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HS Code |
926790 |
| Product Name | Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid |
| Cas Number | 134385-68-9 |
| Molecular Formula | C24H20BrNO4 |
| Molecular Weight | 466.33 |
| Appearance | White to off-white powder |
| Purity | ≥98% |
| Solubility | DMSO, DMF, Methanol |
| Optical Purity | (R)-enantiomer |
| Protecting Group | Fmoc (Fluorenylmethyloxycarbonyl) |
| Storage Temperature | 2-8°C |
| Synonyms | N-Fmoc-(R)-4-bromo-homoalanine |
| Application | Peptide synthesis |
| Functional Group | Amino acid derivative |
| Smiles | C1=CC=C2C(=C1)C=CC3=C2C=CC=C3C(=O)OCC(C(N)CC1=CC=C(C=C1)Br)=O |
As an accredited Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White powder, sealed in an amber glass vial, labeled "Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid, 1g," with hazard and handling instructions. |
| Shipping | Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid is shipped in sealed, chemical-resistant containers to ensure stability and prevent contamination. The package is labeled according to regulatory guidelines and delivered at room temperature unless otherwise specified. Standard shipping is available worldwide, with expedited and temperature-controlled options upon request. |
| Storage | Store Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid in a tightly sealed container, protected from light and moisture. Keep at 2-8°C (refrigerator) in a cool, dry, and well-ventilated area. Avoid exposure to incompatible substances such as strong acids or bases. Make sure to clearly label the container and follow appropriate safety and handling practices. |
Applications of Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid in Industrial ManufacturingFmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid serves as a key chiral intermediate in industrial peptide synthesis and specialized organic chemistry. As the original producer, we apply validated methods to supply this compound for demanding synthesis routes across regulated industrial sectors. Below, we present precise, real-world downstream applications where this intermediate adds direct manufacturing value, with documented compliance, established dosage guidance, process context, and typical finished products. 1. Pharmaceutical Peptide Active Pharmaceutical Ingredient (API) SynthesisThis compound offers a critical enantiopure building block for the industrial synthesis of complex peptides, supporting the development of pharmaceutical APIs targeting therapeutic indications that require non-canonical amino acid incorporation. Manufacturing protocols use it in solid-phase peptide synthesis (SPPS) to introduce functionalized β-amino acid motifs, often in late-stage platform manufacturing for oncology and metabolic disorder drugs. Industry compliance standards
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2. Custom Peptide Reagents for Diagnostic Kit ProductionDiagnostic kit manufacturers require highly pure, sequence-defined peptides containing chiral β-amino acids to enhance specificity and accuracy in immunoassays. Our material supports custom peptide synthesis for MRM standards, peptide calibrators, and in vitro diagnostic reagents. Compliance relies on traceable batch production and validated impurity control, as demanded by quality-focused downstream users in clinical and laboratory assay supply. Industry compliance standards
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3. Chiral Ligand Precursor for Asymmetric Catalysis ManufacturingThis amino acid analog is a favored chiral precursor in specialty ligand synthesis for asymmetric catalysis processes. It allows catalyst developers to introduce precise stereochemical control elements critical for pharmaceutical and fine chemical production. Manufacturing partners scale up its use within ligand functionalization toolkits, following established catalyst technology protocols and real process validation steps. Industry compliance standards
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4. Specialty Chemical for High-Value Fine Chemical SynthesisIn the fine chemicals sector, advanced β-amino acid derivatives enable the creation of functionalized organic intermediates with defined halogen patterns. Fmoc-(R)-3-Amino-3-(4-Bromo-Phenyl)-Propionic Acid delivers site-specific bromination and stereochemistry, making it suitable for downstream brominated building block production in specialty polymer, agrochemical, and advanced material manufacturing flows. Process engineers optimize its use to maximize yield and stereopurity in challenging multi-step organic syntheses. Industry compliance standards
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Tel: +8615371019725
Email: admin@sinochem-nanjing.com
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