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Journal articles on the topic '2-methyl-1-butanol'

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Published: 4 June 2021

Last updated: 9 February 2022

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1

Aucejo, Antonio, M. Cruz Burguet, Juan B. Monton, Rosa Munoz, Margarita Sanchotello, and M. Isabel Vazquez. "Vapor-Liquid Equilibria for Systems of 1-Butanol with 2-Methyl-1-butanol, 3-Methyl-1-butanol, 2-Methyl-2-butanol, and 3-Methyl-2-butanol at 30 and 100 kPa." Journal of Chemical & Engineering Data 39, no. 2 (1994): 271–74. http://dx.doi.org/10.1021/je00014a017.

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2

Aucejo, Antonio, M. C. Burguet, Juan B. Monton, Rosa Munoz, Margarita Sanchotello, and M. Isabel Vazquez. "Isothermal Vapor-Liquid Equilibria of 1-Pentanol with 2-Methyl-1-butanol, 2-Methyl-2-butanol, and 3-Methyl-2-butanol." Journal of Chemical & Engineering Data 39, no. 3 (1994): 578–80. http://dx.doi.org/10.1021/je00015a040.

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3

Weng, Wen-Lu, Liang-Tau Chang, and I.-Min Shiah. "Viscosities and Densities for Binary Mixtures of Benzylamine with 1-Pentanol, 2-Pentanol, 2-Methyl-1-butanol, 2-Methyl-2-butanol, 3-Methyl-1-butanol, and 3-Methyl-2-butanol." Journal of Chemical & Engineering Data 44, no. 5 (1999): 994–97. http://dx.doi.org/10.1021/je990031d.

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4

Aucejo, Antonio, M. Cruz Burguet, Juan B. Monton, Rosa Munoz, Margarita Sanchotello, and M. Isabel Vazquez. "Isothermal Vapor-Liquid Equilibria for 2-Methyl-2-butanol + 2-Methyl-1-butanol + 1-Pentanol." Journal of Chemical & Engineering Data 39, no. 3 (1994): 581–83. http://dx.doi.org/10.1021/je00015a041.

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5

Rhodes, Jonathon M., Venkat R. Bhethanabotla, and Scott W. Campbell. "Total Vapor Pressure Measurements for Heptane + 1-Pentanol, + 2-Pentanol, + 3-Pentanol, + 2-Methyl-1-butanol, + 2-Methyl-2-butanol, + 3-Methyl-1-butanol, and + 3-Methyl-2-butanol at 313.15 K." Journal of Chemical & Engineering Data 42, no. 4 (1997): 731–34. http://dx.doi.org/10.1021/je970016d.

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6

Barton, Demensio P., Venkat R. Bhethanabotla, and Scott W. Campbell. "Binary Total Pressure Measurements for Methanol with 1-Pentanol, 2-Pentanol, 3-Pentanol, 2-Methyl-1-butanol, 2-Methyl-2-butanol, 3-Methyl-1-butanol, and 3-Methyl-2-butanol at 313.15 K." Journal of Chemical & Engineering Data 41, no. 5 (1996): 1138–40. http://dx.doi.org/10.1021/je960128p.

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7

Lee, Hyun-Song, Sung Yong Mun, and Huen Lee. "High-pressure phase equilibria for the carbon dioxide–2-methyl-1-butanol, carbon dioxide–2-methyl-2-butanol, carbon dioxide–2-methyl-1-butanol–water, and carbon dioxide–2-methyl-2-butanol–water systems." Fluid Phase Equilibria 157, no. 1 (1999): 81–91. http://dx.doi.org/10.1016/s0378-3812(99)00041-2.

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8

Miyano, Yoshimori, Takahiro Kobashi, Hiroshi Shinjo, et al. "Henry’s law constants and infinite dilution activity coefficients of cis-2-butene, dimethylether, chloroethane, and 1,1-difluoroethane in methanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, isobutanol, tert-butanol, 1-pentanol, 2-pentanol, 3-pentanol, 2-methyl-1-butanol, 3-methyl-1-butanol, and 2-methyl-2-butanol." Journal of Chemical Thermodynamics 38, no. 6 (2006): 724–31. http://dx.doi.org/10.1016/j.jct.2005.08.004.

