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EC / List no.: 202-849-4
CAS no.: 100-41-4
Mol. formula: C8H10
Ethylbenzene is an organic compound with the formula C6H5CH2CH3.
Ethylbenzene is a highly flammable, colorless liquid with an odor similar to that of gasoline.
This monocyclic aromatic hydrocarbon is important in the petrochemical industry as an intermediate in the production of styrene, the precursor to polystyrene, a common plastic material.
In 2012, more than 99% of ethylbenzene produced was consumed in the production of styrene.
Occurrence and applications
Ethylbenzene occurs naturally in coal tar and petroleum.
The dominant application of ethylbenzene is its role as an intermediate in the production of polystyrene.
Catalytic dehydrogenation of ethylbenzene gives hydrogen and styrene:
C6H5CH2CH3 → C6H5CH=CH2 + H2
As of May 2012, more than 99% of all the ethylbenzene produced is used for this purpose.
Ethylbenzene hydroperoxide, a reagent and radical initiator, is produced by autoxidation of ethylbenzene:
C6H5CH2CH3 + O2 → C6H5CH(O2H)CH3
Niche uses
Ethylbenzene is added to gasoline as an anti-knock agent to reduce engine knocking and increase the octane rating.
Ethylbenzene is often found in other manufactured products, including pesticides, cellulose acetate, synthetic rubber, paints, and inks.
Used in the recovery of natural gas, ethylbenzene may be injected into the ground.
Production
Ethylbenzene is produced on a large scale by combining benzene and ethylene in an acid-catalyzed chemical reaction:
C6H6 + C2H4 → C6H5CH2CH3
In 2012, more than 99% of ethylbenzene was produced in this way.
Thus, manufacturers of ethylbenzene are the major buyers of benzene, claiming more than half of total output.
Small amounts of ethylbenzene are recovered from the mix of xylenes by superfractioning, an extension of the distillation process.
In the 1980s a zeolite-based process using vapor phase alkylation offered a higher purity and yield.
Then a liquid phase process was introduced using zeolite catalysts.
This offers low benzene-to-ethylene ratios, reducing the size of the required equipment and lowering byproduct production.
Industrial Accidents
On January 5, 2011 a major fire took place at the Chemie-Pack storage facility in the Dutch Moerdijk industrial area.
The fire started in a chemical reactor operated by Shell which overheated due to an exothermal runaway reaction between the metal oxide catalyst and ethylbenzene. Firefighting activities lead to massive environmental pollution.
Total damage is estimated at 70 million Euro.
Chemical Properties
Ethylbenzene is a colorless, volatile, highly flammable liquid having a gasoline-like odor.
Less dense than water and insoluble in water. Hence floats on water. Vapors are heavier than air.
Ethylbenzene is a member of the family of chemicals called alkylbenzenes.
These are aromatic compounds containing a benzene substituted at one or more positions.
Ethylbenzene is found in natural products such as coal tar and petroleum and is also found in manufactured products such as inks, insecticides, and paints.
Ethylbenzene is used primarily to make another chemical, styrene.
Other uses include as a solvent, in fuels, and to make other chemicals.
Ethylbenzene is manufactured commercially from benzene and ethylene.
A clear colorless liquid with an aromatic odor. Flash point 59°F. Less dense than water (at 7.2 lb / gal) and insoluble in water. Hence floats on water. Vapors heavier than air. Used as a solvent and to make other chemicals.
Uses:
Ethylbenzene is used primarily to make styrene monomer (SM) counting greater than 99%. At less than 1%, it is used as a solvent, in fuels, or as a starting material[4] to make other chemicals.
Ethylbenzene is mainly used in the manufacture of styrene, which is the raw material of producing styrene-based polymers that are widely used in products such as packaging, kitchen utensils and electronic equipment housing.
Ethylbenzene (C6H5C2H5) is the smallest aromatic hydrocarbon molecule with C C key chain structure, and the C C single bond adjacent to benzene ring is far more weaker than those of other chemical bonds thus it is the most easily broken key.
