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Aromi e aromatizzazione : argomenti di tecnologia, chimica analitica, tossicologia / edited by Fernando Tateo
| Aromi e aromatizzazione : argomenti di tecnologia, chimica analitica, tossicologia / edited by Fernando Tateo |
| Autore | Conferenza nazionale sugli aromatizzanti <2. ; 1986 ; Pavia> |
| Pubbl/distr/stampa | Milano : S.E.F., copyr. 1987 |
| Descrizione fisica | XL, 286 p. ; 25 cm |
| Disciplina | 664.5 |
| Soggetto non controllato | Alimenti - Aromatizzazione |
| Formato | Materiale a stampa  |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ita |
| Record Nr. | UNISA-990000080920203316 |
Conferenza nazionale sugli aromatizzanti <2. ; 1986 ; Pavia>
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| Milano : S.E.F., copyr. 1987 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
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Brevi cenni sulla fabbricazione del cioccolatte / Giuseppe Bianchi
| Brevi cenni sulla fabbricazione del cioccolatte / Giuseppe Bianchi |
| Autore | Bianchi, Giuseppe |
| Pubbl/distr/stampa | Milano : Tip. F. Poncelletti, 1881 |
| Descrizione fisica | 21p., [1] c. di tav. : ill. ; 23 cm |
| Disciplina | 664.5 |
| Soggetto non controllato | Cioccolato |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ita |
| Record Nr. | UNINA-990001823960403321 |
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Bianchi, Giuseppe
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| Milano : Tip. F. Poncelletti, 1881 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Chemistry and technology of flavors and fragrances [[electronic resource] /] / edited by David J. Rowe
| Chemistry and technology of flavors and fragrances [[electronic resource] /] / edited by David J. Rowe |
| Pubbl/distr/stampa | Oxford, : Blackwell, 2005 |
| Descrizione fisica | 1 online resource (352 p.) |
| Disciplina | 664.5 |
| Altri autori (Persone) | RoweDavid J <1958-> (David John) |
| Soggetto topico |
Flavor - Analysis
Odors |
| ISBN |
1-280-21299-3
9786610212996 1-4443-0551-4 1-4051-4807-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Half title; Title; Contents; Contributors; Preface; 1 Introduction, David J. Rowe; 1.1 History: in the beginning; 1.2 The classical world; 1.3 The mediaeval world; 1.4 From the Renaissance to the Enlightment; 1.5 The industrial age; 1.6 The post-war world; 1.6.1 Technical factors; 1.6.2 Social factors; 1.7 The future; 1.8 The structure of the flavour and fragrance industry; 1.9 A note on regulations; 1.10 A note on quality; References; 2 Identification of Aroma Chemicals, Neil C. Da Costa and Sanja Eri; 2.1 Introduction; 2.2 Isolation of aroma chemicals; 2.2.1 Solvent extraction
