≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads 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.
Probucol is an anti-hyperlipidemic drug initially developed in the treatment of coronary artery disease by lowering the level of cholesterol in the bloodstream by increasing the rate of LDL catabolism.
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 | Organic acids and derivatives |
| Klasse | Carboxylic acids and derivatives |
| Subclass | Tetracarboxylic acids and derivatives |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Tetracarboxylic acids and derivatives |
| Alternative Parents | Phenol esters Phenylpropanes Thiophenol ethers Phenoxy compounds Fatty acid esters Dithioketals Alkylarylthioethers Carboxylic acid esters Sulfenyl compounds Carboxylic acids Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Tetracarboxylic acid or derivatives - Phenol ester - Phenylpropane - Phenoxy compound - Aryl thioether - Thiophenol ether - Dithioketal - Fatty acid ester - Alkylarylthioether - Fatty acyl - Monocyclic benzene moiety - Benzenoid - Thioacetal - Carboxylic acid ester - Thioether - Carboxylic acid - Sulfenyl compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Organosulfur compound - Organooxygen compound - Carbonyl group - Aromatic homomonocyclic compound |
| Beschreibung | This compound belongs to the class of organic compounds known as tetracarboxylic acids and derivatives. These are carboxylic acids containing exactly four carboxyl groups. |
| External Descriptors | Not available |
| Activity Type | Relation | Activity value | Units | Action Type | Journal | PubMed Id | doi | Assay Aladdin ID |
|---|
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Datum | Artikel |
|---|---|---|---|
 G2431458 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| G2431468 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| G2431469 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| G2431470 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| G2431471 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| G2431472 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| G2431473 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| G2431474 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| G2431475 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| G2431476 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| G2431477 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| G2431478 | Certificate of Analysis | Apr 22, 2024 | P343020 |
| Löslichkeit | DMSO: 2.5 mg/mL (3.49 mM), sonification is recommended. |
|---|---|
| Empfindlichkeit | Moisture sensitive |
| Molekulargewicht | 717.000 g/mol |
| XLogP3 | 10.400 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 10 |
| Rotatable Bond Count | 18 |
| Exact Mass | 716.342 Da |
| Monoisotopic Mass | 716.342 Da |
| Topological Polar Surface Area | 178.000 Ų |
| Heavy Atom Count | 49 |
| Formal Charge | 0 |
| Complexity | 1020.000 |
| 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 |