Ethylbenzene is the characteristic structure of single chain alternative fuels such as n-propylbenzene n-butylbenzene in diesel oil and aviation kerosene.
Ethylbenzene may be used as a starting material to synthesize:
(1) Acetophenone via selection oxidation in the presence of potassium dichromate supported on neutral alumina and using air as the oxidizing agent.
(2) Styrene via dehydrogenation over nanodiamonds in an oxygen-lean environment.
Primarily used in the production of styrene; also used as an industrial solvent, as a constituent of asphalt and naptha, and as an antiknock agent in aviation and motor fuels
thylbenzene is used as a solvent and as anintermediate to produce styrene monomer.
Anesthetic.
Ethylbenzene is almost exclusively (> 99%) used as an intermediate for the production of styrene monomer. Less than 1 % of the ethylbenzene produced is used as a paint solvent or as an intermediate for the production of diethylbenzene and acetophenone (IARC 2000).
Ethylbenzene is a constituent (15-20%) of commercial xylene (“mixed xylenes”), and hence used as a component of solvents, as a diluent in paints and lacquers, and as a solvent in the rubber and chemical manufacturing industries (WHO 1996).
Ethylbenzene has been added to motor and aviation fuels because of its anti-knock properties. Estimates of ethylbenzene in gasoline have ranged from <1-2.7%. (IARC 2000).
raw materials for the production of styrene, p-nitroacetophenone, methyl benzophenone.
Ethylbenzene is used as an intermediate in medicine for the synthesis of chloromycetin and chloromycetin.
In addition, it can also be used as a solvent.
Ethylbenzene is used primarily in the production of styrene.
Ethylbenzene is also used as a solvent, as a constituent of asphalt and naphtha, and in fuels.
Definition
ethylbenzene: A colourless flammableliquid, C6H5C2H5; r.d. 0.867;m.p. –95°C; b.p. 136°C.
Ethylbenzene is madefrom ethene and ethybenzene by aFriedel–Crafts reaction and is usedin making phenylethene (for polystyrene).
Preparation
By Friedel-Crafts reaction on benzene, ethylbromide and aluminium chloride (Arc tander, 1969).
Ethylbenzene is manufactured by alkylation from benzene and ethylene.
Production Methods Ethylbenzene is produced by alkylation of benzene with ethylene, except for a very small fraction that is recovered from mixed C8 aromatics by superfractionation.
The reaction takes place on acidic catalysts and can be carried out either in the liquid or vapor phase.
colorless liquid, with aromatic odor, vapor slightly heavier than air. The boiling point is 136.2 ℃ and the refractive index is 1. 5009. The relative density was 0.8671.
Freezing point -95 °c.
Flash point 15 °c.
Spontaneous ignition point was 432. 22 ℃.
Specific heat capacity: 1.717J/(g. °C).
Viscosity 0.64 MPAs (25 °c).
Soluble in ethanol, benzene, carbon tetrachloride and ether, almost insoluble in water.
Preparation Method
alkylation of benzene and ethylene in the presence of aluminum chloride catalyst, the liquid phase temperature 95~100 deg C for alkylation reaction, the reactants after hydrolysis, neutralization, it enters the benzene recovery Tower to remove low boiling matters, and the solution in the tower is subjected to rectification to obtain ethylbenzene as a refined product.
The initial distillation point of the atmospheric pressure column top oil by the reforming recovery method is to 138 ℃, and the 60~138 ℃ fraction is pre-hydrogenated by pre-fractionating, then the fraction is reformed by platinum, and then the aromatic hydrocarbon is extracted with diethylene glycol ether, xylene is obtained by distillation, and then the xylene is further distilled to obtain the product ethylbenzene.
Preparation
Preparation of Ethylbenzene from Acetophenone.
Principle:
The carbonyl function can be completely reduced to methylene under acidic, basic or neutral conditions.
Amongst these the most common methods are Clemmensen's reduction, Wolf Kishner reduction and Mozingo reduction.
The reduction of carbonyl group using hydrazine in basic medium using KOH is called as Wolf-Kishner reduction.