2.2.2 Steam distillation methods2.2.3 Headspace techniques; 2.2.4 Direct thermal desorption (DTD); 2.2.5 Sorptive techniques; 2.3 Gas chromatography-olfactometry; 2.4 Techniques for identification of aroma compounds; 2.5 A case study: Generessence®; 2.5.1 Sample preparation; 2.5.2 Valencia orange; 2.5.3 Roast chicken; 2.5.4 Narcissus; 2.5.5 Post-analysis work; References; 3 Flavor Generation in Food, Liam O'Hare and John Grigor; 3.1 Introduction; 3.2 Taste and aroma; 3.3 Cooked meat; 3.3.1 Flavour precursors; 3.3.2 Influence of method of cooking; 3.4 Cheese 3.4.1 Lactose and citrate fermentation3.4.2 Protein degradation; 3.4.3 Lipid degradation; Acknowledgements; References; 4 Aroma Chemicals I: C, H, O Compounds, David J. Rowe; 4.1 Introduction; 4.2 Alcohols; 4.2.1 Saturated alkyl alcohols; 4.2.2 Unsaturated alkyl alcohols; 4.2.3 Complex fragrance alcohols; 4.2.4 Aromatic and aralkyl alcohols; 4.2.5 Phenolics; 4.3 Acids; 4.3.1 Saturated aliphatic acids; 4.3.2 Unsaturated acids; 4.3.3 Aromatic acids; 4.4 Esters; 4.4.1 Saturated esters; 4.4.2 Unsaturated esters; 4.4.3 Aromatic esters; 4.4.4 Lactones - gamma and delta; 4.4.5 Synthesis of esters 4.5 Aldehydes4.5.1 Aliphatic aldehydes; 4.5.2 Unsaturated aldehydes; 4.5.3 Acetals; 4.5.4 Aromatics; 4.5.5 Nitriles; 4.6 Ketones; 4.6.1 Carotenoids, ionones, irones, damascones and related compounds; 4.7 Hydrocarbons; Acknowledgements; References; 5 Aroma Chemicals II: Heterocycles, Michael Zviely; 5.1 Introduction; 5.2 Introduction to heterocyclic compounds; 5.2.1 Terminology of heterocycles; 5.2.2 Non-aromatic heterocyclic compounds; 5.3 Oxygen-containing heterocyclic aroma chemicals; 5.4 Heterocyclic compounds containing nitrogen and/or sulfur; References 6 Aroma Chemicals III: Sulfur Compounds, Simon B. Jameson6.1 Thiols and thioesters; 6.2 Acyclic sulfides and polysulfides; 6.3 Saturated heterocyclic sulfur compounds; 6.4 Quality and stability; Acknowledgements; References; Bibliography; Websites; 7 Aroma Chemicals IV: Musks, Philip Kraft; 7.1 Introduction; 7.2 Natural musks; 7.3 Nitro musks; 7.4 PCM - Polycyclic aromatic musks; 7.5 Evolution of the industrial synthesis of macrocycles; 7.6 Modern macrocyclic musks; 7.7 New musk structures; Acknowledgements; References; 8 Aroma Chemicals V: Natural Aroma Chemials, John Margetts 8.1 Introduction |
| Record Nr. | UNINA-9910143286103321 |
| Oxford, : Blackwell, 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chemistry and technology of flavors and fragrances [[electronic resource] /] / edited by David J. Rowe
| Chemistry and technology of flavors and fragrances [[electronic resource] /] / edited by David J. Rowe |
| Pubbl/distr/stampa | Oxford, : Blackwell, 2005 |
| Descrizione fisica | 1 online resource (352 p.) |
| Disciplina | 664.5 |
| Altri autori (Persone) | RoweDavid J <1958-> (David John) |
| Soggetto topico |
Flavor - Analysis
Odors |
| ISBN |
1-280-21299-3
9786610212996 1-4443-0551-4 1-4051-4807-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Half title; Title; Contents; Contributors; Preface; 1 Introduction, David J. Rowe; 1.1 History: in the beginning; 1.2 The classical world; 1.3 The mediaeval world; 1.4 From the Renaissance to the Enlightment; 1.5 The industrial age; 1.6 The post-war world; 1.6.1 Technical factors; 1.6.2 Social factors; 1.7 The future; 1.8 The structure of the flavour and fragrance industry; 1.9 A note on regulations; 1.10 A note on quality; References; 2 Identification of Aroma Chemicals, Neil C. Da Costa and Sanja Eri; 2.1 Introduction; 2.2 Isolation of aroma chemicals; 2.2.1 Solvent extraction
