13360-61-7

Usage

Uses

Used in Chemical Production:
1-Pentadecene is used as a raw material for the production of other chemicals, leveraging its chemical structure to create a variety of compounds for different uses.
Used as a Lubricant or Additive in Plastics, Rubber, and Coatings Industry:
1-Pentadecene is used as a lubricant or additive to enhance the performance characteristics of plastics, rubber, and coatings, improving their durability and functionality.
Used in Surfactant Synthesis:
1-Pentadecene is used as a chemical intermediate in the synthesis of surfactants, contributing to the development of products that reduce surface tension in various applications.
Used in Specialty Chemicals Production:
1-Pentadecene serves as a chemical intermediate in the production of specialty chemicals, where its unique properties are utilized to create specific compounds for niche applications.
Used in Personal Care Product Formulation:
1-Pentadecene is used as an ingredient in the formulation of personal care products, taking advantage of its solubility in organic solvents and its subtle odor.
Used as a Flavoring Agent in Food and Beverage Industry:
1-Pentadecene is used as a flavoring agent in the food and beverage industry, adding unique taste profiles to various products while ensuring safety and quality standards are met.

InChI:InChI=1/C15H30/c1-3-5-7-9-11-13-15-14-12-10-8-6-4-2/h3H,1,4-15H2,2H3

Upstream product

• 36653-82-4 1-Hexadecanol 
• 2624-31-9 potassium palmitate 
• 15890-72-9 laurylmagnesium bromide 
• 106-95-6 allyl bromide 
• 18996-28-6 dodecylmagnesium chloride 
• 28467-72-3 1,2-dibromopentadecane 
• 7373-13-9 octadecan-2-one 
• 629-72-1 pentadecyl bromide 
• 2181-42-2 trimethylsulphonium iodide 
• 16212-05-8 (allylsulfonyl)benzene 
• 1529-59-5 tridodecyl-aluminum 
• 4200-77-5 di(n-dodecyl)aluminum chloride 
• 77953-89-0 1-pentadecyl phenyl telluride 
• 103227-40-3 dodecanoyl 4-pentenoyl peroxide 

Downstream Products

• 629-72-1 pentadecyl bromide 
• 95177-35-8 pentadecylphenyl sulphide 
• 544-63-8 n-tetradecanoic acid 
• 761407-92-5 [1-(tert-butyl-diphenyl-silanyloxymethyl)-2-(4-methoxy-benzyloxy)-heptadec-3-enyl]-carbamic acid 9H-fluoren-9-ylmethyl ester 
• 866957-61-1 2,2-Dimethyl-propionic acid (2R,3S,4S,5R,6R)-3,5-bis-(2,2-dimethyl-propionyloxy)-2-(2,2-dimethyl-propionyloxymethyl)-6-[(E)-(2S,3R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(4-methoxy-benzyloxy)-octadec-4-enyloxy]-tetrahydro-pyran-4-yl ester 
• 866957-63-3 2,2-Dimethyl-propionic acid (2R,3S,4S,5R,6R)-3,5-bis-(2,2-dimethyl-propionyloxy)-2-(2,2-dimethyl-propionyloxymethyl)-6-[(E)-(2S,3R)-2-hexadecanoylamino-3-(4-methoxy-benzyloxy)-octadec-4-enyloxy]-tetrahydro-pyran-4-yl ester 
• 867067-82-1 5-[((E)-Hexadec-2-enyl)oxycarbonylamino]-isophthalic acid diethyl ester 
• 4201-58-5 (2S,3R,4E)-2-(hexadecanoylamido)-4-octadecene-1,3-diol 
• 116467-63-1 N-tert-butyloxycarbonylsphingosine 
• 16611-84-0 6-Pentadecylsalicylic Acid 
• 765-13-9 pentadec-1-yne 
• 1101185-56-1 dimethyl (3S,4R,5E)-4-(benzyloxycarbonyloxy)-3-(tert-butyloxycarbonylamino)nonadec-5-enylphosphonate 
• 946074-89-1 N-[(2S,3R,4E)-3-(tert-butyloxycabonyloxy)-2-(tert-butyloxycabonylamino)octadec-4-enyl]-4-nitrobenzenesulfonamide 
• 498582-80-2 tert-butyl (2S,4R,5S)-4-((E)-pentadec-1-enyl)-2-phenyl-4-vinyl-1,3-dioxan-5-ylcarbamate 

Related news

Concentrations of substituted p-benzoquinones and 1-Pentadecene (cas 13360-61-7) in the flour beetles Tribolium madens (charp.) and Tribolium brevicornis (lec.) (coleoptera, tenebrionidae)07/26/2019

