Isolation, Separation, and Characterization of Organic Acids*

Similar documents
BIOCHEMISTRY & MEDICINE:

Supporting Information for. Boronic Acid Functionalized Aza-Bodipy (azabdpba) based Fluorescence Optodes for the. analysis of Glucose in Whole Blood

EXPERIMENT 4 DETERMINATION OF REDUCING SUGARS, TOTAL REDUCING SUGARS, SUCROSE AND STARCH

A STUDY OF THE METABOLISM OF THEOBROMINE, THEOPHYLLINE, AND CAFFEINE IN MAN* Previous studies (1, 2) have shown that after the ingestion of caffeine

1 Preparation and Characterization of Lignin-Carbohydrate Complexes

Catalytic decarboxylative alkylation of β-keto acids with sulfonamides via the cleavage of carbon nitrogen and carbon carbon bonds

DISTRIBUTION OF NON-SUGARS IN THE ARI COUPLED LOOP MOLASSES DESUGARIZATION SYSTEM

Study of Phytochemical Screening and Antimicrobial Activity of Citrus aurantifolia Seed Extracts

THERMALLY OXIDIZED SOYA BEAN OIL interacted with MONO- and DIGLYCERIDES of FATTY ACIDS

Supplementary Material (ESI) for Chemical Communications This journal is (c) The Royal Society of Chemistry 2008

THERMALLY OXIDIZED SOYA BEAN OIL

Masatoshi Shibuya,Takahisa Sato, Masaki Tomizawa, and Yoshiharu Iwabuchi* Department of Organic Chemistry, Graduate School of Pharmaceutical Sciences,

Key Words: Brassica oleraceae, glucosinolate, liquid chromatography mass spectrometry, FNH-I-003

Figure 2. Figure 1. Name: Bio AP Lab Organic Molecules

Determination of Tanninoids. Analytical Pharmacognosy

Chapter 2 pt 2. Atoms, Molecules, and Life. Gregory Ahearn. John Crocker. Including the lecture Materials of

Chemicals Based on Ethylene

Chapter 18. Carboxylic Acids and Their Derivatives. Nucleophilic Addition-Elimination at the Acyl Carbon

CELLULOSE, MICROCRYSTALLINE. Cellulosum microcristallinum. Cellulose, microcrystalline EUROPEAN PHARMACOPOEIA 7.0

CARBOXYLIC ACIDS AND THEIR DERIVATIVES: NUCLEOPHILIC ADDITION-ELIMINATION AT THE ACYL CARBON

Novel D-erythro N-Octanoyl Sphingosine Analogs As Chemo- and Endocrine. Resistant Breast Cancer Therapeutics

Circular 80. STATE OF ILLINOIS WILLIAM G. STRATTON, Governor DEPARTMENT OF REGISTRATION AND EDUCATION VERA M. BINKS, Director

THE RELATIONSHIP BETWEEN TWO METHODS FOR EVALUATING FIVE-CARBON SUGARS IN EUCALYPTUS EXTRACTION LIQUOR

Working with Hazardous Chemicals

Organic Chemistry Laboratory Fall Lecture 3 Gas Chromatography and Mass Spectrometry June

(b) The following two alcohols are members of an homologous series and they are isomers.

SUPPLEMENTAL FIGURE 1 Structures and IC50 values of compounds 13 32

PURPOSE: To synthesize soap from fat and lye. To observe the physical and chemical properties of soap.

This is a repository copy of Scalable anthocyanin extraction and purification methods for industrial applications.

Organic Molecule Composition of Milk: Lab Investigation

Supporting Information

3. PRELIMINARY PHYTOCHEMICAL SCREENING

ARTENIMOLUM ARTENIMOL. Adopted revised text for addition to The International Pharmacopoeia

Organic and biochemical synthesis of monolignol biosynthetic pathway intermediates

Supplementary Material

Chapter 18 Carboxylic Acids and Their Derivatives. Nucleophilic Addition- Elimination at the Acyl Carbon

FUNGAL AND TERMITE RESISTANCE OF WOOD REACTED WITH PERIODIC ACID OR SODIUM PERIODATE George C. Chen and Roger M. Rowell

Catalogue. Resins and Columns For High Performance Liquid Chromatography

Studies on the Urea-Dewaxing of Lubricating Oils*

Chapter 2: Biochemistry

Heparin Sodium ヘパリンナトリウム

ETHYLENE GLYCOL. Table 1.1 Physical properties of Ethylene glycol

Petrolatum. Stage 4, Revision 1. Petrolatum is a purified semi solid mixture of hydrocarbons obtained from petroleum.

