1005-30-7

Basic information

• Product Name: Benzoic acid, 4-iodo-, sodiuM salt
• Synonyms: Benzoic acid, 4-iodo-, sodiuM salt
• CAS NO: 1005-30-7
• Molecular Formula: C₇H₄IO₂*Na
• Molecular Weight: 269.9997
• EINECS: -0
• Mol File: 1005-30-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 318.5°Cat760mmHg
• Flash Point: 146.4°C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.00015mmHg at 25°C
• CAS DataBase Reference: Benzoic acid, 4-iodo-, sodiuM salt(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-iodo-, sodiuM salt(1005-30-7)
• EPA Substance Registry System: Benzoic acid, 4-iodo-, sodiuM salt(1005-30-7)

Safety Data

• Hazardous Substances Data: 1005-30-7(Hazardous Substances Data)

Usage

Description

Benzoic acid, 4-iodo-, sodium salt is a chemical compound derived from benzoic acid with an iodine atom substituted at the 4th position, existing in the form of a sodium salt. It is characterized by its strong antifungal and antibacterial properties, making it a versatile compound for various applications in pharmaceuticals, dyes, food preservation, and personal care products.

Uses

Used in Pharmaceutical Industry:
Benzoic acid, 4-iodo-, sodium salt is used as a pharmaceutical intermediate for the synthesis of various drugs. Its unique structure and properties contribute to the development of new therapeutic agents.
Used in Dye Production:
This chemical compound serves as an intermediate in the production of dyes, where its iodine substitution at the 4th position plays a crucial role in the formation of color-producing compounds.
Used in Food and Beverage Industry:
Benzoic acid, 4-iodo-, sodium salt is utilized as a preservative in food and beverages due to its strong antifungal and antibacterial properties. It helps maintain the freshness and quality of products by inhibiting the growth of spoilage-causing microorganisms.
Used in Personal Care Products:
In the personal care industry, this sodium salt is employed in the manufacturing of products such as creams, lotions, and shampoos. Its antimicrobial properties help prevent the growth of harmful microorganisms, ensuring the safety and efficacy of these products.
Used in Organic Synthesis:
Benzoic acid, 4-iodo-, sodium salt can also be used as a starting material for the preparation of other organic compounds. Its unique structure allows for further chemical reactions and modifications, leading to the synthesis of new compounds with potential applications in various fields.
Used as a Reagent in Organic Synthesis:
This chemical compound functions as a reagent in organic synthesis, facilitating specific chemical reactions and transformations. Its presence can enhance the efficiency and selectivity of certain synthetic processes, contributing to the development of novel organic compounds.

InChI:InChI=1/C7H5IO2.Na/c8-6-3-1-5(2-4-6)7(9)10;/h1-4H,(H,9,10);/q;+1/p-1

Upstream product

• 619-58-9 4-iodobenzoic acid 
• 824-78-2 4-nitrophenol sodium salt 
• 124-41-4 sodium methylate 
• 119267-73-1 Acetic acid 2-(4-iodo-phenyl)-2-oxo-1-phenyl-ethyl ester 

Downstream Products

• 3540-62-3 <4-(4-Jod-benzoyloxy)-buttersaeure>-methylester 
• 3540-55-4 <4-(4-Jod-benzoyloxy)-buttersaeure>-butylester 
• 3540-68-9 <4-(4-Jod-benzoyloxy)-buttersaeure>-<3-methyl-butylester> 
• 3540-71-4 <4-(4-Jod-benzoyloxy)-buttersaeure>-<2-aethoxy-aethylester> 
• 3540-73-6 <5-(4-Jod-benzoyloxy)-valeriansaeure>-butylester 
• 3609-60-7 <4-Jod-benzoyloxy)-essigsaeure-aethylester 
• 619-58-9 4-iodobenzoic acid 
• 824-78-2 4-nitrophenol sodium salt 
• 70916-98-2 4′-formyl-(1,1′-biphenyl)-4-carboxylic Acid 
• 609365-68-6 5,10,15,20-tetrakis(4-carboxybiphenyl)porphyrin 
• 120363-52-2 (S)-2-((S)-3-{4-[5-((S)-2-Amino-2-methoxycarbonyl-ethyl)-2-hydroxy-phenoxy]-phenyl}-2-tert-butoxycarbonylamino-propionylamino)-3-(4-hydroxy-phenyl)-propionic acid pentafluorophenyl ester; hydrochloride 
• 120363-51-1 (S)-2-((S)-3-{4-[5-((S)-2-Amino-2-methoxycarbonyl-ethyl)-2-hydroxy-phenoxy]-phenyl}-2-tert-butoxycarbonylamino-propionylamino)-3-(4-hydroxy-phenyl)-propionic acid; hydrochloride 
• 129151-09-3 (9S,12S,15S)-15-Amino-4-hydroxy-12-(4-hydroxy-benzyl)-11,14-dioxo-2-oxa-10,13-diaza-tricyclo[15.2.2.1^3,7]docosa-1⁽²⁰⁾,3⁽²²⁾,4,6,17⁽²¹⁾,18-hexaene-9-carboxylic acid methyl ester; hydrochloride 

Relevant articles and documents

The effect of 4-halogenobenzoate ligands on luminescent and structural properties of lanthanide complexes: Experimental and theoretical approaches

The ligands 4-fluorobenzoate (4-fba), 4-chlorobenzoate (4-cba), 4-bromobenzoate (4-bba) and 4-iodobenzoate (4-iba) were chosen in order to synthesize europium(iii), gadolinium(iii) and terbium(iii) complexes and compare the effect of halogens on their phy

Electronic and steric effects: How do they work in ionic liquids? the case of benzoic acid dissociation

(Figure Presented) The need to have a measure of the strength of some substituted benzoic acids in ionic liquid solution led us to use the protonation equilibrium of sodium p-nitrophenolate as a probe reaction, which was studied by means of spectrophotometric titration at 298 K. In order to evaluate the importance of electronic effect of the substituents present on the aromatic ring, both electron-withdrawing and -donor substituents were taken into account. Furthermore, to have a measure of the importance of the steric effect of the substituents both para- and ortho-substituted benzoic acids were analyzed. The probe reaction was studied in two ionic liquids differing for the ability of the cation to give hydrogen bond and π-π interactions, namely [bm 2im][NTf2] and [bmpyrr][NTf2]. Data collected show that benzoic acids are less dissociated in ionic liquid than in water solution. Furthermore, the equilibrium constant values seem to be significantly affected by both the nature of ionic liquid cation and the structure of the acid. In particular, the ortho-steric effect seems to operate differently in water and in the aromatic ionic liquid, determining in this solvent medium a particular behavior for ortho-substituted benzoic acids.