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Dequalinium chloride

CAS No.
522-51-0
Chemical Name:
Dequalinium chloride
Synonyms
DECA;Dequalinium chloride for performance test CRS;dequadin;Dequalinum;dequafungan;DEQUALINIUM DICHLORIDE;Dequalinium chloride CRS;DEQUALINIUM CHLORIDE HYDRATE;efisol;evazol
CBNumber:
CB3193093
Molecular Formula:
C30H40Cl2N4
Molecular Weight:
527.57
MDL Number:
MFCD00063502
MOL File:
522-51-0.mol
MSDS File:
SDS
TDS File:
TDS
Last updated:2026-05-28 01:02:23
Product description Number Pack Size Price
Dequalinium chloride Pharmaceutical Secondary Standard; Certified Reference Material PHR1300 500mg $153
Dequalinium chloride European Pharmacopoeia (EP) Reference Standard D0430000 d0430000 $220
Dequalinium (chloride) ≥95% 17557 250mg $131
Dequalinium (chloride) ≥95% 17557 500mg $249
Dequalinium (chloride) ≥95% 17557 1g $471
More product size

Dequalinium chloride Properties

Melting point ≥300 °C(lit.)
storage temp. 2-8°C
solubility Slightly soluble in water and in ethanol (96 per cent).
form Solid
color Beige
Merck 13,2930
Stability Stable for 2 years as supplied. Solutions in DMSO or distilled water may be stored at -20° for up to 3 months.
Major Application pharmaceutical (small molecule)
Cosmetics Ingredients Functions ANTIMICROBIAL
ANTIPLAQUE
DEODORANT
ORAL CARE
InChIKey LTNZEXKYNRNOGT-UHFFFAOYSA-N
SMILES C12C=CC=CC1=C(C=C(C)[N+]=2CCCCCCCCCC[N+]1C(C)=CC(N)=C2C=CC=CC=12)N.[Cl-].[Cl-]
CAS DataBase Reference 522-51-0(CAS DataBase Reference)
EWG's Food Scores 1
FDA UNII XYS8INN1I6
UNSPSC Code 41116107
NACRES NA.24

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P280-P301+P312-P302+P352-P305+P351+P338
Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36-37/39
WGK Germany  3
RTECS  VA0700000
8
Storage Class 11 - Combustible Solids
NFPA 704
0
2 0

Dequalinium chloride price More Price(57)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich PHR1300 Dequalinium chloride Pharmaceutical Secondary Standard; Certified Reference Material 522-51-0 500mg $153 2026-04-30 Buy
Sigma-Aldrich D0430000 Dequalinium chloride European Pharmacopoeia (EP) Reference Standard 522-51-0 d0430000 $220 2024-03-01 Buy
Cayman Chemical 17557 Dequalinium (chloride) ≥95% 522-51-0 250mg $131 2026-04-30 Buy
Cayman Chemical 17557 Dequalinium (chloride) ≥95% 522-51-0 500mg $249 2026-04-30 Buy
Cayman Chemical 17557 Dequalinium (chloride) ≥95% 522-51-0 1g $471 2026-04-30 Buy
Product number Packaging Price Buy
PHR1300 500mg $153 Buy
D0430000 d0430000 $220 Buy
17557 250mg $131 Buy
17557 500mg $249 Buy
17557 1g $471 Buy

Dequalinium chloride Chemical Properties,Uses,Production

Description

Dequalinium Chloride is a a potent and selective non-peptide blocker of the apamin-sensitive small conductance Ca2+-activated K+ channel (IC50 = 1.1 mM).

Chemical Properties

White or yellowish-white powder, hygroscopic.

Originator

Dequsan,Sante

Uses

Dequalinium Chloride is a quaternary ammonium cation and the active ingredient in various medications including antiseptic and anti-malarial agents.

Definition

ChEBI: Dequalinium chloride is an organic chloride salt that is the dichloride salt of dequalinium. It has a role as an antiseptic drug, a mitochondrial NADH:ubiquinone reductase inhibitor, an antifungal agent and an antineoplastic agent. It contains a dequalinium.

