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CAS 76784-95-7

(1alpha,2alpha,4alpha)-1,2,4-Cyclohexanetricarboxylic Acid TCI C2062

(1alpha,2alpha,4alpha)-1,2,4-Cyclohexanetricarboxylic Acid TCI C2062
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Description

TCI C2062 is (1alpha,2alpha,4alpha)-1,2,4-Cyclohexanetricarboxylic Acid, an alicyclic tricarboxylic acid carrying three carboxyl groups on a cyclohexane framework at positions 1, 2, and 4, with a uniform spatial orientation on one face of the ring. In organic synthesis and materials science laboratories, this compound serves as a non-heterocyclic building block — a small starting material that carries several reactive points at once, allowing it to be developed into far larger molecules. Its three acid groups are readily converted into esters, amides, acid chlorides, or metal salts, making it an efficient point of departure for researchers constructing branched structures and cross-linked networks alike.

The characteristics that make this material a preferred choice are the combination of a saturated cyclohexane framework and a defined stereochemical arrangement. Unlike its aromatic analogues, the saturated aliphatic ring does not absorb ultraviolet light strongly and is more resistant to yellowing, so polymers or resins derived from it tend to retain optical clarity for longer. The (1alpha,2alpha,4alpha) stereochemical designation ensures that all three carboxyl groups point to the same face of the ring, giving a predictable and reproducible spatial geometry that is valuable whenever the shape of the resulting molecule governs its performance. Sourcing the material from TCI gives laboratories a consistent, well-characterised grade suitable for reproducible synthetic work.

In Indonesian laboratories, this building block is typically used in university and institutional research groups working on organic synthesis, polymer chemistry, and coordination chemistry, as well as in industrial R&D units developing coatings, resins, and specialty materials. It is generally handled at bench scale for method development and small-batch preparation, where a defined multi-functional starting material shortens synthetic routes and where consistent supply of a catalogued reference compound supports work that must be repeated and reported.

Laboratory Applications

  • Polyester and polyamide synthesis — its three carboxyl groups act as multiple condensation points, allowing researchers to introduce branching or cross-linking into a polymer backbone from a single well-defined monomer.
  • Coordination polymer and metal–organic framework studies — the carboxyl groups convert readily into metal salts and coordinate to metal centres, while the fixed stereochemistry gives predictable connectivity between nodes.
  • Optically clear coating and resin development — the saturated aliphatic ring resists ultraviolet absorption and yellowing, helping formulators produce cured films that keep their clarity over extended service periods.
  • Multi-step organic synthesis as a scaffold — chemists selectively derivatise the acid groups into esters, amides, or acid chlorides to build larger, structurally elaborate target molecules from a compact core.
  • Structure–property investigations in materials science — the defined (1alpha,2alpha,4alpha) geometry lets researchers correlate spatial arrangement of functional groups with the mechanical and optical behaviour of the resulting material.

Specifications

  • Brand: TCI (Tokyo Chemical Industry)
  • CAS Number: 76784-95-7
  • Product Code: C2062
  • Chemical Name: (1alpha,2alpha,4alpha)-1,2,4-Cyclohexanetricarboxylic Acid
  • Category: Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
  • Pack Sizes: Available in standard TCI research-scale packaging; please confirm the size options when ordering
  • Storage: Keep the container tightly closed in a cool, dry, well-ventilated place

Handling and Storage

Store the material in its original tightly closed container in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong bases and strong oxidising agents. Glass or chemically resistant containers with secure closures are suitable, and the container should be reclosed promptly after each use to limit moisture uptake. Handle the solid in a fume hood or a well-ventilated area, and weigh it carefully to avoid generating airborne dust. Laboratory personnel should wear safety goggles, chemical-resistant gloves, and a laboratory coat, and should avoid contact with skin and eyes as well as inhalation of dust. Wash hands thoroughly after handling. Always consult the manufacturer's Safety Data Sheet before use, and dispose of residues and contaminated materials in accordance with applicable institutional and local chemical waste regulations.

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