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TCI

CAS 6832-98-0

Palmitanilide TCI P0844

Palmitanilide TCI P0844

Chemical Identity

CAS No.
6832-98-0
PubChem
CID 96171·SID 87574972
Formula
C22H37NO
Molecular weight
331.5 g/mol
Purity
>98.0%(HPLC)(qN
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
N-phenylhexadecanamide
SMILES
CCCCCCCCCCCCCCCC(=O)NC1=CC=CC=C1
InChIKey
VENJCACPSJGPCM-UHFFFAOYSA-N
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Palmitanilide (TCI P0844), with CAS number 6832-98-0, is a chemical compound widely used in organic synthesis as a building block in laboratory settings. It belongs to the category of non-heterocyclic building blocks and is essential for creating complex organic molecules. Its long hydrocarbon chain provides structural versatility, making it a valuable tool for chemists working on a variety of synthetic routes. This compound is commonly used in the development of pharmaceuticals, materials science, and other organic chemistry applications due to its reactivity and compatibility with a wide range of chemical reactions.

Palmitanilide is known for its stable molecular structure and its ability to participate in various chemical reactions such as substitution, esterification, and others. Its solubility in organic solvents makes it an ideal choice for laboratory processes that require efficient reaction conditions. The compound’s chemical properties allow it to be easily modified through functional group transformations, which is why it is highly sought after in research laboratories. Its reliability and consistent performance make it a preferred material for synthetic chemists seeking to develop new compounds with specific properties.

In Indonesian laboratories, Palmitanilide is extensively used in organic chemistry research, particularly in the development of new compounds with potential applications in medicine and industry. Its availability and effectiveness in various reactions make it a key component in the chemical research toolkit. Researchers rely on its predictable behavior and compatibility with different reagents, ensuring reliable results in their experiments. Its role in supporting innovation in chemical synthesis is crucial for advancing scientific knowledge and practical applications.

  • Organic synthesis is a primary application where Palmitanilide is used to construct complex molecules with long hydrocarbon chains, enabling the development of pharmaceuticals and specialty chemicals.
  • Drug development benefits from Palmitanilide’s ability to participate in esterification and substitution reactions, aiding in the synthesis of bioactive compounds with therapeutic potential.
  • Material science research utilizes Palmitanilide to create polymers and coatings with specific functional properties, enhancing the performance of industrial materials.
  • Analytical chemistry applications leverage its stable molecular structure for use in chromatographic and spectroscopic analysis, providing reliable reference standards.
  • Industrial chemical production relies on Palmitanilide for the synthesis of derivatives used in fragrance, lubricant, and surfactant formulations due to its reactivity and solubility.

Brand TCI
CAS number 6832-98-0
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various sizes as per supplier specifications
Physical form Solid (may vary depending on supplier packaging)
Storage Store in a cool, dry place away from light and moisture

Palmitanilide should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Storage conditions should maintain a stable temperature to preserve its chemical integrity. Regular inspection of the container is advised to ensure no contamination or degradation occurs. Proper labeling and storage practices help maintain the compound’s effectiveness and safety in laboratory environments.

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