I3750
3-Indoleacetic acid
98%
Synonym(s):
Heteroauxin, IAA
Sign Into View Organizational & Contract Pricing
All Photos(3)
About This Item
Empirical Formula (Hill Notation):
C10H9NO2
CAS Number:
Molecular Weight:
175.18
Beilstein:
143358
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
98%
mp
165-169 °C (lit.)
SMILES string
OC(=O)Cc1c[nH]c2ccccc12
InChI
1S/C10H9NO2/c12-10(13)5-7-6-11-9-4-2-1-3-8(7)9/h1-4,6,11H,5H2,(H,12,13)
InChI key
SEOVTRFCIGRIMH-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
3-Indoleacetic acid (IAA) is a naturally occurring hydrophilic organic compound consists of an unsaturated aromatic ring that is commonly used in the synthesis of indolylated diarylmethanes, α-acetoxyl ketones, and Indolmethyl-Chromones via copper catalyzed coupling reactions.
Application
3-Indoleacetic acid (IAA) can be used as a building block to synthesize ,(±) harmacine using 4,4-diethoxybutan-1-amine via an acid-catalyzed acyl iminium ion cyclization reaction.
(±)-Harmacine is a vital step in the synthesis of a variety of indole alkaloids and dopamine/serotonin receptor ligands. IAA can also be used in the preparation of alkaloid (±)-19-hydroxyibogamine.
(±)-Harmacine is a vital step in the synthesis of a variety of indole alkaloids and dopamine/serotonin receptor ligands. IAA can also be used in the preparation of alkaloid (±)-19-hydroxyibogamine.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
Copper-Mediated Decarboxylative Coupling of 3-Indoleacetic Acids with Sulfoxonium Ylides for the Synthesis of alpha-Acetoxyl Ketones
Qiwen G, et al.
Organic Letters, 26, 5940-5945 (2024)
Microwave-assisted copper catalyzed decarboxylative reductive coupling of para-quinone methides with 3-indoleacetic acids: rapid access to polycyclic spiroindolequinone derivatives
Gui-Ting S, et al.
Inorganic chemistry frontiers, 10, 1512-1520 (2023)
Copper-Mediated Cyclization of o-Hydroxyaryl Enaminones with 3-Indoleacetic Acids toward the Synthesis of 3-Indolmethyl-Chromones
Kangmei W, et al.
The Journal of Organic Chemistry, 87, 9270-9281 (2022)
Effects of exogenous 3-indoleacetic acid and cadmium stress on the physiological and biochemical characteristics of Cinnamomum camphora
Jihai Z, et al.
Ecotoxicology and Environmental Safety, 191, 109998-109998 (2020)
A novel synthesis of (?)-harmacine and (?) 1, 2, 3, 4, 6, 7, 12, 12b-octahydroindole [2, 3-a] quinolizine
King Frank D
Journal of Heterocyclic Chemistry, 44(6), 1459-1463 (2007)
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service