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TCI

CAS 15383-49-0

1,2,4,5-Cyclohexanetetracarboxylic Acid TCI C2198

1,2,4,5-Cyclohexanetetracarboxylic Acid TCI C2198
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Description

1,2,4,5-Cyclohexanetetracarboxylic Acid is an alicyclic tetracarboxylic acid that carries four carboxyl groups on a saturated cyclohexane ring. This high density of functional groups makes it a valuable building block for the preparation of cross-linked polymers, particularly aliphatic polyimides, as well as a multivalent linker in coordination chemistry. In the laboratory it is frequently used as a precursor to cycloaliphatic dianhydrides and as a monomer that contributes structural rigidity without introducing aromatic groups that absorb visible light.

The property most often behind its selection is its ability to yield transparent materials with good thermal stability. Polyimides built from a cycloaliphatic backbone of this kind are generally clearer and less prone to yellowing than conventional aromatic polyimides, which makes them attractive for research on optical films and flexible electronic substrates. Having four carboxyl groups at once also provides numerous coordination points for metal ions, allowing stable three-dimensional networks to be assembled from a single, well-defined ligand.

Its solid form makes precise weighing straightforward, and the lot-to-lot quality consistency associated with TCI helps researchers reproduce formulations reliably. In Indonesian laboratories this material fits naturally into university and institutional research programmes working on polymer synthesis, materials chemistry, and coordination chemistry, where a defined building block supports repeatable preparations. Its solid presentation also simplifies handling, storage, and portioning across successive experiments in shared laboratory settings.

Laboratory Applications

  • Aliphatic polyimide synthesis: the four carboxyl groups on a saturated ring supply the functionality needed for imide formation while avoiding aromatic absorption in the visible region.
  • Cycloaliphatic dianhydride preparation: the compound serves as a direct precursor, with its carboxyl pairs positioned for conversion into the anhydride functionality required by downstream monomer chemistry.
  • Cross-linked polymer research: the high density of reactive carboxyl groups allows a single molecule to connect several polymer chains, building network structures from a defined starting material.
  • Coordination chemistry and network assembly: four carboxyl groups give many coordination points for metal ions, enabling the construction of stable three-dimensional frameworks in the laboratory.
  • Optical film and flexible substrate studies: cycloaliphatic-derived polyimides are typically clearer and resist yellowing better than aromatic analogues, supporting transparent film and electronic substrate investigations.

Specifications

  • Brand: TCI
  • Product code: C2198
  • CAS number: 15383-49-0
  • Category: Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
  • Physical form: solid, allowing precise weighing
  • Pack sizes: available in the pack sizes offered by TCI for this catalogue item
  • Storage: keep in the original tightly closed container in a cool, dry place

Handling and Storage

Store the material in its original, tightly closed container in a cool, dry, and well-ventilated area, away from moisture and incompatible substances. Glass or other chemically resistant containers with secure closures are appropriate, and containers should be reclosed promptly after each portion is weighed to limit exposure to atmospheric humidity. Handle the solid in a fume hood or a well-ventilated workspace, wearing safety glasses, gloves, and a laboratory coat, and avoid generating or inhaling dust. Use clean, dry spatulas to prevent contamination between lots, label all secondary containers clearly, and consult the manufacturer's safety data sheet before first use.

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