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Organic compound
Cumene (isopropylbenzene) is an organic compound that contains a benzene ring with an isopropyl substituent. It is a constituent of crude oil and refined
Cumene
Industrial process
The cumene process (cumene-phenol process, Hock process) is an industrial process for synthesizing phenol and acetone from benzene and propylene. The term
Cumene_process
Aromatic organic chemical compound
Cumene hydroperoxide is the organic compound with the formula C6H5C(CH3)2OOH; this oily liquid is classified as an organic hydroperoxide. Products of decomposition
Cumene_hydroperoxide
Organic compound (C6H5OH)
for its production, but the cumene process is the dominant technology. Accounting for 95% of production (2003) is the cumene process, also called Hock process
Phenol
Hydrocarbon compound (C6H6)
manufacture of chemicals with more complex structures, such as ethylbenzene and cumene, of which billions of kilograms are produced annually. Although benzene
Benzene
Chemical compound
chemical compound that belongs to the alcohol group. It is a derivative of cumene. 2-Phenyl-2-propanol can be synthesized through Grignard reaction between
2-Phenyl-2-propanol
Chemical product derived from petroleum
styrene as a monomer cumene – isopropylbenzene; a feedstock in the cumene process phenol – hydroxybenzene; often made by the cumene process acetone – dimethyl
Petrochemical
Chemical compound
scintillator in particle physics experiments such as NOνA and Borexino. Cumene The Merck Index: An Encyclopedia of Chemicals, Drugs, and Biologicals (11th ed
1,2,4-Trimethylbenzene
Organic compound ((CH3)2CO); simplest ketone
acetone is produced via the cumene process; as a result, acetone production is tied to phenol production. In the cumene process, benzene is alkylated
Acetone
Simplest secondary alcohol
above methods, as acetone is itself normally prepared from propene via the cumene process. IPA cost is primarily driven by raw material cost, and this way
Isopropyl_alcohol
Chemical manufacturing plant in Australia
to store cumene before it was sent to Oxidation. This section of the plant converts cumene into a mixture of cumene hydroperoxide and cumene. The reaction
Huntsman_(chemical_plant)
Chemical compound (CH3CH=CH2)
for the production of chemicals such as propylene oxide, acrylonitrile, cumene, butyraldehyde, and acrylic acid. In the year 2013 about 85 million tonnes
Propylene
Chemical reactor
oxidation of harmful chemical compounds in wastewater streams or of cumene in the cumene process. Also in the treatment of waste water trickle bed reactors
Trickle-bed_reactor
Chemical compound
by-product of the cumene process. In this procedure, cumene is converted to its radical, through a reaction with oxygen. Normally these cumene radicals are
Α-Methylstyrene
Product of a reaction used in another
chemical intermediates. Cumene is made from benzene and propylene and used to make acetone and phenol in the cumene process. The cumene itself is of relatively
Chemical_intermediate
Organic compound consisting entirely of hydrogen and carbon
butane, terephthalic acid from xylenes, acetone together with phenol from cumene (isopropylbenzene), and cyclohexanone from cyclohexane. The process, which
Hydrocarbon
Organic compounds of the form R–O–O–R′
in major commercial processes. In the cumene process, acetone and phenol are produced by decomposition of cumene hydroperoxide (Me = methyl): C6H5CMe2(O2H)
Organic_peroxides
Chemical compound
useful resins and fragrances. Acetophenone is formed as a byproduct of the cumene process, the industrial route for the synthesis of phenol and acetone. In
Acetophenone
Class of chemical compounds
vs tert-BuOH (b.p. 82-83 °C) CH3OOH (b.p. 46 °C) vs CH3OH (b.p. 65 °C) cumene hydroperoxide (b.p. 153 °C) vs cumyl alcohol (b.p. 202 °C) (C6H5)3COOH (m
Hydroperoxide
Flammable liquid hydrocarbon mixture
reddish brown liquid that is a mixture of hydrocarbons (toluene, xylene, and cumene, etc.), could also be intended in some contexts. Generally, in pre 19th
Naphtha
Chemical compound
It is synthesized as a by-product in the autoxidation of cumene, which mainly affords cumene hydroperoxide. Alternatively, it can be produced by the addition
