals, such as aluminum, zinc, cerium, zirconium, titanium, iron or bismuth, although salts of tin, lead and cadmium are also effective.
  • the acid radical of the astringent salt is preferably chosen from the mineral acid group, such as sulfuric, phosphoric or hydrochloric acid, although salts of strong organic acids, such as sulfonic acids, may also be used.
  • Examples of water soluble heavy metal salts which give excellent results are aluminum sulfate, aluminum chloride and aluminum phosphate.
  • the normally neutral protective ingredient of our composition is preferably a chemical selected from one of two groups of amino compounds, namely the amides and the amino acids.
  • the suitable chemicals in these groups are those which are neutral, which are materially soluble in water or in the strong acid salt of the heavy metal comprising the astringent ingredient of our composition, and which possess one or more intact amino groups.
  • Examples of amides which are suitable for use as the protective ingredient of our composition are the lower aliphatic and aromatic amides, such as formamide, acetamide, carbamide (urea) and derivatives thereof.
  • Suitable derivatives of carbamide include those obtained by replacing one amino group thereof with an alkyl, acyl, or aryl group, such as ethyl carbamate, and those derived by the replacement of one or more hydrogenatoms of one amino group of carbamide, such as ethyl urea and methyl urea.
  • Another suitable derivative of carbamide is one in which both amino groups are intact and oxygen has been replaced by sulfur.
  • amino acids which are suitable for use in our composition as the protective ingredient thereof are aminoacetic acid and aminopropionic acid.
  • the acid salt ingredient and the normally neutral ingredient in such proportions that one reactive amino group of the protective ingredient is available for each potential acid ion of the salt.
  • the astringent and protective ingredients comprise aluminum sulfate and glycine (aminoacetic acid) respectively, the proportions of these ingredients should be such that six molecules of glycine are provided for each molecule of the salt, since upon hydrolysis, a molecule of aluminum sulfate produces three molecules of dibasic sulfuric acid.
  • urea (carbamide) is used as the protective ingredient with aluminum sulfate
  • the proportions should be such as to provide six molecules of urea for each molecule of aluminum sulfate, since although each molecule of urea contains two amino groups, only one of them is chemically active in this reaction.
  • a specific example of our improved composition using aluminum sulfate and urea may be prepared by dissolving grams of aluminum sulfate in approximately 50 cubic centimeters of water and adding and dissolving 15 grams of 25 urea in such solution, the volume of the solution being finally brought up to 100 cubic centimeters by the addition of water.
  • composition employing an amino acid as the protective ingredient may be prepared by dissolving 13 grams of aluminum sulfate in about 20 cubic centimeters of water and dissolving 9 grams of glycine (aminoacetic acid) in such solution.
  • our composition may be used in the form described or a suitable wetting agent may be added thereto if desired.
  • Our improved compound may also be incorporated in an emulsion with wax or oil and applied to the skin in this form.
  • a perspiration inhibiting composition comprising a non-toxic water soluble protein coagulating metallic salt of a strong acid and a neutral, water soluble amino compound taken from the group consisting of the aliphatic amides and the aliphatic amino acids and having at least one intact, reactive amino group.
  • a perspiration inhibiting composition comprising a solution of aluminum sulfate and a normally neutral amino compound, soluble in said salt solution, taken from the group consisting of the aliphatic amides and the aliphatic amino acids and having at least one intact, re- 6 active amino group.
  • a perspiration inhibiting composition comprising a solution of aluminum sulfate and a normally neutral water soluble aliphatic amide having at least one intact, reactive amino group. 10
  • a perspiration inhibiting composition comprising a solution of aluminum sulfate and a normally neutral water soluble aliphatic amino acid having at least one intact, reactive amino group.
  • a perspiration inhibiting composition com- 15 prising a solution of aluminum sulfate and urea.
