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Flavouring

CioHi O. White leaflets, with a strong smell and sweet taste, m.p. 22 C, b.p. 235 C. The chief constituent of anise and fennel oils and other essential oils, from which it is manufactured. It can also be prepared from anisole (meihoxybenzene). It is widely used for flavouring pharmaceuticals and dentifrices, and in perfumery. [Pg.34]

CH3 CH0H CH20H, a colourless, almost odourless liquid. It has a sweet taste, but is more acrid than ethylene glycol b.p. 187. Manufactured by heating propylene chlorohydrin with a solution of NaHCO under pressure. It closely resembles dihydroxyethane in its properties, but is less toxic. Forms mono-and di-esters and ethers. Used as an anti-freeze and in the preparation of perfumes and flavouring extracts, as a solvent and in... [Pg.139]

MSG, C8H8NNa04,H20. Flavouring agent extensively used as a food additive. Prepared from natural or synthetic L-glutamic acid. [Pg.364]

CaH803. Fine white needles, m.p. 82°C, b.p. 285°C, strong vanilla odour, characteristic taste. It occurs extensively in nature, and is the odoriferous principle of the vanilla pod it can be obtained from the glucoside coniferin. Vanillin is made commercially from the ligno-sulphonic acid obtained as a by-product in the manufacture of wood pulp. It is one of the most important flavouring and perfuming... [Pg.417]

An informative second-level text with a practical flavour. [Pg.1465]

We will obtain a flavour of tire nonlinear phenomena by exploring tire processes generated via tire matter-field... [Pg.2864]

There are a number of different ways that the molecular graph can be conununicated between the computer and the end-user. One common representation is the connection table, of which there are various flavours, but most provide information about the atoms present in the molecule and their connectivity. The most basic connection tables simply indicate the atomic number of each atom and which atoms form each bond others may include information about the atom hybridisation state and the bond order. Hydrogens may be included or they may be imphed. In addition, information about the atomic coordinates (for the standard two-dimensional chemical drawing or for the three-dimensional conformation) can be included. The connection table for acetic acid in one of the most popular formats, the Molecular Design mol format [Dalby et al. 1992], is shown in Figure 12.3. [Pg.659]

Review Problem 2 This allyl bromide is an important intermediate in the synthesis of terpenes (including many flavouring and perfumery compounds), as the five carbon fi agment occurs widely in nature. How would you make it ... [Pg.12]

We made this important intermediate (A) in a slightly different way (frame 318), but this is how it s made industrially for use in perfumes and flavours (Pure. Annl. Chem.. 1975, 43, 527). How would you extend this synthesis to make TM 324 ... [Pg.106]

Strategy Problem 7 Synthesis of a single enantiomer. Many compounds such as pharmaceuticals, flavourings, and insect control chemicals must not only have the right relative stereochemistry but must be optically active too if tliey are to be of any use. Consider the strategy of synthesising one enantiomer ... [Pg.134]

G. H. Reazin, in J. R. Piggott, ed.. Flavour of Distilled Beverages Origin and Development, Vedag Chemie International, Deerfield Beach, Fla., 1983, p. 225. [Pg.90]

The oceurrence of a large number of pyrazines as flavouring or aroma eonstituents and as pheromones in extremely low coneentrations has led to mass spectrometry being the method of ehoiee for determining the gross struetural details of a pyrazine nueleus. The method appears to be generally applieable and relatively specifie and sensitive. [Pg.162]


See other pages where Flavouring is mentioned: [Pg.32]    [Pg.33]    [Pg.71]    [Pg.71]    [Pg.100]    [Pg.156]    [Pg.163]    [Pg.180]    [Pg.191]    [Pg.261]    [Pg.286]    [Pg.304]    [Pg.419]    [Pg.1500]    [Pg.1957]    [Pg.2714]    [Pg.2844]    [Pg.2853]    [Pg.94]    [Pg.440]    [Pg.501]    [Pg.7]    [Pg.7]    [Pg.20]    [Pg.20]    [Pg.575]    [Pg.576]    [Pg.437]    [Pg.341]    [Pg.158]    [Pg.160]    [Pg.627]    [Pg.702]    [Pg.365]    [Pg.365]    [Pg.376]    [Pg.22]    [Pg.41]   
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8-Resin Resinous flavours

