<?xml version="1.0" encoding="utf-8"?>
<?xml-stylesheet href="ipcentry.xsl" type="text/xsl"?>
<ipcEntries displayMode="e20080401;a20080401;c20060101" ipcLevel="a" split="subclass" languages=",en,fr," size="113294">
	<ipcEntry kind="s" symbol="C" ipcLevel="C" entryType="K" lang="EN" nocore="yes">
		<textBody>
			<title>
				<titlePart>
					<text>SECTION C <emdash/> CHEMISTRY</text>
				</titlePart>
				<titlePart>
					<text>METALLURGY</text>
				</titlePart>
			</title>
		</textBody>
		<ipcEntry kind="n" symbol="C" ipcLevel="C" entryType="K" lang="EN" nocore="yes">
			<textBody>
				<note type="number">
					<noteParagraph>
						<text>In section C, the definitions of groups of chemical elements are as follows:</text>
						<subnote type="none" indent="1">
							<noteParagraph>
								<text><u>Alkali metals:</u> Li, Na, K, Rb, Cs, Fr</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Alkaline earth metals:</u> Ca, Sr, Ba, Ra</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Lanthanides:</u> elements with atomic numbers 57 to 71 inclusive</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Rare earths:</u> Sc, Y, Lanthanides</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Actinides:</u> elements with atomic numbers 89 to 103 inclusive</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Refractory metals:</u> Ti, V, Cr, Zr, Nb, Mo, Hf, Ta, W</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Halogens:</u> F, Cl, Br, I, At</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Noble gases:</u> He, Ne, Ar, Kr, Xe, Rn</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Platinum group:</u> Os, Ir, Pt, Ru, Rh, Pd</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Noble metals:</u> Ag, Au, Platinum group</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Light metals:</u> alkali metals, alkaline earth metals, Be, Al, Mg</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Heavy metals:</u> metals other than light metals</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Iron group:</u> Fe, Co, Ni</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Non-metals:</u> H, B, C, Si, N, P, O, S, Se, Te, noble gases, halogens</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Metals:</u> elements other than non-metals</text>
							</noteParagraph>
							<noteParagraph>
								<text><u>Transition elements:</u> elements with atomic numbers 21 to 30 inclusive, 39 to 48 inclusive, 57 to 80 inclusive, 89 upwards</text>
							</noteParagraph>
						</subnote>
					</noteParagraph>
					<noteParagraph>
						<text>Section C <u>covers</u>:</text>
						<subnote type="alpha" indent="1">
							<noteParagraph>
								<text>pure chemistry, which covers inorganic compounds, organic compounds, macromolecular compounds, and their methods of preparation;</text>
							</noteParagraph>
							<noteParagraph>
								<text>applied chemistry, which covers compositions containing the above compounds, such as: glass, ceramics, fertilisers, plastics compositions, paints, products of the petroleum industry. It also <u>covers</u> certain compositions on account of their having particular properties rendering them suitable for certain purposes, as in the case of explosives, dyestuffs, adhesives, lubricants, and detergents;</text>
							</noteParagraph>
							<noteParagraph>
								<text>certain marginal industries, such as the manufacture of coke and of solid or gaseous fuels, the production and refining of oils, fats and waxes, the fermentation industry (e.g., brewing and wine-making), the sugar industry;</text>
							</noteParagraph>
							<noteParagraph>
								<text>certain operations or treatments, which are either purely mechanical, e.g., the mechanical treatment of leather and skins, or partly mechanical, e.g., the treatment of water or the prevention of corrosion in general;</text>
							</noteParagraph>
							<noteParagraph>
								<text>metallurgy, ferrous or non-ferrous alloys.</text>
							</noteParagraph>
						</subnote>
					</noteParagraph>
					<noteParagraph>
						<text/>
						<subnote type="alpha" indent="1">
							<noteParagraph>
								<text>In the case of operations, treatments, products or articles having both a chemical and a non-chemical part or aspect, the general rule is that the chemical part or aspect is covered by section C.</text>
							</noteParagraph>
							<noteParagraph>
								<text>In some of these cases, the chemical part or aspect brings with it a non-chemical one, even though purely mechanical, because this latter aspect either is essential to the operation or treatment or constitutes an important element thereof. It has seemed, in fact, more logical not to dissociate the different parts or aspects of a coherent whole. This is the case for applied chemistry and for the industries, operations and treatments mentioned in Notes (1)(c), (d) and (e). For example, furnaces peculiar to the manufacture of glass are covered by class <sref ref="C03"/> and not by class <sref ref="F27"/>.</text>
							</noteParagraph>
							<noteParagraph>
								<text>There are, however, some exceptions in which the mechanical (or non-chemical) aspect carries with it the chemical aspect, for example:</text>
								<subnote type="bullet" indent="2">
									<noteParagraph>
										<text>Certain extractive processes, in subclass <sref ref="A61K"/>;</text>
									</noteParagraph>
									<noteParagraph>
										<text>The chemical purification of air, in subclass <sref ref="A61L"/>;</text>
									</noteParagraph>
									<noteParagraph>
										<text>Chemical methods of fire-fighting, in subclass <sref ref="A62D"/>;</text>
									</noteParagraph>
									<noteParagraph>
										<text>Chemical processes and apparatus, in class <sref ref="B01"/>;</text>
									</noteParagraph>
									<noteParagraph>
										<text>Impregnation of wood, in subclass <sref ref="B27K"/>;</text>
									</noteParagraph>
									<noteParagraph>
										<text>Chemical methods of analysis or testing, in subclass <sref ref="G01N"/>;</text>
