Lidocaine hydrochloride CAS No:73-78-9

Lidocaine hydrochloride, CAS 73-78-9 ,Local anesthesia,Lidocaine hydrochloride CAS No:73-78-9

Product Name: Lidocaine hydrochloride

Product Purity: ≥ 99.0%

CAS No 73-78-9



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Description

Lidocaine Hydrochloride Powder

Premium Amide-Type Local Anesthetic & Antiarrhythmic API | GMP Standards
Assay ≥99.5%
USP/EP/BP/CP Standards
Annual Output 300+ Tons
CAS 73-78-9
Lidocaine hydrochloride
Handling & Storage:
Highly soluble in water and ethanol. Store in a dry and cool place, protected from direct sunlight and high temperatures. Shelf life is 24 months in sealed containers.

Product Introduction

Lidocaine Hydrochloride is a high-purity pharmaceutical-grade amide-type local anesthetic and Class Ib antiarrhythmic API. Synthesized via a refined GMP-compliant process, it provides consistent pharmacological activity for injectable, topical, and mucosal formulations. Our product ensures extremely low impurity profiles, meeting the highest global regulatory expectations.

CAS Number73-78-9
Chemical Name2-(diethylamino)-N-(2,6-dimethylphenyl)acetamide HCl
Molecular FormulaC₁₄H₂₃ClN₂O (Anhydrous)
Molecular Weight270.80
AppearanceWhite crystalline powder
Standard Pack1 kg/bag; 25 kg/drum
Shelf Life24 Months

Product Advantages

Pharmacopoeia Purity

Assay ≥99.5%. Meets USP43, EP11, and BP requirements. Total related substances ≤0.5% and heavy metals ≤10 ppm for maximum clinical safety.

Scale Production

100,000-level clean production workshop with an annual output exceeding 300 tons, ensuring reliable supply for global partners.

Regulatory Support

Full documentation package including batch-specific COA, MSDS, GMP certificate, and DMF assistance for major global markets.

Typical Certificate of Analysis (COA)

Test ItemSpecificationResultMethod
AppearanceWhite crystalline powderConformsVisual
IdentificationMatches IR SpectrumConformsUSP 43 <197K>
Assay (HPLC)99.0% – 101.0%99.5%Chromatography
pH (1% Solution)4.0 – 5.54.8USP 43 <791>
Loss on Drying≤1.0% (Monohydrate)0.45%105℃ for 2 hrs
Residue on Ignition≤0.1%0.04%USP 43 <281>

Safety Warning & Usage

Note: The anhydrous form (MW 270.80) is less stable; the monohydrate form is the industry standard for medicinal applications. This product is a pharmaceutical raw material and should only be handled by qualified professionals in GMP-regulated environments.

Shaanxi Sunrise Pharmaceutical Co., Ltd.

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