2,3-Dibromopropyl Acrylate TCI A0910

Chemical Identity

CAS No.: 19660-16-3
PubChem: CID 29728·SID 87562419
Formula: C6H8Br2O2
Molecular weight: 271.93 g/mol
Purity: >85.0%(GC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2,3-dibromopropyl prop-2-enoate
SMILES: C=CC(=O)OCC(CBr)Br
InChIKey: MUKJDVAYJDKPAG-UHFFFAOYSA-N

Rp 6.253.800,00

~~Rp 4.373.250,00~~ Rp 6.253.800,00

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2,3-Dibromopropyl Acrylate is a chemical compound widely used in laboratory settings for its versatile applications in chemical experimentation and material science. As a monomer, it contains an acrylate group, which is essential for polymerization processes, enabling the formation of various polymers. This compound plays a crucial role in organic synthesis, particularly in polymerization and polymer modification reactions. Its reactivity makes it a valuable reagent in the development of composite materials and specialized chemical substances.

The compound's unique structure, featuring bromine atoms at the 2 and 3 positions of the propyl chain, contributes to its high reactivity. These bromine groups enhance its ability to participate in substitution and polymerization reactions, making it a preferred choice for chemists. Its liquid form and distinct odor also make it easy to handle and incorporate into experimental protocols. The chemical's reactivity and versatility support its use in a wide range of laboratory applications.

In Indonesian laboratories, 2,3-Dibromopropyl Acrylate is frequently utilized in material research, organic chemistry, and polymer technology. Its availability in liquid form and ease of use make it a popular choice for researchers working on polymer synthesis and modification. The compound's properties align well with the needs of modern chemical laboratories, supporting both academic and industrial research activities.

TCI brochures (PDF)

Monomers 2025-05-28 · p. 3

Related TCI products

Polymer synthesis and modification due to its acrylate group and reactivity for cross-linking and chain extension.
Organic chemistry research for substitution reactions and functional group transformations.
Composite material development because of its ability to form reactive intermediates with other monomers.
Specialty chemical production where brominated acrylates are required for specific functional properties.
Material science experiments involving polymerization processes and polymer characterization techniques.

Brand	TCI
CAS number	19660-16-3
Molecular formula	—
Purity	—
Category	Materials Science > Polymer/Macromolecule Reagents > Monomers
Pack sizes	Available in standard laboratory quantities
Physical form	Liquid
Storage	Store in a cool, dark place away from heat and direct sunlight

2,3-Dibromopropyl Acrylate should be stored in a cool, dark location, away from heat and direct sunlight to maintain its chemical integrity. It is recommended to use sealed, airtight containers to prevent exposure to moisture and air, which can affect its stability. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment such as gloves and goggles should be worn. Avoid contact with skin and eyes, and ensure that spill containment measures are in place. The compound is flammable, so it should be kept away from open flames and potential ignition sources. Proper labeling and storage conditions are essential to ensure safe handling and long-term usability in laboratory environments.

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