10265-70-0

Basic information

• Product Name: 1H-Indole-3-butanoic acid monosodium salt
• Synonyms: SODIUM 3-INDOLEBUTYRATE;1H-Indole-3-butanoic acid monosodium salt;Sodium 4-(3-indolyl)butanoate
• CAS NO: 10265-70-0
• Molecular Formula: C₁₂H₁₂NO₂*Na
• Molecular Weight: 225.22
• Mol File: 10265-70-0.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1H-Indole-3-butanoic acid monosodium salt(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole-3-butanoic acid monosodium salt(10265-70-0)
• EPA Substance Registry System: 1H-Indole-3-butanoic acid monosodium salt(10265-70-0)

Safety Data

• Hazardous Substances Data: 10265-70-0(Hazardous Substances Data)

Usage

General Description

1H-Indole-3-butanoic acid monosodium salt is a specific chemical compound broadly used in the field of biochemistry and organic chemistry. It is a monosodium salt derivative of indole-3-butanoic acid, an essential compound in plant physiology and often used to study plant growth and development. It is recognized by its molecular formula C12H12N2O2.Na, and it appears as an off-white or beige colored powder. It is soluble in water and has a slightly acidic pH. As an organic compound, it's crucial in biochemistry research and other chemical reactions or procedures in various laboratory and industrial contexts.

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 articles and documents

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.]