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A7096112

Quinidine , ≥98.0%(including 5-15%dihydroquinidine) , 56-54-2

CAS NO.:56-54-2

Empirical Formula: C20H24N2O2

Molecular Weight: 324.42

MDL number: MFCD00135581

EINECS: 200-279-0

Pack Size Price Stock Quantity
1G RMB52.00 In Stock
5G RMB79.20 In Stock
25G RMB256.80 In Stock
100G RMB676.80 In Stock
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Update time: 2022-07-08

PRODUCT Properties

Melting point: 168-172 °C(lit.)
Boiling point: 462.75°C (rough estimate)
alpha  256 º (c=1, EtOH)
Density  1.1294 (rough estimate)
refractive index  1.5700 (estimate)
storage temp.  Keep in dark place,Sealed in dry,2-8°C
solubility  insoluble in H2O; ≥10.32 mg/mL in EtOH with ultrasonic; ≥11.95 mg/mL in DMSO
form  Powder
pka 5.4, 10.0(at 20℃)
color  White to off-white
optical activity [α]20/D +265±5°, c = 0.8% in ethanol (dry matter)
Water Solubility  0.05 g/100 mL (20 ºC)
Sensitive  Light Sensitive
Merck  14,8060
BRN  91866
BCS Class 1
Stability: Stable. Incompatible with strong oxidizing agents.
LogP 3.440
CAS DataBase Reference 56-54-2(CAS DataBase Reference)
NIST Chemistry Reference Quinine(56-54-2)
EPA Substance Registry System Quinidine (56-54-2)

Description and Uses

Quinidine is a stereoisomer of the antimalarial agent quinine and a class Ia antiarrhythmic agent. Quinidine blocks the voltage-gated sodium (Nav) channel Nav1.5 in a use-dependent manner. It decreases the amplitude and duration of action potentials in isolated canine ventricular myocytes. It inhibits KKr, peak INa, and late INa (IC50s = 4.5, 11, and 12 μM, respectively) and can induce torsade de pointes in isolated rabbit hearts when used at a concentration of 1 μM. Quinidine induces QT prolongation in dogs. It also binds to M2 muscarinic acetylcholine receptors (Ki = 7.5 μM for human recombinant receptors expressed in HM2-B10 cells). Formulations containing quinidine have been used in the treatment of atrial fibrillation and ventricular arrhythmias.

antiarrhythmic, antimalarial

Safety

Symbol(GHS) 
GHS06
Signal word  Danger
Hazard statements  H301-H317
Precautionary statements  P261-P264-P270-P280-P301+P310-P302+P352
Hazard Codes  Xn
Risk Statements  22-20/21/22
Safety Statements  36-22
RIDADR  UN 2811 6.1/PG 3
WGK Germany  3
RTECS  VA4725000
8
TSCA  Yes
HazardClass  6.1(b)
PackingGroup  III
HS Code  29392000
Hazardous Substances Data 56-54-2(Hazardous Substances Data)
Toxicity LD50 in rats (mg/kg): 30 i.v., 263 orally (Dietmann)

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