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T3577

Sigma-Aldrich

Tolperisone hydrochloride

≥98% (HPLC), solid

Synonyme(s) :

2-Methyl-1-(4-methylphenyl)-3-(1-piperidyl)propan-1-one hydrochloride

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About This Item

Formule empirique (notation de Hill):
C16H23NO · HCl
Numéro CAS:
3644-61-9
Poids moléculaire :
281.82
Numéro CE :
222-876-5
Numéro MDL:
MFCD00058211
Code UNSPSC :
12352200
ID de substance PubChem :
329826771
Nomenclature NACRES :
NA.77

Pureté

≥98% (HPLC)

Forme

solid

Conditions de stockage

desiccated

Couleur

white

Solubilité

H2O: >20 mg/mL

Température de stockage

room temp

Chaîne SMILES 

Cl.CC(CN1CCCCC1)C(=O)c2ccc(C)cc2

InChI

1S/C16H23NO.ClH/c1-13-6-8-15(9-7-13)16(18)14(2)12-17-10-4-3-5-11-17;/h6-9,14H,3-5,10-12H2,1-2H3;1H

Clé InChI

ZBUVYROEHQQAKL-UHFFFAOYSA-N

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Actions biochimiques/physiologiques

Tolperisone is derived from piperidine and possesses membrane stabilizing action. It helps in reducing the effect of spasticities associated with the nervous and muscular system. It exhibits muscle relaxant action through attenuating voltage-gated sodium channels in the brain stem.
Tolperisone regulates ionic currents in myelinates axons and subsequently decreases excitability and mediates its antispastic functions3.
Tolperisone is an ion channel blocker and centrally acting muscle relaxant.

Notes préparatoires

Tolperisone hydrochloride dissolves in water at a concentration that is greater than 20 mg/ml.

Pictogrammes

Exclamation mark
GHS07

Mention d'avertissement

Warning

Mentions de danger

H302 + H312 + H332

Classification des risques

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Code de la classe de stockage

11 - Combustible Solids

Classe de danger pour l'eau (WGK)

WGK 3

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable

Équipement de protection individuelle

dust mask type N95 (US), Eyeshields, Gloves

Certificats d'analyse (COA)

Recherchez un Certificats d'analyse (COA) en saisissant le numéro de lot du produit. Les numéros de lot figurent sur l'étiquette du produit après les mots "Lot" ou "Batch".

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Tolperisone: a typical representative of a class of centrally acting muscle relaxants with less sedative side effects
Quasthoff S, et al.
CNS Neuroscience & Therapeutics, 14(2), 107-119 (2008)
HPLC determination of tolperisone in human plasma
Bae JW, et al.
Archives of Pharmacal Research, 29(4), 339-342 (2006)
D Hinck et al.
General physiology and biophysics, 20(4), 413-429 (2002-05-07)
The actions of tolperisone on single intact Ranvier nodes of the toad Xenopus were investigated by means of the Hodgkin-Huxley formalism. Adding tolperisone to the bathing medium (100 micromol/l) caused the following fully reversible effects: 1. The sodium permeability P'Na
A randomized, double-blind, placebo-controlled study of the efficacy and safety of tolperisone in spasticity following cerebral stroke
Stamenova P, et al.
European Journal of Neurology, 12(6), 453-461 (2005)
Pál Kocsis et al.
The Journal of pharmacology and experimental therapeutics, 315(3), 1237-1246 (2005-08-30)
The spinal reflex depressant mechanism of tolperisone and some of its structural analogs with central muscle relaxant action was investigated. Tolperisone (50-400 microM), eperisone, lanperisone, inaperisone, and silperisone (25-200 microM) dose dependently depressed the ventral root potential of isolated hemisected
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Articles

Sodium Channels

Voltage-gated sodium channels are present in most excitable cell membranes and play an important role in generating action potentials.

Sodium Channels

Voltage-gated sodium channels are present in most excitable cell membranes and play an important role in generating action potentials.

Sodium Channels

Voltage-gated sodium channels are present in most excitable cell membranes and play an important role in generating action potentials.

Sodium Channels

Voltage-gated sodium channels are present in most excitable cell membranes and play an important role in generating action potentials.

Chromatograms

application for HPLC

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