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Atomfair Isovaline C5H11NO2
Description Isovaline (CAS 403519-98-2), also known as 2-amino-2-methylbutanoic acid, is a non-proteinogenic amino acid with the molecular formula C5H11NO2. This rare amino acid is a structural analog of valine, distinguished by its unique ??-methyl substitution , which confers distinctive biochemical properties. Isovaline is available as a racemic mixture ( DL-Isovaline ) and is of significant interest in astrobiological research , neuroscience , and pharmaceutical studies due to its potential role in chiral selectivity and neuroprotective effects. With a purity grade suitable for laboratory and research applications, this compound is supplied in high-quality crystalline form, ensuring consistency for experimental use. Store…
Description
Description
Isovaline (CAS 403519-98-2), also known as 2-amino-2-methylbutanoic acid, is a non-proteinogenic amino acid with the molecular formula C5H11NO2. This rare amino acid is a structural analog of valine, distinguished by its unique ??-methyl substitution, which confers distinctive biochemical properties. Isovaline is available as a racemic mixture (DL-Isovaline) and is of significant interest in astrobiological research, neuroscience, and pharmaceutical studies due to its potential role in chiral selectivity and neuroprotective effects. With a purity grade suitable for laboratory and research applications, this compound is supplied in high-quality crystalline form, ensuring consistency for experimental use. Store in a cool, dry environment to maintain stability.
- CAS No: 403519-98-2
- Molecular Formula: C5H11NO2
- Molecular Weight: 117.15
- Exact Mass: 117.078978594
- Monoisotopic Mass: 117.078978594
- IUPAC Name: 2-amino-2-methylbutanoic acid
- SMILES: CCC(C)(C(=O)O)N
- Synonyms: Isovaline, 2-Amino-2-methylbutanoic acid, DL-Isovaline, 595-39-1, Isovaline, DL-
Application
Isovaline is primarily used in astrobiology and origin-of-life studies as a marker for extraterrestrial organic material due to its rarity in terrestrial biology. In neuroscience, it has been investigated for its potential neuroprotective and anticonvulsant properties, particularly in modulating glycine receptors. Additionally, its chiral properties make it valuable for pharmaceutical research into enantioselective synthesis and drug development.
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