10265-70-0

Usage

Uses

Used in Biochemistry Research:
1H-Indole-3-butanoic acid monosodium salt is used as a research compound for studying plant physiology and development. It aids in understanding the role of indole-3-butanoic acid in plant growth and its interactions with other biochemical processes.
Used in Organic Chemistry:
1H-Indole-3-butanoic acid monosodium salt is used as a reagent in various organic chemistry reactions. Its solubility in water and slightly acidic pH make it a valuable component in the synthesis of other compounds and in the development of new chemical procedures.
Used in Laboratory and Industrial Applications:
1H-Indole-3-butanoic acid monosodium salt is used as a key ingredient in the formulation of various laboratory and industrial products. Its properties, such as solubility and pH, contribute to the effectiveness and stability of these products, making it an essential component in their development and production.

InChI:InChI=1/C12H13NO2.Na/c14-12(15)7-3-4-9-8-13-11-6-2-1-5-10(9)11;/h1-2,5-6,8,13H,3-4,7H2,(H,14,15);/q;+1/p-1

Upstream product

• 133-32-4 4-indol-3-yl-butyric acid 

Relevant academic research and scientific papers

Synthesis, characterization, thermal, and antibacterial studies of organotin(Iv) complexes of indole-3-butyric acid and indole-3-propionic acid

Six organotin(IV) complexes of type Me2SnL2, Bu 2SnL2, and Ph3SnL [where L = indole-3-butyric acid (1, 2 and 3) or indole-3-propionic acid (4, 5 and 6)] have been synthesized by the reactions of the corresponding diorganotin(IV) oxide and triphenyltin(IV) hydroxide with respective indole-3-butyric acid (IBH) or indole-3-propionic acid (IPH) in the desired molar ratios of 1:2/1:1. All of the compounds have been characterized by elemental analysis, IR, 1H NMR, 13C NMR, and 119Sn NMR spectroscopy. Thermal studies of all synthesized complexes have been carried out using thermogravimetry (TG) technique under a nitrogen atmosphere. The thermal decompositions for compounds Me2SnL2 and Bu2SnL2 occurred in two steps, whereas in compounds Ph3SnL, it exhibited as three steps decomposition and resulted into the formation of pure SnO2. The complexes were also screened against three gram-positive (Staphylococcus aureus, Staphylococcus epidermidis, and Micrococcus luteus) and three gram-negative (Escherichia coli, Pseudomonas aeruginosa, and Enterobacter aerogenes) bacteria using minimum inhibition concentration (MIC) method, and all of these complexes showed significant antibacterial activity. [Supplementary materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements for the following free supplemental files: Additional text, tables, and figures.]