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Catalog Number:
33499
CAS Number:
2250436-45-2
Nα -Fmoc- Nε -4-methoxyltrityl-aminooxyacetyl-L-lysine
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-L-Lys(Mtt-Aoa)-OH
Documents
$161.64 /100MG
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Product Information

Na -Fmoc- Ne -4-methoxyltrityl-aminooxyacetyl-L-lysine is a versatile amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued for its protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which facilitates the selective deprotection of amino acids during solid-phase peptide synthesis. Its unique structure, featuring a methoxyltrityl group, enhances stability and solubility, making it an excellent choice for researchers focused on developing complex peptides and biologically active compounds.

In pharmaceutical research, Na -Fmoc- Ne -4-methoxyltrityl-aminooxyacetyl-L-lysine is utilized for the synthesis of peptide-based therapeutics, particularly those targeting specific biological pathways. Its ability to incorporate into peptide chains while maintaining functional integrity allows for the design of innovative drug candidates. Additionally, its application in the development of prodrugs and targeted delivery systems highlights its potential in advancing therapeutic efficacy. Researchers and industry professionals will find this compound indispensable for enhancing the efficiency and specificity of their peptide synthesis processes.

Synonyms
Fmoc-L-Lys(Mtt-Aoa)-OH
CAS Number
2250436-45-2
Purity
≥ 97% (HPLC)
Molecular Formula
C43H43N3O6
Molecular Weight
697.8
MDL Number
MFCD31380722
PubChem ID
155885830
Melting Point
67 - 73 °C
Appearance
White amorphous powder
Optical Rotation
[a]20D = -8 ± 1 ° (C=1 in DMF)
Conditions
Store at 2-8 °C
General Information
Synonyms
Fmoc-L-Lys(Mtt-Aoa)-OH
CAS Number
2250436-45-2
Purity
≥ 97% (HPLC)
Molecular Formula
C43H43N3O6
Molecular Weight
697.8
MDL Number
MFCD31380722
PubChem ID
155885830
Melting Point
67 - 73 °C
Appearance
White amorphous powder
Optical Rotation
[a]20D = -8 ± 1 ° (C=1 in DMF)
Conditions
Store at 2-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Na -Fmoc- Ne -4-methoxyltrityl-aminooxyacetyl-L-lysine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing researchers to selectively modify amino acids without interfering with other functional groups. This is particularly beneficial in creating complex peptides for pharmaceuticals.
  • Drug Development: Its unique structure aids in the development of targeted drug delivery systems, enhancing the efficacy of therapeutic agents while minimizing side effects, making it valuable in the pharmaceutical industry.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and diagnostic tools.
  • Research in Cancer Therapy: Researchers are exploring its potential in cancer therapy, as it can be used to create compounds that selectively target cancer cells, improving treatment outcomes.
  • Materials Science: It finds applications in materials science for creating functionalized polymers that can be used in drug delivery systems or as scaffolds in tissue engineering, showcasing its versatility in various fields.

Citations