Mixed polyglyceryl polyester quats

Abstract

The present invention is directed to a class of mixed polyglyceryl polyester quats that provide multifunctional benefit in personal care applications, including but not limited to (1) conditioning, (2) antistatic properties, (3) bacteriostatic properties and (4) exceptional mildness to skin and eyes. The products are made by the reaction reacting some on the many hydroxyl groups present on polyglycerin with (1) with fatty acids, then (2) diacids then reacted with epoxy cationic compounds to make film forming cationic polymers that are bacteriostatic and of interest in inhibiting biofilm formation on environmental surfaces.

Claims

1. A polyglycerol quat prepared by the sequential reaction of: A. a prepolymer made by the reaction of: a. polyglycerin; b. an alkyl group having the following structure: ##STR00012## wherein: n is an integer ranging from 6 to 24; c. a cross-linking alkyl having the following structure: ##STR00013## wherein; R.sup.3 is independently selected from the groups consisting of: a. an alkyl ranging from 2 to 16 carbons; b. hydrogenated dimer acid c. dimer acid and mixtures thereof; B. an alkyl quat intermediate having the following structure: ##STR00014## wherein: R.sup.4 is alkyl containing 1 to 18 carbons; and mixtures thereof.

2. The polyglycerol of claim 1 wherein n is 6.

3. The polyglycerol of claim 1 wherein n is 8.

4. The polyglycerol of claim 1 wherein n is 10.

5. The polyglycerol of claim 1 wherein n is 12.

6. The polyglycerol of claim 1 wherein n is 14.

7. The polyglycerol of claim 1 wherein n is 16.

8. The polyglycerol of claim 1 wherein n is 18.

9. The polyglycerol of claim 1 wherein n is 20.

10. The polyglycerol of claim 1 wherein n is 22.

11. The polyglycerol of claim 1 wherein n is 18.

12. The polyglycerol of claim 1 wherein n is a mixture of 6 and 20.

13. The polyglycerol of claim 1 wherein n is a mixture of 10 and 22.

Description

OBJECT OF THE INVENTION

(1) It is the object to provide a group of polyglyceryl esters linked together by a di-acid then in subsequent reaction reacted with an alkyl quat intermediate having the following structure;

(2) ##STR00001## wherein: R.sup.4 is alkyl containing 1 to 18 carbons; and mixtures thereof.

(3) The crosslinking of the polymers of the present invention with a diacid contributes significant barrier properties that render the hair and skin conditioned, smooth, and having a dry aesthetic.

(4) An additional aspect of the present invention is to provide an additive to shampoos, body washes, and conditioners providing highly desirable properties, including outstanding mildness.

(5) Finally, it is the object of the invention to provide materials that are bacteriostatic. That is, formulations using the compounds of the present invention are resistant to bacterial challenges.

DESCRIPTION OF THE INVENTION

Summary of the Invention

(6) The current invention combines two very different sequential reaction steps that require different processes and process conditions to produce a heretofore unknown polymer having highly desirable properties. Firstly, in the polyglycerin is crosslinked with a diacid. This process called esterification is carried out at high temperature without a solvent. Water is the by product and is efficiently stripped off. This provides a polymeric material that has both hydrophilic (polyglycerin) and hydrophobic (fatty diacid) moieties. It is the balance of these moieties that allows for the creation of products with differing solubilities and HLB values. Secondly, in a the intermediate of step one is reacted with and alkyl quat intermediate in water to produce the desired cationic polymers. The alkyl quat intermediate has the following structure;

(7) ##STR00002## Wherein: R.sup.4 is alkyl containing 1 to 18 carbons; and mixtures thereof.

DETAILED DESCRIPTION OF THE INVENTION

(8) One aspect of the present invention is directed towards a polyglycerol quat made by the reaction of:

(9) 1. A polyglycerol quat prepared by the sequential reaction of: A. a prepolymer made by the reaction of: a. polyglycerin b. an alkyl group having the following structure:

(10) ##STR00003## wherein: n is an integer ranging from 6 to 24; c. a cross-linking alkyl having the following structure:

(11) ##STR00004## wherein; R.sup.3 is independently selected from the groups consisting of: a. an alkyl ranging from 2 to 16 carbons; b. hydrogenated dimer acid c. dimer acid and mixtures thereof; B. an alkyl quat intermediate having the following structure:

(12) ##STR00005## wherein R.sup.4 is alkyl containing 1 to 18 carbons; and mixtures thereof.

Preferred Embodiments

(13) In a preferred embodiment n is 6.

(14) In a preferred embodiment n is 8.

(15) In a preferred embodiment n is 10.

(16) In a preferred embodiment n is 12.

(17) In a preferred embodiment n is 14.

