Chemical Name:N-(2,6-Dimethylphenylcarbamoylmethyl)triethylammonium chloride
Purity: ≥99% (HPLC)
Biological Activity
Technical Data
Solubility
Calculators
Datasheets
References
Biological Activity
Membrane impermeable quaternary derivative of lidocaine, a blocker of voltage-activated Na+ channels.
Technical Data
M. Wt
298.85
Formula
C16H27N2OCl
Storage
Store at RT
Purity
≥99% (HPLC)
CAS Number
5369-03-9
PubChem ID
21462
InChI Key
LLPPOMUAOGMYQI-UHFFFAOYSA-N
Smiles
[Cl-].CC[N+](CC)(CC)CC(=O)NC1=C(C)C=CC=C1C
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All Tocris products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
water
30
100
Preparing Stock Solutions
The following data is based on the product molecular weight 298.85. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
3.35 mL
16.73 mL
33.46 mL
5 mM
0.67 mL
3.35 mL
6.69 mL
10 mM
0.33 mL
1.67 mL
3.35 mL
50 mM
0.07 mL
0.33 mL
0.67 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products' biological activity.
Stichartzet al (1973) The inhibition of sodium currents in myelinated nerve by quaternary derivatives of lidocaine. J.Gen.Physiol. 62 37 PMID: 4541340
Alreja and Aghajanian
(1994) QX-314 blocks the potassium but not the sodium dependent components of the opiate response in locus coeruleus neurons. Brain Res. 639 320 PMID: 8205485
Perkins and Wong
(1995) Intracellular QX-314 blocks the hyperpolarization activated inward current Iq in hippocampal CA1 pyramidal cells. J.Neurophysiol. 72 911 PMID: