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Hoechst 33258

Aventis Pharma Deutschland GmbH DI A Lead Generation Chemoinfonmatics Industriepark Hoechst, G879 65926 Frankfurt / Main Jaroslaw.Tomczak aventis.com... [Pg.674]

Hoechst slurry process Hoeppler viscometer Hoffman degradation Hoffman eliminations Hofmann degradation... [Pg.481]

Mordant Red 27 [6539-224] 45180 Brightener 74 Chromoxane 4.5 4.5 American Hoechst Corp. [Pg.407]

Acetaldehyde, first used extensively during World War I as a starting material for making acetone [67-64-1] from acetic acid [64-19-7] is currendy an important intermediate in the production of acetic acid, acetic anhydride [108-24-7] ethyl acetate [141-78-6] peracetic acid [79-21 -0] pentaerythritol [115-77-5] chloral [302-17-0], glyoxal [107-22-2], aLkylamines, and pyridines. Commercial processes for acetaldehyde production include the oxidation or dehydrogenation of ethanol, the addition of water to acetylene, the partial oxidation of hydrocarbons, and the direct oxidation of ethylene [74-85-1]. In 1989, it was estimated that 28 companies having more than 98% of the wodd s 2.5 megaton per year plant capacity used the Wacker-Hoechst processes for the direct oxidation of ethylene. [Pg.48]

The direct liquid phase oxidation of ethylene was developed in 1957—1959 by Wackei-Chemie and Faibwerke Hoechst in which the catalyst is an aqueous solution of PdClj and CuCl (86). [Pg.51]

Throughout the remainder of this article the term homopolymer refers to Delrin acetal resin manufactured and sold by Du Pont the term copolymer refers to Celcon acetal copolymer resins (registered trademark of Hoechst Celanese Corporation). [Pg.56]

Nominal MI, g/10 min Hoechst Celanese Celcon Du Pont Delrin BASF Ultraform... [Pg.59]

Supply and demand statistics for 1988 for all regions of the wodd as compiled by SRI International are given in Table 5. The wodd producers of acetal resins and their aimual capacities are Hsted in Table 6 (29). Hoechst Celanese and Ultraform Corporation (a joint venture of Degussa and BASF) have aimounced capacity expansions in the United States to 77,000 t and 16,000 t, respectively both were due in place in 1990. Part of general capacity expansion plans, aimounced by Du Pont for completion in 1991, are beHeved to apply to acetal resins. [Pg.59]

E.I. du Pont de Nemours Company, Inc. Hoechst Celanese Corporation Ultraform Company Mexico... [Pg.59]

Hoechst, Oberhausen-Holten, Germany 200 2-ethylhexanol propjiene... [Pg.454]

Polygas Olefins. Refinery propylene and butenes are polymerized with a phosphoric acid catalyst at 200°C and 3040—6080 kPa (30—60 atm) to give a mixture of branched olefins up to used primarily in producing plasticizer alcohols (isooctyl, isononyl, and isodecyl alcohol). Since the olefins are branched (75% have two or more CH groups) the alcohols are also branched. Exxon, BASE, Ruhrchemie (now Hoechst), ICl, Nissan, Getty Oil, U.S. Steel Chemicals (now Aristech), and others have all used this olefin source. [Pg.458]

The world s largest producers are Perstorp AB (Sweden, United States, Italy), Hoechst Celanese Corporation (United States, Canada), Degussa (Germany), and Hercules (United States) with estimated 1989 plant capacities of 65,000, 59,000, 30,000, and 22,000 t/yr, respectively. Worldwide capacity for pentaerythritol production was 316,000 t in 1989, about half of which was from the big four companies. Most of the remainder was produced in Asia (Japan, China, India, Korea, and Taiwan), Europe (Italy, Spain), or South America (Brazil, Chile). The estimated rate of production for 1989 was about 253,000 t or about 80% of nameplate capacity. [Pg.466]

The direct oxidation of ethylene is used to produce acetaldehyde (qv) ia the Wacker-Hoechst process. The catalyst system is an aqueous solution of palladium chloride and cupric chloride. Under appropriate conditions an olefin can be oxidized to form an unsaturated aldehyde such as the production of acroleia [107-02-8] from propjiene (see Acrolein and derivatives). [Pg.472]


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Acetaldehyde Hoechst process

American Hoechst Corp

Boots-Hoechst-Celanese

Boots-Hoechst-Celanese ibuprofen

Carbonylation Hoechst process

Chromosome Hoechst staining

Counterstaining Hoechst fluorescence

Ethylene Wacker—Hoechst process

Examples from Hoechst

Farbwerke Hoechst Company

Formaldehyde Hoechst

Halothan Hoechst - Halothane

Hoechst 33342 nuclear stain

Hoechst Aktiengesellschaft

Hoechst Celanese Alcohols

Hoechst Celanese Corporation

Hoechst Celanese Esters

Hoechst Celanese Methyl Isobutyl Ketone

Hoechst Chemical company

Hoechst Company

Hoechst Marion Roussel

Hoechst Marion Roussell

Hoechst Marion Roussell, Inc

Hoechst agents

Hoechst and N-banding

Hoechst applications

Hoechst corporate center

Hoechst dye

Hoechst in Germany

Hoechst materials

Hoechst mergers

Hoechst method

Hoechst mounting

Hoechst stains

Hoechst, Farbwerke

Hoechst-Celanese

Hoechst-Celanese Ketones

Hoechst-Massachusetts General

Hoechst-Uhde cells

Hoechst’s ether

Ibuprofen Boots-Hoechst-Celanese process

Ibuprofen Hoechst-Celanese process

Minor Hoechst

NUCLEAR YELLOW (HOECHST

Processes Hoechst

Propylene Wacker-Hoechst oxidation

Technical Applications (Wacker-Hoechst-Processes)

Wacker Hoechst

Wacker-Hoechst Acetaldehyde Process

Wacker-Hoechst process

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