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Cyclopentanecarboxylic Acid, 1-[[(9H-Fluoren-9-Ylmethoxy)Carbonyl]Amino]-3-Hydroxy- (9Ci) CAS NO 369403-17-8
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CAS No.:369403-17-8
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Cyclopentanecarboxylic Acid, 1-[[(9H-Fluoren-9-Ylmethoxy)Carbonyl]Amino]-3-Hydroxy- (9Ci) is a specialized Fmoc-protected amino acid derivative, a critical building block in modern solid-phase peptide synthesis (SPPS). Its value lies in enabling the precise and efficient construction of complex peptide sequences, particularly those requiring the incorporation of a cyclopentane ring and a hydroxyl group for structural diversity and bioactivity. This high-purity intermediate is essential for research and development in pharmaceutical discovery, biotechnology, and advanced materials science, where it is used to create novel therapeutic peptides, peptidomimetics, and bioactive probes.
Application
- Solid-Phase Peptide Synthesis (SPPS): A key protected amino acid for the automated, sequential assembly of custom peptide chains in pharmaceutical R&D.
- Pharmaceutical Intermediate: Serves as a crucial building block in the synthesis of novel peptide-based drug candidates and active pharmaceutical ingredients (APIs).
- Peptidomimetic Design: Used to create non-natural peptide analogs where the cyclopentane ring introduces conformational constraints to enhance stability, potency, and selectivity.
- Bioconjugation & Probe Development: Facilitates the site-specific introduction of functional handles into peptides for labeling, imaging, or creating peptide-drug conjugates.
- Academic & Industrial Research: A vital reagent for studying protein-protein interactions, enzyme substrates/inhibitors, and structure-activity relationships (SAR) in life sciences.
- Combinatorial Chemistry Libraries: Employed to generate diverse libraries of cyclic and constrained peptides for high-throughput screening in drug discovery.
Basic Information
| Item | Details |
|---|---|
| Product Name | Cyclopentanecarboxylic Acid, 1-[[(9H-Fluoren-9-Ylmethoxy)Carbonyl]Amino]-3-Hydroxy- (9Ci) |
| CAS No. | 369403-17-8 |
| Molecular Formula | C21H21NO5 |
| Molecular Weight | 367.40 g/mol |
| Synonyms | Fmoc-3-Hydroxy-cyclopentanecarboxylic acid; Fmoc-Cpa(3-OH)-OH; 1-(Fmoc-amino)-3-hydroxycyclopentanecarboxylic acid; (1S,3S)-1-[[(9H-Fluoren-9-ylmethoxy)carbonyl]amino]-3-hydroxycyclopentanecarboxylic acid; Fmoc-3-hydroxy-1-aminocyclopentanecarboxylic acid; N-α-Fmoc-3-hydroxycyclopentylglycine; Protected amino acid 369403-17-8 |
| EINECS | Contact for details |
Quality Control
Our Cyclopentanecarboxylic Acid, 1-[[(9H-Fluoren-9-Ylmethoxy)Carbonyl]Amino]-3-Hydroxy- (9Ci) is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity suitable for sensitive synthetic applications. Each lot undergoes rigorous analytical testing, including HPLC for purity and chiral integrity, NMR for structural confirmation, and mass spectrometry. A comprehensive Certificate of Analysis (COA) detailing all specifications is provided with every shipment to support your quality assurance and regulatory documentation needs.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry place at 2-8°C (refrigerated) or as specified on the label. This compound is hygroscopic (moisture-sensitive); ensure the container is sealed under inert atmosphere (argon or nitrogen) after each use to maintain stability and prevent degradation. Keep away from heat and incompatible materials.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Identification (HPLC) | Retention time matches reference standard |
| Purity (HPLC) | ≥ 98.0% |
| Chiral Purity (Chiral HPLC) | ≥ 99.0% ee (specify isomer) |
| Water Content (KF) | ≤ 0.5% |
| Heavy Metals | ≤ 10 ppm |
| Residual Solvents (GC) | Complies with ICH guidelines |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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