CAS 522-51-0
:Cloreto de dequalínio
Descrição:
Cloreto de dequalínio é um composto de amônio quaternário caracterizado por suas propriedades antimicrobianas de amplo espectro. Aparece como um pó cristalino branco a off-white e é solúvel em água, tornando-o adequado para várias aplicações, particularmente em produtos farmacêuticos e de cuidados pessoais. O composto é conhecido por sua eficácia contra uma variedade de bactérias e fungos, o que o torna valioso em formulações antissépticas e como conservante. Cloreto de dequalínio funciona ao interromper as membranas celulares microbianas, levando à morte celular. É frequentemente utilizado em pastilhas para a garganta, enxaguantes bucais e antissépticos tópicos. Além disso, foi investigado para uso potencial no tratamento de infecções e como desinfetante. Embora geralmente seja considerado seguro quando usado conforme as instruções, pode causar irritação em alguns indivíduos, particularmente em áreas sensíveis. Assim como com qualquer substância química, o manuseio adequado e a adesão às diretrizes de segurança são essenciais para minimizar os riscos associados à exposição.
Fórmula: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
Chave InChI: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-]
Sinónimos:- 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
- Ver mais sinónimos
Ordenar por
Pureza (%)
0
100
|
0
|
50
|
90
|
95
|
100
14 produtos.
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>Fórmula:C30H40Cl2N4Pureza:99.79% - 99.9%Cor e Forma:SolidPeso molecular: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) ChloridePureza:98%Peso molecular:527.57g/molDequalinium Dichloride
CAS:Fórmula:C30H40N4·2ClCor e Forma:Off-White SolidPeso molecular:456.68 2*35.45Dequalinium chloride
CAS:Fórmula:C30H40Cl2N4·xH2OPureza:95.0 - 101.0 % (dried basis)Cor e Forma:White, off-white or light yellow powderPeso molecular: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>Fórmula:C30H40Cl2N4Pureza:Min. 95%Cor e Forma:PowderPeso molecular: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>Fórmula:C30H40Cl2N4Pureza:Min. 95.0 Area-%Peso molecular:527.57 g/molRef: 3D-W-105841
5gA consultar10gA consultar25gA consultar50gA consultar100gA consultar-Unit-ggA consultar










