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AE08813

105931-64-4 | H-Val-pro-oh hcl

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $98.00 $68.00 -   +
250mg 95% in stock $169.00 $118.00 -   +
1g 95% in stock $355.00 $248.00 -   +
5g 95% in stock $1,179.00 $825.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE08813
Chemical Name: H-Val-pro-oh hcl
CAS Number: 105931-64-4
Molecular Formula: C10H19ClN2O3
Molecular Weight: 250.7225
MDL Number: MFCD00191045
SMILES: CC([C@@H](C(=O)N1CCC[C@H]1C(=O)O)N)C.Cl

 

Upstream Synthesis Route
  • H-Val-Pro-OH.HCl, also known as N-Acetyl-L-histidine-L-proline hydrochloride, is a key component in chemical synthesis processes. This compound is widely utilized in peptide synthesis and pharmaceutical research due to its unique properties and functionalities.One of the primary applications of H-Val-Pro-OH.HCl is in the preparation of peptide derivatives. As a protected dipeptide, it serves as a crucial building block for constructing longer peptide chains through solid-phase peptide synthesis (SPPS) or liquid-phase peptide synthesis (LPPS) methods. By incorporating H-Val-Pro-OH.HCl into the peptide sequence, chemists can control the stereochemistry and regulate the reactivity of the amino acids, allowing for the precise design and production of custom peptides with specific biological activities.Moreover, H-Val-Pro-OH.HCl plays a crucial role in the development of peptide-based pharmaceuticals and bioactive molecules. Its presence in the synthetic pathway ensures the production of high-quality peptides that exhibit enhanced stability, solubility, and bioavailability. Researchers and pharmaceutical companies often rely on H-Val-Pro-OH.HCl to synthesize peptide analogs, enzyme inhibitors, and drug candidates with targeted therapeutic effects.In summary, H-Val-Pro-OH.HCl is a versatile and indispensable tool in chemical synthesis, particularly in the creation of peptides and pharmaceutical compounds. Its strategic use in peptide assembly and modification processes highlights its significance in advancing research and innovation within the fields of chemistry, biochemistry, and drug discovery.
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