D-(-)-Mandelic Acid TCI M0662

Chemical Identity

CAS No.: 611-71-2
PubChem: CID 11914·SID 87572674
Formula: C8H8O3
Molecular weight: 152.15 g/mol
Purity: >99.0%(GC)(T)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2R)-2-hydroxy-2-phenylacetic acid
SMILES: C1=CC=C(C=C1)[C@H](C(=O)O)O
InChIKey: IWYDHOAUDWTVEP-SSDOTTSWSA-N

Rp 875.700,00

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D-(-)-Mandelic Acid is a chiral compound widely used in chemical reactions, particularly in asymmetric synthesis. It serves as a key chiral building block in the development of optically active compounds, playing a crucial role in the synthesis of pharmaceuticals and organic molecules. This compound is essential for chemists and pharmacologists who require precise control over molecular stereochemistry. Its unique structure enables it to interact effectively with various reagents, making it a versatile tool in synthetic chemistry.

The physical and chemical properties of D-(-)-Mandelic Acid make it a preferred choice for laboratory use. It exhibits stability under normal conditions and dissolves well in organic solvents, which simplifies its handling and application. Its high purity and consistent structure ensure reliable results in experimental processes. These characteristics contribute to its widespread use in both academic and industrial research settings.

In Indonesian laboratories, D-(-)-Mandelic Acid is commonly used in research focused on asymmetric synthesis and pharmaceutical development. Its availability and reliable performance make it a popular choice among scientists working in chemical and pharmaceutical fields. Its role in creating complex molecular structures supports advancements in drug discovery and organic chemistry.

Related TCI products

Asymmetric synthesis applications benefit from D-(-)-Mandelic Acid's chiral properties, enabling the creation of optically active compounds with high stereocontrol.
Pharmaceutical research utilizes this compound to develop new drugs, as its chiral nature is essential for producing molecules with specific biological activities.
Organic chemistry experiments rely on its ability to interact with various reagents, making it a valuable tool in synthetic pathways.
Structural analysis in laboratories uses its consistent molecular structure for accurate identification and characterization of compounds.
Chemical education programs incorporate it as a teaching aid to demonstrate the principles of chirality and asymmetric synthesis.

Brand	TCI
CAS number	611-71-2
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per standard laboratory requirements
Physical form	Solid, crystalline
Storage	Store in a cool, dry place away from direct sunlight

D-(-)-Mandelic Acid should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in a sealed container to avoid moisture exposure, which could affect its purity. Suitable storage containers include glass or high-density polyethylene vessels that are resistant to chemical reactions. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper labeling of storage containers ensures safe handling and easy identification. Regular monitoring of storage conditions helps maintain the integrity of the compound for consistent performance in chemical reactions.

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