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The article contains sections titled: 1. Introduction 2. History 3. Preparation 4. Properties 5. Uses 6. Economic Aspects 7. Cationic Methine Dyes 7.1. Streptocyanine Dyes 7.1.1. Trimethinestreptocyanine Dyes 7.1.2. Pentamethinestreptocyanine Dyes and Higher Vinylogs 7.1.3. Triazolium Dyes 7.1.4. Aminoarylenamine Dyes 7.2. Hemicyanine Dyes 7.2.1. Cyclomethine Dyes 7.2.2. Dimethinehemicyanine Dyes 7.2.3. Higher Vinylogs of Hemicyanine Dyes 7.3. Phenylogous Hemicyanine Dyes 7.3.1. Zeromethine (Apocyanine) Dyes 7.3.2. Phenylogous Dimethinehemicyanine Dyes 7.3.3. Higher Vinylogs of Phenylogous Hemicyanine Dyes 7.3.4. Phenylogous Hemicyanine Dyes with Rings in the Methine Chain 7.4. Cyanine Dyes 7.4.1. Zeromethinecyanine Dyes 7.4.2. Monomethinecyanine Dyes 7.4.3. Dimethinecyanine Dyes 7.4.4. Trimethinecyanine Dyes 7.4.5. Pentamethinecyanine Dyes 7.4.6. Higher Vinylogs of Cyanine Dyes 7.4.7. Cyanine Dyes with Rings in the Methine Chain 7.4.8. Cyanine Dyes with Several Methine Chains 8. Anionic Methine Dyes (Oxonols) 8.1. Monomethineoxonol Dyes 8.2. Trimethineoxonol Dyes and Higher Vinylogs 9. Methine Dyes with Betaine Structure 10. Neutral Methine Dyes 10.1. Enamineneutrocyanines 10.2. Aminoarylneutrocyanines 10.2.1. Aminoarylneutrocyanines with Open‐Chain Terminal Groups 10.2.2. Aminoarylneutrocyanines with Cyclic Terminal Groups 10.3. Merocyanine Dyes 10.3.1. Merocyanine Dyes with Open‐Chain Terminal Groups 10.3.2. Merocyanine Dyes with Cyclic Terminal Groups
The article contains sections titled: 1. Introduction 2. History 3. Preparation 4. Properties 5. Uses 6. Economic Aspects 7. Cationic Methine Dyes 7.1. Streptocyanine Dyes 7.1.1. Trimethinestreptocyanine Dyes 7.1.2. Pentamethinestreptocyanine Dyes and Higher Vinylogs 7.1.3. Triazolium Dyes 7.1.4. Aminoarylenamine Dyes 7.2. Hemicyanine Dyes 7.2.1. Cyclomethine Dyes 7.2.2. Dimethinehemicyanine Dyes 7.2.3. Higher Vinylogs of Hemicyanine Dyes 7.3. Phenylogous Hemicyanine Dyes 7.3.1. Zeromethine (Apocyanine) Dyes 7.3.2. Phenylogous Dimethinehemicyanine Dyes 7.3.3. Higher Vinylogs of Phenylogous Hemicyanine Dyes 7.3.4. Phenylogous Hemicyanine Dyes with Rings in the Methine Chain 7.4. Cyanine Dyes 7.4.1. Zeromethinecyanine Dyes 7.4.2. Monomethinecyanine Dyes 7.4.3. Dimethinecyanine Dyes 7.4.4. Trimethinecyanine Dyes 7.4.5. Pentamethinecyanine Dyes 7.4.6. Higher Vinylogs of Cyanine Dyes 7.4.7. Cyanine Dyes with Rings in the Methine Chain 7.4.8. Cyanine Dyes with Several Methine Chains 8. Anionic Methine Dyes (Oxonols) 8.1. Monomethineoxonol Dyes 8.2. Trimethineoxonol Dyes and Higher Vinylogs 9. Methine Dyes with Betaine Structure 10. Neutral Methine Dyes 10.1. Enamineneutrocyanines 10.2. Aminoarylneutrocyanines 10.2.1. Aminoarylneutrocyanines with Open‐Chain Terminal Groups 10.2.2. Aminoarylneutrocyanines with Cyclic Terminal Groups 10.3. Merocyanine Dyes 10.3.1. Merocyanine Dyes with Open‐Chain Terminal Groups 10.3.2. Merocyanine Dyes with Cyclic Terminal Groups
The article contains sections titled: 1. Structure and Color 2. History 3. Uses 4. Hydroxynitro Dyes 5. Aminonitro Dyes 5.1. Alkylaminonitro Dyes 5.2. Arylaminonitro Dyes 5.2.1. Arylaminonitro Disperse Dyes 5.2.2. Anionic Arylaminonitro Dyes 5.2.3. Cationic Arylaminonitro Dyes 5.3. Heterocyclic Nitro Dyes 6. Azonitro Dyes 6.1. Azonitro Disperse Dyes 6.2. Anionic Azonitro Dyes 6.3. Cationic Azonitro Dyes 7. Nitro Dyes with Other Color Systems 8. Nitro Dyes in Hair Coloring 8.1. Nitroaniline Hair Dyes 8.2. Diaminonitrobenzene Hair Dyes 8.3. Aminonitrophenol Hair Dyes 8.4. Nitrodiphenylamine Hair Dyes 8.5. Formulation with Nitro Hair Dyes 9. Biologically Active Nitro Dyes 10. Nitroso Dyes
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