									</noteParagraph>
									<noteParagraph>
										<text>Photographic materials and processes, in class <sref ref="G03"/>, and, generally, the chemical treatment of textiles and the production of cellulose or paper, in section D.</text>
									</noteParagraph>
								</subnote>
							</noteParagraph>
							<noteParagraph>
								<text>In still other cases, the pure chemical aspect is covered by section C and the applied chemical aspect by another section, such as A, B or F, e.g., the use of a substance or composition for:</text>
								<subnote type="bullet" indent="2">
									<noteParagraph>
										<text>treatment of plants or animals, covered by subclass <sref ref="A01N"/>;</text>
									</noteParagraph>
									<noteParagraph>
										<text>foodstuffs, covered by class <sref ref="A23"/>;</text>
									</noteParagraph>
									<noteParagraph>
										<text>ammunition or explosives, covered by class <sref ref="F42"/>.</text>
									</noteParagraph>
								</subnote>
							</noteParagraph>
							<noteParagraph>
								<text>When the chemical and mechanical aspects are so closely interlocked that a neat and simple division is not possible, or when certain mechanical processes follow as a natural or logical continuation of a chemical treatment, section C may cover, in addition to the chemical aspect, a part only of the mechanical aspect, e.g., after-treatment of artificial stone, covered by class <sref ref="C04"/>. In this latter case, a note or a reference is usually given to make the position clear, even if sometimes the division is rather arbitrary.</text>
							</noteParagraph>
						</subnote>
					</noteParagraph>
				</note>
			</textBody>
		</ipcEntry>
		<ipcEntry kind="t" symbol="C01" ipcLevel="C" entryType="K" lang="EN" nocore="yes">
			<textBody>
				<title>
					<titlePart>
						<text>CHEMISTRY</text>
					</titlePart>
				</title>
			</textBody>
		</ipcEntry>
		<ipcEntry kind="c" symbol="C12" ipcLevel="C" entryType="K" lang="EN" nocore="yes">
			<textBody>
				<title>
					<titlePart>
						<text>BIOCHEMISTRY</text>
					</titlePart>
					<titlePart>
						<text>BEER</text>
					</titlePart>
					<titlePart>
						<text>SPIRITS</text>
					</titlePart>
					<titlePart>
						<text>WINE</text>
					</titlePart>
					<titlePart>
						<text>VINEGAR</text>
					</titlePart>
					<titlePart>
						<text>MICROBIOLOGY</text>
					</titlePart>
					<titlePart>
						<text>ENZYMOLOGY</text>
					</titlePart>
					<titlePart>
						<text>MUTATION OR GENETIC ENGINEERING</text>
					</titlePart>
				</title>
			</textBody>
			<ipcEntry kind="n" symbol="C12" ipcLevel="C" entryType="K" lang="EN" nocore="yes">
				<textBody>
					<note type="number">
						<noteParagraph edition="19800101">
							<text>In subclasses <mref ref="C12M" endRef="C12Q"/> or <sref ref="C12S"/>, and within each of these subclasses, in the absence of an indication to the contrary, classification is made in the last appropriate place.</text>
						</noteParagraph>
						<noteParagraph edition="19800101,19900101">
							<text>In this class, viruses, undifferentiated human, animal or plant cells, protozoa, tissues and unicellular algae are considered as micro-organisms.</text>
						</noteParagraph>
						<noteParagraph edition="19900101">
							<text>In this subclass, unless specifically provided for, undifferentiated human, animal or plant cells, protozoa, tissues and unicellular algae are classified together with micro-organisms. Sub-cellular parts, unless specifically provided for, are classified with the whole cell.</text>
						</noteParagraph>
					</note>
				</textBody>
			</ipcEntry>
			<ipcEntry kind="n" symbol="C12" endSymbol="C12S" ipcLevel="A" entryType="K" lang="EN" nocore="yes">
				<textBody>
					<note>
						<noteParagraph edition="19800101">
							<text>The codes of subclass <sref ref="C12R"/> are <u>only</u> for use as indexing codes associated with subclasses <mref ref="C12C" endRef="C12Q"/> or <sref ref="C12S"/>, so as to provide information concerning the micro-organisms used in the processes classified in these subclasses.</text>
						</noteParagraph>
					</note>
				</textBody>
			</ipcEntry>
			<ipcEntry kind="u" symbol="C12P" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
				<textBody>
					<title>
						<titlePart>
							<text>FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE</text>
							<entryReference>fermentation processes to form a food composition <sref ref="A21"/>, <sref ref="A23"/></entryReference>
							<entryReference>compounds in general, <u>see</u> the relevant compound class, e.g. <sref ref="C01"/>, <sref ref="C07"/></entryReference>
							<entryReference>brewing of beer <sref ref="C12C"/></entryReference>
							<entryReference>producing vinegar <sref ref="C12J"/></entryReference>
							<entryReference>processes for producing enzymes <sref ref="C12N0009000000"/></entryReference>
							<entryReference>DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification <sref ref="C12N0015000000"/></entryReference>
						</titlePart>
					</title>
				</textBody>
				<ipcEntry kind="n" symbol="C12P" ipcLevel="C" entryType="K" lang="EN" nocore="yes">
					<textBody>
						<note type="number">
							<noteParagraph edition="19800101">
								<text>This subclass <u>covers</u> both major and minor chemical modifications.</text>
							</noteParagraph>
							<noteParagraph edition="19800101">
								<text>Group <sref ref="C12P0001000000"/><u>covers</u> processes for producing organic compounds not sufficiently identified to be classified in groups <mref ref="C12P0003000000" endRef="C12P0037000000"/>. Compounds identified only by their empirical formulae are not considered to be sufficiently identified.</text>
							</noteParagraph>
							<noteParagraph edition="19850101">
								<text>Attention is drawn to Notes (1) to (3) following the title of class <sref ref="C12"/>.</text>
							</noteParagraph>
							<noteParagraph edition="19800101">
