Antiperspirant active compositions and manufacture thereof

Abstract

An antiperspirant active composition comprising an aluminum salt, the aluminum salt (i) having an aluminum to chloride molar ratio of 0.3:1 to 3:1; and (ii) having a species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR that is present in a relative abundance on a .sup.27Al NMR spectrograph that is greater than any other polyhydroxyoxoaluminum cation detectable by .sup.27Al NMR. Also, disclosed are methods of making the antiperspirant active.

Claims

1. A method of making an antiperspirant active composition comprising: I) heating an aqueous solution containing i) a first aluminum salt containing an Al.sub.30 polyhydroxyoxoaluminum cation and having an aluminum to chloride molar ratio of 0.3:1 to 3:1, ii) an inorganic salt, and iii) a buffer, wherein the heating forms a fourth aluminum salt, and is one of a) at a temperature of 100 C. to 250 C. in an isochoric reactor or under hydrothermal reaction for a time sufficient to form a species of polyhydroxyoxoaluminum cation detectable at 76 ppm by NMR; or b) at 100 C. at reflux for about 10 days or greater.

2. A method of making an antiperspirant active composition comprising: I) heating an aqueous solution containing a first aluminum salt having an aluminum to chloride molar ratio of 0.3:1 to 3:1 and a buffer, at a temperature of 50 C. to 100 C. for a period of time of 1 hour to 6 hours to obtain a first aluminum salt solution; II) adding to the first aluminum salt solution an aqueous solution of an inorganic base to obtain a second pH adjusted aluminum sat solution having an OH:Al molar ratio of at most 2.6:1; III) heating the second pH adjusted aluminum salt solution at a temperature of 50 C. to 100 C. for a period of time of at least 6 hours to obtain a third aluminum salt solution containing an Al.sub.30 polyhydroxyoxoaluminum cation; IV) heating the third aluminum salt solution to form a fourth aluminum salt at one of a) at a temperature of 100 C. to 250 C. in an isochoric reactor or under hydrothermal reaction for a time sufficient to form a species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR; or b) at 100 C. at reflux for about 10 days or greater; and V) optionally adding an aqueous solution containing a zirconium compound to the second pH adjusted aluminum salt solution to thereby obtain a second pH adjusted aluminum-zirconium salt solution having a molar ratio of aluminum to zirconium of 5:1 to 10:1.

3. The method of claim 1, wherein the inorganic salt is at least one chloride salt chosen from calcium chloride, strontium chloride, barium chloride, and yttrium chloride.

4. The method of claim 1, wherein the buffer is at least one of an amino acid, betaine, quat, and glycine, and a molar ratio of buffer to aluminum is at least 0.1:1.

5. The method of claim 2, wherein the buffer is at least one of an amino acid, betaine, quat, and glycine, and a molar ratio of buffer to aluminum is at least 0.1:1.

6. The method of claim 1, wherein the inorganic salt is calcium chloride and the buffer is glycine.

7. The method of claim 1, wherein heating in the isochoric reactor or under hydrothermal reaction is one of i) at 100 C. for about 5 days, ii) at 120 C. for about 12 hours, or iii) at 150 C. for about 20 minutes.

8. The method of claim 2, wherein heating in the isochoric reactor or under hydrothermal reaction is one of i) at 100 C. for about 5 days, ii) at 120 C. for about 12 hours, or iii) at 150 C. for about 20 minutes.

9. The method of claim 1, wherein the fourth aluminum salt exhibits a SEC chromatogram having a SEC Peak 4 area of at least 90% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram.

10. The method of claim 2, wherein the fourth aluminum salt exhibits a SEC chromatogram having a SEC Peak 4 area of at least 90% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram.

11. The method of claim 2, wherein the inorganic base includes at least one member chosen from calcium hydroxide, strontium hydroxide, barium hydroxide, calcium oxide, strontium oxide, barium oxide, calcium carbonate, barium carbonate, strontium carbonate, yttrium hydroxide, yttrium oxide, and yttrium carbonate.

12. The method of claim 11, wherein the inorganic base is calcium hydroxide.

13. The method of claim 2, wherein the second pH adjusted aluminum salt solution has an OH to Al molar ratio of 2:1 to 2.5:1.

14. The method of claim 2, wherein the first aluminum salt is an aluminum chloride compound chosen from aluminum trichloride, aluminum chlorohexahydrate, and aluminum dichlorohydrate.

