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1,085 Results
Section: Fragrance
Regulatory & Research
Patent Pick: Clean, Floral 1-(2,4-Dimethyl-cyclohex-3-enyl)-propan-1-ol
Patent Picks are chosen by the editors from publicly available sources. Today's invention, from IFF, is a novel 1-(2,4-dimethyl-cyclohex-3-enyl)-propan-1-ol compound having clean, fresh and floral characteristics.
Ingredients
1-(2-Furfurylthio) Propanone
From Symrise, this material has a distinctly rich coffee odor.
Ingredients
6-Methoxy-2,6-Dimethylheptanal
Use in fragrance compositions
Ingredients
Methyl 2,4-dihydroxy-3,6-dimethylbenzoate
Chemistry and application in fragrance.
Fine Fragrance
Odor Properties of 1-(p-Alkyl)Phenylethanols and Their Esters
All the substances have, principally, similar odor characters, possessing fruity, flowery, woody, penetrant odor notes with minor rotten, moldy notes. Other characteristic notes were observed in some compounds. Odor thresholds show mostly medium values, suitable for application in perfumery products.
Ingredients
Fragrant Esters of 3-Cyclohexyl-1-propanol and 3-Cyclohexyl-1-butanol
Preparation and fragrance properties of some esters of 3-cyclohexyl-1-propanol and 3-cyclohexyl-1-butanol are described in this study. The compounds reported in this study possess interesting fragrant properties and may enrich the assortment of synthetic fragrant compounds used in perfumev industry
Ingredients
3,6-Dimethyl Octan-3-ol
A profile: 3,6-Dimethyl octan-3-ol. Thus is the history of 3,6-dimethyl octan-3-ol and its chemical evolution over forty years of changes in the flavor and fragrance industry. One wonders what might have been the fate of AR-1 if synthetic linalool had not been made available from the vitamin intermediate stream.
Fine Fragrance
1, 3, 6, 7, and 8
Three perfumers discuss their translations of couture into scent.
Ingredients
Hangzhou Grascent's Dimethyl heptanol
Fragrance
Submit Your Proposal to
WPC
2022
Get your speaker submission in before September 28, 2021 for your chance to present at
WPC
2022.
Ingredients
Eurofragance Closes 2020 with €78M Consolidated Sales
The company experienced healthy forecasts and higher than expected sales in the first half of 2021.
June
Hangzhou Grascent Co., Ltd's Dimethyl Heptanol
Trends
Global Aroma Ingredients to Reach $7.69B by 2028
Per the report, the global aroma ingredients market growth is driven by increased demand from the personal care industry.
Ingredients
Aroma Ingredients Market to Reach $7.69B by 2028
The demand for synthetic ingredients is increasing which is due to the low cost of synthetic ingredients, easy availability, and consistency of product quality.
Ingredients
MilliporeSigma's Phenyl Ethyl Dimethyl Carbinyl Isobutyrate, ≥97%, FG
Papaya isobutyrate is a subtle, sweet, fruity and nectar-like floral, with slight honey and green tropical fruit nuances. This ingredient’s succulent and slightly sweet mouth-feel works well in white grape, papaya, pineapple, mango, passion fruit, kiwi, lychee and rambutan flavors.
Ingredients
MilliporeSigma's Ethyl dimethyl dioxolane acetate, mixture of isomers, ≥97%, FG
This ingredient provides fruity and apple notes, which can be used in a range of flavor and fragrance formulations.
Ingredients
Synthesis and Odor Characteristics of New Gem-Dimethylcyclohexane Derivatives
Searching for cyclic analogs of the insect juvenile hormones, we synthesized a series of new compounds containing the cyclogeraniolene system. This system can be considered as a cyclic form of acyclic terpenes, such as dihydrocitronellol, dihydrogeraniol, and menthocitronellol. The isoprenoid chain in these compounds is rolled to form the cyclohexane ring by connection of the carbon atoms C-7 and C-10. As compared with the classical cyclic systems of the cyclogeraniol type, the compounds obtained by us contain the gem-dimethyl groups in the 3-position in relation to a chain with the functional group.
Ingredients
Cycloheptadecanone from Dimethyl Octadecanedioate via a One-Step Catalytic Process
Although the reaction was not studied, it does establish that a one-step conversion of the long chain diesters to the cyclic ketone containing one less carbon atom can occur. It opens the possibility to simpler processes for the preparation of macrocyclic ketones.
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