2.2.2 Steam distillation methods2.2.3 Headspace techniques; 2.2.4 Direct thermal desorption (DTD); 2.2.5 Sorptive techniques; 2.3 Gas chromatography-olfactometry; 2.4 Techniques for identification of aroma compounds; 2.5 A case study: Generessence®; 2.5.1 Sample preparation; 2.5.2 Valencia orange; 2.5.3 Roast chicken; 2.5.4 Narcissus; 2.5.5 Post-analysis work; References; 3 Flavor Generation in Food, Liam O'Hare and John Grigor; 3.1 Introduction; 3.2 Taste and aroma; 3.3 Cooked meat; 3.3.1 Flavour precursors; 3.3.2 Influence of method of cooking; 3.4 Cheese 3.4.1 Lactose and citrate fermentation3.4.2 Protein degradation; 3.4.3 Lipid degradation; Acknowledgements; References; 4 Aroma Chemicals I: C, H, O Compounds, David J. Rowe; 4.1 Introduction; 4.2 Alcohols; 4.2.1 Saturated alkyl alcohols; 4.2.2 Unsaturated alkyl alcohols; 4.2.3 Complex fragrance alcohols; 4.2.4 Aromatic and aralkyl alcohols; 4.2.5 Phenolics; 4.3 Acids; 4.3.1 Saturated aliphatic acids; 4.3.2 Unsaturated acids; 4.3.3 Aromatic acids; 4.4 Esters; 4.4.1 Saturated esters; 4.4.2 Unsaturated esters; 4.4.3 Aromatic esters; 4.4.4 Lactones - gamma and delta; 4.4.5 Synthesis of esters 4.5 Aldehydes4.5.1 Aliphatic aldehydes; 4.5.2 Unsaturated aldehydes; 4.5.3 Acetals; 4.5.4 Aromatics; 4.5.5 Nitriles; 4.6 Ketones; 4.6.1 Carotenoids, ionones, irones, damascones and related compounds; 4.7 Hydrocarbons; Acknowledgements; References; 5 Aroma Chemicals II: Heterocycles, Michael Zviely; 5.1 Introduction; 5.2 Introduction to heterocyclic compounds; 5.2.1 Terminology of heterocycles; 5.2.2 Non-aromatic heterocyclic compounds; 5.3 Oxygen-containing heterocyclic aroma chemicals; 5.4 Heterocyclic compounds containing nitrogen and/or sulfur; References 6 Aroma Chemicals III: Sulfur Compounds, Simon B. Jameson6.1 Thiols and thioesters; 6.2 Acyclic sulfides and polysulfides; 6.3 Saturated heterocyclic sulfur compounds; 6.4 Quality and stability; Acknowledgements; References; Bibliography; Websites; 7 Aroma Chemicals IV: Musks, Philip Kraft; 7.1 Introduction; 7.2 Natural musks; 7.3 Nitro musks; 7.4 PCM - Polycyclic aromatic musks; 7.5 Evolution of the industrial synthesis of macrocycles; 7.6 Modern macrocyclic musks; 7.7 New musk structures; Acknowledgements; References; 8 Aroma Chemicals V: Natural Aroma Chemials, John Margetts 8.1 Introduction |
| Record Nr. | UNISA-996214592703316 |
| Oxford, : Blackwell, 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. di Salerno | ||
| ||
Chemistry and technology of flavors and fragrances [[electronic resource] /] / edited by David J. Rowe
| Chemistry and technology of flavors and fragrances [[electronic resource] /] / edited by David J. Rowe |
| Pubbl/distr/stampa | Oxford, : Blackwell, 2005 |
| Descrizione fisica | 1 online resource (352 p.) |
| Disciplina | 664.5 |
| Altri autori (Persone) | RoweDavid J <1958-> (David John) |
| Soggetto topico |
Flavor - Analysis
Odors |
| ISBN |
1-280-21299-3