15. The method of claim 2, wherein the composition further comprises zirconium and step V) is present in the method.

16. The method of claim 15, wherein the zirconium compound is at least one of ZrOCl.sub.2.8H.sub.2O and Oxo-Hexameric Zirconium-Octaamino Acid.

17. The method of claim 1, wherein the .sup.27Al NMR spectrum has a species distribution including at most 5% Al.sub.13 polyhydroxyoxoaluminum cation in the species detectable by .sup.27Al NMR within the fourth aluminum salt.

18. The method of claim 2, wherein the .sup.27Al NMR spectrum has a species distribution including at most 5% Al.sub.13 polyhydroxyoxoaluminum cation in the species detectable by .sup.27Al NMR within the fourth aluminum salt.

19. The method of claim 1, wherein the fourth aluminum salt has a SEC Peak 4 area of at least 95% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram.

20. The method of claim 2, wherein the fourth aluminum salt has a SEC Peak 4 area of at least 95% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram.

21. The method of claim 1, wherein the fourth aluminum salt has a SEC Peak 3 area of less than 5% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram.

22. The method of claim 2, wherein the fourth aluminum salt has a SEC Peak 3 area of less than 5% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram.

23. The method of claim 2, wherein the third aluminum salt has a SEC Peak 5 area of less than 5% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram.

24. The method according to claim 2, wherein in step III) the period of time is at least 12 hours.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

(1) FIG. 1 is a .sup.27Al NMR spectrograph of material 1 from the examples before heating.

(2) FIG. 2 is a .sup.27Al NMR spectrograph of material 1 from the examples after heating.

(3) FIG. 3 is a .sup.27Al NMR spectrograph of material 2 from the examples before heating.

(4) FIG. 4 is a .sup.27Al NMR spectrograph of material 2 from the examples after heating.

BRIEF SUMMARY OF THE INVENTION

(5) The present invention is based on modifying the composition from the inventors' earlier work, which was filed as PCT/US2010/55030 on 2 Nov. 2011. It has been discovered that the Al.sub.30 in antiperspirant salt can be converted to a species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR. This species also will elute at Peak 4 on a SEC chromatogram.

(6) The previous material can be aged for a sufficient time at sufficient temperature to convert the Al.sub.30. In one embodiment, the material can be aged at about 100 C. for a sufficient period of time, such as about 10 days or greater, or about 30 days or greater. In another embodiment, the material can aged by supercritical heating in an isochoric reaction vessel or under hydrothermal reaction at sufficient temperature and time, such as at 100 C. for 5 days. In another embodiment, the material can be aged at ambient conditions (such as 15 C. to 60 C.) for a period of time of several months, such as at least 6 months, to more than one year.

(7) The present invention accordingly provides antiperspirant active composition comprising an aluminum salt, the aluminum salt (i) having an aluminum to chloride molar ratio of 0.3:1 to 3:1; and (ii) having a species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR that is present in a relative abundance on a .sup.27Al NMR spectrograph that is greater than any other polyhydroxyoxoaluminum cation detectable by .sup.27Al NMR.

(8) In other embodiments, the species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR is present in an amount that is a majority of a total amount of all species of polyhydroxyoxoaluminum cations detectable by .sup.27Al NMR. In other embodiments, the species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR is present in an amount that is at least 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 97, 98, 99, 99.5, 99.9, 99.99, or 99.999% of a total amount of all species of polyhydroxyoxoaluminum cations detectable by .sup.27Al NMR.

(9) Optionally, the aluminum salt exhibits a SEC chromatogram having a SEC Peak 4 area of at least 90% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram.

(10) In this specification, the SEC chromatogram is measured using an aqueous solution of the aluminum salt.

(11) In some embodiments, the .sup.27Al NMR spectrum has a species distribution including at most 5% Al.sub.13 polyhydroxyoxoaluminum cation in the species detectable by .sup.27Al NMR within the aluminum salt. In some embodiments, the .sup.27Al NMR spectrum has a species distribution including no Al.sub.13 polyhydroxyoxoaluminum cation in the species detectable by .sup.27Al NMR within the aluminum salt. In some embodiments, the .sup.27Al NMR spectrum has a species distribution including at most 5% Al.sub.m, Al.sub.m comprising an aluminum- and chloride-containing monomer, in the species detectable by .sup.27Al NMR within the aluminum salt.

(12) In some embodiments, the aluminum salt has an OH to Al ratio of at most 2.6:1, and in other embodiments 2:1 to 2.6:1, optionally an OH to Al ratio of 2:1 to 2.5:1, or 2.3:1 to 2.5:1.

