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Catalog Number:
02655
CAS Number:
52498-32-5
Boc-N-methyl-L-isoleucine
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-N-Me-L-Ile-OH
Documents
$45.47 /1G
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Product Information

Boc-N-methyl-L-isoleucine is a valuable amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound, known for its protective Boc (tert-butyloxycarbonyl) group, enhances the stability and solubility of peptides during synthesis, making it an essential building block for researchers in the field of medicinal chemistry. Its unique structure allows for the selective modification of peptides, facilitating the development of novel therapeutics and biologically active compounds.

In addition to its applications in peptide synthesis, Boc-N-methyl-L-isoleucine is also employed in the production of various bioactive molecules, including those used in drug discovery and development. Its ability to mimic natural amino acids while providing enhanced stability makes it an attractive choice for researchers aiming to create more effective and targeted therapies. With its versatile applications and significant advantages over similar compounds, Boc-N-methyl-L-isoleucine stands out as a crucial tool for professionals in the pharmaceutical and biotechnology industries.

Synonyms
Boc-N-Me-L-Ile-OH
CAS Number
52498-32-5
Purity
≥ 99% (HPLC)
Molecular Formula
C12H23NO4
Molecular Weight
245.3
MDL Number
MFCD00066105
PubChem ID
3348571
Appearance
White solid
Optical Rotation
[a]D24 = -80 ± 1 º (C=1 in MeOH) (Lit.)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-N-Me-L-Ile-OH
CAS Number
52498-32-5
Purity
≥ 99% (HPLC)
Molecular Formula
C12H23NO4
Molecular Weight
245.3
MDL Number
MFCD00066105
PubChem ID
3348571
Appearance
White solid
Optical Rotation
[a]D24 = -80 ± 1 º (C=1 in MeOH) (Lit.)
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-N-methyl-L-isoleucine 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 development of biologically active compounds. Its protective Boc group allows for selective reactions, enhancing the efficiency of peptide assembly.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates, especially in the field of anti-cancer and anti-inflammatory agents. Its unique structure can lead to improved potency and selectivity compared to other amino acids.
  • Bioconjugation: The compound is employed in bioconjugation processes, where it helps link biomolecules to therapeutic agents. This application is crucial in developing targeted therapies that minimize side effects.
  • Protein Engineering: Researchers utilize Boc-N-methyl-L-isoleucine in the design of modified proteins with enhanced stability and functionality. This is particularly important in creating enzymes with improved catalytic properties.
  • Analytical Chemistry: It is also used in analytical methods to study protein interactions and modifications, providing insights into biological processes and aiding in the development of diagnostic tools.

Citations