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Irone alpha

The following synthetic sequence corresponds to the ionone syntheses. Depending on the cyclisation conditions, isomeric double bonds and diastereomers are formed. The racemic cis- and trans-a-irone, for example, are commercially available from Givaudan under the name Irone alpha . [Pg.73]

Like the a-ionones, the enantiomers of a-irone are distinguishable by their olfactory properties. The commercially available racemic mixture does not fiilfil the demands of fine perfumery. Enantiomerically pure a-irones may be obtained by means of a twice-repeated chromatographic separation of the epoxides starting from Irone alpha , and enzymatic kinetic resolution. The alcohols are reoxidised with manganese dioxide and the epoxides reconverted into the alkenes by sodium iodide and chlorotrimethylsUane under mild conditions. [Pg.75]

Iron carries half the charge of a whole electron. The calculation produces a set of molecular orbitals appropriate for this pseudowave function. HyperChem then assigns the unpaired electron its proper spin (alpha), substitutes this electron in the orbital formerly occupied by the half electrons, and calculates energy and other properties. [Pg.47]

Anhydrous sulfonic acids, particularly linear alkylben2enesulfonic acids, are typically stored ia stainless steel containers, preferably type 304 or 316 stainless steel. Use of other metals, such as mild steel, contaminates the acid with iron (qv), causiag a darkening of the acid over time (27). The materials are usually viscous oils which may be stored and handled at 30—35°C for up to two months (27). AH other detergent-grade sulfonic acids, eg, alcohol sulfates, alcohol ether sulfates, alpha-olefin sulfonates, and alpha-sulfomethyl esters, are not stored owiag to iastabiUty. These are neutrali2ed to the desired salt. [Pg.98]

Chemical Reactivity - Reactivity with Water No reaction Reactivity with Common Materials No reactions Stability During Transport Stable Neutralizing Agents for Acids and Caustics Not pertinent Polymerization Polymerization is accelerated by heat and exposure to oxygen, as well as the presence of contamination such as iron rust. Iron surfaces should be treated with an appropriate reducing agent such as sodium nitrate, before being placed into isoprene service Inhibitor of Polymerization Tertiary butyl catechol (0.06 %). Di-n-butylamine, phenyl-beta-naphthylamine andphenyl-alpha-naphthylamine are also recommended. [Pg.222]

Fischer Tropsch technology is best exemplified by the SASOL projects in South Africa. After coal is gasified to a synthesis gas mixture, it is purified in a rectisol unit. The purified gas mixture is reacted in a synthol unit over an iron-based catalyst. The main products are gasoline, diesel fuel, and jet fuels. By-products are ethylene, propylene, alpha olefins, sulfur, phenol, and ammonia which are used for the production of downstream chemicals. [Pg.125]

A term applied to iron in the alpha state (aFe) containing approximately 0.2% carbon together with other elements in solid solution. [Pg.734]

Deming TJ (1999) Cobalt and iron initiators for the controlled polymerization of alpha-amino acid-N-carboxyanhydrides. Macromolecules 32 4500-4502... [Pg.24]

Early measurements of " Th were on seawater samples and Th was co-precipitated from 20-30 L of seawater with iron hydroxide (Bhat et al. 1969). This procedure may not recover all of the " Th in the sample, and an alpha emitting Th isotope (e g., °Th or Th) is added as a yield monitor. Following chemical purification of the Th fraction by ion exchange chromatography, the Th is electrodeposited onto platinum or stainless steel planchets. The planchets are then counted in a low background gas-flow beta detector to measure the beta activity and subsequently with a silicon surface barrier detector to determine the alpha activity of the yield monitor. The " Th activity is thus determined as ... [Pg.462]

AGB stars constitute excellent laboratories to test the theory of stellar evolution and nucleosynthesis. Their particular internal structure allows two important processes to occur in them. First is the so-called 3(,ldredge-up (3DUP), a mixing mechanism in which the convective envelope penetrates the interior of the star after each thermal instability in the He-shell (thermal pulse, TP). The other is the activation of the s-process synthesis from alpha captures on 13C or/and 22Ne nuclei that generate the necessary neutrons which are subsequently captured by iron-peak nuclei. The repeated operation of TPs and the 3DUP episodes enriches the stellar envelope in newly synthesized elements and transforms the star into a carbon star, if the quantity of carbon added into the envelope is sufficient to increase the C/O ratio above unity. In that way, the atmosphere becomes enriched with the ashes of the above nucleosynthesis processes which can then be detected spectroscopically. [Pg.262]

Miyake, R., Murakami, K., Owens, J.T., Greiner, D.P., Ozoline, O.N., Ishihama, A., and Meares, C.F. (1998) Dimeric association of Escherichia coli RNA polymerase alpha subunits, studied by cleavage of single-cysteine alpha subunits conjugated to iron-(S)-l-[p-(bromoacetamido)benzyl]ethylenediaminetet raacetate. Biochemistry 37(5), 1344-1349. [Pg.1095]

Luo, M., O Brien, R.J., Bao, S., and Davis, B.H. 2003. Fischer-Tropsch synthesis Induction and steady-state activity of high-alpha potassium promoted iron catalysts. Appl. Catal. A Gen. 239 111-20. [Pg.145]

The use of a Fischer-Tropsch (FT) process to produce long-chain hydrocarbons is well known in industry, and achieving the desired selectivity from the FT reaction is crucial for the process to make economic sense. It is, however, well known that a one-alpha model does not describe the product spectrum well. From either a chemicals or fuels perspective, hydrocarbon selectivity in the FT process needs to be thoroughly understood in order to manipulate process conditions and allow the optimization of the required product yield to maximize the plant profitability. There are many unanswered questions regarding the selectivity of the iron-based low-temperature Fischer-Tropsch (Fe-LTFT) synthesis. [Pg.229]

Figure 5.27. Iron alloy binary systems. Position in the Periodic Table of the alpha-forming and gamma-forming elements in iron alloys. Figure 5.27. Iron alloy binary systems. Position in the Periodic Table of the alpha-forming and gamma-forming elements in iron alloys.
Ferrite Solid solution of carbon in alpha iron (bcc). [Pg.453]


See other pages where Irone alpha is mentioned: [Pg.27]    [Pg.52]    [Pg.1175]    [Pg.1175]    [Pg.1175]    [Pg.1099]    [Pg.1099]    [Pg.1099]    [Pg.624]    [Pg.27]    [Pg.52]    [Pg.1175]    [Pg.1175]    [Pg.1175]    [Pg.1099]    [Pg.1099]    [Pg.1099]    [Pg.624]    [Pg.58]    [Pg.422]    [Pg.332]    [Pg.122]    [Pg.396]    [Pg.184]    [Pg.71]    [Pg.165]    [Pg.29]    [Pg.464]    [Pg.7]    [Pg.155]    [Pg.138]    [Pg.228]    [Pg.55]    [Pg.312]    [Pg.344]    [Pg.229]    [Pg.270]    [Pg.192]    [Pg.230]    [Pg.334]    [Pg.485]    [Pg.162]    [Pg.360]   
See also in sourсe #XX -- [ Pg.73 , Pg.75 ]




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