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TCI

CAS 58123-77-6

3-Hydroxy-4-iodobenzoic Acid TCI H1496

3-Hydroxy-4-iodobenzoic Acid TCI H1496

Chemical Identity

CAS No.
58123-77-6
PubChem
CID 736854·SID 253660445
Formula
C7H5IO3
Molecular weight
264.02 g/mol
Purity
>98.0%(HPLC)(T)
Reference databases
ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
3-hydroxy-4-iodobenzoic acid
SMILES
C1=CC(=C(C=C1C(=O)O)O)I
InChIKey
UABBBWVTEWIIMN-UHFFFAOYSA-N
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3-Hydroxy-4-iodobenzoic Acid is a chemical compound widely used as a building block in the synthesis of complex organic molecules. Its molecular structure contains both hydroxyl and iodine groups, making it a versatile reagent in various chemical reactions. In the laboratory, this compound plays a crucial role in organic synthesis, particularly in the development of new pharmaceuticals and bioactive compounds. Due to its functional groups, it can participate in multiple reaction pathways, including nucleophilic substitution, esterification, and hydrolysis.

The presence of the iodine group, which is highly electronegative, contributes to the compound’s reactivity. This makes it an ideal candidate for reactions that require high reactivity and functional group manipulation. Its ability to undergo various chemical transformations makes it a preferred choice for researchers working on synthetic routes that require precise control over molecular structure. The compound’s versatility and reactivity are key factors in its widespread use across different fields of chemistry.

In Indonesian laboratories, 3-Hydroxy-4-iodobenzoic Acid is commonly used in organic chemistry research, particularly in academic and research institutions. It is frequently applied in projects related to drug synthesis, bioactive compound development, and industrial chemical production. Its availability and chemical properties make it a valuable resource for scientists and researchers in Indonesia.

  • Organic synthesis projects benefit from this compound due to its reactive hydroxyl and iodine groups, allowing for diverse chemical transformations.
  • Pharmaceutical research utilizes this material for the development of new drugs, as its functional groups can be modified to create bioactive molecules.
  • Bioactive compound synthesis relies on this reagent for its ability to participate in nucleophilic substitution and esterification reactions.
  • Industrial chemical production incorporates this compound for its versatility in creating complex molecular structures.
  • Academic research in chemistry uses this material to explore reaction mechanisms and synthetic pathways in organic chemistry.

Brand TCI
CAS number 58123-77-6
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to humidity and air. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to minimize any potential risks. Proper labeling of containers is essential for safe handling and to prevent accidental exposure. Laboratories should follow standard safety protocols to ensure safe use and storage of this compound.

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