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9

Vogt, Michael, Christian Brüsseler, Jan van Ooyen, Michael Bott, and Jan Marienhagen. "Production of 2-methyl-1-butanol and 3-methyl-1-butanol in engineered Corynebacterium glutamicum." Metabolic Engineering 38 (November 2016): 436–45. http://dx.doi.org/10.1016/j.ymben.2016.10.007.

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10

Resa, José M., José M. Goenaga, and Miguel Iglesias. "Vapor−Liquid Equilibria at 101.3 kPa for Binary Mixtures Containing 2-Methyl-1-propanol + 2-Methyl-1-butanol, 2-Methyl-1-propanol + 3-Methyl-1-butanol, and 2-Methyl-1-propanol + 1-Pentanol." Journal of Chemical & Engineering Data 51, no. 5 (2006): 1892–95. http://dx.doi.org/10.1021/je060238o.

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11

Domínguez, M., A. Camacho, M. C. López, F. M. Royo, and J. S. Urieta. "Excess molar volumes and excess viscosities of ternary mixtures (2-butanol + 1-chlorobutane + 1-butylamine) and (2-methyl-2-propanol + 1-chlorobutane + 1-butylamine) at 298. 15 K." Canadian Journal of Chemistry 73, no. 6 (1995): 896–901. http://dx.doi.org/10.1139/v95-112.

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Excess molar volumes and excess viscosities, at 298.15 K, of the ternary mixtures (2-butanol + 1-chlorobutane + 1-butylamine) and (2-methyl-2-propanol + 1-chlorobutane + 1-butylamine) and of the binary mixtures (2-butanol + 1-butylamine), (2-methyl-2-propanol + 1-butylamine), and (1-chlorobutane + 1-butylamine) have been measured. The ternary excess properties were fitted to the polynomial equation of Cibulka. The experimental results were also compared with those predicted by the empirical equations of Redlich–Kister, Tsao–Smith, Kohler, and Colinet. Keywords: binary and ternary mixtures, exc

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12

Dejoz, Ana, Vicenta González-Alfaro, Francisco J. Llopis, Pablo J. Miguel, and M. Isabel Vázquez. "Vapor–liquid equilibrium of binary mixtures of chlorobenzene with 3-methyl-1-butanol, 3-methyl-2-butanol and 2-methyl-2-butanol, at 100 kPa." Fluid Phase Equilibria 153, no. 2 (1998): 265–77. http://dx.doi.org/10.1016/s0378-3812(98)00430-0.

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13

Kato, Masahiro, Daisuke Kodama, Hisako Serizawa, Chiaki Yaginuma, and Takeshi Ono. "Vapor−Liquid Equilibrium Behaviors of Vanillin in 1-Butanol, 2-Butanol, and 2-Methyl-1-propanol." Journal of Chemical & Engineering Data 52, no. 4 (2007): 1486–87. http://dx.doi.org/10.1021/je700063c.

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14

Rodriguez, V., J. Pardo, M. C. Lopez, F. M. Royo, and J. S. Urieta. "Vapor pressures of binary mixtures of hexane + 1-butanol, + 2-butanol, + 2-methyl-1-propanol, or +2-methyl-2-propanol at 298.15 K." Journal of Chemical & Engineering Data 38, no. 3 (1993): 350–52. http://dx.doi.org/10.1021/je00011a003.

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15

Végh, Daniel, Michal Uher, Oľga Rajniaková, Miloslava Dandárová, and Milan Kováč. "Preparation of vic-Mercaptoisopentanols." Collection of Czechoslovak Chemical Communications 58, no. 2 (1993): 404–8. http://dx.doi.org/10.1135/cccc19930404.

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This paper describes the preparation of some mercaptoisopentanols: 2-mercapto-3-methyl-1-butanol (I), 1-mercapto-3-methyl-2-butanol (II), 3-mercapto-3-methyl-2-butanol (III) and the unsaturated analogue of compound I - 2-mercapto-3-methyl-2-buten-1-ol (IV). These compounds belong to the flavonoid group present in food responsible for deterioration of their gustatory properties.

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16

Dejoz, Ana, Vicenta González-Alfaro, Francisco J. Llopis, Pablo J. Miguel, and M. Isabel Vázquez. "Vapor−Liquid Equilibrium of Binary Mixtures of Tetrachloroethylene with 1-Pentanol, 3-Methyl-1-butanol, and 2-Methyl-1-butanol." Journal of Chemical & Engineering Data 44, no. 2 (1999): 286–90. http://dx.doi.org/10.1021/je980170f.

