Boc-L-2-aminobutyric acid (also known as Boc-L-Abu-OH or (S)-2-(Boc-amino)butyric acid) is a Boc-protected unnatural amino acid featuring a tert-butyloxycarbonyl (Boc) group protecting the α-amino functionality and an ethyl side chain at the α-carbon. The molecular formula is C₉H₁₇NO₄ with a molecular weight of 203.30 g/mol.
Boc-L-2-aminobutyric acid is a protected chiral building block widely utilized in Boc solid-phase peptide synthesis (Boc SPPS) for introducing L-2-aminobutyric acid residues into peptides and pharmaceutical intermediates. The Boc group in Boc-L-2-aminobutyric acid serves as a protecting group for the amino functionality during peptide synthesis, allowing for selective modification of amino acids without interference from other functional groups. As a pharmaceutical intermediate, Boc-L-2-aminobutyric acid is employed in the manufacturing of various pharmaceutical compounds. The chiral L-configuration of Boc-L-2-aminobutyric acid is essential for maintaining biological activity in peptide-based therapeutics, making it a critical building block in drug discovery and development programs. The compound‘s stability and crystalline nature make Boc-L-2-aminobutyric acid convenient to handle and store for long-term research and manufacturing campaigns.
Product Parameters
Parameter
Specification
Product Name
Boc-L-2-aminobutyric acid
CAS Number
34306-42-8
Molecular Formula
C₉H₁₇NO₄
Molecular Weight
203.24 g/mol
Appearance
White to off-white solid
Melting Point
70–74°C
Boiling Point
334.5±25.0℃
Optical Rotation
[α]²⁰/D −18.5±2° (c = 1% in methanol)
Solubility
Slightly soluble in water
Flash Point
113 °C
Storage Condition
Keep in dark place,Sealed in dry,Room Temperature
pKa
4.00±0.10
Density
1.101±0.06 g/cm3
Synthetic Route
Boc-L-2-aminobutyric acid is typically synthesized from DL-2-aminobutyric acid via the following procedure: dissolve 10.3 g of DL-2-aminobutyric acid in a mixture of 95 mL of 1 M NaOH solution and 65 mL of methanol; add 27.5 mL of diisopropyl carbonate (i.e., Boc anhydride, see Equation 1 in Chemical Book 2) under ice bath heating, then gradually升温 to room temperature while stirring for 12 hours. After reaction completion, remove methanol by rotary evaporation, adjust pH to 1–2 with 1 M hydrochloric acid, extract three times with 50 mL of ethyl acetate each, wash twice with saturated saline solution (40 mL each), dehydrate with anhydrous sulfuric acid, and finally obtain 18.9 g of colorless solid (93.4%).
Application
(1) Synthesis of the antitumor drug idelalisib
(2) Synthesis of the antitumor drug edelizib
(3) Synthesis of the intermediate compound of o-fluoro-o-iminobenzoic acid
Product Quality Assurance
Cosperpharm has established a comprehensive quality assurance system for Boc-L-2-aminobutyric acid that meets the rigorous expectations of pharmaceutical intermediate and research-grade applications:
Thorough analytical characterization. Each batch undergoes multi-technique analytical release testing: HPLC purity (≥98%), optical rotation verification ([α]²⁰/D −18.5±2°, c = 1% in methanol), melting point verification (70–79 °C), and appearance inspection (white to off-white powder).
Full batch traceability. From raw material procurement through Boc protection, purification, crystallization, drying, and final packaging, every step is fully documented and traceable. Each batch receives a unique lot number with retention samples maintained in accordance with Cosperpharm quality procedures.
Documentation ready for regulatory submission. As a pharmaceutical intermediate, Boc-L-2-aminobutyric acid is used in drug substance manufacturing and requires comprehensive documentation. Every shipment includes a Certificate of Analysis (COA) with batch-specific purity and characterization data, a Material Safety Data Sheet (SDS), and customs documentation. DMF-ready documentation, stability summaries, and custom quality agreements are available upon request.
Customer-initiated quality audits. Qualified customers are welcome to audit Cosperpharm‘s manufacturing, quality control, and documentation facilities. Please contact our regulatory team to schedule an audit.
Contact Us
Interested in sourcing Boc-L-2-aminobutyric acid for your next peptide synthesis campaign or pharmaceutical manufacturing project? Cosperpharm is here to help. Reach out to our team for pricing, documentation, or technical support — we look forward to supporting your success.
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