Introduction The isolation of an active ingredient in analgesic drugs is an important technique to determine a drug’s composition. This technique can be exercised through column chromatography, a method used to purify a specific compound in a mixture. In column chromatography, alumina is typically used to separate less polar compounds by acting as a purifying agent. Most analgesic drugs work as pain relievers and generally fall into four categories. However, these drugs are made up of many more chemicals then just the pain relieving chemicals. All tablets must contain at least one active pharmaceutical ingredient (API) that will make up its pharmacological properties such as, acetylsalicylic acid, acetaminophen, ibuprofen or naproxen. These …show more content…
A possible reason that such a low percent recovery was obtained was most likely due to evaporating too much of the solvent out when it was lodged into the warm water bath. However, the most likely reason that a low percent recovery was obtained is because the unknown was purified of everything except the API. Meaning that, the API only made up approximately 10.4% of the pill. Table 2 represents the melting point of unknown B, which was found to be acetyl salicylic acid. According to Chemicalbook, the melting point of acetyl salicylic acid is 134-136°C. However, the melting point of unknown B (acetyl salicylic acid) melted faster than the literate melting point of acetyl salicylic acid. The most likely explanation for this is that the crystals did not have an adequate drying time on the Buncher funnel, and that they were still somewhat wet when placed into the DigiMelt, a melting apparatus. This is because when the unknown B was placed into the DigiMelt, it was not fully solid, it contained liquid. Therefore, the unknown did not require as much heat to melt as it normally would because the unknown was already partly liquid. However, the unknown B had a narrow melting range, indicating that the substance was relatively pure and did not contain many contaminants. Potential contaminants that could be present in the crystallized unknown B could be, methanol, colorants, coating, buffering
Identification of an Unknown Compound using Quantitative and Qualitative Analysis Lauren Tremaglio Chemistry 1011 Lab, Section 16 Instructor: Steven Belina October 3, 2014 Our signatures indicate that this document represents the work completed by our group this semester. Experimental Design and Discussion of Results The objective of this experiment was to identify an unknown compound through quantitative and qualitative analysis. In order to find the identity of the unknown compound, an initial qualitative test for solubility was performed.
Since, acetaminophen takes away pain acetaminophen is a drug that can be used and sold. Acetaminophen is a product that people can sell to make money and that assists them economically. Or, acetaminophen can be used so that people can go to work, For example, say that someone has a pain somewhere like a headache and that person does not believe that they are able to go to work then they can take acetaminophen feel better and be able to go to work and get paid. Acetaminophen is a useful molecule because it is a great tool to kill pain and stay afloat
Introduction The purpose of this experiment was to identify the composition of over-the-counter analgesics by the method of Thin Layer Chromatography (TLC). The TLC method is used for rapid qualitative analysis of mixtures to determine and identify its components and purity. A development solvent was used to separate the analgesics found in both the known drug sample and an unknown sample of over-the-counter medications.
Materials and methods: 1. Materials: Urethane was purchased form Hychem Laboratories. AST, ALT, and ALP was purchased from ----------. All the others reagents use are of high purity and of analytical grade. 2.
It has an infinite solubility with a density of 1.05. Its pH in a 1.0 M solution is at 2.4 with a vapor pressure of 11mmHg at 20 °C or 68 °F and a vapor density of 2.1 in air. It is stable under ordinary conditions of use and storage. Heat and sunlight may contribute to its instability. Heat, flame, ignition sources, freezing and incompatibles are conditions that must be avoided.
Experiment 4: Formal Report Preparation and Recrystallisation of Aspirin Aim of the experiment: In this experiment, a pure sample of aspirin is to be obtained through esterification to synthesise the sample, then purify the sample by recrystallisation. Lastly, determine the melting point of the sample to characterise the aspirin. Introduction: Background Aspirin (acetylsalicylic acid) is an aromatic compound that contains an ester- functional group and a carboxylic acid- functional group. Aspirin is commonly used as a pain reliever (analgesic), an anti-inflammatory, an anti-coagulant (prevent platelet aggregation) and an antipyretic (to reduce fever) pill.
