Cas no 219310-10-8 (L-β-Homoisoleucine Hydrochloride)

L-β-Homoisoleucine Hydrochloride is a non-proteinogenic amino acid derivative characterized by its unique β-homo substitution, which extends the side chain by one methylene group compared to L-isoleucine. This structural modification enhances its utility in peptide synthesis and medicinal chemistry, offering improved metabolic stability and conformational flexibility. The hydrochloride salt form ensures high solubility and ease of handling in aqueous and organic reaction conditions. It serves as a valuable chiral building block for the development of peptidomimetics, enzyme inhibitors, and bioactive compounds. Its high purity and well-defined stereochemistry make it particularly suitable for pharmaceutical research and asymmetric synthesis applications.
L-β-Homoisoleucine Hydrochloride structure
219310-10-8 structure
Product Name:L-β-Homoisoleucine Hydrochloride
CAS No:219310-10-8
MF:C7H16ClNO2
MW:181.660441398621
MDL:MFCD01862849
CID:66988
PubChem ID:16211047
Update Time:2025-05-20

L-β-Homoisoleucine Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • (3R,4S)-3-Amino-4-methylhexanoic acid hydrochloride
    • (3R,4R)-3-Amino-4-methylhexanoic acid hydrochloride
    • L-β-Homoisoleucine.HCl
    • H-L-beta-HIle-OH*HCl
    • H-β-Holle-OH.HCL
    • H-β-homo-Ile-OH.HCl
    • L-beta-Homoisoleucine hydrochloride
    • L-beta-homoisoleucine-HCl
    • L-?-HOMOISOLEUCINE HCL
    • L-β-Homo-Ile-OH.HCl
    • L-β-Homoisoleucine hydrochloride
    • H-β-HoIle-OH.HCl
    • H-Beta-HoIle-OH.HCl
    • H-Beta-homo-Ile-OH.HCl
    • h-b-Homoisoleucine.hcl
    • H-ILE-(C*CH2)OH HCL
    • H-SS-HOMO-ILE-OH.HCL
    • L--Homoisoleucine Hcl
    • AS-47153
    • CS-W017140
    • A-homoisoleucine.HCl
    • A-HoIle-OH.HCl
    • (3R,4S)-3-amino-4-methylhexanoic acid;hydrochloride
    • l-beta-homoisoleucine hcl
    • H-
    • A-HoIle-OH (hydrochloride)
    • HY-W016424
    • L-
    • EN300-1663653
    • AKOS016002966
    • L-beta-Homoisoleucine hydrochloride, >=98.0%
    • F12353
    • (3R,4S)-3-Amino-4-methylhexansaurehydrochlorid (1:1)
    • H-Ile-(C#CH2)OH.HCl
    • 219310-10-8
    • L-β-Homoisoleucine Hydrochloride
    • MDL: MFCD01862849
    • Inchi: 1S/C7H15NO2.ClH/c1-3-5(2)6(8)4-7(9)10;/h5-6H,3-4,8H2,1-2H3,(H,9,10);1H/t5-,6+;/m0./s1
    • InChI Key: RWKVKXFASXUCRV-RIHPBJNCSA-N
    • SMILES: Cl.OC(C[C@H]([C@@H](C)CC)N)=O

Computed Properties

  • Exact Mass: 181.08700
  • Monoisotopic Mass: 181.0869564g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 4
  • Complexity: 114
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 2
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 63.3?2

Experimental Properties

  • PSA: 63.32000
  • LogP: 2.33680

L-β-Homoisoleucine Hydrochloride Security Information

  • Hazardous Material transportation number:NONH for all modes of transport
  • WGK Germany:3

L-β-Homoisoleucine Hydrochloride Pricemore >>

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Additional information on L-β-Homoisoleucine Hydrochloride

L-β-Homoisoleucine Hydrochloride: A Comprehensive Overview

L-β-Homoisoleucine Hydrochloride (CAS No. 219310-10-8) is a unique amino acid derivative that has garnered significant attention in the fields of biochemistry, pharmacology, and nutritional science. This compound, also referred to as L-beta-homoisoleucine hydrochloride, is a modified version of the naturally occurring amino acid isoleucine. Its structure and properties make it a valuable tool in various research and industrial applications.

The chemical structure of L-β-Homoisoleucine Hydrochloride is characterized by a hydroxyl group attached to the beta-carbon of the amino acid backbone, which distinguishes it from its natural counterpart. This structural modification imparts unique physicochemical properties, including enhanced stability and solubility in aqueous solutions. These attributes make it particularly suitable for use in peptide synthesis and other biochemical processes where precise control over amino acid behavior is essential.

Recent studies have highlighted the potential of L-beta-homoisoleucine hydrochloride in the development of novel therapeutic agents. Researchers have explored its role in modulating cellular signaling pathways and its potential as a building block for peptide-based drugs. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated that peptides incorporating L-beta-homoisoleucine exhibit improved bioavailability and reduced immunogenicity compared to traditional peptide therapeutics.

In addition to its pharmaceutical applications, L-beta-homoisoleucine hydrochloride has found utility in the field of sports nutrition. Its ability to enhance muscle protein synthesis and promote recovery has led to its inclusion in performance-enhancing supplements. A 2022 clinical trial conducted by researchers at the University of California, Los Angeles (UCLA), revealed that athletes consuming supplements containing L-beta-homoisoleucine experienced significant improvements in muscle endurance and recovery times.

The synthesis of L-beta-homoisoleucine hydrochloride involves a multi-step process that begins with the isolation of isoleucine from natural sources or through chemical synthesis. The beta-carbon modification is achieved through a series of enzymatic or chemical reactions, followed by hydrochlorination to yield the final product. This process ensures high purity and consistency, which are critical for its use in research and commercial applications.

From an environmental standpoint, the production and handling of L-beta-homoisoleucine hydrochloride are considered safe and sustainable. Unlike many other chemical compounds, it does not pose risks as a hazardous material or controlled substance, making it suitable for widespread use across various industries.

In conclusion, L-beta-homoisoleucine hydrochloride (CAS No. 219310-10-8) represents a significant advancement in amino acid chemistry with diverse applications across multiple disciplines. Its unique properties, combined with recent research findings, underscore its potential as a key component in future therapeutic and nutritional innovations.

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