CAS 522-51-0
:Dequalinium chloride
Description:
Dequalinium chloride is a quaternary ammonium compound characterized by its broad-spectrum antimicrobial properties. It appears as a white to off-white crystalline powder and is soluble in water, making it suitable for various applications, particularly in pharmaceuticals and personal care products. The compound is known for its effectiveness against a range of bacteria and fungi, which makes it valuable in antiseptic formulations and as a preservative. Dequalinium chloride functions by disrupting microbial cell membranes, leading to cell death. It is often used in throat lozenges, mouthwashes, and topical antiseptics. Additionally, it has been investigated for its potential use in treating infections and as a disinfectant. While generally considered safe when used as directed, it can cause irritation in some individuals, particularly in sensitive areas. As with any chemical substance, proper handling and adherence to safety guidelines are essential to minimize risks associated with exposure.
Formula:C30H40N4·2Cl
InChI:InChI=1S/C30H38N4.2ClH/c1-23-21-27(31)25-15-9-11-17-29(25)33(23)19-13-7-5-3-4-6-8-14-20-34-24(2)22-28(32)26-16-10-12-18-30(26)34;;/h9-12,15-18,21-22,31-32H,3-8,13-14,19-20H2,1-2H3;2*1H
InChI key:InChIKey=LTNZEXKYNRNOGT-UHFFFAOYSA-N
SMILES:C(CCCCCCCCC[N+]=1C2=C(C(N)=CC1C)C=CC=C2)[N+]=3C4=C(C(N)=CC3C)C=CC=C4.[Cl-]
Synonyms:- 1,1'-Decane-1,10-Diylbis(4-Amino-2-Methylquinolinium) Dichloride
- 1,1′-Decamethylenebis[4-aminoquinaldinium chloride]
- Badq 10
- Baqd 10
- Decamethylenebis[4-aminoquinaldinium chloride]
- Decamine
- Decamine (pharmaceutical)
- Decatylen
- Dekadin
- Dekamiln
- Dekamin
- Dequacets
- Dequadin
- Dequadin chloride
- Dequafungen
- Dequalinum Chloride
- Dequavagyn
- Dequavet
- Efisol
- Eriosept
- Evazol
- Fluomizin
- Fluomycin N
- Grocreme
- Ivazil
- Labosept
- Ldn 0096422
- NSC 166454
- Optipect
- Oralgol
- Phylletten
- Polycidine
- Quinaldinium, 1,1′-decamethylenebis[4-amino-, dichloride
- Quinolinium, 1,1′-(1,10-decanediyl)bis[4-amino-2-methyl-, chloride (1:2)
- Quinolinium, 1,1′-(1,10-decanediyl)bis[4-amino-2-methyl-, dichloride
- Rumilet
- Sanoral
- Sentril
- See more synonyms
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Found 14 products.
Dequalinium chloride
CAS:<p>Dequalinium chloride: topical bacteriostat, blocks apamin-sensitive K+ channels, used for wounds, oral infections, potential antifungal, risk of skin ulcers.</p>Formula:C30H40Cl2N4Purity:99.79% - 99.9%Color and Shape:SolidMolecular weight:527.591,1'-(Decane-1,10-Diyl)Bis(4-Amino-2-Methylquinolin-1-Ium) Chloride
CAS:1,1'-(Decane-1,10-Diyl)Bis(4-Amino-2-Methylquinolin-1-Ium) ChloridePurity:98%Molecular weight:527.57g/molDequalinium Dichloride
CAS:Formula:C30H40N4·2ClColor and Shape:Off-White SolidMolecular weight:456.68 2*35.45Dequalinium chloride
CAS:Formula:C30H40Cl2N4·xH2OPurity:95.0 - 101.0 % (dried basis)Color and Shape:White, off-white or light yellow powderMolecular weight:527.57 (anhydrous)Dequalinium chloride
CAS:<p>Dequalinium chloride is a quaternary ammonium compound that has been discovered to be an inhibitor of the cytopathic effects of some syndrome viruses. It is able to inhibit the replication of the virus in various clinical isolates and in cell culture models. Dequalinium chloride also inhibits acetylcholine receptor-mediated endocytosis, which is one of the mechanisms by which cells resist infection. The mechanism by which dequalinium chloride inhibits acetylcholine receptor-mediated endocytosis is not yet known, but it has been suggested that it might be due to its inhibitory activity on mitochondrial uncoupler proteins. This property may make dequalinium chloride an effective treatment against bacterial infections and respiratory diseases such as cystic fibrosis and asthma.</p>Formula:C30H40Cl2N4Purity:Min. 95%Color and Shape:PowderMolecular weight:527.57 g/molDequalinium chloride
CAS:<p>Dequalinium chloride is a novel, broad spectrum antimicrobial agent with a mechanism of action that inhibits the mitochondria-dependent respiratory chain. Studies have shown that it inhibits the growth of resistant microorganisms in cell-based experiments and in bacterial infections. Dequalinium chloride also has cytopathic effects on thp-1 cells, which are specific for Mycobacterium tuberculosis. In addition to inhibiting mitochondria-dependent respiration, this compound also increases acetylcholine receptor sensitivity in A549 lung cancer cells. Dequalinium chloride is a quaternary ammonium cation and has been shown to be effective against clinical isolates and inhibitory concentrations of a variety of virus species, including human rhinovirus (HRV) and Coxsackie virus type B4 (CoxB4).</p>Formula:C30H40Cl2N4Purity:Min. 95.0 Area-%Molecular weight:527.57 g/mol










