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Catalog Number:
05763
CAS Number:
129223-22-9
Fmoc-Pro-Pro-OH
Purity:
≥ 98% (HPLC)
Documents
$95.00 /250MG
Pack Size Availability Price
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Product Information

Fmoc-Pro-Pro-OH is a versatile compound widely utilized in peptide synthesis and research applications. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability and ease of handling during the synthesis process. Its unique structure allows for selective deprotection, making it an ideal choice for the construction of complex peptides and proteins. Researchers often leverage Fmoc-Pro-Pro-OH in the development of peptide-based therapeutics, where precise amino acid sequences are crucial for biological activity.

In addition to its role in peptide synthesis, Fmoc-Pro-Pro-OH is also valuable in the study of protein folding and interactions, contributing to advancements in drug design and biomolecular research. Its compatibility with various coupling reagents and solid-phase synthesis techniques enhances its utility in laboratory settings. By incorporating Fmoc-Pro-Pro-OH into their workflows, researchers can streamline their peptide synthesis processes, ensuring high yields and purity in their final products.

CAS Number
129223-22-9
Purity
≥ 98% (HPLC)
Molecular Formula
C25H26N2O5
Molecular Weight
434.49
MDL Number
MFCD00237673
PubChem ID
20775119
Melting Point
188 - 190 ?C
Appearance
White to off-white powder
Optical Rotation
[a]20D = -62 ± 2 ° (C=1 in DMF)
Conditions
Store at 0 - 8 °C
General Information
CAS Number
129223-22-9
Purity
≥ 98% (HPLC)
Molecular Formula
C25H26N2O5
Molecular Weight
434.49
MDL Number
MFCD00237673
PubChem ID
20775119
Melting Point
188 - 190 ?C
Appearance
White to off-white powder
Optical Rotation
[a]20D = -62 ± 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-Pro-Pro-OH 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 coupling of amino acids while preventing unwanted reactions.
  • Drug Development: Its role in synthesizing peptide-based drugs is crucial, especially in designing therapeutics that target specific biological pathways.
  • Bioconjugation: The compound is used to create bioconjugates, enhancing the delivery of drugs or imaging agents to specific cells or tissues, which is particularly beneficial in cancer therapy.
  • Research in Neuroscience: It aids in the development of neuropeptides, which are vital for understanding neurological functions and disorders, thereby contributing to advancements in neuropharmacology.
  • Custom Peptide Libraries: Researchers utilize it to create diverse peptide libraries for high-throughput screening, facilitating the discovery of novel bioactive compounds.

Citations