2-Bromohexane (contains 3-Bromohexane) (stabilized with Copper chip) TCI B1235

Chemical Identity

CAS No.: 3377-86-4
PubChem: CID 18805·SID 87564171
Formula: C6H13Br
Molecular weight: 165.07 g/mol
Purity: >70.0%(GC)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromohexane
SMILES: CCCCC(C)Br
InChIKey: NEBYCXAKZCQWAW-UHFFFAOYSA-N

Rp 3.763.200,00

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Berat 25g

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2-Bromohexane (CAS No. 3377-86-4) is an organic compound widely used as a building block in the synthesis of complex organic molecules. It serves as a versatile reagent in various chemical reactions, particularly in nucleophilic substitution and elimination reactions. This compound is a key component in the development of new compounds with applications in pharmaceuticals, materials science, and chemical industries. Its simple molecular structure allows for easy reactivity with a wide range of reagents, making it a valuable asset in organic chemistry laboratories.

The presence of 3-Bromohexane in the mixture enhances the stability of 2-Bromohexane, especially when stored with a copper catalyst. This stabilization significantly extends the shelf life and minimizes degradation during storage. The compound's stability and reactivity make it a preferred choice for researchers seeking reliable and consistent results in their experiments. Its compatibility with various reaction conditions ensures that it remains a staple in chemical synthesis processes.

In Indonesian laboratories, 2-Bromohexane is extensively used in organic chemistry research, particularly by academic institutions and research organizations. Its availability, stability, and broad applicability make it a go-to reagent for a variety of chemical reactions. It is commonly used as a starting material for the synthesis of complex organic compounds, supporting both teaching and research activities in the field of chemistry.

Related TCI products

Organic synthesis of complex compounds as a key starting material due to its reactivity and versatility in chemical reactions.
Nucleophilic substitution reactions where brominated alkanes are essential for forming new carbon-carbon bonds.
Elimination reactions where 2-Bromohexane serves as a precursor for the formation of alkenes through dehydrohalogenation.
Research in pharmaceutical development for the synthesis of bioactive molecules with specific functional groups.
Educational purposes in academic institutions for teaching fundamental concepts in organic chemistry and reaction mechanisms.

Brand	TCI
CAS number	3377-86-4
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per standard chemical supply practices
Physical form	Liquid
Storage	Store with copper catalyst to ensure stability and prevent degradation

2-Bromohexane should be stored in a cool, dark place away from direct sunlight to maintain its stability. It is recommended to use amber-colored glass containers to minimize exposure to light, which can cause degradation. The compound should be kept in a well-ventilated area to prevent the accumulation of vapors. It is important to handle the material with appropriate personal protective equipment, such as gloves and safety goggles, to ensure safety during use and storage. Avoid contact with incompatible substances, and ensure proper labeling of containers to prevent accidental use. Regular monitoring of storage conditions is advised to maintain the integrity and effectiveness of the compound in laboratory settings.

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