9786610212996 1-4443-0551-4 1-4051-4807-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Half title; Title; Contents; Contributors; Preface; 1 Introduction, David J. Rowe; 1.1 History: in the beginning; 1.2 The classical world; 1.3 The mediaeval world; 1.4 From the Renaissance to the Enlightment; 1.5 The industrial age; 1.6 The post-war world; 1.6.1 Technical factors; 1.6.2 Social factors; 1.7 The future; 1.8 The structure of the flavour and fragrance industry; 1.9 A note on regulations; 1.10 A note on quality; References; 2 Identification of Aroma Chemicals, Neil C. Da Costa and Sanja Eri; 2.1 Introduction; 2.2 Isolation of aroma chemicals; 2.2.1 Solvent extraction
2.2.2 Steam distillation methods2.2.3 Headspace techniques; 2.2.4 Direct thermal desorption (DTD); 2.2.5 Sorptive techniques; 2.3 Gas chromatography-olfactometry; 2.4 Techniques for identification of aroma compounds; 2.5 A case study: Generessence®; 2.5.1 Sample preparation; 2.5.2 Valencia orange; 2.5.3 Roast chicken; 2.5.4 Narcissus; 2.5.5 Post-analysis work; References; 3 Flavor Generation in Food, Liam O'Hare and John Grigor; 3.1 Introduction; 3.2 Taste and aroma; 3.3 Cooked meat; 3.3.1 Flavour precursors; 3.3.2 Influence of method of cooking; 3.4 Cheese 3.4.1 Lactose and citrate fermentation3.4.2 Protein degradation; 3.4.3 Lipid degradation; Acknowledgements; References; 4 Aroma Chemicals I: C, H, O Compounds, David J. Rowe; 4.1 Introduction; 4.2 Alcohols; 4.2.1 Saturated alkyl alcohols; 4.2.2 Unsaturated alkyl alcohols; 4.2.3 Complex fragrance alcohols; 4.2.4 Aromatic and aralkyl alcohols; 4.2.5 Phenolics; 4.3 Acids; 4.3.1 Saturated aliphatic acids; 4.3.2 Unsaturated acids; 4.3.3 Aromatic acids; 4.4 Esters; 4.4.1 Saturated esters; 4.4.2 Unsaturated esters; 4.4.3 Aromatic esters; 4.4.4 Lactones - gamma and delta; 4.4.5 Synthesis of esters 4.5 Aldehydes4.5.1 Aliphatic aldehydes; 4.5.2 Unsaturated aldehydes; 4.5.3 Acetals; 4.5.4 Aromatics; 4.5.5 Nitriles; 4.6 Ketones; 4.6.1 Carotenoids, ionones, irones, damascones and related compounds; 4.7 Hydrocarbons; Acknowledgements; References; 5 Aroma Chemicals II: Heterocycles, Michael Zviely; 5.1 Introduction; 5.2 Introduction to heterocyclic compounds; 5.2.1 Terminology of heterocycles; 5.2.2 Non-aromatic heterocyclic compounds; 5.3 Oxygen-containing heterocyclic aroma chemicals; 5.4 Heterocyclic compounds containing nitrogen and/or sulfur; References 6 Aroma Chemicals III: Sulfur Compounds, Simon B. Jameson6.1 Thiols and thioesters; 6.2 Acyclic sulfides and polysulfides; 6.3 Saturated heterocyclic sulfur compounds; 6.4 Quality and stability; Acknowledgements; References; Bibliography; Websites; 7 Aroma Chemicals IV: Musks, Philip Kraft; 7.1 Introduction; 7.2 Natural musks; 7.3 Nitro musks; 7.4 PCM - Polycyclic aromatic musks; 7.5 Evolution of the industrial synthesis of macrocycles; 7.6 Modern macrocyclic musks; 7.7 New musk structures; Acknowledgements; References; 8 Aroma Chemicals V: Natural Aroma Chemials, John Margetts 8.1 Introduction |
| Record Nr. | UNINA-9910830632203321 |
| Oxford, : Blackwell, 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chemistry and technology of flavors and fragrances [[electronic resource] /] / edited by David J. Rowe
| Chemistry and technology of flavors and fragrances [[electronic resource] /] / edited by David J. Rowe |
| Pubbl/distr/stampa | Oxford, : Blackwell, 2005 |
| Descrizione fisica | 1 online resource (352 p.) |
