METHOD OF PREPARING CREATINE ESTER SALTS AND USES THEREOF.
This invention discloses the method of preparation of creatine ester-salts. Creatine is an extremely popular ergogenic aid, and is found most often in the form of creatine monohydrate. Creatine monohydrate is poorly soluble in water however and while esters gain solubility, there functionality is greatly decreased. The material can be administered in a variety of ways including capsules, tablets, powdered beverages, bars, gels, liquids, liposomes or drinks.
1 . A dietary supplement comprising an ester salt of creatine of the following structure,
wherein R— contains alkyl and aryl groups or combinations thereof between 1 to 35 carbon atoms; n- represents 1 to 6 creatine; X— represents 1 to 6; and A- represents an organic acid with 1 to 6 carboxylic radicals.
2 . A process of preparing a creatine ester salts comprising the following structure,
wherein R— contains alkyl and aryl groups or combinations thereof between 1 to 35 carbon atoms; n- represents 1 to 6 creatine; X— represents 1 to 6; and A- represents an organic acid with 1 to 6 carboxylic radicals; and
wherein the creatine ester salt is prepared at a temperature from −60° C. to 300° C. in a water solution or organic solution, or without any solvent.
3 . The process according to claim 2 where, R is straight or branched, saturated or unsaturated.
4 . The process according to claim 2 where, R further includes 1 to 6 hydroxy radicals.
5 . The process according to claim 2 where R further includes substituent radicals selected from the group consisting of keto, halide, and amine.
6 . The process according to claim 2 where, 1 to 6 carbon atoms in the 1 to 35 carbon atoms in R are replaced by a nitrogen, an oxygen, a sulphur or a phosphor atom.
7 . (canceled)
8 . (canceled)
9 . A method for enhancing performance, muscle size or strength, comprising administering the dietary supplement according to claim 1 .
10 . A method according to claim 9 , wherein from about 10 mg to about 20000 mg of the dietary supplement according to claim 1 is administered on a routine basis.
11 . The process according to claim 2 wherein the R is selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl glyceryl, and benzyl.
12 . The process according to claim 2 wherein the A is selected from the group consisting of malic acid, maleic acid, fumaric acid, pyruvic acid, citric acid, tartaric acid, alpha-ketoglutaric acid and ascorbic acid.
13 . The dietary supplement according to claim 1 wherein R is straight or branched, saturated or unsaturated.
14 . The dietary supplement according to claim 1 wherein R has 1 to 6 hydroxy radicals.
15 . The dietary supplement according to claim 1 wherein R has a substituent radical selected from the group consisting of keto, halide, and amine.
16 . The dietary supplement according to claim 1 wherein 1 to 6 carbon atoms in the 1 to 35 carbon atoms in R are replaced by a nitrogen, an oxygen, a sulphur, or a phosphor atom.
17 . The dietary supplement according to claim 1 wherein the R is selected from the group consisting of methyl, ethyl, propyl, isopropyl, butyl, isobutyl, tert-butyl, glyceryl, and benzyl.
18 . The dietary supplement according to claim 1 wherein the A is selected from the group consisting of malic acid, maleic acid, fumaric acid, pyruvic acid, citric acid, tartaric acid, alpha-ketoglutaric acid and ascorbic acid.
19 . The dietary supplement according to claim 1 wherein R— represents ethyl; n- represents 1; X— represents 1; and A- represents malic acid.
20 . The method according to claim 9 , wherein from about 1 g to about 20 g of the dietary supplement according to claim 1 is administered on a routine basis.