  • a perspiration inhibiting composition comprising a non-toxic water soluble protein coagulating metallic salt of a strong acid and 9. normally neutral water soluble organic compound 20 taken from the group of amino compounds consisting of the aliphatic amides and the aliphatic amino acids and having at least one intact, reactive amino group, the proportion of said organic compound in the composition being sufli- 25 cient to provide at least one intact, reactive amino group for each potential acid ion of the metallic salt.
  • a perspiration inhibiting composition comprising a water solution containing a solute com- 30 prising about 62% by weight of aluminum sulfate and about 38% by weight of urea.
  • a cosmetic astringent preparation containing an astringent material comprising an acidreacting inorganic salt of a polyvalent metal and 35 a proportion of a soluble aliphatic amide.
  • a cosmetic astringent preparation including aluminum chloride and a soluble aliphatic amide.
  • a cosmetic astringent preparation including aluminum chloride and urea. 40
  • a cosmetic astringent preparation including as its essential astringent ingredient an acid reacting inorganic salt of a polyvalent metal together with a proportion of a water soluble aliphatic amide.
  • a cosmetic astringent preparation including aluminum sulphate as its essential astringent ingredient together with urea.
  • a cosmetic astringent preparation containing an astringent material comprising an acid 50 reacting inorganic salt of a polyvalent metal and a proportion of urea.
  • a cosmetic astringent preparation containing an astringent material comprising an acid reacting inorganic salt of a polyvalent metal and 55 a proportion of a water soluble aliphatic amino acid.
  • a cosmetic astringent preparation containing as its essential astringent ingredient an acid reacting inorganic salt of a polyvalent metal together with a proportion of urea.

Description

Patented Mar. 25, 194i TION INHIBITING COMPOSITIGN John H. Wallace, In, Princeton, N. .lL, and Wilfred 0. Hand, New York N. Y.; said Hand assignor to said Wallace, Jr.
N Drawing. Application May 3, 1938, Serial N0. 205,702
16 Claims.
This invention relates to improved perspiration retarding or inhibiting compounds.
It has heretofore been proposed to control or retard the flow of perspiration from certain skin areas by the application of solutions containing an acid salt of a heavy metal, usually aluminum chloride or aluminum sulfate. Such solutions are effective in stopping perspiration but are unsatisfactory and hazardous in that the use thereof frequently produces acute skin irritation or dermatitis and rots clothing fabrics which come in contact with the treated areas. In an attempt to mitigate the corrosive action of these compounds on fabrics, directions for their use usually urge that the solutions be permitted to dry on the skin and that the treated skin areas be thereafter wiped ofi with a damp cloth before clothing is brought in contact therewith. The solutions dry slowly and these precautions are frequently disregarded. In any case, the recommended procedure does not prevent skin irritation.
Prior to the present invention, the above described corrosive action of efiective perspiration inhibiting preparations was considered inherent and unavoidable. The action of such preparations apparently depends upon the presence of both the metallic aluminum or aluminum hydroxide ion and the strong mineral acid ion. Considering aluminum sulfate, for example, the aluminum or aluminum hydroxide ion apparently combines with and coagulates the skin proteins only in the presence of the sulfate radical, and as a result of this action, a residue of sulfuric as acid remains which irritates the skin and rots the clothing. The use of metallic salts of weak acids offers no solution since such compounds are ineffective to restrict the flow of perspiration. The problem is further complicated by the fact that if alkaline substances are added, insoluble basic aluminum compounds, such as aluminum hydroxide, are formed, and no perspiration retarding action is obtained. As-a consequence, all previously known effective perspiration inhibiting preparations are characterized by the above described undesirable corrosive action. With the above and other considerations in mind, it is proposed in accordance with the present invention to provide an improved perspira- 5 tion retarding or inhibiting compound which. While retaining in full the desirable inhibitory action of previously known preparations, avoids their corrosive action and is harmless to the skin and fabrics. Other objects of the invention include the provision of a perspiration treating or inhibiting compound which is inexpensive to produce, which may be easily applied in liquid, semiliquid or other forms and which has no undesirable odor or other physical or chemical properties which would impair its usefulness as a cosmetic preparation.
