4727-17-7

Usage

Uses

Used in Detergent Production:
Cyclopentadecanol is used as a raw material in the production of detergents for its ability to enhance cleaning properties and improve the formulation's overall performance.
Used in Lubricant Manufacturing:
It serves as a component in lubricants, providing the necessary viscosity and reducing friction between moving parts.
Used as a Chemical Intermediate:
Cyclopentadecanol is utilized as an intermediate in the synthesis of other chemicals, contributing to the creation of a variety of compounds used across different industries.
Used in Cosmetics Industry:
In the cosmetics sector, Cyclopentadecanol is used as an ingredient for its emollient properties, helping to improve the texture and feel of cosmetic products.
Used in Pharmaceutical Development:
It has potential applications in the pharmaceutical industry, where it may be used in the development of new drugs or as a component in existing formulations.
Used in Surfactant Production:
Cyclopentadecanol is also used in the manufacturing of surfactants, which are essential in creating stable mixtures of otherwise immiscible substances, such as oil and water.
While Cyclopentadecanol is not considered highly toxic, it is important to note that prolonged exposure to high concentrations may cause irritation to the skin, eyes, and respiratory system.

InChI:InChI=1/C15H30O/c16-15-13-11-9-7-5-3-1-2-4-6-8-10-12-14-15/h15-16H,1-14H2

Upstream product

• 4727-18-8 2-hydroxycyclopentadecanone 
• 287-08-1 cis-1,2-epoxycyclopentadecane 
• 22591-33-9 acetic acid cyclopentadecyl ester 
• 502-72-7 cyclopentadecanone 
• 64-17-5 ethanol 
• 60-29-7 diethyl ether 
• 7732-18-5 water 
• 524-38-9 N-hydroxyphthalimide 
• 295-48-7 cyclopentadecane 
• 98348-19-7 2-Acetoxy-cyclopentadecanon-⁽¹⁾ 

Downstream Products

• 502-72-7 cyclopentadecanone 
• 6573-72-4 cyclopentadecene 
• 22591-33-9 acetic acid cyclopentadecyl ester 
• 1460-18-0 pentadecanedioic acid 
• 1259516-71-6 cyclopentadecyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 
• 1259516-70-5 cyclopentadecyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside 
• 14224-81-8 cyclopentadecanone 2,4-dinitrophenylhydrazone 
• 502-41-0 cycloheptanol 

Relevant academic research and scientific papers

Synthesis of α-Cyclooctyl- and α-Cyclopentadecylglycosides of N-Acetylmuramyl-L-Alanyl-D-Isoglutamine

N-Acetylmuramyl-L-alanyl-D-isoglutamine α-cyclooctyl- and α-cyclopentadecylglycosides were synthesized. The starting peracetylated α-N-glucosaminides were synthesized by reacting the cycloalkanols with peracetyl α-D-glucosaminyl chloride in the presence of Hg(II) iodide in CH3NO2 with heating or by using ZnCl2/tetrabutylammonium bromide in CH2Cl2 at room temperature. Sequential deacetylation, isopropyl protection, and alkylation by (S)-2-bromopropanoic acid gave α-cycloalkyl-4,6-O-isopropylidene-N-acetyl-D-muramic acids, condensation of which with the benzyl ester of L-Ala-D-iGln using the HOSu/DCC method and deprotection afforded the target glycopeptides.

Pincerlike molybdenum complex and preparation method thereof, catalytic composition and application thereof, and alcohol preparation method

The invention discloses a clamp-type molybdenum complex, a preparation method, a corresponding catalyst composition and application. The method comprises the steps: obtaining 9 molybdenum complexes with different structures through coordination reaction of 2-(substituent ethyl)-(5, 6, 7, 8-tetrahydroquinolyl) amine and a corresponding carbonyl molybdenum metal precursor; and catalyzing a ketone compound transfer hydrogenation reaction through a molybdenum complex to generate 40 alcohol compounds. The preparation method of the molybdenum complex is simple, high in yield and good in stability. For a transfer hydrogenation reaction of ketone, the molybdenum-based catalytic system has high catalytic activity and small molybdenum loading capacity, is used for production of aromatic and aliphatic alcohols, and has the advantages of simple method, small environmental pollution and high yield.