(18) In a preferred embodiment n is 16.

(19) In a preferred embodiment n is 18.

(20) In a preferred embodiment n is 20.

(21) In a preferred embodiment n is 22.

(22) In a preferred embodiment n is 32.

Examples

(23) Raw Materials

(24) Polyglycerol

(25) Polyglycerol are commercially available from a variety of sources including Solvay, of Alpharetta, Ga. It has the following structure:

(26) ##STR00006##

(27) TABLE-US-00001 Example X Polyglycerol Molecular Weight 1 1 Polyglycerol-3 240 2 2 Polyglycerol-4 314 3 4 Polyglycerol-6 462 4 6 Polyglycerol-8 610 5 8 Polyglycerol-10 758

(28) Fatty Acids

(29) Fatty acids useful in the practice of the present invention are items of commerce commercially available from Cognis.

(30) Fatty Acid Names

(31) Fatty acids useful as raw materials in the preparation of compounds of the present invention are commercially available from a variety of sources including Procter and Gamble of Cincinnati Ohio. The structures are well known to those skilled in the art.

(32) ##STR00007##

(33) TABLE-US-00002 N Common Name Molecular Weight Example 6 6 Caprylic 144 7 8 Capric 172 8 10 Lauric 200 9 12 Myristic 228 10 13 Pentadecanoic 242 11 14 Palmitic 256 12 16 Stearic 284 13 16 Isosteric 284 14 18 Arachidinic 312 15 20 Behenic 340 16 15 cetrotic 396 17 32 geddic acid 508 Unsaturated Example 18 16 Oleic 282 19 16 Linoleic 280 20 16 Linolenic 278 21 14 Palmitoleic 254 22 12 Myristicoleic 226 23 20 Erucic 338

(34) Dicarboxylic Acids

(35) Dicarboxylic acids are useful raw materials in the synthesis of the compounds of the present invention and are commercially available from a variety of sources including Cognis. They have the following structure:

(36) ##STR00008##

(37) Saturated Dicarboxylic Acids

(38) TABLE-US-00003 Example Common Name a Molecular Weight 24 Malonic 1 104 25 Succinic 2 118 26 Glutaric 3 132 27 Adipic 4 146 28 Pimelic 5 160 29 Subric 6 174 30 Azelaic 7 188 31 Sebacic 8 202 32 Undecanedioic 9 216 33 Dodecanedioic 10 230

(39) Example 34 Dimer Acid

(40) Dimer acid is an item of commerce available commercially from Cognis Corporation. It conforms to the following structure:

(41) ##STR00009##

(42) Example 35 Hydrogenated Dimer Acid

(43) Hydrogenated dimer acid is an item of commerce available commercially from Henkel Corporation. It conforms to the following structure:

(44) ##STR00010##

(45) Quat Intermediates

(46) Quat Intermediates are items of commerce available commercially from Colonial Chemical South Pittsburgh Tn. They conform to the following structure:

(47) ##STR00011##

(48) TABLE-US-00004 Example R.sup.4 MW 36 CH.sub.3 158 37 Lauryl 358 38 Coco 426

(49) Polyglycerol Prepolymer (Step 1)

(50) General Procedure

(51) To a flask equipped with thermometer, heat and distillation ability is added the specified number of grams of polyglycerol (examples 1-5) and the specified number of grams of the specified a fatty acid (examples 6-23). The mixture is heated to 160-200 C. under agitation. The temperature is held in this range for 8-10 hours as water distills off. The resulting product is cooled and used without additional purification.

(52) TABLE-US-00005 Polyglycerol Fatty acid Example Example Grams Example Grams Unreacted-OH 39 1 53.57 6 96.43 2 40 3 46.39 7 103.61 2 41 3 60.26 7 89.74 4 42 5 31.60 12 118.40 2 43 5 46.18 12 103.82 6 44 1 32.92 13 117.08 2 45 3 46.39 15 103.61 2 46 3 60.36 15 89.74 4 47 5 27.45 18 122.55 2 48 5 27.45 18 103.59 6 49 1 33.52 20 116.48 2

(53) TABLE-US-00006 Polyglycerol Fatty acid Fatty Acid Example Example Grams Example Grams Example Grams Unreacted-OH 50 1 41.24 6 37.11 20 71.65 2 51 3 37.99 7 42.43 18 69.57 2 52 3 50.58 7 37.66 18 61.75 4 53 5 32.54 12 73.15 15 44.30 2 54 5 53.48 12 60.11 15 36.41 6 55 1 32.92 13 58.54 12 58.54 2 56 3 49.15 15 54.89 6 45.96 2 57 3 63.35 15 47.17 6 39.49 4 58 5 37.55 18 69.85 7 42.60 2 59 5 53.63 18 59.86 7 36.51 6 60 1 33.22 20 57.72 12 59.07 2 61 3 31.05 12 50.02 13 50.02 2 62 3 43.31 12 53.34 13 53.34 4 63 5 31.56 12 59.22 13 59.22 2 64 5 46.13 12 51.94 13 51.94 6

