Description

Ipravacaine is a pharmaceutical-grade local anesthetic agent, identified by CAS NO 166181-63-1. It is valued for its precise pharmacological profile and reliable performance in controlled medical applications. This compound is essential for manufacturers and research institutions in the pharmaceutical and life sciences sectors developing advanced anesthetic formulations and conducting related biochemical research.

Application

• Pharmaceutical Intermediates: Serves as a critical building block in the synthesis of advanced local anesthetic drugs.
• Research & Development: Used in preclinical and clinical studies to investigate anesthetic efficacy, pharmacokinetics, and safety profiles.
• Reference Standard: Employed as a high-purity analytical standard for quality control and method validation in pharmaceutical testing laboratories.
• Formulation Development: Integral to the development of injectable solutions, topical creams, or other delivery systems for regional anesthesia.

Basic Information

Product Name	Ipravacaine
CAS No.	166181-63-1
Molecular Formula	C15H24N2O
Molecular Weight	248.37 g/mol
Synonyms	Ipravacaine; 1-Butyl-N-(2,6-dimethylphenyl)-2-piperidinecarboxamide; (RS)-1-Butyl-2',6'-pipecoloxylidide; Bupivacaine Impurity K; Bupivacaine Related Compound K; Levobupivacaine Impurity; Bupivacaine EP Impurity K
EINECS	Contact for details

Quality Control

Our Ipravacaine is produced and tested under a strict quality management system to ensure it meets the high standards required for pharmaceutical research and development. Each batch is accompanied by a comprehensive Certificate of Analysis (COA) detailing purity, identity, and impurity profiles, with testing performed according to validated methods. We support compliance with relevant pharmacopeial guidelines (e.g., USP, EP) for impurity and reference standards.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry place at controlled room temperature (15-25°C). Due to its hygroscopic (moisture-sensitive) nature, the container must be kept tightly sealed after opening to prevent degradation from atmospheric moisture.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to structure
Identification (HPLC)	Retention time matches reference standard
Assay (HPLC)	≥ 98.0%
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 1.0%
Residual Solvents (GC)	Complies with ICH guidelines
Loss on Drying	≤ 1.0%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.