Bupivacaine Hydrochloride / Bupivacaine Base ≥99% Pure Powder CAS 2180-92-9

Bupivacaine,2180-92-9 ,Anaesthetic,Bupivacaine Anaesthetic 99% CAS No: 2180-92-9

Product Name: Bupivacaine API Powder

Product Purity: ≥ 99%

CAS No: 2180-92-9



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Description



Bupivacaine API Powder

High-Purity Anaesthetic Raw Material | CAS: 2180-92-9
Standard: USP / EP / BP Grade Validated
BUSINESS DISCLOSURE: Shaanxi Sunrise Pharmaceutical Co., Ltd. operates strictly as an industrial raw material manufacturer and supplier. We DO NOT manufacture, distribute, or sell finished pharmaceutical products or medical devices. This product is for compounding and industrial manufacturing use only.
GMP Compliant Facility
HPLC Tested Purity >99.5%
Secure Global Logistics
Comprehensive COA/MSDS
Bupivacaine 3

Available Chemical Forms:

  • Bupivacaine Base (CAS 2180-92-9) - Highly lipophilic, optimized for specific non-aqueous formulations.

  • Bupivacaine Hydrochloride (CAS 14252-80-3) - Water-soluble form, the industry standard for injectable manufacturing.

Product NameBupivacaine / 1-butyl-N-(2,6-dimethylphenyl)piperidine-2-carboxamide
CAS Registry No.2180-92-9 (Base) | 14252-80-3 (HCl)
Purity (HPLC)≥ 99.5% (Single impurity < 0>
Molecular FormulaC₁₈H₂₈N₂O | MW: 288.43 g/mol
AppearanceWhite crystalline powder, odorless
Quality StandardIn-house / USP / EP Standard Compliant
Production SourceTotal Chemical Synthesis
Supply Capacity500kg - 1000kg / Month (Stable bulk supply)

* Note: Laboratory samples (10g-50g) are available for R&D evaluation and pre-manufacturing quality audits.

Technical Description & Application Profile

Bupivacaine is a highly potent, long-acting amide-type local anesthetic. Due to its superior receptor binding affinity, it provides a significantly extended duration of analgesia compared to Lidocaine or Mepivacaine.

As a raw material supplier, Shaanxi Sunrise Pharmaceutical provides this API exclusively for downstream pharmaceutical manufacturers. Our meticulously synthesized Bupivacaine powder features a highly stable crystalline structure, excellent thermal stability, and a consistent particle size distribution. It serves as the critical active pharmaceutical ingredient (API) for compounding facilities and manufacturers producing epidural, spinal, and peripheral nerve block formulations.

Quality Control & Compliance

Strict Impurity Profiling

Every commercial batch undergoes rigorous validation via High-Performance Liquid Chromatography (HPLC) and Gas Chromatography (GC). We guarantee heavy metal limits are strictly < 10ppm, with residual solvents well within ICH guidelines.

Documentation & Regulatory Support

We understand the complexities of global pharmaceutical procurement. Shaanxi Sunrise provides comprehensive technical data packages to streamline your regulatory filings and quality audits.

Detailed COA SDS / MSDS TDS HPLC Method Logs

Logistics & Supply Chain

Industrial Scale Packaging

  • R&D / Small Scale: 1kg vacuum-sealed Aluminum Foil Bags.

  • Commercial Bulk: 25kg standard Fiber Drums equipped with double PE inner liners to prevent moisture degradation.

  • Customized OEM packaging and labeling are available upon request.

Global Distribution Network

With extensive experience in handling sensitive pharmaceutical raw materials, we provide secure, specialized shipping routes to North America, Europe, and Asia. Our logistics team offers robust support for smooth and compliant customs clearance.