(13) The antiperspirant active composition may optionally further comprise a buffer, wherein a molar ratio of buffer to aluminum is at least 0.1:1. In other embodiments, the molar ratio is 0.1:1 to 3:1. The buffer may be at least one buffer chosen from an amino acid, betaine, and quat. Optionally, the buffer is an amino acid and a molar ratio of amino acid to aluminum is at least 0.1:1. In some embodiments, the amino acid is glycine.

(14) In some embodiments, the composition has a SEC Peak 4 area of at least 95% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram. In some embodiments, the composition has a SEC Peak 3 area of less than 5% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram, and most preferably has no SEC Peak 3 area in the SEC chromatogram.

(15) In some embodiments, the composition has a SEC Peak 5 area of less than 5% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram, and most preferably has no SEC Peak 5 area in the SEC chromatogram.

(16) In some embodiments, the antiperspirant active composition has a SEC Peak 4 area of 95 to 100%, no SEC Peak 3 area, and a SEC Peak 5 area of from 0 to 5% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram.

(17) The antiperspirant active composition may further comprise zirconium, and optionally a molar ratio of aluminum to zirconium is 5:1 to 10:1.

(18) A method of making an antiperspirant active composition comprising: I) heating an aqueous solution containing i) a first aluminum salt containing an Al.sub.30 polyhydroxyoxoaluminum cation and having an aluminum to chloride molar ratio of 0.3:1 to 3:1, ii) an inorganic salt, and iii) a buffer, wherein the buffer is at least one of an amino acid, betaine, and quat and a molar ratio of buffer to aluminum is at least 0.1:1, wherein the heating is one of a) at a temperature of 100 C. to 250 C. in an isochoric reactor or under hydrothermal reaction for a time sufficient to form a species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR; or b) at 100 C. at reflux for about 10 days or greater, optionally about 30 days or greater to form a fourth aluminum salt.

(19) The present invention also provides a method of making an antiperspirant active composition comprising: I) heating an aqueous solution containing a first aluminum salt having an aluminum to chloride molar ratio of 0.3:1 to 3:1 and a buffer, wherein the buffer is at least one of an amino acid, betaine, and quat and a molar ratio of buffer to aluminum is at least 0.1:1, at a temperature of 50 C. to 100 C. for a period of time of 1 hour to 6 hours to obtain a first aluminum salt solution; II) adding to the first aluminum salt solution an aqueous solution of an inorganic base to obtain a second pH adjusted aluminum salt solution having an OH:Al molar ratio of at most 2.6:1, or optionally 2:1 to 2.6:1, and a pH of 2 to 5; III) heating the second pH adjusted aluminum salt solution at a temperature of 50C to 100 C. for a period of time of at least 6 hours to obtain a third aluminum salt solution containing an Al.sub.30 polyhydroxyoxoaluminum cation; IV) heating the third aluminum salt solution at one of a) at a temperature of 100 C. to 250 C. in an isochoric reactor or under hydrothermal reaction for a time sufficient to form a species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR; or b) at 100 C. at reflux for about 10 days or greater, optionally about 30 days or greater; to form a fourth aluminum salt; and V) optionally adding an aqueous solution containing a zirconium compound to the second pH adjusted aluminum salt solution to thereby obtain a second pH adjusted aluminum-zirconium salt solution having a molar ratio of aluminum to zirconium of 5:1 to 10:1.

(20) The present invention also provides a method of making a polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR comprising storing an aqueous solution containing i) the aluminum salt containing an Al.sub.30 polyhydroxyoxoaluminum cation and having an aluminum to chloride molar ratio of 0.3:1 to 3:1, ii) an inorganic salt, and iii) a buffer, wherein the buffer is at least one of an amino acid, betaine, and quat, and a molar ratio of buffer to aluminum is at least 0.1:1 at a temperature of 15 C. to 60 C. for a period of time until the polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR that is present in a relative abundance on a .sup.27Al NMR spectrograph that is greater than any other polyhydroxyoxoaluminum cation detectable by .sup.27Al NMR.

