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Purification And Calculation Of Aspirin
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Introduction Aspirin is an organic compound created through the process of esterification. In this reaction, an ester is formed from an alcohol and a carboxylic acid combined with an acid catalyst (Timberlake). Aspirin, or acetylsalicylic acid, is made from the reaction of salicylic acid and acetic anhydride, with a byproduct of acetic acid also. Various techniques have historically been used to produce aspirin. Filtration is the process of removing any excess water from the crystals by vacuuming or suctioning it out. Recrystallization is the cooling and hardening of the crystals to give a purified product by using a solvent to pull out any impurities. To calculate the theoretical yield of a product, the mass of the acid is multiplied by the …show more content…
After crystallization, the product was a white solid. After recrystallization, it was very lumpy, but there were distinct white chunks present. This product changed several times in appearance because of the purification of it. The material was left with no impurities so the product kept getting more solid and distinct chunks. The percent yield is calculated by taking the weight of the aspirin after recrystallization divided by the theoretical yield and multiplying it by 100. The yield before and after recrystallization was a significant difference. Before recrystallization, the product weighed 8.9 grams because there was several impurities present in the product, with the percent yield being 135%. The product weighed so much more than expected as a result of excess impurities that had not been filtered out yet. After the product was recrystallized, however, and the product was purified, it weighed 1.14 grams, with the percent yield being 17.3%. The percent yield after the final recrystallization was so far below 100% as a result of the first step not fully working where the solution did not dissolve completely. This caused the following steps to also have problems and the yield was so low as a result. The weight of the final product was expected to go down after recrystallization because any excess water and other impurities were being taken out. There may have been some loss of the product when it was being filtered because some was still left in the container for
The experiment was not a success, there was percent yield of 1,423%. With a percent yield that is relatively high at 1,423% did not conclude a successful experiment, because impurities added to the mass of the actual product. There were many errors in this lab due to the product being transferred on numerous occasions as well, as spillage and splattering of the solution. Overall, learning how to take one product and chemically create something else as well as how working with others effectively turned out to be a
Every 5 minutes, a small amount of mixture was dissolved in acetone (0.5 mL) and was spotted onto a thin layer chromatography (TLC) plate, which contained an eluent mixture of ethyl acetate (2 mL) and hexanes (8 mL). The bezaldehyde disappearance was monitored under an ultraviolet (UV) light. Water (10 mL) was added after the reaction was complete, and vacuum filtrated with a Buchner funnel. Cold ethanol (5 mL) was added drop-by-drop to the dried solid and stirred at room temperature for about 10 minutes. Then, the solution was removed from the stirrer and place in an ice bath until recrystallization. The recrystallized product was dried under vacuum filtration and the 0.057 g (0.22 mmol, 43%) product was analyzed via FTIR and 1H NMR
Then, I added 8 drops of concentrated phosphoric acid to the mixture. swirling it a few times. Then, I carefully took the flask to the station as I avoided trying to breath the vapors of the acetic anhydride. I put the e-flask into the beaker of water sitting on the hot plate in order to heat it for seven minutes. Once the seven minutes was up, my partner carried the e-flask to the fume hood, and added 3 mL of de-ionized water to the flask. She swirled it for a couple of minutes there. She brought it back tot he station where I gradually added 60 Ml of de-ionozed water to the mixture while my partner stirred the mixture constantly. I was able to see some of the aspirin beginning to form. In order to complete the crystallization process we cooled the flask in an ice-water bath from 4:00 until 4:20. As we waited I began to set up our filtration system. I used a ring stand, right angel clamp, three finger clamp, Buchner funner, filtering flask,rubber tubing, and filter paper in the Buchner funnel. I turned on the aspirator and pored some water over the filtering paper in order to create a good
Esterification was used to synthesize aspirin which was by reacting salicylic acid with acetic anhydride. To speed up the reaction, dehydrating agent and conc. sulphuric acid was present. The purity of a substance, which is the aspirin in this particular experiment, can be determined by the identification of its melting point.
Aspirin contains the substance acetylsalicylic acid (ASA), which can relieve inflammation, fever, pain, and known as a “blood thinner”. Aspirin was not officially trademarked until March 6, 1899 when the Imperial Office of Berlin made it official. It has been used for the last 110 years, but its natural form, salicylic acid has been around for thousands by Egyptians, Greeks, and Romans. Aspirin is available in over 80 countries and known as the best non-prescription drug. The most common use of aspirin is to cure headaches and use it as a pain reliever, but aspirin is known to prevent heart attack and strokes. It was first proposed in 1940, but wasn’t confirmed until 1970 when doctors would recommend taking aspirin daily [1].
