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· · COA & SDS für jedes Produkt verfügbar · Versand am selben Tag für Lagerartikel QX 314 bromide - ≥98% , CAS No.24003-58-5
Synonyms
DTXSID10151315 | NCGC00094039-01 | UNII-6V3HD5WBY8 | C16H27N2OBr | HY-101350 | NCGC00261364-01 | BCP05527 | HMS3402J13 | Lidocaine N-ethyl bromide | N-(2,6-Dimethylphenylcarbamoylmethyl)triethylammonium bromide | NCGC00094039-02 | QX-314 | QX-314 BROMIDE
Storage
Store at 2-8°C,Desiccated
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Desiccated Ships Wet ice Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyme
DTXSID10151315 | NCGC00094039-01 | UNII-6V3HD5WBY8 | C16H27N2OBr | HY-101350 | NCGC00261364-01 | BCP05527 | HMS3402J13 | Lidocaine N-ethyl bromide | N-(2,6-Dimethylphenylcarbamoylmethyl)triethylammonium bromide | NCGC00094039-02 | QX-314 | QX-314 BROMIDE
Spezifikationen & Reinheit
≥98%
Biochemische und physiologische Mechanismen
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.
Storage
Store at 2-8°C,Desiccated
Verschickt in
Wet ice
Dieses Produkt erfordert Kühlkettenversand. Grundversand und andere Economy-Optionen sind nicht verfügbar.
Namen und Kennungen Pubchem Sid 528766826 Kanonisches Lächeln CC[N+](CC)(CC)CC(=O)NC1=C(C=CC=C1C)C.[Br-] IUPAC Name [2-(2,6-dimethylanilino)-2-oxoethyl]-triethylazanium;bromide InChIKey DLHMKHREUTXMCH-UHFFFAOYSA-N INCHI 1S/C16H26N2O.BrH/c1-6-18(7-2,8-3)12-15(19)17-16-13(4)10-9-11-14(16)5;/h9-11H,6-8,12H2,1-5H3;1H Isomere SMILES CC[N+](CC)(CC)CC(=O)NC1=C(C=CC=C1C)C.[Br-] PubChem CID 9884487 Molekulargewicht 343.31
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Organic acids and derivatives Klasse Carboxylic acids and derivatives Subclass Amino acids, peptides, and analogues Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives Direct Parent Alpha amino acid amides Alternative Parents Anilides m-Xylenes N-arylamides Tetraalkylammonium salts Secondary carboxylic acid amides Organopnictogen compounds Organic zwitterions Organic oxides Organic bromide salts Hydrocarbon derivatives Carbonyl compounds Amines Molecular Framework Aromatic homomonocyclic compounds Substituents Alpha-amino acid amide - Anilide - N-arylamide - Xylene - M-xylene - Monocyclic benzene moiety - Benzenoid - Tetraalkylammonium salt - Quaternary ammonium salt - Carboxamide group - Secondary carboxylic acid amide - Hydrocarbon derivative - Amine - Organic zwitterion - Organic oxygen compound - Organic salt - Organic bromide salt - Organooxygen compound - Organonitrogen compound - Organopnictogen compound - Carbonyl group - Organic nitrogen compound - Organic oxide - Aromatic homomonocyclic compound Beschreibung This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D-Struktur Zugehörige Ziele (menschlich) Zugehörige Ziele (nicht menschlich) Wirkungsmechanismen Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm) Chemische und physikalische Eigenschaften Löslichkeit Solvent:water, Max Conc. mg/mL: None, Max Conc. mM: 100 Empfindlichkeit Moisture sensitive Molekulargewicht 343.300 g/mol XLogP3 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 6 Exact Mass 342.131 Da Monoisotopic Mass 342.131 Da Topological Polar Surface Area 29.100 Ų Heavy Atom Count 20 Formal Charge 0 Complexity 268.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 0 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 0 Covalently-Bonded Unit Count 2
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