								<text>If a particular reaction is considered of interest, it is also classified in the relevant chemical compound class, e.g. <sref ref="C07"/>, <sref ref="C08"/>.</text>
							</noteParagraph>
							<noteParagraph>
								<text>In this subclass:</text>
								<subnote type="bullet" indent="1">
									<noteParagraph>
										<text>metal or ammonium salts of a compound are classified as that compound.</text>
									</noteParagraph>
									<noteParagraph edition="19800101">
										<text>compositions are classified in the relevant compound groups.</text>
									</noteParagraph>
								</subnote>
							</noteParagraph>
						</note>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="n" symbol="C12P" endSymbol="C12P0041000000" ipcLevel="A" entryType="K" lang="EN" nocore="yes">
					<textBody>
						<note type="none" indent="1">
							<noteParagraph edition="19950101">
								<text>In this subclass, it is desirable to add the indexing codes of subclass <sref ref="C12R"/>.</text>
							</noteParagraph>
						</note>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="i" symbol="C12P" ipcLevel="C" entryType="K" lang="EN" nocore="yes">
					<textBody>
						<index>
							<indexEntry>
								<text>BIOSYNTHESIS OF CHEMICAL SUBSTANCES</text>
								<indexEntry>
									<text>Inorganic compounds </text>
									<references><sref ref="C12P0003000000"/></references>
								</indexEntry>
								<indexEntry>
									<text>Acyclic or carbocyclic organic compounds </text>
									<references><mref ref="C12P0005000000" endRef="C12P0015000000"/></references>
								</indexEntry>
								<indexEntry>
									<text>peptides or proteins </text>
									<references><sref ref="C12P0021000000"/></references>
								</indexEntry>
								<indexEntry>
									<text>Carotenes </text>
									<references><sref ref="C12P0023000000"/></references>
								</indexEntry>
								<indexEntry>
									<text>Tetracyclines </text>
									<references><sref ref="C12P0029000000"/></references>
								</indexEntry>
								<indexEntry>
									<text>Prostaglandins </text>
									<references><sref ref="C12P0031000000"/></references>
								</indexEntry>
								<indexEntry>
									<text>Steroids </text>
									<references><sref ref="C12P0033000000"/></references>
								</indexEntry>
								<indexEntry>
									<text>Heterocyclic organic compounds </text>
									<references><sref ref="C12P0017000000"/></references>
								</indexEntry>
								<indexEntry>
									<text>containing saccharide radicals </text>
									<references><sref ref="C12P0019000000"/></references>
								</indexEntry>
								<indexEntry>
									<text>Riboflavin </text>
									<references><sref ref="C12P0025000000"/></references>
								</indexEntry>
								<indexEntry>
									<text>Giberellin </text>
									<references><sref ref="C12P0027000000"/></references>
								</indexEntry>
								<indexEntry>
									<text>Cephalosporin; penicillin </text>
									<references><sref ref="C12P0035000000"/>; <sref ref="C12P0037000000"/></references>
								</indexEntry>
							</indexEntry>
							<indexEntry>
								<text>SEPARATION OF OPTICAL ISOMERS </text>
								<references><sref ref="C12P0041000000"/></references>
							</indexEntry>
							<indexEntry>
								<text>OTHER PROCESSES FOR BIOSYNTHESIS PREPARATIONS </text>
								<references><sref ref="C12P0001000000"/>, <sref ref="C12P0039000000"/></references>
							</indexEntry>
						</index>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0001000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="200" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of compounds or compositions, not provided for in groups <mref ref="C12P0003000000" endRef="C12P0039000000"/>, by using micro-organisms or enzymes</text>
							</titlePart>
							<titlePart>
								<text>General processes for the preparation of compounds or compositions by using micro-organisms or enzymes</text>
							</titlePart>
						</title>
					</textBody>
					<ipcEntry kind="1" symbol="C12P0001020000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>by using fungi</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0001040000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>by using bacteria</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0001060000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>by using actinomycetales</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0003000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="190" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of elements or inorganic compounds except carbon dioxide</text>
							</titlePart>
						</title>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0005000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="180" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of hydrocarbons</text>
							</titlePart>
						</title>
					</textBody>
					<ipcEntry kind="1" symbol="C12P0005020000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>acyclic</text>
									<entryReference>producing methane by anaerobic treatment of sludge <sref ref="C02F0011040000"/></entryReference>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0007000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="170" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of oxygen-containing organic compounds</text>
							</titlePart>
						</title>
					</textBody>
					<ipcEntry kind="1" symbol="C12P0007020000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>containing a hydroxy group</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0007040000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>acyclic</text>
									</titlePart>
								</title>
							</textBody>
							<ipcEntry kind="3" symbol="C12P0007060000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>Ethanol, i.e. non-beverage</text>
										</titlePart>
									</title>
								</textBody>
								<ipcEntry kind="4" symbol="C12P0007080000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>produced as by-product or from waste or cellulosic material substrate</text>