Dicumyl_peroxide
Set of reactions to attach substituents to an aromatic ring
from benzene and ethylene and for the production of cumene from benzene and propene in cumene process: Industrial production typically uses solid acids
Friedel–Crafts_reaction
Chemical compound
industrially in two main ways. The most widely used route is similar to the cumene process in reaction mechanism and involves the dialkylation of benzene with
Hydroquinone
Chemical compound
as a solution in (aromatic) solvents, commonly toluene but also xylene, cumene, or mesitylene, Used in large excess, it activates precatalysts for alkene
Methylaluminoxane
American chemical company
integrated chemical manufacturer. It produces phenol in Frankford through the cumene process, where it is converted to caprolactam in Hopewell, polymerized to
AdvanSix
Chemical compound
analogous to the cumene process begins with cyclohexylbenzene, which is oxidized to a hydroperoxide, akin to the production of cumene hydroperoxide. Via
Cyclohexylbenzene
Chemical compound
a colorless liquid. A more common structural isomer of this compound is cumene. n-Propylbenzene is used as a nonpolar organic solvent in various industries
N-Propylbenzene
Chemical substance
estimated to be 1.42 ug/Kg bw/day. Calcium xylene sulfonate and sodium cumene sulfonate have been shown to cause temporary, slight eye irritation in animals
Hydrotrope
Chemical compound
dehydrated to give styrene, a useful monomer. Cumene hydroperoxide derived from oxygenation of cumene (isopropylbenzene), which affords cumyl alcohol
Propylene_oxide
Chemical compound
by dechlorination of polychlorophenols. Alternatively, it arises via the cumene process, which starts with the alkylation of chlorobenzene with propylene
3-Chlorophenol
Compound containing rings with delocalized pi electrons
benzene ring. Representative arene compounds Benzene Toluene Ethylbenzene Cumene p-Xylene m-Xylene o-Xylene Mesitylene Durene Biphenyl Phenol Aniline Benzaldehyde
Aromatic_compound
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
2,2,4-Trimethylpentane
Topics referred to by the same term
centre-left party Collagen hybridizing peptide CHP (gene) Chp (GTPase) Cumene hydroperoxide Capillary hydrostatic pressure, a component of the Starling
CHP
Chemical compound (CH3C(O)CH2CH3)
isobutylbenzene, which is analogous to the industrial production of acetone. The cumene process can be modified to produce phenol and a mixture of acetone and butanone
Butanone
Chemical compound
organic synthesis. It is chiral. Together with tert-butyl hydroperoxide and cumene hydroperoxide, ethylbenzene hydroperoxide is important commercially. The
Ethylbenzene_hydroperoxide
Spontaneous oxidation by oxygen at normal temperature
chemicals are produced by autoxidation: in the cumene process, isopropylbenzene undergoes autoxidation to give cumene hydroperoxide. This compound is then converted
Autoxidation
Organic compounds with the formula (CH3)2C6H4
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Xylene
Substance that can explode
5-Bis(trinitromethyl)tetrazole Chlorine oxides Copper(I) acetylide Copper(II) azide Cumene hydroperoxide Cycloprop(-2-)enyl nitrate (CXP or CPN) Cyanogen azide Cyanuric
Explosive
Petrochemical process to break down saturated hydrocarbons in smaller molecules
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Steam_cracking
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Pentadienyl
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Azulene
Index of chemical compounds with the same name
to: n-Propylbenzene, the straight chain isomer (IUPAC name propylbenzene) Cumene (isopropylbenzene) This set index article lists chemical compounds articles
Propylbenzene
Hydrocarbon compound containing one or more C≡C bonds
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Alkyne
Chemical compounds in which hydroxyl group is attached directly to an aromatic ring
typically produced by the alkylation of benzene/toluene with propylene to form cumene then O 2 is added with H 2SO 4 to form phenol (Hock process). In addition
Phenols
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
