Barbituric acid
For spectrophotometric determination of cyanide, ≥99.5%
- Product Code: 93344
Alias:
Barbituric acid; malonyl urea, pyrimidinetrione, malonyl uret, barbituric acid
CAS:
67-52-7
| Molecular Weight: | 128.09 g./mol | Molecular Formula: | C₄H₄N₂O₃ |
|---|---|---|---|
| EC Number: | 200-658-0 | MDL Number: | MFCD00006666 |
| Melting Point: | 248-252 °C (dec.)(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
Barbituric acid serves as a fundamental building block in the synthesis of barbiturate drugs, which are historically used as sedatives, hypnotics, and anesthetics. Its derivatives play a crucial role in central nervous system depressants, helping to manage conditions like insomnia, anxiety, and seizures. Additionally, it is utilized in organic chemistry research as a precursor for creating various heterocyclic compounds. In analytical chemistry, barbituric acid is employed as a reagent for detecting certain metals and organic compounds. It also finds application in the dye industry, where it acts as an intermediate in the production of colorants.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to red crystals or powder |
| Ca | 0 ppm 10 ppm |
| Cd | 0 ppm 5 ppm |
| ChlorideCl | 0 ppm 50 ppm |
| Co | 0 ppm 5 ppm |
| Cr | 0 ppm 5 ppm |
| Cu | 0 ppm 5 ppm |
| Fe | 0 ppm 5 ppm |
| IGN. RESIDUE | 0 % 0.05 % |
| IGNITION RESIDUE AS SULFATE | 0 % 0.5 % |
| MELTING POINT | 248-255 |
| Mg | 0 ppm 10 ppm |
| Mn | 0 ppm 5 ppm |
| Ni | 0 ppm 5 ppm |
| Pb | 0 ppm 5 ppm |
| PROTON NMR SPECTRUM | Conforms to Structure |
| PURITYHPLC | 99.5 % 100 % |
| SULFATE SO42- | 0 ppm 50 ppm |
| Zn | 0 ppm 5 ppm |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 25.000 | 10-20 days | Ft29,952.02 |
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-
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| 100.000 | 10-20 days | Ft96,536.01 |
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-
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| 500.000 | 10-20 days | Ft301,459.54 |
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Barbituric acid
Barbituric acid serves as a fundamental building block in the synthesis of barbiturate drugs, which are historically used as sedatives, hypnotics, and anesthetics. Its derivatives play a crucial role in central nervous system depressants, helping to manage conditions like insomnia, anxiety, and seizures. Additionally, it is utilized in organic chemistry research as a precursor for creating various heterocyclic compounds. In analytical chemistry, barbituric acid is employed as a reagent for detecting certain metals and organic compounds. It also finds application in the dye industry, where it acts as an intermediate in the production of colorants.
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