											</titlePart>
										</title>
									</textBody>
									<ipcEntry kind="5" symbol="C12P0007100000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
										<textBody>
											<title>
												<titlePart>
													<text>substrate containing cellulosic material</text>
												</titlePart>
											</title>
										</textBody>
									</ipcEntry>
									<ipcEntry kind="5" symbol="C12P0007120000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
										<textBody>
											<title>
												<titlePart>
													<text>substrate containing sulfite waste liquor or citrus waste</text>
												</titlePart>
											</title>
										</textBody>
									</ipcEntry>
								</ipcEntry>
								<ipcEntry kind="4" symbol="C12P0007140000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>Multiple stages of fermentation</text>
											</titlePart>
											<titlePart>
												<text>Multiple types of micro-organisms or reuse for micro-organisms</text>
											</titlePart>
										</title>
									</textBody>
								</ipcEntry>
							</ipcEntry>
							<ipcEntry kind="3" symbol="C12P0007160000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>Butanols</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
							<ipcEntry kind="3" symbol="C12P0007180000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>polyhydric</text>
										</titlePart>
									</title>
								</textBody>
								<ipcEntry kind="4" symbol="C12P0007200000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>Glycerol</text>
											</titlePart>
										</title>
									</textBody>
								</ipcEntry>
							</ipcEntry>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0007220000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>aromatic</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0007240000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>containing a carbonyl group</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0007260000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Ketones</text>
									</titlePart>
								</title>
							</textBody>
							<ipcEntry kind="3" symbol="C12P0007280000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>Acetone-containing products</text>
										</titlePart>
									</title>
								</textBody>
								<ipcEntry kind="4" symbol="C12P0007300000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>produced from substrate containing inorganic compounds other than water</text>
											</titlePart>
										</title>
									</textBody>
								</ipcEntry>
								<ipcEntry kind="4" symbol="C12P0007320000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>produced from substrate containing inorganic nitrogen source</text>
											</titlePart>
										</title>
									</textBody>
								</ipcEntry>
								<ipcEntry kind="4" symbol="C12P0007340000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>produced from substrate containing protein as nitrogen source</text>
											</titlePart>
										</title>
									</textBody>
								</ipcEntry>
								<ipcEntry kind="4" symbol="C12P0007360000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>produced from substrate containing grain or cereal material</text>
											</titlePart>
										</title>
									</textBody>
								</ipcEntry>
							</ipcEntry>
							<ipcEntry kind="3" symbol="C12P0007380000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>Cyclopentanone- or cyclopentadione- containing products</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0007400000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>containing a carboxyl group</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0007420000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Hydroxy carboxylic acids</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0007440000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Polycarboxylic acids</text>
									</titlePart>
								</title>
							</textBody>
							<ipcEntry kind="3" symbol="C12P0007460000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>Dicarboxylic acids having four or less carbon atoms, e.g. fumaric acid, maleic acid</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
							<ipcEntry kind="3" symbol="C12P0007480000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>Tricarboxylic acids, e.g. citric acid</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
							<ipcEntry kind="3" symbol="C12P0007500000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>having keto groups, e.g. 2-ketoglutaric acid</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0007520000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Propionic acid</text>
									</titlePart>
									<titlePart>
										<text>Butyric acids</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0007540000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Acetic acid</text>
										<entryReference>vinegar <sref ref="C12J"/></entryReference>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0007560000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Lactic acid</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0007580000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Aldonic, ketoaldonic or saccharic acids</text>
										<entryReference>uronic acids <sref ref="C12P0019000000"/></entryReference>
									</titlePart>
								</title>
							</textBody>
							<ipcEntry kind="3" symbol="C12P0007600000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>2-Ketogulonic acid</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0007620000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Carboxylic acid esters</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0007640000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Fats</text>
								</titlePart>
								<titlePart>
									<text>Fatty oils</text>
								</titlePart>
								<titlePart>