REACTIONS OF CARBOXYLIC ACID DERIVATIVES WITH NUCLEOPHILES A. Reactions of Acid Chlorides with Nucleophiles

you-try-it-02.xlsx Step-by-Step Guide ver. 8/26/2009

1/3/2011. Chapter 17 Carboxylic Acids and Their Derivatives. Nucleophilic Addition- Elimination at the Acyl Carbon

H O. rapidly reduces. They dissolve. because they can hydrogen bond to the water molecules.

The Amendment of Standards for Specification, Scope, Application and Limitation of Food Additives

Test Bank for Lehninger Principles of Biochemistry 5th Edition by Nelson

--> Buy True-PDF --> Auto-delivered in 0~10 minutes. GB Translated English of Chinese Standard: GB1886.

University of Queensland

Analysis of fatty acid metabolism using Click-Chemistry and HPLC-MS

Oxalate (urine, plasma)

STUDIES OF THE MECHANISM OF ACTION OF COBAMIDE COENZYMES

PB1617-Irrigation Water Quality for Greenhouse Production

QUALITATIVE ANALYSIS OF AMINO ACIDS AND PROTEINS

THE CHEMISTRY OF THE LIPIDS OF TUBERCLE BACILLI

SUMMARY AND CONCLUSION

Qualitative test of protein-lab2

22. The Fischer Esterification

Revision of monograph in the 4 th Edition of The International Pharmacopoeia (August 2008)

ISOLATION AND PROPERTIES OF FURTHER COMPONENTS OF THE ANTIBIOTIC MOENOMYCIN. U. Schacht and G. Huber Farbwerke Hoechst AG., Frankfurt am Main, Germany

Ex17. Analgesics, TLC Analysis. Analgesics. The Experiment. Part A. Carboxylic Acids. Part B. Willow Bark Esters & Esterification

Rebaudioside a From Multiple Gene Donors Expressed in Yarrowia Lipolytica

Challenges with Chelated &/or Complexed Minerals (Chelated and Soluble Methods of Analysis Used in FL)

The Oxidation of Quinic Acid

All chemicals were obtained from Aldrich, Acros, Fisher, or Fluka and were used without

Prerequisites Protein purification techniques and protein analytical methods. Basic enzyme kinetics.

Biological molecules = Biomolecules = Compounds of life

Lignin Isolation from Pulp

This place covers: Reducing the size of material from which sugars are to be extracted; Presses and knives therefor,

Effect of Washing on Quality Improvement of Mechanically Deboned Chicken Meat

MONOGRAPHS (USP) Saccharin Sodium

PHOTOCATALYTIC DECONTAMINATION OF CHLORANTRANILIPROLE RESIDUES IN WATER USING ZnO NANOPARTICLES. DR. A. RAMESH, Ph.D, D.Sc.,

Synthetic chemistry-led creation of a difluorinated biaryl ether non-nucleoside reverse transcriptase inhibitor

PURIFICATION OF PROTHROMBIN AND THROMBIN : CHEMICAL PROPERTIES OF PURIFIED PREPARATIONS*

Supporting information (protein purification, kinetic characterization, product isolation, and characterization by NMR and mass spectrometry):

SYNTHESIS OF QUATERNARY AMMONIUM COMPOUNDS FROM NATURAL MATERIALS

Pectins. Residue Monograph prepared by the meeting of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 82 nd meeting 2016

Supporting Information: Investigation into the Sources of Biochar Water Soluble Organic Compounds and Their

SYNOPSIS STUDIES ON THE PREPARATION AND CHARACTERISATION OF PROTEIN HYDROLYSATES FROM GROUNDNUT AND SOYBEAN ISOLATES

SPE Cartridges. All Finneran Products Are Certified. Conditioning Sample application Wash Elution

Extraction and Standardization of Medicinal Herbal Products

Prelab 6: Carboxylic Acids

Studies on the Determination of Bile Pigments I. Standard of Purity for Bilirubin

Lipid Analysis ISOLATION, SEPARATION, IDENTIFICATION AND. Bridgwater, England LIPIDOMIC ANALYSIS. Fourth Edition. Invergowrie, Dundee, Scotland

Determination of 6-Chloropicolinic Acid (6-CPA) in Crops by Liquid Chromatography with Tandem Mass Spectrometry Detection. EPL-BAS Method No.

