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CAS 21210-43-5

Methyl L-(+)-Mandelate TCI M1350

Methyl L-(+)-Mandelate TCI M1350

Chemical Identity

CAS No.
21210-43-5
PubChem
CID 643570·SID 87573306
Formula
C9H10O3
Molecular weight
166.17 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl (2S)-2-hydroxy-2-phenylacetate
SMILES
COC(=O)[C@H](C1=CC=CC=C1)O
InChIKey
ITATYELQCJRCCK-QMMMGPOBSA-N
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TCI M1350 21210-43-5 Methyl L-(+)-Mandelate is a chiral building block used in asymmetric synthesis to construct molecules with specific biological activities. This compound plays a crucial role in organic chemistry laboratories, particularly in the development of pharmaceuticals and bioactive compounds. Its chiral nature allows for the creation of enantiomerically pure substances, which are essential in drug development and advanced chemical research. Due to its optical activity, it is a key component in the synthesis of molecules that require precise stereochemical control.

The compound's unique optical properties and stability make it a preferred choice for researchers working in asymmetric synthesis. Its ability to participate in enantioselective reactions enables the production of compounds with high enantiomeric purity. This characteristic is vital for applications where the stereochemistry of a molecule significantly affects its biological activity. The compound is also easy to handle and available in high purity, making it a reliable option for laboratory use.

In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in pharmaceutical and asymmetric synthesis projects. It is a valuable tool for academic institutions and research centers aiming to develop new drugs or bioactive compounds. Its availability and reliability make it a staple in laboratories that require high-quality chiral building blocks for advanced chemical studies.

TCI brochures (PDF)

  • Asymmetric Synthesis: Used for creating enantiomerically pure compounds due to its chiral structure and optical activity.
  • Pharmaceutical Research: Essential in drug development for producing molecules with specific stereochemistry and biological activity.
  • Organic Chemistry Studies: Widely applied in research involving chiral compounds and stereoselective reactions.
  • Bioactive Compound Development: Utilized in the synthesis of molecules with pharmacological or biochemical properties.
  • Academic Research: Frequently used in universities and research institutions for teaching and experimental purposes.

Brand TCI
CAS number 21210-43-5
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 appearance
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and purity. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its chiral nature, it is important to handle the compound with care to avoid contamination or degradation. In laboratory settings, proper personal protective equipment should be worn when handling this material. It is also advisable to store it in a designated chemical storage area to ensure safety and compliance with laboratory protocols.

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