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INTERNATIONAL STANDARD IS0 13685 First edition 1997-08- 15 Dit document mag slechts op een stand-alone PC worden geinstalleerd. Gebruik op een netwerk is alleen. toestaan als een aanvullende licentieovereenkomst voor netwerkgebruik met NEN is afgesloten. This document may only be used on a stand-alone PC. Use in a network is only permitted when a supplementary license agreement for us in a network with NEN has been concluded. Ginger and its oleoresins - Determination of the main pungent components (gingerols and shogaols) - Method using highperformance liquid chromatography Gingembre et okorksines de gingembre - Dosage des principaux compos& piquants (gingkrols et shogaols) - Mkthode par chromatographie en phase liquide A haute performance Reference number IS0 13685:1997(E)

IS0 13685:1997(E) Foreword IS0 (the International Organization for Standardization) is a worldwide federation of national standards bodies (IS0 member bodies). The work of preparing International Standards is normally carried out through IS0 technical committees. Each member body interested in a subject for which a technical committee has been established has the right to be represented on that committee. International organizations, governmental and non-governmental, in liaison with ISO, also take part in the work. IS0 collaborates closely with the International Electrotechnical Commission (IEC) on all matters of electrotechnical standardization. Draft International Standards adopted by the technical committees are circulated to the member bodies for voting. Publication as an International Standard requires approval by at least 75 % of the member bodies casting a vote. International Standard IS0 13685 was prepared by Technical Committee ISOmC 34, Agriculfural food products, Subcommittee SC 7, Spices and condiments. Annexes A to E of this International Standard are for information only. 0 IS0 1997 All rights reserved. Unless otherwise specified, no part of this publication may be reproduced or utilized in any electronic or mechanical, including photocopying and microfilm, without permission in writing from the publisher. International Organization for Standardization Case postale 56 l CH-1211 Geneve 20 l Switzerland Internet central @ iso.ch x.400 c=ch; a=400net; p=iso; o=isocs; s=central Printed in Switzerland form or by any means, ii

@ IS0 IS0 13685: 1997(E) Introduction This method, initially based on Wood s publications [Overseas Development Natural Resources Institutes (ODNRI)], enables one to know without any ambiguity the identity of the peaks obtained by HPLC, for the quality control of ginger extracts It is particular-y useful in this case as the pungent compounds of interest are very sensitive to heat. The method has been validated by two international interlaboratory tests carried out by seven laboratories. After examination of the results, it is estimated that the method may be considered as the best that can be achieved for the moment but it could be improved, in particular for the precision data.

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INTERNATIONAL STANDARD o Iso IS0 13685:1997(E) Ginger and its oleoresins - Determination of the main pungent components (gingerols and shogaols) - Method using high= performance liquid chromatography 1 Scope This international Standard describes a method for the determination of gingerols [61-G, [81-G and [101-G and the corresponding shogaols [61-S, [81-S and [101-S in dried ginger or in oleoresins of ginger, by high-performance liquid chromatography (HPLC) in the reverse phase. NOTE - Chemical structures of gingerols and shogaols are shown in annex A. 2 Normative references The following standards contain provisions which, through reference in this text, constitute provisions of this International Standard. At the time of the publication, the editions indicated were valid. All standards are subject to revision, and parties to agreements based on the International Standard are encouraged to investigate the possibility of applying the most recent editions of the standards indicated below. Members of IEC and IS0 maintain registers of currently valid International Standards. IS0 939:1980, Spices and condiments - Determination of moisture con tent - En trainmen t method. IS0 2825: 1981, Spices and condiments - Preparation of a ground sample for analysis. 3 Principle From ground and dried ginger, extraction of the pungent components by methanol at atmospheric temperature and concentration at reduced pressure of part of the extract. The oleoresins are dissolved in the methanol. The resulting solutions are analysed directly (without any cleaning) by reverse-phase HPLC on a column filled with octadecylsilyl silica, with a mixture of acetonitrile and aqueous acetic acid as the mobile phase and by UV detection at 280 nm. Quantification is carried out using an external standard, nonanoic acid vanillylamide, which has a retention time comparable to that of gingerol-[6] (and a similar UV absorption spectrum).

IS0 13685:1997(E) 0 IS0 4 Reagents and products Use only reagents of recognized analytical grade, unless otherwise specified, and water of HPLC grade. 4.1 External standard: Nonanoic acid vanillylamide (NVA), with melting point between 42 OC and 44 C and giving primarily a unique peak (at least 98 % of the total area of the peak between 3 min and 8 min) when analysed by HPLC under the conditions described in this International Standard. WARNING: Nonanoic acid vanillylamide is a product which can cause irritation. NOTE - NVA is also known as nonyl vanillylamide or pelargonic acid vanillylamide. 4.2 Solvents WARNING: Acetonitrile is a toxic product which must be used with caution. Studies are underway to replace it by another product. 4.2.1 Methanol, HPLC grade, for preparation of the NVA standard. 4.2.2 Methanol, analytical grade, for dilution and extraction of the test samples. 4.2.3 Acetonitrile, HPLC grade. 4.2.4 Glacial acetic acid. 5 Apparatus Usual laboratory equipment and, in particular, the following. 5.1 Chromatograph Apparatus equipped for HPLC analysis: - an injection system capable of delivering portions of 20 ~1 of the sample solution with considerable precision; - an ultraviolet (UV) detector measuring absorbance at a wavelengh of 280 nm; - a recorder/integrator capable of precisely measuring the area of the peaks with appropriate baseline corrections, with a sensitivity of 0,25 to 0,5 a.u.f.s. 5.2 Stainless-steel column, of 250 mm length and 4,6 mm diameter (or of comparable dimensions) filled with type C,, stationary phase with particles of 5 urn?) I) ODS distributed by Phase Separations Ltd UK, is an example of a suitable product available commekcially.this information is given for the konvenience of users of International Standard and does not constitute an endorsement by IS0 of this product. 2

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