3-Bromopentane TCI B4340

Chemical Identity

CAS No.: 1809-10-5
PubChem: CID 15738·SID 253660376
Formula: C5H11Br
Molecular weight: 151.04 g/mol
Purity: >90.0%(GC)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 3-bromopentane
SMILES: CCC(CC)Br
InChIKey: VTOQFOCYBTVOJZ-UHFFFAOYSA-N

Rp 3.498.600,00

~~Rp 2.446.500,00~~ Rp 3.498.600,00

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3-Bromopentane is an organic compound widely utilized in chemical synthesis for constructing complex molecules. As a key building block, it serves as a fundamental component in the development of both heterocyclic and non-heterocyclic compounds. In laboratory settings, it plays a crucial role in various synthetic pathways, particularly in nucleophilic substitution and elimination reactions. Its reactivity and versatility make it an essential reagent for chemists working on the synthesis of haloalkanes and alcohols.

The compound’s simplicity in molecular structure belies its high reactivity, which is primarily attributed to the bromine atom at the third carbon position. This bromine group significantly enhances its chemical reactivity, enabling it to participate in a wide range of chemical transformations. Additionally, its volatile nature requires careful handling, especially in environments where controlled conditions such as vacuum or low temperatures are necessary.

In Indonesian laboratories, 3-Bromopentane is a vital material for organic chemistry research, particularly in academic institutions and research centers. Its availability supports the development of new compounds and the testing of chemical reactions relevant to local scientific needs. Its use is integral to advancing chemical research and innovation in the region.

Related TCI products

Nucleophilic Substitution Reactions: 3-Bromopentane is ideal for these reactions due to its reactive bromine atom, which readily participates in substitution processes.
Elimination Reactions: The compound’s structure makes it suitable for elimination reactions, allowing the formation of alkenes through dehydrohalogenation.
Haloalkane Synthesis: Its bromine functionality makes it a preferred reagent for the synthesis of haloalkane derivatives.
Alcohol Synthesis: 3-Bromopentane can be used in the preparation of alcohols through nucleophilic attack by hydroxide ions.
Vacuum and Low-Temperature Reactions: Its volatility necessitates controlled environments, making it suitable for reactions requiring vacuum or cryogenic conditions.

Brand	TCI
CAS number	1809-10-5
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	As per supplier specifications
Physical form	Liquid
Storage	Store in a cool, well-ventilated area away from heat and direct sunlight

3-Bromopentane should be stored in a cool, well-ventilated area, away from heat and direct sunlight. It is recommended to use sealed, airtight containers to prevent evaporation due to its volatile nature. Due to its reactivity, it should be handled in a fume hood to minimize exposure. Proper personal protective equipment, such as gloves and goggles, should be worn during handling. The compound should not be stored near incompatible materials such as strong oxidizers. Regular monitoring of storage conditions is essential to ensure safety and maintain the integrity of the material.

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