Cas no 13031-62-4 (4-Aminobutyramide Hydrochloride)

4-Aminobutyramide Hydrochloride is a hydrochloride salt derivative of 4-aminobutyramide, commonly utilized in pharmaceutical and biochemical research. This compound serves as a key intermediate in the synthesis of GABA (γ-aminobutyric acid) analogs and related neuroactive substances. Its high purity and stability make it suitable for applications in drug development, particularly in studies targeting neurological pathways. The hydrochloride form enhances solubility, facilitating its use in aqueous-based reactions. Analytical standards of this compound are often employed in chromatographic and spectroscopic studies to ensure reproducibility in research. Proper handling and storage under controlled conditions are recommended to maintain its integrity.
4-Aminobutyramide Hydrochloride structure
13031-62-4 structure
Product Name:4-Aminobutyramide Hydrochloride
CAS No:13031-62-4
MF:C4H11ClN2O
MW:138.595939874649
MDL:MFCD00792526
CID:211032
PubChem ID:3014709
Update Time:2025-05-25

4-Aminobutyramide Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 4-Aminobutanamide hydrochloride
    • 4-Aminobutyramide Hydrochloride
    • Butanamide, 4-amino-,hydrochloride (1:1)
    • 4-Amino-Butanamide Hydrochloride
    • 4-Aminobutyramide HCl
    • 4-aminobutyramide monohydrochloride
    • 4-aminobutyric acid amide hydrochloride
    • EINECS 235-895-9
    • Gabamide Hydrochloride
    • Gabamide Hydrochlorid
    • 4-Aminobutanamide Monohydrochloride
    • ButanaMide, 4-aMino-, Monohydrochloride
    • AMY15220
    • SY174709
    • EN300-39439
    • 4-aminobutanamidehydrochloride
    • Gabaminde hydrochloride
    • J-005789
    • FT-0661642
    • C72206
    • MVEPJLNIXKEKMI-UHFFFAOYSA-N
    • Butanamide, 4-amino-, hydrochloride (1:1)
    • 4-AMINOBUTANAMIDE HCL
    • Z398513418
    • CBB62LLN98
    • AS-64833
    • CS-0103894
    • MFCD00792526
    • 13031-62-4
    • NS00085182
    • AKOS016008821
    • 4-aminobutanamide;hydrochloride
    • DTXSID60156451
    • SCHEMBL856415
    • 4-Aminobutanamide Monohydrochloride; Gabamide Hydrochloride;
    • BUTANAMIDE, 4-AMINO- (9CI) HYDROCHLORIDE
    • 4-AMINOBUTYRAMIDE, HYDROCHLORIDE
    • MDL: MFCD00792526
    • Inchi: 1S/C4H10N2O.ClH/c5-3-1-2-4(6)7;/h1-3,5H2,(H2,6,7);1H
    • InChI Key: MVEPJLNIXKEKMI-UHFFFAOYSA-N
    • SMILES: Cl.O=C(CCCN)N

Computed Properties

  • Exact Mass: 138.05600
  • Monoisotopic Mass: 138.056
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 3
  • Complexity: 62.7
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 69.1A^2

Experimental Properties

  • Boiling Point: 300.8°Cat760mmHg
  • Flash Point: 135.7°C
  • PSA: 69.11000
  • LogP: 1.41320

4-Aminobutyramide Hydrochloride Pricemore >>

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4-Aminobutyramide Hydrochloride Production Method

Additional information on 4-Aminobutyramide Hydrochloride

4-Aminobutyramide Hydrochloride: A Comprehensive Overview

4-Aminobutyramide Hydrochloride, also known by its CAS number CAS No. 13031-62-4, is a compound that has garnered significant attention in the fields of pharmacology and biochemistry. This compound, which belongs to the class of amino acid derivatives, has been extensively studied for its potential applications in drug development and therapeutic interventions. Recent advancements in research have shed light on its unique properties and mechanisms of action, making it a subject of interest for both academia and industry.

The chemical structure of 4-Aminobutyramide Hydrochloride comprises a butyramide backbone with an amino group attached at the fourth carbon position. This structural arrangement imparts distinctive chemical properties, including its ability to interact with various biological systems. Researchers have explored its role in modulating cellular signaling pathways, particularly those involving neurotransmitters and neuromodulators. These findings have implications for treating conditions such as neurological disorders and metabolic diseases.

One of the most promising areas of research involving 4-Aminobutyramide Hydrochloride is its potential as a precursor to gamma-aminobutyric acid (GABA). GABA is a key inhibitory neurotransmitter in the central nervous system, playing a crucial role in regulating neuronal activity. Studies have demonstrated that this compound can be metabolized into GABA under specific physiological conditions, suggesting its utility in managing conditions associated with GABA deficiency, such as anxiety and epilepsy.

In addition to its neuropharmacological applications, 4-Aminobutyramide Hydrochloride has also been investigated for its metabolic effects. Recent studies indicate that it may influence energy metabolism by interacting with enzymes involved in lipid synthesis and degradation. This property has led to explorations into its potential as an adjunct therapy for obesity and related metabolic disorders.

The synthesis of 4-Aminobutyramide Hydrochloride involves a multi-step chemical process that ensures high purity and stability. Researchers have optimized synthetic protocols to enhance yield and minimize byproducts, making it more accessible for large-scale production. The compound's stability under various storage conditions further adds to its suitability for pharmaceutical applications.

From a regulatory standpoint, 4-Aminobutyramide Hydrochloride has undergone rigorous safety assessments to evaluate its toxicity profile. Preclinical studies suggest that it exhibits low toxicity at therapeutic doses, with minimal adverse effects observed in animal models. These findings are encouraging for its progression into clinical trials.

In conclusion, 4-Aminobutyramide Hydrochloride, CAS No. 13031-62-4, represents a versatile compound with diverse applications in medicine and pharmacology. Its ability to influence neurotransmitter systems and metabolic pathways positions it as a valuable tool in addressing a range of health conditions. As research continues to uncover new insights into its mechanisms and therapeutic potential, this compound is poised to play a significant role in future drug development efforts.

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