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Isopropyl benzene

Dimethylpentane Isopropyl benzene fraMS-2-Pentene 1,2,4-Trimethylbenzene... [Pg.169]

Chemical Designations - Synonyms Cymol p-Isopropyltoluene Isopropyltoluol l-Methyl-4-Isopropyl-benzene Methyl Propyl Benzene Chemical Formula p-CH3C4H,CH(CH3)2. [Pg.101]

The cymidiu sulphouic acid is then diazotised in the usual manner by treating with sodium nitrite in acid solution and the diazo body reduced with alkaline tin chloride solution, or with formic acid and powdered copper, or with other relatively gentle reducing agents. The 3 or 5 cymidin sulphonic acid gives by the above process one and the same cymene sulphonic acid, viz., l-methyl-3-sulphonic-4-isopropyl benzene. [Pg.255]

The sodium salt of the cymene sulphonic acid is then fused with sodium hydroxide in the usual manner, and the hydroxyl group substituted for the sulphonic group. This gives l-methyl-3-hydroxy-4-isopropyl-benzene or thymol. [Pg.255]

Quantity Benzene Toluene Isopropyl- benzene Ethyl- benzene P- Xylene m- o-Xylene Xylene Tetra- line... [Pg.20]

The column used was a Pecosphere 3 mm in diameter and 3 cm long carrying a Cl8 stationary phase. The mobile phase was a mixture of methanol (75%) and water (25%) at a flow rate of 2 ml/min. The solutes were 1 benzene, 2 toluene, 3 ethyl benzene, 4 isopropyl benzene, 5 t-butylbenzene, 6 anthracene, and 7 sodium chloride. [Pg.191]

In order to test this concept a series of compounds was prepared in a 5 L Shaw Intermix (rubber internal mixer, Mark IV, Kl) with EPDM (Keltan 720 ex-DSM elastomers an amorphous EPDM containing 4.5 wt% of dicyclopentadiene and having a Mooney viscosity ML(1 +4) 125°C of 64 MU 100 phr), N550 carbon black (50 phr), diisododecyl phthalate (10 phr), stearic acid (2 phr), and l,3-bis(tert-butylperoxy-isopropyl)benzene (Perkadox 14/40 MB ex Akzo Nobel 40% active material 6 or 10 phr). A polar co-agent (15 phr) was admixed to the masterbatch on an open mill and compounds were cured for 20 min at 180°C in a rheometer (MDR2000, Alpha Technologies). The maximum torque difference obtained in the rheometer experiments was used as a measure of... [Pg.404]

Atkyl-araUcyl peroxide Bis(tert-butylperoxy isopropyl) benzene 160 180... [Pg.439]

The cumene (isopropyl benzene) cracking reaction is often used as a model reaction for determining the relative activities of cracking catalysts. [Pg.436]

Hock Also known as the Hock Lang process, and the cumene peroxidation process. A process for converting isopropyl benzene (cumene) to a mixture of phenol and acetone m-di-isopropyl benzene likewise yields resorcinol, and p-di-isopropyl benzene yields hydro-quinone. The basis of the process is the liquid-phase air oxidation of cumene to cumene hydroperoxide ... [Pg.129]

Isopropyl benzene (CUMENE) 59 112 102 6 3-Methyl- tram-2-pentene 6 97 82 6... [Pg.36]

Using isopropyl fluoride and BF3, the yield of isopropyl benzene can be raised to about 82%. [Pg.314]

If the side chain is in an iso form, a more complex aromatic olefin forms. Isopropyl benzene leads to a methyl styrene and styrene [70], The long-chain alkylate aromatics decay to styrene, phenyl, benzyl, benzene, and alkyl fragments. The oxidation processes of the xylenes follow somewhat similar mechanisms [71, 72],... [Pg.139]

Draw the chemical structure of heptane, 3-octene, and isopropyl benzene. [Pg.141]

During World War II, isopropyl benzene, more commonly and commercially known as cumene, was manufactured in large volumes for use in aviation gasoline. The combination of a benzene ring and an iso-paraffin structure made for a very high octane number at a relatively cheap cost. After the war, the primary interest in cumene was to manufacture cumene hydroperoxide. This compound was used in small amounts as a catalyst in an early process of polymerizing butadiene with styrene to make synthetic rubber. Only by accident did someone discover that mild treating of cumene hydroperoxide with phosphoric acid resulted in the formation of... [Pg.105]

Excess benzene is always used in the reactors, also for two reasons. First, the benzene acts like a heat sponge, mitigating the rate at which the temperature increases due to the exothermic reaction. Second, excess benzene helps eliminate some of the undesirable side reactions that can take place, mainly the formation of di- or tri-isopropyl benzene (benzene hooking up with two or three propylenes) or other miscellaneous compounds. [Pg.107]

Alkylation, In petrochemicals, any reaction involving the thermal or catalytic addition of an olefin to a branch-chain hydrocarbon or aromatic hydrocarbon. The most notable example in petrochemicals is the addition of ethylene or propylene to benzene to produce ethylbenzene or isopropyl benzene (cumene). Other examples include the production of detergent alkylates. [Pg.389]

Even sulphonate esters 109 are powerful directing groups, competing well with tertiary amides. No substitution accompanies ortholithiation of ethyl or isopropyl benzene-sulphonate by BuLi. Hydrolysis and chlorination of the products 110 gives functionalized sulphonyl chlorides 111 (Scheme 48) °°. [Pg.526]

On the basis of products formed in a number of condensation reactions only confusion results for any step by step mechanism involving specific identifiable species as intermediates. Here are some of the facts. Benzene condenses with cyclopropane to form n-propylbenzene (Simons et al., 44). Normal propyl bromide gives chiefly isopropyl benzene (Simons and Archer, 36) as does propylene (Simons and Archer, 28). Ethyl alcohol gives ethylbenzene, but methyl alcohol does not give... [Pg.225]

Faujasite X and Y, with 12 ring channels of 7.4 A diameter, admit o- and m-xylenes, but not tri-isopropyl benzene. [Pg.103]


See other pages where Isopropyl benzene is mentioned: [Pg.441]    [Pg.388]    [Pg.300]    [Pg.134]    [Pg.174]    [Pg.63]    [Pg.206]    [Pg.335]    [Pg.248]    [Pg.438]    [Pg.302]    [Pg.32]    [Pg.230]    [Pg.243]    [Pg.63]    [Pg.335]    [Pg.368]    [Pg.388]    [Pg.102]    [Pg.39]    [Pg.237]    [Pg.250]    [Pg.128]    [Pg.254]    [Pg.254]    [Pg.182]   
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See also in sourсe #XX -- [ Pg.243 ]

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See also in sourсe #XX -- [ Pg.281 , Pg.282 ]

See also in sourсe #XX -- [ Pg.66 ]

See also in sourсe #XX -- [ Pg.248 , Pg.249 ]




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Benzene-isopropyl-alcohol-water mixture

Bromo-isopropyl benzene

Chloro-isopropyl benzene

Isopropyl benzene alkylation

Isopropyl benzene cracking

Isopropyl benzene toxicity

Isopropylation, benzene, rate

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