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Ac-Phe-Phe-OH; CAS 10030-31-6 is N-acetyl-L-phenylalanyl-L-phenylalanine, an N-capped aromatic dipeptide related to the widely studied diphenylalanine self-assembly motif.
N-acetylation changes terminal charge and intermolecular interaction patterns relative to free Phe-Phe, providing a defined derivative for aggregation, self-assembly and analytical comparison studies.
Product Information
| Product Name | Ac-Phe-Phe-OH |
| Catalog No. | AS4040 |
| CAS No. | 10030-31-6 |
| Molecular Formula | C20H22N2O4 |
| Molecular Weight | 354.41 g/mol |
| Sequence / Identity | Ac-Phe-Phe |
| Synonym | N-acetyl-L-phenylalanyl-L-phenylalanine |
| Primary Research Use | aromatic dipeptide aggregation/self-assembly model |
Aromatic Self-Assembly and Stereochemical Context
Phenylalanine side chains support π-interactions and hydrophobic packing, which is why diphenylalanine is widely used in supramolecular peptide research. Configuration and terminal capping can change packing, morphology and solubility; comparisons should therefore use matched concentration, solvent history and purity.
What Changes with Configuration or Terminal Capping?
Self-assembly is sensitive to molecular geometry, solvent, concentration and sample history. A stereoisomer or N-capped derivative should therefore be treated as a distinct experimental system rather than as an interchangeable version of L-Phe-L-Phe.
Procurement and QC Considerations
For research use, match the requested purity and documentation to the experiment. Analytical or quantitative studies benefit from lot-specific HPLC and MS data, while metabolomics or sequence-isomer work may require additional identity controls.
For identity and purity documentation, review our peptide QC methods for HPLC and mass-spectrometric characterization principles.
For broader sequence or project work, see analytical peptide references.
Analytical Fit and Sample Preparation
For comparative or quantitative work, review the lot-specific purity method together with identity data. Chromatographic purity is method-dependent and should be interpreted separately from molecular-mass confirmation or gravimetric vial content.
Solvent and working concentration should be validated for the intended assay. Solution history can influence small peptide models through aggregation, oxidation or concentration-dependent behavior even when the dry material meets its release specification.
Product Documents
The Safety Data Sheet provides product identification, laboratory handling guidance, exposure controls, transport information and safety information for research use.
Certificates of Analysis (COAs) are batch-specific. Please contact us to request the COA for your product, and we will provide it by email.
Frequently Asked Questions
What is Ac-Phe-Phe-OH?
It is N-acetyl-L-phenylalanyl-L-phenylalanine, a defined research compound with sequence or structural identity Ac-Phe-Phe.
What is the main value of this product?
Its main value is as a chemically defined reference for aromatic dipeptide aggregation/self-assembly model.
What should be checked before quantitative use?
Confirm lot-specific identity, purity basis and analytical documentation appropriate to the method.