Laboratory Exercise: Chromatographic Separation

Similar documents
Thin Layer Chromatography

Thin Layer Chromatography

CHEMICAL SEPARATION EXPERIMENT 2

Exp 1 Column Chromatography for the Isolation of Excedrin Components. Reading Assignment: Column Chromatography, TLC (Chapter 18)

Chromatography Extraction and purification of Chlorophyll CHM 220

Exercise 4: Thin layer chromatography of organic compounds

Is There a Chemist in You?

Chemistry 3200 High Performance Liquid Chromatography: Quantitative Determination of Headache Tablets

Experiment Nine Thin Layer Chromatography

Chromatography: Thin-Layer Chromatography (TLC) & Column Chromatography

Chromatography Lab # 4

Laboratory Exercise: Synthesis of Zinc Iodide

Practical 1 Procedure Iron by Titrimetry

Experiment 1: Extraction and Thin Layer Chromatography

Physical Separations and Chromatography

PROGRAMMING THE RINSE ROBOT INTRODUCTION

Chromatography 1 of 26 Boardworks Ltd 2016

Chromatographic Methods of Analysis Section 2: Planar Chromatography. Prof. Tarek A. Fayed

Name Period Date. Lab 10: Paper Chromatography

Separations: Chromatography of M&M and Ink Dyes

Experiment 1: Thin Layer Chromatography

3. Separation of a Mixture into Pure Substances

LAB #6 Chromatography Techniques

What s In That Pill?

THIN LAYER CHROMATOGRAPHY

Exp 2 Acid-Base Extraction and Isolation of Excedrin Components

Principles of Thin Layer Chromatography

Drug tests Students Notes By Doaa George, based on the workshop investigation by Claire Lenehan

Ester Synthesis And Analysis: Aspirin and Oil of Wintergreen. Vanessa Jones November 19, 2015 Thursday 8:30 Lab Section Lab Partner: Melissa Blanco

LIQUID CHROMATOGRAPHY

Chromatography: Candy Coating and Marker Colors Student Advanced Version

Paper Chromatography Lab. Prepared for: Mrs. Freeman

PURPOSE: To separate the pigments of spinach by Column Chromatography. To analyze Column Chromatography fractions by Thin Layer Chromatography.

Chromatography. What is Chromatography?

Experiment 1: The Borohydride Reduction of 9-Fluorenone to 9-Fluorenol

EXPERIMENT #1 SEPARATION AND RECOVERY OF ORGANIC COMPOUNDS, THIN LAYER CHROMATOGRAPHY, COLUMN CHROMATOGRAPHY, CRYSTALLIZATION AND MELTING POINTS

not to be republished NCERT THE technique of chromatography is vastly used for the separation, Chromatography UNIT-5 EXPERIMENT 5.

Chromatography What is it?

36B-BioOrganic Modifications for Technique Experiments. Technique of Thin-Layer Chromatography

Chemistry 151 Lab 4: Chromatography

Abstract. Introduction

Chromatography: Candy Coating and Marker Colors Student Version

Chromatography- Separation of mixtures CHEM 212. What is solvent extraction and what is it commonly used for?

Magnet Junior High/High School Lesson Plan

University of Wisconsin Chemistry 116 Preparation and Characterization of Aspirin and Some Flavoring Esters *

The Basis for Paper Chromatography

Experiment 8 Synthesis of Aspirin

For Chromatography, you might want to remember Polar Dissolves More, not like dissolves like.