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17

Hiaki, Toshihiko, Akira Taniguchi, Tomoya Tsuji, and Masaru Hongo. "Isothermal vapor–liquid equilibria of octane with 1-butanol, 2-butanol, or 2-methyl-2-propanol." Fluid Phase Equilibria 144, no. 1-2 (1998): 145–55. http://dx.doi.org/10.1016/s0378-3812(97)00253-7.

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18

Miyano, Yoshimori. "Henry's Law Constants and Infinite Dilution Activity Coefficients of Propane, Propene, Butane, Isobutane, 1-Butene, Isobutene,trans-2-Butene, and 1,3-Butadiene in 2-Methyl-1-butanol, 3-Methyl-1-butanol, and 2-Methyl-2-butanol." Journal of Chemical & Engineering Data 50, no. 1 (2005): 211–15. http://dx.doi.org/10.1021/je049723e.

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19

Tanaka, Hiroyuki, Teruaki Muramatsu, and Masahiro Kato. "Isobaric vapor-liquid equilibria for three binary systems of 2-butanone with 3-methyl-1-butanol, 1-butanol, or 2-butanol." Journal of Chemical & Engineering Data 37, no. 2 (1992): 164–66. http://dx.doi.org/10.1021/je00006a007.

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20

Sankarshana, T., E. Yadagiri, and J. S. N. Murthy. "Phase Transfer Catalysis: Oxidation of 2-Methyl-1-butanol." Chinese Journal of Chemical Engineering 22, no. 9 (2014): 1000–1004. http://dx.doi.org/10.1016/j.cjche.2014.06.023.

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21

Senol, Aynur. "Vapor−Liquid Equilibria of the Systems Ethyl Ethanoate + 2-Methyl-2-butanol, 2-Methyl-1-propanol + 3-Methyl-1-butanol, and Cyclohexanol + Benzyl Alcohol at 101.32 KPa." Journal of Chemical & Engineering Data 43, no. 5 (1998): 763–69. http://dx.doi.org/10.1021/je9702798.

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22

Seal, Prasenjit, Ewa Papajak, Tao Yu, and Donald G. Truhlar. "Statistical thermodynamics of 1-butanol, 2-methyl-1-propanol, and butanal." Journal of Chemical Physics 136, no. 3 (2012): 034306. http://dx.doi.org/10.1063/1.3674995.

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23

Chen, Chan-Cheng, Horng-Jang Liaw, Chi-Min Shu, and Yen-Cheng Hsieh. "Autoignition Temperature Data for Methanol, Ethanol, Propanol, 2-Butanol, 1-Butanol, and 2-Methyl-2,4-pentanediol." Journal of Chemical & Engineering Data 55, no. 11 (2010): 5059–64. http://dx.doi.org/10.1021/je100619p.

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24

Hiaki, Toshihiko, Akira Taniguchi, Tomoya Tsuji, Masaru Hongo, and Kazuo Kojima. "Isobaric Vapor−Liquid Equilibria of Octane + 1-Butanol, +2-Butanol, and +2-Methyl-2-propanol at 101.3 kPa." Journal of Chemical & Engineering Data 41, no. 5 (1996): 1087–90. http://dx.doi.org/10.1021/je960112z.

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25

Cann, Anthony F., and James C. Liao. "Production of 2-methyl-1-butanol in engineered Escherichia coli." Applied Microbiology and Biotechnology 81, no. 1 (2008): 89–98. http://dx.doi.org/10.1007/s00253-008-1631-y.

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26

Mellouki, A., F. Oussar, X. Lun, and A. Chakir. "Kinetics of the reactions of the OH radical with 2-methyl-1-propanol, 3-methyl-1-butanol and 3-methyl-2-butanol between 241 and 373 K." Physical Chemistry Chemical Physics 6, no. 11 (2004): 2951. http://dx.doi.org/10.1039/b316514k.

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27

Fikar, Jiří, Petr Trška, Pavel Pech, and František Liška. "Radical Addition of 2-Propanol to Trifluoroethylene. Preparation of Trifluoroethylene Oligomersfrom Chlorotrifluoroethylene Oligomers." Collection of Czechoslovak Chemical Communications 61, no. 8 (1996): 1215–22. http://dx.doi.org/10.1135/cccc19961215.