Efficient Transfer Hydrogenation of Ketones using Methanol as Liquid Organic Hydrogen Carrier

Herein, we demonstrate an efficient protocol for transfer hydrogenation of ketones using methanol as practical and useful liquid organic hydrogen carrier (LOHC) under Ir(III) catalysis. Various ketones, including electron-rich/electron-poor aromatic ketones, heteroaromatic and aliphatic ketones, have been efficiently reduced into their corresponding alcohols. Chemoselective reduction of ketones was established in the presence of various other reducible functional groups under mild conditions.

Synthesis of β-cycloalkylglycosides of Muramyl Dipeptide

β-Cyclooctyl-, β-cyclodecyl-, and β-cyclopentadecylglycosides of N-acetylmuramyl-L-alanyl-D-isoglutamine were prepared in yields of 39, 18, and 25%, respectively, (calculated for muramic acid) via the reaction of β-cycloalkyl-4,6-O-isopropylidene-N-acetyl-D-muramic acids with the benzyl ester of L-Ala-D-iGln using the HOSu/DCC method followed by deprotection.

CIRCULAR ECONOMY METHODS OF PREPARING UNSATURATED COMPOUNDS

Methods of preparing unsaturated compounds or analogs through dehydrogenation of corresponding saturated compounds and/or hydrogenation of aromatic compounds are disclosed.

Catalytic transfer hydrogenation of cycloalkanones on MgO. Vapour and liquid phase modes of reaction

The reactivity of a series of cycloalkanones of the general formula (CH2)nCO, where n = 4, 5, 6, 7, 11 and 14 in the transfer hydrogenation reaction over magnesium oxide as the catalyst, either in vapour or liquid phase (VP or LP) has been studied. In the VP mode of reaction the activity of MgO treated with triethylamine, water, phenol or benzoic acid in the reduction of cyclopentanone by propan-2-ol has been determined. A strongly diminished or residual activity of MgO has been observed after the catalyst's treatment with phenol or benzoic acid, respectively. The occurrence of side reactions of cyclopentanone in the LP mode of reaction resulted in high conversions of the ketone (up to 91%), very low yields of cyclopentanol (I) (below 6%) and very high yields of 2-cyclopentyli- dene-cyclopentanone (II) (>80%).

Method for oxidizing hydrocarbons

The invention relates to a method for oxidizing substrates such as hydrocarbons, waxes or soot. The method involves the use of a compound of formula (I) in which: R1 and R2 represent H, an aliphatic or aromatic alkoxy radical, carboxyl radical, alkoxycarbonyl radical or hydrocarbon radical, each having 1 to 20 hydrocarbon atoms, SO3H, NH2, OH, F, Cl, Br, I and/or NO2, whereby R1 and R2 designate identical or different radicals or R1 and R2 can be linked to one another via a covalent bonding; Q1 and Q2 represent C, CH, N, CR5, each being the same or different; X and Z represent C, S, CH2, each being the same or different; Y represents O and OH; k=0, 1, 2; l=0, 1, 2; m=1 to 3, and; R5 represents one of the meanings of R1. Said compound is used as a catalyst in the presence of a radical initiator, whereby the molar ratio of the catalyst to the hydrocarbon is less than 10 mol %. Peroxy compounds or azo compounds can be used as the radical initiator. Preferred substrates are aliphatic or aromatic hydrocarbons.

213. The reductive Conversion of Some Cyclic and Acyclic vic-Epoxides to Alcohols by Means of Lithium Aluminium Hydride/Aluminium Trichloride

Unsubstituted medium-ring 1,2-epoxycycloalkanes and certain vic-epoxyalkanes are reduced to the corresponding alcohols very slowly when LiAlH4 alone is used as reducing agent.However, the combination of LiAlH4 and AlCl3, in a 2:1 molar ratio (with respect to 1 mol-equiv. of epoxide) used in refluxing Et2O, greatly enhances these reductions, rendering them of interest for practical purposes.