Dimethyl L-(+)-Tartrate TCI T0006

Chemical Identity

CAS No.: 608-68-4
PubChem: CID 11851·SID 87576032
Formula: C6H10O6
Molecular weight: 178.14 g/mol
Purity: >98.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: dimethyl (2R,3R)-2,3-dihydroxybutanedioate
SMILES: COC(=O)[C@@H]([C@H](C(=O)OC)O)O
InChIKey: PVRATXCXJDHJJN-QWWZWVQMSA-N

Rp 980.700,00

~~Rp 685.650,00~~ Rp 980.700,00

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Dimethyl L-(+)-Tartrate is a chiral compound widely used in asymmetric synthesis to construct molecules with specific biological activities. This chemical plays a crucial role in laboratories where precise control over stereochemistry is required. Its unique optical properties make it an essential tool for synthesizing chiral compounds, which are vital in pharmaceutical and biochemical research. As a building block in chiral synthesis, it enables the creation of complex molecular structures with defined stereo configurations.

The compound’s stability and predictable optical behavior make it a preferred choice for researchers. Its dimethylated structure provides enhanced stability, allowing it to remain active in various chemical reactions. The optical activity of Dimethyl L-(+)-Tartrate ensures that it can be reliably used in chiral synthesis without unwanted side reactions. These properties make it a reliable and consistent reagent for laboratories requiring high precision in their synthetic processes.

In Indonesian laboratories, Dimethyl L-(+)-Tartrate is commonly used in chemical and pharmaceutical research. It is a key component in experiments involving asymmetric synthesis, particularly in academic and industrial settings. Its availability and reliability have made it a standard material in many research institutions, supporting the development of new drugs and bioactive compounds.

TCI brochures (PDF)

Chiral Auxiliaries and Optical Resolving Agents 2025-06-17 · p. 7
Chiral Building Blocks 2025-04-14 · p. 10

Related TCI products

Asymmetric Synthesis: Used to create chiral molecules with specific stereochemical configurations, essential for drug development.
Chiral Compound Synthesis: Provides a stable and optically active building block for complex molecular structures.
Pharmaceutical Research: Supports the development of bioactive compounds requiring precise stereochemistry control.
Organic Chemistry Experiments: Offers a reliable reagent for reactions requiring optical purity and stability.
Academic Research: Widely utilized in universities and research institutions for teaching and experimental studies.

Brand	TCI
CAS number	608-68-4
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in standard laboratory quantities
Physical form	Solid
Storage	Store in a cool, dry place away from light

Dimethyl L-(+)-Tartrate should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent moisture absorption and contamination. Due to its optical activity, it should be protected from light to avoid degradation. Proper labeling of containers is essential for safe handling and identification. Laboratories should ensure that it is stored in a well-ventilated area to prevent any potential exposure. General laboratory safety practices, such as using appropriate personal protective equipment, should be followed when handling this compound.

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