H-Met-Ala-Pro-Arg-Gly-Phe-Ser-Cys-Leu-Leu-Leu-Leu-Thr-Gly-Glu-Ile-Asp-Leu-Pro-Val-Lys-Arg-Arg-Ala-OH(CAS: 330936-70-4)

H-Met-Ala-Pro-Arg-Gly-Phe-Ser-Cys-Leu-Leu-Leu-Leu-Thr-Gly-Glu-Ile-Asp-Leu-Pro-Val-Lys-Arg-Arg-Ala-OH is a linear peptide with a molecular weight of approximately 1683.5 Da. It is moderately soluble in water and organic solvents. The compound is prone to hydrolysis under acidic and basic conditions, and it is susceptible to proteolytic degradation. It can form crystalline structures under appropriate conditions.

H-Met-Ala-Pro-Arg-Gly-Phe-Ser-Cys-Leu-Leu-Leu-Leu-Thr-Gly-Glu-Ile-Asp-Leu-Pro-Val-Lys-Arg-Arg-Ala-OH is synthesized through solid-phase peptide synthesis (SPPS) using Fmoc chemistry. Commonly, the peptide is synthesized on a solid support, with each amino acid step protected by Fmoc groups. The reaction sequence involves coupling reactions and deprotection steps, typically yielding products with high purity.

H-Met-Ala-Pro-Arg-Gly-Phe-Ser-Cys-Leu-Leu-Leu-Leu-Thr-Gly-Glu-Ile-Asp-Leu-Pro-Val-Lys-Arg-Arg-Ala-OH finds applications in pharmaceuticals, where it is used as a research tool for drug discovery and development. It is also utilized in sensors and semiconductor industries for its unique chemical properties.

When handling H-Met-Ala-Pro-Arg-Gly-Phe-Ser-Cys-Leu-Leu-Leu-Leu-Thr-Gly-Glu-Ile-Asp-Leu-Pro-Val-Lys-Arg-Arg-Ala-OH, it is essential to wear appropriate personal protective equipment (PPE) such as gloves and safety goggles. Ensure the use of adequate ventilation, ideally a fume hood, to minimize exposure risk. Follow proper storage procedures and dispose of waste according to local regulations. Always refer to the SDS for detailed handling instructions.