3-Indoleacetic acid
ALDRICH/I3750 - 98%
Synonym: Heteroauxin; IAA
CAS Number: 87-51-4
Empirical Formula (Hill Notation): C10H9NO2
Molecular Weight: 175.18
EC Number: 201-748-2
MDL Number: MFCD00005636
Linear Formula: C10H9NO2
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material.
This image depicts SKU: I3750-100G-A
This image depicts SKU: I3750-100G-A
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: I3750-5G-A
| assay | 98% |
| InChI | 1S/C10H9NO2/c12-10(13)5-7 |
| InChI key | SEOVTRFCIGRIMH-UHFFFAOYSA |
| mp | 165-169 °C (lit.) |
| SMILES string | OC(=O)Cc1c[nH]c2ccccc12 |
| 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. |
| 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. |
| Packaging: | 25, 100 g in poly bottle |
| Packaging: | 5 g in glass bottle |
| RIDADR | NONH for all modes of transport |
| WGK Germany | WGK 3 |
| Flash Point(F) | Not applicable |
| Flash Point(C) | Not applicable |
| Purity | 98% |
| mp | 165-169 °C (lit.) |
| UNSPSC | 12352100 |