71072-22-5 Usage
Uses
Used in Chemical Industry:
1-HEXYLTETRAHYDRO-4(1H)-PYRIDINONE is used as a solvent for its capacity to dissolve a wide range of substances, facilitating various chemical reactions and processes.
Used in the Production of Resins:
1-HEXYLTETRAHYDRO-4(1H)-PYRIDINONE is used as a component in the production of resins, contributing to their formation and performance characteristics.
Used in Coatings Industry:
1-HEXYLTETRAHYDRO-4(1H)-PYRIDINONE is used as a solvent in coatings to improve their application properties and drying times, enhancing the final product's quality.
Used in Adhesives:
1-HEXYLTETRAHYDRO-4(1H)-PYRIDINONE is used as a solvent in adhesive formulations to adjust viscosity and improve bonding performance.
Used in Inks:
1-HEXYLTETRAHYDRO-4(1H)-PYRIDINONE is used in ink formulations to ensure proper flow and dispersion of pigments, affecting print quality and durability.
Used as a Surfactant:
1-HEXYLTETRAHYDRO-4(1H)-PYRIDINONE is used to reduce surface tension between liquids and solids, improving the wetting and spreading properties in various applications.
Used as a Coupling Agent:
1-HEXYLTETRAHYDRO-4(1H)-PYRIDINONE is used to improve the compatibility between different substances, enhancing the performance of blended materials.
Used as an Emulsifier:
1-HEXYLTETRAHYDRO-4(1H)-PYRIDINONE is used to stabilize mixtures of immiscible liquids, such as oil and water, by reducing the interfacial tension.
It is crucial to handle 1-HEXYLTETRAHYDRO-4(1H)-PYRIDINONE with care and within appropriate settings to mitigate any potential health and safety risks associated with its use.
Check Digit Verification of cas no
The CAS Registry Mumber 71072-22-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,0,7 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71072-22:
(7*7)+(6*1)+(5*0)+(4*7)+(3*2)+(2*2)+(1*2)=95
95 % 10 = 5
So 71072-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H21NO/c1-2-3-4-5-8-12-9-6-11(13)7-10-12/h2-10H2,1H3
71072-22-5Relevant academic research and scientific papers
Lightening Agents and/or Dyes that Contain Aldehyde(s)
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, (2010/12/29)
Agents for dyeing and/or lightening keratin fibers, in particular human hair, containing, relative to the weight thereof, 0.001 to 15 wt. % of at least one aldehyde of the formula (I): wherein X represents —CH(R2)—SO2—Y—R1, —CR3R4R5, or wherein Y represents —CH(CHO)— or —CH2— or a chemical bond, and wherein each of R1, R2, R3, R4, R5, R6, R7, R8, R9, and R10 independently represents —H or —CN or —F or —Cl or —Br or —I or —CHO or —NH2 or —NO2 or —CF3 or —CCl3 or —CF2CF3 or —CCl2CCl3 or an optionally substituted (C1-C6) alkyl group or a hydroxyalkyl group or a polyhydroxyalkyl group or an optionally substituted (C1-C6) alkylene group, and wherein the agent contains no oxidation dye precursors of developer and coupler type.
Catalytic Epoxidation of Alkenes with Oxone
Denmark, Scott E.,Forbes, David C.,Hays, David S.,DePue, Jeffrey S.,Wilde, Richard G.
, p. 1391 - 1407 (2007/10/02)
A practical, general and efficient protocol for the catalytic epoxidation of alkenes has been developed.The in situ generation of reactive dioxiranes capable of epoxidizing a variety of alkenes under biphasic conditions has been accomplished using phase transfer catalysts bearing a carbonyl group.Optimal epoxidation conditions employ 10 mol percent of 1-dodecyl-1-methyl-4-oxopiperidinium triflate (8d(+)OTf(-)) in a CH2Cl2/pH 7.5-8.0 biphase using potassium monoperoxosulfate (Oxone) as the oxidant.Optimization of the conditions identified (1) slow addition rate, (2) pH 7.5-8.0, (3) N-dodecyl chain, and (4) the triflate salt as key experimental and structural variables.A selection of nine olefins was successfully oxidized to the corresponding epoxides in 83-96percent yield.
