23708-56-7

Usage

Uses

Used in Pharmaceutical Industry:
6-Undecanol is used as a pharmaceutical ingredient for its mild properties and solubility in organic solvents, aiding in the formulation and delivery of medications.
Used in Perfume Industry:
6-Undecanol is used as a fragrance ingredient for its mild, fatty odor, contributing to the development of various scent profiles in perfumes.
Used in Cosmetics Industry:
6-Undecanol is used as a cosmetic ingredient for its ability to dissolve in organic solvents, enhancing the texture and performance of cosmetic products.
Used in Plasticizer Production:
6-Undecanol is used as a component in the manufacture of plasticizers, which are additives that increase the flexibility and workability of plastics.
Used in Lubricant Production:
6-Undecanol is used as a component in the production of lubricants, providing a smooth and efficient operation of machinery and reducing friction.
Used in Surfactant Production:
6-Undecanol is used as a component in the manufacture of surfactants, which are compounds that reduce the surface tension of liquids, improving the effectiveness of cleaning and emulsifying agents.
Used in Flavoring Compound Synthesis:
6-Undecanol is used as a chemical intermediate in the synthesis of flavoring compounds, contributing to the development of various taste profiles in food and beverage products.
Used in Chemical Intermediate Production:
6-Undecanol serves as a chemical intermediate in the production of other chemicals, facilitating the synthesis of a wide range of compounds for diverse applications.

InChI:InChI=1/C11H24O/c1-3-5-7-9-11(12)10-8-6-4-2/h11-12H,3-10H2,1-2H3

Upstream product

• 73587-64-1 undec-4t-en-6-one 
• 64-17-5 ethanol 
• 927-49-1 dipentyl ketone 
• 60045-12-7 tert-Butyl-dimethyl-(1-pentyl-hexyloxy)-silane 
• 110-53-2 1-Bromopentane 
• 109-94-4 formic acid ethyl ester 
• 621-84-1 O-benzyl carbamate 
• 142-61-0 Hexanoyl chloride 
• 64214-56-8 N-methoxy-N-methylhexanoamide 
• 142-62-1 hexanoic acid 
• 67-64-1 acetone 
• 71-36-3 butan-1-ol 
• 543-59-9 1-Chloropentane 
• 66-25-1 hexanal 

Downstream Products

• 65633-70-7 2-[4-(4-Chloro-phenoxy)-phenoxy]-propionic acid 1-pentyl-hexyl ester 
• 20351-26-2 6-chloro-undecane 
• 927-49-1 dipentyl ketone 
• 4941-53-1 5-undecene 
• 1051938-75-0 undec-6-yl benzoate 
• 61405-58-1 sulfuric acid mono-(1-pentyl-hexylester); sodium-salt 
• 5422-52-6 α-n-pentylheptanoic acid 
• 27610-92-0 2-butyloctanoic acid 
• 1315330-96-1 N,N'-bis(2,6-diisopropylphenyl)-1,7-bis(6-undecanoxy)perylene-3,4,9,10-tetracarboxylic diimide 
• 1315330-98-3 N-(2,6-diisopropylphenyl)-N'-{4-[2-methyl-5-(cyanoacrylic acid)-3-thienyl]-phenyl}-1,7-bis(6-undecanoxy)perylene-3,4,9,10-tetracarboxylic diimide 
• 1315330-97-2 N-(2,6-diisopropylphenyl)-1,7-bis(6-undecanoxy)perylene-3,4,9,10-tetracarboxylic 3,4-anhydride 9,10-imide 
• 1315331-00-0 N-(2,6-diisopropylphenyl)-N'-(3-carboxy-2-pyrazyl)-1,7-bis(6-undecanoxy)perylene-3,4,9,10-tetracarboxylic diimide 
• 1315330-99-4 N-(2,6-diisopropylphenyl)-N'-(3-carboxy-2-pyridil)-1,7-bis(6-undecanoxy)perylene-3,4,9,10-tetracarboxylic diimide 
• 1259516-73-8 1-pentylhexyl 2,3,4,6-tetra-O-benzyl-β-D-glucopyranoside 

Relevant academic research and scientific papers

Volatile constituents of used frying oils

The volatile constituents of used frying oils obtained from a local food-processing plant were isolated by simultaneous distillation-extraction and fractionated by silica gel column chromatography. The isolates were analyzed by capillary gas chromatography and combined capillary gas chromatography-mass spectrometry, resulting in the identification of 140 compounds. The major constituents identified were 1-pentanol, hexanal, furfuryl alcohol, (E)-2-heptenal, 5-methylfurfural, 1-octen-3-ol, octanal, 2-pentylfuran, (E)-2-octenal, nonanal, (E)-2-nonenal, and hexadecanoic acid.

METHOD FOR PRODUCING HIGHER LINEAR FATTY ACIDS OR ESTERS

The present invention relates to a method of producing linear fatty acids comprising 7 to 28 carbon atoms or esters thereof using a combined biotechnological and chemical method. In particular, the present invention relates to a method of producing dodecanoic acid (i.e. lauric acid), via higher alkanones, preferably 6-undecanone.