Manufacturing Process

a) 15 g of 4-aminoquinaldine, 15 g of decamethylene diiodide and 200 ml of methyl ethyl ketone were refluxed together for 400 hours. The mixture was allowed to cool, the precipitate filtered off, washed with methyl ethyl ketone, and 1,1'-decamethylenebis(4-aminoquinaldinium chloride) recrystallized from ethyl alcohol containing a little methyl alcohol.
b) 160 g of 4-aminoquinaldine, 174 g of decamethylene diiodide and 1,500 ml of methyl isobutyl carbinol were heated together at 120°C for 90 hours. The mixture was allowed to cool, the precipitate filtered off, washed with methyl ethyl ketone and 1,1'-decamethylenebis(4-aminoquinaldinium chloride) recrystallized from ethyl alcohol containing a little methyl alcohol.
b) 160 g of 4-aminoquinaldine, 174 g of decamethylene diiodide and 1,500 ml of methyl isobutyl carbinol were heated together at 120°C for 90 hours. The mixture was allowed to cool, the precipitate filtered off, washed with methyl ethyl ketone and 1,1'-decamethylenebis(4-aminoquinaldinium chloride) recrystallized from ethyl alcohol containing a little methyl alcohol.

brand name

Decabis;Dequacaine;Dequafungan;Dequin;Faringina;Gargilon;Grocreme;Labosept;Maltyl;Phylletten;Soor-gel;Sorot;Tetesept.

Therapeutic Function

Antiseptic, Antifungal

World Health Organization (WHO)

Skin reactions to dequalinium chloride, including necrotic lesions, have been reported. It remains available as a mouth and throat disinfectant in many countries.

General Description

Dequalinium Chloride is a topical bacteriostat that is available as various salts. It is used in wound dressings and mouth infections and may also have antifungal action, but may cause skin ulceration.

Biological Activity

Dequalinium is a quaternary ammonium cation with diverse biological activities. It has antifungal activity against C. albicans, C. glabrata, and C. krusei (MICs = 0.5-2, 64-256, and 128 μg/ml, respectively), antitrichomonal activity against T. vaginalis (MICs = 28.8-230.4 μg/ml), and antibacterial activity against a panel of aerobic and facultative anaerobic bacteria (MICs = 0.25-256 μg/ml). Dequalinium inhibits apamin binding to, and net potassium loss mediated by, SKCa channels in guinea pig hepatocytes stimulated by angiotensin II (Item No. 17150). In vivo, dequalinium (1-10 mg/kg) inhibits primary and recurrent tumor growth in a W163 rat colon carcinoma isograft model.

References

1) Miyataet al.(2014),Pharmacologic rescue of an enzyme-trafficking defect in primary hyperoxaluria 1; Proc. Natl. Acad. Sci. USA11114406
2) Frey Tirriet al.(2011),Antimicrobial topical agents used in the vagina; Curr. Probl. Dermatol.4036
3) Castleet al.(1993),Dequalinium: a potent inhibitor of apamin-sensitive K+ channels in hepatocytes and of nicotinic responses in skeletal muscle; Eur. J. Pharmacol.236201
4) Orzaezet al.(2011),Characterization of dequalinium as a XIAP antagonist that targets the BIR2 domain; Apoptosis16460

