1-Bromo-2-butanol (contains ca. 30% 2-Bromo-1-butanol) TCI B0932

Chemical Identity

CAS No.: 2482-57-7
PubChem: CID 520149·SID 87563895
Formula: C4H9BrO
Molecular weight: 153.02 g/mol
Purity: >70.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 1-bromobutan-2-ol
SMILES: CCC(CBr)O
InChIKey: DMRXISNUOWIOKV-UHFFFAOYSA-N

Rp 2.359.350,00

~~Rp 1.649.550,00~~ Rp 2.359.350,00

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Berat 25g

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1-Bromo-2-butanol is a chemical compound widely used in organic laboratory reactions. It serves as a versatile building block in the synthesis of more complex molecules. This compound is particularly valued for its ability to participate in nucleophilic substitution reactions, making it a key reagent in organic chemistry. Its bromine functional group enhances its reactivity, allowing it to interact with various nucleophiles such as alcohols, amines, and hydroxide ions. This makes it an essential tool for researchers aiming to construct intricate molecular structures.

The chemical properties of 1-Bromo-2-butanol make it a preferred choice in laboratory settings. Its reactivity with nucleophilic reagents enables a wide range of synthetic applications. The presence of approximately 30% 2-Bromo-1-butanol in the mixture adds versatility, allowing for multiple reaction pathways. This dual composition provides flexibility in experimental design, making it suitable for both academic and industrial research. Its stability under controlled conditions ensures reliable performance in various chemical processes.

In Indonesian laboratories, 1-Bromo-2-butanol is commonly used in organic chemistry research. It is frequently found in academic institutions and research centers where synthetic chemistry is practiced. Its role in creating complex molecular structures supports both teaching and research activities. The compound’s availability and reactivity make it a go-to material for chemists working on diverse projects. Its widespread use highlights its importance in the Indonesian scientific community.

Related TCI products

Organic synthesis is a primary application where 1-Bromo-2-butanol is used to create complex molecules through nucleophilic substitution reactions.
Heterocyclic compound synthesis benefits from this reagent due to its ability to form new carbon-carbon bonds.
Nucleophilic substitution experiments rely on 1-Bromo-2-butanol as a reactive brominated compound that reacts with various nucleophiles.
Teaching laboratories use this compound to demonstrate reaction mechanisms and synthetic pathways in organic chemistry courses.
Research institutions incorporate it into their synthetic protocols to develop new compounds and materials for scientific advancement.

Brand	TCI
CAS number	2482-57-7
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Liquid
Storage	Store in a cool, dry place away from light and incompatible materials

1-Bromo-2-butanol should be stored in a cool, dry environment to maintain its stability. It is recommended to keep it in a sealed container to prevent exposure to air and moisture. The compound should be stored away from incompatible substances such as strong oxidizers and bases. Suitable containers include glass or polyethylene bottles with tight-fitting lids. Laboratory personnel should handle the material with care, using appropriate personal protective equipment. Due to its reactivity, it is important to avoid direct contact with skin and eyes. Proper ventilation should be maintained in the workspace to minimize inhalation risks.

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