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Photochemically initiated addition of 2-propanol to trifluoroethylene afforded the 1 : 1 adducts 3,3,4-trifluoro-2-methyl-2-butanol 1 and 3,4,4-trifluoro-2-methyl-2-butanol 2, as well as the 1 : 2 telomers 3,4,4,5,5,6-hexafluoro-2-methyl-2-hexanol 3 and 3,4,4,5,6,6-hexafluoro-2-methyl-2-hexanol 4. The other possible 1 : 2 and 1 : 3 telomers, in which the CF2-CFH- groups regularly alternate ("head-tail") - 3,3,4,5,5,6-hexafluoro-2-methyl-2-hexanol 13 and 3,3,4,5,5,6,7,7,8-nonafluoro-2-methyl-2-octanol 14 - and which did not arise in the reaction, were obtained by photochemical reduction of addi

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28

Schilling, K., M. Kayser, K. Deckardt, K. Küttler, and H.-J. Klimisch. "Subchronic toxicity studies of 3-Methyl-1- butanol and 2-Methyl-1-propanol in rats." Human & Experimental Toxicology 16, no. 12 (1997): 722–26. http://dx.doi.org/10.1177/096032719701601205.

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1 90-day subchronic toxicity studies with 3-methyl-1- butanol (MEB) and 2-methyl-1-propanol (MEP) were performed on rats to evaluate the toxicological profile of the compounds under conditions of drinking water studies, to identify the potential target organs, and to determine no-observable-adverse-effect-levels (NOAELs) respective of the substances. The test substances were administered to groups of 10 male and 10 female Wistar rats in drinking water at concentrations of 0, 1000 p.p.m. (about 80 mg/kg/d), 4000 p.p.m. (about 340 mg/kg/d) and 16 000 p.p.m. (about 1250 and 1450 mg/kg/d of MEB an

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29

Yang, Xingchuan, Huanxin Li, Chunmei Cao, Li Xu, and Guoji Liu. "Experimental and correlated liquid-liquid equilibrium data for water + 1,6-hexanediol + 1-pentanol/3-methyl-1-butanol/2-methyl-2-butanol at different temperatures." Journal of Chemical Thermodynamics 154 (March 2021): 106341. http://dx.doi.org/10.1016/j.jct.2020.106341.

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30

Dejoz, Ana, Vicenta González-Alfaro, Francisco J. Llopis, Pablo J. Miguel, and M. Isabel Vázquez. "Vapor–liquid equilibrium of binary mixtures of trichloroethylene with 1-pentanol, 2-methyl-1-butanol and 3-methyl-1-butanol at 100 kPa." Fluid Phase Equilibria 155, no. 2 (1999): 229–39. http://dx.doi.org/10.1016/s0378-3812(98)00473-7.

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31

Dell’Era, Claudia, Anna Zaytseva, Petri Uusi-Kyyny, Juha-Pekka Pokki, Minna Pakkanen, and Juhani Aittamaa. "Vapour–liquid equilibrium for the systems butane+methanol, +2-propanol, +1-butanol, +2-butanol, +2-methyl-2-propanol at 364.5K." Fluid Phase Equilibria 254, no. 1-2 (2007): 49–59. http://dx.doi.org/10.1016/j.fluid.2007.02.028.

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32

Terblans, Yvette M., Michelle Huyser, Desmond A. Young, and Michael J. Green. "The synthesis of butene glycol ethers with aluminium triflate." Canadian Journal of Chemistry 84, no. 6 (2006): 859–66. http://dx.doi.org/10.1139/v06-086.

