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T-anol

Koeduka T, Baiga TJ, Noel JP et al (2009) Biosynthesis of r-Anethole in anise characterization of t-Anol/Isoeugenol synthase and an O-Methyltransferase specific for a C7-C8 propenyl side chain. Plant Physiol 149 384-394... [Pg.197]

Silica Gel G CHClj-Isopro-T>anol-5%NH OH (74.4 25 0.6) Dragendorff s Reagent l t... [Pg.245]

Ord, T. J. and Martins, E. P. (2006) Tracing the origins of signal diversity in anole lizards phylogenetic approaches to inferring the evolution of complex behaviour. Anim. Behav. 71,1411-1429. [Pg.365]

Anke, H. (1997) Zearal Kxie and zo anoL In Fungal Biotechnology. Anke, T., ed.. Chapman Hall, London, pp. 186-92. [Pg.306]

Fig. 18.10 Time dependence of hydrogen evolution under steady state irradiation at 30°C. The sample solution consisting of NADPH (2.0 mmol dir-3), TPPSC6V(2.5 /tmol dm-3), and hydrogenase (C.35 unit) in 4.0 ml of 25 mmol dm-3 Tris- HC1 (pH = 7.4) containing 1% Triton X-100 (I). NADPH (2.0 mmol dm-3, TPPS (2.5 /anol dm-3), t/V2+ (2.5 /imol dm-3), and hydrogenase (0.35 unit) in 4.0 ml of 25 mmol dm-3Tris- HC1 (pH - 7.4) containing 1% Triton X-100. Fig. 18.10 Time dependence of hydrogen evolution under steady state irradiation at 30°C. The sample solution consisting of NADPH (2.0 mmol dir-3), TPPSC6V(2.5 /tmol dm-3), and hydrogenase (C.35 unit) in 4.0 ml of 25 mmol dm-3 Tris- HC1 (pH = 7.4) containing 1% Triton X-100 (I). NADPH (2.0 mmol dm-3, TPPS (2.5 /anol dm-3), t/V2+ (2.5 /imol dm-3), and hydrogenase (0.35 unit) in 4.0 ml of 25 mmol dm-3Tris- HC1 (pH - 7.4) containing 1% Triton X-100.
Solvent System I = n-butanol-acetic acid-water 4 1 1 Solvent System II = t-but anol-0.004N HCl-saturated NaCl solution 2 1 1 on paper impregnated with acetone-water-saturated NaCl solution 6 3 1, Ref. (149). [Pg.70]

Anoll Incid t With Nitrogen Backup for a Compressed Air Supply... [Pg.41]

Cellosolue 2-ethoxye anol 41 a if 60 s 6 .. 8 t. -. Solvay Fortilene Phillips Mariex Solvay Fortilene... [Pg.627]

Fig. 8a. Scaling behavior of qm(t) vs the rescaled time f = tD q (0) = 2X(0) [XsM>o) — 3 for the polymer mixture as shown in Fig. 6a and a quench to T = 25 °C. Different symbols refer to different sample geometries. The solid curve is a fit to a formula ohtained by Furukawa [168] corresponding data for polyvinylmethylether (PVME)-polystyrene (PS), dash-dotted [158] and cyclohexane/meth-anol, dashed curve [169], are included. From Bates and Wiltzius [36]. b Coarsening behavior of mixtures of SBR (a random copolymer of styrene and polybutadiene) and polyisoprene (PI) at various compositions, at T = 60 °C. a shows qm(t) and b. corresponding intensity I (t), in arbitrary units, while arrows indicate the times where pinning (t,) or crossover (t ) from intermediate to late stages occurs. From Hashimoto et al. [173]... Fig. 8a. Scaling behavior of qm(t) vs the rescaled time f = tD q (0) = 2X(0) [XsM>o) — 3 for the polymer mixture as shown in Fig. 6a and a quench to T = 25 °C. Different symbols refer to different sample geometries. The solid curve is a fit to a formula ohtained by Furukawa [168] corresponding data for polyvinylmethylether (PVME)-polystyrene (PS), dash-dotted [158] and cyclohexane/meth-anol, dashed curve [169], are included. From Bates and Wiltzius [36]. b Coarsening behavior of mixtures of SBR (a random copolymer of styrene and polybutadiene) and polyisoprene (PI) at various compositions, at T = 60 °C. a shows qm(t) and b. corresponding intensity I (t), in arbitrary units, while arrows indicate the times where pinning (t,) or crossover (t ) from intermediate to late stages occurs. From Hashimoto et al. [173]...
Cycl opent anet hi ol Cycl opent anol Cycl opent anone Cycl opent anon xi me Cyclopentene 1-Cyclopent enecarboni t ri I e 1-Cyclopent ene-1-carboxal dehyde... [Pg.264]

Et hyl -4-hept anol Et hylh ran t / ans2,4-hexadi enoat e... [Pg.388]

Met hyl-3-pent anol 3-Met hyl-3-pent anol 2-Met hyl-1-pent amabet at e 3-Met hyl-2-pentanon t)... [Pg.520]

Maodel,K., Pearson. T.D.U. and Dema8,LN 1980. Lonunesoeot quantum connteis based on organic [Pg.59]

Sano, T., Yanagishita, H., Kiyozumi, Y, Mizukami, F. and Haraya, K. 1991. Separation of eth-anol/water mixture by silicate membrane on pervaporation. 95 221-238. [Pg.326]

A. Hihara, T. Kitamori, Onneutral ionophore-based ion pair extraction reaction. Anol. Chem., 2001, 73, 1382-1386. [Pg.342]

A neat method for cleaving acid-sensitive triterpenoid and steroid aglycones from L-arabinopyranosides and D-galactopyranosides involved oxidation (DMSO-acetic anhydride) of the corresponding 3,4-0-isopropylidene derivative to the glycopyranosidulose, which can be cleaved on u.v.-irradiation in t-but-anol. Photolysis of the model acetals (61) gave, depending on the substituents... [Pg.31]

See other pages where T-anol is mentioned: [Pg.264]    [Pg.191]    [Pg.232]    [Pg.543]    [Pg.553]    [Pg.264]    [Pg.264]    [Pg.264]    [Pg.191]    [Pg.232]    [Pg.543]    [Pg.553]    [Pg.264]    [Pg.264]    [Pg.192]    [Pg.627]    [Pg.244]    [Pg.125]    [Pg.429]    [Pg.1201]    [Pg.1662]    [Pg.21]    [Pg.196]    [Pg.105]    [Pg.331]    [Pg.49]    [Pg.563]    [Pg.123]    [Pg.191]    [Pg.419]    [Pg.347]    [Pg.2341]    [Pg.57]    [Pg.381]    [Pg.147]    [Pg.200]    [Pg.643]    [Pg.1947]    [Pg.2255]    [Pg.187]   
See also in sourсe #XX -- [ Pg.232 ]



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