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CAS 220141-70-8

5-Fluoroorotic Acid Monohydrate TCI F0382

5-Fluoroorotic Acid Monohydrate TCI F0382

Chemical Identity

Other names
5-Fluorouracil-6-carboxylic Acid Monohydrate
CAS No.
220141-70-8
Formula
C5H3FN2O4.H2O
Molecular weight
192.11 g/mol
Purity
>95.0%(HPLC)(T)
Storage
0-10°C
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
5-fluoro-2,4-dioxo-1H-pyrimidine-6-carboxylic acid;hydrate
SMILES
C1(=C(NC(=O)NC1=O)C(=O)O)F.O
InChIKey
LODRRYMGPWQCTR-UHFFFAOYSA-N
MDL
MDL00150658
PubChem
CID 16212749
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5-Fluoroorotic Acid Monohydrate is a chemical compound widely used in laboratory experiments and scientific research. It belongs to the category of fluorinated building blocks, playing a crucial role in the synthesis of complex molecules. This compound is particularly valued for its ability to participate in chemical reactions that require fluorine substitution, making it essential for the development of fluorinated compounds. Its unique chemical properties make it a versatile reagent in various scientific applications.

The compound is chemically stable and soluble in organic solvents such as ethylamine, which enhances its usability in different experimental setups. Its fluorinated structure provides distinct advantages in specific chemical reactions, enabling precise control over molecular synthesis. This stability and reactivity make it a preferred choice for researchers aiming for accuracy and reproducibility in their experiments. Additionally, its compatibility with a range of solvents allows for flexibility in experimental design.

In Indonesian laboratories, 5-Fluoroorotic Acid Monohydrate is commonly used in organic and biochemical research. It is a key component in the synthesis of bioactive compounds and is frequently employed in academic and research institutions. Its availability supports a wide range of scientific investigations, contributing to advancements in both chemical and biological sciences.

  • Organic synthesis applications benefit from its fluorinated structure, enabling the creation of complex fluorinated compounds with high specificity.
  • Biochemical research utilizes it for the synthesis of bioactive molecules, supporting studies in pharmacology and molecular biology.
  • Fluorination studies rely on its reactivity, allowing for controlled substitution of hydrogen atoms with fluorine in various organic frameworks.
  • Analytical chemistry experiments use it as a standard for fluorine-containing compound identification and quantification.
  • Drug development projects incorporate it in the design of fluorinated pharmaceuticals, enhancing compound stability and biological activity.

Brand TCI
CAS number 220141-70-8
Molecular formula —
Purity —
Category Chemistry > Building Blocks > Fluorinated Building Blocks
Pack sizes Available in various quantities as per supplier specifications
Physical form Solid, monohydrate form
Storage Store in a cool, dry place away from moisture and direct light

5-Fluoroorotic Acid Monohydrate 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 moisture, which could affect its integrity. Storage away from direct sunlight and in a well-ventilated area is essential to avoid any potential degradation. The compound is generally handled in standard laboratory conditions, with appropriate personal protective equipment worn when handling. Due to its chemical nature, it should be stored separately from incompatible substances to ensure safety. Proper labeling and storage practices help maintain the compound’s quality and usability for research purposes.

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