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tert-Butylbenzol

Tert-Butylbenzene

HCID 7366
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Grundinformationen

CAS
98-06-6
Standard-SMILES
CC(C)(C)c1ccccc1
InChIKey
YTZKOQUCBOVLHL-UHFFFAOYSA-N
Summenformel
C10H14
Durchschnittliche Molmasse
134,22 g/mol
Monoisotopische Masse
134,10955045

Namen und Bezeichner

Bevorzugter Name
Tert-Butylbenzene
IUPAC
tert-butylbenzene
Lokaler Name
tert-Butylbenzol
Englischer Name
tert-Butylbenzene
Summenformel
C10H14
Molmasse
134.22

Namen und Synonyme

tert-Butylbenzene98-06-6T-BUTYLBENZENE2-Methyl-2-phenylpropaneBenzene, (1,1-dimethylethyl)-PseudobutylbenzenePhenyltrimethylmethaneTrimethylphenylmethaneBenzene, tert-butyl-Dimethylethylbenzene(1,1-dimethylethyl)benzeneDTXSID3047138
Weitere Namen anzeigen
Phenyltrim-Trimethyltoluenetert-butyl-benzentert.-ButylbenzolAKOS BBS-00004358Reaxys ID: 4964438
M1R2NME7S2NSC-6557DTXCID1027138RefChem:6292202-632-4tertiary-Butylbenzene1,1-Dimethylethylbenzene(tert-butyl)benzene

Datenbank-Bezeichner

CAS
98-06-6
PubChem CID
7366
DTXSID
DTXSID3047138
ChEMBL
CHEMBL1797277
UNII
M1R2NME7S2
EC Number
202-632-4
Nikkaji
J43.279B

Eigenschaften

Berechnete Struktureigenschaften

XLogP
4,1
Polarare Oberfläche (TPSA)
0 Ų
H-Brücken-Donoren
0
H-Brücken-Akzeptoren
0
Frei drehbare Bindungen
1
Schwere Atome
10
Formalladung
0
Komplexität
91,1

Experimentelle und physikochemische Eigenschaften

Chemical Classes · 2 Einträge

Flammable agents - 3rd degree

Volatile Organic Compound (VOC)

SolventsSolvents -> Aromatic Solvents
SpringerMaterials Properties13C nuclear magnetic resonance spectrum
LogP · 2 Einträge

log Kow= 4.11

4.11

Density · 2 Einträge

0.8669 @ 20 °C/4 °C

0.8665 @ 20°C

Color/Form · 2 Einträge

Liquid

Colorless liquid

Solubility · 4 Einträge

Miscible with alc, ether, benzene

Insoluble in water; very soluble in ethanol and ethyl ether; miscible in acetone

Soluble in alcohol.

In water, 29.5 mg/l @ 25 °C.

Flash Point140 °F (60 °C) OPEN CUP
Boiling Point · 2 Einträge

Sicherheit und Regulatorisches

Sicherheitsangaben dienen nur zur Orientierung und ersetzen weder das Sicherheitsdatenblatt (SDB) des Lieferanten noch geltende Vorschriften oder eine fachliche Bewertung.

GHS-Klassifizierung

GHS Classification · 6 Einträge

This chemical does not meet GHS hazard criteria for 0.4% (1 of 233) of reports.

Danger

H226 (91.8%): Flammable liquid and vapor [Warning Flammable liquids]

P210, P233, P240, P241, P242, P243, P264, P264+P265, P273, P280, P301+P316, P302+P352, P303+P361+P353, P305+P351+P338, P321, P331, P332+P317, P337+P317, P362+P364, P370+P378, P391, P403+P235, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 233 reports by companies from 12 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Danger

Gefahrenhinweise

Regulatory Information · 6 Einträge

Chemical: Benzene, (1,1-dimethylethyl)-

Hazard Traits - Nephrotoxicity and Other Toxicity to the Urinary System

Benzene, (1,1-dimethylethyl)- is listed on the EPA's Chemical Data Reporting (CDR) system. Manufacturers and importers of Benzene, (1,1-dimethylethyl)- are required to report information about their production and use of this chemical to the EPA under the Toxic Substances Control Act (TSCA). (40 eCFR Part 711)

REACH registered substance: tert-butylbenzene (EC: 202-632-4)

Benzene, (1,1-dimethylethyl)-: Does not have an individual approval but may be used under an appropriate group standard

The New Jersey Worker and Community Right to Know Act requires public and private employers to provide information about hazardous substances at their workplaces. (N.J.S.A. 34:5A-1 et. seq.)

