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TCI

CAS 77-85-0

Trimethylolethane TCI T0479

Trimethylolethane TCI T0479

Chemical Identity

CAS No.
77-85-0
PubChem
CID 6502·SID 87576420
Formula
C5H12O3
Molecular weight
120.15 g/mol
Purity
>98.0%(GC)
Reference databases
ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
2-(hydroxymethyl)-2-methylpropane-1,3-diol
SMILES
CC(CO)(CO)CO
InChIKey
QXJQHYBHAIHNGG-UHFFFAOYSA-N
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Trimethylolethane (TCI T0479), with CAS number 77-85-0, is a versatile chemical compound widely used in laboratory settings for its ability to participate in various synthetic reactions. As a non-heterocyclic building block, it serves as a foundational material in the creation of complex organic molecules. Its molecular structure, featuring three methyl groups and one hydroxyl group, allows for multiple functionalization pathways, making it a valuable tool in chemical synthesis. This compound is commonly found in organic chemistry laboratories where researchers aim to develop new materials or compounds through controlled chemical reactions.

One of the key reasons Trimethylolethane is preferred in laboratory applications is its reactivity and compatibility with a wide range of chemical environments. It exhibits good solubility in organic solvents such as ethyl acetate and methanol, which facilitates its use in solution-based reactions. Additionally, its chemical stability under controlled conditions ensures consistent results in experimental processes. These properties make it an ideal candidate for use in both academic and industrial research settings, where precision and reliability are essential.

In Indonesian laboratories, Trimethylolethane is frequently utilized in the synthesis of polymers, esters, and heterocyclic compounds. Its ability to undergo various chemical transformations makes it a go-to material for chemists working on complex molecular structures. The compound's availability and reliability have made it a staple in many research facilities across Indonesia, supporting a wide range of chemical investigations and innovations.

TCI brochures (PDF)

  • Polymer synthesis where Trimethylolethane acts as a multifunctional monomer due to its three hydroxyl groups, enabling cross-linking and chain extension.
  • Esterification reactions where the hydroxyl groups can be converted into ester functionalities through acid-catalyzed processes.
  • Organic synthesis of heterocyclic compounds due to its ability to participate in condensation and substitution reactions.
  • Cross-linking agents in the development of thermosetting resins because of its multiple reactive hydroxyl groups.
  • Structural modification of existing molecules to create new derivatives through various chemical transformations.

Brand TCI
CAS number 77-85-0
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various sizes as per supplier specifications
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight and incompatible materials

Trimethylolethane should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in tightly sealed containers made of materials compatible with organic solvents, such as glass or high-density polyethylene. Due to its reactivity, it should be stored away from strong oxidizing agents and heat sources. In laboratory settings, proper ventilation is essential to minimize exposure to vapors. Always use appropriate personal protective equipment when handling this compound to ensure safety and compliance with standard laboratory protocols.

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