()-Di-p-toluoyl-D-tartaric acid

98.0%

Reagent Code: #70771
label
Alias Dip-toluoyl-D-tartaric acid
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CAS Number 32634-68-7

science Other reagents with same CAS 32634-68-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 386.35 g/mol
Formula C₂₀H₁₈O₈
badge Registry Numbers
EC Number 251-132-2
MDL Number MFCD00008552
thermostat Physical Properties
Melting Point 169-171 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used extensively in the pharmaceutical industry as a chiral resolving agent to separate enantiomers of racemic compounds, particularly in the production of optically pure drugs. It is highly effective in forming diastereomeric salts with basic compounds, enabling the purification of specific enantiomers through crystallization. This chemical is also employed in asymmetric synthesis and catalysis, aiding in the development of enantioselective reactions. Additionally, it finds application in analytical chemistry for the determination of enantiomeric purity in chiral molecules. Its stability and efficiency make it a valuable tool in research and industrial processes focused on chiral separations and synthesis.

format_list_bulleted Product Specification

Test Parameter Specification
Specific Optical Rotation (20°C, 1% EtOH) 134-142
Purity (HPLC) 98-100
Purity (Titration with NaOH) 97.5-102.5
Appearance White crystal or crystal powder
Infrared Spectrum Conforms to Structure
Solubility Almost transparent (hot methanol)

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿290.00
inventory 25g
10-20 days ฿380.00
inventory 100g
10-20 days ฿560.00
inventory 500g
10-20 days ฿2,460.00
inventory 2.5kg
10-20 days ฿11,520.00

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()-Di-p-toluoyl-D-tartaric acid
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Used extensively in the pharmaceutical industry as a chiral resolving agent to separate enantiomers of racemic compounds, particularly in the production of optically pure drugs. It is highly effective in forming diastereomeric salts with basic compounds, enabling the purification of specific enantiomers through crystallization. This chemical is also employed in asymmetric synthesis and catalysis, aiding in the development of enantioselective reactions. Additionally, it finds application in analytical che

Used extensively in the pharmaceutical industry as a chiral resolving agent to separate enantiomers of racemic compounds, particularly in the production of optically pure drugs. It is highly effective in forming diastereomeric salts with basic compounds, enabling the purification of specific enantiomers through crystallization. This chemical is also employed in asymmetric synthesis and catalysis, aiding in the development of enantioselective reactions. Additionally, it finds application in analytical chemistry for the determination of enantiomeric purity in chiral molecules. Its stability and efficiency make it a valuable tool in research and industrial processes focused on chiral separations and synthesis.

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