Understanding the fundamental chemical properties and synthesis pathways of key reagents is vital for successful research and development. NINGBO INNO PHARMCHEM CO.,LTD. provides insights into Boc-D-Abu-OH (CAS 45121-22-0), a crucial amino acid derivative, shedding light on its molecular characteristics and how it is produced.

Boc-D-Abu-OH, chemically known as (2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]butanoic acid, possesses a molecular formula of C9H17NO4 and a molecular weight of approximately 203.24 g/mol. Its structure features a D-2-aminobutyric acid core with a tert-butoxycarbonyl (Boc) protecting group attached to the amine nitrogen. This Boc group is key to its utility in organic synthesis, particularly in peptide synthesis and the creation of pharmaceutical intermediates. The compound typically appears as a white powder and is soluble in organic solvents like DMF, a common characteristic for such compounds when researchers aim to buy Boc-D-Abu-OH online.

The synthesis of Boc-D-Abu-OH generally involves the protection of the amino group of D-2-aminobutyric acid with a Boc anhydride reagent, such as di-tert-butyl dicarbonate. This reaction is typically carried out in a suitable solvent system, often with a mild base like sodium bicarbonate to neutralize the acid byproduct. For instance, a common method involves reacting D-2-aminobutyric acid with Boc anhydride in a mixture of dioxane and water under controlled temperature conditions. The reaction is monitored for completion, after which the product is isolated and purified. The yield is often high, with the resulting product being the desired Boc-protected D-amino acid. The efficiency of this synthesis route is a critical factor for manufacturers like NINGBO INNO PHARMCHEM CO.,LTD. to ensure a stable supply for chemical synthesis needs.

The stereochemistry of the starting material, D-2-aminobutyric acid, is preserved throughout the synthesis, resulting in optically pure Boc-D-Abu-OH. This stereochemical purity is paramount for its application in chiral synthesis and in the development of stereospecific pharmaceuticals. The precise control over enantiomeric purity is a hallmark of quality for suppliers of amino acid derivatives.

Beyond its use in peptide synthesis, Boc-D-Abu-OH can also be employed in the creation of specialized chemical reagents, in academic research exploring reaction mechanisms, and as a building block for novel materials. Its predictable reactivity and the ability to easily remove the Boc group make it a versatile tool in the hands of organic chemists. For those engaged in custom peptide synthesis or requiring specific chiral building blocks, understanding the synthesis and properties of this compound is essential.

In conclusion, Boc-D-Abu-OH is a chemically well-defined and synthetically accessible compound with significant utility. Its properties and straightforward synthesis make it an indispensable component in various chemical research and development endeavors. NINGBO INNO PHARMCHEM CO.,LTD. is committed to providing researchers with high-quality Boc-D-Abu-OH, facilitating advancements across scientific disciplines.