| Disciplina | 664.5 |
| Altri autori (Persone) | RoweDavid J <1958-> (David John) |
| Soggetto topico |
Flavor - Analysis
Odors |
| ISBN |
1-280-21299-3
9786610212996 1-4443-0551-4 1-4051-4807-1 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Half title; Title; Contents; Contributors; Preface; 1 Introduction, David J. Rowe; 1.1 History: in the beginning; 1.2 The classical world; 1.3 The mediaeval world; 1.4 From the Renaissance to the Enlightment; 1.5 The industrial age; 1.6 The post-war world; 1.6.1 Technical factors; 1.6.2 Social factors; 1.7 The future; 1.8 The structure of the flavour and fragrance industry; 1.9 A note on regulations; 1.10 A note on quality; References; 2 Identification of Aroma Chemicals, Neil C. Da Costa and Sanja Eri; 2.1 Introduction; 2.2 Isolation of aroma chemicals; 2.2.1 Solvent extraction
2.2.2 Steam distillation methods2.2.3 Headspace techniques; 2.2.4 Direct thermal desorption (DTD); 2.2.5 Sorptive techniques; 2.3 Gas chromatography-olfactometry; 2.4 Techniques for identification of aroma compounds; 2.5 A case study: Generessence®; 2.5.1 Sample preparation; 2.5.2 Valencia orange; 2.5.3 Roast chicken; 2.5.4 Narcissus; 2.5.5 Post-analysis work; References; 3 Flavor Generation in Food, Liam O'Hare and John Grigor; 3.1 Introduction; 3.2 Taste and aroma; 3.3 Cooked meat; 3.3.1 Flavour precursors; 3.3.2 Influence of method of cooking; 3.4 Cheese 3.4.1 Lactose and citrate fermentation3.4.2 Protein degradation; 3.4.3 Lipid degradation; Acknowledgements; References; 4 Aroma Chemicals I: C, H, O Compounds, David J. Rowe; 4.1 Introduction; 4.2 Alcohols; 4.2.1 Saturated alkyl alcohols; 4.2.2 Unsaturated alkyl alcohols; 4.2.3 Complex fragrance alcohols; 4.2.4 Aromatic and aralkyl alcohols; 4.2.5 Phenolics; 4.3 Acids; 4.3.1 Saturated aliphatic acids; 4.3.2 Unsaturated acids; 4.3.3 Aromatic acids; 4.4 Esters; 4.4.1 Saturated esters; 4.4.2 Unsaturated esters; 4.4.3 Aromatic esters; 4.4.4 Lactones - gamma and delta; 4.4.5 Synthesis of esters 4.5 Aldehydes4.5.1 Aliphatic aldehydes; 4.5.2 Unsaturated aldehydes; 4.5.3 Acetals; 4.5.4 Aromatics; 4.5.5 Nitriles; 4.6 Ketones; 4.6.1 Carotenoids, ionones, irones, damascones and related compounds; 4.7 Hydrocarbons; Acknowledgements; References; 5 Aroma Chemicals II: Heterocycles, Michael Zviely; 5.1 Introduction; 5.2 Introduction to heterocyclic compounds; 5.2.1 Terminology of heterocycles; 5.2.2 Non-aromatic heterocyclic compounds; 5.3 Oxygen-containing heterocyclic aroma chemicals; 5.4 Heterocyclic compounds containing nitrogen and/or sulfur; References 6 Aroma Chemicals III: Sulfur Compounds, Simon B. Jameson6.1 Thiols and thioesters; 6.2 Acyclic sulfides and polysulfides; 6.3 Saturated heterocyclic sulfur compounds; 6.4 Quality and stability; Acknowledgements; References; Bibliography; Websites; 7 Aroma Chemicals IV: Musks, Philip Kraft; 7.1 Introduction; 7.2 Natural musks; 7.3 Nitro musks; 7.4 PCM - Polycyclic aromatic musks; 7.5 Evolution of the industrial synthesis of macrocycles; 7.6 Modern macrocyclic musks; 7.7 New musk structures; Acknowledgements; References; 8 Aroma Chemicals V: Natural Aroma Chemials, John Margetts 8.1 Introduction |
| Record Nr. | UNINA-9910840946003321 |