(54) General Procedure Dimer Prepolymers

(55) To a flask equipped with thermometer, heat and distillation ability is added the specified number of grams of polyglycerol (examples 1-5), di-acid (examples 24-35) and the specified number of grams of the specified a fatty acid (examples 6-23). The mixture is heated to 160-200 C. under agitation. The temperature is held in this range for 8-10 hours as water distills off. The resulting product is cooled and used without additional purification.

(56) TABLE-US-00007 Polyglycerol Fatty acid Fatty Acid Di-Acid Example Example Grams Example Grams Example Grams Example Grams Unreacted-OH 65 5 29.17 12 109.27 35 11.56 2 66 5 45.87 12 85.94 35 18.19 10 67 1 25.85 13 91.78 35 32.37 2 68 1 32.48 13 76.86 35 40.66 4 69 1 25.82 12 45.92 13 45.92 35 32.34 2 70 1 32.45 12 38.46 13 38.46 35 40.63 4 71 3 60.05 6 28.08 20 54.20 25 7.67 2 72 3 72.41 6 22.57 20 43.57 27 11.44 4 73 5 28.61 12 53.69 15 64.16 30 3.55 2 74 5 47.11 12 44.21 15 52.82 33 5.84 10 75 3 49.71 18 23.24 7 44.87 34 32.17 2 76 3 58.58 18 18.26 7 35.25 34 37.91 4 77 3 42.88 12 39.61 13 39.61 35 27.89 2 78 3 32.45 12 38.46 13 38.46 35 40.63 4 79 5 29.13 12 54.66 13 54.66 35 11.55 2 80 5 69.86 12 26.22 14 26.22 35 27.70 10

(57) Alkyl Quat Intermediate (Step 2)

(58) General Procedure

(59) An alkyl quat intermediate (examples 37 or 38) is added into a round bottom flask. Sodium hydroxide solution is added to adjust the pH. Water is added to adjust to 15% wt. Polyglycerol prepolymer (examples 39-80) is added into the round bottom and stirred. The round bottom flask is placed under reflux and heated to 85-95 C. Once the reaction clears, example 36 is added and allowed to react for 4-6 hours.

(60) TABLE-US-00008 Example Example Example Polyglycerol Prepolymer 36 37 38 Example Example Grams Grams Grams Grams 81 39 72.62 77.38 82 41 74.42 20.45 55.13 83 42 131.19 5.76 13.05 84 43 84.97 10.91 24.71 29.41 85 45 98.38 23.57 28.05 86 52 80.97 18.68 50.35 87 55 101.91 14.73 33.36 88 57 77.19 22.30 50.52 89 62 75.76 33.90 40.34 90 64 85.02 10.90 24.70 29.39 91 69 126.57 7.17 16.25 92 70 102.57 14.58 33.04 93 73 139.73 2.78 7.49 94 74 87.45 5.73 25.95 30.88 95 77 120.72 13.37 15.91 96 78 87.89 28.36 33.75 97 79 140.70 2.85 6.45 98 90 72.80 7.07 32.03 38.11

(61) Unexpectantly, the presence of the two different substitution patterns in the quaternary compounds of the current invention, one having R.sup.4 defined as methyl and other in which R.sup.4 is defined as higher alkyl provides for materials where the former group (methyl) is water soluble and bacteriostatic and the latter higher alkyl is surface active, foaming and conditioning. The compounds of this type of structure are very effective in the treatment of non-woven sheets to allow for the wetting of the hydrophobic sheets by water, generally used for baby wipes. The presence of the higher alkyl groups provides mild conditioning, foam and cleansing. The ratio between the two groups allows for the ability to fine tune the desired properties, matching it to the hydrophobicity of the non-woven sheet. Finally, unlike amino silicones that are also used in the preparation of non-woven sheets, these products are biodegradable and do not release methanol during storage when the methoxy group present in such silicones reacts with water.

(62) While the illustrative embodiments of the invention have been described with particularity, it will be understood that various other modifications will be apparent to and can be readily made by those skilled in the art without departing from the spirit and scope of the invention. Accordingly, it is not intended that the scope of the claims appended hereto be limited to the examples and descriptions set forth hereinabove but rather that the claims be construed as encompassing all the features of patentable novelty which reside in the present invention, including all features which would be treated as equivalents thereof by those skilled in the art to which the invention pertains.