Classifications

• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K8/00—Cosmetics or similar toiletry preparations
  • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
  • A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
  • A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
  • A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
  • A61K8/8182—Copolymers of vinyl-pyrrolidones. Compositions of derivatives of such polymers
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
  • A61Q5/00—Preparations for care of the hair
  • A61Q5/12—Preparations containing hair conditioners

Definitions

• This invention relates to a process for making substantially homogeneous terpolymers of vinyl pyrrolidone, a quaternary amino monomer and a hydrophobic monomer, for use in hair care applications.
• These synthetic polymers generally are made by a "one-pot" polymerization process in which selected amounts of the several monomers are reacted together.
• the composition of the thus-formed polymer is considered as being the same as the composition of the charged monomers.
• such conventional non-homogeneous polymerization processes can provide only a mixture of polymers of various compositions, and, additionally, an indeterminate amount of homopolymers and undesired copolymers.
• Another object of this invention is to provide a clear, aqueous solution of substantially homogeneous terpoly ers of vinyl pyrrolidone (VP) , 3-methacrylamido- propyl trimethylammonium chloride (MAPTAC) , and RMA where R is C -C 32 , and MA is methacrylate, preferably octadecyl methacrylate (ODMA) , in a compositional range, by weight, of 55-99% VP, 0.5-49% MAPTAC and 0.5-49% ODMA.
• VP vinyl pyrrolidone
• MATAC 3-methacrylamido- propyl trimethylammonium chloride
• RMA where R is C -C 32
• MA is methacrylate, preferably octadecyl methacrylate (ODMA) , in a compositional range, by weight, of 55-99% VP, 0.5-49% MAPTAC and 0.5-49% ODMA.
• Still another object herein is to provide clear, aqueous solutions of substantially homogeneous terpolymers of VP, MAPTAC and RMA in a predetermined compositional range and at a selected solids level, which, upon formulation into hair styling and conditioning compositions, will provide enhanced water solubility, and improved fixative, conditioning, and hair holding properties for the user.
• a homogeneous polymerization process is described for making substantially homogeneous terpolymers comprising, by weight, 55-99%, preferably 65-95% of vinyl pyrrolidone, 0.5-49%, preferably 1-25% of a quaternary amino monomer, preferably 3-methacrylamido- propyl trimethylammonium chloride; and 0.5-49%, preferably 1-25%, of a hydrophobic monomer, preferably RMA, where R is C 4 -C 32 alkyl, and, most preferably, octadecyl methacrylate.
• Such homogeneous terpolymers provide both hair styling and conditioning for the user.
• the homogeneous terpolymer solution herein also has better clarity, and provides hair care products with greater water solubility, and improved polymer adsorption onto hair, when compared to non-homogeneous copolymers of the same composition, or related existing commercial products.
• the homogeneous polymerization process of the invention includes precharging VP, and solvent, and introducing the MAPTAC and ODMA monomers incrementally at rates corresponding to the rate of disappearance of VP, over a given period of time.
• FIGURE 1 is a graphical representation of a conventional non-homogeneous ("one-pot") polymerization process for making a terpolymer of vinylpyrrolidone (VP) , 3-methacrylamidopropyl trimethylammonium chloride (MAPTAC) , and octadecyl methacrylate (ODMA) monomers from precharged amounts of the monomers.
• VP vinylpyrrolidone
• MAAC 3-methacrylamidopropyl trimethylammonium chloride
• ODMA octadecyl methacrylate
• FIGURE 2 is a graphical representation of the homogeneous process of the invention for making the same terpolymer.
• Vinylpyrrolidone is the most preferred vinyl lactam.
• the vinyl lactam monomer is present in an amount of about 55-99%, and, preferably, 65-95%, by weight of the terpolymer.
• the quaternary amino (or organic quaternary ammonium) acrylamide or acrylate monomer in the terpolymer of the invention has the formula:
• R is C 2 -C 20 alkyl or —(-CH 2 CHO- ⁇ -CH 2 -CH- , where n is 0-10,
• X and X 1 are independently H, or C- ⁇ to C 8 alkyl
• R l t R 2 and R 3 are independently C- ⁇ C ⁇ alkyl
• Z is a halide, sulfate or sulfonate.
• Suitable examples of amino acrylamides, acrylates, methacrylamides, or methacrylates which are employed as monomers in the terpolymer of the invention include quaternized salts of
