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CAS 4358-87-6

Methyl DL-Mandelate TCI M0040

Methyl DL-Mandelate TCI M0040

Chemical Identity

CAS No.
4358-87-6
PubChem
CID 78066·SID 87572156
Formula
C9H10O3
Molecular weight
166.17 g/mol
Purity
>98.0%(GC)
Reference databases
ChEBI·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl 2-hydroxy-2-phenylacetate
SMILES
COC(=O)C(C1=CC=CC=C1)O
InChIKey
ITATYELQCJRCCK-UHFFFAOYSA-N
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Methyl DL-Mandelate is a chemical compound widely used in laboratory settings for its versatility in organic synthesis. As a building block, it plays a crucial role in constructing complex molecular structures through various chemical reactions. It is commonly employed in esterification and substitution reactions, making it an essential component in synthetic chemistry. Its ability to participate in multiple reaction pathways enhances its utility across different research areas.

This compound is favored for its stable chemical structure and favorable reactivity, which contribute to efficient synthetic processes. Its non-heterocyclic nature allows it to be used in a wide range of chemical reactions without interfering with other molecular structures. These properties make it a reliable and adaptable material for researchers aiming to develop new compounds with biological activity.

In Indonesian laboratories, Methyl DL-Mandelate is frequently used in organic chemistry research and the development of pharmacological compounds. It is also integral to projects focused on synthesizing bioactive molecules. Its reliability and compatibility with various experimental conditions make it a preferred choice among scientists and researchers in the field.

  • Organic synthesis projects benefit from Methyl DL-Mandelate due to its role in esterification and substitution reactions, enabling the creation of complex molecular structures.
  • Drug development initiatives utilize this compound for synthesizing bioactive molecules, contributing to the discovery of new pharmacological agents.
  • Research in medicinal chemistry often incorporates Methyl DL-Mandelate to explore its potential in developing compounds with therapeutic applications.
  • Academic laboratories use it as a standard reagent for teaching and experimental purposes, demonstrating its importance in chemical education.
  • Analytical chemistry applications may involve Methyl DL-Mandelate as a reference standard for identifying and quantifying compounds in various samples.

Brand TCI
CAS number 4358-87-6
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Non-Heterocyclic Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Liquid
Storage Store in a cool, dry place away from direct sunlight

Methyl DL-Mandelate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep the compound in a tightly sealed container to prevent exposure to air and moisture. Due to its potential reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid contact with incompatible substances such as strong oxidizing agents. Always use appropriate personal protective equipment, including gloves and safety goggles, when handling this compound. Proper storage and handling ensure the compound remains effective and safe for use in laboratory applications.

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