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CAS 1579-40-4

Di-p-tolyl Ether TCI D2178

Di-p-tolyl Ether TCI D2178
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Di-p-tolyl Ether from TCI is a symmetrical diaryl ether compound consisting of two methyl-substituted aromatic rings joined by a single oxygen atom. This simple yet stable structure makes it a useful building block and model compound in organic chemistry and materials chemistry laboratories. Researchers employ it as a starting material for aromatic substitution reactions, as a reference compound in studies of aryl ether bonding, and as a model component for investigating the thermal behaviour and stability of oxygen-bridged aromatic systems. Its well-defined structure supports reproducible experimental work across synthetic and analytical settings.

The characteristics that make this compound a preferred choice begin with the high stability of its aryl ether linkage toward heat and ordinary reaction conditions, allowing the molecule to survive reasonably harsh reaction steps without decomposing. The two methyl groups in the para positions provide additional reactive sites for oxidation, benzylic halogenation, or further functionalisation, while the molecular symmetry simplifies the interpretation of spectroscopic data. Its solid form at room temperature makes weighing and storage straightforward, and its good solubility in non-polar to semi-polar organic solvents supports both solvent-based reactions and physical property studies.

In Indonesian laboratories, Di-p-tolyl Ether is typically used in university and institutional research settings where organic synthesis and materials characterisation work is carried out. It serves teaching and research groups that require a dependable diaryl ether reference for method development, spectroscopic training, and small-scale synthetic sequences. Because the material is a stable solid, it suits laboratories that handle chemicals across varied storage environments and need compounds that remain reliable between experimental campaigns.

  • Aromatic substitution synthesis — the intact aryl ether core withstands reaction conditions while the activated rings provide predictable positions for electrophilic functionalisation in multi-step organic sequences.
  • Aryl ether bonding studies — its symmetrical, unambiguous structure makes it a clean reference compound for examining how the diaryl ether linkage behaves chemically and spectroscopically.
  • Thermal stability investigations — the compound serves as a model for oxygen-bridged aromatic systems, allowing researchers to study decomposition behaviour under elevated temperature conditions.
  • Benzylic functionalisation work — the two para methyl groups offer accessible sites for oxidation or halogenation, giving chemists a convenient handle for building more elaborate molecules.
  • Spectroscopic method development — molecular symmetry reduces the number of distinct signals, so the compound is well suited to calibrating and teaching NMR and infrared interpretation techniques.

Brand TCI
CAS number 1579-40-4
Molecular formula
Purity
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory research pack sizes; please confirm the current options when ordering
Physical form Solid at room temperature
Storage Keep in a tightly closed container in a cool, dry, well-ventilated place
  • Product Code: D2178

Store Di-p-tolyl Ether in its original tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and strong oxidising agents. Amber glass or the supplier's original packaging is suitable for maintaining material integrity, and containers should be resealed promptly after each use to limit moisture uptake and contamination. Handle the solid inside a fume hood or a well-ventilated workspace, using a laboratory coat, chemical-resistant gloves, and safety glasses. Avoid generating dust during weighing and transfer, keep the working area clean, and wash hands thoroughly after handling. Always consult the manufacturer's safety data sheet before use and follow institutional waste disposal procedures for organic chemical residues.