Procedure:
Place 0.5 ml acetophenone, 5.0 ml ethylene glycol and 1.0 ml of 90% hydrazine hydrate solution and 1.1 g KOH pellets in a round bottom flask fitted with water condenser.
Warm the reaction mixture of boiling water bath till KOH dissolves and then reflux for 1 h on wire gauze. Distill using Hickmann head till the temperature is 175oC.
Keep the distillate and again reflux for 2 h. Cool this and extract twice with 10 ml ether.
Combine the ether extracts with the distillate removed earlier and dry over sodium sulphate, decant and evaporate the ether.
Ethylbenzene Production
Ethylbenzene is currently used on a large scale industrially for the production of styrene monomer.
Ethylbenzene may be produced by a number of chemical processes but one process which has achieved a significant degree of commercial success is the alkylation of benzene with ethylene in the presence of a solid, acidic zeolite catalyst.
A preferred catalyst includes the synthetic zeolite identified in this specification as MCM-22.
In the production of ethylbenzene by this process, ethylene is used as the alkylating agent and is reacted with benzene in the presence of the catalyst at certain temperatures.
Production of ethylbenzene involves the liquid-phase reaction of ethylene with benzene
C2H4 + C6H6 C8H10
Undesirable reaction occurred by the formation of Di-ethyl benzene from reaction of ethylbenzene with ethylene.
C8H10 + C2H4 C10H14
A third reaction also occurs, in which Di-ethyl benzene reacts with benzene to form ethylbenzene.
C10H14 + C6H6 2C8H10
Physical properties
Clear, colorless liquid with a sweet, gasoline-like odor.
At 40 °C, the average odor threshold concentration and the lowest concentration at which an odor was detected were 550 and 150 μg/L, respectively.
Similarly, at 25 °C, the average taste threshold concentration and the lowest concentration at which a taste was detected were 780 and 390 μg/L, respectively (Young et al., 1996).
The average least detectable odor threshold concentrations in water at 60 °C and in air at 40 °C were 2.4 and 72 μg/L, respectively (Alexander et al., 1982).
Cometto-Mu?iz and Cain (1994) reported an average nasal pungency threshold concentration of 10,100 ppmv.
Ethylbenzene is a colorless, flammable liquid that smells like gasoline.
Ethylbenzene is naturally found in coal tar and petroleum and is also found in manufactured products such as inks, pesticides, and paints.
Ethylbenzene is used primarily to make another chemical, styrene.
Other uses include as a solvent, in fuels, and to make other chemicals.
Ethylbenzene is a colorless liquid, which has an aromatic odor.
Ethylbenzene is widely used in the manufacturing of styrene and as a solvent.
Ethylbenzene is insoluble in water.
Ethylbenzene may be used as an analytical standard for the determination of the analyte in paints, engine oils, biological samples, water and air samples by various chromatography techniques.
Ethylbenzene may also be used as a standard to spike pump oil to form excellent standard generator for solid-phase microextraction (SPME).
Ethylbenzene is a clear, colorless liquid with a sweet odor, similar to gasoline.
Ethylbenzene evaporates easily and catches fire easily.
Formula: C8H10
Formula Weight: 106.17
Melting point: -95°
Boiling Point: 135-136°
Flash Point: -5°(59°F)
Density: 0.867
Refractive Index: 1.4950
Storage & Sensitivity: Ambient temperatures.
Solubility
Miscible with alcohol, ethylalcohol, benzene, ethyl ether, carbon tetrachloride, organic solvents, sulfur dioxide and ether.
Slightly miscible with chloroform. Immiscible with water and ammonia.
Applications
Ethylbenzene is used as a solvent for rubber adhesives, varnishes, resins, paints and coatings.
Ethylbenzene acts as an intermediate in the preparation of styrene.
Ethylbenzene is also used as a fuel additive.
Ethylbenzene is added to gasoline as an anti-knock agent, thereby reducing engine knocking and increase the octane rating.
In addition to this, it is used in natural gas recovery process.
Ethylbenzene is almost exclusively (> 99%) used as an intermediate for the manufacture of styrene monomer.
Styrene production, which uses ethylbenzene as a starting material, consumes approximately 50% of the world’s benzene production.