• N-[ (dimethylamino)alkyl]methacrylamides or acrylamides, methacrylates and acrylates of their quaternized halide, sulfate and sulfonate salts are preferred.
• MATAC 3-methacrylamidopropyl) trimethylammonium chloride
• quaternized amino acrylamide is (3- ethacrylamidopropyl)trimethylammonium chloride
• the formula is represented by X and x being CH 3 ; Y being NH; R being C 3 alkyl; R 1/ R 2 and R 3 being methyl; and Z being chloride.
• the quaternary amino monomer suitably is present in the terpolymer in an amount of about 0.5-49%, and, preferably 1-25%, by weight of the terpolymer.
• the vinyl lactam and quaternary amino acrylamide or acrylate monomers constitute the hydrophilic portion of the terpolymer of the invention.
• hydrophobic monomer in the terpolymer of the invention suitably has the formula: RMA where R is a C 4 -C 32 alkyl, preferably C 12 -C 32 alkyl, or a mixture thereof; and MA is an acrylate, methacrylate, acrylamide or methacrylamide.
• Suitable hydrophobic monomers include 2-ethylhexyl methacrylate, dodecyl acrylate, tetradecyl acrylate, octadecyl methacrylate (ODMA) , octadecyl methacrylamide, dodecyl acrylamide and 2-ethylhexyl methacrylamide.
• a preferred hydrophobic monomer is octadecyl methacrylate.
• the hydrophobic monomer is present in an amount of about 0.5-49%, preferably 1-25%, by weight of the terpolymer.
• the homogeneous polymerization process of the invention is illustrated by making substantially homogeneous terpolymers of VP, MAPTAC and ODMA in a predetermined composition.
• the least reactive monomer of the terpolymer (VP) is precharged into a reactor at a suitable reaction temperature, generally about 50-80°C, and preferably 55-75 ⁇ C.
• the more reactive monomers (MAPTAC and ODMA) then are introduced incrementally into the VP-charged reactor at a rate which corresponds to the observed rate of disappearance of VP, over the period of polymerization.
• the entire predetermined amount of the MAPTAC and ODMA monomers are added before substantially all the VP monomer has been consumed so that all monomers can react to form a substantially homogeneous terpolymer in a desired compositional ratio of VP:MAPTAC:ODMA. Consequently, a substantially homogeneous terpolymer is obtained whose composition approaches the nominal monomer ratio of the desired terpolymer composition and whose structure has the three individual monomeric units of the copolymer distributed substantially uniformly in a homogeneous chain along the backbone of the polymer.
• the precharge in the process of the invention may include some MAPTAC and ODMA therein, generally in an amount of up to about 15% of the total amount of MAPTAC and ODMA required for a predetermined terpolymer composition without affecting the homogeneous polymerization process. However, it is still necessary that the rate of addition of MAPTAC and ODMA after any precharge be carried out at substantially the rate of disappearance of VP during polymerization.
• the schedule of addition of MAPTAC and ODMA to accomplish the desired matched rate of reaction of VP is determined in the following manner.
• VP 553.5 g
• MAPTAC 124.5 g
• ODMA ODMA
• ethanol 753.5 g
• the pH of the solution was adjusted to about 7.5 with KOH.
• a stream of nitrogen then was bubbled through the solution during the reaction.
• the solution was gradually heated to 68 ⁇ C, and 0.25 ml of Lupersol 11 as catalyst was added; then another 0.25 ml of the catalyst was added after 10 minutes; and another 6 units of 0.25 ml amount was added each 30 minutes.
• the reaction was carried out for an additional 3 hours.
• the relative percentage amounts of residual monomers present during the course of the one-pot reaction was determined by gas chromatographic analysis after sampling the reaction mixture periodically. The analytical data obtained then was plotted as the graph of FIGURE 1.
• the MAPTAC and ODMA monomers react much more rapidly than VP. Accordingly, after 100 minutes, for example, all the MAPTAC and ODMA monomers are consumed while residual VP monomer still is available for homopolymerization.
• the terpolymer formed is of a composition different from the desired monomer ratios selected by the precharged amounts of the two monomers.
• the polymer product obtained is a complex mixture of a homopolymer which is polyvinylpyrrolidone, various copolymers, and a terpolymer of the several monomers of uncertain composition.
• the curve of rate of reaction vs. time for both MAPTAC and ODMA substantially coincide or match the rate of reaction curve for VP.
• the VP is precharged and substantially all the MAPTAC and RMA monomers are fed external to the precharge at a feeding schedule determined by analysis of the data of FIGURE 1.
