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2-Methyl-5-Nitroimidazol-1-Ylacetic Acid CAS NO 1010-93-1
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CAS No.:1010-93-1
Grade:Pharmacy Grade
Content:99.0%
Brand:Customizable
Packaging:Customizable
Description
2-Methyl-5-Nitroimidazol-1-Ylacetic Acid is a key nitroimidazole derivative, a versatile chemical building block with significant synthetic utility. Its primary value lies in its role as a crucial intermediate in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). This compound is essential for manufacturers and research institutions engaged in developing and producing nitroimidazole-based therapeutics, particularly in the antimicrobial and antiprotozoal sectors.
Application
- Pharmaceutical Intermediate: A critical precursor in the synthesis of nitroimidazole-class antibiotics and antiparasitic drugs.
- Antimicrobial Agent Synthesis: Used in the research and production of compounds targeting anaerobic bacteria and protozoa.
- Chemical Research & Development: Serves as a versatile scaffold for medicinal chemists exploring new bioactive molecules.
- Active Pharmaceutical Ingredient (API) Manufacturing: Employed in the commercial-scale production of finished drug substances.
- Reference Standard: Utilized as an analytical standard in quality control laboratories for method development and validation.
- Biochemical Research: Applied in studies investigating the mechanism of action of nitroimidazole compounds.
Basic Information
| Product Name | 2-Methyl-5-Nitroimidazol-1-Ylacetic Acid |
| CAS No. | 1010-93-1 |
| Molecular Formula | C6H7N3O4 |
| Molecular Weight | 185.14 g/mol |
| Synonyms | 1-Carboxymethyl-2-methyl-5-nitroimidazole; 2-Methyl-5-nitro-1H-imidazole-1-acetic Acid; (2-Methyl-5-nitro-1H-imidazol-1-yl)acetic Acid; Metronidazole Impurity C (EP); Metronidazole Related Compound C (USP); MNZ Impurity C; 1-Acetic Acid-2-methyl-5-nitroimidazole |
| EINECS | Contact for details |
Quality Control
Our 2-Methyl-5-Nitroimidazol-1-Ylacetic Acid is manufactured under strict quality management systems. Each batch undergoes comprehensive analytical testing to ensure identity, purity, and consistency, meeting the stringent requirements for pharmaceutical intermediates. Certificates of Analysis (COA) detailing specifications such as assay, related substances, and residual solvents are provided with every shipment to support your regulatory and quality assurance needs.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep away from incompatible materials and sources of ignition.
Specification
| Item | Specification |
|---|---|
| Appearance | Yellow to light brown crystalline powder |
| Identification (IR) | Conforms to structure |
| Assay (HPLC) | ≥ 98.0% |
| Related Substances (HPLC) | Total impurities ≤ 2.0% Any individual impurity ≤ 0.5% |
| Loss on Drying | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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