Sparteine sulfate

≥98%

Reagent Code: #236070
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CAS Number 299-39-8

science Other reagents with same CAS 299-39-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.46 g/mol
Formula C₁₅H₂₈N₂O₄S
thermostat Physical Properties
Melting Point 135 °C
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a chiral base in asymmetric synthesis, particularly in enantioselective deprotonation reactions. Commonly employed in the preparation of chiral intermediates for pharmaceuticals. Acts as a ligand in organometallic chemistry to influence stereoselectivity. Also utilized in the resolution of racemic mixtures, especially in the separation of alkaloids. Has been used in cardiac research due to its antiarrhythmic properties, though clinical use is limited. Serves as a diagnostic tool in coordination chemistry for studying metal ion complexation behavior. Additionally, it serves as a probe substrate in pharmacokinetic studies to evaluate CYP2D6 enzyme activity, which is crucial for understanding inter-individual variability in drug metabolism, efficacy, and side effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿26,000.00

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Sparteine sulfate
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Used as a chiral base in asymmetric synthesis, particularly in enantioselective deprotonation reactions. Commonly employed in the preparation of chiral intermediates for pharmaceuticals. Acts as a ligand in organometallic chemistry to influence stereoselectivity. Also utilized in the resolution of racemic mixtures, especially in the separation of alkaloids. Has been used in cardiac research due to its antiarrhythmic properties, though clinical use is limited. Serves as a diagnostic tool in coordination c

Used as a chiral base in asymmetric synthesis, particularly in enantioselective deprotonation reactions. Commonly employed in the preparation of chiral intermediates for pharmaceuticals. Acts as a ligand in organometallic chemistry to influence stereoselectivity. Also utilized in the resolution of racemic mixtures, especially in the separation of alkaloids. Has been used in cardiac research due to its antiarrhythmic properties, though clinical use is limited. Serves as a diagnostic tool in coordination chemistry for studying metal ion complexation behavior. Additionally, it serves as a probe substrate in pharmacokinetic studies to evaluate CYP2D6 enzyme activity, which is crucial for understanding inter-individual variability in drug metabolism, efficacy, and side effects.

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