| Oxford, : Blackwell, 2005 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Chimica analitica degli aromi / Fernando Tateo, Monica Bonomi
| Chimica analitica degli aromi / Fernando Tateo, Monica Bonomi |
| Autore | Tateo, Fernando |
| Pubbl/distr/stampa | Bussolengo (Verona) : Giuseppe Maria Ricchiuto Ed., 1995-1999 |
| Descrizione fisica | 2 v. ; 25 cm |
| Disciplina | 664.5 |
| Altri autori (Persone) | Bonomi, Monica |
| Soggetto non controllato |
Tecnologia alimentare
Aromi |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | ita |
| Record Nr. | UNINA-990001824770403321 |
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Tateo, Fernando
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| Bussolengo (Verona) : Giuseppe Maria Ricchiuto Ed., 1995-1999 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Common fragrance and flavor materials : preparation, properties and uses / / Horst Surburg, Johannes Panten
| Common fragrance and flavor materials : preparation, properties and uses / / Horst Surburg, Johannes Panten |
| Autore | Surburg Horst |
| Edizione | [Six completely revised and updated edition.] |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH, , 2016 |
| Descrizione fisica | 1 online resource (389 p.) |
| Disciplina | 664.5 |
| Soggetto topico |
Flavoring essences
Essences and essential oils Perfumes Odors |
| ISBN |
3-527-69318-1
1-5231-1011-2 3-527-69315-7 3-527-69317-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Copyright; Contents; Preface; Chapter 1 Introduction; 1.1 History; 1.2 Definition; 1.3 Physiological Importance; 1.4 Natural, Nature-Identical, and Artificial Products; 1.5 Sensory Properties and Chemical Structure; 1.6 Volatility; 1.7 Threshold Concentration; 1.8 Sensory Properties; 1.8.1 Fragrance Ingredients; 1.8.2 Flavoring Substances; Chapter 2 Individual Fragrance and Flavor Materials; 2.1 Aliphatic Compounds; 2.1.1 Hydrocarbons; 2.1.1.1 (E,Z)-1,3,5-Undecatriene [51447-08-6]; 2.1.1.2 1,3-Undecadien-5-yne [166432-52-6]; 2.1.2 Alcohols; 2.1.2.1 3-Octanol [589-98-0]
2.1.2.2 2,6-Dimethyl-2-heptanol [13254-34-7]2.1.2.3 (E)-2-Hexen-1-ol [928-95-0]; 2.1.2.4 (Z)-3-Hexen-1-ol [928-96-1], Leaf Alcohol; 2.1.2.5 1-Octen-3-ol [3391-86-4]; 2.1.2.6 9-Decen-1 (cipher)-ol [13019-22-2]; 2.1.2.7 10-Undecen-1-ol [112-43-6]; 2.1.2.8 3,4,5,6,6-Pentamethylheptan-2-ol [87118-95-4]; 2.1.2.9 (2E,6Z)-2,6-Nonadien-1-ol [28069-72-9], Violet Leaf Alcohol; 2.1.2.10 4-Methyl-3-decen-5-ol [81782-77-6]; 2.1.3 Aldehydes and Acetals; 2.1.3.1 Hexanal [66-25-1], Caproaldehyde, Aldehyde C6; 2.1.3.2 Octanal [124-13-0], Caprylaldehyde, Aldehyde C8 2.1.3.3 Nonanal [124-19-6], Pelargonaldehyde, Aldehyde C92.1.3.4 Decanal [112-31-2], Caprinaldehyde, Aldehyde C10; 2.1.3.5 Undecanal [112-44-7], Aldehyde C11; 2.1.3.6 Dodecanal [112-54-9], Lauraldehyde, Lauric Aldehyde, Aldehyde C12; 2.1.3.7 Tridecanal [10486-19-8]; 2.1.3.8 2-Methyldecanal [19009-56-4], Methyloctylacetaldehyde, Aldehyde MOA; 2.1.3.9 2-Methylundecanal [110-41-8], Methylnonylacetaldehyde, Aldehyde MNA; 2.1.3.10 (E)-2-Hexenal [6728-26-3], Leaf Aldehyde; 2.1.3.11 (Z)-4-Heptenal [6728-31-0]; 2.1.3.12 2,6-Dimethyl-5-hepten-1-al [106-72-9]; 