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Catalog Number:
33581
CAS Number:
151171-11-8
Ácido Boc-(S)-2-amino-2-metilbutírico
Purity:
≥ 99,5 % (HPLC quiral)
Synonym(s):
Boc-L-Isovalina
Documents
$58.39 /100 mg
Tamaño
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Product Information

Boc-(S)-2-Amino-2-methylbutyric acid is a versatile amino acid derivative widely utilized in the fields of pharmaceuticals and biochemistry. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and solubility, making it an ideal choice for peptide synthesis and drug development. Its unique structure allows for the selective modification of amino acids, facilitating the creation of complex biomolecules and therapeutic agents. Researchers often employ Boc-(S)-2-Amino-2-methylbutyric acid in the synthesis of peptide-based drugs, where its chiral center can impart specific biological activity, thus enhancing the efficacy of the final product.

In addition to its applications in drug formulation, this compound is also valuable in the development of advanced materials and bioconjugates. Its ability to form stable linkages with various functional groups opens up possibilities for creating innovative delivery systems and diagnostic tools. With its favorable properties and broad applicability, Boc-(S)-2-Amino-2-methylbutyric acid stands out as a crucial building block for researchers and industry professionals aiming to advance their projects in medicinal chemistry and biotechnology.

Synonyms
Boc-L-Isovalina
CAS Number
151171-11-8
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C10H19Nº 4
Molecular Weight
217.26
MDL Number
MFCD12031697
PubChem ID
11063876
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = 11 ± 1 ° (C=1 en CHCl 3 )
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Boc-L-Isovalina
CAS Number
151171-11-8
Purity
≥ 99,5 % (HPLC quiral)
Molecular Formula
C10H19Nº 4
Molecular Weight
217.26
MDL Number
MFCD12031697
PubChem ID
11063876
Appearance
Polvo blanco
Optical Rotation
[a] D 20 = 11 ± 1 ° (C=1 en CHCl 3 )
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-(S)-2-Amino-2-methylbutyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and facilitating the creation of complex structures in pharmaceuticals.
  • Drug Development: It plays a crucial role in the development of new drugs, particularly those targeting neurological disorders, by enhancing the stability and bioavailability of active pharmaceutical ingredients.
  • Biotechnology: In the biotechnology sector, it is used to modify proteins and enzymes, improving their functionality and efficiency in various biocatalytic processes.
  • Research in Chiral Chemistry: The compound is valuable in studies involving chiral molecules, helping researchers understand stereochemistry and its implications in drug interactions.
  • Cosmetic Formulations: Its properties make it a suitable ingredient in cosmetic products, where it can enhance skin absorption and provide moisturizing benefits.

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