(21) In some embodiments, the buffer is glycine. In some embodiments, the inorganic salt is at least one chloride salt chosen from calcium chloride, magnesium chloride, strontium chloride, barium chloride, stannous chloride, and yttrium chloride. In some embodiments, the inorganic base includes at least one member chosen from calcium hydroxide, magnesium hydroxide, strontium hydroxide, barium hydroxide, stannous hydroxide, yttrium hydroxide, calcium oxide, magnesium oxide, strontium oxide, barium oxide, stannous oxide, yttrium oxide, calcium carbonate, magnesium carbonate, strontium carbonate, barium carbonate, stannous carbonate, and yttrium carbonate. Typically, the inorganic base is calcium hydroxide. In some embodiments, the aluminum salt solution has an OH to Al molar ratio of 2.0:1 to 2.5:1 or 2.1:1 to 2.5:1.

(22) In some embodiments, the first aluminum salt is an aluminum chloride compound chosen from aluminum trichloride, aluminum chlorohexahydrate, aluminum dichlorohydrate, and aluminum monochlorohydrate. Optionally, the composition further comprises zirconium. The zirconium compound may be ZrOCl.sub.2.8H.sub.2O or Oxo-Hexameric Zirconium-Octaamino Acid.

(23) In some embodiments, the fourth aluminum salt has a SEC Peak 4 area of at least 95% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram. In some embodiments, the fourth aluminum salt has a SEC Peak 3 area of less than 5% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram, and preferably the fourth aluminum salt has no SEC Peak 3 area in the SEC chromatogram. In some embodiments, the fourth aluminum salt has a SEC Peak 5 area of less than 5% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram.

(24) In some embodiments, in step Ill) the period of time is at least 12 hours, or in some embodiments at least 24 hours.

(25) The present invention further provides the use of a heating step to convert Al.sub.30 polyhydroxyoxoaluminum cations in the species detectable by .sup.27Al NMR within an aqueous aluminum salt solution into a species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR, the aqueous aluminum salt solution i) having an aluminum to chloride molar ratio of 0.3:1 to 3:1; ii) an inorganic salt, and iii) a buffer, wherein the buffer is at least one of an amino acid, betaine, and quat, and a molar ratio of buffer to aluminum is at least 0.1:1; an OH:Al molar ratio of at most 2.6:1, or optionally, 2:1 to 2.6:1; and the heating step is one of: a) at a temperature of 100 C. to 250 C. in an isochoric reactor or under hydrothermal reaction for a time sufficient to form a species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR; or b) at 100 C. at reflux for about 10 days or greater, optionally about 30 days or greater.

(26) In some embodiments, the heating step converts all the Al.sub.13 polyhydroxyoxoaluminum cation species present in the aqueous aluminum salt solution into the Al.sub.30 polyhydroxyoxoaluminum cation species. In some embodiments, the heating step reduces a SEC Peak 5 area in the SEC chromatogram. Optionally, the period of time is at least 12 hours or, in other embodiments, at least 24 hours. In some embodiments, the buffer is glycine.

(27) In some embodiments, the OH:Al molar ratio has been achieved by adding to the aqueous aluminum salt solution an inorganic base including at least one member chosen from calcium hydroxide, magnesium hydroxide, strontium hydroxide, barium hydroxide, stannous hydroxide, yttrium hydroxide, calcium oxide, magnesium oxide, strontium oxide, barium oxide, stannous oxide, yttrium oxide, calcium carbonate, magnesium carbonate, strontium carbonate, barium carbonate, stannous carbonate, and yttrium carbonate. Typically, the inorganic base is calcium hydroxide. Optionally, the OH to Al molar ratio is 2.0:1 to 2.5:1 or 2.1:1 to 2.5:1.

(28) In some embodiments, the aluminum salt is an aluminum chloride compound chosen from aluminum trichloride, acidified aluminum chlorohexahydrate, aluminum dichlorohydrate, and aluminum monochlorohydrate.

(29) In some embodiments, the heating increases the Al.sub.30 polyhydroxyoxoaluminum cation species in the .sup.27Al NMR spectrum from at least 90% to at least 95% of the species detectable by .sup.27Al NMR within the aluminum salt.

(30) In some embodiments, after the heating step the aluminum salt has a SEC Peak 4 area of at least 95% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram. In some embodiments, after the heating step the aluminum salt has a SEC Peak 3 area of less than 5% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram, and preferably has no SEC Peak 3 area in the SEC chromatogram. In some embodiments, after the heating step the aluminum salt has a SEC Peak 5 area of less than 5% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram.

(31) The present invention further provides an antiperspirant active composition including an aluminum salt produced by the method of the invention or the use of the invention.