Aceclofenac is a non-steroidal anti-inflammatory drug, widely used in the management of osteoarthritis, rheumatoid arthritis and ankylosing spondylitis. Usual therapeutic dose is 100 mg twice daily and half life is 3-4 hrs; thus it is necessary to be administered frequently in order to maintain the desired concentration. Therefore, Aceclofenac is an ideal candidate for sustained release formulation, resulting in more reproducible drug absorption and reducing the risk of local irritations.5
Opiates are a class of drugs that are used for chronic pain. Opioids are substances that are used to relieve pain by binding opiate receptors throughout the body, and in the brain. These areas in the brain control pain and also emotions, producing a feeling of excitement or happiness. As the brain gets used to these feelings, and the body builds a tolerance to the opioids, there is a need for more opioids and then the possibility of addiction.
Discuss the possible drug and excipient-related constrains of the formulation (no identity of the drug was given to you at this
What would you give to rid yourself of acne? What would you do? The bane of every adolescent’s existence, these red spots develop to some degree in 85% of the population between ages 12 and 25 (Lamberg). Teenagers wake up every morning, look at the mirror, and sigh at the acne on their faces and often other places on their bodies. They dread these awful things that are absolutely ugly. They get desperate and eventually, if the acne grows worse than ever before, they resort to Accutane. Accutane, also known as isotretinoin, is a medication for acne. However, despite isotretinoin’s helpfulness in controlling acne that is unresponsive to other treatments, this medication should not be used because of its harmful physical side effects, its association with psychiatric adverse effects, and its effects on reproduction.
The actual amount of crude product was determined to be 3.11 grams. The percent yield of the crude product was determined to be 67.75 %. The actual amount of pure product formed was found to be 4.38 grams. The percent yield of the pure product was determined to be 95.42%. Regarding the thin layer chromatography, the line from the solvent front is 8 centimeters.
The purpose of this experiment was to learn and preform an acid-base extraction technique to separate organic compounds successfully and obtaining amounts of each component in the mixture. In this experiment, the separation will be done by separatory funnel preforming on two liquids that are immiscible from two layers when added together. The individual components of Phensuprin (Acetylsalicylic acid, Acetanilide, and Sucrose as a filler) was separated based upon their solubility and reactivity, and the amount of each component in the mixture was obtained. Also, the purity of each component will be determined by the melting point of the component.
The solvent should be easily removed from the purified product, not react with the target substances, and should only dissolve the target substance near it’s boiling point, but none at freezing. A successful recrystallization uses minimum amount of solvent, and cools the solution slowly, if done to fast, many impurities will be left in the crystals. Using the correct solvent, in this case ice water and ethyl acetate, the impurities in the compound can be dissolved to obtain just the pure compound. A mixed solvent was used to control the solubility of the product. The product is soluble in ethanol an insoluble in water. Adding water reduced solubility and saturates the solution and then the crystals
Background Information Aspirin is an analgesic (pain relieving) and an antipyretic drug (a drug that lowers body temperature). The main constituent of aspirin is 2 - ethanoythydroxybenzoic acid, also known as acetylsalicyclic acid (shown below right). It was originally made from just salicylic acid (which is found in the bark of a willow tree) when used by the Ancient Greeks to counter fever and pain, but its bitterness and tendency to irritate the stomach caused problems. These were resolved by the German chemist Felix Hoffman, who made the acetyl derivative of salicylic acid in the
·Aspirin (salicylic acid acetate) is an anti-inflammatory (decreases swelling and inflammation), anti-pyretic (fever reducing), and anti-platelet (decreases platelets in the body to thin blood). Many heart treatment patients take an aspirin a day to prevent blood clotting. However, if aspirin is taken in large quantities over long periods of time, it may cause gastric ulcers or other internal damage. The molecular formula of aspirin is C9H8O4. Some examples of Aspirin are Bayer, Ecotrin, and Aspergum.
Bam! Bam! Bam! Have you ever hear this deaf- making, irritating sound from water bottle flipping? Hearing this noise in schools and houses, is so annoying for millions of people. Even some schools banned bottle flipping. Bam! I get it why some adults and kids don’t like this sound and I don’t get why you get so happy when it landed. That’s why I want to talk to my friends and kids, to not flip water bottles anywhere from public to private places.