Bromoacetonitrile TCI B1058

Chemical Identity

CAS No.: 590-17-0
PubChem: CID 11534·SID 87564005
Formula: C2H2BrN
Molecular weight: 119.95 g/mol
Purity: >97.0%(GC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 2-bromoacetonitrile
SMILES: C(C#N)Br
InChIKey: REXUYBKPWIPONM-UHFFFAOYSA-N

Rp 1.881.600,00

~~Rp 1.331.400,00~~ Rp 1.881.600,00

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Bromoacetonitrile (CAS 590-17-0) is a chemical compound widely used as a foundational material in various laboratory reactions. It serves as a versatile building block in organic chemistry, enabling the synthesis of complex molecules through its reactive nature. This compound is particularly valuable in the development of new chemical structures due to its ability to participate in multiple reaction pathways. Its simplicity in molecular structure belies its significant role in advancing chemical research and innovation.

The reactivity of Bromoacetonitrile, especially at the nitrile group and the bromine atom, makes it a preferred choice for nucleophilic and electrophilic substitution reactions. These properties allow chemists to tailor its behavior in different synthetic contexts, making it an essential tool in organic synthesis. Its high reactivity also means that it must be handled with care to ensure safety and efficiency in laboratory settings.

In Indonesian laboratories, Bromoacetonitrile is commonly used in organic chemistry research, particularly in the synthesis of new compounds. Its application extends to both academic and industrial research, where its reactivity and versatility are highly valued. Researchers in Indonesia often rely on this compound for its ability to form stable intermediates and participate in a wide range of chemical transformations.

TCI brochures (PDF)

Biomaterials Research Reagents 2025-02-19 · p. 29

Related TCI products

Synthesis of heterocyclic compounds for drug development due to its reactivity and ability to form stable intermediates.
Nucleophilic substitution reactions where the bromo group acts as a good leaving group for efficient reaction pathways.
Electrophilic substitution reactions benefiting from the nitrile group's ability to participate in various chemical transformations.
Organic synthesis of new compounds in research settings requiring versatile and reactive building blocks.
Industrial applications involving high reactivity and the potential for forming complex molecular structures.

Brand	TCI
CAS number	590-17-0
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 light and incompatible materials

Bromoacetonitrile should be stored in a cool, dry place away from direct light and incompatible substances. It is recommended to use sealed containers made of materials compatible with its chemical properties, such as glass or high-density polyethylene. Due to its reactivity, it should be handled in a well-ventilated area and with appropriate personal protective equipment. Avoid contact with moisture and strong oxidizing agents. Ensure that storage conditions are controlled to prevent degradation and maintain the compound’s effectiveness in laboratory applications.

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