Less than 1% of the ethylbenzene produced is used as a paint solvent or as an intermediate for the production of diethylbenzene and acetophenone. The ethylbenzene present in recovered mixed xylenes is largely converted to xylenes or benzene.
Ethylbenzene has been added to motor and aviation fuels because of its anti-knock properties.
Estimates of ethylbenzene in gasoline have ranged from < 1–2.7%.
Ethylbenzene is also used as a negative photoresist solvent in the semiconductor industry and as a general solvent and diluent.
Ethylbenzene is also present in commercial mixed xylenes at levels up to 25%, and, as such, is present in many paints and lacquers, printing inks, insecticides and solvents in the rubber and chemical manufacturing industries.
Ethylbenzene is used primarily in the production of styrene and synthetic polymers.
Ethylbenzene is used as a solvent, a constituent of asphalt and naphtha; and in synthetic rubber, fuels, paints, inks, carpet glues, varnishes, tobacco products, and insecticides.
Ethylbenzene is a component of automotive and aviation fuels.
Ethylbenzene is also used to make other chemicals, including acetophenone, cellulose acetate, diethyl-benzene, ethyl anthraquinone, ethylbenzene sulfonic acids, propylene oxide, and alpha-methylbenzyl alcohol.
Substance details
Substance name: Ethylbenzene
CASR number: 100-41-4
Molecular formula: C8H10
Synonyms: EB, ethylbenzol, phenylethane, Ethyl Benzene
Physical properties
Ethylbenzene is a colourless liquid that smells like petrol.
Boiling Point: 136.2°C
Melting Point: 94.97°C
Vapour Density: 3.66
Vapour Pressure: 9.53 mm Hg at 25°C
Specific Gravity: 0.867 at 20°C
Chemical properties
Ethylbenzene is a flammable and combustible liquid.
Its vapours are heavier than air and may travel to a source of ignition and flash back.
In liquid form, it floats on water and may travel to a source of ignition and spread fire.
Its combustion may produce irritants and toxic gases.
Ethylbenzene may accumulate static electricity and will react with oxidising materials.
Ethylbenzene is miscible with organic solvents and soluble in alcohol and ether.
Ethylbenzene evaporates at room temperature and burns easily.
Ethylbenzene moves easily into the air from water and soil and is most commonly found as a vapour in the air.
he majority of ethylbenzene is manufactured and used on site to produce the styrene monomer for polystyrene.
Ethylbenzene as a component of “mixed xylenes” is used as a motor fuel additive, component of solvents, as a diluent in paints and lacquers and as a solvent in the rubber and chemical manufacturing industries .
Ethylbenzene is also a constituent of asphalt and commercial naphtha.
What is Ethylbenzene?
Ethylbenzene is a colorless, flammable liquid that smells like gasoline.
Ethylbenzene is found in natural products such as coal tar and petroleum and is also found in manufactured products such as inks, insecticides, and paints.
Ethylbenzene is used primarily to make another chemical, styrene.
Uses:
Ethylbenzene is used primarily in the production of styrene.
Ethylbenzene is also used as a solvent, as a constituent of asphalt and naphtha, and in fuels.
What is Ethyl Benzene?
Ethyl Benzene is a colourless liquid made by a catalytic reaction between ethylene and benzene and subsequent distillation.
How is Ethyl Benzene Used?
Ethylbenzene is almost exclusively consumed as an intermediate in the manufacture of styrene, the main use of which is in the manufacture of styrene-based polymers.
These polymers are in turn used in products such as packaging, kitchen utensils and electronic equipment housing.
Ethyl Benzene is also used as a process solvent in industrial settings, its application as a solvent in the professional or consumer sector is not supported.
Ethylebenzene is the pre-cursor to the production of styrene monomer.
Ethylbenzene is also used in other applications such as fuel blending components and solvents.
Ethylbenzene is a colorless flammable liquid with a pleasant aromatic odor.
Ethylbenzene is an aromatic hydrocarbon, that is, a compound consisting of carbon and hydrogen only with a molecular structure similar to that of benzene (C6H6).