The objects of the invention are carried out by providing a compound in which are combined one or more water soluble heavy metal salts of strong acids, usually mineral acids, and a normally neutral water soluble amino compound possessing one or more intact reactive amino (NHz) groups.
The metallic salt astringent or coagulant ingredient of our composition preferably comprises ,a water soluble strong acid salt of one or more metals, such as aluminum, zinc, cerium, zirconium, titanium, iron or bismuth, although salts of tin, lead and cadmium are also effective. The acid radical of the astringent salt is preferably chosen from the mineral acid group, such as sulfuric, phosphoric or hydrochloric acid, although salts of strong organic acids, such as sulfonic acids, may also be used. Examples of water soluble heavy metal salts which give excellent results are aluminum sulfate, aluminum chloride and aluminum phosphate.
The normally neutral protective ingredient of our composition is preferably a chemical selected from one of two groups of amino compounds, namely the amides and the amino acids. The suitable chemicals in these groups are those which are neutral, which are materially soluble in water or in the strong acid salt of the heavy metal comprising the astringent ingredient of our composition, and which possess one or more intact amino groups. Examples of amides which are suitable for use as the protective ingredient of our composition are the lower aliphatic and aromatic amides, such as formamide, acetamide, carbamide (urea) and derivatives thereof. Suitable derivatives of carbamide include those obtained by replacing one amino group thereof with an alkyl, acyl, or aryl group, such as ethyl carbamate, and those derived by the replacement of one or more hydrogenatoms of one amino group of carbamide, such as ethyl urea and methyl urea. Another suitable derivative of carbamide is one in which both amino groups are intact and oxygen has been replaced by sulfur.
Examples of amino acids which are suitable for use in our composition as the protective ingredient thereof are aminoacetic acid and aminopropionic acid.
We find it preferable to combine the acid salt ingredient and the normally neutral ingredient in such proportions that one reactive amino group of the protective ingredient is available for each potential acid ion of the salt. For ex- 5 ample, if the astringent and protective ingredients comprise aluminum sulfate and glycine (aminoacetic acid) respectively, the proportions of these ingredients should be such that six molecules of glycine are provided for each molecule of the salt, since upon hydrolysis, a molecule of aluminum sulfate produces three molecules of dibasic sulfuric acid. If urea (carbamide) is used as the protective ingredient with aluminum sulfate, the proportions should be such as to provide six molecules of urea for each molecule of aluminum sulfate, since although each molecule of urea contains two amino groups, only one of them is chemically active in this reaction.
A specific example of our improved composition using aluminum sulfate and urea may be prepared by dissolving grams of aluminum sulfate in approximately 50 cubic centimeters of water and adding and dissolving 15 grams of 25 urea in such solution, the volume of the solution being finally brought up to 100 cubic centimeters by the addition of water.
An example of the composition employing an amino acid as the protective ingredient may be prepared by dissolving 13 grams of aluminum sulfate in about 20 cubic centimeters of water and dissolving 9 grams of glycine (aminoacetic acid) in such solution.
The above and other solutions of our composition may be used in the form described or a suitable wetting agent may be added thereto if desired. Our improved compound may also be incorporated in an emulsion with wax or oil and applied to the skin in this form.
Our improved composition is highly effective in stopping perspiration and is harmless to the skin and fabrics. It is our belief that when the composition is applied to the skin, the ionized metallic salt gives up metallic ions or metallic hydroxide ions which combine with the skin proteins to form coagulant materials and so inhibit the flow of perspiration. The acid ions present make possible this coagulating action, probably either acting as solubilizing agents or reacting with the skin proteins. The reaction of the metallic ions with the skin proteins leaves an excess of sulfuric acid which immediately reacts with the normally neutral protective ingredient, probably forming a neutral addition compound therewith through the reactive amino groups thereof. Although we believe that the foregoing explanation is correct, it should be understood that the invention is in no way dependent upon the accuracy of the theory here expressed.
