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CAS 28508-48-7

Sodium 4-Hydroxy-3-methoxybenzoate TCI H0265

Sodium 4-Hydroxy-3-methoxybenzoate TCI H0265

Chemical Identity

Other names
4-Hydroxy-3-methoxybenzoic Acid Sodium Salt · Sodium Vanillate · Vanillic Acid Sodium Salt
CAS No.
28508-48-7
PubChem
CID 23675709·SID 87570692
Formula
C8H7NaO4
Molecular weight
190.13 g/mol
Purity
>98.0%(GC)(T)
Reference databases
ChEBI·ChemSpider
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
sodium 4-hydroxy-3-methoxybenzoate
SMILES
COC1=C(C=CC(=C1)C(=O)[O-])O.[Na+]
InChIKey
ZFRVFUWCVYLUIH-UHFFFAOYSA-M
MDL
MDL00016534
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Sodium 4-Hydroxy-3-methoxybenzoate is a chemical compound widely used in laboratory settings for its versatility in organic synthesis and chemical reactions. It serves as a building block in the creation of aromatic compounds and phenolic derivatives, making it essential for researchers and students in Indonesia. This compound plays a crucial role in the development of complex chemical structures, supporting both academic and industrial research. Its presence in various laboratory applications highlights its importance in the field of chemistry.

The compound's stability and reactivity make it a preferred choice for chemical experiments requiring high reactivity. Its molecular structure, consisting of hydroxyl and methoxy groups, provides both polar and reactive characteristics. These properties allow it to dissolve in organic solvents such as ethyl acetate and ethanol, facilitating mixing and reaction processes. This solubility enhances its usability in a range of chemical reactions, including substitution, esterification, and the synthesis of complex compounds.

In Indonesian laboratories, Sodium 4-Hydroxy-3-methoxybenzoate is commonly used in educational and research environments. It is a staple in both academic institutions and research facilities, supporting a wide array of chemical processes. Its reliability and consistent performance make it a trusted material for chemical synthesis and experimentation in the region.

  • Organic synthesis applications benefit from its reactivity and solubility in organic solvents, allowing for efficient reaction processes.
  • Phenolic derivative production relies on its ability to form stable compounds, making it ideal for creating aromatic structures.
  • Educational experiments utilize its predictable behavior, providing students with a reliable material for learning chemical reactions.
  • Industrial research uses it as a building block for developing new chemical compounds and materials.
  • Analytical chemistry procedures benefit from its stability and reactivity, supporting accurate and reproducible results.

Brand TCI
CAS number 28508-48-7
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in standard laboratory quantities
Physical form Solid
Storage Store in a cool, dry place away from moisture and light

Sodium 4-Hydroxy-3-methoxybenzoate should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and light exposure. Since it is a solid, it should be kept in a secure location away from potential contaminants. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment when necessary. Proper storage ensures the compound remains effective for use in chemical reactions and synthesis processes. Regular inspection of storage conditions is advised to maintain optimal performance and safety standards.

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