DETAILED DESCRIPTION OF THE INVENTION

(32) In this specification, the use of .sup.27Al NMR data is not quantitative but considers only NMR-visible Al species and in particular resonances at 0 ppm, 62.5 ppm, 70 ppm, and 76 ppm. Octahedrally coordinated nuclei are detected via .sup.27Al NMR. The Al monomer resonance at 0 ppm is octahedrally coordinated. Octahedral bands in Al.sub.13 and Al.sub.30 are broad and overlapping, so they're not useful when identifying Al species. The breadth of octahedral bands in Al.sub.13 & Al.sub.30 is due to structural and environmental variation. Because the Al nuclei in monomeric Al exist structurally in one form, the signal is narrow, and easily identified. Tetrahedrally coordinated nuclei in Al.sub.13 and Al.sub.30 also feature minimal variation, which leads to narrow, identifiable NMR signals. .sup.27Al NMR data do not indicate the amount of undetected Al embodied in NMR-invisible species.

(33) When calculating the relative amounts of Al embodied in compositions containing .sup.27Al NMR visible species that have known structures, such as Al.sub.13 and Al.sub.30 polyhydroxyoxoaluminum cations, the tetrahedral resonance peak of the aluminum is integrated and multiplied by a scaling factor to account for other octahedrally coordinated Al present in the structure. In the Al.sub.13 polyhydroxyoxoaluminum cation, there is one tetrahedral resonance peak in the structure. In the Al.sub.30 polyhydroxyoxoaluminum cation, there are two tetrahedral resonance peaks in the structure. To convert, the resonance from the Al.sub.13 polyhydroxyoxoaluminum cation is multiplied by 13, whereas the resonance from the Al.sub.30 polyhydroxyoxoaluminum cation is multiplied by 15. When the structure of the 76 ppm material is identified, a scaling factor can be determined.

(34) For now, the amounts of each species of polybydroxyoxoaluminum cation in a composition will be characterized by the relative abundance of tetrahedral aluminum resonance peaks on a .sup.27Al NMR spectrograph. This means that the area of the tetrahedral aluminum resonance peak for a polyhydroxyoxoaluminum cation is compared to the area of the tetrahedral aluminum resonance peaks for other polyhydroxyoxoaluminum cations. The .sup.27Al NMR spectrograph should be collected at sufficient enough field strength so that all relevant signals can be integrated. One procedure for operating a .sup.27Al NMR is described in the examples below. In the current state of the art, the resonance frequency is at least 104.2 Mhz to provide a sufficient field strength.

(35) The present invention is directed to antiperspirant active composition comprising an aluminum salt, the aluminum salt (i) having an aluminum to chloride molar ratio of 0.3:1 to 3:1; and (ii) having a species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR that is present in a relative abundance on a .sup.27Al NMR spectrograph that is greater than any other polyhydroxyoxoaluminum cation detectable by .sup.27Al NMR.

(36) In certain embodiments, the species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR is present in an amount that is at least 50, 55, 60, 65, 70, 75, 80, 85, 90, 95, 96, 97, 98, 99, 99.5, 99.9, 99.99, or 99.999% of a total amount of all species of polyhydroxyoxoaluminum cation detectable by .sup.27Al NMR. In other embodiments, the species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR is present in an amount that is a majority of a total amount of all species of polyhydroxyoxoaluminum cations detectable by .sup.27Al NMR.

(37) The species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR can be made by heating an aqueous solution containing i) a first aluminum salt containing an A.sub.30 polyhydroxyoxoaluminum cation and having an aluminum to chloride molar ratio of 0.3:1 to 3:1, ii) an inorganic salt, and iii) a buffer, wherein the buffer is at least one of an amino acid, betaine, and quat, and a molar ratio of buffer to aluminum is at least 0.1:1, wherein the heating is one of a) at a temperature of 100 C. to 250 C. in an isochoric reactor or under hydrothermal reaction for a time sufficient to form a species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR; or b) at 100 C. at reflux for about 10 days or greater, optionally about 30 days or greater.

(38) The reaction in the isochoric reactor is conducted at 100 C. to 250 C. As the temperature increases, the time need to convert Al.sub.30 polyhydroxyoxoaluminum cation to the polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR decreases. Below are some examples of temperature and time: i) at 100 C. for about 5 days, ii) at 120 C. for about 12 hours, or iii) at 150 C. for about 20 minutes.

