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3-Hexadecanone, a chemical compound with the molecular formula C16H32O, is a saturated ketone derived from hexadecanoic acid. It is characterized by its fruity and fatty odor and is commonly found in various essential oils. Due to its unique scent and potential health benefits, 3-Hexadecanone has a wide range of applications in different industries.

18787-64-9

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18787-64-9 Usage

Uses

Used in Fragrance and Flavor Industries:
3-Hexadecanone is used as a fragrance ingredient for its characteristic fruity and fatty odor, making it popular in the creation of various scents.
Used in Food Products:
3-Hexadecanone is used as a flavoring agent in food products, enhancing the taste and aroma of various dishes.
Used in Cosmetic and Personal Care Products:
3-Hexadecanone is used as a component in cosmetic and personal care products, contributing to their scent and potentially providing antimicrobial and anti-inflammatory effects.
Used in Therapeutic Applications:
3-Hexadecanone has been studied for its potential therapeutic properties, including its antimicrobial and anti-inflammatory effects, making it a candidate for use in various health and wellness applications.

Check Digit Verification of cas no

The CAS Registry Mumber 18787-64-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,8 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18787-64:
(7*1)+(6*8)+(5*7)+(4*8)+(3*7)+(2*6)+(1*4)=159
159 % 10 = 9
So 18787-64-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H32O/c1-3-5-6-7-8-9-10-11-12-13-14-15-16(17)4-2/h3-15H2,1-2H3

18787-64-9 Well-known Company Product Price

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  • Alfa Aesar

  • (L05098)  3-Hexadecanone, 95%   

  • 18787-64-9

  • 5g

  • 313.0CNY

  • Detail
  • Alfa Aesar

  • (L05098)  3-Hexadecanone, 95%   

  • 18787-64-9

  • 25g

  • 1259.0CNY

  • Detail

18787-64-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name hexadecan-3-one

1.2 Other means of identification

Product number -
Other names Ethyl tridecyl ketone

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:18787-64-9 SDS

18787-64-9Relevant academic research and scientific papers

Organoruthenium-supported polyoxotungstate - Synthesis, structure and oxidation of n-hexadecane with air

Meng, Rui-Qi,Wang, Bin,Sui, Hui-Min,Li, Bao,Song, Wei,Wu, Li-Xin,Zhao, Bing,Bi, Li-Hua

, p. 1935 - 1942 (2013/05/23)

A ruthenium complex, KNa[Ru2(C6H6) 2(CH3COO)6] (Ru-KNa), and its polyoxotungstate derivative, Na6[{Ru(C6H6)}2W 8O28(OH)2]·16H2O (Ru-Na), have been successfully isolated from routine synthetic reactions and characterized by X-ray single-crystal structure analysis, IR spectroscopy and elemental analysis. A remarkable aspect of Ru-KNa is that it has two ligand types, benzene and acetate, and the acetate ligands are connected exclusively by a central Na cation to form a dimeric sandwich-type structure, which is further connected by K cations to construct the 3D structures. Based on complex Ru-KNa, the compound Ru-Na was synthesized, and it consists of two {Ru(C 6H6)} units linked to a [W8O 28(OH)2]10- fragment by three Ru-O(W) bonds to result in an assembly with idealized C2 symmetry in which the polyanions form 3D structures by the connection of Na chains. Subsequently, the compound Ru-Na was anchored on (3-aminopropyl)triethoxysilane (apts) modified SBA-15 to prepare the solid catalysts, which were characterized by powder XRD, N2 adsorption measurements and FTIR spectroscopy. Finally, the catalytic efficiency of Ru-Na was assessed in the oxidation of n-hexadecane with air without any additives and solvents. The results indicated that Ru-Na is a heterogeneous catalyst and exhibits higher catalytic activity than previously reported Ru-containing polyoxotungstates. Copyright

A new vanadium(IV)-bridged polyoxotungstate containing mixed valence-antimony(III,V)

Wang, Bin,Xu, Ling-Xiao,Meng, Rui-Qi,Suo, Lin,Li, Bao,Wu, Li-Xin,Bi, Li-Hua

, p. 274 - 278 (2013/10/22)

A new mixed-valence SbV/III containing vanadium-substituted polyoxotungstate Na10[{SbV(OH)3} 2{VIV-O(H2O)}2{Sb IIIW9O33}2]·32H2O (1-Na) has been synthesized by routine synthetic reaction and characterized by IR, XPS, elemental analysis. The polyoxoanion [{SbV(OH)3}2{V IVO(H2O)}2{SbIIIW9O33}2]10 (1) consists of two trilacunary species β-B-SbIIIW9O 33 connected by two VIVO(H2O) groups and two SbV(OH)3 units. The cyclic voltammetry and catalytic activity of 1-Na for the oxidation of n-hexadecane under green condition have been measured.

Nanosized gold-catalyzed selective oxidation of alkyl-substituted benzenes and n-alkanes

Biradar, Ankush V.,Asefa, Tewodros

scheme or table, p. 19 - 26 (2012/10/08)

We report the synthesis of nanoporous silica-supported gold nanoparticle catalysts and their selective and efficient catalytic properties toward oxidation reactions of various substituted alkylbenzenes and linear alkanes. The Au nanoparticles were synthesized by reducing Au(III) ions in situ within the nanopores of hemiaminal-functionalized mesoporous silica by using the supported hemiaminal groups as reducing agents. The resulting mesoporous silica-supported gold nanoparticles efficiently catalyzed the oxidation reactions of different alkyl-substituted benzenes and linear alkanes with t-butyl hydroperoxide (TBHP) as an oxidant. The catalytic reactions gave up to ~99% reactant conversion and up to ~100% selectivity toward ketone products in some cases. This high selectivity toward ketone products by the catalysts was unprecedented, especially considering the fact that only mild reaction conditions and no additives were employed during the reactions.

Cycloalkanones. 8. Hypocholesterolemic activity of long chain ketones related to pentadecanone

Wyrick,Hall,Piantadosi,Fenske

, p. 219 - 222 (2007/10/12)

Aliphatic analogs of 2,8 dibenzylcyclooctanone which included C15-C18 ketones have been investigated for hypocholesterolemic activity in rats. The position of the carbonyl group in the chain for maximum activity appears to be the 2 position. 2 Hexadecanone reduced serum cholesterol levels significantly without altering serum triglyceride levels. This drug was not estrogenic at effective doses which is in contrast to the cyclooctanones which possess this activity.

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