									<text>Ester-type waxes</text>
								</titlePart>
								<titlePart>
									<text>Higher fatty acids, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group</text>
								</titlePart>
								<titlePart>
									<text>Oxidised oils or fats</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0007660000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>containing the quinoid structure</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0009000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="160" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of organic compounds containing a metal or atom other than H, N, C, O, S, or halogen</text>
							</titlePart>
						</title>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0011000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="150" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of sulfur-containing organic compounds</text>
							</titlePart>
						</title>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0013000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="140" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of nitrogen-containing organic compounds</text>
							</titlePart>
						</title>
					</textBody>
					<ipcEntry kind="1" symbol="C12P0013020000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Amides, e.g. chloramphenicol</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0013040000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Alpha- or beta-amino acids</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0013060000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Alanine</text>
									</titlePart>
									<titlePart>
										<text>Leucine</text>
									</titlePart>
									<titlePart>
										<text>Isoleucine</text>
									</titlePart>
									<titlePart>
										<text>Serine</text>
									</titlePart>
									<titlePart>
										<text>Homoserine</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0013080000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Lysine</text>
									</titlePart>
									<titlePart>
										<text>Diaminopimelic acid</text>
									</titlePart>
									<titlePart>
										<text>Threonine</text>
									</titlePart>
									<titlePart>
										<text>Valine</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0013100000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Citrulline</text>
									</titlePart>
									<titlePart>
										<text>Arginine</text>
									</titlePart>
									<titlePart>
										<text>Ornithine</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0013120000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Methionine</text>
									</titlePart>
									<titlePart>
										<text>Cysteine</text>
									</titlePart>
									<titlePart>
										<text>Cystine</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0013140000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Glutamic acid</text>
									</titlePart>
									<titlePart>
										<text>Glutamine</text>
									</titlePart>
								</title>
							</textBody>
							<ipcEntry kind="3" symbol="C12P0013160000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>using surfactants, fatty acids or fatty acid esters, i.e. having at least seven carbon atoms in an unbroken chain bound to a carboxyl group or a carboxyl ester group</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
							<ipcEntry kind="3" symbol="C12P0013180000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>using biotin or its derivatives</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0013200000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Aspartic acid</text>
									</titlePart>
									<titlePart>
										<text>Asparagine</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0013220000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Tryptophan</text>
									</titlePart>
									<titlePart>
										<text>Tyrosine</text>
									</titlePart>
									<titlePart>
										<text>Phenylalanine</text>
									</titlePart>
									<titlePart>
										<text>3,4-Dihydroxyphenylalanine</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0013240000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Proline</text>
									</titlePart>
									<titlePart>
										<text>Hydroxyproline</text>
									</titlePart>
									<titlePart>
										<text>Histidine</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
					</ipcEntry>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0015000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="130" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of compounds containing at least three condensed carbocyclic rings</text>
							</titlePart>
						</title>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0017000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="120" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of heterocyclic carbon compounds with only O, N, S, Se, or Te as ring hetero atoms</text>
								<entryReference><mref ref="C12P0013040000" endRef="C12P0013240000"/> take precedence</entryReference>
							</titlePart>
						</title>
					</textBody>
					<ipcEntry kind="1" symbol="C12P0017020000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Oxygen as only ring hetero atoms</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0017040000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>containing a five-membered hetero ring, e.g. griseofulvin</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0017060000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>containing a six-membered hetero ring, e.g. fluorescein</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0017080000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>containing a hetero ring of at least seven ring members, e.g. zearalenone, macrolide aglycons</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0017100000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Nitrogen as only ring hetero atom</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0017120000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>containing a six-membered hetero ring</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0017140000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Nitrogen or oxygen as hetero atom and at least one other diverse hetero ring atom in the same ring</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0017160000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>containing two or more hetero rings</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0017180000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0019000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="110" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of compounds containing saccharide radicals</text>