(39) The inorganic salt and buffer help to stabilize the species of polyhydroxyoxoaluminum cation detectable at 76 ppm by .sup.27Al NMR. In certain embodiments, the inorganic salt is at least one chloride salt chosen from calcium chloride, strontium chloride, barium chloride, magnesium chloride, stannous chloride, and yttrium chloride. In one embodiment, the salt is calcium chloride. In certain embodiments, the buffer is glycine. In certain embodiments, the inorganic salt is calcium chloride and the buffer is glycine.

(40) The present invention can provide an antiperspirant active composition having a high SEC peak 4 in aqueous solution. The composition is obtained by a stepwise procedure to neutralize aluminum chloride in a solution (optionally buffered) using inorganic bases. In some embodiments, the antiperspirant active compositions obtained by this stepwise procedure include aluminum salts having an aluminum to chloride molar ratio of 0.3:1 to 3:1, optionally, the aluminum salt exhibits a SEC chromatogram having a SEC Peak 4 area of at least 90% of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram in aqueous solution. The composition may optionally include zirconium.

(41) The description below describes methods of obtaining an A.sub.30 polyhydroxyoxoaluminum cation containing composition.

(42) The Al.sub.30 containing compositions may be made in a variety of ways involving a stepwise procedure to neutralize aluminum chloride in solution (optionally buffered) using inorganic basic salts. The procedure generally includes the step of heating an aqueous solution containing an aluminum chloride compound (optionally with a buffer agent) at a temperature of 50 C. to 100 C. optionally 50 C. to 95 C., for a period of time of 1 hour to 6 hours. The heating may be under stirring, such as vigorous stirring, or under reflux. In one such embodiment, an aqueous solution containing an aluminum chloride compound and a buffer agent is heated at a temperature of 75 C. to 95 C. to reflux for a period of time of 2 hours to 4 hours. In one embodiment, the temperature is 95 C. under vigorous stirring for a period of time of 2.5 hours.

(43) To adjust the pH of the aluminum salt solution, an aqueous solution of an inorganic base is added to the heated solution to thereby obtain a pH adjusted aluminum salt solution having a hydroxide to aluminum molar ratio of 1:1 to 4:1, and a pH of 2 to 5. In one such embodiment, the hydroxide to aluminum molar ratio of 2:1 to 3:1. In another such embodiment, the hydroxide to aluminum molar ratio is 2.1:1 to 2.6:1.

(44) In one embodiment, the inorganic base can be at least one base chosen from metal hydroxides, calcium hydroxide, magnesium hydroxide, strontium hydroxide, barium hydroxide, stannous hydroxide, yttrium hydroxide, calcium oxide, magnesium oxide, strontium oxide, barium oxide, stannous oxide, yttrium oxide, calcium carbonate, magnesium carbonate, strontium carbonate, barium carbonate, stannous carbonate, and yttrium carbonate.

(45) Optionally, a buffer can be included. Buffers that can be used can be chosen from amino acids, such as glycine, and betaine, such as betaine monohydrate, or quats. The buffer to aluminum molar ratio in certain embodiments can be at least 0.1:1, or 0.1:1 to 3:1. In another embodiment, the buffer to aluminum molar ratio is 0.1:1 to 2:1.

(46) In one embodiment, the inorganic base is calcium hydroxide. In one such embodiment, the addition of calcium hydroxide provides an aqueous solution having a Ca(OH).sub.2:glycine molar ratio of at least 0.1:1.

(47) When a buffer is absent, significant Peak 3 species in the SEC chromatogram begin to form when the total Al concentration is above 0.2M. When a buffer is present, the total Al concentration can reach up to 2.5M while maintaining a predominant Peak 4 in the SEC chromatogram. In one embodiment, an aqueous aluminum chloride salt solution is buffered with glycine and held at 50 C. to 95 C. under vigorous stirring for a period time of 1 to 6 hours. To the heated solution, an aqueous solution of an inorganic base is added dropwise over a period of time of 1 to 3 hours while maintaining the aluminum-glycine solution at 50 C. to 95 C. under vigorous stirring. In one such embodiment, the solution has a glycine to aluminum molar ratio of 1.5. In another such embodiment, the solution has a glycine to aluminum molar ratio of 0.5.

(48) In some embodiments, a zirconium salt may also be added to the pH adjusted aluminum salt solution. In one other such embodiment, the molar ratio of Al:Zr is 5:1 to 10:1. The zirconium salt may be simple Zr salts: ZrOCl.sub.2.8H.sub.2O or Oxo-Hexameric Zirconium-Octaamino Acid. In one such embodiment, the molar ratio of Al:Zr is 8. In another such embodiment, the molar ratio of Al:Zr is 7. In one other such embodiment, the molar ratio of Al:Zr is 9.

