565-60-6 Usage
Description
3-METHYL-2-PENTANOL, also known as isoamyl alcohol or isopentanol, is a secondary alcohol with the chemical formula C5H12O. It is a clear, colorless liquid and is derived from 3-methylpentane, which is substituted at position 2 by a hydroxy group. This organic compound is widely used in various industries due to its unique properties.
Uses
Used in Flavor and Fragrance Industry:
3-METHYL-2-PENTANOL is used as a flavoring agent for its pleasant, fruity odor and taste. It is commonly used in the production of artificial fruit flavors, particularly in beverages, confectionery, and ice cream.
Used in Chemical Synthesis:
3-METHYL-2-PENTANOL is used as a chemical intermediate in the synthesis of various organic compounds, such as esters, ethers, and other alcohols. It plays a crucial role in the production of solvents, resins, and plasticizers.
Used in Pharmaceutical Industry:
3-METHYL-2-PENTANOL is used as a solvent in the pharmaceutical industry for the preparation of medications and pharmaceutical formulations. Its ability to dissolve a wide range of substances makes it a versatile component in drug manufacturing processes.
Used in Cleaning and Disinfectant Products:
3-METHYL-2-PENTANOL is used as a component in cleaning and disinfectant products due to its ability to dissolve grease, oils, and other organic materials. It is commonly found in household and industrial cleaning products, as well as in personal care products such as hand sanitizers and disinfectants.
Used in Fuel Additives:
3-METHYL-2-PENTANOL is used as a fuel additive in the production of gasoline and other fuels. It helps improve the octane rating, reduce engine knocking, and enhance the overall performance of the fuel.
Used in Paints and Coatings:
3-METHYL-2-PENTANOL is used as a solvent in the paint and coatings industry to help dissolve and disperse pigments, resins, and other components. It contributes to the improved flow, leveling, and drying properties of the paint, resulting in a smoother and more durable finish.
Check Digit Verification of cas no
The CAS Registry Mumber 565-60-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,6 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 565-60:
(5*5)+(4*6)+(3*5)+(2*6)+(1*0)=76
76 % 10 = 6
So 565-60-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H14O/c1-4-5(2)6(3)7/h5-7H,4H2,1-3H3/t5-,6-/m0/s1
565-60-6Relevant articles and documents
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Arcus,C.L. et al.
, p. 1213 - 1216 (1963)
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Mild-temperature hydrogenation of carbonyls over Co-ZIF-9 derived Co-ZIF-x nanoparticle catalyst
Hu, Ao,Lu, Xinhuan,Pan, Haijun,Wang, Chenlong,Xia, Qinghua,Xia, Yongde,Yang, Lu,Yue, Fanfan,Zhang, Haifu,Zhou, Dan
, (2020/08/21)
Benzimidazole and metal cobalt salts were employed in the synthesis of Co-ZIF-9 by solvothermal crystallization. Highly active catalysts for selective hydrogenation of carbonyl compounds were developed. The optimal nanocatalyst Co-ZIF-350 manifested remarkable activity and selectivity for the hydrogenation of cyclohexanone under mild conditions. Catalytic conversion of cyclohexanone reached the highest over the catalyst of Co-ZIF-9-pyrolyzed at 350 °C for 2 h, in which the conversion of cyclohexanone was 100 % and the selectivity of cyclohexanol was ＞99 % at 50 °C. A wide scope of ketones/aromatic aldehydes could be selectively reduced to the corresponding alcohols with high yields. Importantly, the nanocatalyst Co-ZIF-350 presented good tolerance of substrates with various functional groups under mild conditions.
Photooxygenation of alkanes by dioxygen with: P -benzoquinone derivatives with high quantum yields
Ohkubo, Kei,Hirose, Kensaku,Fukuzumi, Shunichi
, p. 731 - 734 (2016/07/06)
Alkanes were oxygenated by dioxygen with p-benzoquinone derivatives such as p-xyloquinone in alkanes which are used as solvents to yield the corresponding alkyl hydroperoxides, alcohols and ketones under visible light irradiation with high quantum yields (Φ = 1000, 1600%). The photooxygenation is started by hydrogen atom abstraction from alkanes by the triplet excited states of p-benzoquinone derivatives as revealed by laser-induced transient absorption spectral measurements.
