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TCI

CAS 3976-69-0

Methyl (R)-(-)-3-Hydroxybutyrate TCI H0705

Methyl (R)-(-)-3-Hydroxybutyrate TCI H0705

Chemical Identity

Other names
(R)-(-)-3-Hydroxybutyric Acid Methyl Ester
CAS No.
3976-69-0
Formula
C5H10O3
Molecular weight
118.13 g/mol
Purity
>98.0%(GC)
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
methyl (3R)-3-hydroxybutanoate
SMILES
CC(CC(=O)OC)O
InChIKey
LDLDJEAVRNAEBW-SCSAIBSYSA-N
MDL
MDL00063289
PubChem
CID 2724279
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TCI H0705 3976-69-0 Methyl (R)-(-)-3-Hydroxybutyrate is a chiral building block used in asymmetric synthesis to create molecules with specific optical properties. This compound plays a crucial role in organic chemistry laboratories, where it serves as a key component in the development of chiral compounds. Its importance lies in its ability to influence the stereochemistry of the final product, making it indispensable for researchers working on complex molecular structures. Due to its unique optical activity, it is widely utilized in the synthesis of biologically active molecules, including pharmaceuticals and agrochemicals.

The compound is preferred for its high purity and consistent performance in synthetic reactions. Its chiral nature allows for precise control over the stereochemistry of the reaction, which is essential in the production of enantiomerically pure compounds. The structural complexity of this molecule enables it to interact effectively with other reagents, facilitating the formation of desired products with specific stereochemical configurations. These properties make it a reliable and efficient choice for advanced chemical synthesis.

In Indonesian laboratories, TCI H0705 3976-69-0 Methyl (R)-(-)-3-Hydroxybutyrate is commonly used by chemists and pharmacologists for research and development. It is a fundamental material in organic chemistry experiments and studies related to bioactive compounds. Many educational and research institutions in Indonesia rely on this compound to support their scientific investigations and innovation in the field of chemistry and pharmaceutical sciences.

  • Asymmetric synthesis of chiral pharmaceutical compounds due to its optical activity and stereochemical control.
  • Development of enantiomerically pure molecules for drug discovery and formulation processes.
  • Organic chemistry research involving chiral building blocks for complex molecule synthesis.
  • Bioactive compound studies where precise stereochemistry is required for biological activity.
  • Academic research in Indonesian universities focusing on synthetic chemistry and medicinal chemistry.

Brand TCI
CAS number 3976-69-0
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes —
Physical form —
Storage Store in a cool, dry place away from light

This compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Storage conditions should maintain a stable temperature to preserve the compound's integrity and effectiveness. Proper labeling of containers is essential for safe handling and easy identification. Always follow standard laboratory safety protocols when working with chiral compounds to minimize risks.

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