Absolute flavourings

Acetaldehyde flavour

Acetic flavour

Acidic flavour

Active flavours

Alcoholic flavour

Aliphatic flavour compounds

Alkaline flavour

Apple flavour compounds

Application of Flavourings

Aroma flavour precursors

Artificial flavouring agents

Artificial flavouring substance

Artificial flavourings

As flavouring agents

Astringent flavours

Banana flavour

Base Notes Flavour Body and Taste Enhancement

Biotechnological natural flavours

Bitter flavour

Blue cheese flavour

Blueberry flavour

Bread flavour

Broccoli flavour

Burnt flavours

Butterscotch flavour

Buttery flavour

Butyric flavour

Cabbage flavour compounds

Caprylic flavour

Caramel flavoured compounds

Caramel flavours

Carbonation flavours

Cardboard flavour

Carrots flavour

Cereal flavours

Characteristics of Microbial Flavour Production

Cheddar cheese flavour

Cheese flavour

Cheese flavour amines

Cheese flavour amino acids

Cheese flavour organic acids

Cheese flavour peptides

Cheesy flavours

Chemical Senses and Flavour

Chemically Defined Flavouring Substances

Citrus flavours

Colouring and Flavouring

Commission Proposal flavouring preparation

Concrete flavours

Cooked vegetable flavours

Coumarins flavours

Council proposal flavouring preparation

Cucumber flavour

Current Flavouring Directive

Definitions flavouring preparations

Definitions flavourings

Definitions natural flavouring substances

Definitions nature-identical flavouring

Definitions other flavourings

Definitions process flavourings

Detection of heavy flavours

Developments in Flavours

Diacetyl flavour

Dimethyl sulphide flavour

Dry Flavours

EU Flavour Directive

Elderberry flavour

Emulsifiers, Colours and Flavours

Enantioselective and Isotope Analysis—Key Steps to flavour Authentication

Enzyme-derived flavours from lipids

Enzymes and Flavour Biotechnology

Esters flavour compounds

Estery flavours

Ethyl acetate flavour

Ethyl hexanoate flavour

European Flavour Industry

European Flavour and Fragrance

European Flavour and Fragrance Association

European Union flavourings

Examples of Flavour Chemicals Derived from Sugars

Extraction of Flavourings

Extracts, flavouring, liquid

Fantasy Flavourings

Fatty acids flavours

Flavour

Flavour

Flavour / flavouring compounds analysis

Flavour / flavouring compounds enhancement

Flavour / flavouring compounds grapes

Flavour / flavouring compounds thresholds

Flavour / flavouring compounds volatiles

Flavour Fragrance Industry

Flavour Fragrance Market

Flavour Generation by Fermentation of Food Raw Materials

Flavour Generation in Bioreactors

Flavour Production

Flavour Release Food Texture, Composition and Physiological Effects

Flavour Release and Perception

Flavour World

Flavour additive

Flavour adjunct

Flavour aldehydes

Flavour analysis

Flavour and Extract Manufacturers

Flavour and aroma

Flavour and aroma profiles

Flavour and fragrance

Flavour and fragrance companies

Flavour and fragrance market

Flavour binding and release

Flavour change

Flavour chemical

Flavour classification of hadrons

Flavour coffee

Flavour compounds

Flavour compounds, defined

Flavour creation

Flavour definition

Flavour deterioration

Flavour dilution factor

Flavour enhancers

Flavour esters

Flavour esters, synthesis

Flavour extracts

Flavour format

Flavour formulated

Flavour fruit

Flavour industry

Flavour ingredients

Flavour instability

Flavour interaction

Flavour intrinsic

Flavour legislation

Flavour manufacturers

Flavour market

Flavour mass spectrometry

Flavour materials

Flavour microemulsions

Flavour microencapsulation

Flavour microencapsulation spray drying

Flavour migration

Flavour modifier

Flavour of Spirit Drinks Raw Materials, Fermentation, Distillation, and Ageing

Flavour of meat

Flavour oils

Flavour perception deconstruction

Flavour perception description

Flavour potentiator

Flavour precursors

Flavour preference

Flavour profile

Flavour pyramid

Flavour quality

Flavour reference compounds

Flavour release

Flavour releasers

Flavour research

Flavour stability

Flavour stimulants

Flavour substance

Flavour sulfur compounds

Flavour symmetry

Flavour units

Flavour vegetable

Flavour volatile compounds

Flavour-Impact Compounds

Flavour-Isolation Techniques

Flavour-modifying

Flavouring Components for Dairy Products

Flavouring Composition

Flavouring Directive

Flavouring Ingredients

Flavouring Preparations and Some Source Materials

Flavouring Production

Flavouring Raw Materials

Flavouring Stability

Flavouring agents

Flavouring essence

Flavouring extracts

Flavouring extracts, essential oils

Flavouring legislation

Flavouring liquids

Flavouring mixtures

Flavouring preparations

Flavouring substance

Flavouring terpenoid

Flavouring, synthetic

