2-Bromo-2-methylbutane TCI B0612

Chemical Identity

CAS No.: 507-36-8
PubChem: CID 68180·SID 87563623
Formula: C5H11Br
Molecular weight: 151.04 g/mol
Purity: >95.0%(GC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromo-2-methylbutane
SMILES: CCC(C)(C)Br
InChIKey: JOUWCKCVTDSMHF-UHFFFAOYSA-N

Rp 3.180.450,00

~~Rp 2.223.900,00~~ Rp 3.180.450,00

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2-Bromo-2-methylbutane is a chemical compound widely used as a building block in various chemical reactions, particularly in the synthesis of complex organic compounds. Its simple molecular structure plays a crucial role in forming more intricate carbon chain structures, making it a versatile reagent in synthetic chemistry. In the laboratory, it is commonly employed in nucleophilic substitution and elimination reactions, which are fundamental steps in organic synthesis. This compound is essential for researchers and students aiming to explore the mechanisms and outcomes of different chemical transformations.

The chemical properties of 2-Bromo-2-methylbutane make it a preferred choice for laboratory use. It exhibits chemical stability and does not react spontaneously under normal conditions, which simplifies handling and storage. Its relatively high boiling point allows it to be used in reactions requiring specific temperature conditions. These characteristics ensure that it remains a reliable and safe reagent for a wide range of chemical experiments and research applications.

In Indonesian laboratories, 2-Bromo-2-methylbutane is frequently utilized in both educational and research settings. It is an important tool for teaching fundamental chemical reactions and for conducting advanced research in organic chemistry. Its availability and reliability make it a valuable resource for academic institutions and research facilities across Indonesia.

Related TCI products

Organic synthesis reactions benefit from 2-Bromo-2-methylbutane as it serves as a versatile intermediate in the creation of complex organic molecules.
Nucleophilic substitution reactions utilize this compound due to its bromine atom, which is a good leaving group, facilitating substitution processes.
Elimination reactions often involve this compound as it can act as a substrate for dehydrohalogenation, leading to the formation of alkenes.
Teaching laboratories use it to demonstrate fundamental reaction mechanisms and to provide hands-on experience for students.
Research laboratories employ it in the development of new synthetic methodologies and in the study of reaction kinetics and selectivity.

Brand	TCI
CAS number	507-36-8
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	Available in various quantities as per supplier specifications
Physical form	Liquid
Storage	Store in a cool, dry place away from direct sunlight

2-Bromo-2-methylbutane should be stored in a cool, dry place, away from direct sunlight and incompatible materials. It is recommended to use sealed containers made of materials that are chemically inert, such as glass or stainless steel, to prevent any potential reactions. Due to its chemical stability, it does not require special handling under normal laboratory conditions. However, it is important to ensure proper ventilation when working with this compound to avoid inhalation of vapors. Always follow standard safety protocols when handling any chemical reagent to maintain a safe laboratory environment.

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