Perfume compositions – Perfume compositions – With preservative – stabilizer – or fixative
Reexamination Certificate
2002-04-15
2003-06-24
Killos, Paul J. (Department: 1625)
Perfume compositions
Perfume compositions
With preservative, stabilizer, or fixative
C512S003000
Reexamination Certificate
active
06583106
ABSTRACT:
FIELD OF THE INVENTION
The present invention is directed to novel compositions of urethane emollients, solubilizers, clarifiers and emulsifiers derived from monohydric alcohols and having no free isocyanate groups. These urethane emollients are substantially free of terminal hydroxyl groups and are derived from linear, branch-chained or aromatic monohydric alcoholic compounds of synthetic or natural origin. In particular aspects of the present invention, the use of monohydric urethane compounds according to the present invention, in fragrance compositions, will unexpectedly prolong the fragrance of a fragrance composition on the skin.
BACKGROUND OF THE INVENTION
Standard emollients for the cosmetic, toiletry and personal care industries have been esters (monohydric) such as isopropyl myristate, butyl stearate, cetyl octanoate and isostearyl isostearate covering a wide breadth of molecular weights. Monohydric esters have also been manufactured from high molecular weight compounds such as behenic acid and behenyl alcohol which yield a solid ester useful as an emollient for increasing the melting point characteristics of a given formulation. Synthetic spermacetic waxes have been utilized for the past thirty years to replace the natural rare variety. Such products as cetyl palmitate, cetyl myristate and mixed cetyl esters have essentially replaced the use of spermacetic wax.
In the mid-seventies, there was a critical shortage of beeswax, and the synthesis of a synthetic version of this natural wax and emollients derived from this wax was sought. As one solution, the relatively high molecular weight dodecanedicarboxylic acid was esterified with a mixture of cetyl, stearyl and polyoxyethylene glycols to render a product that was found to be a suitable replacement. With the mixture of relatively high molecular weight alcohols and polyethers, the dicarboxylic acid of C
12
yielded a perfectly usable product for skin applications-where natural beeswax had been used for numerous years.
For many years, monohydric alcohol diesters used in the cosmetic and personal care industries have been synthesized from such difunctional carboxylic acids as adipic, sebacic, azeleic, dodecanedicarboxylic acid and dimer acid, as well as anhydrides such as maleic, succinic and phthallic, among others. Based on the molecular weight of the difunctional carboxylic acid and the alcohol used, it was possible for the synthetic organic chemist to obtain a wide range of properties from these compositions, including, for example, dryness, oiliness, spreadability, lubricity, freezing point depression, insect repellency (e.g., dicapryl adipate), melting and slip point modification, emulsion synergism, solvency and color dispersion.
As the molecular weight of the dicarboxylic acid and corresponding alcohol increase, a greater degree of heaviness is imparted to the emollient, along with a higher degree of viscosity. As the degree of unsaturation of the alcohol used increases and becomes more olefinic in character, spreadability is enhanced. For example, diesters derived from oleyl or linoleyl alcohols have a greater degree of spreadability than does a corresponding diester derived from stearyl or isostearyl alcohol.
It is possible to further influence the melting point and indeed the viscosity of a diester through the use of branched rather than linear structures. With the introduction of an ether linkage, the liquidity of a given diester is also enhanced. Diesters made from ethoxylated and/or propoxylated adducts of alcohols have also been used as emollients and emulsifiers.
As a result of molecular weight and structure, diisopropyl adipate has been found to be an extremely dry ester with excellent solvency characteristics. Because of its physical properties, diisopropyl adipate finds use in products ranging from floating bath oils, after shaves, creams, lotions, deodorants, pre-electric shave lotions, to antiperspirants. Diisopropyl adipate has been widely used for numerous years in these applications because of the availability of raw materials and relatively low production cost. Diisostearyl adipate, on the other hand, is a relatively heavy, water white diester with little or no odor that imparts a luster and sheen to the skin and, as a result of its molecular weight and viscosity, has a tendency to linger on the skin. Dicapryl adipate is a diester derived from natural sources (through the cracking of castor oil to yield caprylene, then conversion to the corresponding alcohol) which has been found to exhibit insect repellency and has met with huge success in repellents for use in human and animal products. Diesters derived from dimer acids, such as diisopropyl dimerate and diisostearyl dimerate, in addition to being excellent, long lasting emollients because of their relatively high molecular weight, were shown to add anti-irritation characteristics to given skin formulations.
Typical end-use applications of diesters of dicarboxylic acids in the personal care, cosmetic as well as toiletry industries include: skin care products, eye makeups, body shampoo, stick deodorants, protective skin formulations, lipsticks, lip glosses, pre-electric and after shave lotions, after-bath splashes, shampoos and rinses, presun and sun products, antiperspirants and sunscreens.
OBJECTS OF THE INVENTION
It is an object of the present invention to provide fragrance compositions which exhibit enhanced fragrance values and prolong the fragrance of a composition on the skin of a user.
It is a further object of the present invention to provide urethanes of monohydric alcohols, which, when added to compositions, may function to reduce, counteract and neutralize malodors on the skin or in a closed environment such as a home, a bedroom, a bathroom, or a boat.
These and/or other objects of the invention may be readily gleaned from the description of the invention, which follows.
SUMMARY OF THE INVENTION
The present invention relates to a dimeric urethane compounds derived from monohydric alcohols, generally fatty alcohols, and a diisocyanate according to the following reaction scheme:
wherein R
1
is selected from the group consisting of saturated, unsaturated, aromatic or halogen substituted linear, cyclic, aromatic or branch-chained hydrocarbons and R
2
is a linear, cyclic, aromatic, branch-chained alkyl, aminoalkyl, amino alkanol or alkoxide group ranging from two to 500 carbon atoms, preferably two to 50 carbons, more preferably 6 to 36 carbons, even more preferably from about 6 to 22 carbons, said urethane compound being substantially free of terminal hydroxyl groups.
Compounds according to the present invention exhibit primary utility as emollients, wetting agents, dispersants, lubricants, plasticizers, stabilizers, emulsifiers, clarifying agents, solubilizing agents and adhesion and melting point modifiers in formulations of cosmetic, toiletry and personal care products. The emollient properties of compounds according to the present invention are primarily due to the hydrophobic nature of the fatty alkyl groups, which maintain a desirable moisture balance as it softens and soothes the skin and related mucous membranes.
By proper selection of the diisocyanate and monohydric alcohol, it is possible to obtain a wide variety of properties in the resultant urethane compound, ranging from such characteristics as a glasslike, resinous product suitable as an extremely heavy emollient and replacement for diisostearyl adipate to a solid product such as an arichidyl urethane suitable as a substitute for beeswax in formulations. The monohydric alcohols reacted to produce the compounds with a diisocyanate group according to the present invention may be synthetically or naturally derived.
One of the more innovative properties of compounds according to the present invention is the stability of the dimeric urethane of the monohydric alcohols over a wide pH range and temperature. Under conditions causing the prior art diesters of corresponding alcohols to readily decompose, their urethane counterparts will remain relatively stable. Consequently, the
Alzo International Inc.
Coleman Henry
Coleman Sudol Sapone P.C.
Killos Paul J.
LandOfFree
Monohydric alcohol derived urethanes and their use in... does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Monohydric alcohol derived urethanes and their use in..., we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Monohydric alcohol derived urethanes and their use in... will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-3087407