2.1.3.13 (E)-4-Decenal [65405-70-1] 2.1.3.14 10-Undecenal [112-45-8]2.1.3.15 2-Dodecenal [20407-84-5]; 2.1.3.16 2,6,10-Trimethyl-5,9-undecadienal [24048-13-3] and [54082-68-7]; 2.1.3.17 1,1-Dimethoxy-2,2,5-trimethyl-4-hexene [67674-46-8]; 2.1.4 Ketones; 2.1.4.1 3-Hydroxy-2-butanone [52217-02-4], Acetoin; 2.1.4.2 2,3-Butanedione [431-03-8], Diacetyl; 2.1.4.3 (2E)-5-Methyl-2-hepten-4-one [81925-81-7]; 2.1.4.4 3,4,5,6,6-Pentamethyl-3-hepten-2-one [81786-73-4]; 2.1.4.5 2,4,4,7-Tetramethyl-6-octen-3-one [74338-72-0]; 2.1.5 Acids and Esters; 2.1.5.1 2-Methyl-2-pentenoic Acid [3142-72-1]; 2.1.5.2 Ethyl Formate [109-94-4] 2.1.5.3 (Z)-3-Hexenyl Formate [33467-73-1]2.1.5.4 Ethyl Acetate [141-78-6]; 2.1.5.5 Butyl Acetate [123-86-4]; 2.1.5.6 Isoamyl Acetate [123-92-2]; 2.1.5.7 Hexyl Acetate [142-92-7]; 2.1.5.8 3,5,5-Trimethylhexyl Acetate [58430-94-7], Isononyl Acetate; 2.1.5.9 (E)-2-Hexenyl Acetate [2497-18-9]; 2.1.5.10 (Z)-3-Hexenyl Acetate [3681-71-8]; 2.1.5.11 Ethyl Propionate [105-37-3]; 2.1.5.12 Ethyl Butyrate [105-54-4]; 2.1.5.13 Butyl Butyrate [109-21-7]; 2.1.5.14 Isoamyl Butyrate [106-27-4]; 2.1.5.15 Hexyl Butyrate [2639-63-6]; 2.1.5.16 (Z)-3-Hexenyl Isobutyrate [41519-23-7] 2.1.5.17 Ethyl Isovalerate [108-64-5] |
| Record Nr. | UNINA-9910136445103321 |
|
Surburg Horst
|
||
| Weinheim, Germany : , : Wiley-VCH, , 2016 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
| ||
Common fragrance and flavor materials : preparation, properties and uses / / Horst Surburg, Johannes Panten
| Common fragrance and flavor materials : preparation, properties and uses / / Horst Surburg, Johannes Panten |
| Autore | Surburg Horst |
| Edizione | [Six completely revised and updated edition.] |
| Pubbl/distr/stampa | Weinheim, Germany : , : Wiley-VCH, , 2016 |
| Descrizione fisica | 1 online resource (389 p.) |
| Disciplina | 664.5 |
| Soggetto topico |
Flavoring essences
Essences and essential oils Perfumes Odors |
| ISBN |
3-527-69318-1
1-5231-1011-2 3-527-69315-7 3-527-69317-3 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Nota di contenuto |
Cover; Title Page; Copyright; Contents; Preface; Chapter 1 Introduction; 1.1 History; 1.2 Definition; 1.3 Physiological Importance; 1.4 Natural, Nature-Identical, and Artificial Products; 1.5 Sensory Properties and Chemical Structure; 1.6 Volatility; 1.7 Threshold Concentration; 1.8 Sensory Properties; 1.8.1 Fragrance Ingredients; 1.8.2 Flavoring Substances; Chapter 2 Individual Fragrance and Flavor Materials; 2.1 Aliphatic Compounds; 2.1.1 Hydrocarbons; 2.1.1.1 (E,Z)-1,3,5-Undecatriene [51447-08-6]; 2.1.1.2 1,3-Undecadien-5-yne [166432-52-6]; 2.1.2 Alcohols; 2.1.2.1 3-Octanol [589-98-0]
2.1.2.2 2,6-Dimethyl-2-heptanol [13254-34-7]2.1.2.3 (E)-2-Hexen-1-ol [928-95-0]; 2.1.2.4 (Z)-3-Hexen-1-ol [928-96-1], Leaf Alcohol; 2.1.2.5 1-Octen-3-ol [3391-86-4]; 2.1.2.6 9-Decen-1 (cipher)-ol [13019-22-2]; 2.1.2.7 10-Undecen-1-ol [112-43-6]; 2.1.2.8 3,4,5,6,6-Pentamethylheptan-2-ol [87118-95-4]; 2.1.2.9 (2E,6Z)-2,6-Nonadien-1-ol [28069-72-9], Violet Leaf Alcohol; 2.1.2.10 4-Methyl-3-decen-5-ol [81782-77-6]; 2.1.3 Aldehydes and Acetals; 2.1.3.1 Hexanal [66-25-1], Caproaldehyde, Aldehyde C6; 2.1.3.2 