O-Xylene
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
1,7-Octadiene
Group of isomeric chemical compounds
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Trimethylbenzene
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Twistane
Group of atoms giving a molecule characteristic properties
alkynyl- -yne H − C ≡ C − H {\displaystyle {\ce {H-C#C-H}}} Acetylene (Ethyne) Benzene derivative Phenyl RC6H5 RPh phenyl- ‑benzene Cumene (Isopropylbenzene)
Functional_group
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Styrene
Hydrocarbon compound containing a non-aromatic ring with a C=C bond
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Cycloalkene
Chemical compound
producing the acetone by-product appears attractive and is similar to the cumene process as a hydroperoxide is formed and then decomposed to yield two key
Cyclohexanone
Substances harmful to people, property or the environment
2 Organic peroxides, either in liquid or solid form (benzoyl peroxides, cumene hydroperoxide). Class 6: Toxic and Infectious Substances Hazardous Materials
Dangerous_goods
Index of chemical compounds with the same molecular formula
C9H12O2 (molar mass: 152.18 g/mol, exact mass: 152.0837 u) may refer to: Cumene hydroperoxide (CHP) 4-Ethylguaiacol Lanierone This set index page lists
C9H12O2
Chemical compound
p-cymene, which can be oxidatively dealkylated in a manner similar to the cumene process. p-Cresol is consumed mainly in the production of antioxidants,
P-Cresol
Tidal island in northeast England
of the West Saxon Anglo-Saxon Chronicle record: Her wæron reðe forebecna cumene ofer Norðhymbra land, ⁊ þæt folc earmlic bregdon, þæt wæron ormete þodenas
Lindisfarne
Type of saturated hydrocarbon compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Alkane
Standard measure of the performance of an engine or aviation fuel
6 99.9 105 propane 112 97 105 ethylbenzene 112 99 106 isopropylbenzene (cumene) 112 102 107 2,2,3-trimethylbutane 112.1 101.3 106 VP C16 Race Fuel 117
Octane_rating
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
1,2,3-Trimethylbenzene
Organic compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Tert-Butylbenzene
Hydrocarbon ring molecule containing a C≡C bond
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Cycloalkyne
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
2-Methylhexane
Chemical compound
by the reduction of 4-isopropylbenzoyl chloride or by the formylation of cumene. Merck Index, 11th Edition, 2623 "cuminaldehyde". Scents and Flavors. Scents
Cuminaldehyde
Organic compounds of the form >C=O
aerobic oxidation of cyclohexane. Acetone is prepared by air-oxidation of cumene. For specialized or small scale organic synthetic applications, ketones
Ketone
Chemical compound
starting material for the synthesis of acetone before the development of the cumene process: Ca(CH3COO)2 → CaCO3(s) + (CH3)2CO A saturated solution of calcium
Calcium_acetate
Class of chemical compounds
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Acene
Classification of agents that are possibly carcinogenic to humans
salts Coconut oil diethanolamine condensate para-Cresidine Crotonaldehyde Cumene Cupferron Cycasin Dacarbazine Dantron (Chrysazin, 1,8-Dihydroxyanthraquinone)
IARC_group_2B
Organic compound, C6H4(CH=CH2)2
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Divinylbenzene
Family of organic compounds
p-xylene Trimethylbenzenes hemimellitene pseudocumene mesitylene Tetramethylbenzenes prehnitene isodurene durene Miscellaneous ethylbenzene cumene p-cymene
Alkylbenzene
Aromatic hydrocarbon
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Toluene
Transfer of an alkyl group from one molecule to another
fundamental benzene-based feedstocks such as ethylbenzene (precursor to styrene), cumene (precursor to phenol and acetone), linear alkylbenzene sulfonates (for detergents)
Alkylation
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Cyclooctyne
Hydrocarbon compound with 3 or more consecutive double bonds
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Cumulene
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
2-Methylpentane
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
