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1-Hexadecanone, 1-(3-methylphenyl)-, also known as 1-(3-methylphenyl)hexadecan-1-one, is an organic compound with the molecular formula C23H38O. It is a derivative of hexadecanone, featuring a 3-methylphenyl group attached to the first carbon atom. 1-Hexadecanone, 1-(3-methylphenyl)- is a colorless to pale yellow liquid with a mild, floral odor. It is used in the fragrance industry as a fixative and in the synthesis of various perfumes and flavorings. Due to its relatively high molecular weight and lipophilic nature, 1-hexadecanone, 1-(3-methylphenyl)- is known for its ability to provide long-lasting scents and enhance the stability of fragrances.

5775-30-4

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5775-30-4 Usage

Chemical Structure

A ketone consisting of a hexadecyl group attached to a carbonyl group at the first carbon position and a 3-methylphenyl group attached at the 1-position.

Usage

Flavor and fragrance ingredient in consumer products such as perfumes, soaps, and cosmetics.

Aroma

Strong, sweet, floral with fruity and woody undertones.

Antimicrobial Properties

Exhibits antimicrobial activity, useful in pest control and preservation applications.

Insecticidal Properties

Demonstrates insecticidal properties, making it valuable in pest control.

Applications

Enhances the scent of personal care and household products.

Check Digit Verification of cas no

The CAS Registry Mumber 5775-30-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,7 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 5775-30:
(6*5)+(5*7)+(4*7)+(3*5)+(2*3)+(1*0)=114
114 % 10 = 4
So 5775-30-4 is a valid CAS Registry Number.

5775-30-4Downstream Products

5775-30-4Relevant academic research and scientific papers

Catalytic Decarboxylative Cross-Ketonisation of Aryl- and Alkylcarboxylic Acids using Magnetite Nanoparticles

Goossen, Lukas J.,Mamone, Patrizia,Oppel, Christoph

supporting information; experimental part, p. 57 - 63 (2011/03/22)

In the presence of catalytic amounts of magnetite nanopowder, mixtures of aromatic and aliphatic carboxylic acids are converted selectively into the corresponding aryl alkyl ketones. As by-products, only carbon dioxide and water are released. This catalytic cross-ketonisation allows the regioselective acylation of aromatic systems and, thus, represents a sustainable alternative to Friedel-Crafts acylations.

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