We claim: I
1. A perspiration inhibiting composition comprising a non-toxic water soluble protein coagulating metallic salt of a strong acid and a neutral, water soluble amino compound taken from the group consisting of the aliphatic amides and the aliphatic amino acids and having at least one intact, reactive amino group.
2. A perspiration inhibiting composition comprising a solution of aluminum sulfate and a normally neutral amino compound, soluble in said salt solution, taken from the group consisting of the aliphatic amides and the aliphatic amino acids and having at least one intact, re- 6 active amino group.
3. A perspiration inhibiting composition comprising a solution of aluminum sulfate and a normally neutral water soluble aliphatic amide having at least one intact, reactive amino group. 10
4. A perspiration inhibiting composition comprising a solution of aluminum sulfate and a normally neutral water soluble aliphatic amino acid having at least one intact, reactive amino group.
5. A perspiration inhibiting composition com- 15 prising a solution of aluminum sulfate and urea.
6. A perspiration inhibiting composition comprising a non-toxic water soluble protein coagulating metallic salt of a strong acid and 9. normally neutral water soluble organic compound 20 taken from the group of amino compounds consisting of the aliphatic amides and the aliphatic amino acids and having at least one intact, reactive amino group, the proportion of said organic compound in the composition being sufli- 25 cient to provide at least one intact, reactive amino group for each potential acid ion of the metallic salt.
7. A perspiration inhibiting composition comprising a water solution containing a solute com- 30 prising about 62% by weight of aluminum sulfate and about 38% by weight of urea.
8. A cosmetic astringent preparation containing an astringent material comprising an acidreacting inorganic salt of a polyvalent metal and 35 a proportion of a soluble aliphatic amide.
9. A cosmetic astringent preparation including aluminum chloride and a soluble aliphatic amide.
10. A cosmetic astringent preparation including aluminum chloride and urea. 40
11. A cosmetic astringent preparation including as its essential astringent ingredient an acid reacting inorganic salt of a polyvalent metal together with a proportion of a water soluble aliphatic amide.
12. A cosmetic astringent preparation including aluminum sulphate as its essential astringent ingredient together with urea.
13. A cosmetic astringent preparation containing an astringent material comprising an acid 50 reacting inorganic salt of a polyvalent metal and a proportion of urea.
14. A cosmetic astringent preparation containing an astringent material comprising an acid reacting inorganic salt of a polyvalent metal and 55 a proportion of a water soluble aliphatic amino acid.
15. A cosmetic astringent preparation containing aluminum sulphate as its essential astringent ingredient together with a soluble aliphatic 6 amide.
16. A cosmetic astringent preparation containing as its essential astringent ingredient an acid reacting inorganic salt of a polyvalent metal together with a proportion of urea. 65
JOHN H. WALLACE, JR. WILFRED C. HAND.
