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    Preparation of Sodium Chloride through titration Abstract: acid-base titration is a technique commonly used to determine the moles of acid in a sample by adding a known volume of strong base of a known concentration. The strong base provides the hydroxide ion‚ to react quantitatively with the acid. The point at which the acid is completely and exactly consumed the known quantity of base is called the equivalence end point and is signalled by a colour change in the solution (end point). This colour

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    than the published melting point of acetaminophen. After conducting a TLC plate‚ the Rf value was calculated to be .4268‚ the same as the standard Rf. Introduction: The purpose of this lab was to identify an analgesic drug and to understand how to interpret infrared spectroscopy. The lab consisted of several steps‚ which include extraction‚ distillation and filtration. Based on the active ingredient crystals that were obtained at the end of filtration‚ the melting point was found. The

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    for Standard Analgesics‚ Reference Mix & Unknown Components* Standard Substance | Distance Spot Travels (cm) | Distance Solvent Front Travels (cm) | Fluorescence? | I2 Staining Appearance | Acetaminophen | 48 | 150 | No | Dark Yellow | Aspirin | 86 | 150 | No | Not Significant | Caffeine | 14 | 150 | No | Not Significant | Ibuprofen | 92 | 148 | No | Not Significant | Salicylamide | 81 | 148 | Yes |

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    Essay On Kawasaki Disease

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    Kawasaki disease is a rare disease of childhood. It is the leading cause of acquired heart disease in children. Kawasaki disease causes swelling and inflammation of the walls of the blood vessels. It also affects the mucous membranes‚ lymph nodes‚ and the heart. The heart problems are the most worrisome part of the disease. The inflammation of blood vessels in the arteries of the heart (coronary arteries) can lead to aneurysms. An aneurysm is a weak area in the blood vessel that balloons out. Such

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    Wintergreen Oil Synthesis

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    Experiment #1: Synthesis of Salicylic Acid From Wintergreen Oil By: Asad Razzaq TA: Date: 18/01/2015 222/Lab Section 8 Introduction Salicylic acid‚ used in production of substances used worldwide such as commonly used analgesic drug aspirin(cite)‚ can be obtained from natural resources such as wintergreen oil or can be synthesized. Through a series of chemical reactions with cheap raw materials beginning with beginning with methyl salicylate and‚ it is a cheaper and more

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    Tenebrio Molitor

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    Tenebrio molitor is the scientific name for mealworm. While conducting the experiment‚ the Tenebrio molitor is given a drug name aspirin to see the changes in the worm after taking the drug. The independent variable is aspirin and the dependent variable is death rate. Aspirin is given to Tenebrio molitor to see if they die from taking the drug. In many countries‚ mealworms are being served for meals. It’s surprisingly tasty and is a very high source of protein. Mealworms live in places surrounded

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    Synthesis of a

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    Acetylsalicylic acid is an acetyl derivative of salicylic acid which appears as a white and crystalline and a weakly acidic substance with a melting point of 135°C and is also known to be aspirin. It is one of the most widely used drugs that can lower fever and is used as a painkiller. According to (Escobel‚ 2011)‚ Aspirin is synthesized through the reaction of salicylic acid with acetyl anhydride that causes a chemical reaction that turns salicylic acid’s hydroxyl group into an acetyl group‚ (R—OH → R—OCOCH3)

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    Asrin Research Paper

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    Aspirin (ASA) is one of the most commonly used medication in our lives.it is found as analgesic and pain killer in 1899; today‚ it has developed other uses in addition to pain relief‚ such as reduction of inflammation and swelling‚ cancer prevention and treatment for heart attack and stroke. Especially‚ its effect on preventing and treating heart attack has been proven outstanding and efficient. Since aspirin is also an anti-coagulant‚ which means it lubricates the blood and effectively prevents

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    Antiplatelet Therapy

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    BMS3021 – Research Topic: Aspirin TOPIC SUMMARY Aspirin is able to inhibit the synthesis of the Thromboxane A2 precursor‚ by irreversibly binding to the COX-1 enzyme Lack of Thromboxane A2 means that there is no signalling for platelet aggregation so there is no blood clot formation‚ leading to its ability to act as a ‘blood thinner‘ SALT found that in a low-dose of 75mg of Aspirin a day‚ secondary prophylaxis of new cardiovascular events were reduced by 16-20% By decreasing the daily dose to 75mg

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    1cm/7.4cm = .689 Rf1 Unknown 5.0cm/7.4cm = .676 Rf2 Aspirin 5.0cm/7.4cm = .676 Rf3 Acetaminophen 2.9cm/7.4cm = .392 Rf4 Ibuprofen 2.9cm/7.4cm = .392 Rf5 Salicylamide 5.0cm/7.4cm = .676 Rf6 Caffeine 1.0cm/7.4cm = .135 Trial 2: Rf1 Unknown 5.0cm/7.4cm = .676 Rf1 Unknown 5.0cm/7.4cm = .676 Rf2 Aspirin 5.2cm/7.4cm = .703 Rf3 Acetaminophen 3.3cm/7

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