								<entryReference>ketoaldonic acids <sref ref="C12P0007580000"/></entryReference>
							</titlePart>
						</title>
					</textBody>
					<ipcEntry kind="n" symbol="C12P0019000000" ipcLevel="C" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<note type="none">
								<noteParagraph edition="19800101">
									<text>Attention is drawn to Note (3) following the title of subclass <sref ref="C07H"/>, which defines the expression "saccharide radical".<nbsp/></text>
								</noteParagraph>
							</note>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019020000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Monosaccharides</text>
									<entryReference>2-ketogulonic acid <sref ref="C12P0007600000"/></entryReference>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019040000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Polysaccharides, i.e. compounds containing more than five saccharide radicals attached to each other by glycosidic bonds</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0019060000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Xanthan, i.e. Xanthomonas-type heteropolysaccharides</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0019080000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Dextran</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0019100000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Pullulan</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019120000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Disaccharides</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019140000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>produced by the action of a carbohydrase, e.g. by alpha-amylase</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019160000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>produced by the action of an alpha-1, 6-glucosidase, e.g. amylose, debranched amylopectin</text>
									<entryReference>non-biological hydrolysis of starch <sref ref="C08B0030000000"/></entryReference>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019180000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>produced by the action of a glycosyl transferase, e.g. alpha-, beta- or gamma-cyclodextrins</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019200000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>produced by the action of an exo-1, 4 alpha-glucosidase, e.g. dextrose</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019220000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>produced by the action of a beta-amylase, e.g. maltose</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019240000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>produced by the action of an isomerase, e.g. fructose</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019260000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Preparation of nitrogen-containing carbohydrates</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0019280000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>N-glycosides</text>
									</titlePart>
								</title>
							</textBody>
							<ipcEntry kind="3" symbol="C12P0019300000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>Nucleotides</text>
										</titlePart>
									</title>
								</textBody>
								<ipcEntry kind="4" symbol="C12P0019320000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>having a condensed ring system containing a six-membered ring having two nitrogen atoms in the same-ring, e.g. purine nucleotides, nicotineamide-adenine dinucleotide</text>
											</titlePart>
										</title>
									</textBody>
								</ipcEntry>
								<ipcEntry kind="4" symbol="C12P0019340000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>Polynucleotides, e.g. nucleic acids, oligoribonucleotides</text>
											</titlePart>
										</title>
									</textBody>
								</ipcEntry>
								<ipcEntry kind="4" symbol="C12P0019360000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>Dinucleotides, e.g. nicotineamide-adenine dinucleotide phosphate</text>
											</titlePart>
										</title>
									</textBody>
								</ipcEntry>
							</ipcEntry>
							<ipcEntry kind="3" symbol="C12P0019380000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>Nucleosides</text>
										</titlePart>
									</title>
								</textBody>
								<ipcEntry kind="4" symbol="C12P0019400000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>having a condensed ring system containing a six-membered ring having two nitrogen atoms in the same ring, e.g. purine nucleosides</text>
											</titlePart>
										</title>
									</textBody>
								</ipcEntry>
							</ipcEntry>
							<ipcEntry kind="3" symbol="C12P0019420000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>Cobalamins, i.e. vitamin B<sub>12</sub>, LLD factor</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019440000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Preparation of O-glycosides, e.g. glucosides</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0019460000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>having an oxygen atom of the saccharide radical bound to a cyclohexyl radical, e.g. kasugamycin</text>
