ChemicalBook >> CAS DataBase List >>QX-314
QX-314
- CAS No.
- 21306-56-9
- Chemical Name:
- QX-314
- Synonyms
- QX-314;QX-314.Br;QX 314 BROMIDE;Lidocaine N-ethyl bromid;LIDOCAINE N-ETHYL BROMIDE;QX-314 - CAS 21306-56-9 - Calbiochem;QX-314 bromide (N-Ethyllidocaine bromide);LIDOCAINE N-ETHYL BROMIDE (QUATERNARY SALT);Lidocaine N ethyl bromide,Lidocaine Nethyl bromide;N-(2,6-DIMETHYLPHENYL)ACETAMIDE-2-TRIETHYLAMMONIUM BROMIDE
- CBNumber:
- CB0421458
- Molecular Formula:
- C16H27N2O+
- Molecular Weight:
- 263.4
- MDL Number:
- MFCD00083182
- MOL File:
- 21306-56-9.mol
- MSDS File:
- SDS
Last updated:2023-04-23 13:52:06
Melting point | 220 - 222°C |
---|---|
storage temp. | Desiccate at RT |
solubility | DMSO (Slightly), Methanol (Slightly) |
color | White to Off-White |
Specific Activity | 40-60 Ci/mmol |
Solvent | Ethanol:water (1:1) |
Concentration | 1 mCi/ml |
FDA UNII | 46ZIF6Y2X9 |
SAFETY
Risk and Safety Statements
Symbol(GHS) | GHS07 |
---|---|
Signal word | Warning |
Hazard statements | H315-H319-H335 |
Precautionary statements | P261-P280a-P304+P340-P305+P351+P338-P405-P501a |
Hazard Codes | Xi |
Risk Statements | 36/37/38 |
Safety Statements | 26-36 |
WGK Germany | 3 |
QX-314 price More Price(8)
Manufacturer | Product number | Product description | CAS number | Packaging | Price | Updated | Buy |
---|---|---|---|---|---|---|---|
Sigma-Aldrich | L5783 | Lidocaine N-ethyl bromide analytical standard, for drug analysis | 21306-56-9 | 50mg | $56.5 | 2024-03-01 | Buy |
Sigma-Aldrich | 552233 | QX-314 | 21306-56-9 | 100mg | $142 | 2024-03-01 | Buy |
Alfa Aesar | J60678 | Lidocaine N-ethyl bromide, 99+% | 21306-56-9 | 100mg | $104.65 | 2024-03-01 | Buy |
Sigma-Aldrich | L5783 | Lidocaine N-ethyl bromide analytical standard, for drug analysis | 21306-56-9 | 250mg | $225 | 2024-03-01 | Buy |
Tocris | 1014 | QX314bromide ≥99%(HPLC) | 21306-56-9 | 100 | $125 | 2021-12-16 | Buy |
QX-314 Chemical Properties,Uses,Production
Uses
Blocker of voltage-activated sodium channels
Uses
QX-314 bromide is a derivative of Lidocaine. It is a local anesthetic.
Biological Activity
Membrane impermeable quaternary derivative of lidocaine, a blocker of voltage-activated Na + channels. Intracellular QX 314 bromide also inhibits calcium currents in hippocampal CA1 pyramidal neurons.
QX-314 Preparation Products And Raw materials
Raw materials
Preparation Products
Global( 74)Suppliers
Supplier | Tel | Country | ProdList | Advantage | |
---|---|---|---|---|---|
Capot Chemical Co.,Ltd. | 571-85586718 +8613336195806 | sales@capotchem.com | China | 29798 | 60 |
Career Henan Chemica Co | +86-0371-86658258 +8613203830695 | laboratory@coreychem.com | China | 30253 | 58 |
TargetMol Chemicals Inc. | +1-781-999-5354 | support@targetmol.com | United States | 19973 | 58 |
LEAPCHEM CO., LTD. | +86-852-30606658 | market18@leapchem.com | China | 43348 | 58 |
Shanghai Acmec Biochemical Technology Co., Ltd. | +undefined18621343501 | product@acmec-e.com | China | 33350 | 58 |
J & K SCIENTIFIC LTD. | 010-82848833 400-666-7788 | jkinfo@jkchemical.com | China | 94717 | 76 |
3B Pharmachem (Wuhan) International Co.,Ltd. | 821-50328103-801 18930552037 | 3bsc@sina.com | China | 15848 | 69 |
Ascent Scientific | 4401179829988 | customerservice@ascentscientific.co.uk | United Kingdom | 279 | 60 |
Hangzhou Yuhao Chemical Technology Co., Ltd | 0571-82693216 | info@yuhaochemical.com | China | 9394 | 52 |
HangZhou YuHao Chemical Technology Co., Ltd. | 0571-82693216 | info@yuhaochemical.com | China | 2031 | 58 |
21306-56-9(QX-314)Related Search:
2-[(2,6-Dimethylphenyl)amino]-N,N,N-triethyl-2-oxoethanaminium
QX-314;LIDOCAINE N-ETHYL BROMIDE;N-(2,6-DIMETHYLPHENYLCARBAMOYLMETHYL)TRIETHYLAMMONIUM BROMIDE
QX-314.Br
QX-314 bromide (N-Ethyllidocaine bromide)
N-(2,6-DIMETHYLPHENYLCARBAMOYLMETHYL)TRIETHYLAMMONIUM BROMIDE
N-(2,6-DIMETHYLPHENYL)ACETAMIDE-2-TRIETHYLAMMONIUM BROMIDE
QX-314
QX 314 BROMIDE
LIDOCAINE N-ETHYL BROMIDE
LIDOCAINE N-ETHYL BROMIDE (QUATERNARY SALT)
QX-314 - CAS 21306-56-9 - Calbiochem
Lidocaine N-ethyl bromid
Lidocaine N ethyl bromide,Lidocaine Nethyl bromide
Ethanaminium,2-[(2,6-dimethylphenyl)amino]-N,N,N-triethyl-2-oxo-
21306-56-9
C16H27BrN2O
C16H27N2OBr
C16H27N2O
A quaternary derivative of lidocaine that is not membrane permeable. Blocks both fast Na+-dependent action potentials and voltage-dependent, non-inactivating Na+ conductance.
Analytical Chromatography Product Catalog
Analytical Standards
Alphabetic
Sodium channel
Ion Channels