(49) For the above methods, the aluminum chloride salt and inorganic base may be obtained from a variety of sources. In one embodiment, the aluminum chloride salt includes aluminum trichloride, acidified aluminum chlorohexahydrate, aluminum dichlorohydrate, and aluminum monochlorohydrate. In one such embodiment, the aluminum chloride salt is aluminum chlorohexahydrate.

(50) The present invention provides for aluminum antiperspirant active compositions and/or aluminum-zirconium antiperspirant active compositions having high levels of low molecular weight Al and Zr species. The high levels of low molecular weight Al and Zr species is reflected in a SEC trace that has an intense Peak 4 and low Peaks 1, 2, 3 and 5. The polymerization of the antiperspirant actives in aqueous solutions and the correspondent gelation process were followed by monitoring the molecular weight profile of the polyoxohalides in time by SEC. The relative retention time (Kd) for each of these peaks varies depending on the experimental conditions, but the peaks remain relative to each other. The SEC data for the examples was obtained using an SEC chromatogram using the following parameters: Waters600 analytical pump and controller, Rheodyne 77251 injector, Protein-Pak 125 (Waters) column, Waters 2414 Refractive Index Detector. 5.56 mM nitric acid mobile phase, 0.50 ml/min flow rate, 2.0 microliter injection volume. Data was analyzed using Waters Empower software (Waters Corporation, Milford, Mass.). The concentration of the antiperspirant in aqueous solution does not affect the retention time in the machine.

(51) The design of modern antiperspirant (AP) salts aims at actives with high levels of low molecular weight Al and Zr species, which is reflected in a SEC trace that has intense Peak 4 and low Peaks 1, 2, and 3, and optionally low Peak 5. Throughout the present study, the levels of the species corresponding to these peaks are estimated based on the following ratios (or percentages):

(52) $f_{\mathrm{Pi}}=\frac{\mathrm{Pi}}{.Math.\mathrm{Pj}}i=1,2,3,4,5;j=2,3,4,5$
where f.sub.Pi is the fraction of peak i, and Pi or Pj are the intensity of peaks Pi or Pj, respectively. The amount of low molecular weight Al species will be correlated with the fraction, f.sub.P4, or percentage, f.sub.P4100, of SEC-Peak 4. In brief, a preferred antiperspirant salt would have a very low f.sub.P1, f.sub.P2, f.sub.P3, and/or f.sub.P5, and a high f.sub.P4.

(53) In certain embodiments, the ratio of Peak 4 to Peak 3 is at least 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 25, 30, 35, 40, 45, 50, 60, 70, 80, 90, 100, or any number up to infinity. Preferably, Peak 3 is so low as to be undetectable.

(54) In one embodiment, an aluminum salt and/or aluminum-zirconium salt, in aqueous solution, exhibit a SEC profile wherein the SEC Peak 4 to Peak 3 intensity ratio is even as high as infinity, because the Peak 3 is undetectable. In some embodiments, the percentage of SEC Peak 4 of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram is: at least at least 90%; at least 95%, or 95 to 100%. In another such embodiment, the SEC Peak 4 area is 100%.

(55) In another embodiment, the aluminum salt and/or the aluminum-zirconium salt, in aqueous solution, exhibits a SEC profile which exhibits low percentage of SEC Peak 3. In such embodiments, the composition has the percentage of SEC Peak 3 area of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram is: less than 5%; less than 2%; less than 1%; less than 0.9%; less than 0.8%; less than 0.7%; less than 0.6%; of less than 0.5%; less than 0.4%; less than 0.3%; less than 0.2%; or less than 0.1%. In another such embodiment, the composition has no SEC Peak 3 area.

(56) In another embodiment, the aluminum salt and/or the aluminum-zirconium salt, in aqueous solution, exhibits a SEC profile which exhibits low percentages of SEC Peak 5. In such embodiments, the percentage of SEC Peak 5 area of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram is: less than 5%; or less than 1%. In another such embodiment, the composition has no SEC Peak 5 area.

