D-Mandelic Acid | 611-71-2

Description :

Overview of D-Mandelic Acid

D-Mandelic Acid is a pharmaceutical-grade chiral organic acid widely used in pharmaceutical synthesis and formulation development. It is the dextrorotatory isomer of mandelic acid and is valued for its optical purity and controlled reactivity.

In pharmaceutical manufacturing, D-Mandelic Acid is used as an intermediate and functional ingredient where stereochemical specificity is important. It is produced under regulated conditions to meet purity, enantiomeric excess, and quality requirements. D-mandelic acid manufacturers in India supply this compound for both domestic and export pharmaceutical markets.

As a pharma chemical, D-Mandelic Acid is primarily used in API synthesis, formulation support, and specialty pharmaceutical applications.

Applications of D-Mandelic Acid

Pharmaceutical Intermediate in API Synthesis

D-Mandelic Acid is used as a chiral intermediate in the synthesis of active pharmaceutical ingredients. Its defined stereochemistry supports the development of enantiomerically pure drugs and controlled reaction pathways in pharmaceutical manufacturing.

Antimicrobial & Urological Formulation Support

D-Mandelic Acid is used in pharmaceutical formulations intended for urinary tract–related applications, where its mild antimicrobial and acidifying properties are beneficial. It supports controlled pH management in specialised formulations.

Resolution Agent & Chiral Separation

D-Mandelic Acid is used as a resolving agent in the separation of racemic mixtures during pharmaceutical synthesis. Its chiral nature allows selective interaction with target compounds, improving yield and purity.

Regulated Pharmaceutical Manufacturing Use

D-Mandelic Acid is manufactured as a high-purity pharmaceutical raw material with strict control over optical rotation, impurity profile, and residual solvents. It is suitable for GMP-compliant pharmaceutical production environments.

In chiral synthesis and acid-based formulation development, it is often evaluated alongside Mandelic Acid, L-Mandelic Acid, and Benzoic Acid for functional comparison.

Safety & Handling Guidelines

• Store in a cool, dry, and controlled environment

• Protect from moisture and excessive heat

• Keep containers tightly sealed and clearly labelled

• Avoid inhalation of dust during handling

• Use appropriate personal protective equipment

• Handle under controlled pharmaceutical manufacturing conditions

• Dispose of waste according to regulatory guidelines
  
  
  

Where to Buy D-Mandelic Acid?

D-Mandelic Acid Manufacturer

D-Mandelic Acid is manufactured for pharmaceutical applications where chiral purity, consistent quality, and regulatory compliance are essential.

D-Mandelic Acid Supplier & Distributor

Pharmaceutical-grade D-Mandelic Acid is supplied in suitable packaging for formulation manufacturers and API producers. As a pharmaceutical chemicals supplier and distributor, Chemicalbull Pvt. Ltd. supports reliable sourcing with standard documentation.

MSDS for D-Mandelic Acid

The MSDS for D-Mandelic Acid provides information on chemical hazards, handling precautions, storage conditions, exposure controls, and emergency response measures. It should be reviewed before pharmaceutical manufacturing use.

Frequently Asked Questions (FAQs)

1. What is D-Mandelic Acid used for?

   D-Mandelic Acid is used in pharmaceutical synthesis, chiral resolution processes, and specialised formulation applications.
   
   

2. What is the formula of D-Mandelic Acid?

   The D-mandelic acid formula is C₈H₈O₃.
   
   

3. What is the structure of D-Mandelic Acid?

   D-mandelic acid structure consists of a benzene ring attached to a hydroxyl-substituted acetic acid moiety with defined chirality.
   
   

4. Is D-Mandelic Acid manufactured in India?

   Yes, D-mandelic acid manufacturers in India produce pharmaceutical-grade material under regulated conditions.
   
   

5. Is D-Mandelic Acid different from L-Mandelic Acid?

   Yes, D-Mandelic Acid and L-Mandelic Acid are optical isomers with different stereochemical orientations.