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The use of aluminium triflate as a ring-opening catalyst for butene oxide (BuO) was evaluated in the presence of different alcohols such as methanol, ethanol, n-propanol, n-butanol, 2-propanol, 2-methyl-1-propanol, and 2-methyl-2-propanol. The reaction with methanol was studied kinetically by varying the temperature, catalyst concentration, and methanol butene oxide molar ratio. These reactions yielded two major products (2-methoxy-1-butanol and 1-methoxy-2-butanol) in a approximate ratio of 1:1. It was noted that at low catalyst concentrations (<5 ppm), low temperatures (<90 °C), and

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33

Pan, Chuanrong, Gangfeng Ouyang, Jielan Lin, et al. "Excess Molar Volumes and Surface Tensions of 1,2,4-Trimethylbenzene and 1,3,5-Trimethylbenzene with 1-Butanol, 2-Methyl-1-propanol, 2-Butanol, and 2-Methyl-2-propanol at 298.15 K." Journal of Chemical & Engineering Data 49, no. 6 (2004): 1744–47. http://dx.doi.org/10.1021/je049807n.

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34

Gomis, V., F. Ruiz, N. Boluda, and M. D. Saquete. "Unusual S-shaped binodal curves of the systems water+lithium chloride+1-butanol or 2-butanol or 2-methyl-1-propanol." Fluid Phase Equilibria 155, no. 2 (1999): 241–49. http://dx.doi.org/10.1016/s0378-3812(99)00008-4.

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35

Canosa, J., A. Rodríguez, and J. Tojo. "Dynamic Viscosities of (Methyl Acetate or Methanol) with (Ethanol, 1-Propanol, 2-Propanol, 1-Butanol, and 2-Butanol) at 298.15 K." Journal of Chemical & Engineering Data 43, no. 3 (1998): 417–21. http://dx.doi.org/10.1021/je9702302.

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36

Lopes, José A., and Manuel Nunes da Ponte. "Ternary-phase equilibria for CO2+3-methyl-1-butanol+2-phenylethanol." Journal of Supercritical Fluids 34, no. 2 (2005): 189–94. http://dx.doi.org/10.1016/j.supflu.2004.11.022.

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37

Martínez de la Ossa, Enrique, Clara Pereyra, and Inmaculada Santiago. "Vapor−Liquid Equilibrium of the Ethanol + 2-Methyl-1-butanol System." Journal of Chemical & Engineering Data 48, no. 1 (2003): 14–17. http://dx.doi.org/10.1021/je010272x.

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38

Martínez de la Ossa, C. Pereyra, and I. Santiago. "Vapor−Liquid Equilibrium of the Ethanol + 2-Methyl-1-butanol System." Journal of Chemical & Engineering Data 48, no. 5 (2003): 1364. http://dx.doi.org/10.1021/je0304769.

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39

Rodríguez,, A., J. Canosa,, and J. Tojo. "Speeds of sound and isentropic compressibilities of (methyl ethanoate + methanol+ 1-propanol, or 2-propanol, or 2-butanol, or 2-methyl-2-butanol) atT= 298.15 K." Journal of Chemical Thermodynamics 32, no. 8 (2000): 999–1012. http://dx.doi.org/10.1006/jcht.2000.0668.

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40

Proctor, Amy, Brooke H. Blake-Taylor, and William E. Acree. "Solubility of Anthracene in Ternary Cyclohexane + Propanol + 2-Methyl-1-propanol and Cyclohexane + Butanol + 2-Methyl-1-propanol Mixtures." Journal of Chemical & Engineering Data 53, no. 12 (2008): 2910–12. http://dx.doi.org/10.1021/je800667r.

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41

Song, Hang, Liangming Liu, Yongkui Zhang, and Chao Fu. "Isobaric Vapor−Liquid Equilibria for the Ternary System of 2-Methyl-1-butanol, 3-Methyl-1-butanol, and Ethylene Glycol at 101.3 kPa." Journal of Chemical & Engineering Data 49, no. 6 (2004): 1535–38. http://dx.doi.org/10.1021/je030216r.

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42

Zhang, Ying, Taotao Zhan, Junshuai Chen, and Maogang He. "Mutual diffusion coefficients of 3–methyl–1–butanol + n–heptane and 2–methyl–1–butanol + n–heptane from 288.15 K to 318.15 K." Journal of Chemical Thermodynamics 131 (April 2019): 97–103. http://dx.doi.org/10.1016/j.jct.2018.10.023.

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43

Nain, Anil Kumar, Tanu Srivastava, Jata Dhari Pandey, and Swarita Gopal. "Densities, ultrasonic speeds and excess properties of binary mixtures of methyl acrylate with 1-butanol, or 2-butanol, or 2-methyl-1-propanol, or 2-methyl-2-propanol at temperatures from 288.15 to 318.15K." Journal of Molecular Liquids 149, no. 1-2 (2009): 9–17. http://dx.doi.org/10.1016/j.molliq.2009.07.005.

