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Section: Fragrance > Ingredients

CSA Roundtable 2009 in May

The Chemical Sources Association’s next roundtable will be held on May 14 at the Sheraton Newark Airport Hotel, in Newark, New Jersey.

Symrise Achieves USDA Organic Certification

Move boosts sustainable fragrance strategy.

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Patent Pick: Nitrile Cumin Scent

Patent Picks are chosen by the editors from publicly available sources. Today's invention, from Kao Corp., relates to a nitrile compound that imparts a spicy, cumin odor.

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Patent Pick: Cyclopentanols for Fragrance

Patent Picks are chosen by the editors from publicly available sources. Today's technology relates to cyclopentanols to enhance fragrance in perfume, cologne, fabric care and other applications.

Honeysuckle in Perfumery and Cosmetics

Honeysuckle belongs to the family of floral odors like lilac and lily of the valley for which there are no natural materials available and are considered important in perfumery. In the past honeysuckle absolute produced commercially in small quantities was used in deluxe fragrances. The advent of aromatic chemicals enabled the perfumer to develop synthetic compounds, which are now used in perfumery.

The Composition of Bergamot Oil

In this paper, we report the results relative to the composition of the volatile fraction of 1,082 samples of bergamot oil produced between 1984 and 1993.

Amber Perfumes, Compounds and Specialties

This article will discuss the development and applications of amber perfumes, synthetic amber compounds and specialties.

New Aroma Chemicals: Thujone Alternatives

This article will examine the uses of thujone and thujonecontaining materials in perfumery, and describe some synthetic materials — old and new— that are intended to provide this note.

New Aroma Chemicals: Thujone Alternatives

Perfumers often use the descriptor “thujone” to describe a particular note in fragrances. However, the odor of thujone itself seems to be inseparable from the character of the essential oils in which it is found. This article will examine the uses of thujone and thujone containing materials in perfumery, and describe some synthetic materials — old and new— that are intended to provide this note.

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Editor's Note: A Natural Conversation

As the muse of F&F, naturals are the headliner on the product label. In the last issue, we explored the safety, sustainability and efficiency of synthetics. This issue features creativity in research and application inspired by naturals.

China: important raw material producer?

These changes and China’s new awareness of the outside are very important in considering my topic: “China: important raw material producer?” Before examining how this specifically refers to essential oils and aroma chemicals, we must go back to economics and understand what has happened in China and what will happen in the future.

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Are Your Products REACH Compliant?

With the May 2018 deadline for REACH compliance quickly approaching is your business ready for the changes?

This development allows Treatt to conduct business, hire local employees and generate revenue without a subsidiary company in China.

Treatt Establishes WOFE in China

This development allows Treatt to conduct business, hire local employees and generate revenue without a subsidiary company in China.

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Iberchem to offer COSMOS Fragrances

Iberchem will now offer COSMOS fragrances certified by Ecocert as part of their commitment to reducing their ecological footprint

With this designation, officials at Agrumaria Reggina stated that these values are embedded in the company’s corporate statute.

Agrumaria Reggina Becomes Benefit Corporation

The designation highlights the company's commitment to social and environmental values.

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Mamta Polycoats' Triethyl Citrate, Natural

Triethyl Citrate ≥ 99.5 %, FDA (FEMA# 3083, CAS# 77-93-0) is a modified natural organic ingredient having 100% renewable carbon source.

Delbia Do's Clean Fragrance Formulation

Delbia Do's Clean Fragrance Formulation

Synthetic Routes to Carvone

Methods leading to (–)-, (+)-, and (±)-carvone have been reviewed, The technical production of (–)-carvone is based on the widely available (+)-limonene; the most favored route is that epitomized in Chart 1. Though the steps involved are simple, their exploitation is a wellguarded secret, There is no similar commercialscale production of (+)-carvone because the basic materials for its synthesis are not as readily available. However, sooner or later the rising demand for this ketone will ensure that it, too, will be produced synthetically.

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