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Catalog Number:
35212
CAS Number:
139573-78-7
Fmoc-S-[(S-2,3-bis(palmitoyloxy)propyl]-L-cysteine
Purity:
≥ 96% (HPLC)
Synonym(s):
Fmoc-(SPam2Cys-OH, Fmoc-Cys((S-2,3-di(palmitoyloxy)-propyl)-OH
Documents
$93.14 /25MG
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Product Information

Fmoc-S-[(S)-2,3-bis(palmitoyloxy)propyl]-L-cysteine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and bioconjugation applications. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely recognized for its stability and ease of removal under mild conditions, making it an excellent choice for solid-phase peptide synthesis. The palmitoyloxy groups enhance its hydrophobic properties, allowing for better integration into lipid membranes, which is particularly beneficial in drug delivery systems and membrane protein studies.

Researchers and industry professionals can leverage this compound in the development of novel therapeutics, particularly in the fields of cancer research and immunology, where targeted delivery of peptides is essential. Its unique structure not only facilitates the synthesis of complex peptides but also improves their stability and bioavailability. With its versatile applications in both academic and industrial settings, Fmoc-S-[(S)-2,3-bis(palmitoyloxy)propyl]-L-cysteine stands out as a valuable tool for advancing peptide-based research and development.

Synonyms
Fmoc-(SPam2Cys-OH, Fmoc-Cys((S-2,3-di(palmitoyloxy)-propyl)-OH
CAS Number
139573-78-7
Purity
≥ 96% (HPLC)
Molecular Formula
C53H83NO8S
Molecular Weight
894.31
MDL Number
MFCD00269874
PubChem ID
23505305
Melting Point
76 - 80 ?C
Appearance
Off-white powder
Optical Rotation
[a]20D = 10 ± 1 ° (C= 0.55 in CHCl3)
Conditions
Store at ≤ -20 °C
General Information
Synonyms
Fmoc-(SPam2Cys-OH, Fmoc-Cys((S-2,3-di(palmitoyloxy)-propyl)-OH
CAS Number
139573-78-7
Purity
≥ 96% (HPLC)
Molecular Formula
C53H83NO8S
Molecular Weight
894.31
MDL Number
MFCD00269874
PubChem ID
23505305
Melting Point
76 - 80 ?C
Appearance
Off-white powder
Optical Rotation
[a]20D = 10 ± 1 ° (C= 0.55 in CHCl3)
Conditions
Store at ≤ -20 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-S-[(S)-2,3-bis(palmitoyloxy)propyl]-L-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing researchers to create complex peptide sequences efficiently.
  • Drug Delivery Systems: Its unique structure enables the development of liposomal formulations, improving the delivery of therapeutic agents in targeted drug delivery applications, especially in cancer therapy.
  • Bioconjugation: The chemical is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, enhancing the functionality of biosensors and diagnostic tools.
  • Cosmetic Formulations: With its palmitoyloxy groups, it can be incorporated into cosmetic products to improve skin penetration and moisturization, appealing to the beauty and personal care industry.
  • Research in Cell Biology: This compound is valuable in cell culture studies, where it can be used to modify cell membranes, aiding in the investigation of cellular processes and interactions.

Citations