sec-Butyl Acetoacetate TCI A0815

Chemical Identity

CAS No.: 13562-76-0
PubChem: CID 139498·SID 87562340
Formula: C8H14O3
Molecular weight: 158.19 g/mol
Purity: >98.0%(GC)
Reference databases: ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: butan-2-yl 3-oxobutanoate
SMILES: CCC(C)OC(=O)CC(=O)C
InChIKey: QSTNBMLCULGCQE-UHFFFAOYSA-N

Rp 2.093.700,00

~~Rp 1.479.450,00~~ Rp 2.093.700,00

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Volume 25mL

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Sec-Butyl Acetoacetate is a chemical compound widely used in laboratory settings for various organic synthesis reactions. It serves as a building block in the creation of complex organic molecules, particularly in the development of esters and heterocyclic compounds. Its molecular structure enables it to participate in substitution reactions and other essential chemical processes, making it a valuable reagent in synthetic chemistry. This compound is commonly found in research laboratories where precision and control over chemical reactions are critical.

The compound’s chemical stability under specific conditions, along with its reactivity towards acids and bases, makes it a preferred choice for controlled chemical environments. Its ability to undergo various reactions without degrading quickly allows researchers to maintain the integrity of their experiments. Additionally, the distinct aroma of Sec-Butyl Acetoacetate aids in its identification during laboratory procedures, enhancing safety and accuracy. These properties make it an essential component in many chemical synthesis protocols.

In Indonesian laboratories, Sec-Butyl Acetoacetate is extensively used in chemical research, especially in the fields of organic synthesis and the development of new chemical products. Its reliability and ease of handling make it a popular choice among researchers and students. The compound’s versatility and stability ensure that it remains a key material in both academic and industrial research settings.

Related TCI products

Organic synthesis is a primary application where Sec-Butyl Acetoacetate is used to create complex molecules through substitution and other chemical reactions.
Heterocyclic compound development benefits from its reactivity, allowing for the formation of ring structures essential in pharmaceutical and industrial chemistry.
Ester synthesis relies on this compound’s ability to undergo esterification reactions, making it a key reagent in the production of ester-based compounds.
Research in chemical innovation often incorporates Sec-Butyl Acetoacetate due to its stability and versatility in various reaction conditions.
Educational laboratories use it to teach fundamental organic chemistry concepts and reaction mechanisms to students.

Brand	TCI
CAS number	13562-76-0
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes	—
Physical form	Liquid
Storage	Store in a cool, dry place away from direct sunlight

Sec-Butyl Acetoacetate should be stored in a cool, dry place away from direct sunlight to maintain its chemical stability. It is recommended to use sealed containers to prevent exposure to air and moisture, which could affect its properties. Due to its reactivity with acids and bases, it should be handled in a well-ventilated area and kept separate from incompatible substances. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling this compound. Proper labeling of containers is essential to ensure safe storage and usage. Regular monitoring of storage conditions helps maintain the integrity of the compound for reliable experimental results.

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