• the % MAPTAC and ODMA monomers to be fed at time t of the polymerization is determined from the Asymmetric Double Sigmoidal Distribution formula, A ⁇ below, which has four adjustable parameters, a l f a 2 , a 3 an( a 4 : At -
• t time in minutes during copolymerization
• a ⁇ is a parameter which determines the center of the distribution
• a 2 is a parameter which affects the width of the distribution
• a 3 is a parameter which determines the ascending portion of the distribution
• a 4 is a parameter which determines the descending portion of the distribution.
• N time when the polymerization is completed.
• % unreacted MAPTAC or ODMA at time t is too large, then the value of a 3 (ascendency) in the A t formula is increased, a (descendency) is decreased, a 1 (center) is decreased, and a 2 (width) is decreased. Conversely, if the initial guess values of a A through a 4 give a reaction rate for MAPTAC or ODMA which is too fast, then changes in the values of a ⁇ through a are made in a direction opposite to those discussed above.
• the matched curves of VP, MAPTAC and ODMA in FIGURE 2 will have at least one set of values for a ⁇ a 2 , a 3 and a 4 (the last set of the iterative fitting process) for suitable feeding of MAPTAC and ODMA over the entire period of polymerization.
• One such set is:
• VP (303.6 g)
• MAPTAC (7.8 g)
• ODMA 3.1 g
• ethanol 1001.0 g
• the pH of the solution is adjusted to about 7.5 with KOH.
• a stream of nitrogen is introduced which bubbles through the solution during the reaction.
• the solution is gradually heated to 65°C.
• MAPTAC (63.2 g) and octadecyl methacrylate (ODMA) (51.4 g) are introduced incrementally into the pot with vigorous stirring over a period of 5 hours so that the relative concentrations of the onomeric VP, MAPTA and ODMA monomer remain practically constant throughout the reaction at predetermined levels.
• Lupersol 11 t-butylperoxy pivalate in mineral spirits
• the rate of the addition of the catalyst is such that 2 ml of Lupersol is completely delivered in 4 hours.
• the solution is held for an additional 3 hours at the 68°C.
• the product is an alcoholic solution of the homogeneous terpolymer of VP, MAPTAC and ODMA.
• the homogeneous terpolymer of the invention contains a predetermined dominant blend of a hydrophilic part, i.e. VP/MAPTAC, and a small proportion of a hydrophobic monomer, i.e. RMA.
• This homogeneous terpolymer composition enables the terpolymer to be readily adsorbed onto the negatively charged hair in high amounts as clear films, and to provide both styling and conditioning functions, while still being capable of being readily rinsed or washed-off with water or shampoo after use.
• the homogeneous terpolymer of the invention comprises about 0.2-20%, preferably 1-10%, and, most preferably, about 2-8%, by weight of the hair care product, the rest being water, and, optionally including an organic solvent such as ethanol, and/or other acceptable adjuvant components such as silicones, surface active agents, viscosity modifiers, dyes, chelating agents, distributing aids, pearlescent aids, opacifiers, perfumes, fatty alcohols, pH adjusting agents, and the like.
• an organic solvent such as ethanol
• other acceptable adjuvant components such as silicones, surface active agents, viscosity modifiers, dyes, chelating agents, distributing aids, pearlescent aids, opacifiers, perfumes, fatty alcohols, pH adjusting agents, and the like.
• the homogeneous terpolymer of the invention finds particular utility in multifunctional hair care products such as water-based, rinse-off hair styling and conditioning products, and in leave-on hair care products such as a mousse, and may be included as a concentrate, or as a gel, and applied as a self-actuated pump hair spray, or in an aerosol product with a propellant.
• Various actuator and packaging devices known in the art may be used therewith.

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• Health & Medical Sciences (AREA)
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• Epidemiology (AREA)
• Dermatology (AREA)
• Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
• Cosmetics (AREA)

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Cited By (6)

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• 1995
  • 1995-12-13 JP JP8520476A patent/JPH10511422A/ja active Pending
  • 1995-12-13 EP EP95943076A patent/EP0800540A4/de not_active Withdrawn
  • 1995-12-13 WO PCT/US1995/016127 patent/WO1996020227A1/en not_active Application Discontinuation
  • 1995-12-13 CN CN 95197087 patent/CN1171120A/zh active Pending
  • 1995-12-13 AU AU44216/96A patent/AU700245B2/en not_active Ceased

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