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29 Results
Regulatory & Research
EFSA: Citrus Flavor Perilla Aldehyde is Unsafe, Genotoxic
Perilla aldehyde, a flavor used in baked goods and more that has woody, spicy, citrus taste characteristics, has been shown to be genotoxic in a new study on animals [includes video] according to EFSA.
Regulatory & Research
Patent Pick: Aldehyde as Perfume
Patent Picks are chosen by the editors from publicly available sources. Today's patent, from Firmenich, explores the use of aldehyde as a perfuming agent to evoke cardamom or lily of the valley notes.
March
Natural Advantage's Hexyl cinnamic aldehyde
Regulatory & Research
Patent Pick: Carotenoid Enzyme-produced Aldehydes, Flavors
Patent Picks are chosen by the editors from publicly available sources. Today's highlight is a method for catalyzing the synthesis of aldehydes and flavor additives using isolated carotenoid cleavage dioxygenase enzymes derived from natural plants.
Regulatory & Research
Regulatory Watch: EFSA Opinion on Perilla Aldehyde
This article highlights the international evaluation of perilla aldehyde.
Regulatory & Research
European Commission Orders to Remove Perilla Aldehyde Flavoring
The European Commission has determined p-mentha-1,8-dien-7-al, also known as perilla aldehyde, does not comply with the general conditions of use for flavorings and should be removed from its list of approved flavorings.
Regulatory & Research
IFRA to Prohibit 2,4-Double Conjugated alpha, beta Unsaturated Aldehydes
The International Fragrance Association (IFRA) is expected to prohibit the use of 2,4-hexadienal (CAS# 80466-34-8) and other 2,4-double conjugated alpha, beta unsaturated aldehydes as part of the 44th Amendment to the IFRA Code of Practice.
Regulatory & Research
IOFI Dissents EFSA Opinion on Perilla Aldehyde's Genotoxity
After the European Food Safety Authority (EFSA) issued an opinion citing citrusy flavor Perilla aldehyde as a genotoxic concern, The International Organization of the Flavor Industry (IOFI) said it "respectfully disagrees."
Ingredients
Kesom Oil—A Natural Source of Aliphatic Aldehydes
The recent investigation of the plant habitats and the chemical analysis of the essential oils obtained from the leaves and stems provided some new findings that could prove highly useful to the flavour and fragrance industry. In this report the habitats of Polygonum minus Huds. and the chemical composition of leaf and stem oils are presented, and the possible relevance of Kesom oil as a new product is discussed.
Regulatory & Research
Research article: Biotransformation of Unsaturated Aliphatic Aldehydes Using Baker’s Yeast
Actively fermenting baker’s yeast (
Saccharomyces cerevisiae
) not only converts aliphatic aldehydes to the corresponding alcohols, but also may reduce certain carbon-carbon double bonds in the same molecule. Furthermore, an in situ acyloin condensation reaction occurs; this bioconversion reaction gives rise to relatively good yields of unsaturated 2,3-diols, which have two carbon atoms more than the corresponding aliphatic aldehyde used as substrate. Baker’s yeast has been used as a reagent in organic synthesis since the beginning of the 20th century, when fundamental studies were initiated on the mechanism of formation of fusel alcohols from the corresponding l-amino acids during the formation of ethanol.
Beverage
Sweet and Fruity With Natural Advantage's Hexyl Cinnamic Aldehyde
This ingredient provides a fresh jasmine and gardenia odor and can be described as sweet, fruity, floral, citrus, green and smooth.
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