Octanal [124-13-0], Caprylaldehyde, Aldehyde C8 2.1.3.3 Nonanal [124-19-6], Pelargonaldehyde, Aldehyde C92.1.3.4 Decanal [112-31-2], Caprinaldehyde, Aldehyde C10; 2.1.3.5 Undecanal [112-44-7], Aldehyde C11; 2.1.3.6 Dodecanal [112-54-9], Lauraldehyde, Lauric Aldehyde, Aldehyde C12; 2.1.3.7 Tridecanal [10486-19-8]; 2.1.3.8 2-Methyldecanal [19009-56-4], Methyloctylacetaldehyde, Aldehyde MOA; 2.1.3.9 2-Methylundecanal [110-41-8], Methylnonylacetaldehyde, Aldehyde MNA; 2.1.3.10 (E)-2-Hexenal [6728-26-3], Leaf Aldehyde; 2.1.3.11 (Z)-4-Heptenal [6728-31-0]; 2.1.3.12 2,6-Dimethyl-5-hepten-1-al [106-72-9]; 2.1.3.13 (E)-4-Decenal [65405-70-1] 2.1.3.14 10-Undecenal [112-45-8]2.1.3.15 2-Dodecenal [20407-84-5]; 2.1.3.16 2,6,10-Trimethyl-5,9-undecadienal [24048-13-3] and [54082-68-7]; 2.1.3.17 1,1-Dimethoxy-2,2,5-trimethyl-4-hexene [67674-46-8]; 2.1.4 Ketones; 2.1.4.1 3-Hydroxy-2-butanone [52217-02-4], Acetoin; 2.1.4.2 2,3-Butanedione [431-03-8], Diacetyl; 2.1.4.3 (2E)-5-Methyl-2-hepten-4-one [81925-81-7]; 2.1.4.4 3,4,5,6,6-Pentamethyl-3-hepten-2-one [81786-73-4]; 2.1.4.5 2,4,4,7-Tetramethyl-6-octen-3-one [74338-72-0]; 2.1.5 Acids and Esters; 2.1.5.1 2-Methyl-2-pentenoic Acid [3142-72-1]; 2.1.5.2 Ethyl Formate [109-94-4] 2.1.5.3 (Z)-3-Hexenyl Formate [33467-73-1]2.1.5.4 Ethyl Acetate [141-78-6]; 2.1.5.5 Butyl Acetate [123-86-4]; 2.1.5.6 Isoamyl Acetate [123-92-2]; 2.1.5.7 Hexyl Acetate [142-92-7]; 2.1.5.8 3,5,5-Trimethylhexyl Acetate [58430-94-7], Isononyl Acetate; 2.1.5.9 (E)-2-Hexenyl Acetate [2497-18-9]; 2.1.5.10 (Z)-3-Hexenyl Acetate [3681-71-8]; 2.1.5.11 Ethyl Propionate [105-37-3]; 2.1.5.12 Ethyl Butyrate [105-54-4]; 2.1.5.13 Butyl Butyrate [109-21-7]; 2.1.5.14 Isoamyl Butyrate [106-27-4]; 2.1.5.15 Hexyl Butyrate [2639-63-6]; 2.1.5.16 (Z)-3-Hexenyl Isobutyrate [41519-23-7] 2.1.5.17 Ethyl Isovalerate [108-64-5] |
| Record Nr. | UNINA-9910817155903321 |
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Surburg Horst
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| Weinheim, Germany : , : Wiley-VCH, , 2016 | ||
| Materiale a stampa | ||
| Lo trovi qui: Univ. Federico II | ||
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Development and optimization of phytosterols microencapsulation for the formulation of chocolate functional food [Tesi di dottorato] / student: Roberta Tolve ; coordinator: Marco Borghetti ; tutor: Fernanda Galgano ; co-tutors: Maria Carmela Caruso, Fabio Favati
| Development and optimization of phytosterols microencapsulation for the formulation of chocolate functional food [Tesi di dottorato] / student: Roberta Tolve ; coordinator: Marco Borghetti ; tutor: Fernanda Galgano ; co-tutors: Maria Carmela Caruso, Fabio Favati |
| Autore | Tolve, Roberta |
| Descrizione fisica | IX, 169 p. : ill. ; 30 cm. |
| Disciplina | 664.5 |
| Formato | Materiale a stampa |
| Livello bibliografico | Monografia |
| Lingua di pubblicazione | eng |
| Record Nr. | UNIBAS-000044758 |
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Tolve, Roberta
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| Materiale a stampa | ||
| Lo trovi qui: Univ. della Basilicata | ||
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