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Description
TCI D1362 1,3-Dipropoxybenzene is an aromatic ether derived from resorcinol, in which both hydroxyl groups have been substituted with propyl chains. The compound belongs to the non-heterocyclic building block group — benzene ring-based construction materials whose functional groups are already protected as ethers. In the laboratory, molecules of this type serve as ready-to-use aromatic frameworks for constructing more complex derivatives, and equally as comparison compounds in studies examining how alkoxy chain length influences the physical properties, solubility, and reactivity of aromatic systems.
The principal properties that make this material a preferred choice are its symmetrical meta substitution pattern and its electron-donating propoxy groups. This combination activates the ring toward electrophilic substitution and directs reactions to predictable positions, so that synthetic planning becomes considerably more orderly. The ether functionality is also stable under many reaction conditions, allowing it to act as a protecting arrangement for the hydroxyl groups of resorcinol while transformations proceed. The reasonably long propyl chains add lipophilic character and alter solubility behaviour, an aspect that proves useful in both materials design and structure–property relationship studies.
In Indonesian laboratories, a reagent of this kind is typically handled within organic synthesis and materials chemistry work at university research groups, institutional laboratories, and industrial development units. It is generally drawn upon when a defined aromatic scaffold is required as a starting point rather than being prepared in-house, and when consistent, reproducible material is needed across repeated experiments. Its role is usually that of an intermediate or reference substance supporting a longer synthetic route.
Laboratory Applications
Organic synthesis intermediate — the pre-protected aromatic ring provides a defined starting scaffold, letting researchers build more complex derivatives without first carrying out separate protection steps on resorcinol.
Electrophilic aromatic substitution studies — the two electron-donating propoxy groups activate the ring and direct incoming electrophiles to predictable positions, giving clean and interpretable outcomes for methodology work.
Structure–property relationship investigations — serves as a defined comparison compound when examining how alkoxy chain length affects physical properties, solubility behaviour, and reactivity across a series of aromatic systems.
Protecting group chemistry — the ether linkages remain stable under many reaction conditions, so the compound illustrates and supports strategies where resorcinol hydroxyls must survive subsequent chemical transformations.
Materials chemistry development — the lipophilic character contributed by the propyl chains makes it useful where solubility behaviour must be tuned deliberately during the design of functional organic materials.
Specifications
Brand: TCI
CAS Number: 56106-37-7
Chemical name: 1,3-Dipropoxybenzene
Catalogue code: D1362
Category: Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Storage: refer to the manufacturer's label and accompanying safety data sheet for the recommended storage conditions and available pack sizes
Handling and Storage
Store the container tightly closed in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, ignition sources, and strong oxidising agents. Keep the material in its original manufacturer packaging or in a chemically compatible sealed glass container, clearly labelled and kept upright to prevent leakage. Handle the compound inside a fume hood while wearing appropriate personal protective equipment, including safety goggles, chemical-resistant gloves, and a laboratory coat. Avoid inhaling vapours and prevent contact with skin and eyes. Always consult the manufacturer's safety data sheet before use, and dispose of residues and contaminated materials in accordance with applicable laboratory chemical waste procedures.
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