In 2004 it ranked fifteenth among chemicals produced in the United States.
Its primary use is in the manufacture of another aromatic hydrocarbon, styrene (C6H5CH=CH2), widely used to make a number of polymers, such as polystyrene, styrene-butadiene latex, SBR rubber, and ABS rubber.
More than 99 percent of the ethylbenzene made is used for a single purpose—the production of styrene.
Styrene is a very important industrial chemical, ranking seventeenth among all chemicals produced in the United States in 2004.
Ethylbenzene is used to make a number of important and popular polymers, the best known of which may be polystyrene.
Much smaller amounts of ethylbenzene are used in solvents or as additives to a variety of products.
Some products that contain ethylbenzene include synthetic rubber, gasoline and other fuels, paints and varnishes, inks, carpet glues, tobacco products, and insecticides.
Ethylbenzene, also known as ethylbenzol or phenylethane, belongs to the class of organic compounds known as benzene and substituted derivatives.
These are aromatic compounds containing one monocyclic ring system consisting of benzene.
Chronic exposure to etylbenzene can lead to an increase in the mean number of lymphocytes and a decrease in hemoglobin levels.
Ethylbenzene is possibly neutral.
Outside of the human body, Ethylbenzene is found, on average, in the highest concentration within black walnuts and safflowers. Ethylbenzene has also been detected, but not quantified in, several different foods, such as garden tomato (var.), cauliflowers, cucumbers, cherry tomato, and garden tomato.
This could make ethylbenzene a potential biomarker for the consumption of these foods.
This aromatic hydrocarbon is important in the petrochemical industry as an intermediate in the production of styrene, which in turn is used for making polystyrene, a commonly used plastic material.
Ethylbenzene is formally rated as a possible carcinogen and is also a potentially toxic compound.
Treat dermal irritation or burns with standard topical therapy.
Ethylbenzene is naturally found in crude oil.
Ethylbenzene is included in a group of chemicals known as BTEX, which stands for benzene, toluene, ethylbenzene, and xylenes.
The chemicals in BTEX are commonly found in gasoline and petroleum products.
Ethylbenzene is used in the production of styrene, which is used to make Styrofoam.
Ethylbenzene can be found in consumer products including plastics, paints, glues, and some automobile products.
Ethylbenzene is a component of tobacco smoke.
Ethylbenzene is a volatile organic compound (VOC) in the ‘BTEX’ substance group which includes benzene, toluene, ethylbenzene, and xylene.
Ethylbenzene is a colourless liquid that smells similar to gasoline.
Ethylbenzene exists naturally in petroleum, and is also an industrial chemical with a variety of uses.
Ethylbenzene may be referred to as phenylethane or EB.
See the Hazardous Substances Data Bank (HSDB) for other synonyms and more information.
Ethylbenzene has been classified by the International Agency for Research on Cancer (IARC) as Group 2B, possibly carcinogenic to humans.
Additionally, short term exposure to high concentrations of ethylbenzene can irritate eyes and throat.
Chronic exposure may also cause haematological effects and damage to the inner ear.
Ethylbenzene is commercially produced from benzene and ethylene in industrial plants, and a minor amount is isolated by purifying petroleum by-product streams.
Ethylbenzene is also present naturally in crude oil, some natural gas streams, and coal tar.
Over 98% of synthetic ethylbenzene is used as a raw material in the manufacture of styrene monomer.
Minor ethylbenzene applications also include the production of chemicals other than styrene or as a solvent, as well as some agricultural and home insecticide sprays, dyes, household degreasers, rubber adhesives, and rust preventives.
Naturally-occurring ethylbenzene is a component of automotive, diesel, and aviation fuels (up to about 5% ethylbenzene).
In addition, ethylbenzene is present in crude petroleum streams and is a major component of mixed xylenes (15–20% ethylbenzene), which are used as a solvent for some spray paints, coatings, wood stains and varnishes, paint removers and thinners, as well as agricultural and home insecticide sprays, dyes, rubber adhesives, rust preventatives, and household and automotive cleaners.
