Cas no 42271-58-9 (L-Alloisoleucine, methyl ester)

L-Alloisoleucine methyl ester is a chiral ester derivative of the non-proteinogenic amino acid L-alloisoleucine. This compound is primarily utilized in organic synthesis and pharmaceutical research as a versatile building block for peptidomimetics and bioactive molecules. Its methyl ester group enhances solubility in organic solvents, facilitating reactions such as peptide coupling or derivatization. The stereochemistry of L-alloisoleucine contributes to its utility in studying enzyme specificity or asymmetric synthesis. The ester form also improves stability and handling compared to the free amino acid. This product is particularly valuable for researchers requiring controlled stereochemical configurations in complex molecular frameworks.
L-Alloisoleucine, methyl ester structure
42271-58-9 structure
Product Name:L-Alloisoleucine, methyl ester
CAS No:42271-58-9
MF:C7H15NO2
MW:145.199502229691
MDL:MFCD15147094
CID:3982325
Update Time:2025-05-21

L-Alloisoleucine, methyl ester Chemical and Physical Properties

Names and Identifiers

    • L-Alloisoleucine, methyl ester
    • YXMMTUJDQTVJEN-RITPCOANSA-N
    • L-Alloisoleucine methyl ester
    • MDL: MFCD15147094
    • Inchi: 1S/C7H15NO2/c1-4-5(2)6(8)7(9)10-3/h5-6H,4,8H2,1-3H3/t5-,6+/m1/s1
    • InChI Key: YXMMTUJDQTVJEN-RITPCOANSA-N
    • SMILES: C(OC)(=O)[C@H]([C@H](C)CC)N

Experimental Properties

  • Density: 0.955±0.06 g/cm3(Predicted)
  • Boiling Point: 169.2±13.0 °C(Predicted)
  • pka: 7.98±0.39(Predicted)

L-Alloisoleucine, methyl ester Pricemore >>

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eNovation Chemicals LLC
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eNovation Chemicals LLC
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eNovation Chemicals LLC
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Additional information on L-Alloisoleucine, methyl ester

L-Alloisoleucine, methyl ester (CAS 42271-58-9): A Comprehensive Guide to This Unique Amino Acid Derivative

In the world of amino acid derivatives, L-Alloisoleucine, methyl ester (CAS 42271-58-9) stands out as a compound of significant scientific interest. This stereoisomer of isoleucine has garnered attention from researchers across multiple disciplines due to its unique structural properties and potential applications. As interest in specialized amino acids grows within the pharmaceutical and nutritional sectors, understanding this compound's characteristics becomes increasingly valuable.

The methyl ester form of L-Alloisoleucine offers distinct advantages in various chemical processes. Unlike its free acid counterpart, the esterified version demonstrates improved solubility in organic solvents, making it particularly useful in peptide synthesis and other organic chemistry applications. Recent studies have highlighted its role as a building block for more complex molecules, especially in the development of novel therapeutic agents.

From a structural perspective, L-Alloisoleucine methyl ester maintains the crucial chiral center that defines its biological activity. This characteristic makes it valuable for research into enzyme-substrate interactions and metabolic pathways. Scientists investigating protein folding mechanisms or developing chiral catalysts frequently turn to this compound for its well-defined stereochemistry.

The production of CAS 42271-58-9 typically involves sophisticated synthetic routes that preserve its optical purity. Modern manufacturing techniques emphasize green chemistry principles, reducing environmental impact while maintaining high yields. These advancements answer growing market demands for sustainably produced specialty chemicals, a trend particularly strong among younger researchers and environmentally conscious companies.

In analytical chemistry, L-Alloisoleucine, methyl ester serves as an important reference standard for chromatographic methods. Its well-characterized properties make it ideal for method development and quality control in amino acid analysis. Laboratories performing metabolomics studies or nutritional profiling often include this compound in their standard panels.

Beyond research applications, this compound has shown promise in specialized nutritional formulations. While not a mainstream supplement ingredient, methylated amino acid derivatives like this one attract interest from sports nutrition researchers investigating novel performance-enhancing compounds. The esterification potentially alters absorption kinetics, a property under investigation for targeted delivery systems.

The stability profile of L-Alloisoleucine methyl ester makes it suitable for various storage conditions, though proper handling remains essential. Like all amino acid derivatives, it requires protection from moisture and extreme temperatures to maintain purity over time. These storage considerations are particularly important for researchers requiring consistent batch-to-batch performance.

Market analysis indicates steady growth in demand for specialty amino acid derivatives like CAS 42271-58-9. Pharmaceutical applications drive much of this demand, followed by academic research and niche industrial uses. Suppliers report increasing inquiries from biotechnology startups focusing on peptide-based therapeutics, reflecting broader industry trends.

Quality specifications for L-Alloisoleucine, methyl ester typically emphasize optical purity, chemical purity, and absence of residual solvents. Reputable manufacturers provide comprehensive analytical certificates with each batch, including HPLC chromatograms and mass spectrometry data. These quality assurances are critical for researchers requiring materials of known composition for reproducible experiments.

Future research directions for this compound may explore its potential in asymmetric synthesis or as a precursor for more complex chiral molecules. The growing field of biocatalysis might also find applications for this well-defined stereochemical building block. As synthetic biology advances, such specialized amino acid derivatives could play roles in engineered metabolic pathways.

For researchers considering L-Alloisoleucine methyl ester for their work, proper handling procedures should be followed. While not classified as hazardous, standard laboratory precautions apply when working with any chemical substance. Material safety data sheets provide specific guidance for this amino acid derivative, including appropriate personal protective equipment.

The pricing structure for CAS 42271-58-9 reflects its specialty status, with costs varying based on quantity and purity requirements. Bulk purchases for industrial applications typically command different pricing than small-scale research quantities. Market dynamics suggest prices may stabilize as production scales to meet growing demand for such fine chemicals.

In conclusion, L-Alloisoleucine, methyl ester represents an important tool in modern chemical and biological research. Its unique properties continue to find new applications as scientific understanding advances. For researchers and manufacturers alike, this compound exemplifies the value of specialized amino acid chemistry in addressing contemporary scientific challenges across multiple disciplines.

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