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CAS RN: 24003-58-5 | Product Number: Q0118
QX 314 Bromide
Purity: >98.0%(T)(HPLC)
Synonyms:
- 2-(2,6-Dimethylanilino)-N,N,N-triethyl-2-oxoethanaminium Bromide
- 2-[(2,6-Dimethylphenyl)amino]-N,N,N-triethyl-2-oxoethan-1-aminium Bromide
Product Documents:
Size | Unit Price | Same Day | 2-3 Business Days | Other Lead Time | Shipping Information |
---|---|---|---|---|---|
100MG |
NT$3,640
|
24 | 0 | Contact Us |
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Product Number | Q0118 |
Purity / Analysis Method | >98.0%(T)(HPLC) |
Molecular Formula / Molecular Weight | C__1__6H__2__7BrN__2O = 343.31 |
Physical State (20 deg.C) | Solid |
Storage Temperature | Refrigerated (0-10°C) |
Store Under Inert Gas | Store under inert gas |
Condition to Avoid | Air Sensitive,Hygroscopic,Heat Sensitive |
Packaging and Container | 100MG-Glass Bottle with Plastic Insert (View image) |
CAS RN | 24003-58-5 |
Reaxys Registry Number | 3789225 |
MDL Number | MFCD00083182 |
Specifications
Appearance | White to Light yellow powder to crystal |
Purity(HPLC) | min. 98.0 area% |
Purity(Precipitation Titration) | min. 98.0 % |
NMR | confirm to structure |
Properties (reference)
Melting Point | 215 °C |
GHS
Related Laws:
Transport Information:
H.S.code* | 2924.29-000 |
Application
QX 314 Bromide: A Membrane-Impermeable Sodium Channel Blocker
QX 314 bromide is a membrane-impermeable lidocaine [L0156] derivative and sodium channel blocker. QX 314 bromide has been reported to selectively block sodium channels on nociceptive neurons when delivered intracellularly through the pore of the noxious heat-sensitive TRPV1 (transient receptor potential vanilloid subfamily member 1) channel, but is ineffective when applied extracellularly.1) In addition, the combination of lidocaine (as a TRPV1 agonist) and QX-314 in an injectable formulation may be a useful adjunct for regional pain control.2,3) (The product is for research use only.)
References
- 1) Inhibition of nociceptors by TRPV1-mediated entry of impermeant sodium channel blockers
- 2) The quaternary lidocaine derivative, QX-314, produces long-lasting local anesthesia in animal models in vivo
- 3) Targeting of sodium channel blockers into nociceptors to produce long-duration analgesia: a systematic study and review
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