Indole-3-propionic acid
ALDRICH/57410 - ≥97.0% (T)
Synonym: NSC 3252; NSC 47831; 3-
CAS Number: 830-96-6
Empirical Formula (Hill Notation): C11H11NO2
Molecular Weight: 189.21
EC Number: 212-600-1
MDL Number: MFCD00005660
Linear Formula: C11H11NO2
Product Type: Chemical
| assay | ≥97.0% (T) |
| form | solid |
| functional group | carboxylic acid |
| InChI | 1S/C11H11NO2/c13-11(14)6- |
| InChI key | GOLXRNDWAUTYKT-UHFFFAOYSA |
| Quality Level | 100  |
| SMILES string | OC(=O)CCc1c[nH]c2ccccc12 |
| Application: | Reactant for preparation of: • Fluorescent analogues of strigolactones • Anti-tumor agents • Melanocortin receptors ligands • Immunosuppressive agents • Iinhibitors of hepatitis C virus • Histamine H4 receptor agonists • NR2B/NMDA receptor antagonists • CB1 antagonist for the treatment of obesity • Antibacterial agents • Inhibitor of TGF-β receptor binding Indole-3-propionic acid may be used in the synthesis of oxindole-3-propionic acid via reaction with N-bromosuccinimide in acetic acid followed by treatment with H2/Pd catalyst. |
| Biochem/physiol Actions: | Studied as an adjunct to improve perfusion after liver transplant. |
| Biochem/physiol Actions: | Was studied as an adjunct to improve perfusion after liver transplant. |
| General description: | Indole-3-propionic acid can be obtained from tryptophan by deamination reaction. |
| Packaging: | 100 g in poly bottle |
| Packaging: | 25 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 | ≥97.0% (T) |
| UNSPSC | 12352100 |