≥99%(T) for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Lagerung bei 2-8°C Ships Nasses Eis 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Pubchem Sid | 504754331 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504754331 |
| Kanonisches Lächeln | CC[N+]1=C(C=CC2=CC=CC=C21)C.[I-] |
| IUPAC Name | 1-ethyl-2-methylquinolin-1-ium;iodide |
| InChIKey | OEVSHJVOKFWBJY-UHFFFAOYSA-M |
| INCHI | 1S/C12H14N.HI/c1-3-13-10(2)8-9-11-6-4-5-7-12(11)13;/h4-9H,3H2,1-2H3;1H/q+1;/p-1 |
| Isomere SMILES | CC[N+]1=C(C=CC2=CC=CC=C21)C.[I-] |
| RTECS | VA0740000 |
| PubChem CID | 69076 |
| Molekulargewicht | 299.16 |
| Reaxy-Rn | 3575423 |
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 |
| Klasse | Quinolines and derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Quinolines and derivatives |
| Alternative Parents | Methylpyridines Pyridinium derivatives Benzenoids Heteroaromatic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organic iodide salts Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Quinoline - Methylpyridine - Benzenoid - Pyridinium - Pyridine - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organic iodide salt - Organic salt - Organonitrogen compound - Aromatic heteropolycyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as quinolines and derivatives. These are compounds containing a quinoline moiety, which consists of a benzene ring fused to a pyrimidine ring to form benzo[b]azabenzene. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
 D2402083 | Certificate of Analysis | Jan 16, 2026 | Q160816 |
| F2005050 | Certificate of Analysis | Jan 19, 2024 | Q160816 |
| F2217057 | Certificate of Analysis | Jun 09, 2022 | Q160816 |
| F2217058 | Certificate of Analysis | Jun 09, 2022 | Q160816 |
| Löslichkeit | Soluble in Water |
|---|---|
| Schmelzpunkt (°C) | 231℃ |
| Molekulargewicht | 299.150 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 1 |
| Rotatable Bond Count | 1 |
| Exact Mass | 299.017 Da |
| Monoisotopic Mass | 299.017 Da |
| Topological Polar Surface Area | 3.900 Ų |
| Heavy Atom Count | 14 |
| Formal Charge | 0 |
| Complexity | 167.000 |
| 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 | 2 |