(57) In other embodiments, the aluminum salt and/or the aluminum-zirconium salt, in aqueous solution, exhibits a SEC profile which exhibits a low percentage of SEC Peak 1 and a low percentage of SEC Peak 2. In such embodiments, the percentage of SEC Peak 1 area of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram is less than 5%; less than 2%; or less than 1%, or the salt has no SEC Peak 1 area. In other embodiments, the percentage of SEC Peak 2 area of a total area of Peaks 1, 2, 3, 4 and 5 in the SEC chromatogram is less than 5%; less than 2% or less than 1%; or the salt has no SEC Peak 2 area. Preferably, the salt has no Peak 1 area and no Peak 2 area. More preferably, the salt has no Peak 1 area, no Peak 2 area and no Peak 3 area. Yet more preferably, the salt has no Peak 1 area, no Peak 2 area, no Peak 3 area and no Peak 5 area.

(58) The aluminum antiperspirant active compositions and/or aluminum-zirconium antiperspirant active compositions may be used in a variety of antiperspirant products. If the product is used as a solid powder, the size of the particles of antiperspirant active of the invention can be any desired size, and may include conventional sizes such as in the range of 2 to 100 microns, with selected grades having an average particle size of 30-40 microns; finer sized grades having an average particle size distribution of 2-10 microns with an average size of 7 microns as made by a suitable dry-grinding method; and micronized grades having an average particle size of less than or equal to 2 microns, or less than or equal to 1.5 microns.

(59) The compositions of this invention may be used to formulate antiperspirants having improved efficacy. Such antiperspirants include solids such as sticks and creams (creams sometimes being included in the term soft solid), gels, liquids (such as are suitable for roll-on products), and aerosols. The forms of these products may be suspensions or emulsions. These antiperspirant actives can be used as the antiperspirant active in any antiperspirant composition. Examples of formulations can be found in WO2009/076591.

(60) The present invention is exemplified by the following non-limiting Examples.

EXAMPLES

(61) Two materials prepared in accordance with PCT/US2010/55030 are provided. The materials are aqueous systems that contain the glycine buffer and the calcium chloride byproduct of the manufacturing process.

(62) The raw integration values for .sup.27Al NMR spectroscopy peaks for these materials are listed below in Table 1, and Table 2 shows the relative abundance. The materials are analyzed by taking a 1 M solution and diluting in a 1:4 ratio using D.sub.2O. The final Al concentration for all samples is 0.25M. The samples are analyzed at a .sup.27Al resonance frequency of 104.2 MHz at 90 C. A coaxial insert containing NaAlO.sub.2 is included to provide a reference resonance peak at 80 ppm. The instrument collects 1500 transients, with a pulse width of 6.4 s and a delay time of 2 seconds. The data for the relevant peaks are shown in the tables below. The full spectrographs can be seen in FIGS. 1 to 4.

(63) Materials 1 is held at reflux for 30 days at 100 C. Material 2 is subjected to 100 C. for 5 days in an isochoric reaction vessel. For comparative purposes, the following discussion relates only with the relative integrations instead of raw data.

(64) For Material 1, the Al.sub.30 signal (encompassing 96.10% of the total visible tetrahedral Al) is converted to a signal at 76 ppm (97.76% Td Al). Also, the amount of Al.sub.13 is reduced from 3.90% to 2.24%.

(65) For Material 2, the Al.sub.30 signal at 70 ppm (encompassing 98.44% of the total visible tetrahedral Al) is converted to a signal at 76 ppm (99.37% Td Al). Also, the amount of Al.sub.13 is reduced from 1.56% to 0.63%.

(66) TABLE-US-00001 TABLE 1 Total Visible Material 76 ppm 70 ppm 63 ppm T.sub.d Al Material 1 untreated None detected 906.11 36.75 942.86 Material 1 treated 1054.37 None detected 24.15 1078.52 Material 2 untreated None detected 1585.97 25.09 1611.06 Material 2 Treated 1453.69 None detected 9.20 1462.89

(67) TABLE-US-00002 TABLE 2 Relative Abundance % Material 76 ppm 70 ppm 63 ppm Material 1 untreated 0 96.10 3.90 Material 1 treated 97.76 0 2.24 Material 2 untreated 0 98.44 1.56 Material 2 Treated 99.37 0 0.63

(68) As used throughout, ranges are used as shorthand for describing each and every value that is within the range. Any value within the range can be selected as the terminus of the range. In addition, all references cited herein are hereby incorporated by referenced in their entireties. In the event of a conflict in a definition in the present disclosure and that of a cited reference, the present disclosure controls.

(69) Unless otherwise specified, all percentages and amounts expressed herein and elsewhere in the specification should be understood to refer to percentages by weight. The amounts given are based on the active weight of the material.