phone
Email
Online Inquiry
Verification code

Tranexamic acid

Catalog Number
ACM1197188-1
CAS
1197-18-8
Structure
IUPAC Name
4-(Aminomethyl)cyclohexane-1-carboxylic acid
Synonyms
Hexapromin
Molecular Weight
157.21
Molecular Formula
C8H15NO2
Canonical SMILES
C1CC(CCC1CN)C(=O)O
InChI
InChI=1S/C8H15NO2/c9-5-6-1-3-7(4-2-6)8(10)11/h6-7H,1-5,9H2,(H,10,11)
InChI Key
GYDJEQRTZSCIOI-UHFFFAOYSA-N
Boiling Point
281.88 °C
Melting Point
>300 °C(lit.)
Flash Point
135.357 °C
Purity
98%
Density
1.0806 g/cm³
Solubility
water, 2.5e+004 mg/L @ 25 °C (est)
Appearance
White crystalline powder
Storage
2-8 °C
Active Content
95%
Physical State
Solid
Typical Applications
Use as dispersing agent, emulsion stabilizer.
Spec Sheet
Case Study

Preparation of Tranexamic Acid-Modified Porous Starch

Preparation of Tranexamic Acid-Modified Porous Starch Zhao, Xinhong, et al. International Journal of Biological Macromolecules 200 (2022): 273-284.

Materials with good hemostatic properties have recently attracted widespread attention in the scientific community. In this study, a new material, tranexamic acid (TA)-modified porous starch (TAMPS), was prepared by esterification. By exploring the relevant hemostatic mechanisms, TAMPS can promote coagulation through rapid fluid absorption and high red blood cell aggregation capacity.
Synthesis of TAMPS:
1. Dissolve 2 g of starch in 100 mL of sodium hydrogen phosphate and citric acid buffer solution (pH 4.5). Place the solution in a 50 °C water bath and stir mechanically at 500 rpm. Then, under magnetic stirring, add α-amylase and glucoamylase to the solution for 6 hours. Adjust the alkalinity of the solution to pH 12 by adding 0.5 M sodium hydroxide. Continue stirring for 30 minutes, then centrifuge at 5500 rpm for 5 minutes. Wash three times with deionized water and freeze-dry to obtain enzyme-hydrolyzed starch, which is the porous starch (PS).
2. Dissolve 5 g of BOC-tranexamic acid (BOC-TA) in 50 mL of dichloromethane and stir magnetically at 500 rpm at 30 °C. Then, add 200 μL of N,N-dimethylformamide and 2.8 mL of thionyl chloride (SOCl2) to the solution and stir for 3 hours. After evaporation, obtain the BOC-amidocarbonyl chloride powder.
3. Add 2 g of PS to 100 mL of dimethyl sulfoxide at 80 °C and stir magnetically at 500 rpm. Add 10 g of BOC-amidocarbonyl chloride and stir for 8 hours. Centrifuge at 5500 rpm for 10 minutes, wash three times with deionized water, centrifuge again, and freeze-dry for 24 hours to obtain TAMPS.

Preparation of Tranexamic Acid-Containing Soluble Microneedle (DMNs) Patches

Preparation of Tranexamic Acid-Containing Soluble Microneedle (DMNs) Patches Xing, Mengzhen, et al. International Journal of Pharmaceutics 600 (2021): 120406.

Tranexamic acid (TA)-containing soluble microneedle (DMN) patches can be used for the treatment of melasma.
Preparation of Soluble Microneedles: Dissolve polyvinyl alcohol (PVA) in deionized water at high temperature (80 °C), and dissolve polyvinylpyrrolidone (PVP) at room temperature to obtain a matrix solution composed of 8% PVA and 2% PVP. Add tranexamic acid (TA) and licorice extract (LIC) into the matrix solution to obtain an active ingredient solution containing 44 mg/mL TA and 2 mg/mL LIC. Adjust the pH of the solution to 5.5 to obtain a uniform and stable microneedle solution. Pour the microneedle solution into a mold made of polydimethylsiloxane (PDMS). Then, using a vacuum method, fill each microneedle unit and dry it at room temperature by blowing air.

Preparation of Tranexamic Acid-Loaded Mesoporous Silica Microspheres as Hemostatic Materials

Preparation of Tranexamic Acid-Loaded Mesoporous Silica Microspheres as Hemostatic Materials Mohamed, Sara Saber Younes, et al. Materials Today Communications 34 (2023): 105198.

The aim of this study was to develop a hemostatic agent based on macroporous mesoporous silica particles for use in bleeding control. Mesoporous silica microspheres (MSM) with a particle size of 1.5 - 5 µm and a pore size of 25 nm were successfully synthesized and, for the first time, loaded with 4.7% w/w tranexamic acid (TXA). The hemostatic activity of the pure material and the TXA-loaded material (TXA@MSM) was evaluated. Based on the results, TXA@MSM can be considered a promising material for the development of novel hemostatic agents.
TXA Loading: TXA was loaded using water as the solvent through an initial wet impregnation technique. This method is simple, fast, economical, and green because it does not require any organic solvents, making it suitable for potential future industrial transfer. During impregnation, 15 mg of TXA was dissolved in 0.36 mL of water, and the solution was added dropwise to 285 mg of MSM, achieving a nominal TXA content of approximately 5% w/w. The slurry was vigorously stirred with a spatula, and the sample was dried overnight at room temperature. The resulting material was designed as TXA@MSM.

❈ Please kindly note that our products are for research use only.

PAGE TOP