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TCI

CAS 496-46-8

Glycoluril TCI G0243

Glycoluril TCI G0243

Chemical Identity

Other names
Acetyleneurea · Tetrahydroimidazo[4,5-d]imidazole-2,5(1H,3H)-dione
CAS No.
496-46-8
PubChem
CID 62347·SID 87570421
Formula
C4H6N4O2
Molecular weight
142.12 g/mol
Purity
>98.0%(N)
Reference databases
ChEBI·ChemSpider·ECHA·Wikipedia
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
1,3,3a,4,6,6a-hexahydroimidazo[4,5-d]imidazole-2,5-dione
SMILES
C12C(NC(=O)N1)NC(=O)N2
InChIKey
VPVSTMAPERLKKM-UHFFFAOYSA-N
MDL
MDL00005539
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Glycoluril is a chemical compound classified under the heterocyclic category, widely used in various laboratory reactions. It serves as a fundamental building block in organic chemistry, enabling the synthesis of complex molecules. Its unique molecular structure, consisting of two urea groups connected by a carbon chain, provides high reactivity under different conditions. This makes it a versatile compound for chemical transformations in both research and industrial settings. Glycoluril is particularly valuable in the development of heterocyclic compounds, which are essential in pharmaceutical and organic chemistry. Its role as a building block allows chemists to create a wide range of derivatives through specific chemical reactions.

Glycoluril is preferred due to its chemical stability under controlled conditions and its reactivity towards various reaction parameters such as temperature, catalysts, and solvents. These properties make it suitable for substitution reactions, hydrolysis, and condensation processes. Its ability to participate in multiple reaction types enhances its utility in synthetic chemistry. The compound’s versatility and predictable behavior in different reaction environments make it a reliable choice for researchers and students alike. Its stability ensures consistent results, while its reactivity allows for the exploration of diverse chemical pathways.

In Indonesian laboratories, Glycoluril is commonly used by researchers and students for organic chemistry experiments. It is an essential component in the synthesis of heterocyclic compounds, which are crucial in drug development and material science. Its availability and reliability make it a preferred choice for both academic and industrial applications. The compound’s role in supporting chemical innovation underscores its importance in the scientific community.

  • Organic synthesis is a key application where Glycoluril is used to create complex molecules due to its reactivity and structural versatility.
  • Pharmaceutical research benefits from Glycoluril as it is a building block for synthesizing heterocyclic compounds essential in drug development.
  • Analytical chemistry uses Glycoluril in various reactions to test and characterize chemical compounds under controlled conditions.
  • Teaching laboratories incorporate Glycoluril in experiments to demonstrate the principles of heterocyclic chemistry and synthetic pathways.
  • Industrial chemical processes rely on Glycoluril for the production of specialized materials due to its stability and reactivity in different environments.

Brand TCI
CAS number 496-46-8
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid
Storage Store in a cool, dry place away from moisture and direct sunlight

Glycoluril should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent moisture absorption, which could affect its reactivity. Due to its potential reactivity with certain solvents and catalysts, it should be handled in a well-ventilated area. Laboratory personnel should use appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Avoid exposure to high temperatures and direct sunlight to ensure long-term stability. Proper storage and handling are essential to maintain the compound's effectiveness and safety in laboratory settings.

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