P-Cymene
Manufacturer and marketer of chlorovinyls and aromatics
PVC resins, PVC rigid and flexible compounds) and aromatics (acetone, cumene, phenol). With the acquisition of Royal Group Technologies the company is
Axiall
Polish chemist (1810–1847)
nitrotoluene, cedrene, potassium hydroxide dihydrate, chromyl chloride, cumene, benzyl chloride, benzyl bromide, and menthene. In 1847 he was decorated
Filip_Neriusz_Walter
Index of chemical compounds with the same name
1-Ethyl-2-methylbenzene 1-Ethyl-3-methylbenzene 1-Ethyl-4-methylbenzene Cumene n-Propylbenzene Cyclopropylbenzene trans-Propenylbenzene cis-Propenylbenzene
C3-Benzenes
Hydrocarbon compound; precursor to styrene and polystyrene
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Ethylbenzene
Organic compound (C6H5NH2); simplest aromatic amine
can alternatively be prepared from ammonia and phenol derived from the cumene process. Many analogues and derivatives of aniline are known where the phenyl
Aniline
Process of producing goods
Cracking (chemistry) – the generic term for breaking up the larger molecules Cumene process – making phenol and acetone from benzene Friedel–Crafts reaction
Industrial_processes
Chemical reaction
hydrocarbons: benzaldehyde from toluene, acrolein from propylene, acetone from cumene, cyclohexanone from cyclohexanol. In teaching laboratories and small scale
Alcohol_oxidation
Chemical group (–CH2–CH=CH2)
particularly large scale, e.g. production of terephthalic acid, benzoic acid, and cumene hydroperoxide. Many substituents can be attached to the allyl group to give
Allyl_group
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Heptacene
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Hexamethylbenzene
Index of chemical compounds with the same name
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
C4-Benzenes
Chemical compound
such as toluene or xylene in the presence of acidic montmorillonite or in cumene in the presence of methanesulfonic acid. In both variants yields of 95-97 %
Itaconic_anhydride
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Naphthalene
Chemical used in plastics, xenoestrogen
economy and large amounts of both starting materials are available from the cumene process. As the only by-product is water, it may be considered an industrial
Bisphenol_A
Chemical compound
and surfactants. Some formulations include solvents such as xylenes and cumene. It is also used as a fungicide for Sclerotinia white moulds on soybean
Lactofen
Unsaturated hydrocarbon compound (H2C=C(CH3)2)
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Isobutylene
Chemical compound
2-naphthol. 2-Naphthol can also be produced by a method analogous to the cumene process. The Sudan dyes are popular dyes noted for being soluble in organic
2-Naphthol
Saturated alicyclic hydrocarbon
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Cycloalkane
Covalent compound that contains two double bonds
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Diene
Privately owned multinational chemicals company
paraformaldehyde, and triallylcyanurate Phenol Acetone, alpha-methylstyrene, cumene and phenol Salt * Granular salt, pure dried vacuum salt, salt tablets, and
Ineos
Organic compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Isodurene
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Diisobutene
Group of chemical compounds
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Tetramethylbenzene
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
Methylcyclopropane
Chemical compound
C3-Benzenes Trimethylbenzenes Mesitylene Pseudocumene Hemellitene Other Cumene n-Propylbenzene 4-Ethyltoluene C4-Benzenes Cymenes o-Cymene m-Cymene p-Cymene
1,3,5-Triethylbenzene
CUMENE
CUMENE
CUMENE
CUMENE
CUMENE
CUMENE
CUMENE
CUMENE
CUMENE
a.
Pertaining to, derived from, or related to, xylene; specifically, designating any one of several metameric acids produced by the partial oxidation of mesitylene and pseudo-cumene.
n.
A colorless oily hydrocarbon, C6H5.C3H7, obtained by the distillation of cuminic acid; -- called also cumol.
n.
A hydrocarbon of the aromatic series, metameric with mesitylene and cumene, found in coal tar, and obtained as a colorless liquid.