The purpose of this experiment was to perform the separation of aspirin, sucrose and an unknown analgesic, which are constituents of Panacetin using the methods of filtration, extraction, and purification…
The problem proposed in the experiment is an unknown ingredient found in generic Panacetin tablets that must be discovered. Panacetin tablets are known to contain aspirin, acetaminophen, and sucrose; therefore, the tablets tested, containing aspirin and sucrose, are thought to contain an unknown of something similar to that of acetaminophen such as acetanilide or phenacetin. Another problem trying to be sought out in the experiments is whether or not the composition of Panacetin as stated on the label is accurate.…
This experiment was based on the unknown component of “Panacetin”. In addition to our unknown, we used phenacetin, acetanilide and water. The structures of phenacetin and acetanilide are shown respectively.…
To be able to understand how organic soluble compounds could be isolated from non-organic components, a chromatographic separation process was used. The objective of the analgesic drug identification is to isolate the organic compounds/ active ingredients in an unknown drug. The identity of the drug was determined through melting point, percent recover, and Rf values. The comparable data for acetaminophen from the manufacturer is 500mg of active ingredient. After conducting the experiment-extraction, distillation, and evaporation- 451mg of active ingredient. This relates to a 68.1% recovery. The melting point was between 158 and 165 degrees Celsius, which is almost ten degrees lower 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.…
First, the unknown sample from experiment 2 was boiled with just enough water dissolve it completely. After all of…
Pre-Lab: Analgesic drugs are known for reducing pain, while antiseptic drugs reduce symptoms such as fevers and swelling. However, some of these drugs can reduce both illnesses. To obtain a pure compound in these drugs, the scientist needs to separate the desired compound by taking advantage of the different physical and chemical properties. Such as; different boiling points, melting points and their solubility properties. To do this a chemist can also asses the differences between acidic and basic substances when they are added to water soluble mixtures. Within this current experiment I will asses the pharmaceutical preparation of Panacetin, by using it 's solubility along with other organic molecules. We know that Panacetin is made up of sucrose, aspirin and some other unknown substance. We know the substance has to be Phenacetin or Acetanilide. To help solidify our reasoning, we need a % recovery of 8-12% sucrose, 35-45% aspirin and 45-55% unknown.…
0.30093 g of panacetin was weighed and mixed well with 50 ml of dichloromethane. After stirring the solution thoroughly, some solid is formed (solid sucrose) and liquid. With using a preweighed filter paper to filter the mixture, and after the sucrose had dried, it was weighed out to 0.7756g. For the aqueous layer, adding 10ml of 6M HCl(pH 2) and filtered using vacuum filtration and after cooled in the ice bath. Leaving behind is the solid aspirin which was weighed out as 1.2469g. Lastly, to measure the weight of the unknown solid component of panacetin, putting the organic layer in a warm water bath to evaporate the solvent and the remain is the solid residue. Extract the unknown solid component of panacetin, which was weighed to be 0.8946g.…
The Consulting Chemists Institute has been asked to analyze the drug preparation of Aspirin to find out what percentages of aspirin, sucrose, and drug preparation. The purpose of this experiment was to determine the unknown component of panacetin. Panacetin contains aspirin, sucrose, and an unknown component. Dichloromate reacts with Panacetin to produce the sucrose as an insoluble solid. Aspirin is removed from the solution by reacting with sodium bicarbonate. The aqueous layer reacts with hydrochloric acid, the unknown component can then be isolated by evaporating the solvent from the dichloromethane solution.…
Aspirin, Caffeine and Salicylamide were extracted from an over-the-counter pain reliever (BC Powder). These components were separated by manipulating their solubilities by adjusting the acidity and basicity of the solution. By doing this, the three components were forced into conjugate acid (or base) forms, causing selective solubility in either an aqueous or organic solvent. These layers were then separated by use of a separation funnel. Once separated, the components extracted were characterized by measuring the melting point and performing a TLC analysis. Also, the recovered aspirin from the first part of the experiment was recrystallized and compared to that of the isolated aspirin.…
Aim Counterfeit pharmaceuticals are a big concern regarding the issue of medicines due to fake versions containing either the wrong ingredients or inaccuracy of the active ingredient which can cause toxicity issues in patients using these products. The aim of this experiment is to find if the percentage composition of the label (50% paracetamol, 40% aspirin and 10% sucrose) matches that of the percentage composition of the powder by following 10% ranges of each component in the powder. I am going to do this via a number of methods including vacuum filtration, heating, extraction and evaporation.…
To separate the sucrose the lab needed to use ~2.95 grams of Panacetin and 50 mL of dichloromethane. This mixture was then used extract the sucrose via gravity filtration. To separate the aspirin, the lab used two separate portions of sodium bicarbonate. Two different liquid layers formed, one with an aqueous solution and the other with the organic dichloromethane. The aqueous solution was then separated into one container and the dichloromethane solution into another. The lab then added HCl to the aqueous solution until it was acidic, reaching a pH ≤ 2. The aqueous solution was then cooled and the aspirin precipitate was separated. To isolate the unknown, the lab heated the dichloromethane…
Of the three components likely to be present in your sample of Panacetin (aspirin, acetanilide, and starch), only starch is insoluble in the organic solvent dichloromethane (or methylene chloride), CH2 Cl2. If a sample of Panacetin is dissolved as completely as possible in dichloromethane, the insoluble starch can be filtered out, leaving acetanilide and aspirin in solution. The purpose of this experiment is to extract the components of Panacetin.…
The cat Jasper is a male cat that was given an over-the-counter analgesic which had caused him to keep getting sicker. He is one years old and weighs seven pounds, five ounces. His symptoms included vomiting and having diarrhea for several days. His lab tests showed a metabolic acidosis meaning there was too much acid in his body fluid. This meant Jasper could have been given acetaminophen, aspirin, or ibuprofen. To identify what analgesic Jasper was given we took samples of the different analgesics and crushed them. We used a melting point apparatus to find out what the melting point was and matched it with acetaminophen, aspirin, or ibuprofen. Then we used the Infrared Spectroscopy to determine the function group of the molecules to help us identify which analgesic was used. Between the symptoms, melting point, and results of the infrared spectroscopy we were able to identify what analgesic Jasper ingested.…
Throughout this experiment we saw recrystallization of the solid into a white crystalline structure suspended in liquid, and then vacuum filtered the unknown and put it into the Mel-Temp device in order to determine the correct melting point. We had pre-calculated that if it was acetanilide, there would need to be 31.6mL used to dissolve it, and if it was phenacetin, it would need 129.5mL to dissolve it. We ended up putting 129 mL of water in order to dissolve the crystals to begin the purification process. When we put the water into it, there was some of the unknown lost on the stirring rod, as well as solid impurities floating at the top of the mixture. Crystals began to form almost immediately, even before the mixture was put into the ice bath. The…
Acetaminaphen was crushed then extracted for the active ingredient by mixing it with methanol. Then separated from the binders by centrifugation and a filtration technique using a Pasteur pipet packed with alumina. The remaining solvent was then evaporated to yield the solid analgesic(.2295g, 45.9% yield) which was collected by filtration and tested for the purity of the drug by the melting point determination. The melting point was (135-142 C) compared to the literature melting point values for acetaminophen (169-171 C) the lower melting point show that their were still impurities in the isolated ingredient.…