Determine the necessary mass, volume, or concentration for preparing a solution.
10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Protected from light,Store at -80°C Ships Dry ice packs + Cold packs 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
(+)-Sparteine is a natural alkaloid acting as a ganglionic blocking agent. (+)-Sparteine competitively blocks nicotinic ACh receptor in the neurons.
| Canonical Smiles | C1CCN2CC3CC(C2C1)CN4C3CCCC4 |
|---|---|
| IUPAC Name | (1R,2S,9R,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane |
| InChIKey | SLRCCWJSBJZJBV-TUVASFSCSA-N |
| INCHI | 1S/C15H26N2/c1-3-7-16-11-13-9-12(14(16)5-1)10-17-8-4-2-6-15(13)17/h12-15H,1-11H2/t12-,13-,14-,15+/m1/s1 |
| Isomeric SMILES | C1CCN2C[C@H]3C[C@@H]([C@H]2C1)CN4[C@H]3CCCC4 |
| RTECS | RT0620000 |
| PubChem CID | 7014 |
| Molecular Weight | 234.39 |
| Reaxy-Rn | 82448 |
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 |
| Class | Lupin alkaloids |
| Subclass | Sparteine, lupanine, and related alkaloids |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Sparteine, lupanine, and related alkaloids |
| Alternative Parents | Quinolizidines Piperidines Trialkylamines Azacyclic compounds Organopnictogen compounds Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteropolycyclic compounds |
| Substituents | Sparteine-lupanine skeleton - Quinolizidine - Piperidine - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Amine - Aliphatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as sparteine, lupanine, and related alkaloids. These are alkaloids with a structure based on either sparteine, lupanine, or derivatives thereof. These are tetracyclic compounds made of two fused quinolizidine ring systems. |
| External Descriptors | Not available |
| Sensitivity | Light sensitive&Moisture & Heat sensitive |
|---|---|
| Refractive Index | 1.53 |
| Specific Rotation[α] | +18° (C=1,EtOH) |
| Flash Point(°C) | 148 °C |
| Boil Point(°C) | 174°C/8mmHg |
| Molecular Weight | 234.380 g/mol |
| XLogP3 | 2.500 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 0 |
| Exact Mass | 234.21 Da |
| Monoisotopic Mass | 234.21 Da |
| Topological Polar Surface Area | 6.500 Ų |
| Heavy Atom Count | 17 |
| Formal Charge | 0 |
| Complexity | 263.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 4 |
| 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 |
| 1. Hongzhu Lai, Li Jiang, Wenyan Huang, Bibiao Jiang, Daoyong Chen. (2025) Synthesis and Directed One-Dimensional Self-Assembly of Dumbbell-Shaped Single-Chain Particles. JOURNAL OF POLYMER SCIENCE, 63 (8): (1938-1946). [PMID:] [10.1002/pol.20250020] |