2-Thiobarbituric Acid TCI T0192

Chemical Identity

CAS No.: 504-17-6
PubChem: CID 1268265·SID 87576183
Formula: C4H4N2O2S
Molecular weight: 144.15 g/mol
Purity: >98.0%(T)

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 6-hydroxy-2-sulfanylidene-1H-pyrimidin-4-one
SMILES: C1=C(NC(=S)NC1=O)O
InChIKey: STUQITWXBMZUGY-UHFFFAOYSA-N

Rp 1.378.650,00

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2-Thiobarbituric Acid is a chemical compound widely used in laboratory experiments, particularly in organic and analytical chemistry. It serves as a key building block for the synthesis of various heterocyclic compounds, including barbiturates and their derivatives. This compound plays a crucial role in forming complex chemical structures during synthetic processes. Its stability and controlled reactivity make it a reliable choice for researchers aiming to develop new chemical compounds.

One of the main reasons for its popularity is its ability to react with a variety of chemical reagents under both acidic and basic conditions. This versatility allows it to be used in a wide range of chemical reactions. Additionally, its solubility in organic solvents such as ethyl acetate and ethanol facilitates separation and isolation processes in the laboratory. These properties make it a preferred material for many chemical applications.

In Indonesian laboratories, 2-Thiobarbituric Acid is commonly used in scientific research across multiple disciplines, including pharmacology, analytical chemistry, and organic chemistry. It is frequently applied in studies related to drug development, chemical analysis, and structural synthesis. Its predictable chemical behavior ensures consistent results, making it a valuable tool for researchers in Indonesia.

Related TCI products

Organic synthesis applications benefit from 2-Thiobarbituric Acid due to its role in forming complex heterocyclic structures, which are essential in pharmaceutical research.
Analytical chemistry uses this compound for its reactivity and solubility properties, aiding in the detection and quantification of various chemical species.
Pharmaceutical research relies on 2-Thiobarbituric Acid as a precursor for synthesizing barbiturate derivatives, which are important in drug development.
Chemical characterization processes utilize its predictable chemical behavior to ensure accurate and reproducible results in laboratory settings.
Research in medicinal chemistry employs this compound to explore new compounds with potential therapeutic applications.

Brand	TCI
CAS number	504-17-6
Molecular formula	—
Purity	—
Category	Chemistry > Building Blocks > Heterocyclic Building Blocks
Pack sizes	—
Physical form	—
Storage	Store in a cool, dry place away from direct sunlight

2-Thiobarbituric Acid should be stored in a cool, dry place away from direct sunlight to maintain its chemical stability. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its reactivity, it should be handled with care in a well-ventilated area. Proper personal protective equipment, such as gloves and safety goggles, should be worn when handling this compound. Avoid exposure to incompatible substances, and ensure that it is kept in a secure location to prevent accidental spills or contamination. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for laboratory use.

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