Aurantiol

СинтетичнийКВІТИквітковий · цвіт апельсина
Ноти серця·Базові нотиПіраміда
4/5Сила
—Стійкість
—Походження
Зразок
Aurantiol як парфумерна сировина
Від нот серця до базових нот
Визначення

Aurantiol is the Schiff base of hydroxycitronellal and methyl anthranilate. It has an orange blossom and neroli character.

КВІТКОВИЙ СОЛОДКИЙ ПУДРОВИЙ БАЛЬЗАМІЧНИЙ ФРУКТОВИЙ
Hydroxycitronellal methyl anthranilate, Aurantium, Aurantine, Aurantion, Auralva, Hydroxycitronellylidene methyl anthranilate
Type
Складник
Olfactive family
Квіткові
Source
Synthetic
Chemical class
Schiff base
Інструменти
Піраміда
ВВерхні ноти
СНоти серця
ББазові ноти
4/5Сила
Висока
інтенсивність запаху

Запах

The odour is floral, of orange blossom, slightly sweet, powdery and faintly balsamic. The aroma is reminiscent of orange blossom absolute, with soft fruity-floral nuances and balsamic undertones. It has a powerful floral-orange blossom aroma.

Докладно

Aurantiol has the IUPAC name methyl 2-[(7-hydroxy-3,7-dimethyloctylidene)amino]benzoate. Methyl anthranilate is one of the two amines most commonly used to form Schiff bases in the fragrance industry, the other being ethyl anthranilate.

A Schiff base is a compound with the general structure R1R2C=NR3, in which R3 is an alkyl or aryl group but not hydrogen. Schiff bases can be considered a sub-class of imines.

Schiff bases of methyl anthranilate are typically yellow-to-orange, viscous liquids that are more stable than their parent aldehydes and have greater tenacity on skin, though they darken over time. Formation of a Schiff base is reversible, and the compound can be readily hydrolyzed back to its starting materials in aqueous environments, mainly in acidic conditions. In water-ethanol solutions the hydrolysis is very slow, while it is very fast when an acid is added, as it is complete within 24 hours.

Other Schiff bases of methyl anthranilate are known. Verdantiol, formed with Lilial, has a linden blossom character with orange blossom undertones. Lyrame, formed with the aldehyde Lyral, has a fresh lily-of-the-valley character with notes of orange blossom.

Explore all seven extraits in the Discovery Set.

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Related: Accord Eudora · African Marigold · Alpha Amylcinnamaldehyde · Alyssum · Angels Trumpet · Aquaflora · Ashoka Flower · Azalea

Цікавий факт

Schiff bases are named after the chemist Hugo Schiff, who discovered them. The reaction between methyl anthranilate and an aldehyde continues even after a perfume has been bottled, so older samples may show Schiff bases that were not present when the fragrance was originally formulated.

Отримання й хімія

Спосіб отримання

When methyl anthranilate reacts with an aldehyde, water is released and a single, heavier compound is formed. Schiff bases can be synthesized from odorant aldehydes and primary amines through a condensation reaction. The Schiff base of hydroxycitronellal and methyl anthranilate can be prepared by direct condensation of the neat liquid reagents at 110 °C, without solvents or dehydrating agents. Of four methyl anthranilate Schiff bases made in one study, three gave their best yield with a 2:1 excess of the aldehyde, and one with a 2:1 excess of methyl anthranilate. Perfumers can also add methyl anthranilate as a separate ingredient alongside an aldehyde such as hydroxycitronellal, so that the Schiff base forms gradually inside the finished compound over weeks or months, in a process known as maceration.

Формула
C₁₈H₂₇NO₃
CAS
89-43-0
Зовнішній вигляд
Pale yellow to amber viscous liquid
Сила запаху
Висока
Синоніми
Hydroxycitronellal methyl anthranilate, Aurantium, Aurantine, Aurantion, Auralva, Hydroxycitronellylidene methyl anthranilate
Статус IFRA
Див. примітку

No IFRA Standard for the material itself (51st Amendment)

У парфумерії

Aurantiol is used extensively in a large variety of floral notes, such as orange-blossom, linden-blossom and tuberose. Schiff bases of methyl anthranilate with four aldehydes, hydroxycitronellal among them, may be applied as profragrances, which release the aldehyde and methyl anthranilate on hydrolysis.

Роль у формулі
01модифікатор
02сполучний компонент
03формувач об’єму
Форми випуску
синтетична речовина

Див. також

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