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Cited By (39)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2498514A (en) * 1946-01-18 1950-02-21 Nat Lead Co Zirconium compound deodorant and antiperspirant
US2504107A (en) * 1946-10-04 1950-04-18 Purdue Research Foundation Aluminum methionate
US2508787A (en) * 1948-07-08 1950-05-23 Chattanooga Medicine Co Dichloro aluminum aminoacetate hydrate deodorant composition
US2586288A (en) * 1948-12-11 1952-02-19 Colgate Palmolive Peet Co Aluminum sulfamate antiperspirant
US2586287A (en) * 1948-12-11 1952-02-19 Colagte Palmolive Peet Company Aluminum sulfamate antiperspirant preparation
US2586289A (en) * 1949-05-03 1952-02-19 Colgate Palmolive Peet Co Zinc sulfamate antiperspirant
US2734847A (en) * 1956-02-14 Ptoatw
US2790747A (en) * 1952-08-06 1957-04-30 Carter Products Zirconium containing anti-perspirant compositions
US2814585A (en) * 1954-04-30 1957-11-26 Procter & Gamble Buffered antiperspirant compositions
US2814584A (en) * 1954-04-30 1957-11-26 Procter & Gamble Buffered antiperspirant compositions
US2885323A (en) * 1952-10-13 1959-05-05 Nat Lead Co Process for inactivating urushiol on skin with cerium compounds
US2889253A (en) * 1956-06-14 1959-06-02 Carter Prod Inc Zirconium containing anti-perspirant compositions
US3009860A (en) * 1957-06-14 1961-11-21 Chattanooga Medicine Co Zirconyl trichloro aluminate and method of making the same
US3018223A (en) * 1958-02-24 1962-01-23 Bristol Myers Co Aluminum dihydroxy-titanium dilactate antiperspirant
US3090728A (en) * 1957-02-20 1963-05-21 Berger Frank Milan Titanic acid complexes of hydroxy aliphatic carboxylic acids antiperspirant compostions
US3211620A (en) * 1960-09-19 1965-10-12 Colgate Palmolive Co Stabilized antiperspirant-deodorant composition
US3235458A (en) * 1962-08-22 1966-02-15 Colgate Palmolive Co Process for preparing an aluminum sulfate-aluminum chlorhydrate antiperspirant cream
US3499961A (en) * 1963-12-09 1970-03-10 Crown Zellerbach Corp Dimethyl sulfoxide-enhanced astringent aluminum,zinc or zirconium antiperspirant salt cosmetics
US3934004A (en) * 1973-03-09 1976-01-20 Orren Leonard J Stain resistant anti-perspirant composition
US3981986A (en) * 1973-11-23 1976-09-21 Armour Pharmaceutical Company Zirconium-aluminum-polyol buffered anti-perspirant complexes
US4017599A (en) * 1973-11-23 1977-04-12 Armour Pharmaceutical Company Aluminum-zirconium anti-perspirant systems with salts of amino acids
US4021536A (en) * 1975-04-18 1977-05-03 Armour Pharmaceutical Company Magnesium-zirconium complexes useful as antiperspirants
US4027007A (en) * 1970-12-09 1977-05-31 Colgate-Palmolive Company Antiperspirants formulated with borax
US4028390A (en) * 1975-03-26 1977-06-07 Armour Pharmaceutical Company Methods of making basic zirconium complexes
US4089942A (en) * 1976-01-29 1978-05-16 L'oreal Deodorant composition and process
US4490354A (en) * 1980-04-11 1984-12-25 American Cyanamid Company Antiperspirant method containing vanadium salts
US4565693A (en) * 1981-11-09 1986-01-21 Colgate-Palmolive Company Deodorant composition
US4606915A (en) * 1981-04-23 1986-08-19 Bristol-Myers Company Antiperspirant combination containing an aluminum halohydrate and a stannic halide
US4650671A (en) * 1981-07-17 1987-03-17 Claus Riemann & Co. Aps Antiperspirant kit and method for controlling perspiration
US5135741A (en) * 1984-04-24 1992-08-04 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Antiperspirant product
WO1993007853A1 (en) * 1991-10-23 1993-04-29 Monell Chemical Senses Center Inhibition of odor formation and bacterial growth
US5463098A (en) * 1992-11-16 1995-10-31 Giovanniello; Rocco Clear antiperspirant gel stick and method for making same
