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Catalog Number:
31699
CAS Number:
864876-91-5
Fmoc-L-Ile-O-CH2-Ph-OCH2-CH2-COOH
Purity:
≥ 98% (HPLC)
Documents
$43.87 /1G
Pack Size Availability Price
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Product Information

Fmoc-L-Ile-O-CH2-Ph-OCH2-CH2-COOH is a versatile compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during solid-phase peptide synthesis. Its unique structure, which includes a phenoxy and a propanoic acid moiety, enhances its solubility and stability, making it particularly valuable in the formulation of complex peptides and pharmaceuticals. Researchers and industry professionals appreciate its ability to facilitate the synthesis of bioactive peptides, which are crucial in therapeutic applications, including cancer treatment and hormone regulation.

In addition to its role in peptide synthesis, Fmoc-L-Ile-O-CH2-Ph-OCH2-CH2-COOH is also explored for its potential in drug delivery systems due to its favorable physicochemical properties. Its compatibility with various solvents and reagents allows for flexibility in experimental design, making it an ideal choice for researchers aiming to develop innovative therapeutic strategies. The compound's ability to enhance the stability and efficacy of peptide-based drugs positions it as a key player in the pharmaceutical industry, paving the way for advancements in targeted therapies.

CAS Number
864876-91-5
Purity
≥ 98% (HPLC)
Molecular Formula
C31H33NO7
Molecular Weight
531.61
MDL Number
MFCD08457848
PubChem ID
155892341
Appearance
Slightly yellow powder
Optical Rotation
[a]20D = -13 ± 2 ° (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
864876-91-5
Purity
≥ 98% (HPLC)
Molecular Formula
C31H33NO7
Molecular Weight
531.61
MDL Number
MFCD08457848
PubChem ID
155892341
Appearance
Slightly yellow powder
Optical Rotation
[a]20D = -13 ± 2 ° (C=1 in DMF)
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-L-Ile-O-CH2-Ph-OCH2-CH2-COOH is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective formation of peptide bonds while preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in the development of drugs targeting specific biological pathways.
  • Bioconjugation: The compound can be used to create bioconjugates, enhancing the delivery of drugs or imaging agents to specific cells or tissues, which is vital in targeted therapy.
  • Research in Cancer Therapy: Its application in creating peptide derivatives can lead to the development of novel anticancer agents, improving treatment efficacy while minimizing side effects.
  • Material Science: This chemical can be incorporated into polymer systems for creating smart materials that respond to environmental stimuli, useful in various industrial applications.

Citations