1. 2-Methyl-1,4-benzoquinone (MBQ), 2-ethyl-1,4-benzoquinone (EBQ) and 1-pentadecene (PD) were identified in Tribolium madens and T. brevicornis by gas-liquid chromatography.2. MBQ, EBQ and PD were extremely low in newly eclosed adults (detailed

Concentrations of substituted p-benzoquinones and 1-Pentadecene (cas 13360-61-7) in the flour beetles tribolium confusum J. Du Val and tribolium castaneum (herbst)07/25/2019

1.1. 2-Methyl-1,4-benzoquinone (MBQ), 2-ethyl-1,4-benzoquinone (EBQ) and 1-pentadecene (PD) concentrations in Tribolium confusum and T. castaneum were found to be extremely low in newly eclosed adults (detailed

Relevant academic research and scientific papers

Effective deoxygenation of fatty acids over Ni(OAc)2 in the absence of H2 and solvent

Different metal acetate salts were systematically examined for the catalytic deoxygenation of stearic acid in the absence of H2 and solvent for the first time. Ni(OAc)2 exhibited the highest activity with 62% yield achieved at 350°C for 4.5 h with only 1 mol% (0.2 wt%) of the catalyst. Even with 0.25 mol% (0.05 wt%) catalyst, around 28% yield was achieved within 2 h at 350°C with 89% selectivity to C17 hydrocarbons. The activity based on C17 yields per Ni was 14.5 mol mol-1 h-1, considerably higher than that in previous reports. The catalytically active species were identified to be in situ generated Ni nanoparticles (8-10 nm) formed from the decomposition of the metal precursor with stearic acid as a stabilizer. A new reaction pathway of alkane formation from stearic acid via anhydride intermediate decarbonylation under an inert gas atmosphere was proposed. The excellent stability of the catalyst was demonstrated by re-adding a substrate to the system, during which the activity remained constant through four consecutive runs. The novel catalytic system was found to be applicable to a range of fatty acids and triglycerides with varying activities.

The Sphingosine and Acyl Chains of Ceramide [NS] Show Very Different Structure and Dynamics That Challenge Our Understanding of the Skin Barrier

The lipid phase of the uppermost human skin layer is thought to comprise highly rigid lipids in an orthorhombic phase state to protect the body against the environment. By synthesizing sphingosine-d28 deuterated N-lignoceroyl-d-erythro-sphingosine (ceramide [NS]), we compare the structure and dynamics of both chains of that lipid in biologically relevant mixtures using X-ray diffraction, 2H NMR analysis, and infrared spectroscopy. Our results reveal a substantial fraction of sphingosine chains in a fluid and dynamic phase state at physiological temperature. These findings prompt revision of our current understanding of the skin lipid barrier, where an extended ceramide [NS] conformation is preferred and a possible domain structure is proposed. Mobile lipid chains may be crucial for skin elasticity and the translocation of physiologically important molecules.

Anodic Cyclization of Unsaturated α-Stannyl Ethers. Termination by Bromide derived from Dibromomethane

Anodic oxidation of unsaturated α-stannyl ethers in Bu4NClO4-CH2Br2 results in effective cyclization and the introduction of bromide into one of the original olefinic carbons; a mechanism involving the coupling between the cyclized carbocation and Br- generated by cathodic reduction of CH2Br2 is suggested.

A Method for preparing alpha-olefins from Biomass-derived fat and oil

The present invention relates to a method for preparing alpha-olefins from biomass-derived fats and oils. According to the preparation method, all of the various saturated or unsaturated fatty acids in the biomass-derived fats and oils can be prepared into alpha-olefins, and a conventional problem that the saturated fatty acids do not participate in a reaction or a mixture is generated due to polyunsaturated fatty acids can be solved. Thus, the present invention can be advantageously used to prepare alpha-olefins from biomass.

Alkene synthesis by photocatalytic chemoenzymatically compatible dehydrodecarboxylation of carboxylic acids and biomass

Direct conversion of renewable biomass and bioderived chemicals to valuable synthetic intermediates for organic synthesis and materials science applications by means of mild and chemoselective catalytic methods has largely remained elusive. Development of artificial catalytic systems that are compatible with enzymatic reactions provides a synergistic solution to this enduring challenge by leveraging previously unachievable reactivity and selectivity modes. We report herein a dual catalytic dehydrodecarboxylation reaction that is enabled by a crossover of the photoinduced acridine-catalyzed O-H hydrogen atom transfer (HAT) and cobaloxime-catalyzed C-H-HAT processes. The reaction produces a variety of alkenes from readily available carboxylic acids. The reaction can be embedded in a scalable triple-catalytic cooperative chemoenzymatic lipase-acridine-cobaloxime process that allows for direct conversion of plant oils and biomass to long-chain terminal alkenes, precursors to bioderived polymers.