Ethylbenzene , also known as ethylbenzol or alpha-methyltoluene, belongs to benzene and substituted derivatives class of compounds.
Those are aromatic compounds containing one monocyclic ring system consisting of benzene.
Ethylbenzene can be found in black walnut and safflower, which makes ethyl benzene a potential biomarker for the consumption of these food products.
Ethylbenzene can be found primarily in blood and feces.
Ethylbenzene exists in all eukaryotes, ranging from yeast to humans.
Ethylbenzene is formally rated as possibly a carcinogenic potentially toxic compound.
Ethylbenzene is an organic compound with the formula C6H5CH2CH3.
Ethylbenzene is a highly flammable, colorless liquid with an odor similar to that of gasoline.
This monocyclic aromatic hydrocarbon is important in the petrochemical industry as an intermediate in the production of styrene, the precursor to polystyrene, a common plastic material.
In 2012, more than 99% of ethylbenzene produced was consumed in the production of styrene.
Ethylbenzene is also used to make other chemicals, in fuel, and as a solvent in inks, rubber adhesives, varnishes, and paints. Ethylbenzene exposure can be determined by testing for the breakdown products in urine .
Following oral exposure, a gastric lavage is recommended.
Protect airway by placement in Trendelenburg and left lateral decubitus position or by endotracheal intubation.
Control any seizures first.
Following inhalation, move patient to fresh air.
Monitor for respiratory distress. If cough or difficulty breathing develops, evaluate for respiratory tract irritation, bronchitis, or pneumonitis.
Administer oxygen and assist ventilation as required. Following eye exposure, irrigate exposed eyes with copious amounts of room temperature water for at least 15 minutes.
In case of dermal exposure, remove contaminated clothing and wash exposed area thoroughly with soap and water. Treat dermal irritation or burns with standard topical therapy.
Patients developing dermal hypersensitivity reactions may require treatment with systemic or topical corticosteroids or antihistamines.
Some chemicals can produce systemic poisoning by absorption through intact skin.
Carefully observe patients with dermal exposure for the development of any systemic signs or symptoms and administer symptomatic treatment as necessary
About Ethylbenzene
Helpful information
Ethylbenzene is registered under the REACH Regulation and is manufactured in and / or imported to the European Economic Area, at ≥ 1 000 000 tonnes per annum.
Ethylbenzene is used in articles, by professional workers (widespread uses), in formulation or re-packing, at industrial sites and in manufacturing.
Consumer Uses
ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which Ethylbenzene is most likely to be released to the environment.
Article service life
Release to the environment of Ethylbenzene can occur from industrial use: in processing aids at industrial sites, as an intermediate step in further manufacturing of another substance (use of intermediates) and manufacturing of the substance.
ECHA has no public registered data indicating whether or into which articles the substance might have been processed.
Widespread uses by professional workers
Ethylbenzene is used in the following products: coating products.
Ethylbenzene is used in the following areas: building & construction work.
Ethylbenzene is used for the manufacture of: plastic products, mineral products (e.g. plasters, cement) and furniture.
Other release to the environment of Ethylbenzene is likely to occur from: indoor use and outdoor use resulting in inclusion into or onto a materials (e.g. binding agent in paints and coatings or adhesives).
Formulation or re-packing
Ethylbenzene is used in the following products: polymers, coating products, fuels and inks and toners.
Release to the environment of Ethylbenzene can occur from industrial use: formulation of mixtures and formulation in materials.
Uses at industrial sites
Ethylbenzene is used in the following products: coating products, polymers and inks and toners.
Ethylbenzene has an industrial use resulting in manufacture of another substance (use of intermediates).
Ethylbenzene is used in the following areas: formulation of mixtures and/or re-packaging.
Ethylbenzene is used for the manufacture of: chemicals.
Release to the environment of Ethylbenzene can occur from industrial use: in processing aids at industrial sites and as an intermediate step in further manufacturing of another substance (use of intermediates).
Manufacture
Release to the environment of Ethylbenzene can occur from industrial use: manufacturing of the substance.
