• 2,2-Bis(bromomethyl)-1,3-propanediol (CAS 3296-90-0) - TCI D1808 - AMI Scientific
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TCI

CAS 3296-90-0

2,2-Bis(bromomethyl)-1,3-propanediol TCI D1808

2,2-Bis(bromomethyl)-1,3-propanediol TCI D1808
Rp 502.950,00
Rp 502.950,00
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2,2-Bis(bromomethyl)-1,3-propanediol is a chemical compound widely used as a building block in the synthesis of complex organic molecules. It plays a crucial role in various laboratory processes, particularly in the formation of heterocyclic compounds and long-chain structures. This compound is commonly employed in substitution reactions, coupling reactions, and electrophilic substitution reactions due to its reactivity and stability. Its versatility makes it an essential reagent in organic chemistry laboratories, supporting a wide range of synthetic pathways.

The compound’s chemical properties, including its non-polar nature and good solubility in organic solvents, make it a preferred choice for laboratory applications. Its controlled reactivity ensures predictable outcomes in chemical reactions, which is vital for reproducibility in research. The presence of two bromomethyl groups on the propanediol backbone allows for targeted substitution or coupling reactions, making it highly adaptable to different synthetic strategies. These characteristics contribute to its reliability and effectiveness in laboratory settings.

In Indonesian laboratories, 2,2-Bis(bromomethyl)-1,3-propanediol is frequently used in organic chemistry research, especially in the synthesis of synthetic compounds and chemical materials. Its stable chemical properties and controlled reactivity make it a trusted reagent for both academic and industrial research. It is commonly found in laboratories focused on developing new chemical products and conducting advanced organic synthesis experiments. Its utility in various reaction types ensures its continued relevance in chemical research in Indonesia.

  • Organic synthesis is a key application where this compound is used to build complex molecular structures through substitution and coupling reactions.
  • Heterocyclic compound formation benefits from its bromomethyl groups, enabling the creation of ring structures essential in pharmaceutical and industrial chemistry.
  • Coupling reactions rely on its reactivity to connect different molecular fragments, facilitating the synthesis of larger, more complex molecules.
  • Electrophilic substitution reactions utilize its bromomethyl groups as reactive sites, allowing for controlled modification of molecular structures.
  • Synthetic material development leverages its versatility in creating polymers and other chemical materials with specific functional properties.

Brand TCI
CAS number 3296-90-0
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Liquid
Storage Store in a cool, dry place away from light and incompatible materials

This compound should be stored in a cool, dry place, away from direct sunlight and sources of heat. It is recommended to keep it in a tightly sealed container to prevent exposure to air and moisture. Due to its brominated nature, it should be stored separately from strong oxidizing agents and incompatible chemicals. Proper ventilation is essential when handling the compound to minimize inhalation risks. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when working with this substance. Regular monitoring of storage conditions ensures the compound remains stable and safe for use in laboratory applications.

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