Hydrophobic Interaction Chromatography

Alehydes, Ketones and Carboxylic Acid

Supporting Information for. Use of the Curtius Rearrangement of Acryloyl Azides in the Synthesis of. 3,5-Disubstituted Pyridines: Mechanistic Studies

vii LIST OF TABLES TABLE NO DESCRIPTION PAGE 1.1 System Suitability Parameters and Recommendations Acidic and Alkaline Hydrolysis 15

Industrial Pharmacy (3) Solutions as a dosage form. DR.Saad.M.YACOUB

THE IDENTIFICATION OF PHENOLIC ACIDS BY HPLC METHOD FROM STRAWBERRIES. Abstract

MONOGRAPHS (NF) Pharmacopeial Forum 616 HARMONIZATION Vol. 31(2) [Mar. Apr. 2005]

Rapid and Robust Detection of THC and Its Metabolites in Blood

from Miscanthus Cellulose - Lignin

SUPPLEMENTARY MATERIAL

Carboxylic Acids and their Derivatives I

Chapter MEMBRANE TRANSPORT

QUALITATIVE TEST OF PROTEIN

Transcription:

In Dashek, William V., ed. Methods in plant biochemistry and molecular biology. Boca Raton, FL: CRC Press: pp. 107-113. Chapter 9.1997. Isolation, Separation, and Characterization of Organic Acids* William V. Dashek and Jessie A. Micales Contents 9.1 Overview Chemistry, Occurrence, and Function Many plants contain a variety of free acids which are colorless compounds soluble in water, ethanol, and ether. but insoluble in the nonpolar solvents benzene or petroleum ether. These acids are weakly acidic and can accumulate in the cellular vacuoles of certain plants. Some of the acids are components of the citric acid cycle, while others are intermediates in the pathway leading from carbohydrates to either aromatic compounds or isoprenoid derivatives. 1 Figure 9.1 presents the chemistry of certain of these organic acids. Table 9.1 summarizes their possible functions. Oxalic acid appears to be of marked significance in fungal-induced wood decay. i.e.. the acid could serve as a proton donor for oxidative (Fenton's reaction) cleavages of wood cellulose. 2,3 * The Forest Products Laboratory is maintained in cooperation with the University of Wisconsin. The chapter was coauthored by J. A. Micales. a U.S. government employee, on official time and is, therefore, in the public domain and not subject to copyright.

Isolation, Separation, and Characterization of Organic Acids 9.2 Protocols 9.2.1 Isolation This chapter is concerned with the isolation, purification, and assay of organic acids. Whereas Protocol 9.1 presents an acidified, ether extraction procedure for isolating organic acids from either heat-dried or freeze-dried plant material, Protocol 9.2 summarizes an ion exchange chromatographic protocol for extracting the acids. 9.2.2 Separation and Preparation Techniques and Characterization Subsequent to extraction, organic acids can be separated and detected via a variety of techniques. Table 9.2 lists the references for procedures that separate the acids in ether extracts. A gas chromatographic separation of organic acids is depicted in Figure 9.2 and an HPLC elution profile of seven organic acids can be seen in Figure 9.3 For rigorous identification of organic acids, gas chromatography can be coupled to mass spectrometry. In addition to the above techniques, paper and thin-layer chromatographies have been employed to separate certain organic acids. Table 9.3 summarizes the conditions for paper and thin-layer chromatographies. If Whatman 3MM chromatography paper is employed, paper chromatography can serve as a preparative procedure, partially purifying as much as 100 mg of organic acids.

Methods in Plant Biochemistry and Molecular Biology L

Isolation, Separation, and Characterization of Organic Acids

Methods in Plant Biochemistry and Molecular Biology Heat-dried or freeze-fried plant material. Make strongly acidic (ph 1.0) with H 2 SO 4 and extract up to several days with peroxide-free ether. Ether extract contains free acids. Transfer from ether to water by shaking with sodium hydroxide. Remove sodium sulfate by adjusting aqueous solution to ph 1 H 2 SO 4 two volumes of ethanol maintaining overnight in the cold. Separate organic acids by filtation from precipitated sodium sulfate. Note: (1) drying with heat can remove volatile acids, destroy keto acids, and cause ester formation: (2) volatile acids or esters may be lost during freeze drying. Neutralizing the plant marerial before drying yields acids as nonvolatile salts. Protocol 9.1 Isolation of organic acids by acidification and subsequent partitioning of plant extracts with ether. (Adapted from Robinson, T., The Organic Constituents of Higher Plants, Their Chemistry and Interrelationships. Cordus Press. North Amherst, MA. 1980, 43-49. With permission.) Prepare an aqueous extract of plant acids Pass through a column of weakly basic anion exchange in the hydroxide form (cast separate several hundred milligrams of mixed organic acids with 10 g resin). Wash column. Elute free acids with 0.1 N HCl (order of elution mono, di, and tricarboxylic acids). Note if a strongly basic anion exchange resin is utilized in the hydroxide form, sugars may form sugar acids. Protocol 9.2 Anion exchange chromatography protocol for extracting organic acids. (Adapted from Robinson, T., The Organic Constituents of Higher Plants, Their Chemistry and Interrelationships. Cordus Press,,North Amherst, MA. 1980, 43-49. With permission.) References

Isolation, Separation, and Characterization of Organic Acids