2-Bromobutyryl Chloride TCI B4105

Chemical Identity

CAS No.: 22118-12-3
PubChem: CID 90734·SID 253660059
Formula: C4H6BrClO
Molecular weight: 185.45 g/mol
Purity: >98.0%(GC)(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromobutanoyl chloride
SMILES: CCC(C(=O)Cl)Br
InChIKey: DROZQELYZZXYSX-UHFFFAOYSA-N

Rp 2.969.400,00

~~Rp 2.091.600,00~~ Rp 2.969.400,00

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2-Bromobutyryl Chloride (TCI B4105) is a chemical compound widely used in organic laboratory reactions. As a halogenated carboxylic acid derivative, it serves as a versatile building block for the synthesis of complex organic molecules. This compound is particularly valuable in synthetic chemistry due to its ability to participate in substitution and nucleophilic reactions. Its role as a bromo group donor makes it an essential reagent for functional group transformations in various chemical processes.

The chemical properties of 2-Bromobutyryl Chloride make it a preferred choice for researchers. It is chemically stable under controlled conditions but is highly reactive, especially in the presence of moisture and air. The presence of bromine enhances its reactivity, allowing it to interact with a wide range of nucleophiles such as amines and alkoxides. Its solid form and solubility characteristics make it convenient for use in different reaction setups. These properties ensure its reliability and effectiveness in laboratory applications.

In Indonesian laboratories, 2-Bromobutyryl Chloride is commonly used in organic chemistry research, particularly in the synthesis of heterocyclic compounds and other complex molecules. It is a key reagent in academic and industrial research settings, supporting the development of new chemical structures. Its availability and performance make it a popular choice among researchers working on synthetic pathways and molecular design.

Related TCI products

Organic synthesis reactions where bromo group introduction is essential for functional group modification.
Nucleophilic substitution reactions involving amines, alkoxides, and other reactive nucleophiles.
Preparation of heterocyclic compounds through bromide-based synthetic pathways.
Development of complex molecular structures requiring brominated intermediates.
Research in pharmaceutical and agrochemical industries for compound modification and optimization.

Brand	TCI
CAS number	22118-12-3
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	—

2-Bromobutyryl Chloride should be stored in a cool, dry place away from moisture and air exposure. It is recommended to keep the compound in a tightly sealed container to prevent degradation. Due to its reactivity, it should be handled in a well-ventilated area, and appropriate personal protective equipment should be worn. Storage in a desiccator or under an inert atmosphere can further enhance its stability. Regular monitoring of storage conditions ensures the compound remains effective for laboratory use.

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