Dequalinium chloride Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 236)Suppliers
Supplier Tel Email Country ProdList Advantage
Hebei Chuanghai Biotechnology Co., Ltd
+8615350571055 Sibel@chuanghaibio.com China 8738 58
HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
+86-15350851019; +8615350851019 admin@86-ss.com China 999 58
Hebei Zhuanglai Chemical Trading Co Ltd
+86-16264648883 niki@zlchemi.com China 7245 58
Henan Tianfu Chemical Co.,Ltd.
+86-0371-55170693 +86-19937530512 info@tianfuchem.com China 21586 55
ATK CHEMICAL COMPANY LIMITED
+undefined-21-51877795 ivan@atkchemical.com China 33024 60
Changzhou Ansciep Chemical Co., Ltd.
+86 519 86305871 sales@ansciepchem.com CHINA 4241 58
Nanjing Dolon Biotechnology Co.,Ltd.
18905173768 52513593@qq.com CHINA 2972 58
CONIER CHEM AND PHARMA LIMITED
+8618523575427 sales@conier.com China 49979 58
career henan chemical co
+86-0371-86658258 +8613203830695 factory@coreychem.com China 29792 58
SIMAGCHEM CORP
+86-5922680277 +86-13806087780 sale@simagchem.com China 17346 58

View Lastest Price from Dequalinium chloride manufacturers

Image Update time Product Price Min. Order Purity Supply Ability Manufacturer
Dequalinium chloride pictures 2026-06-15 Dequalinium chloride
522-51-0
$75.00-100.00 1kg 99% 5000Ton HEBEI SHENGSUAN CHEMICAL INDUSTRY CO.,LTD
Dequalinium chloride pictures 2026-05-18 Dequalinium chloride
522-51-0
$39.00-73.00 99.90% 10g TargetMol Chemicals Inc.
Dequalinium chloride pictures 2026-05-18 Dequalinium chloride
522-51-0
$39.00-73.00 99.90% 10g TargetMol Chemicals Inc.
1,1'-DECAMETHYLENEBIS(4-AMINOQUINALDINIUM CHLORIDE) 1,1'-DECAMETHYLENEBIS(4-AMINOQUINALDINIUM) DICHLORIDE 1,1'-(1,10-DECANEDIYL)BIS(4-AMINO-2-METHYLQUINOLINIUM) DICHLORIDE DEQUALINIUM CHLORIDE DEQUALINIUM DICHLORIDE DECA dequadinchloride dequafungan dequavagyn dequavet efisol eriosept evazol 1,1'-[1,10-Decanediyl] bis[4-amino-2-methylquinolinium chloride] Dequalinum Quinolinium, 1,1-(1,10-decanediyl)bis4-amino-2-methyl-, dichloride QUINALDINIUM,1,1'-DECAMETHYLENEBIS(4-AMINO-,DICHLORIDE 1,1μ-Decamethylenebis(4-aminoquinaldinium) dichloride hydrate 1,1'-(1,10-Decanediyl)bis(4-amino-2-methylquinolinium)·2chloride 1,1'-(Decane-1,10-diyl)bis(4-amino-2-methylquinoline-1-ium)·2chloride 1,1'-Decamethylenebis(2-methyl-4-aminoquinolinium)·dichloride BADQ-10 DequaliniuM (graMs of bacteria May be) QuinoliniuM,1,1'-(1,10-decanediyl)bis[4-aMino-2-Methyl-, chloride (1:2) 1,1'-(decane-1,10-diyl)bis(4-aMino-2-Methylquinolin-1-iuM) chloride 1-[10-(4-amino-2-methyl-1-quinolin-1-iumyl)decyl]-2-methyl-4-quinolin-1-iumamine dichloride hydrate 1,1’-decamethylenebis(4-amino-quinaldiniudichloride 1,10-decamethylene-bis(4-aminoquinaldiniumchloride) baqd10 decamethylenebis(4-aminoquinaldiniumchloride) decamine(pharmaceutical) dekadin dekamin dequadin grocreme labosept optipect phylletten polycidine Dequalinum Chloride DEQUALINIUM CHLORIDE HYDRATE Dequalinium chloride for performance test CRS Dequalinium chloride CRS Danical Decabis Dequalinium chloride USP/EP/BP MitoBloCK-12 equaliniumchloride Diquinone chloride Dequalinium chloride for ID Dequalinium for system suitability 522-51-0 C30H40CI2N4 C30H40Cl2N4 C30H40N42Cl 52757 Heterocyclic Ammonium Salts Ion Channels