57105-45-0

Basic information

• Product Name: N-(3-Indolylacetyl)-L-isoleucine
• Synonyms: IAA-L-ILE;INDOLE-3-ACETYL-L-ISOLEUCINE;N-(3-INDOLYLACETYL)-L-ISOLEUCINE;N-(3-Indolylacetyl)-L-isoleucine, Indole-3-acetyl-L-isoleucine, 99%;INDOLE-3-ACETYL-L-ISOLEUCINE (IAIleu)
• CAS NO: 57105-45-0
• Molecular Formula: C16H20N2O3
• Molecular Weight: 288.34
• Product Categories: Indoles and derivatives;Leucine Derivatives;Peptide Synthesis;Unnatural Amino Acid Derivatives
• Mol File: 57105-45-0.mol
• Article Data: 0

Chemical Properties

• Melting Point: 182-183 °C(lit.)
• Boiling Point: 591.4°Cat760mmHg
• Flash Point: 311.4°C
• Appearance: /
• Density: 1.226g/cm³
• Vapor Pressure: 7.87E-15mmHg at 25°C
• Refractive Index: 1.605
• CAS DataBase Reference: N-(3-Indolylacetyl)-L-isoleucine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(3-Indolylacetyl)-L-isoleucine(57105-45-0)
• EPA Substance Registry System: N-(3-Indolylacetyl)-L-isoleucine(57105-45-0)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 57105-45-0(Hazardous Substances Data)

Usage

Description

N-(3-Indolylacetyl)-L-isoleucine, also known as Indole-3-acetyl-L-isoleucine, is an indole-3-acetyl-amino acid conjugate that plays a crucial role in the regulatory mechanisms controlling auxin activity. N-(3-Indolylacetyl)-L-isoleucine is involved in various physiological and pathophysiological responses, making it a significant molecule in the study of plant biology and potentially in the development of agricultural applications.

Uses

Used in Plant Biology Research:
N-(3-Indolylacetyl)-L-isoleucine is used as a research tool for understanding the complex regulatory mechanisms of auxin activity in plants. Its role in controlling auxin activity is essential for various physiological and pathophysiological responses, which can provide insights into plant growth, development, and stress responses.
Used in Agricultural Applications:
N-(3-Indolylacetyl)-L-isoleucine has potential applications in the agricultural industry, particularly in the development of crops with improved stress resistance and growth characteristics. By modulating auxin activity, this compound could be used to enhance crop yields and resilience against environmental stressors.
Used in Pharmaceutical Development:
Given its involvement in regulatory mechanisms, N-(3-Indolylacetyl)-L-isoleucine may also have potential applications in the pharmaceutical industry. Further research into its specific roles and interactions could lead to the development of new drugs targeting various physiological and pathophysiological conditions.

InChI:InChI=1/C16H20N2O3/c1-3-10(2)15(16(20)21)18-14(19)8-11-9-17-13-7-5-4-6-12(11)13/h4-7,9-10,15,17H,3,8H2,1-2H3,(H,18,19)(H,20,21)