boc-L-hydroxyproline NEW

Boc-Hyp-OH, also known as Boc-hydroxyproline, is a chemical compound used primarily in peptide synthesis and organic chemistry. It is a derivative of hydroxyproline with a Boc (tert-butoxycarbonyl) protecting group attached to the amino group of the hydroxyproline molecule.

Key Characteristics and Uses:

1. Chemical Structure:

• Boc Group: The Boc (tert-butoxycarbonyl) group is a common protective group used in peptide synthesis to protect amino groups from reacting during the synthesis process.

• Hydroxyproline: Hydroxyproline is an amino acid that is a modified form of proline, containing a hydroxyl group (-OH) on the proline ring.

2. Role in Peptide Synthesis:

• Protective Group: The Boc group protects the amino group of hydroxyproline during peptide synthesis, preventing unwanted reactions and ensuring that the amino group remains free for coupling with other amino acids.

• Deprotection: After the peptide synthesis is completed, the Boc group can be removed under acidic conditions, revealing the free amino group for further reactions or for use in the final peptide product.

3. Applications:

• Organic Chemistry: Used in the synthesis of peptides and other complex molecules, particularly when hydroxyproline is a component of the target molecule.

• Pharmaceutical Research: Useful in the synthesis of bioactive peptides and pharmaceuticals where precise control over amino acid sequences is required.

4. General Properties:

• Appearance: Boc-Hyp-OH is typically a white to off-white powder.

• Solubility: It is usually soluble in organic solvents like dimethylformamide (DMF) and dichloromethane (DCM).

In summary, Boc-Hyp-OH is a key reagent in peptide synthesis, offering a way to control and protect the functional groups during the formation of complex peptide structures. Its use in organic chemistry and pharmaceutical research highlights its importance in creating specific and high-purity compounds.

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