Guangdong, China
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Trading Company
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Management System Certification:
ISO 9001, ISO 14000
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Peak season lead time: within 15 workday
Off season lead time: within 15 workday
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Dyclonine, Dyclonine Hydrochloride, Dyclonine Hydroch manufacturer / supplier in China, offering Dyclonine Pharmaceutical Raw Materials Dyclonine Hydrochloride, 850-52-2 Progestone/Progesterone Hormon Altrenogest for Women, Top Quality Powder Toremifen Citrate CAS 89778-27-8 and so on.

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Dyclonine Pharmaceutical Raw Materials Dyclonine Hydrochloride

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Min. Order: 10 Pieces
Port: Shanghai, China
Production Capacity: 500~1000kg Per Month
Payment Terms: L/C, T/T, D/P, Western Union, Paypal, Money Gram
Powder: Powder
Customized: Non-Customized
Certification: GMP, HSE, ISO 9001, USP, BP
Suitable for: Elderly, Children, Adult
State: Powder
Purity: >99%

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Basic Info

Model NO.: CAS; 536-43-6 Dyclonine Hydrochloride
Name;: Dyclonine Hydrochloride
Biology Description: Sodium Channel Blocker
CAS;: 536-43-6
Molecular Weight;: 325.87
Formula;: C18h27no2.HCl
Solubility Overview;: Soluble in Water to 10 mm
Chemical Name;: -(4-Butoxyphenyl)-3-P
Trademark: SMQ
Transport Package: Special Package
Specification: SGS
Origin: Shenzhen
HS Code: 2937290090

Product Description

Pharmaceutical Raw Materials Dyclonine Hydrochloride CAS; 536-43-6

Quick detail;

Name;Dyclonine hydrochloride
Biology description;Sodium channel blocker. HSP90 chaperone protein inhibitor. Shows local anesthetic effects in vivo. Orally active.
Chemical Name;1-(4-Butoxyphenyl)-3-piperidin-1-ylpropan-1-one hydrochloride
CAS; 536-43-6
Molecular weight; 325.87
Formula; C18H27NO2.HCl
Solubility Overview; Soluble in water to 10 mM, in DMSO to 25 mM and in ethanol to 100 mM
Product NameDyclonine hydrochloride
Molecular FormulaC18H27NO2.HCl
Molecular Weight325.87
usePharmaceutical Intermediate
Appearance:Colorless crystal

Dyclonine Hydrochloride is the hydrochloride salt of Dyclonine, an unclassified compound with local anesthetic effect. Dyclonine reversibly binds to activated sodium channels on the neuronal membrane, thereby decreasing the neuronal membrane's permeability to sodium ions, leading to an increased threshold for excitation. This reversibly stabilizes the membrane and inhibits depolarization, leading to the failure of a propagated action potential and subsequent conduction blockade. This results in a transient and reversible loss of sensation in a localized area of the body.


Dental procedure - Local anesthesia: 0.5% solution ORALLY as a spray or gargle
Local anesthesia: dosage varies and depends upon the area to be anesthetized, vascularity of the tissues, individual tolerance, and the technique of anesthesia
Local anesthesia: 4 to 20 mL of 1% spray TOPICALLY to accesible mucous membranes; MAX dose 300 mg; single dose MAX 200 mg
Local anesthesia: apply 0.5% solution TOPICALLY as wet compresses or as a spray to episiotomy or perineorrhaphy wounds
Local anesthesia: apply pledgets of cotton or sponges moistened with 0.5% solution TOPICALLY to postoperative wounds following proctology procedures
Pain in throat: one 2 to 3 mg lozenge ORALLY dissolved in mouth slowly every 2 h as needed
Pain in throat: 4 sprays of 0.1% spray ORALLY with swallow; may be used as gargle or rinse on the affected area for 15 sec and spit out 6 times a day as needed
Pharyngeal gag reflex finding: 0.5% solution ORALLY as mouthwash or gargle
Stomatitis: 5 to 15 mL of 0.5% solution ORALLY with swallow for lesions of the esophagus; as a rinse or swab applied to inflamed or ulcerated mucous membranes of the mouth

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