									</titlePart>
								</title>
							</textBody>
							<ipcEntry kind="3" symbol="C12P0019480000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>the cyclohexyl radical being substituted by two or more nitrogen atoms, e.g. destomycin, neamin</text>
										</titlePart>
									</title>
								</textBody>
								<ipcEntry kind="4" symbol="C12P0019500000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
									<textBody>
										<title>
											<titlePart>
												<text>having two saccharide radicals bound through only oxygen to adjacent ring carbon atoms of the cyclohexyl radical, e.g. ambutyrosin, ribostamycin</text>
											</titlePart>
										</title>
									</textBody>
									<ipcEntry kind="5" symbol="C12P0019520000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
										<textBody>
											<title>
												<titlePart>
													<text>containing three or more saccharide radicals, e.g. neomycin, lividomycin</text>
												</titlePart>
											</title>
										</textBody>
									</ipcEntry>
								</ipcEntry>
							</ipcEntry>
							<ipcEntry kind="3" symbol="C12P0019540000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>the cyclohexyl radical being bound directly to a nitrogen atom of two or more <img src="fig79.gif"/> radicals, e.g. streptomycin</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0019560000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>having an oxygen atom of the saccharide radical directly bound to a condensed ring system having three or more carbocyclic rings, e.g. daunomycin, adriamycin</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0019580000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>having an oxygen atom of the saccharide radical directly bound through only acyclic carbon atoms to a non-saccharide heterocyclic ring, e.g. bleomycin, phleomycin</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0019600000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>having an oxygen of the saccharide radical directly bound to a non-saccharide heterocyclic ring or a condensed ring system containing a non-saccharide heterocyclic ring, e.g. coumermycin, novobiocin</text>
									</titlePart>
								</title>
							</textBody>
							<ipcEntry kind="3" symbol="C12P0019620000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>the hetero ring having eight or more ring members and only oxygen as ring hetero atoms, e.g. erythromycin, spiramycin, nystatin</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0019640000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Preparation of S-glycosides, e.g. lincomycin</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0021000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="100" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of peptides or proteins</text>
								<entryReference>single-cell protein <sref ref="C12N0001000000"/></entryReference>
							</titlePart>
						</title>
					</textBody>
					<ipcEntry kind="1" symbol="C12P0021020000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>having a known sequence of two or more amino acids, e.g. glutathione</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0021040000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Cyclic or bridged peptides or polypeptides, e.g. bacitracin</text>
										<entryReference>cyclised by <emdash/>S<emdash/>S<emdash/> bonds only <sref ref="C12P0021020000"/></entryReference>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0021060000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>produced by the hydrolysis of a peptide bond, e.g. hydrolysate products</text>
									<entryReference>preparing foodstuffs by protein hydrolysis <sref ref="A23J0003000000"/></entryReference>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0021080000" ipcLevel="C" edition="19900101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Monoclonal antibodies</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0023000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="90" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of compounds containing a cyclohexene ring having an unsaturated side chain containing at least ten carbon atoms bound by conjugated double bonds, e.g. carotenes</text>
								<entryReference>containing hetero-rings <sref ref="C12P0017000000"/></entryReference>
							</titlePart>
						</title>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0025000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="80" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of compounds containing alloxazine or isoalloxazine nucleus, e.g. riboflavin</text>
							</titlePart>
						</title>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0027000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="70" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of compounds containing a gibbane ring system, e.g. gibberellin</text>
							</titlePart>
						</title>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0029000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="60" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of compounds containing a naphthacene ring system, e.g. tetracycline</text>
								<entryReference><sref ref="C12P0019000000"/> takes precedence</entryReference>
							</titlePart>
						</title>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0031000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="50" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of compounds containing a five-membered ring having two side-chains in ortho position to each other, and having at least one oxygen atom directly bound to the ring in ortho position to one of the side-chains, one side-chain containing, not directly bound to the ring, a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, and the other side-chain having at least one oxygen atom bound in gamma-position to the ring, e.g. prostaglandins</text>
							</titlePart>
