for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Température ambiante 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Le jaune de pinacryptol est un indicateur dont l'absorption UV est de 385 nm. Le jaune de pinacryptol est idéalement utilisé comme colorant pour identifier les complexes de sulfate de dodécyle et de tétradécyle lors de l'électrophorèse sur gel de polyacrylamide.
| Sourires canoniques | CCOC1=CC2=C(C=C1)[N+](=C(C=C2)C=CC3=CC(=CC=C3)[N+](=O)[O-])C.COS(=O)(=O)[O-] |
|---|---|
| IUPAC Name | 6-ethoxy-1-methyl-2-[(E)-2-(3-nitrophenyl)ethenyl]quinolin-1-ium;methyl sulfate |
| InChIKey | ZXQHSPWBYMLHLB-BXTVWIJMSA-M |
| INCHI | 1S/C20H19N2O3.CH4O4S/c1-3-25-19-11-12-20-16(14-19)8-10-17(21(20)2)9-7-15-5-4-6-18(13-15)22(23)24;1-5-6(2,3)4/h4-14H,3H2,1-2H3;1H3,(H,2,3,4)/q+1;/p-1/b9-7+; |
| Isomères SMILES | CCOC1=CC2=C(C=C1)[N+](=C(C=C2)/C=C/C3=CC(=CC=C3)[N+](=O)[O-])C.COS(=O)(=O)[O-] |
| WGK Allemagne | 3 |
| PubChem CID | 6438045 |
| Poids moléculaire | 446.47 |
| Beilstein | 3881592 |
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 |
| Classe | Quinolines and derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Quinolines and derivatives |
| Alternative Parents | Nitrobenzenes Styrenes Nitroaromatic compounds Alkyl aryl ethers Sulfuric acid monoesters Pyridinium derivatives Alkyl sulfates Heteroaromatic compounds Propargyl-type 1,3-dipolar organic compounds Azacyclic compounds Organic oxoazanium compounds Hydrocarbon derivatives Organonitrogen compounds Organic salts Organopnictogen compounds Organic oxides |
| Molecular Framework | Not available |
| Substituents | Quinoline - Nitrobenzene - Nitroaromatic compound - Styrene - Alkyl aryl ether - Sulfate-ester - Alkyl sulfate - Sulfuric acid ester - Benzenoid - Pyridine - Pyridinium - Monocyclic benzene moiety - Sulfuric acid monoester - Heteroaromatic compound - Organic sulfuric acid or derivatives - Organic nitro compound - C-nitro compound - Ether - Organic oxoazanium - Azacycle - Organic 1,3-dipolar compound - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organonitrogen compound - Hydrocarbon derivative - Organooxygen compound - Organic oxygen compound - Organic salt - Organic nitrogen compound - Organopnictogen compound - Organic oxide - Aromatic heteropolycyclic compound |
| Description | 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 |
| Solubilité | Insoluble in water. |
|---|---|
| Point de fusion (°C) | 260-262° C |
| Poids moléculaire | 446.500 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 7 |
| Rotatable Bond Count | 4 |
| Exact Mass | 446.115 Da |
| Monoisotopic Mass | 446.115 Da |
| Topological Polar Surface Area | 134.000 Ų |
| Heavy Atom Count | 31 |
| Formal Charge | 0 |
| Complexity | 567.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 1 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 1 |
| Covalently-Bonded Unit Count | 2 |
