Description

Diperodon Hydrochloride is a pharmaceutical-grade local anesthetic agent with proven efficacy in topical formulations. Its primary value lies in providing rapid and sustained pain relief by blocking nerve signals, making it a critical component in specialized medical products. This compound is essential for manufacturers in the pharmaceutical and personal care industries developing analgesic creams, ointments, and other topical preparations for minor surgical procedures, dermatological treatments, and pain management.

Application

• Topical Anesthetic Formulations: Primary active ingredient in creams, gels, and ointments for surface anesthesia.
• Dermatological Preparations: Used in products for minor surgical procedures, laser treatments, and skin biopsies to manage procedural pain.
• Ophthalmic Solutions: Component in eye drop formulations for local anesthesia during ophthalmic examinations and surgeries.
• Veterinary Medicine: Employed in topical analgesic products for animal healthcare.
• Dental Applications: Incorporated into oral gels for temporary relief of mouth and gum pain.
• Cosmetic & Personal Care: Used in after-waxing or after-shave products to soothe skin and reduce discomfort.
• Research & Development: Serves as a reference standard and active pharmaceutical ingredient (API) in pharmacological research and new drug development.

Basic Information

Product Name	Diperodon Hydrochloride
CAS No.	537-12-2
Molecular Formula	C₁₈H₂₈N₂O₄ • HCl
Molecular Weight	380.89 g/mol
Synonyms	Diperodon HCl; 3-Piperidino-1,2-propanediol dicarbanilate hydrochloride; 1,2-Propanediol, 3-(1-piperidinyl)-, dicarbanilate, hydrochloride; Dipercaine; Percaine Hydrochloride; Nupercainal (historical trade name); 3-(Piperidin-1-yl)propane-1,2-diyl bis(phenylcarbamate) hydrochloride
EINECS	208-658-4

Quality Control

Our Diperodon Hydrochloride is manufactured under strict quality management systems to ensure it meets the rigorous standards required for pharmaceutical applications. Each batch is tested against comprehensive specifications, including identity, purity, and impurity profiles. A Certificate of Analysis (COA) is provided with every shipment, detailing results for key parameters such as assay, related substances, residual solvents, and microbiological quality. We support compliance with cGMP, ICH guidelines, and relevant pharmacopoeial standards (USP/EP).

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated area at a controlled room temperature (15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed to prevent moisture absorption, which can affect stability and performance. Keep away from incompatible materials.

Specification

Item	Specification
Appearance	White to off-white crystalline powder
Identification (IR)	Conforms to reference standard
Identification (HPLC)	Retention time matches reference
Assay (HPLC)	98.0% - 102.0% (on anhydrous basis)
Water Content (KF)	≤ 1.0%
Residue on Ignition	≤ 0.1%
Heavy Metals	≤ 20 ppm
Related Substances (HPLC)	Total impurities ≤ 2.0% Any single impurity ≤ 0.5%
Microbiological Enumeration	Total aerobic microbial count ≤ 1000 cfu/g Total combined yeasts/molds ≤ 100 cfu/g
Specified Pathogens	Absent (per 1g)

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