(-)-Sparteine TCI S0461

Chemical Identity

CAS No.: 90-39-1
PubChem: CID 7014·SID 87575942
Formula: C15H26N2
Molecular weight: 234.38 g/mol
Purity: >98.0%(GC)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (1R,2S,9R,10R)-7,15-diazatetracyclo[7.7.1.02,7.010,15]heptadecane
SMILES: C1CCN2C[C@H]3C[C@@H]([C@H]2C1)CN4[C@H]3CCCC4
InChIKey: SLRCCWJSBJZJBV-TUVASFSCSA-N

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(-)-Sparteine is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemical configurations. As a key reagent in organic chemistry, it plays a crucial role in catalytic processes that require precise control over molecular structure. Its chiral nature makes it particularly valuable in the development of pharmaceutical compounds, where stereochemistry significantly influences biological activity. This compound is often employed in reactions that demand high selectivity and efficiency, making it a staple in modern synthetic laboratories.

One of the main reasons for its popularity is its ability to coordinate with transition metals, such as palladium, enhancing the effectiveness of catalytic systems. This property allows for more efficient and selective reactions, reducing byproducts and improving yield. Additionally, (-)-Sparteine exhibits good stability under standard laboratory conditions, which simplifies its handling and storage. These characteristics make it a reliable choice for researchers working on complex chemical transformations.

In Indonesian laboratories, (-)-Sparteine is extensively used in organic chemistry research, especially in the development of new compounds with pharmacological activity. It is a common reagent in experiments involving asymmetric synthesis and biological activity testing. Many research institutions and universities rely on this compound as a fundamental building block for their synthetic and analytical work. Its versatility and effectiveness have made it an essential tool in both academic and industrial research settings.

TCI brochures (PDF)

Alkaloids 2025-10-10 · p. 3
Asymmetric Synthesis 2026-03-18 · p. 7
Phytochemicals 2025-12-17 · p. 4
Ligands 2025-12-01 · p. 3

Related TCI products

Asymmetric synthesis in pharmaceutical research due to its chiral properties and ability to control stereochemistry.
Catalytic reactions involving transition metals such as palladium, enhancing reaction efficiency and selectivity.
Development of new organic compounds with specific biological activities, supporting drug discovery efforts.
Organic chemistry experiments requiring precise stereochemical control for high-purity product formation.
Biological activity testing of synthesized compounds, aiding in the evaluation of pharmacological properties.

Brand	TCI
CAS number	90-39-1
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Catalysts, Chiral Ligands, Chiral Reagents
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid
Storage	Store in a cool, dry place away from light and moisture

(-)-Sparteine should be stored in a cool, dry place, away from direct light and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its chemical integrity. Since it is a solid, it should be kept in a secure location to avoid contamination or accidental exposure. Laboratory personnel should handle it with care, using appropriate personal protective equipment when necessary. Regular monitoring of storage conditions ensures optimal performance and safety in research environments. Proper storage practices help preserve the compound’s properties and ensure its suitability for use in various synthetic and analytical applications.

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