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Catalog Number:
28687
CAS Number:
102507-13-1
Boc-(S)-2-amino-3-hydroxy-3-methylbutanoic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Boc-L-Ser(3,3-dimethyl)-OH, (S)-Boc-b,b-dimethyl-serine
Documents
$100.05 /100MG
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Product Information

Boc-(S)-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 Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal choice for researchers looking to develop complex peptides and biologically active compounds. Its unique structure, characterized by a hydroxyl group and a branched side chain, allows for the introduction of specific functionalities that can be tailored for various applications in medicinal chemistry and drug development.

In addition to its role in peptide synthesis, Boc-(S)-2-amino-3-hydroxy-3-methylbutanoic acid has potential applications in the development of novel therapeutics, particularly in the fields of neuropharmacology and metabolic disorders. Researchers appreciate its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups. This compound stands out for its ease of use and compatibility with various coupling reagents, making it a preferred choice for professionals aiming to streamline their synthetic processes and enhance the efficiency of their research.

Synonyms
Boc-L-Ser(3,3-dimethyl)-OH, (S)-Boc-b,b-dimethyl-serine
CAS Number
102507-13-1
Purity
≥ 98% (HPLC)
Molecular Formula
C10H19NO5
Molecular Weight
233.26
MDL Number
MFCD03094792
PubChem ID
13756005
Appearance
White to Off-white powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-L-Ser(3,3-dimethyl)-OH, (S)-Boc-b,b-dimethyl-serine
CAS Number
102507-13-1
Purity
≥ 98% (HPLC)
Molecular Formula
C10H19NO5
Molecular Weight
233.26
MDL Number
MFCD03094792
PubChem ID
13756005
Appearance
White to Off-white powder
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-(S)-2-amino-3-hydroxy-3-methylbutanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the pharmaceutical industry, where it can enhance the stability and bioavailability of therapeutic peptides.
  • Drug Development: Its unique structure allows for the design of novel drug candidates, especially in the development of treatments for metabolic disorders, due to its amino acid properties.
  • Biochemical Research: Researchers use this compound to study enzyme activity and protein interactions, providing insights into metabolic pathways and potential therapeutic targets.
  • Cosmetic Formulations: The compound is explored in cosmetic chemistry for its potential skin benefits, such as moisturizing and anti-aging properties, making it a candidate for innovative skincare products.
  • Food Industry Applications: It can be utilized as a food additive or flavor enhancer, contributing to the development of functional foods that promote health and wellness.

Citations