(-)-Dibenzoyl-L-tartaric acid monohydrate

98%

Reagent Code: #221363
label
Alias (-)-Dibenzoyl-L-tartaric acid monohydrate; L-(-)-Dibenzoyl-tartaric acid monohydrate; (-)-Dibenzoyl-L-tartaric acid monohydrate;
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CAS Number 62708-56-9

science Other reagents with same CAS 62708-56-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 376.31 g/mol
Formula C₁₈H₁₆O₉
badge Registry Numbers
MDL Number MFCD00149119
thermostat Physical Properties
Melting Point 88-89 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in chiral resolution to separate enantiomers of basic organic compounds, especially amines. Its ability to form diastereomeric salts with racemic mixtures allows for the isolation of optically active compounds through selective crystallization. Commonly employed in pharmaceutical synthesis for obtaining enantiomerically pure intermediates. Also utilized as a chiral derivatizing agent in analytical chemistry to determine enantiomeric purity. The monohydrate form enhances stability and reproducibility in crystallization processes.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿300.00
inventory 100g
10-20 days ฿580.00
inventory 500g
10-20 days ฿1,660.00
inventory 2.5kg
10-20 days ฿6,780.00

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(-)-Dibenzoyl-L-tartaric acid monohydrate
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Used in chiral resolution to separate enantiomers of basic organic compounds, especially amines. Its ability to form diastereomeric salts with racemic mixtures allows for the isolation of optically active compounds through selective crystallization. Commonly employed in pharmaceutical synthesis for obtaining enantiomerically pure intermediates. Also utilized as a chiral derivatizing agent in analytical chemistry to determine enantiomeric purity. The monohydrate form enhances stability and reproducibility

Used in chiral resolution to separate enantiomers of basic organic compounds, especially amines. Its ability to form diastereomeric salts with racemic mixtures allows for the isolation of optically active compounds through selective crystallization. Commonly employed in pharmaceutical synthesis for obtaining enantiomerically pure intermediates. Also utilized as a chiral derivatizing agent in analytical chemistry to determine enantiomeric purity. The monohydrate form enhances stability and reproducibility in crystallization processes.

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