≥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.
Information
Hydroprotopine (W1171) is a kind of natural herbal extract.
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 | Alkaloids and derivatives |
| Classe | Protoberberine alkaloids and derivatives |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Protoberberine alkaloids and derivatives |
| Alternative Parents | Tetrahydroisoquinolines Benzodioxoles Benzenoids Tetraalkylammonium salts Oxacyclic compounds Azacyclic compounds Alkanolamines Acetals Organopnictogen compounds Organic salts Hydrocarbon derivatives Organic cations |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Protoberberine skeleton - Tetrahydroprotoberberine skeleton - Tetrahydroisoquinoline - Benzodioxole - Benzenoid - Tetraalkylammonium salt - Acetal - Alkanolamine - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organic salt - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Organic cation - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as protoberberine alkaloids and derivatives. These are alkaloids with a structure based on a protoberberine moiety, which consists of a 5,6-dihydrodibenzene moiety fused to a quinolizinium and forming 5,6-Dihydrodibenzo(a,g)quinolizinium skeleton. |
| 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 | Article |
|---|---|---|---|
 K2218484 | Certificate of Analysis | Sep 04, 2025 | H414365 |
| K2218485 | Certificate of Analysis | Sep 04, 2025 | H414365 |
| K2218594 | Certificate of Analysis | Sep 04, 2025 | H414365 |
| K2218595 | Certificate of Analysis | Sep 04, 2025 | H414365 |
| K2218596 | Certificate of Analysis | Sep 04, 2025 | H414365 |
| Solubilité | Solubility (25°C) In vitro DMSO: 53.7 mg/mL (151.53 mM); |
|---|---|
| DMSO (mg/mL) Solubilité maximale | 53.7 |
| DMSO (mM) Solubilité maximale | 151.533750121693 |
| Poids moléculaire | 354.400 g/mol |
| XLogP3 | 2.200 |
| Hydrogen Bond Donor Count | 1 |
| Hydrogen Bond Acceptor Count | 5 |
| Rotatable Bond Count | 0 |
| Exact Mass | 354.134 Da |
| Monoisotopic Mass | 354.134 Da |
| Topological Polar Surface Area | 57.200 Ų |
| Heavy Atom Count | 26 |
| Formal Charge | 1 |
| Complexity | 589.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 2 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
