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Noberastine CAS NO 110588-56-2
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CAS No.:110588-56-2
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Noberastine is a high-purity pharmaceutical intermediate and active ingredient with the CAS registry number 110588-56-2. This compound is of significant commercial importance for its role in the synthesis of advanced pharmaceutical agents, particularly in the respiratory and anti-allergy therapeutic segments. It is primarily required by manufacturers in the pharmaceutical and fine chemical industries for research, development, and large-scale production of active pharmaceutical ingredients (APIs).
Application
- Pharmaceutical Intermediate: A key building block in the synthesis of novel antihistamine and respiratory drugs.
- Active Pharmaceutical Ingredient (API) Development: Used in R&D for formulating new therapeutic compounds targeting allergic conditions.
- Fine Chemical Synthesis: Employed in multi-step organic synthesis for creating complex, high-value molecules.
- Biochemical Research: Serves as a reference standard and reagent in pharmacological and biochemical studies.
- Contract Manufacturing: Supplied to CDMOs (Contract Development and Manufacturing Organizations) for cGMP production.
- Generic Drug Manufacturing: Utilized in the production of generic versions of established allergy medications.
Basic Information
| Product Name | Noberastine |
| CAS No. | 110588-56-2 |
| Molecular Formula | C21H24N2O2 |
| Molecular Weight | 336.43 g/mol |
| Synonyms | Noberastine; 110588-56-2; 2-[4-(Diphenylmethoxy)-1-piperidinyl]ethyl 1H-benzimidazole-2-carboxylate; Ebastel; Ebastine Impurity; Ebastine Related Compound; Kestine Impurity; LAS-W 090 |
| EINECS | Contact for details |
Quality Control
Our Noberastine is manufactured under strict quality management systems to ensure batch-to-batch consistency and high purity. We provide comprehensive quality documentation, including Certificates of Analysis (COA) that detail purity, identity, and impurity profiles. The product is suitable for use under cGMP guidelines for pharmaceutical manufacturing, and specifications can be aligned with USP/EP monograph requirements upon request.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). This product is hygroscopic (moisture-sensitive) and light-sensitive; therefore, containers must be kept tightly sealed and away from direct light to maintain stability and purity.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white powder |
| Identification (IR) | Conforms to reference spectrum |
| Identification (HPLC) | Retention time matches reference standard |
| Assay (HPLC) | ≥ 98.5% |
| Related Substances (HPLC) | Total impurities ≤ 1.0% Any single impurity ≤ 0.5% |
| Residual Solvents (GC) | Complies with ICH Q3C guidelines |
| Loss on Drying | ≤ 0.5% |
| Heavy Metals | ≤ 20 ppm |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
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