
4-Benzyloxy-2-nitrophenol | CAS 96315-18-3
| Catalog Number | A14-0135 |
| Category | Calcium, Chloride and Other indicators |
| Molecular Formula | C13H11NO4 |
| Molecular Weight | 245.234 |
* Please be kindly noted products are not for therapeutic use. We do not sell to patients.
Product Introduction
4-Benzyloxy-2-nitrophenol is an aromatic compound featuring a nitrophenol core with a benzyloxy substituent, contributing to its potential applications in fluorescence and biochemical labeling. The presence of the nitro group can influence its electronic properties, potentially affecting its absorption and emission characteristics, making it a candidate for further exploration in spectroscopic studies. This compound may serve as a precursor in the synthesis of more complex fluorescent probes or quenchers, where its structural attributes could be leveraged for specific conjugation or labeling strategies.
Chemical Information
Application
Chemical Information
| Synonyms | 4-(Benzyloxy)-2-nitrophenol |
| SMILES | C1=CC=C(C=C1)COC2=CC(=C(C=C2)O)[N+](=O)[O-] |
| InChI | InChI=1S/C13H11NO4/c15-13-7-6-11(8-12(13)14(16)17)18-9-10-4-2-1-3-5-10/h1-8,15H,9H2 |
| InChIKey | VRYYLYCOPKQGPS-UHFFFAOYSA-N |
| Appearance | Solid Powder |
Application
4-Benzyloxy-2-nitrophenol is an aromatic nitro-phenol derivative used in fluorescence and photochemical workflow development where nitro-activated phenolic structures serve as reactive or quenching components in dye-adjacent systems. Its phenolic oxygen and nitro substituent enable incorporation into staining chemistries, polymer or surface formulations, and probe-building strategies that rely on controlled fluorescence attenuation or photoresponsive behavior. In practice, researchers employ it as a functional small-molecule component for constructing fluorescent readouts, tuning background, or preparing labeled materials for microscopy and spectroscopy-based assays.
1. Fluorescence Quenching Systems
4-Benzyloxy-2-nitrophenol is used as a quenching component in fluorescence assay development where suppression of dye emission is required to improve interpretability of signal readouts. In dye-based screening workflows, it can be incorporated into experimental formulations to reduce unwanted fluorescence background from fluorescent labels, conjugates, or polymer matrices, supporting more stable plate-based measurements and cleaner endpoint discrimination. Researchers in chemical biology and materials analytics often pair it with established fluorophores in solution or immobilized formats to evaluate how emission intensity changes under defined chemical environments.
2. Dye-Adjacent Probe Building
4-Benzyloxy-2-nitrophenol serves as a small-molecule building block for constructing dye-adjacent reagents used in fluorescence probe development and molecular imaging reagent optimization. Teams developing fluorescence-based detection tools use it to introduce a nitro-phenolic motif into probe scaffolds or linker regions that are positioned to modulate fluorescence output in the presence of specific assay conditions. This makes it relevant to research efforts that require tunable fluorescence response behavior in conjugate libraries, including probe candidates for microscopy visualization and spectroscopic monitoring.
3. Polymer And Surface Formulation
4-Benzyloxy-2-nitrophenol is incorporated into polymer and surface functionalization studies where aromatic nitro-phenol functionalities are used to create fluorescently responsive or fluorescence-suppressing material interfaces. Materials scientists use it to prepare coated films, blended polymer layers, or surface-modified substrates that interact with fluorescent labels during imaging or optical readout experiments. Such formulations are commonly explored for developing materials with controlled optical background, for studying dye-material interactions, and for engineering test platforms used in fluorescence microscopy and spectroscopy.
4. Photoactive Staining Chemistry
4-Benzyloxy-2-nitrophenol is applied in photochemical staining and light-controlled labeling research where nitro-activated phenolic motifs are leveraged as functional components in staining chemistries. Researchers use it to explore how photoinduced or condition-dependent changes in aromatic nitro-phenol structures influence the fluorescence behavior of co-formulated dyes or labeled targets in microscopy experiments. This supports assay development efforts that require controllable optical contrast in imaging workflows, particularly in studies focused on illumination-dependent signal modulation rather than purely static labeling.
Recommended Services
Recommended Articles
- Hoechst Dyes: Definition, Structure, Mechanism and Applications
- Mastering the Spectrum: A Comprehensive Guide to Cy3 and Cy5 Dyes
- Fluorescent Probes: Definition, Structure, Types and Application
- Fluorescent Dyes: Definition, Mechanism, Types and Application
- Coumarin Dyes: Definition, Structure, Benefits, Synthesis and Uses
- Unlocking the Power of Fluorescence Imaging: A Comprehensive Guide
- Cell Imaging: Definitions, Systems, Protocols, Dyes, and Applications
- Lipid Staining: Definition, Principles, Methods, Dyes, and Uses
- Flow Cytometry: Definition, Principles, Protocols, Dyes, and Uses
- Nucleic Acid Staining: Definition, Principles, Dyes, Procedures, and Uses
Recommended Products
Online Inquiry