Determine the necessary mass, volume, or concentration for preparing a solution.
≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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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.
Vindesine sulfate is a vinca alkaloid derived from vinblastine. Vindesine sulfate is an inhibitor of Tubulin.
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Alkaloids and derivatives |
| Classe | Vinca alkaloids |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Vinca alkaloids |
| Alternative Parents | Quinoline carboxamides Carbazoles 3-alkylindoles Anisoles Dialkylarylamines Alkyl aryl ethers Aralkylamines Piperidines Organic sulfuric acids N-alkylpyrrolidines Tertiary alcohols Pyrroles Heteroaromatic compounds Methyl esters 1,2-aminoalcohols Cyclic alcohols and derivatives Primary carboxylic acid amides Trialkylamines Secondary alcohols Amino acids and derivatives Azacyclic compounds Monocarboxylic acids and derivatives Organopnictogen compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Vinca alkaloid skeleton - Carbazole - Quinoline-6-carboxamide - 3-alkylindole - Indole - Indole or derivatives - Anisole - Dialkylarylamine - Tertiary aliphatic/aromatic amine - Alkyl aryl ether - Sulfuric acid - Aralkylamine - Piperidine - Benzenoid - N-alkylpyrrolidine - Cyclic alcohol - Heteroaromatic compound - Organic sulfuric acid or derivatives - Pyrrole - Pyrrolidine - Tertiary alcohol - Methyl ester - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Amino acid or derivatives - Carboxamide group - Carboxylic acid ester - 1,2-aminoalcohol - Primary carboxylic acid amide - Ether - Organoheterocyclic compound - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Azacycle - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Alcohol - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organopnictogen compound - Amine - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as vinca alkaloids. These are alkaloids with a dimeric chemical structure composed of an indole nucleus (catharanthine), and a dihydroindole nucleus (vindoline), joined together. |
| External Descriptors | alkaloid sulfate salt |
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| Lot Number | Certificate Type | Date | Article |
|---|---|---|---|
| Certificate of Analysis | Apr 01, 2026 | V342764 | |
| Certificate of Analysis | Dec 06, 2025 | V342764 | |
| Certificate of Analysis | Aug 08, 2025 | V342764 | |
| Certificate of Analysis | Jun 09, 2025 | V342764 | |
| Certificate of Analysis | Jun 09, 2025 | V342764 | |
| Certificate of Analysis | Jun 09, 2025 | V342764 | |
| Certificate of Analysis | Jun 09, 2025 | V342764 | |
| Certificate of Analysis | Jun 09, 2025 | V342764 | |
| Certificate of Analysis | Jun 09, 2025 | V342764 |
| Solubilité | Soluble in methanol, DMSO, water, and methyl alcohol. |
|---|---|
| Indice de réfraction | n20D1.71 (Predicted) |
| Point de fusion (°C) | >250° C |
| Poids moléculaire | 852.000 g/mol |
| XLogP3 | |
| Hydrogen Bond Donor Count | 7 |
| Hydrogen Bond Acceptor Count | 14 |
| Rotatable Bond Count | 7 |
| Exact Mass | 851.378 Da |
| Monoisotopic Mass | 851.378 Da |
| Topological Polar Surface Area | 248.000 Ų |
| Heavy Atom Count | 60 |
| Formal Charge | 0 |
| Complexity | 1650.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 9 |
| 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 |