L-(+)-Tartaric Acid TCI T0025

Chemical Identity

CAS No.: 87-69-4
PubChem: CID 444305·SID 87576049
Formula: C4H6O6
Molecular weight: 150.09 g/mol
Purity: >99.0%(T)
Reference databases: ChEBI·ChemSpider·ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: (2R,3R)-2,3-dihydroxybutanedioic acid
SMILES: [C@@H]([C@H](C(=O)O)O)(C(=O)O)O
InChIKey: FEWJPZIEWOKRBE-JCYAYHJZSA-N

Rp 530.250,00

~~Rp 386.400,00~~ Rp 530.250,00

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Berat 25g 500g

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L-(+)-Tartaric Acid is a chiral compound widely used in laboratory settings, particularly in asymmetric synthesis and the production of chiral compounds. It plays a crucial role in organic chemistry by enabling the creation of optically active molecules, which are essential in pharmaceutical and chemical research. Its unique molecular structure allows it to form complexes with metals and act as a reaction control agent, making it a versatile tool for chemists. Due to its stability and reactivity, it is frequently used in the development of chiral building blocks for various synthetic applications.

This compound is preferred for its physical and chemical stability, as well as its ability to interact with a wide range of organic molecules. Its chiral nature allows for precise control over molecular structures, which is vital in the synthesis of enantiomerically pure compounds. Additionally, its solubility in organic solvents facilitates its use in diverse chemical reactions. These properties make it a reliable and effective reagent in both academic and industrial laboratory environments.

In Indonesian laboratories, L-(+)-Tartaric Acid is commonly used in organic chemistry research, especially in asymmetric synthesis and the development of pharmacological compounds. It is a key component in experiments aimed at creating chiral molecules with specific biological activities. Many research institutions and universities in Indonesia rely on this compound for its consistent performance and reliability in chemical processes.

TCI brochures (PDF)

Chiral Auxiliaries and Optical Resolving Agents 2025-06-17 · p. 7
Chiral Building Blocks 2025-04-14 · p. 13

Related TCI products

Asymmetric Synthesis: L-(+)-Tartaric Acid is ideal for asymmetric synthesis due to its chiral structure, enabling the selective formation of enantiomers in organic reactions.
Chiral Compound Development: Its ability to form chiral complexes makes it a valuable tool in the creation of optically active compounds for pharmaceutical applications.
Metal Complex Formation: The compound's capacity to form complexes with metals supports its use in catalytic and coordination chemistry experiments.
Organic Reaction Control: It acts as a reaction control agent, helping to regulate the direction and efficiency of chemical reactions in laboratory settings.
Pharmaceutical Research: Its role in synthesizing chiral molecules is critical in the development of new drugs and bioactive compounds.

Brand	TCI
CAS number	87-69-4
Molecular formula	—
Purity	—
Category	Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes	Available in various quantities as per standard laboratory supply
Physical form	Solid
Storage	Store in a cool, dry place away from moisture and direct sunlight

L-(+)-Tartaric Acid should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a sealed container to avoid moisture exposure, which could affect its purity and reactivity. Due to its solid form, it is typically stored in airtight containers made of glass or high-density polyethylene to ensure long-term preservation. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. While it is generally non-hazardous, proper storage and handling protocols should be followed to ensure safe usage and maintain the integrity of the compound.

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