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44

Fialho, Maurício Batista, Maria Heloisa Duarte de Moraes, Annelise Roberta Tremocoldi, and Sérgio Florentino Pascholati. "Potential of antimicrobial volatile organic compounds to control Sclerotinia sclerotiorum in bean seeds." Pesquisa Agropecuária Brasileira 46, no. 2 (2011): 137–42. http://dx.doi.org/10.1590/s0100-204x2011000200004.

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The objective of this work was to evaluate the potential of an artificial mixture of volatile organic compounds (VOCs), produced by Saccharomyces cerevisiae, to control Sclerotinia sclerotiorum in vitro and in bean seeds. The phytopathogenic fungus was exposed, in polystyrene plates, to an artificial atmosphere containing a mixture of six VOCs formed by alcohols (ethanol, 3-methyl-1-butanol, 2-methyl-1-butanol and phenylethyl alcohol) and esters (ethyl acetate and ethyl octanoate), in the proportions found in the atmosphere naturally produced by yeast. Bean seeds artificially contamined with t

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45

Iloukhani, Hossein, and Mehdi Fattahi. "Excess Molar Enthalpies of 2-Methyl-2-butanol (1) + 1-Alkanols (C1−C5) (2) at 298.15 K." Journal of Chemical & Engineering Data 56, no. 1 (2011): 130–32. http://dx.doi.org/10.1021/je101031j.

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46

Saleh, M. A., M. Habibullah, M. Shamsuddin Ahmed, et al. "Excess molar volumes of the systemsm-xylene + 1-propanol, +2-propanol, +1-butanol, +2-methyl-2-propanol." Physics and Chemistry of Liquids 43, no. 2 (2005): 139–48. http://dx.doi.org/10.1080/00319100512331323986.

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47

Pai, Yung-Hsiang, and Li-Jen Chen. "Liquid–liquid equilibria of two binary systems: water+1-pentanol and water+2-methyl-2-butanol and two ternary systems: water+1-pentanol+2-butyloxyethanol and water+2-methyl-2-butanol+2-butyloxyethanol." Fluid Phase Equilibria 155, no. 1 (1999): 95–105. http://dx.doi.org/10.1016/s0378-3812(98)00456-7.

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48

Sundberg, Aarne T., Helena Laavi, Younghun Kim, Petri Uusi-Kyyny, Juha-Pekka Pokki, and Ville Alopaeus. "Vapor–Liquid Equilibria, Excess Enthalpy, and Excess Volume of Binary Mixtures Containing an Alcohol (1-Butanol, 2-Butanol, or 2-Methyl-2-butanol) and 2-Ethoxy-2-methylbutane." Journal of Chemical & Engineering Data 57, no. 12 (2012): 3502–9. http://dx.doi.org/10.1021/je300670n.

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49

Illini, P., and G. Platz. "Electric Field Induced Anisotropic Concentration Fluctuations in Solutions Containing 2-Butanol, 1-Butanol or 2-Methyl-1-Propanol, Water and Ionic Surfactant." Berichte der Bunsengesellschaft für physikalische Chemie 89, no. 2 (1985): 197–207. http://dx.doi.org/10.1002/bbpc.19850890221.

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50

Ojo, James O., and David A. Oyegoke. "On the Extraction of Vanadium (V) by Alkanols: A comparative Study of 1-pentanol and 3-methyl-1-butanol Isomers as Extractants for Vanadium (V) Extraction from Hydrochloric Acid Solutions." International Journal of Chemistry 8, no. 3 (2016): 9. http://dx.doi.org/10.5539/ijc.v8n3p9.

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<p>Further to the previous study on the extractive recovery of V(V) from HCl solution by some alkanols, the extraction of V(V) from HCl solutions by 1-pentanol and 3-methyl -1-butanol (isomers) dissolved in n-heptane were investigated in the present study, still propelled by the need to proffering viable alternatives to the scarce and relatively costly organophosphorous extractants, and also compare the extraction efficiency of straight- and branched-chain extractants. At the studied pH range (0.5-4.0) with 1-penttanol as extractant, the percentage V(V) extraction (extraction efficiency,

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