()-Dibenzoyl-D-tartaric acid

99%

Reagent Code: #71366
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CAS Number 17026-42-5

science Other reagents with same CAS 17026-42-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 358.30 g/mol
Formula C₁₈H₁₄O₈
badge Registry Numbers
MDL Number MFCD00063222
thermostat Physical Properties
Melting Point 154-156 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used as a resolving agent in the separation of racemic mixtures, particularly for chiral amines and alcohols. It forms diastereomeric salts with enantiomers, allowing their purification through crystallization. Commonly applied in pharmaceutical synthesis to obtain optically pure compounds. Also serves as a chiral catalyst or additive in asymmetric synthesis. Its effectiveness in enantiomeric resolution makes it valuable in producing single-enantiomer drugs and fine chemicals.

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Test Parameter Specification
Purity 98-102
Specific Rotation [α]20/D (c=1, Ethanol) 113-119
Appearance White to off-white to yellow powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500g
10-20 days ฿2,690.00
inventory 5kg
10-20 days ฿19,620.00
inventory 25g
10-20 days ฿320.00
inventory 100g
10-20 days ฿840.00
inventory 1kg
10-20 days ฿5,220.00

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()-Dibenzoyl-D-tartaric acid
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Used as a resolving agent in the separation of racemic mixtures, particularly for chiral amines and alcohols. It forms diastereomeric salts with enantiomers, allowing their purification through crystallization. Commonly applied in pharmaceutical synthesis to obtain optically pure compounds. Also serves as a chiral catalyst or additive in asymmetric synthesis. Its effectiveness in enantiomeric resolution makes it valuable in producing single-enantiomer drugs and fine chemicals.

Used as a resolving agent in the separation of racemic mixtures, particularly for chiral amines and alcohols. It forms diastereomeric salts with enantiomers, allowing their purification through crystallization. Commonly applied in pharmaceutical synthesis to obtain optically pure compounds. Also serves as a chiral catalyst or additive in asymmetric synthesis. Its effectiveness in enantiomeric resolution makes it valuable in producing single-enantiomer drugs and fine chemicals.

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