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Sku CI04894_5_G
Chem Impex
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Product Information

Product Name
4-Iodobenzoic acid
Brand Name
Chem Impex
Product Number
04894
CAS
619-58-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
12085
IUPAC Name
4-iodobenzoic acid
InChI Key
GHICCUXQJBDNRN-UHFFFAOYSA-N
SMILES
C1=CC(=CC=C1C(=O)O)I

Description

4-Iodobenzoic acid is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and analgesic drugs.

Organic Synthesis: It is commonly used in organic chemistry for the preparation of iodinated compounds, which are valuable in the creation of complex molecules.

Material Science: The compound is applied in the production of polymers and materials that require specific functional groups for enhanced properties, such as increased thermal stability.

Analytical Chemistry: 4-Iodobenzoic acid is utilized as a reagent in analytical methods, helping researchers identify and quantify other chemical substances through its distinctive properties.

Biochemical Research: It is used in studies involving enzyme inhibition and receptor binding, providing insights into biological mechanisms and potential therapeutic targets.

References Data Source From Pubchem

Biosensing device based on optical waveguide spectrometry with fluorescent solvatochromic beads for label-free tracking of avidin–biotin interaction

Publication Name: Analytical sciences : the international journal of the Japan Society for Analytical Chemistry
Publication Date: 2026-01-28
DOI: 10.1007/s44211-025-00865-y

S73 | METXBIODB | Metabolite Reaction Database from BioTransformer

Publication Date: 2026
DOI: 10.5281/zenodo.4056560

Molecularly engineered porphyrin photosensitizers featuring multi-anchoring and alkoxy modifications for robust photocatalytic hydrogen production

Publication Name: Science China Materials
Publication Date: 2025-11-21
DOI: 10.1007/s40843-025-3715-5

Arylation of C=C bonds via non-cross-coupling reactions: historical evolution of the Meerwein arylation mechanisms

Publication Name: ChemTexts
Publication Date: 2025-03-20
DOI: 10.1007/s40828-025-00202-w

Quantitative analysis of related substances in acetaminophen tablets using pre-column derivatization coupled with HPLC–ICP-MS

Publication Name: Analytical sciences : the international journal of the Japan Society for Analytical Chemistry
Publication Date: 2025-03-01
DOI: 10.1007/s44211-025-00739-3