Flavourings alcoholic

Flavourings and legislation

Flavourings commercially available

Flavourings continued

Flavourings dairy

Flavourings fermented

Flavourings for Confectioneries, Baked Goods, Ice-cream and Dairy Products

Flavourings for Fine Bakery Products

Flavourings for beverages

Flavourings for confectioneries

Flavourings for dairy products

Flavourings for ice-cream

Flavourings inventory

Flavourings natural

Flavourings natural-identical

Flavourings process

Flavourings smoke

Flavourings vegetable

Flavourings: application

Flavourings: nature identical

Flavourings: water dispersible

Flavours and flavourings

Flavours and fragrances, extraction

Flavours antioxidants

Flavours chocolate

Flavours developments

Flavours intensity

Flavours perception

Flavours toffee

Flavours, extraction

Flavours, food

Flavours/flavouring compounds

Floral flavour

Foodstuffs flavourings

Fragrances and flavours industry

Fruity flavours

Furonol, meat flavour

Future Flavouring Regulation

Geraniol flavour/aroma

Glycosidic / glycosidically bound flavour compounds

Glycosidic / glycosidically flavour precursors, grapes

Glycosidic / glycosidically precursors, flavour compounds, grapes

Glycosidically bound flavouring substance

Grape bound flavour compounds

Grape flavouring compounds

Grapefruit, flavour

Grassy flavours

Green flavour complexes

Grill flavours

Heat-induced changes in flavour of milk

Heavy flavour lifetimes

Heavy flavour masses

Heavy flavours

Heavy flavours at LEP

Heavy flavours production

Heterocyclic Flavour Molecules

Hidden flavour bound states

Hoppy flavours

Hydrogen sulphide flavour

Impact of bacteria on beer appearance and flavour

Impact of yeast on beer flavour

Important Flavour Compounds from Raw Materials

Industrial Process Flavourings

International Organization of the Flavour

International Organization of the Flavour Industry

Isoamyl acetate flavour

Isolating flavouring materials

Isolation of Flavour from Plant Materials for Commercial Use

Isolation of Flavouring Materials from Waste Streams

Isolation of flavouring materials

Isovaleric flavours

Juice flavour

Lager flavour

Leathery flavours

Licorice flavour

Light-activated flavour

Lipid oxidation flavour

Liquid Flavours

Liquorice flavour

Maltol, flavouring

Malty flavours

Masking flavours

Meat flavour

Meaty flavour

Melanoidins flavours

Mercaptans flavour

Metallic flavour

Microbial Flavour Production

Middle Notes Process and Reaction Flavours

Mixed powder flavour

Molasses flavour

Mouldy flavours

Mouthfeel flavours

Multidimensional Chromatography Foods, Flavours and Fragrances Applications

Mushroom flavours

Natural flavour concentrate

Natural flavouring agents

Natural flavouring substance

Natural flavours

Natural meat flavours

Nature identical flavours

Nature-identical flavouring substance

Non-flavouring Ingredients

Non-volatile flavour compounds

Nutty flavours

Off-flavour production

Off-flavours

Oily flavours

Onion flavour

Open heavy flavours

Oral liquids flavour

Other Blended Flavourings

Other Flavour Modifiers

Other Rules Concerning Flavourings

Other regulated substance, aromatic extract or flavouring

Oxidized flavours

Panel on Food Contact Materials, Enzymes Flavourings and Processing Aids

Parsley flavour

Phenolic flavours

Phenols flavour

Phenols flavour compounds

Piquant flavour

Plastic flavour

Potato flavour

Primings flavour

Process Flavour Chemistry

Process flavours

Processed Flavourings

Production of Flavoured Dairy Products

Production of Flavours for Alcoholic Beverages

Production of heavy flavours

Pumpkin flavour

Pyrazines flavour

Pyrazines, food flavour

Quantitative flavour profiling

Rancid flavours

Raw Materials for Flavourings

Reaction flavours

Roquefort flavour

Safety evaluations of flavouring substance

Salt flavour

Savoury flavour

Savoury process flavourings

Sensorially Interesting Fruit Flavours

Soapy flavours

Soft flavour compounds

Solvent-like flavours

Sour flavour compounds

Sour flavours

Strawberry flavour

Subject flavour

Subject flavour compounds

Sulphidic flavours

Sulphitic flavours

Sulphury flavours

Sunlight oxidized flavour

Sunstruck flavour

Sweet flavour

Synthetic flavours

Technological Flavour Products

Terpenes flavour

The Roots of Flavour Work

The Specifics of Flavour Application

Theoretical estimates of heavy flavour production

Tobacco flavour

Tobacco flavouring

Tomato flavour

Tropical Fruit Flavour

Untypical ageing flavour

Use of Flavour Systems at the Consumer Level

Vanilla Flavourings

Vanilla flavour

Warmed-over flavour

Warming flavour

World of Commercially Important Fruit Flavours

Worty flavours

Yeasty flavours

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