ammonium [R-(R*,R*)]-tartrate

98%

Reagent Code: #229959
label
Alias (2R,3R)-2,3-dihydroxysuccinate ammonium salt, diammonium tartate
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CAS Number 14307-43-8

science Other reagents with same CAS 14307-43-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 184.14 g/mol
Formula C₄H₁₂N₂O₆
thermostat Physical Properties
Boiling Point 399.3ºC at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in chiral resolution processes, particularly for the separation of enantiomers in pharmaceutical intermediates. It acts as a resolving agent due to its ability to form diastereomeric salts with racemic mixtures of basic compounds, enabling the isolation of single enantiomers. Commonly applied in the production of optically active drugs, such as certain beta-blockers and antidepressants. Also employed in asymmetric synthesis and crystallization techniques where stereochemical purity is critical. Its effectiveness in enantioselective precipitation makes it valuable in fine chemical and pharmaceutical manufacturing.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25g
10-20 days ฿330.00
100g
10-20 days ฿680.00
500g
10-20 days ฿1,980.00
2.5kg
10-20 days ฿8,800.00
ammonium [R-(R*,R*)]-tartrate
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Used in chiral resolution processes, particularly for the separation of enantiomers in pharmaceutical intermediates. It acts as a resolving agent due to its ability to form diastereomeric salts with racemic mixtures of basic compounds, enabling the isolation of single enantiomers. Commonly applied in the production of optically active drugs, such as certain beta-blockers and antidepressants. Also employed in asymmetric synthesis and crystallization techniques where stereochemical purity is critical. Its

Used in chiral resolution processes, particularly for the separation of enantiomers in pharmaceutical intermediates. It acts as a resolving agent due to its ability to form diastereomeric salts with racemic mixtures of basic compounds, enabling the isolation of single enantiomers. Commonly applied in the production of optically active drugs, such as certain beta-blockers and antidepressants. Also employed in asymmetric synthesis and crystallization techniques where stereochemical purity is critical. Its effectiveness in enantioselective precipitation makes it valuable in fine chemical and pharmaceutical manufacturing.

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