How is tranexamic acid produced?

Discovered in the 1950s, tranexamic acid is a structurally similar derivative of the amino acid lysine. It was initially used in the medical field for its ability to inhibit fibrinolysis. When taken orally, it can manage excessive bleeding induced by events such as severe trauma, surgical procedures, postpartum hemorrhages, and heavy menstruation. This use is based on its coagulating abilities, which help to reduce blood loss.

It is noteworthy that tranexamic acid is listed on the World Health Organization's (WHO) list of essential medicines. However, it was only recently, in 2009, that it was authorized and incorporated into cosmetic product formulations by the Cosmetology Commission. Thanks to its depigmenting action, this acid has the notable ability to diminish the appearance of various forms of skin hyperpigmentation, such as melasma, post-inflammatory hyperpigmented marks, and sun spots.

By acting in this way, it promotes a clearer complexion by limiting the production of melanin. Studies have even suggested that the effectiveness of tranexamic acid could be comparable to that of the hydroquinone, an active ingredient widely used in this context. Moreover, this acid is also sought after for its anti-inflammatory properties.

When applied topically in skincare products, tranexamic acid is generally well tolerated and does not cause major side effects However, in rare cases, it could cause temporary reactions, such as redness or itching. For this reason, it is recommended to perform a test beforehand by applying the product to a small area of the body during the first use.

Tranexamic acid is a synthetic compound produced in a laboratory, derived from the amino acid lysine. However, the specific details of its chemical synthesis are typically protected and not disclosed. Nonetheless, there are studies that provide some insight into its production.

1. The synthesis begins with dimethyl terephthalate (C10H10O4), a diester formed from terephthalic acid and methanol, where potassium hydroxide (KOH) and methanol (CH4O) are added to the solution.

2. After the reaction mixture has been heated to reflux, methyl 4-(chlorocarbonyl)benzoate is formed through the use of bis(trichloromethyl) carbonate (BTC).

3. As the chemical reaction progresses, the reaction mixture transforms into a solid that reacts with an aqueous solution of ammonia (NH3).

4. Acetic anhydride (C4H6O3) is then added and heated.

5. Subsequently, a hydrogenation occurs, which is a chemical reaction that involves the addition of a dihydrogen molecule to another compound, in order to produce potassium 4-(methoxycarbonyl)benzoate (C6H7KO4).

6. The obtained molecule is then hydrolyzed and isomerized.

7. In conclusion, barium hydroxide (BaH2O2) is added to the solution along with water and ethanol (C2H6O) as solvents to produce tranexamic acid.

Note : The steps presented above are only the main phases of the tranexamic acid synthesis process. The manufacturing process may vary from one laboratory to another.