Tertiary amide terminated polyamides in cosmetics

Details Tertiary amide terminated polyamides in cosmetics Tertiary amide terminated polyamides in cosmetics

2001-12-13

2003-07-15

Zitomer, Fred (Department: 1713)

Drug, bio-affecting and body treating compositions

Live hair or scalp treating compositions

Polymer containing

C424S070100, C424S070110, C424S070170, C528S335000

Reexamination Certificate

active

06592857

ABSTRACT:

BACKGROUND OF THE INVENTION
1. Field of the Invention
This invention generally relates to cosmetics, and more particularly to cosmetics incorporating polyamide resins having tertiary amide termination.
2. Description of the Related Art
In many commercially important compositions, the consistency of the product is critical to its commercial success. One example is personal care products, which generally contain one or more active ingredients within a carrier formulation. While the active ingredient(s) determine the ultimate performance properties of the product, the carrier formulation is equally critical to the commercial success of the product in that it largely determines the consistency of the product. The rheology of the carrier (also referred to as the “base”) largely determines the flow properties of the product, and the flow properties largely determine the manner in which the consumer will apply or use the product.
For example, aluminum chlorohydrate, aluminum-zirconium tetrachlorohydrate, aluminum-zirconium polychlorohydrate complexed with glycine, and aluminum-zirconium complexed with any of trichlorohydrate, octachlorohydrate, and sesquichlorohydrate are metal salts that are commonly used as active ingredients in deodorant and antiperspirant products. Consumers have shown a preference for applying deodorant from a stick form. Thus, the carrier in a stick-form deodorant must be a relatively hard substance, and waxy fatty alcohol such as stearyl alcohol has often been used as the carrier in these products. As another example, the active ingredient in a lipstick is the colorant. A lipstick should not be as hard as a stick deodorant, but of course must maintain its shape when undisturbed at room temperature. A blend of wax and oil is known to provide a consistency that is well-suited as a carrier for a lipstick. As a final example, shampoo desirably has a viscosity greater than water, and when the active ingredient(s) in a shampoo does not have a sufficiently high viscosity, a somewhat viscous carrier material is desirably included in the shampoo formulation.
From the above examples, it is seen that formulators of personal care products depend upon the availability of materials having various Theological properties, in order to formulate a successful personal care product. Materials which have a gel-like character, in that they maintain their shape when undisturbed but flow upon being rubbed, are often desired for personal care products.
Transparent (i.e., clear) carriers are desired by formulators who develop a personal care product wherein colorant is an active ingredient, because a transparent carrier (as opposed to an opaque carrier) will minimally, if at all, interfere with the appearance of the colorant. In recent years, consumers have demonstrated an increasing preference for transparent and colorless personal care products such as deodorants and shampoos. There is thus an increasing demand for transparent materials which can provide the theological properties needed for various personal care products, and particularly which can impart gel-like character to a formulation.
Polyamide resin prepared from polymerized fatty acid and diamine is reported to function as a gellant in formulations developed for personal care products. For example, U.S. Pat. No. 3,148,125 is directed to a clear lipstick carrier composition formed from polyamide resin compounded with a lower aliphatic alcohol and a so-called “polyamide solvent.”Likewise, U.S. Pat. No. 5,500,209 is directed to forming a gel or stick deodorant, where the composition contains polyamide gelling agent and a solvent system including monohydric or polyhydric alcohols. Thus, the prior art recognizes to blend certain polyamides with alcohols, to thereby form a gel.
Pure hydrocarbon is desirably included in personal care formulations because it is transparent and relatively inexpensive. Pure hydrocarbons are also available in a wide variety of viscosities and grades. However, pure hydrocarbon often does not have the Theological properties that are desired in a carrier, e.g., it does not naturally exhibit gel-like character. Furthermore, when hydrocarbon is present in a personal care formulation, alcohol is also typically present when a gel-like consistency is desired for the product. Alcohol can be irritating to skin, and accordingly, in some formulations, is desirably omitted.
Accordingly, there is a need in the art for cosmetic materials that have a gel-like consistency. The present invention provides this and related advantages as described herein.
SUMMARY OF THE INVENTION
In one aspect, the invention provides a cosmetic formulation that includes a tertiary amide terminated polyamide (ATPA) resin of the formula (1):
wherein,
n designates a number of repeating units such that terminal amide groups (ie., the amide groups to which R
1
is directly bonded) constitute from 10% to 50% of the total amide groups of the ATPA;
R
1
at each occurrence is independently selected from a C
1-22
hydrocarbon group;
R
2
at each occurrence is independently selected from a C
2-42
hydrocarbon group;
R
3
at each occurrence is independently selected from an organic group containing at least two carbon atoms in addition to hydrogen atoms, and optionally containing one or more oxygen and nitrogen atoms; and
R
3a
at each occurrence is independently selected from hydrogen, C
1-10
alkyl and a direct bond to R
3
or another R
3a
such that the N atom to which R
3
and R
3a
are both bonded is part of a heterocyclic structure defined in part by R
3a
—N—R
3
.
In another aspect, the invention provides a cosmetic formulation that includes an ATPA resin prepared by a method that includes reacting x equivalents of carboxylic acid from diacid or a reactive equivalent thereof, y equivalents of amine from diamine, and z equivalents of a secondary amine-containing molecule having no reactive functional groups except the secondary amine or a reactive equivalent thereof, where the secondary amine-containing molecule (i.e. monoamine) is substantially the only monofunctional reactant used to form the ATPA resin, and wherein each of x, y and z is greater than 0.
In another aspect, the invention provides a cosmetic composition that includes a low polarity liquid in addition to an ATPA resin as described above.
In another aspect, the invention provides a method for preparing a cosmetic composition, where the method includes combining a low polarity liquid with an ATPA resin as described above, and additional components as needed to prepare the specific cosmetic formulation.
These and other aspects of the present invention will become evident upon reference to the following drawing and detailed description.


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