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Catalog Number:
03697
CAS Number:
210532-98-2
Fmoc-S-[2,3-bis(palmitoyloxy)propyl]-L-cysteine
Purity:
≥ 96% (HPLC)
Synonym(s):
Fmoc-Dhc(Pam)2-OH
Documents
$90.60 /25MG
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Product Information

Fmoc-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 effectiveness in solid-phase peptide synthesis. The palmitoyloxy groups enhance the hydrophobicity of the molecule, making it particularly useful in the development of lipid-based drug delivery systems and membrane protein studies. Researchers appreciate its ability to facilitate the formation of stable peptide bonds while maintaining the integrity of sensitive functional groups.

In practical applications, this compound is utilized in the synthesis of bioactive peptides and as a building block for creating novel therapeutic agents. Its unique structure allows for improved solubility and stability in biological environments, which is essential for drug formulation and delivery. Additionally, the incorporation of palmitoyloxy groups can enhance cellular uptake, making it a valuable tool in pharmaceutical research and development. Overall, Fmoc-S-[2,3-bis(palmitoyloxy)propyl]-L-cysteine stands out for its versatility and effectiveness in advancing peptide chemistry and drug design.

Synonyms
Fmoc-Dhc(Pam)2-OH
CAS Number
210532-98-2
Purity
≥ 96% (HPLC)
Molecular Formula
C53H83NO8S
Molecular Weight
894.31
MDL Number
MFCD00153354
PubChem ID
23505305
Melting Point
77 - 82 °C (Lit.)
Appearance
White to off-white powder
Optical Rotation
[a]20D = 13 ± 1 ° (C=0.55 in CHCl3) (Lit.)
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-Dhc(Pam)2-OH
CAS Number
210532-98-2
Purity
≥ 96% (HPLC)
Molecular Formula
C53H83NO8S
Molecular Weight
894.31
MDL Number
MFCD00153354
PubChem ID
23505305
Melting Point
77 - 82 °C (Lit.)
Appearance
White to off-white powder
Optical Rotation
[a]20D = 13 ± 1 ° (C=0.55 in CHCl3) (Lit.)
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

Fmoc-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 for the creation of complex and functional peptides.
  • Drug Delivery Systems: Its unique structure enhances the formulation of drug delivery systems, improving the solubility and bioavailability of therapeutic agents, especially in targeted therapies.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in developing biosensors and diagnostic tools.
  • Nanotechnology: In nanotechnology, it plays a role in the fabrication of lipid-based nanoparticles, which can encapsulate drugs and improve their delivery to specific cells or tissues.
  • Cosmetic Formulations: Its properties are leveraged in cosmetic formulations to enhance skin penetration and stability of active ingredients, making it valuable in the beauty and personal care industry.

Citations