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Quinidine Sulfate Dihydrate

Catalog Number
ACM6591635-1
Product Name
Quinidine Sulfate Dihydrate
Structure
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CAS
6591-63-5
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Synonyms
6-Methoxy-alpha-(5-vinyl-2-quinuclidinyl)-4-quinolinemethanol hemisulfate hydrate
IUPAC Name
(S)-[(2R,4S,5R)-5-ethenyl-1-azabicyclo[2.2.2]octan-2-yl]-(6-methoxyquinolin-4-yl)methanol;sulfuric acid;dihydrate;
Molecular Weight
782.9
Molecular Formula
C40H54N4O10S;
Canonical SMILES
COC1=CC2=C(C=CN=C2C=C1)C(C3CC4CCN3CC4C=C)O.COC1=CC2=C(C=CN=C2C=C1)C(C3CC4CCN3CC4C=C)O.O.O.OS(=O)(=O)O;
InChI
InChI=1S/2C20H24N2O2.H₂O4S.2H₂O/c2*1-3-13-12-22-9-7-14(13)10-19(22)20(23)16-6-8-21-18-5-4-15(24-2)11-17(16)18;1-5(2,3)4;/h2*3-6,8,11,13-14,19-20,23H,1,7,9-10,12H2,2H3;(H2,1,2,3,4);2*1H2/t2*13-,14-,19+,20-;/m0/s1
InChI Key
ZHNFLHYOFXQIOW-AHSOWCEXSA-N
Melting Point
212-214 °C
Purity
98%+
Solubility
Slightly sol in water and soluble in alcohol.;
Color Form
Occurs as fine, needle-like, white crystals which frequently cohere in masses or as a fine, white powder.;
Complexity
538
Covalently-Bonded Unit Count
5
Decomposition
When heated to decomposition it emits very toxic fumes of /nitrogen oxides and sulfur oxides/.;
Defined Atom Stereocenter Count
8
Exact Mass
782.35606511
H-Bond Acceptor
14
H-Bond Donor
6
Heavy Atom Count
55
Isomeric SMILES
COC1=CC2=C(C=CN=C2C=C1)[C@@H]([C@H]3C[C@@H]4CCN3C[C@@H]4C=C)O.COC1=CC2=C(C=CN=C2C=C1)[C@@H]([C@H]3C[C@@H]4CCN3C[C@@H]4C=C)O.O.O.OS(=O)(=O)O
Monoisotopic Mass
782.35606511
Other Experimental
WHITE; VERY BITTER; ODORLESS; FINE CRYSTALS; FREQUENTLY COHERING IN MASSES; PH (1% AQUEOUS SOLN): 6.0-6.8 PKA: 4.2, 8.8; SPECIFIC OPTICAL ROTATION: +212 @ 25 DEG C/D (95% ALCOHOL); ABOUT + 260 @ 25 DEG C/D (DILUTE HYDROCHLORIC ACID); DOES NOT LOSE ALL OF ITS WATER BELOW 120 DEG C 1 G DISSOLVES IN ABOUT 90 ML WATER, 15 ML BOILING WATER, 10 ML ALCOHOL, 3 ML METHANOL, 12 ML CHLOROFORM; INSOL IN ETHER, BENZENE; /DIHYDRATE/;ODORLESS; VERY BITTER TASTE; SOLN ARE NEUTRAL OR ALKALINE TO LITMUS;INDEX OF REFRACTION ALPHA 1.565; BETA 1.607; GAMMA 1.670. OPTIC SIGN +, EXTINCTION PARALLEL, ELONGATION +;Specific optical rotation: + 212 deg at 25 deg C/D (alcohol); prisms; needles from water. /d-quinidine sulfate/;Rods; soluble in 8 parts water with blue fluorescence. /Quinidine acid sulfate tetrahydrate/;
Physical State
Neat
Rotatable Bond Count
8
Stability
PROTECT FROM LIGHT; DARKENS ON EXPOSURE TO LIGHT /DIHYDRATE/;Quinidine gluconate, quinidine polygalacturonate, and quinidine sulfate darken on exposure to light and should be stored in well closed, light-resistant containers. Solutions of quinidine salts slowly acquire a brownish tint on exposure to light. Only colorless, clear solutions of quinidine gluconate injection should be used. Quinidine gluconate injection should be stored at 15-30 deg C. When diluted to a concentration of 16 mg/ml with 5% dextrose injection, quinidine gluconate injection is stable for 24 hr at room temperature and up to 48 hr when refrigerated. /Quindine salts/;
Topological Polar Surface Area
176 Ų
UNII
J13S2394HE
Application
Quinidine sulfate dihydrate is primarily used as a class I antiarrhythmic drug, derived as the sulfate salt from various species of Cinchona and their hybrids. It is a dextrorotatory diastereomer of quinine with a bitter taste, appearing as a white to light yellow crystalline powder. This compound effectively functions as a sodium channel blocker, crucial for addressing heart rhythm disorders. It is particularly noted for its efficacy against bacterial strains resistant to erythromycin, such as staphylococci and streptococci, by inhibiting cellular ATPases. Although it has limited solubility in water and alcohol, it dissolves readily in chloroform and ether. Quinidine sulfate dihydrate is nearly neutral to slightly alkaline and is also known to have been utilized in studies exploring the cardiac sodium channel Nav1.5.
January 18, 2025

Reliable and Efficient Antiarrhythmic Agent for Research

I've been using Quinidine Sulfate Dihydrate in our cardiac research lab, and its effectiveness as a Na+ channel blocker is impressive. It's invaluable for studying Nav1.5 mutations, though handling requires care due to its bitter nature.

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