						</title>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0033000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="40" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of steroids</text>
							</titlePart>
						</title>
					</textBody>
					<ipcEntry kind="n" symbol="C12P0033000000" ipcLevel="C" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<note type="none">
								<noteParagraph edition="19800101">
									<text>Attention is drawn to Note (1) following the title of subclass <sref ref="C07J"/>, which explains what is covered by the term "steroids".</text>
								</noteParagraph>
							</note>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="n" symbol="C12P0033020000" endSymbol="C12P0033200000" ipcLevel="A" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<note type="none">
								<noteParagraph>
									<text>In groups <mref ref="C12P0033020000" endRef="C12P0033200000"/>, the following terms are used with the meaning indicated:</text>
									<subnote type="bullet" indent="1">
										<noteParagraph edition="19800101">
											<text>"acting", "forming", "hydroxylating", "dehydroxylating" or "dehydrogenating" means the action of a micro-organism or enzyme rather than other chemical action.</text>
										</noteParagraph>
									</subnote>
								</noteParagraph>
							</note>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0033020000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Dehydrogenating</text>
								</titlePart>
								<titlePart>
									<text>Dehydroxylating</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0033040000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Forming an aryl ring from A ring</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0033060000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Hydroxylating</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0033080000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>at 11 position</text>
									</titlePart>
								</title>
							</textBody>
							<ipcEntry kind="3" symbol="C12P0033100000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>at 11alpha-position</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0033120000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Acting on D ring</text>
								</titlePart>
							</title>
						</textBody>
						<ipcEntry kind="2" symbol="C12P0033140000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Hydroxylating at 16 position</text>
									</titlePart>
								</title>
							</textBody>
						</ipcEntry>
						<ipcEntry kind="2" symbol="C12P0033160000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
							<textBody>
								<title>
									<titlePart>
										<text>Acting at 17 position</text>
									</titlePart>
								</title>
							</textBody>
							<ipcEntry kind="3" symbol="C12P0033180000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
								<textBody>
									<title>
										<titlePart>
											<text>Hydroxylating at 17 position</text>
										</titlePart>
									</title>
								</textBody>
							</ipcEntry>
						</ipcEntry>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0033200000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>containing heterocyclic rings</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0035000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="30" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of compounds having a 5-thia-1-azabicyclo [4.2.0] octane ring system, e.g. cephalosporin</text>
							</titlePart>
						</title>
					</textBody>
					<ipcEntry kind="1" symbol="C12P0035020000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>by desacylation of the substituent in the 7 position</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0035040000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>by acylation of the substituent in the 7 position</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0035060000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>Cephalosporin C</text>
								</titlePart>
								<titlePart>
									<text>Derivatives thereof</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0035080000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>disubstituted in the 7 position</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0037000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="20" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Preparation of compounds having a 4-thia-1-azabicyclo [3.2.0] heptane ring system, e.g. penicillin</text>
							</titlePart>
						</title>
					</textBody>
					<ipcEntry kind="1" symbol="C12P0037020000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>in presence of phenylacetic acid or phenylacetamide or their derivatives</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0037040000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>by acylation of the substituent in the 6 position</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
					<ipcEntry kind="1" symbol="C12P0037060000" ipcLevel="A" edition="19800101" entryType="K" lang="EN" nocore="yes">
						<textBody>
							<title>
								<titlePart>
									<text>by desacylation of the substituent in the 6 position</text>
								</titlePart>
							</title>
						</textBody>
					</ipcEntry>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0039000000" ipcLevel="C" edition="19800101" entryType="K" lang="EN" priorityOrder="10" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Processes involving micro-organisms of different genera in the same process, simultaneously</text>
							</titlePart>
						</title>
					</textBody>
				</ipcEntry>
				<ipcEntry kind="m" symbol="C12P0041000000" ipcLevel="C" edition="19850101" entryType="K" lang="EN" priorityOrder="0" nocore="yes">
					<textBody>
						<title>
							<titlePart>
								<text>Processes using enzymes or micro-organisms to separate optical isomers from a racemic mixture</text>
							</titlePart>
						</title>
					</textBody>
				</ipcEntry>
			</ipcEntry>
		</ipcEntry>
	</ipcEntry>
</ipcEntries>