IUPAC NAMES:
Benzene, ethyl-
Ethylbenzene
ethyl benzene
Ethylbenzene
ethyl benzene
Ethyl-benzene
ethylbenze
Ethylbenzen
ethylbenzen
ETHYLBENZENE
Ethylbenzene
ethylbenzene
Ethylbenzene
ethylbenzene
Ethylbenzol
ethylbenzol
SYNONYMS:
ETHYLBENZENE REFERENCE SUBSTANCE FOR GAS
Ethylbenzene, 99.5%, SpcDry, Water≤50 ppM (by K.F.), SpcSeal
Ethyl Ether Anhydrous, Stabilized
Ethylbenzene in Dimethyl Sulfoxide, USP 467 Standard
Ethylbenzene, 99.8%
ET2O
ETHER
ETHOXYETHANE
ETHYL ETHER 1000
ethylenzene
ETHYLBENZENE
ETHYL OXIDE
DIETHYL ETHER 300
DIETHYL ETHER 5000
DIETHYL OXIDE
Ethylbenzene 1
Ethylbenzene, 99.5%, with Molecular sieves, SpcDry, Water≤50 ppM (by K.F.), SpcSeal
NSC 406903
ethyl-Benzene Phenylethane aethylbenzol
AKOS BBS-00004368
PHENYLETHANE
a.-Methyltoluene
Aethylbenzol
alpha-Methyltoluene
Benzene, ethyl-
benzene,ethyl-
EB
Ethylbenzeen
ethyl-benzen
Ethylbenzol
Etilbenzene
Etylobenzen
etylobenzen(polish)
iithylbenzol
NCI-C56393
1-Ethylbenzene
Ethylbenzene , reagent grade
Ethylbenzene 10g [100-41-4]
Ethylbenzene, anhydrous, AcroSeal, 99.8%
Ethylbenzene, pure, 99.8%
Ethylbenzene ,99.7%
Ethylbenzene (0.5 mL/ampule
Ethylenzee
Ethylbenzene
Ethylbenzene, 99.8%, anhydrous, AcroSeal
Ethylbenzene, 99.8%, pure
Ethylbenzene, 99.8% 25ML
Ethylbenzene, 99.8% 500ML
Ethylbenzene ReagentPlus(R), 99%
Ethylbenzene Standard
Ethylbenzene, 99%, SuperDry, water≤20 ppm, J&KSeal
ETHYLBENZENE, 1X1ML, MEOH, 200UG/ML
ETHYLBENZENE, 5000MG, NEAT
ETHYLBENZENE, STANDARD FOR GC
ETHYLBENZENE, 1X1ML, MEOH, 5000UG/ML
ETHYLBENZENE, ANHYDROUS, 99.8%
ETHYLBENZENE, REAGENTPLUS, 99%
ETHYLBENZENE OEKANAL
100-41-4 [RN]
1901871 [Beilstein]
202-849-4 [EINECS]
Benzene, ethyl- [ACD/Index Name]
ethyl benzene
Ethylbenzene [ACD/IUPAC Name]
Éthylbenzène [French] [ACD/IUPAC Name]
Ethylbenzol [German] [ACD/IUPAC Name]
MFCD00011647 [MDL number]
Phenylethane
1,2,3,4,5-Pentadeuterio-6-ethylbenzene
17203-53-1 [RN]
1861-01-4 [RN]
20302-26-5 [RN]
2348-51-8 [RN]
2618-00-0 [RN]
272-685-6 [EINECS]
38729-11-2 [RN]
4-Ethylphenetole
84272-90-2 [RN]
Aethylbenzol [German]
Ethenylbenzene
Ethyl(benzene-d5)
Ethyl, 2-phenyl- [ACD/Index Name]
Ethyl-1,1-d2 benzene-d5
ethyl-benzene
ETHYLBENZENE-2,3,4,5,6-D5
Ethylbenzene-d10
Ethylbenzenemissing
Ethyl-d5-benzene
Ethyl-α,α-d2-benzene
Ethyl-β,β,β-d3-benzene
Phenylurethane
PYJ
SYN
WLN: 2R
α-Methyltoluene
α-METHYLTOLUENE