Chromatography and Functional Group Analysis

Thin Layer Chromatography

Midlands Regional Heat Schools Analyst Competition Active Compounds in Commercial Medicine Tablets

IDENTIFICATION TESTS FOR DURACOR TABLETS

Prelab Reading Assignment: Laboratory Techniques in Organic Chemistry, 4 th Ed. Chapter 19

Sodium Borohydride Reduction of Benzoin

Coordination Complexes

Lab 10 Guide: Column Chromatography (Nov 3 9)

Experiment #10: Analysis of Antacids

AP Chemistry Lab #5- Synthesis and Analysis of Alum (Big Idea 1 & 2)

CK-12 FOUNDATION. Separating Mixtures. Say Thanks to the Authors Click (No sign in required)

Volumetric Analysis. Quantitative analysis answers the second question

Paper Chromatography. Identifying the components of a mixture

Chromatography. Read pages 366 to 375 in your text to answer the following questions.

Coordination Complexes

Chromatography & instrumentation in Organic Chemistry

Chemistry 11. Unit 3 The Physical Properties and Physical Changes of Substances

The Fluorometric Determination of Acetylsalicylic Acid in an Aspirin Tablet

PAPER AND THIN LAYER CHROMATOGRAPHY (TLC)

CfE Higher Chemistry. Unit 3: Chemistry in Society. Chemical Analysis as part of quality control

Aspirin Synthesis H 3 PO 4

Analytical Technologies in Biotechnology Prof. Dr. Ashwani K. Sharma Department of Biotechnology Indian Institute of Technology, Roorkee

IDENTIFICATION AND DETERMINATION OF HYDROQUINONE IN COSMETIC PRODUCTS 2 14/11/17 ACM 003 BY TLC AND HPLC

Esterification of Salicylic Acid via Acetic Anhydride for the Pro- duction of Acetylsalicylic Anhydride (Aspirin)

Applications in Forensic Science. T. Trimpe

Year 10 practice questions Chemistry

2. Synthesis of Aspirin

The Synthesis and Analysis of Aspirin

Experiment 1 & 2 PURPOSE OF THE EXPERIMENT

solution, Concentrated HNO 3

Thin Layer Chromatography

DATE PERFORMANCE TASK #1

Stationary phase: Non-moving phase that provides support for mixture to move.

IGCSE (9-1) Edexcel - Chemistry

This method describes the identification of the following prohibited colorants in cosmetic products:

Lab 9: Over-the-Counter Drugs

Experiment A. Introduction to the Organic Laboratory and Characterization Techniques

Laboratory Exercise: Diameter of a Carbon Atom

MIXTURES, COMPOUNDS, & SOLUTIONS

Mixtures 1 of 38 Boardworks Ltd 2016

LUMEFANTRINUM LUMEFANTRINE

PLANT PIGMENTS AND PHOTOSYNTHESIS LAB

ARTEMETHER AND LUMEFANTRINE TABLETS: Final text for addition to The International Pharmacopoeia (July 2008)

Lab.2. Thin layer chromatography

Open Column Chromatography, GC, TLC, and HPLC

Elements, Compounds and Mixtures

216 S10-Exam #1 Page 2. Name

Manual Accompanying The GPHF-Minilab

Chromatography. Investigation Photosynthetic Pigments. Do all leaves contain the same pigments?

Minneapolis Community and Technical College. Separation of Components of a Mixture

Experiment: Titration

Photosynthesis. Introduction

Transcription:

CHEM 109 Introduction to Chemistry Revision 1.0 Laboratory Exercise: Chromatographic Separation As we have discussed, chromatographic separations employ a system with two phases of matter; a mobile phase and a stationary phase. Thin layer chromatography uses a stationary phase that involves a very thin layer of solid silica deposited on a glass or plastic plate with a liquid mobile phase that wicks up the plate carrying the mixture to be separated with it. In this exercise we will analyze a commercial pain reliever to determine the identity of the active analgesic in the reliever s prescription. We will limit ourselves to non-narcotic analgesics that contain Ibuprofen, Acetaminophen, Aspirin or Caffeine. We will separate the active ingredient of the analgesic from the binders holding the tablet together using Thin Layer Chromatography. Then, since the distance the analgesic runs along the chromatogram depends on the chemical properties of the analgesic, the distance it runs can be compared with results for standards (above list of compounds) run on the same chromatogram in order to identify it. TLC Chromatogram of Black Ink We will dissolve the analgesic tablet into an appropriate solvent and then apply the resulting liquid solution as a small dot near the bottom of the TLC plate. Something similar will be done for our standards. The chromatogram will then be run by dipping it in an eluting liquid in a TLC chamber. When the elutant has reached to near the top of the plate, the plate will be removed from the eluting chamber and dried. Then, because all the analgesics are whitish in color and

