Cas no 3235-46-9 (4-Amino-4-methylpentanoic acid)

4-Amino-4-methylpentanoic acid is a branched-chain amino acid derivative with applications in organic synthesis and pharmaceutical research. Its structure, featuring both an amino and a carboxyl functional group, makes it a versatile intermediate for the preparation of peptidomimetics and bioactive compounds. The methyl substitution at the 4-position enhances steric hindrance, which can influence conformational stability in synthetic pathways. This compound is particularly valued for its role in studying enzyme inhibition and modulating metabolic pathways. Its purity and well-defined chemical properties ensure reproducibility in research settings. Suitable for controlled reactions, it is commonly used in academic and industrial laboratories for targeted molecular design.
4-Amino-4-methylpentanoic acid structure
3235-46-9 structure
Product Name:4-Amino-4-methylpentanoic acid
CAS No:3235-46-9
MF:C6H13NO2
MW:131.172921895981
CID:323012
PubChem ID:228069
Update Time:2025-05-21

4-Amino-4-methylpentanoic acid Chemical and Physical Properties

Names and Identifiers

    • 4-Amino-4-methylpentanoic acid
    • 4-AMINO-4-METHYLPENTANOIC ACID XHCL
    • Pentanoic acid, 4-amino-4-methyl-
    • 3235-46-9
    • SCHEMBL1933286
    • FZNOWMWZNCOYIJ-UHFFFAOYSA-N
    • CS-0273048
    • EN300-58734
    • 4-amino-4,4-dimethyl butanoic acid
    • NSC20667
    • NSC-20667
    • FT-0684017
    • 4-amino-4-methylpentanoicacid
    • MFCD09036517
    • 4-Amino-4-methylpentanoic acid HCl
    • F8887-3924
    • AKOS000320168
    • DTXSID20281177
    • Pentanoic acid, 4-amino-4-methyl-, hydrochloride
    • DS-012137
    • G72767
    • STK694725
    • ALBB-016157
    • MDL: MFCD09036517
    • Inchi: 1S/C6H13NO2/c1-6(2,7)4-3-5(8)9/h3-4,7H2,1-2H3,(H,8,9)
    • InChI Key: FZNOWMWZNCOYIJ-UHFFFAOYSA-N
    • SMILES: OC(CCC(C)(C)N)=O

Computed Properties

  • Exact Mass: 131.094628657g/mol
  • Monoisotopic Mass: 131.094628657g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 3
  • Complexity: 110
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -2.5
  • Topological Polar Surface Area: 63.3?2

4-Amino-4-methylpentanoic acid Security Information

  • HazardClass:IRRITANT

4-Amino-4-methylpentanoic acid Pricemore >>

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Additional information on 4-Amino-4-methylpentanoic acid

Comprehensive Overview of 4-Amino-4-methylpentanoic acid (CAS No. 3235-46-9): Properties, Applications, and Research Insights

4-Amino-4-methylpentanoic acid (CAS No. 3235-46-9), also known as 4-AMP, is a specialized organic compound with a unique structure combining an amino group and a carboxylic acid functionality. This molecule has garnered significant attention in pharmaceutical research, biochemical studies, and material science due to its versatile properties. The compound's molecular formula C6H13NO2 and molecular weight 131.17 g/mol make it an interesting candidate for various synthetic applications. Researchers often explore its stereochemistry, solubility profiles, and reactivity patterns to develop novel derivatives for targeted applications.

In recent years, the demand for amino acid derivatives like 4-Amino-4-methylpentanoic acid has surged due to their potential in peptide synthesis and drug discovery. The compound's branched-chain structure offers distinct advantages in creating bioactive molecules with enhanced stability. A 2023 study highlighted its role as a building block for neurologically active compounds, aligning with growing interest in central nervous system therapeutics. This connection to brain health research makes it particularly relevant to current pharmaceutical trends addressing neurodegenerative conditions and cognitive enhancement.

The synthetic pathways for 4-Amino-4-methylpentanoic acid typically involve reductive amination or Strecker synthesis modifications. Advanced green chemistry approaches have been developed to improve the atom economy of its production, responding to the industry's push for sustainable manufacturing. Analytical techniques such as HPLC purity analysis, NMR spectroscopy, and mass spectrometry are crucial for characterizing this compound, especially when used in GMP-grade applications. The pharmaceutical industry particularly values its chiral purity when incorporated into active pharmaceutical ingredients (APIs).

Beyond pharmaceutical applications, 4-Amino-4-methylpentanoic acid shows promise in biodegradable polymer development. Its dual functional groups enable participation in polycondensation reactions, creating materials with potential use in medical implants and controlled-release systems. This aligns with the global focus on eco-friendly materials and circular economy principles. Researchers are also investigating its metal-chelating properties, which could lead to applications in water treatment or catalysis.

Quality control standards for CAS 3235-46-9 require strict monitoring of residual solvents and heavy metal content, especially for laboratory reagent and research chemical grades. The compound's storage stability under various conditions (temperature, humidity) has been extensively studied to ensure long-term viability of research samples. Recent innovations in crystal engineering have improved its powder flow properties, benefiting industrial-scale handling.

From a commercial perspective, 4-Amino-4-methylpentanoic acid suppliers have seen increased inquiries from contract research organizations and academic institutions. The compound's price per gram varies significantly based on purity grade (98%, 99%, or >99.5%) and batch size. Market analysts note growing interest from Asia-Pacific research hubs, particularly for custom synthesis projects involving structural analogs. Proper material safety data documentation remains essential for international shipping compliance.

Future research directions for 4-AMP may explore its potential in bioconjugation chemistry or as a linker molecule in antibody-drug conjugates (ADCs). The compound's metabolic stability makes it attractive for developing prodrug systems, while its zwitterionic nature could be exploited for drug delivery optimization. As computational chemistry tools advance, more accurate predictions of its intermolecular interactions will facilitate targeted molecular design.

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