3775-72-2 | (S)-3-Aminobutyric acid

Packsize	Purity	Availability	Price	Discounted Price
250mg	98%	in stock	$9.00	$6.00
1g	98%	in stock	$12.00	$9.00
5g	98%	in stock	$24.00	$17.00
25g	98%	in stock	$119.00	$84.00
100g	98%	in stock	$475.00	$333.00

Description

• Catalog Number: AB47324
• Chemical Name: (S)-3-Aminobutyric acid
• CAS Number: 3775-72-2
• Molecular Formula: C4H9NO2
• Molecular Weight: 103.1198
• MDL Number: MFCD00270347
• SMILES: C[C@@H](CC(=O)O)N

Computed Properties

• Complexity: 72.1
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 1
• Heavy Atom Count: 7
• Hydrogen Bond Acceptor Count: 3
• Hydrogen Bond Donor Count: 2
• Rotatable Bond Count: 2
• XLogP3: -3.1

Upstream Synthesis Route

(S)-3-aminobutyric acid, also known as beta-aminoisobutyric acid or BAIBA, is a valuable building block in chemical synthesis due to its distinct structure and versatile reactivity. This compound is widely used in the pharmaceutical industry for the synthesis of various bioactive molecules and drug candidates. In particular, (S)-3-aminobutyric acid serves as a key intermediate in the production of peptides, which are essential components of many drugs and biologically active compounds.One prominent application of (S)-3-aminobutyric acid is in the synthesis of peptide-based drugs and pharmaceuticals. By incorporating this amino acid derivative into peptide sequences, chemists can modulate the properties and functions of the resulting peptides. This enables the design and creation of novel peptide analogs with enhanced therapeutic effects, improved bioavailability, and specific targeting abilities. Additionally, (S)-3-aminobutyric acid can be utilized to introduce structural constraints and conformational rigidity into peptide structures, leading to improved stability and activity profiles.Furthermore, (S)-3-aminobutyric acid finds utility in the preparation of complex natural products, functional materials, and chiral building blocks. Its unique stereochemistry and amino acid-like properties make it a valuable starting material for the synthesis of diverse organic compounds with specific chirality and biological activities. Through strategic incorporation of (S)-3-aminobutyric acid into molecular frameworks, chemists can access new chemical space and develop innovative synthetic routes for the construction of challenging molecules.Overall, the application of (S)-3-aminobutyric acid in chemical synthesis spans various fields, including pharmaceuticals, materials science, and biotechnology. Its versatility and reactivity make it an essential component in the toolbox of synthetic chemists seeking to access novel compounds and design innovative molecules with tailored properties and functions.