Efficient and Practical Transfer Hydrogenation of Ketones Catalyzed by a Simple Bidentate Mn?NHC Complex

Catalytic reductions of carbonyl-containing compounds are highly important for the safe, sustainable, and economical production of alcohols. Herein, we report on the efficient transfer hydrogenation of ketones catalyzed by a highly potent Mn(I)?NHC complex. Mn?NHC 1 is practical at metal concentrations as low as 75 ppm, thus approaching loadings more conventionally reserved for noble metal based systems. With these low Mn concentrations, catalyst deactivation is found to be highly temperature dependent and becomes especially prominent at increased reaction temperature. Ultimately, understanding of deactivation pathways could help close the activity/stability-gap with Ru and Ir catalysts towards the practical implementation of sustainable earth-abundant Mn-complexes.

IONIZABLE CATIONIC LIPID FOR RNA DELIVERY

What is described is a compound of formula I consisting of a compound in which R1 is a branched chain alkyl consisting of 10 to 31 carbons; R2 is a linear alkyl, alkenyl, or alkynyl consisting of 2 to 20 carbons; L1 and L2 are the same or different, each a linear alkylene of 1 to 20 carbons or a linear alkenylene of 2 to 20 carbons; X1 is S or O; R3 is a linear or branched alkylene consisting of 1 to 6 carbons; and R4 and R5 are the same or different, each a hydrogen or a linear or branched alkyl consisting of 1 to 6 carbons; or a pharmaceutically acceptable salt thereof.

IONIZABLE CATIONIC LIPID FOR RNA DELIVERY

What is described is a compound of formula I consisting of a compound in which R1 is a branched chain alkyl consisting of 10 to 31 carbons;R2 is a linear alkyl, alkenyl, or alkynyl consisting of 2 to 20 carbons, or a branched chain alkyl consisting of 10 to 31 carbons;L1 and L2 are the same or different, each a linear alkane of 1 to 20 carbons or a linear alkene of 2 to 20 carbons;X1 is S or O;R3 is a linear or branched alkylene consisting of 1 to 6 carbons; andR4 and R5 are the same or different, each a hydrogen or a linear or branched alkyl consisting of 1 to 6 carbons; or a pharmaceutically acceptable salt thereof.

Stereoselective direct reductive amination of ketones with electron-deficient amines using Re2O7/NaPF6 catalyst

The first example of direct reductive amination (DRA) of ketones with electron-deficient amines (EDA) such as Cbz-, Boc-, EtOCO-, Fmoc-, Bz-, ArSO2-, etc. protected amines have been achieved using catalytic Re2O7/NaPF6. Excellent chemoselectivities as well as diastereoselectivity (for 2-alkyl cyclohexanones) were obtained. The Royal Society of Chemistry 2013.

METHOD TO CONVERT FERMENTATION MIXTURE INTO FUELS

The present disclosure provides methods to produce ketones suitable for use as fuels and lubricants by catalytic conversion of an acetone-butanol-ethanol (ABE) fermentation product mixture that can be derived from biomass.

Effect of side chain substituents on the electron injection abilities of unsymmetrical perylene diimide dyes

Three near-infrared (NIR) absorbing unsymmetrical perylene diimide D-A-D type dyes containing 6-undecanoxy as donor group were utilized in dye-sensitized nanocrystalline TiO2 solar cells. Structure of the acceptor side of the molecules were improved by adding 4-[2-methyl-5-(cyanoacrylic acid)-3-thienyl]-phenyl (V), 3-carboxy-2-pyridil (VI) and 3-carboxy-2-pyrazyl (VII) moieties attached to one of the N-side of the dye. The relationship between the molecular structure of the acceptor sites of the dyes and the photovoltaic performances were discussed. Electrochemical measurements indicated that band gaps of the dyes were energetically favorable for electron injection from the excited state of the dyes to the conduction band of TiO2 nanoparticles. However, three dyes gave lower conversion efficiency on DSSC applications. Strong electron-withdrawing nature of perylene core might not permit to transfer the photo-generated electrons to the carboxyl groups anchoring to TiO2 surface, and then solar-to-electricity conversion efficiencies of the dyes were reduced.

Novel NIR-absorbing conjugated polymers for efficient polymer solar cells: Effect of alkyl chain length on device performance

Three low bandgap conjugated polymers, i.e., PDTPBT-C8, PDTPBT-C6 and PDTPBT-C5, which consist of alternating N-alkyl dithieno[3,2-b:2′, 3′-d]pyrrole and 2,1,3-benzothiadiazole units and carry 1-octylnonyl, 1-hexylheptyl and 1-pentylhexyl as side chains,

Hydrogen-transfer reduction of carbonyl compounds promoted by nickel nanoparticles

Nickel(0) nanoparticles, generated from nickel(II) chloride, lithium powder and a catalytic amount of 4,4-di-tert-butylbiphenyl (DTBB) in THF at room temperature, have been found to promote the reduction of a variety of ketones and aldehydes by transfer hydrogenation using isopropanol as the hydrogen donor. The nickel nanoparticles were characterised and could be re-utilised with a good performance in the absence of a base. A mechanistic study demonstrates that the reaction proceeds through a dihydride-type mechanism.