Levobupivacaine HCl CAS: 27262-48-2
| Product Parameters | |
|---|---|
| Catalog No. | BK688F |
| CAS.RN | 27262-48-2 |
| Molecular Formula | C18H29ClN2O |
| Molecular Weight | 324.89 g/mol |
| Purity | NLT 98% |
Product Overview
Levobupivacaine hydrochloride, as an important intermediate for local anesthetics, is widely used in pharmaceutical research and development and production, primarily for the synthesis of levobupivacaine and related formulations. This product is suitable for various stages, including drug development, small-scale preparation, pilot-scale amplification, and commercial production. It features high purity, stability, and good scalability, meeting diverse customer needs in process development, route optimization, and project transformation.
Applications
- Pharmaceutical API Synthesis
- Preparation of Prodrug Compounds for Local Anesthetics
- Drug Process Development and Optimization
- Customized Supply of Intermediates
- Preclinical Research and Formulation Development
Quality & Supply Capability
English Name: Levobupivacaine HCl Properties: White crystalline powder, readily soluble in water, with a stable chemical structure containing a levorotatory amide-type local anesthetic core functional group, meeting pharmaceutical intermediate standards. Storage Recommendations: Store in a sealed, light-protected, and dry place, subject to the COA/MSDS. Supply Capabilities: Samples, gram-level, kilogram-level, commercial batches. Packaging Specifications: Aluminum foil bags, fluorinated bottles, cardboard drums, customized packaging. Documentation Support: COA, MSDS, HPLC, NMR, etc. We provide a full-process service from sample supply to small-scale preparation, pilot-scale amplification, and customized batch production. We can flexibly adjust purity levels, impurity control standards, packaging specifications, and delivery cycles according to customer needs, with complete quality documentation support. Furthermore, we have a professional technical support team that can provide comprehensive technical assistance from laboratory research and development to industrial production, helping customers efficiently advance process development and project transformation.
Why Choose Bioncan
Focused on pharmaceutical intermediates, possessing extensive experience in synthesis and purification. Full-scale supply capability, covering all stages from laboratory to commercial production. Provides complete quality control documentation to ensure product quality compliance and controllability. Supports customized needs, adjusting purity, impurity limits, and packaging according to customer requirements. Provides supporting process optimization and scale-up technologies to enhance customer R&D efficiency and production stability.
Customers are responsible for ensuring compliance with applicable patent, regulatory, and import/export requirements in their respective jurisdictions.
Online Consulting
For quotation, inventory, samples, COA, MSDS, or custom synthesis support for CAS 27262-48-2, please submit your requirements. We will respond according to purity, quantity, delivery timeline, and documentation needs.
