Skip to product information
1 of 2

TCI

CAS 6624-84-6

Amyl Acetoacetate TCI A0811

Amyl Acetoacetate TCI A0811

Chemical Identity

CAS No.
6624-84-6
PubChem
CID 138786·SID 87562336
Formula
C9H16O3
Molecular weight
172.22 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
pentyl 3-oxobutanoate
SMILES
CCCCCOC(=O)CC(=O)C
InChIKey
IDZAUPYMMSSVHP-UHFFFAOYSA-N
Regular price Rp 662.550,00
Regular price Rp 478.800,00 Sale price Rp 662.550,00
Sale Sold out
Shipping calculated at checkout.
Volume
Quantity
Pembayaran hanya melalui request quotation dan dilakukan setelah tim kami menghubungi Anda. Mohon cantumkan nomor WhatsApp aktif untuk konfirmasi pesanan & pembuatan invoice. Estimasi pengiriman 2-4 minggu setelah pembayaran.

Dokumen Keamanan & Mutu

CoA (Certificate of Analysis)

Spesifik per batch produksi — diterbitkan dan dikirim bersama barang sesuai nomor lot yang Anda terima.

Contoh CoA segera tersedia.

💬 Minta CoA via WhatsApp

View full details

Amyl Acetoacetate (TCI A0811, CAS 6624-84-6) is an organic compound widely used in laboratory settings for various chemical reactions. As an ester, it serves as a versatile building block in synthetic chemistry, enabling the creation of complex molecules through functional group transformations. Its role in organic synthesis is critical, particularly in the development of pharmaceutical compounds and other specialty chemicals. This compound is commonly found in the category of Non-Heterocyclic Building Blocks, which are essential for constructing molecular frameworks. Its chemical stability and reactivity make it a valuable reagent for researchers working in both academic and industrial laboratories.

The properties of Amyl Acetoacetate that make it a preferred choice include its molecular stability, volatility, and reactivity with a wide range of reagents. Its ester functionality allows for easy modification through hydrolysis, oxidation, or reduction, making it adaptable to different synthetic strategies. Additionally, its characteristic aroma can aid in visual identification during experiments. These features contribute to its widespread use in both qualitative and quantitative chemical analyses. The compound’s ability to participate in multiple reaction types enhances its utility in diverse research applications, particularly in organic and medicinal chemistry.

In Indonesian laboratories, Amyl Acetoacetate is frequently used in research related to organic chemistry and pharmaceutical development. Its high reactivity and molecular versatility make it an essential component in the synthesis of new compounds and the study of chemical reactions. It is particularly relevant in projects requiring compounds with specific functional groups or structural features. Its availability and reliability as a chemical building block support ongoing scientific investigations in both academic and industrial research settings.

  • Organic synthesis applications benefit from Amyl Acetoacetate's reactivity and versatility, enabling the creation of complex molecular structures through ester functional group transformations.
  • Pharmaceutical research utilizes this compound for the development of new drug molecules, leveraging its ability to participate in various synthetic pathways.
  • Analytical chemistry experiments often incorporate Amyl Acetoacetate due to its stable molecular structure and characteristic aroma, aiding in both qualitative and quantitative analysis.
  • Teaching laboratories use Amyl Acetoacetate to demonstrate ester hydrolysis and other fundamental chemical reactions, providing students with hands-on experience.
  • Industrial research and development projects rely on this compound for the synthesis of specialty chemicals, supporting innovation in chemical manufacturing processes.

Brand TCI
CAS number 6624-84-6
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 and incompatible materials

Amyl Acetoacetate should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to minimize exposure to moisture and air, which can affect its reactivity. Due to its volatile nature, it should be kept away from heat sources and direct sunlight. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper ventilation is essential when working with this substance to ensure safe handling and prevent inhalation of vapors. Regular monitoring of storage conditions is advised to maintain the integrity and effectiveness of the compound in research applications.

—