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Catalog Number:
28640
CAS Number:
288159-40-0
Boc-(R)-2-amino-3-hydroxy-3-methylbutanoic acid
Purity:
≥ 98% (Assay)
Synonym(s):
N-Boc-3-hydroxy-D-valine, (R)-Boc-ß-hydroxy-valine
Documents
$105.70 /100MG
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Product Information

Boc-(R)-2-amino-3-hydroxy-3-methylbutanoic acid is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a tert-butyloxycarbonyl (Boc) protecting group, which is crucial for the selective protection of amino groups during the synthesis of complex peptides. Its unique structure, characterized by a hydroxyl and a methyl group, enhances its solubility and reactivity, making it an ideal candidate for various applications in medicinal chemistry and biochemistry.

Researchers and industry professionals can leverage Boc-(R)-2-amino-3-hydroxy-3-methylbutanoic acid in the development of bioactive peptides, particularly those targeting specific biological pathways. Its ability to facilitate the formation of stable peptide bonds while maintaining the integrity of sensitive functional groups makes it a preferred choice in the synthesis of therapeutic agents. Additionally, this compound can be employed in the design of novel drug candidates, contributing to advancements in targeted therapies and personalized medicine.

Synonyms
N-Boc-3-hydroxy-D-valine, (R)-Boc-ß-hydroxy-valine
CAS Number
288159-40-0
Purity
≥ 98% (Assay)
Molecular Formula
C10H19NO5
Molecular Weight
233.26
MDL Number
MFCD02682576
PubChem ID
13756005
Melting Point
115 - 123 °C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = 9 ± 3 º (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
N-Boc-3-hydroxy-D-valine, (R)-Boc-ß-hydroxy-valine
CAS Number
288159-40-0
Purity
≥ 98% (Assay)
Molecular Formula
C10H19NO5
Molecular Weight
233.26
MDL Number
MFCD02682576
PubChem ID
13756005
Melting Point
115 - 123 °C
Appearance
White to off-white powder
Optical Rotation
[a]D20 = 9 ± 3 º (C=1 in DMF)
Conditions
Store at 0 - 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-(R)-2-amino-3-hydroxy-3-methylbutanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the pharmaceutical industry, where it helps create biologically active compounds.
  • Drug Development: Its unique structure allows for the development of novel drugs, especially in the treatment of metabolic disorders, enhancing the efficacy and specificity of therapeutic agents.
  • Biochemical Research: Researchers use it to study enzyme activity and protein interactions, providing insights into metabolic pathways and potential drug targets.
  • Cosmetic Formulations: The compound is also explored in the cosmetic industry for its potential benefits in skin care products, particularly those aimed at anti-aging and hydration.
  • Food Industry Applications: It can be utilized as a food additive or supplement, contributing to flavor enhancement and nutritional benefits in functional foods.

Citations