tetracaine hcl best quality reasonable price136-47-0 High Purity 136-47-0

tetracaine hcl best quality reasonable price136-47-0 High Purity 136-47-0

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0 Metric Ton	Negotiable

0 Metric Ton

Negotiable

Min.Order :0 Metric Ton
Purity: >99%

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tetracaine hcl best quality reasonable price136-47-0 High Purity 136-47-0

Quick Details

Appearance:White solid
Application:pharmaceutical intermediates
PackAge:1kg/Aluminum foil package, 25Kg/Drum
ProductionCapacity:|Metric Ton|Day
Storage:Normal temperature
Transportation:FEDEX,DHL,EMS,Special line guarantee delivery

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tetracaine hcl best quality reasonable price136-47-0 High Purity

A potent local anesthetic. Tetracaine is used to alter the function of calcium release channels (ryanodine receptors) that control the release of calcium from intracellular stores. Tetracaine is an allosteric blocker of channel function. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely.

Tetracaine HCl is a potent local anaesthetic and a channel function allosteric inhibitor.Tetracaine hydrochloride is a calcium channel protein inhibitor and blocks voltage-sensitive release of Ca2+ from sarcoplasmic reticulum. Tetracaine is a potent local Other sizes are available. Please inqury us for quote.

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Factory supply Tetracaine hydrochloride CAS NO.136-47-0 in stock Tetracaine hydrochloride CAS: 136-47-0 MF: C15H25ClN2O2 MW: 300.82 Melting point: 149Â°C storage temp: Refrigerator Chemical Properties: White Solid Purity: 99% Function: Local anesthetic; Mainly used in mucosa anesthetic. The function is stronger than Procaine and Lidocaine.

White to off-white powder. Soluble in water (40mg/ml), DMSO (40mg/ml) or ethanol (20mg/ml). Chemical. CAS: 136-47-0. Formula: C15H24N2O2 . HCl. MW: 264.4 . 36.5. Synthetic. Tetracaine is a potent local anaesthetic and a channel function allosteric inhibitor that blocks voltage-sensitive release of Ca2+ from sarcoplasmic reticulum. At low concentrations, tetracaine causes an initial inhibition of spontaneous calcium release events, while at high concentrations, tetracaine blocks release completely. inhibitor of voltage-gated sodium channels such as NaV1.4 and NaV1.8. Shown also to reversibly block nicotinic acetylcholine (ACh) receptors (nAChRs).

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