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Di-para-toluoyl-D-Tartaric acid, Anhydrous
Di-para-toluoyl-D-Tartaric acid, Anhydrous

Di-para-toluoyl-D-Tartaric acid, Anhydrous

MOQ : 1 Gram

Di-para-toluoyl-D-Tartaric acid, Anhydrous Specification

  • Usage
  • Chiral resolution, research, chemical synthesis
  • Size
  • As per requirement
  • Ph Level
  • Acidic
  • Melting Point
  • >175C (decomposes)
  • Molecular Formula
  • C18H16O6
  • Physical State
  • Solid
  • Density
  • Gram per cubic centimeter(g/cm3)
  • Purity
  • 99%
  • Storage Instructions
  • Store in cool, dry place, in tightly closed container
  • Shelf Life
  • 36 months (if stored properly)
  • Packaging Type
  • Bottle/Drum/Customized packaging
  • Molecular Weight
  • 352.33 g/mol
  • Type
  • Acid
  • Application
  • Resolving agent for chiral amines, pharmaceutical intermediate, research
  • Appearance
  • White Crystalline Powder
  • Purity(%)
  • 99.0
 

Di-para-toluoyl-D-Tartaric acid, Anhydrous Trade Information

  • Minimum Order Quantity
  • 1 Gram
  • Supply Ability
  • 1 Gram Per Week
  • Delivery Time
  • 1 Week
 

About Di-para-toluoyl-D-Tartaric acid, Anhydrous

Di-para-toluoyl-D-Tartaric acid, Anhydrous

CAS Number

32634-68-7

Appearance

White to pale yellow powder

Assay

99.0 % min.

Optical rotation

+]D20=+136o-+143o

Optical purity

99.0 % min.ee

Boiling point

169 - 171

Molecular weight

386.35

Use

Used in chiral medicine, chiral intermediate and asymmetric catalysis, or its titanium complex can be used in the asymmetric oxidization of enol.

Storage

Keep container tightly closed. Store in a cool, dry, well-ventilated area. Ensure adequate ventilation during use. Use only in a chemical fume hood.Avoid sources of ignition.



Exceptional Chiral Resolving Agent

Known for its effectiveness in resolving chiral amines, Di-para-toluoyl-D-Tartaric acid plays a vital role in separating enantiomers, which is crucial for the synthesis of optically active pharmaceutical ingredients and other fine chemicals. The compounds consistent high purity ensures optimal performance in both laboratory and commercial settings.


High Purity and Stability Guaranteed

With a purity of 99% and anhydrous form, this acid ensures minimal contamination and predictable results in sensitive chemical processes. Its stability at elevated temperatures (decomposes above 175C) and acidic pH make it a dependable choice for research and synthesis tasks requiring stringent specifications.


Flexible Packaging and Long Shelf Life

To accommodate diverse user preferences, Di-para-toluoyl-D-Tartaric acid is offered in bottles, drums, or customized packaging with size options as per specific requirements. It boasts a shelf life of up to 36 months when stored in a cool, dry place within tightly closed containers, ensuring long-term usability and convenience.

FAQs of Di-para-toluoyl-D-Tartaric acid, Anhydrous:


Q: How should Di-para-toluoyl-D-Tartaric acid, Anhydrous be stored to maintain its quality?

A: The compound should be kept in a cool, dry place in a tightly sealed container to preserve its integrity. Proper storage conditions help maintain its purity and ensure a shelf life of up to 36 months.

Q: What are the main applications of Di-para-toluoyl-D-Tartaric acid, Anhydrous?

A: This acid is primarily used as a resolving agent for chiral amines, in the preparation of pharmaceutical intermediates, and for advanced chemical research and synthesis.

Q: When is it beneficial to use Di-para-toluoyl-D-Tartaric acid in pharmaceutical processes?

A: Its especially valuable when high purity and precise chiral resolution are essential, such as in the synthesis of optically active compounds or intermediates in drug manufacturing.

Q: Where can I purchase Di-para-toluoyl-D-Tartaric acid in India?

A: The product is available across India through a network of distributors, exporters, importers, manufacturers, retailers, suppliers, traders, and wholesalers. Custom packaging and sizes can be requested as needed.

Q: What is the process for using this acid as a chiral resolving agent?

A: It is typically employed in fractional crystallization or salt formation protocols to separate enantiomers of chiral amines, facilitating subsequent isolation of the desired optical isomer.

Q: What are the benefits of selecting this anhydrous acid for research purposes?

A: Researchers benefit from its high purity (99%), excellent stability, and reliable performance in chiral resolution, which are essential for reproducible results and advanced chemical synthesis.

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