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Procainamide Hydrochloride is the hydrochloride salt form of procainamide, an amide derivative exhibiting class 1A antiarrhythmic property and analog of procaine. Procainamide hydrochloride reversibly binds to and blocks activated (open) voltage-gated sodium channels, thereby blocks the influx of sodium ions into the cell, which leads to an increase in threshold for excitation and inhibit depolarization during phase 0 of the action potential. In addition, the effective refractory period (ERP), action potential duration (APD), and ERP/APD ratios are increased, resulting in decreased impulse conduction velocity. The lasting action potential may also be due to blockage of outward K+ currents. The result is a decrease in automaticity, increase in refractory period and slowing of impulse conduction.
Procainamide Hydrochloride is an oral antiarrhythmic agent that has been in wide use for more than 60 years. Long term procainamide therapy is known to induce hypersensitivity reactions, autoantibody formation and a lupus-like syndrome but is a rare cause of clinically apparent acute liver injury.
1. Procainamide hydrochloride Medical uses
Procainamide is used for treating ventricular arrhythmias: ventricular ectopy and tachycardia and supraventricular arrhythmias: atrial fibrillation, and re-entrant and automatic supraventricular tachycardia. For example, it can be used to convert new-onset atrial fibrillation, though it is suboptimal for this purpose. It is administered by mouth, by intramuscular injection, or intravenously.
2. Procainamide hydrochloride Side effects
There are many side effects following the induction of procainamide. These adverse effects are ventricular dysrhythmia, bradycardia, hypotension and shock. The adverse effects occur even more often if the daily doses are increased. Procainamide may also lead to drug fever and other allergic responses. There is also a chance that systemic lupus erythematosus occurs, which at the same time leads to polyarthralgia, myalgia and pleurisy. Most of these side effects may occur due to the acetylation of procainamide.
Procainamide hydrochloride is used for treating ventricular arrhythmias: Ventricular ectopy and tachycardia and supraventricular arrhythmias: Atrial fibrillation, and re-entrant and automatic supraventricular tachycardia. For example, it can be used to convert new-onset atrial fibrillation, though it is suboptimal for this purpose. Procainamide hydrochloride is administered by mouth, by intramuscular injection, or intravenously.
There are many side effects following the induction of procainamide. These adverse effects are ventricular dysrhythmia, bradycardia, hypotension and shock. The adverse effects occur even more often if the daily doses are increased. Procainamide may also lead to drug fever and other allergic responses. There is also a chance that systemic lupus erythematosus occurs, which at the same time leads to polyarthralgia, myalgia and pleurisy. Most of these side effects may occur due to the acetylation of procainamide.
Product name | Procainamide hydrochloride | |||
CAS No. | 614-39-1 | Outer Packing | 25kg | |
Production date | 2017.7.5 | Shelf life | 2 years | |
Standard adopted | USP 38 | |||
Items of analysis | Specification | Results | ||
Appearance | A white or almost white crystalline | Complies | ||
Identification | A.B in pass | Complies | ||
Melting Point | 165°~169° | 166°~169° | ||
Solution trasparence | 50mg/mL colourless liquid | colourless liquid | ||
Organic volatile impurities | Meets the requirements | Complies | ||
Limit of free p-aminobenzoic acid | ≤0.1% | 0.05% | ||
USP Reference standards | USP Procainamide Hydrochoride RS. | Complies | ||
Loss on drying | ≤0.3% | 0.12% | ||
Residue on ignition | ≤0.1% | 0.03% | ||
Heavy Metals(ppm) | ≤0.002% | 5ppm | ||
Assay | 98.0~102.0% | 99.38% | ||
Conclusion | Qualified |
Proparacaine hydrochloride,Anesthesia for procedures on eye: deep anesthesia, 1 drop 0.5% ophthalmic solution in each eye every 5 to 10 min for 5 to 7 doses.
Proparacaine hydrochloride,Anesthesia for procedures on eye: superficial anesthesia, 1 to 2 drops 0.5% ophthalmic solution in each eye before surgery or diagnostic procedure.Tonometry AND/OR tonography procedure: 1 to 2 drops 0.5% ophthalmic solution in each eye before procedure.
Local anesthesia Powder | |
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Tetracaine HCl | 136-47-0 |
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Dibucaine hydrochloride | 1961/12/1 |
Prilocaine Base | 751-50-6 |
Prilocaine hydrochloride | 1786-81-8 |
Proparacaine hydrochloride | 5875/6/9 |
Procaine | 59-46-1 |
Procainamide hydrochloride | 614-39-1 |
Procaine Hcl | 1951/5/8 |
Benzocaine | 1994/9/7 |
Lignocaine | 73-78-9 |
lidocaine hydrochloride | 73-78-9 |
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Delivery
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Packing
1. 25kg/drum : 25kg net weight,28kg gross weight; Packed in a cardboard-drum with two plasticbags insideSize: 510mm high, 350mm diameter
2. 1kg/bag (1kg net weight, 1.2kg gross weight, packed in an aluminum foil bag) OR as per your request.
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GW1516 | 317318-70-0 | For obesity, diabetes, dyslipidemia and cardiovascular disease |
Andarine(S4) | 401900-40-0 | partial agonist, intended mainly for treatment of benign prostatic hypertrophy |
SR9009 | 1379686-30-2 | under development at The Scripps Research Institute (TSRI), increases the level of metabolic activity in skeletal muscles of mice |
RAD140 | 1182367-47-0 | New generation for gaining mass and cutting edges |
YK11 | 431579-34-9 | YK11: a SARM and myostatin inhibitor in one |
AC262356 | 870888-46-3 | New SARMS |
SR9011 | 1379686-29-9 | New SARMS |
S23 | 1010396-29-8 | New SARMS |
GW0724 | 317318-84-6 | New SARMS |
Product name | CAS No. | Specification |
LGD-4033 | 1165910-22-4 | 98%min |
SR-9009 | 1379686-30-2 | 98%min |
YK-11 | 1370003-76-1 | 98%min |
MK-2866 (ostarine) | 841205-47-8 | 99%min |
GW-501516 | 317318-70-0 | 98%min |
S4 | 401900-40-1 | 98%min |
SR9009 | 1379686-30-2 | 98%min |
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