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Atomfair Boc-aminoisobutyric acid C9H17NO4

Description Boc-aminoisobutyric acid (CAS No. 1231709-25-3) is a high-purity, protected amino acid derivative widely used in peptide synthesis and pharmaceutical research. With the molecular formula C9H17NO4and IUPAC name 2-amino-2-methyl-4-[(2-methylpropan-2-yl)oxy]-4-oxobutanoic acid , this compound features a Boc (tert-butoxycarbonyl) protecting group, ensuring stability during synthetic processes. Ideal for researchers and scientists, our product undergoes rigorous QC testing (HPLC, NMR) to guarantee ??95% purity, making it suitable for sensitive applications. Supplied as a white to off-white crystalline powder, it is packaged under inert conditions to prevent degradation. Store at 2-8??C in a dry environment for optimal shelf life.

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Description

Description

Boc-aminoisobutyric acid (CAS No. 1231709-25-3) is a high-purity, protected amino acid derivative widely used in peptide synthesis and pharmaceutical research. With the molecular formula C9H17NO4 and IUPAC name 2-amino-2-methyl-4-[(2-methylpropan-2-yl)oxy]-4-oxobutanoic acid, this compound features a Boc (tert-butoxycarbonyl) protecting group, ensuring stability during synthetic processes. Ideal for researchers and scientists, our product undergoes rigorous QC testing (HPLC, NMR) to guarantee ??95% purity, making it suitable for sensitive applications. Supplied as a white to off-white crystalline powder, it is packaged under inert conditions to prevent degradation. Store at 2-8??C in a dry environment for optimal shelf life.

  • CAS No: 1231709-25-3
  • Molecular Formula: C9H17NO4
  • Molecular Weight: 203.24
  • Exact Mass: 203.11575802
  • Monoisotopic Mass: 203.11575802
  • IUPAC Name: 2-amino-2-methyl-4-[(2-methylpropan-2-yl)oxy]-4-oxobutanoic acid
  • SMILES: CC(C)(C)OC(=O)CC(C)(C(=O)O)N
  • Synonyms: Boc-aminoisobutyric acid, boc-amino isobutyric acid, SCHEMBL189917, VIQZVYPYYUPDQY-UHFFFAOYSA-N, AS-15794

Application

Boc-aminoisobutyric acid serves as a key intermediate in solid-phase peptide synthesis (SPPS), enabling the incorporation of sterically hindered amino acids. It is particularly valuable in the design of peptidomimetics and constrained peptides for drug discovery. Researchers also utilize it in the development of bioactive compounds targeting protease inhibition and receptor modulation.

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