US5518714A (en) * 1984-04-24 1996-05-21 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Method for inhibiting the dissolution of antiperspirant compounds in alcohols
US5643559A (en) * 1991-10-30 1997-07-01 Colgate-Palmolive Company Deodorant compositions comprising inhibitors of odor-producing axillary bacterial exoenzymes
US20030031727A1 (en) * 1994-12-21 2003-02-13 Cosmederm Technologies, Llc Topical product formulations containing strontium for reducing skin irritation
US20030124202A1 (en) * 1994-12-21 2003-07-03 Hahn Gary S. Formulations and methods for reducing skin irritation
WO2011087702A3 (en) * 2009-12-23 2012-07-05 Colgate-Palmolive Company Aqueous antiperspirant/deodorant composition
WO2017117301A1 (en) * 2015-12-30 2017-07-06 Colgate-Palmolive Company Personal care compositions
WO2017117155A1 (en) * 2015-12-30 2017-07-06 Colgate-Palmolive Company Personal care compositions

Cited By (52)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2734847A (en) * 1956-02-14 Ptoatw
US2498514A (en) * 1946-01-18 1950-02-21 Nat Lead Co Zirconium compound deodorant and antiperspirant
US2504107A (en) * 1946-10-04 1950-04-18 Purdue Research Foundation Aluminum methionate
US2508787A (en) * 1948-07-08 1950-05-23 Chattanooga Medicine Co Dichloro aluminum aminoacetate hydrate deodorant composition
US2586288A (en) * 1948-12-11 1952-02-19 Colgate Palmolive Peet Co Aluminum sulfamate antiperspirant
US2586287A (en) * 1948-12-11 1952-02-19 Colagte Palmolive Peet Company Aluminum sulfamate antiperspirant preparation
US2586289A (en) * 1949-05-03 1952-02-19 Colgate Palmolive Peet Co Zinc sulfamate antiperspirant
US2790747A (en) * 1952-08-06 1957-04-30 Carter Products Zirconium containing anti-perspirant compositions
US2885323A (en) * 1952-10-13 1959-05-05 Nat Lead Co Process for inactivating urushiol on skin with cerium compounds
US2814585A (en) * 1954-04-30 1957-11-26 Procter & Gamble Buffered antiperspirant compositions
US2814584A (en) * 1954-04-30 1957-11-26 Procter & Gamble Buffered antiperspirant compositions
US2889253A (en) * 1956-06-14 1959-06-02 Carter Prod Inc Zirconium containing anti-perspirant compositions
US3090728A (en) * 1957-02-20 1963-05-21 Berger Frank Milan Titanic acid complexes of hydroxy aliphatic carboxylic acids antiperspirant compostions
US3009860A (en) * 1957-06-14 1961-11-21 Chattanooga Medicine Co Zirconyl trichloro aluminate and method of making the same
US3018223A (en) * 1958-02-24 1962-01-23 Bristol Myers Co Aluminum dihydroxy-titanium dilactate antiperspirant
US3211620A (en) * 1960-09-19 1965-10-12 Colgate Palmolive Co Stabilized antiperspirant-deodorant composition
US3235458A (en) * 1962-08-22 1966-02-15 Colgate Palmolive Co Process for preparing an aluminum sulfate-aluminum chlorhydrate antiperspirant cream
US3499961A (en) * 1963-12-09 1970-03-10 Crown Zellerbach Corp Dimethyl sulfoxide-enhanced astringent aluminum,zinc or zirconium antiperspirant salt cosmetics
US4027007A (en) * 1970-12-09 1977-05-31 Colgate-Palmolive Company Antiperspirants formulated with borax
US3934004A (en) * 1973-03-09 1976-01-20 Orren Leonard J Stain resistant anti-perspirant composition
US3981986A (en) * 1973-11-23 1976-09-21 Armour Pharmaceutical Company Zirconium-aluminum-polyol buffered anti-perspirant complexes
US4017599A (en) * 1973-11-23 1977-04-12 Armour Pharmaceutical Company Aluminum-zirconium anti-perspirant systems with salts of amino acids
US4028390A (en) * 1975-03-26 1977-06-07 Armour Pharmaceutical Company Methods of making basic zirconium complexes
US4021536A (en) * 1975-04-18 1977-05-03 Armour Pharmaceutical Company Magnesium-zirconium complexes useful as antiperspirants
