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CAS 17696-62-7

Phenyl 4-Hydroxybenzoate TCI H0218

Phenyl 4-Hydroxybenzoate TCI H0218

Chemical Identity

Other names
4-Hydroxybenzoic Acid Phenyl Ester · Phenylparaben
CAS No.
17696-62-7
PubChem
CID 87250·SID 87570647
Formula
C13H10O3
Molecular weight
214.22 g/mol
Purity
>99.0%(GC)
Reference databases
ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
phenyl 4-hydroxybenzoate
SMILES
C1=CC=C(C=C1)OC(=O)C2=CC=C(C=C2)O
InChIKey
GJLNWLVPAHNBQN-UHFFFAOYSA-N
MDL
MDL00016467
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Phenyl 4-Hydroxybenzoate is a chemical compound widely used in laboratory settings for organic synthesis reactions. It serves as a key building block in the creation of aromatic compounds and their derivatives. Its role in substitution reactions and the formation of complex molecular structures makes it an essential component in many chemical experiments. This compound is particularly valued for its stability and controlled reactivity, which allow for predictable outcomes in synthetic processes. Its versatility and reliability make it a preferred choice among researchers and chemists.

The compound's molecular structure, featuring both hydroxyl and phenyl groups, contributes to its reactivity and functional versatility. It dissolves well in organic solvents such as ethyl acetate and ethanol, which simplifies its use in various chemical reactions. These solubility characteristics also aid in the separation and isolation of final products, making the process more efficient. Its chemical stability ensures that it remains effective under a range of experimental conditions, enhancing its utility in laboratory environments.

In Indonesian laboratories, Phenyl 4-Hydroxybenzoate is frequently used in chemical research, pharmaceutical development, and the production of specialty chemicals. Scientists and researchers in educational institutions and research organizations rely on this compound for experiments requiring high-quality, stable raw materials. Its consistent performance and broad applicability make it a staple in both academic and industrial laboratory settings.

  • Organic synthesis of aromatic compounds due to its reactivity and structural versatility.
  • Pharmaceutical research for the development of drug molecules and active pharmaceutical ingredients.
  • Chemical analysis in quality control processes for the identification and characterization of compounds.
  • Industrial applications in the production of specialty chemicals and functional materials.
  • Educational use in teaching organic chemistry and synthetic reaction mechanisms to students.

Brand TCI
CAS number 17696-62-7
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply options
Physical form Solid
Storage Store in a cool, dry place away from direct sunlight

Phenyl 4-Hydroxybenzoate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in airtight containers to prevent moisture absorption and contamination. Due to its organic nature, it should be stored away from strong oxidizing agents and incompatible substances. Proper labeling of containers is essential for safe handling and identification. In laboratory settings, it is important to use appropriate personal protective equipment when handling this compound. Regular inspection of storage conditions ensures the compound remains in optimal condition for use in experiments.

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