Bromoacetic Acid TCI B0531

Chemical Identity

CAS No.: 79-08-3
PubChem: CID 6227·SID 87563552
Formula: C2H3BrO2
Molecular weight: 138.95 g/mol
Purity: >98.0%(T)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromoacetic acid
SMILES: C(C(=O)O)Br
InChIKey: KDPAWGWELVVRCH-UHFFFAOYSA-N

Rp 662.550,00

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Berat 25g 500g

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Bromoacetic acid (79-08-3) is a chemical compound widely used in various synthetic reactions within laboratory settings. As a carboxylic acid bearing a bromo group, it plays a crucial role in organic chemistry by participating in nucleophilic substitution and halogenation reactions. Its reactivity makes it a valuable reagent for the synthesis of complex organic compounds. Due to its versatility, bromoacetic acid is commonly found in both academic and industrial research environments, supporting the development of new chemical structures and processes.

The compound’s high reactivity is complemented by its chemical stability under controlled conditions, making it a preferred choice for synthetic chemists. It is particularly useful in reactions where the introduction of a bromine atom is necessary, such as in the preparation of substituted acetic acids and other functional groups. Its ability to react with strong bases or alkali metals further enhances its utility in a variety of synthetic pathways. These properties make bromoacetic acid an essential reagent in modern chemical laboratories.

In Indonesian laboratories, bromoacetic acid is routinely used in organic chemistry research, especially in pharmaceutical and chemical manufacturing sectors. It is a key component in the development of new compounds and the optimization of existing synthesis methods. Many research institutions and universities in Indonesia rely on this compound for its effectiveness and reliability in experimental processes.

Related TCI products

Organic synthesis for the preparation of substituted acetic acids and functional groups due to its reactivity and bromo group.
Nucleophilic substitution reactions where bromoacetic acid acts as a good leaving group for further chemical transformations.
Halogenation processes to introduce bromine atoms into organic molecules, enhancing the diversity of synthesized compounds.
Pharmaceutical research for the development of new drugs and chemical intermediates in drug synthesis pathways.
Chemical manufacturing applications in the production of specialty chemicals and industrial compounds requiring brominated structures.

Brand	TCI
CAS number	79-08-3
Molecular formula	—
Purity	—
Category	Chemistry > Synthetic Reagents > Acids, Bases [Synthetic Reagents]
Pack sizes	Available in various quantities as per standard reagent packaging
Physical form	Liquid
Storage	Store in a cool, dry place away from strong bases and reactive materials

Bromoacetic acid should be stored in a cool, dry environment, away from strong bases and reactive materials to prevent unwanted chemical interactions. It is recommended to use appropriate containers such as glass or polyethylene bottles to minimize the risk of corrosion. Due to its corrosive nature, personal protective equipment like gloves, goggles, and a lab coat should be worn during handling. The compound is irritating to the skin and eyes, so proper ventilation and spill containment measures should be in place. It is essential to follow standard laboratory safety protocols to ensure safe handling and storage practices.

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