There are two main types of OTC painkillers; acetaminophen and anti-inflammatory. If those kinds of relievers don’t work doctors can prescribe stronger kinds. The most powerful of all the pain relievers are called narcotics, which must be prescribed by a doctor. Narcotics are extremely effective but almost always have serious side
The wax melted first, followed by the salt, and lastly the sugar. The salt not only burned before the sugar, but developed a brown color throughout most of the substance at a faster pace. In the water solubility test, the salt dissolved in the water, as soon as it was properly mixed and the sugar dissolved in the water as well, but was stirred for a longer period of time until it was completely dissolved. The wax did not dissolve in the water, however bits of the substance broke off from the main piece. With this information, the final results included: wax as a nonpolar covalent compound, since the substance melted first and was not soluble in water; salt as a polar covalent compound, since the substance was soluble in water and the second to melt; and sugar as an ionic compound because the substance melted last and was soluble in
HPLC-grade methanol (15 mL) was added to a quantity of the powdered tablets equivalent to one tablet. This solution is sonicated for 20 min. Filtration through Whatman No. 1 filter paper followed by quantitative transfer of the filtered solution into 25 mL volumetric flask and then dilution was made to volume with methanol. A further dilution was made to reach final concentration of 102.8 µg/mL, 97.2 µg/mL for VAL and SAC respectively. Four aliquots (0.1 ,0.5, 1 and 2 mL) of the diluted solution were transferred to 10 mL volumetric flask and diluted with distilled water to obtain concentrations within the linear range of each studied drug then treated as under General Procedure and the corresponding regression equations were used to calculate the recovered
1. Introduction Mefenamic Acid (MA) a non-steroidal anti-inflammatory drug is used extensively for clinical applications [1]. This particular drug provides relief from pain caused by muscle pain, dental pain, pre-menstrual syndrome, headaches and postoperative surgeries. It is mainly a derivative of fenamic acid where there is coplanarity between the carboxylic group and the nitrogen atom of the aromatic ring [2]. This type of coplanarity is generally found in most of the fenamates which is responsible for their conformational similarities.
Thin Layer Chromatography (TLC) Abstract This experiment uses the TLC chromatography technique to identify the presence of acetylsalicylic and Acetaminophen in analgesic drugs (Tylenol and Anacin). It was found that the Anacin and acetylsalicylic had very closer Rf values (0.8 and 0.79). The Tylenol and acetaminophen had closer Rf values (0.54 and 0.58).
Dosage forms usually are made up of the active compound and other ingredients known as excipients. Excipients can have many functions, they can act as fillers, lubricants, binders, preservatives and antioxidants. A change in the nature of the excipients can significantly affect the stability of the active ingredient as well as its release from the dosage form. Changes in the preparation (the way the compound is made) of the active compound like the use of a different solvent for purification, can affect its bioavailability (The fraction of the dose of a drug that is found in general circulation around the body. It is influenced by such factors such as Absorption, Distribution, Metabolism and Elimination (ADME).
Morpho-physiological and Biochemical Responces of Rubus idaeus under Salinity Stress In vitro Conditions Supplemented by Sodium Nitroprusside Ali Ghadakchi asl , Ali- Akbar Mozafari*1, Nasser Ghaderi1 Abstract. To evaluate the effect of sodium nitroprusside (SNP) on morpho-physiological and biochemical characteristics of Rubus idaeus var. Danehdrosht, shoot tip explant was cultured on Murashige and Skoog (MS) medium supplemented with growth regulator combination including Benzyleadenin (BA)(1 mg.L-1), Indol-3-Butyric Acetic acid (IBA)(0.2 mg.L-1), Sodium Nitroprusside (SNP) (0, 50 and 100 µM) and NaCl (0, 50 and 100 mM).The results showed that salinity stress significantly decreased morpho-physiological and biochemical characteristics such as RWC, MSI, total soluble protein in regenerated explants. Furthermore salinity significantly increased the total
For this purpose 0.1N HCl, pH 4.6 buffer, pH 6.8 buffer and purified water were used. Highest dose of the drug i.e., 400mg was dissolved in 250 mL of medium and was kept untouched for 6 hrs. Later on the insoluble drug was filtered off and the solution was analysed by HPLC technique to find out the solubility. Based on the solubility calculated the D/S ratios were calculated. The FDA guidance on “Dissolution Testing of Immediate Release Solid Oral Dosage Forms” says that a drug substance is considered highly soluble when the dose/solubility volume of solution are less than or equal to 250 mL. 4.2.3 DRUG-EXCIEPIENT COMPATIBILITY STUDY DRUG-EXCIPIENT COMPATIBILITY STUDY