US4089942A (en) * 1976-01-29 1978-05-16 L'oreal Deodorant composition and process
US4490354A (en) * 1980-04-11 1984-12-25 American Cyanamid Company Antiperspirant method containing vanadium salts
US4606915A (en) * 1981-04-23 1986-08-19 Bristol-Myers Company Antiperspirant combination containing an aluminum halohydrate and a stannic halide
US4650671A (en) * 1981-07-17 1987-03-17 Claus Riemann & Co. Aps Antiperspirant kit and method for controlling perspiration
US4565693A (en) * 1981-11-09 1986-01-21 Colgate-Palmolive Company Deodorant composition
US5135741A (en) * 1984-04-24 1992-08-04 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Antiperspirant product
US5518714A (en) * 1984-04-24 1996-05-21 Chesebrough-Pond's Usa Co., Division Of Conopco, Inc. Method for inhibiting the dissolution of antiperspirant compounds in alcohols
WO1993007853A1 (en) * 1991-10-23 1993-04-29 Monell Chemical Senses Center Inhibition of odor formation and bacterial growth
US5643559A (en) * 1991-10-30 1997-07-01 Colgate-Palmolive Company Deodorant compositions comprising inhibitors of odor-producing axillary bacterial exoenzymes
US5676937A (en) * 1991-10-30 1997-10-14 Colgate-Palmolive Company Deodorant compositions comprising inhibitors of odor-producing axillary bacterial exoenzymes
US5463098A (en) * 1992-11-16 1995-10-31 Giovanniello; Rocco Clear antiperspirant gel stick and method for making same
US20100173021A1 (en) * 1994-12-21 2010-07-08 Cosmederm Technologies, Inc. Topical Product formulations containing strontium for reducing skin irritation
US8449923B2 (en) 1994-12-21 2013-05-28 Cosmederm Bioscience, Inc. Methods for inhibiting sensory nerves by topically administering strontium-containing compositions to keratinized skin
US20080131386A1 (en) * 1994-12-21 2008-06-05 Cosmederm Technologies, Inc. Topical product formulations containing strontium for reducing skin irritation
US7404967B2 (en) 1994-12-21 2008-07-29 Cosmederm, Inc. Topical product formulations containing strontium for reducing skin irritation
US20030031727A1 (en) * 1994-12-21 2003-02-13 Cosmederm Technologies, Llc Topical product formulations containing strontium for reducing skin irritation
US8147855B2 (en) 1994-12-21 2012-04-03 Cosmederm Bioscience, Inc. Methods for inhibiting sensory responses in the skin such as pain and itch using topical product formulations containing strontium
US20030124202A1 (en) * 1994-12-21 2003-07-03 Hahn Gary S. Formulations and methods for reducing skin irritation
US8815222B2 (en) 2009-12-23 2014-08-26 Colgate—Palmolive Company Anhydrous liquid antiperspirant composition
US8663610B2 (en) 2009-12-23 2014-03-04 Colgate-Palmolive Company Method of making an anhydrous liquid antiperspirant composition
WO2011087702A3 (en) * 2009-12-23 2012-07-05 Colgate-Palmolive Company Aqueous antiperspirant/deodorant composition
US9585825B2 (en) 2009-12-23 2017-03-07 Colgate-Palmolive Company Method of making an anhydrous liquid antiperspirant composition
WO2017117301A1 (en) * 2015-12-30 2017-07-06 Colgate-Palmolive Company Personal care compositions
WO2017117155A1 (en) * 2015-12-30 2017-07-06 Colgate-Palmolive Company Personal care compositions
US10123952B2 (en) 2015-12-30 2018-11-13 Colgate-Palmolive Company Personal care compositions
US10292912B2 (en) 2015-12-30 2019-05-21 Colgate-Palmolive Company Personal care compositions
RU2731096C2 (en) * 2015-12-30 2020-08-28 Колгейт-Палмолив Компани Compositions for personal hygiene
RU2731093C2 (en) * 2015-12-30 2020-08-28 Колгейт-Палмолив Компани Compositions for personal hygiene

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