≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Argon charged,Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
4-Aminoindole is an indole derivative. Its cytokinin activity has been assessed by tobacco pith callus bioassay.4-Aminoindole can be prepared by reacting 2,6-dinitrotoluene and N,N-dimethylformamide dimethylacetal in anhydrous DMF.
Reactant for preparation of:
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| Pubchem Sid | 488190442 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/488190442 |
| Canonical Smiles | C1=CC(=C2C=CNC2=C1)N |
| IUPAC Name | 1H-indol-4-amine |
| InChIKey | LUNUNJFSHKSXGQ-UHFFFAOYSA-N |
| INCHI | 1S/C8H8N2/c9-7-2-1-3-8-6(7)4-5-10-8/h1-5,10H,9H2 |
| Isomeric SMILES | C1=CC(=C2C=CNC2=C1)N |
| WGK Germany | 3 |
| Molecular Weight | 132.16 |
| Beilstein | 114919 |
| Reaxy-Rn | 114919 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=114919&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Indoles and derivatives |
| Subclass | Indoles |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Indoles |
| Alternative Parents | Benzenoids Pyrroles Heteroaromatic compounds Azacyclic compounds Primary amines Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Indole - Benzenoid - Heteroaromatic compound - Pyrrole - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Primary amine - Organonitrogen compound - Amine - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as indoles. These are compounds containing an indole moiety, which consists of pyrrole ring fused to benzene to form 2,3-benzopyrrole. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
 I2117205 | Certificate of Analysis | Jul 10, 2025 | A115486 |
| I2117206 | Certificate of Analysis | Jul 10, 2025 | A115486 |
| I2117207 | Certificate of Analysis | Jul 10, 2025 | A115486 |
| B2511088 | Certificate of Analysis | Apr 13, 2024 | A115486 |
| C2027083 | Certificate of Analysis | Jan 15, 2024 | A115486 |
| E2311306 | Certificate of Analysis | Jun 25, 2021 | A115486 |
| Sensitivity | air&light sensitive |
|---|---|
| Melt Point(°C) | 106-109°C |
| Molecular Weight | 132.160 g/mol |
| XLogP3 | 2.100 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 0 |
| Exact Mass | 132.069 Da |
| Monoisotopic Mass | 132.069 Da |
| Topological Polar Surface Area | 41.800 Ų |
| Heavy Atom Count | 10 |
| Formal Charge | 0 |
| Complexity | 124.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Xiaoqian Li, Xiaohua Jia, Jin Yang, Yong Li, Hongliang Lin, Haojie Song. (2023) Synergism of non-covalent interaction and ZIF-8@GO to improve tribological and mechanical properties of carbon fiber reinforced recyclable indole-based poly(hexahydrotriazine) composites. POLYMER COMPOSITES, [PMID:] [10.1002/pc.28049] |
| 2. Ting-Ting Li, Qiang Wan, Xin Zhang, Yuan Xiao, Li-Ying Sun, Yu-Rong Zhang, Xiang-Nan Liu, Wan-Chao Yang. (2022) Stellate ganglion block reduces inflammation and improves neurological function in diabetic rats during ischemic stroke. Neural Regeneration Research, [PMID:35142688] [10.4103/1673-5374.335162] |