Synthesis of mesoporous ZSM-5 zeolites and catalytic cracking of ethanol and oleic acid into light olefins

Conversion of biomass-derived chemicals into light olefins is a promising method to maintain sustainable development of light olefin industry. In this study, three mesoporous ZSM-5 zeolites (MZSM-5-A, MZSM-5-B and MZSM-5-C) with major pore diameter about 4.8 nm, 16 nm and 22 nm were synthesized using a hydrothermal method by utilizing different templates. The catalytic activity of catalysts was studied by catalytic cracking of ethanol and oleic acid. The influence of reaction temperature on conversion and product selectivity was investigated. The characterization of ZSM-5 samples showed that the orders of the external surface area and mesopore volume were MZSM-5-C > MZSM-5-B > MZSM-5-A > conventional HZSM-5. In ethanol to light olefin reaction, MZSM-5-C achieved the highest light olefin yield (318.3 mL g?1) and ethylene selectivity (42.3%) at 400 °C. In oleic acid to light olefin reaction, MZSM-5-B achieved a complete conversion of oleic acid at 500 °C, and obtained the highest light olefin selectivity (38.1%) at 550 °C. The difference may be relevant to the size and chemical structure of feedstock molecular as well as the acidity of catalysts. Regardless of ethanol or oleic acid as feedstock, introduction of mesopore in zeolites significantly enhanced the light olefin yield and selectivity.

Electron transfer-induced reduction of organic halides with amines

Reduction of a variety of organo halides was examined by using amines as a sacrificial hydrogen source. UV light-induced reduction of vinyl and aryl halides with triethylamine proceeded smoothly to give the corresponding reduced products. High temperature heating also caused the reduction and DABCO (1,4-diazabicyclo[2.2.2]octane) also served as a good reducing reagent.

An Engineered Self-Sufficient Biocatalyst Enables Scalable Production of Linear α-Olefins from Carboxylic Acids

Fusing the decarboxylase OleTJE and the reductase domain of P450BM3 creates a self-sufficient protein, OleT-BM3R, which is able to efficiently catalyze oxidative decarboxylation of carboxylic acids into linear α-olefins (LAOs) under mild aqueous conditions using O2 as the oxidant and NADPH as the electron donor. The compatible electron transfer system installed in the fusion protein not only eliminates the need for auxiliary redox partners, but also results in boosted decarboxylation reactivity and broad substrate scope. Coupled with the phosphite dehydrogenase-based NADPH regeneration system, this enzymatic reaction proceeds with improved product titers of up to 2.51 g L-1 and volumetric productivities of up to 209.2 mg L-1 h-1 at low catalyst loadings (～0.02 mol%). With its stability and scalability, this self-sufficient biocatalyst offers a nature-friendly approach to deliver LAOs.

A process for the preparation and synthetic ChondriamideA and ChondriamideC method (by machine translation)

The invention provides a process for the preparation of synthetic Chondriamide A and Chondriamide C and method, wherein the invention provides a process for the preparation, including: formula (I) compounds of structure, palladium catalyst, phosphorus ligand, alkali and organic solvent at room temperature the illumination reaction, formula (II) structure obtained olefin; wherein through the selection of a particular phosphorus ligand; make the method of the invention can be under the photocatalysis, room temperature to realize high-efficient catalytic conversion, and the mild reaction conditions, simple operation, in line with the development of green environment-friendly chemical requirements, and the range of choice of substrate and functional group compatibility has more universal, and has outstanding chemical selectivity; and the method can be successfully applied to complex molecular introducing carbon-carbon double bond to the programme, to optimize a part of the drug molecular synthesis strategy, improve the synthesis efficiency, reduce the cost, with industrial synthetic value and prospects. (by machine translation)

Decarboxylative Olefination of Activated Aliphatic Acids Enabled by Dual Organophotoredox/Copper Catalysis

Herein, we demonstrate a dual organophotoredox/copper catalytic strategy toward challenging decarboxylative olefination processes proceeding in high yields and selectivities. This operationally simple method uses photoactive organic molecules and Cu(II)-complexes as catalysts to provide rapid access to a wide variety of olefins from inexpensive synthetic and biomass-derived carboxylic acids under mild light-mediated conditions. Mechanistic investigations suggest that the reaction rate for this process is controlled solely by the incident photon flux.