Methyl Bromoacetate TCI B0533

Chemical Identity

CAS No.: 96-32-2
PubChem: CID 60984·SID 87563554
Formula: C3H5BrO2
Molecular weight: 152.97 g/mol
Purity: >98.0%(GC)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: methyl 2-bromoacetate
SMILES: COC(=O)CBr
InChIKey: YDCHPLOFQATIDS-UHFFFAOYSA-N

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Methyl Bromoacetate (CAS 96-32-2) is a versatile chemical compound widely used in laboratory settings for its reactivity and utility in organic synthesis. As a building block in chemical reactions, it plays a crucial role in the development of various organic compounds. Its bromo group makes it an essential reagent for substitution reactions, esterification, and other chemical transformations. This compound is particularly valuable in synthetic chemistry due to its ability to participate in multiple reaction pathways, making it a fundamental material for researchers and students alike.

The chemical properties of Methyl Bromoacetate make it a preferred choice in laboratory applications. It exhibits good solubility in organic solvents, which facilitates its use in solution-based reactions. Its reactivity towards bases, alkali metals, and high temperatures allows it to be employed in a wide range of experimental conditions. These characteristics enable chemists to manipulate and synthesize complex molecules with precision. Its stability under controlled conditions further enhances its reliability in laboratory experiments.

In Indonesian laboratories, Methyl Bromoacetate is commonly used in organic chemistry research, especially in academic institutions and research centers. It is a key component in practical experiments and studies that require reactive compounds. Its availability and effectiveness make it a standard reagent in both educational and industrial research environments, supporting the development of new chemical products and processes.

TCI brochures (PDF)

Biomaterials Research Reagents 2025-02-19 · p. 29

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Organic synthesis is a primary application where Methyl Bromoacetate is used for its reactivity in substitution and esterification reactions.
Esterification processes benefit from its solubility in organic solvents, enabling efficient reaction conditions.
Substitution reactions rely on its bromo group for introducing functional groups into organic molecules.
Research and development in chemical industries utilize it for creating new compounds with specific properties.
Educational institutions use it in laboratory courses to teach fundamental organic chemistry concepts and techniques.

Brand	TCI
CAS number	96-32-2
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 light and incompatible materials

Methyl Bromoacetate 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 evaporation and contamination. Due to its reactivity, it should be stored separately from strong bases, alkali metals, and oxidizing agents. Proper ventilation is essential when handling this compound to minimize exposure. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, to ensure safe handling. Regular inspection of storage conditions is advised to maintain the integrity and safety of the compound.

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