P a g e 2 cannot be distinguished from the white silica, it will be visualized under UV light. The silica has been impregnated with a fluorescing compound and so will glow with a greenish color under UV light. Because the compounds run on the chromatogram absorb the light's energy, regions of the silica that contain any of the compounds run will appear as a dark spot under UV light. The spot produced by the analgesic can be compared with those of the standards run simultaneously in order to determine its identity.

P a g e 3 Procedure 1. Prepare your chromatography chamber. Obtain a 250 ml beaker and cover it with a piece of Aluminum foil. In the fume hood, add eluting solvent to a depth of about 5 mm in the chamber. We will use a solvent composed of Ethyl Acetate:Acetic Acid (95:5). Set the chamber aside while you prepare the chromatography plate. 2. Prepare the TLC plate. We will use Whatman Polyester backed plates coated with Silica Gel to a thickness of 250 m. These plates have been activated to fluoresce under UV 254 radiation. Handle the plates only by the edges. Cut a TLC plate to the size indicated by your instructor. Using a pencil, very, very, lightly draw a line about 1 cm from the bottom edge of the plate. Mark off 5 five 1 cm intervals. Lightly label each: Ace, Asp, Caff, Ibu, Unk. Your instructor will demonstrate how to draw out a melting point capillary tube into a micropipetter. Using a separate micropipetter, spot your unknown analgesic and each standard analgesic onto the TLC plate. Do this by touching the tip of the micropipetter filled with sample to the plate s surface four or five times. It is important the spot be reasonably concentrated and small. Do not allow the tip of the micropipetter to touch the surface for more than a fraction of a second. If it does, it will produce a spot that is too large. And, allow the spot to dry before spotting it again. Each standard solution has been prepared by dissolving the standard in a 1:1 Ethanol:Dichloromethane mixture. 3. To prepare the unknown analgesic, obtain roughly one-half an analgesic tablet. Prepare a 9 cm pipette with a small cotton plug for filtration. Crush the sample using a pestle in a mortar. Collect the powder in a small beaker or Erlenmeyer flask. Dissolve in 5 ml of 1:1 ethanol/dichloromethane. Pass the sample thru the pipette containing the cotton plug. This will separate any insoluble material from the material soluble in the ethanol/dichloromethane mixture. Collect in a medium test tube. Rinse the beaker or Erlenmeyer flask with another 5 ml of 1:1 ethanol/dichloromethane and pass the solution thru the pipette containing the cotton plug. 3. Develop the chromatogram. Add the TLC plate to the developing chamber. Allow it to run until the solvent front is a reasonable distance (~1 cm) from the top of the plate. Remove the plate from the TLC chamber and allow it to dry. Be sure to mark the position of the solvent front. 4. Observe the plate under a UV lamp. Do not look directly into the lamp as UV radiation can cause blindness. Lightly circle each spot with a pencil. 5. Accurately sketch the thin-layer chromatograms in your notebook.

P a g e 4 Data Sheet Obs. of Analgesic Tablet: Scketch of TLC Chromatogram: Identity of Analgesic: Name: Date: Signature:

P a g e 5 Additional Points to Consider You do not need to submit answers to these questions. However, you should seriously ponder the answers to these questions as they could reappear on an exam. Suppose a mixture being separated by TLC produces two spots on the chromatogram. Is it possible the mixture contained three substances? Explain. How far will a compound run along a chromatographic plate if it has a very low solubility in the eulting solvnet?