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Is Isoeugenol polar?

Is Isoeugenol polar?

Isoeugenol is a commonly used fragrance added to many commercially available products, and occurs naturally in the essential oils of plants such as ylang-ylang….3.1Computed Properties.

Property Name Property Value Reference
Topological Polar Surface Area 29.5 Ų Computed by Cactvs 3.4.8.18 (PubChem release 2021.05.07)

How are the properties of eugenol and Isoeugenol different?

The key difference between eugenol and isoeugenol is that eugenol has a clove-like odour, whereas isoeugenol has a floral odour. In addition, eugenol is a pale yellow color liquid whereas the trans isomer of isoeugenol is a crystalline substance while its cis isomer is an oily liquid.

Is linalool polar or nonpolar?

nonpolar
Geraniol and linalool molecules are primarily nonpolar.

What is Isoeugenol used for?

Isoeugenol is approved by the FDA for use within allergenic epicutaneous patch tests which are indicated for use as an aid in the diagnosis of allergic contact dermatitis (ACD) in persons 6 years of age and older. Build, train, & validate predictive machine-learning models with structured datasets.

What is Isoeugenol found in?

Where is Isoeugenol found? Isoeugenol is used in manufacturing perfumes, flavorings, essential oils (Clove, spicy, sweet, woody) and in medicine (local antiseptic and analgesic) as well as vanillin.

What is the molecular formula of Isoeugenol?

C10H12O2Isoeugenol / Formula

What does Isoeugenol smell like?

Isoeugenol is a substance added to fragrances to give them that unique sweet-yet-spicy scent. While it can be created in a lab, isoeugenol can also be found in essential oils, such as ylang-ylang. It is used by Fragrance Creators to make vanillin in a lab.

Is linalool soluble in water?

Linalool is a colorless liquid, relatively soluble in water (1590 mg L−1 at 25 ◦C) and highly soluble in different organic solvents. This tertiary terpene alcohol has a chiral center at C3 carbon, thus appearing two enantiomeric forms in nature: (+)-Linalool and (−)-linalool [18].

Is linalool banned in EU?

Warning! According to the harmonised classification and labelling (ATP10) approved by the European Union, this substance may cause an allergic skin reaction.

Is Isoeugenol harmful?

Conclusion: The use of isoeugenol at current levels in household cleaning products does not raise any safety concerns with regard to its potential to induce allergic contact dermatitis and adverse systemic effects.

Is Isoeugenol toxic?

Isoeugenol has moderate acute toxicity based on results from animal tests following dermal exposure.

Is borneol soluble in water?

Borneol appears as a white colored lump-solid with a sharp camphor-like odor. Burns readily. Slightly denser than water and insoluble in water.

What is the melting and boiling point of isoeugenol?

The melting point of isoeugenol is 33°C (91.0°F) (trans). The boiling point has been reported to be 133.0°C (271.4°F) (cis) and 140.0°C (284.0°F) (trans). Isoeugenol is slightly soluble in water. Production/Uses/Exposure: Isoeugenol is produced by various companies throughout the United States and Europe.

What is isoeugenol?

Isoeugenol is is a clear to pale yellow oily liquid extracted from certain essential oils especially from clove oil and cinnamon. It is very slightly soluble in water and soluble in organic solvents. It has a spicy odor and taste of clove. Isoeugenol is prepared from eugenol by heating.

How is the toxicity of isoeugenol determined?

The toxicity was determined by comparing the norepinephrine-induced oxygen consumption, after addition of isoeugenol, to that of the control and expressing the ratio as a percentage. Isoeugenol was found to strongly inhibit oxidative metabolism (See A

What is the isoeugenol CAS number 97-54-1?

EXECUTIVE SUMMARY OF SAFETY AND TOXICITY INFORMATION ISOEUGENOL CAS Number 97-54-1 April 10, 1991 Submitted to: NATIONAL TOXICOLOGY PROGRAM Submitted by: Arthur D. Little, Inc. Board of Scientific Counselors Draft Report TABLE OF CONTENTS I. NOMINATION HISTORY AND REVIEW II. CHEMICAL AND PHYSICAL DATA III.