≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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.
Methyl reserpate (NSC 81464) is a Yohimbine type alkaloid, that can be isolated from Rauwolfia vomitoria roots and leaves.
| Pubchem Sid | 528765620 |
|---|---|
| Sorrisi canonici | COC1C(CC2CN3CCC4=C(C3CC2C1C(=O)OC)NC5=C4C=CC(=C5)OC)O |
| IUPAC Name | methyl (1R,15S,17R,18R,19S,20S)-17-hydroxy-6,18-dimethoxy-1,3,11,12,14,15,16,17,18,19,20,21-dodecahydroyohimban-19-carboxylate |
| InChIKey | MDJQWFFIUHUJSB-UQVJXISSSA-N |
| INCHI | 1S/C23H30N2O5/c1-28-13-4-5-14-15-6-7-25-11-12-8-19(26)22(29-2)20(23(27)30-3)16(12)10-18(25)21(15)24-17(14)9-13/h4-5,9,12,16,18-20,22,24,26H,6-8,10-11H2,1-3H3/t12-,16+,18-,19-,20+,22+/m1/s1 |
| Isomeri SMILES | CO[C@H]1[C@@H](C[C@@H]2CN3CCC4=C([C@H]3C[C@@H]2[C@@H]1C(=O)OC)NC5=C4C=CC(=C5)OC)O |
| PubChem CID | 73532 |
| Peso molecolare | 414.49 |
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 | Yohimbine alkaloids |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Yohimbine alkaloids |
| Alternative Parents | Corynanthean-type alkaloids Beta carbolines 3-alkylindoles Anisoles Alkyl aryl ethers Aralkylamines Piperidines Pyrroles Methyl esters Heteroaromatic compounds Trialkylamines Secondary alcohols Amino acids and derivatives Cyclic alcohols and derivatives Monocarboxylic acids and derivatives Dialkyl ethers Azacyclic compounds Hydrocarbon derivatives Organic oxides Organopnictogen compounds Carbonyl compounds |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Yohimbine - Corynanthean skeleton - Yohimbine alkaloid - Beta-carboline - Pyridoindole - 3-alkylindole - Indole - Indole or derivatives - Anisole - Alkyl aryl ether - Aralkylamine - Piperidine - Benzenoid - Pyrrole - Methyl ester - Heteroaromatic compound - Cyclic alcohol - Tertiary aliphatic amine - Tertiary amine - Secondary alcohol - Amino acid or derivatives - Carboxylic acid ester - Organoheterocyclic compound - Azacycle - Carboxylic acid derivative - Monocarboxylic acid or derivatives - Ether - Dialkyl ether - Alcohol - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organooxygen compound - Amine - Organic nitrogen compound - Aromatic heteropolycyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as yohimbine alkaloids. These are alkaloids containing the pentacyclic yohimban skeleton. The Yohimbinoid alkaloids contain a carbocyclic ring E arising through C-17 to C-18 bond formation in a corynantheine precursor. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 H2421256 | Certificate of Analysis | May 08, 2024 | R342807 |
| H2421441 | Certificate of Analysis | May 08, 2024 | R342807 |
| H2421442 | Certificate of Analysis | May 08, 2024 | R342807 |
| H2421443 | Certificate of Analysis | May 08, 2024 | R342807 |
| H2421444 | Certificate of Analysis | May 08, 2024 | R342807 |
| H2421445 | Certificate of Analysis | May 08, 2024 | R342807 |
| H2421446 | Certificate of Analysis | May 08, 2024 | R342807 |
| H2421447 | Certificate of Analysis | May 08, 2024 | R342807 |
| Solubilità | Soluble in chloroform, dichloromethane, DMSO, and methanol. |
|---|---|
| Indice di rifrazione | n20D1.64 (Predicted) |
| Punto di ebollizione (°C) | ~587.8° C at 760 mmHg (Predicted) |
| Punto di fusione (°C) | >200° C (dec.) |
| Peso molecolare | 414.500 g/mol |
| XLogP3 | 1.900 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 6 |
| Rotatable Bond Count | 4 |
| Exact Mass | 414.215 Da |
| Monoisotopic Mass | 414.215 Da |
| Topological Polar Surface Area | 84.000 Ų |
| Heavy Atom Count | 30 |
| Formal Charge | 0 |
| Complexity | 647.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 6 |
| 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 |