Fire PotentialFlammable liquid when exposed to heat or flame.
Hazards SummaryEffects in lethal dose studies include somnolence and tremor; [RTECS] An irritant; [MSDSonline]
TSCA Requirements · 1 Eintrag

Chemie und Industrie

Pharmakologische Informationen

Metabolism/Metabolites · 3 Einträge

YIELDS 2,2-DIMETHYL-2-PHENYLETHANOL IN RABBIT. /FROM TABLE/

.../MONOBUTYLBENZENES/ ARE BELIEVED TO BE READILY METABOLIZED BY SIDE CHAIN HYDROXYLATION AND CONJUGATION FOR URINARY EXCRETION.

FROM CULTURES OF ACHROMOBACTER STRAINS A2 IN THE PRESENCE OF TERT-BUTYLBENZENE, A DIOL WAS ISOLATED AND IDENTIFIED AS 2,3-DIHYDRO-2,3-DIHYDROXY-TERT-BUTYLBENZENE. EVIDENCE FOR META CLEAVAGE OF THE AROMATIC RING AND FOR ACCUMULATION OF PIVALIC ACID IN THE CULTURES WAS ALSO OBTAINED.

Verwendung und Herstellung

Uses · 3 Einträge

Used in organic synthesis; as polymerization solvent; as polymer linking agent; as solvent (e.g., production of hydrogen peroxide); [HSDB]

Organic synthesis, polymerization solvent, polymer linking agent

SOLVENT, EG, IN PRODN OF HYDROGEN PEROXIDE

U.S. Imports · 2 Einträge

(1979) 8.46X10+5 GRAMS (PRINCPL CUSTMS DISTS)

(1981) 4.80X10+7 GRAMS (PRINCPL CUSTMS DISTS)

U.S. Production · 3 Einträge

2023: 75,000 - <500,000 lb

(1979) PROBABLY GREATER THAN 2.27X10+6 GRAMS

(1981) PROBABLY GREATER THAN 2.27X10+6 GRAMS

Industry UsesSolvent
Methods of Manufacturing · 5 Einträge

PREPD FROM BENZENE, ISOBUTYL CHLORIDE AND ALCL3; FROM ISOBUTYL ALCOHOL AND BENZENE BY TREATMENT WITH FUMING SULFURIC ACID ... .

... BY DECARBONYLATION OF BETA-PHENYLISOVALERALDEHYDE IN PRESENCE OF PD/C CATALYST.

PROBABLY BY REACTION OF BENZENE WITH ISOBUTYL OR T-BUTYL CHLORIDE IN THE PRESENCE OF ALUMINUM CHLORIDE

By the action of sodium on gamma-chloro-sec-butylbenzene.

For more Methods of Manufacturing (Complete) data for T-BUTYLBENZENE (6 total), please visit the HSDB record page.

Zugehörige Reaktionen

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Reaktionsgleichung von HRID 41901
HRID 41901als Eduktuspto-grants-2013_09
Reaktionsgleichung von HRID 93195
HRID 93195als EduktTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaktionsgleichung von HRID 94202
HRID 94202als EduktTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
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HRID 121436als EduktTraining data from https://doi.org/10.1039/C8SC04228D (2/10)
Reaktionsgleichung von HRID 133634
HRID 133634als Eduktuspto-grants-2008_06
Reaktionsgleichung von HRID 133635
HRID 133635als Eduktuspto-grants-2008_06
Reaktionsgleichung von HRID 140502
HRID 140502als ProduktTraining data from https://doi.org/10.1039/C8SC04228D (9/10)
Reaktionsgleichung von HRID 185342
HRID 185342als EduktTraining data from https://doi.org/10.1039/C8SC04228D (6/10)
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169.1 °C

169.1 °C @760 [mm Hg]

DecompositionWhen heated to decomposition it emits acrid smoke and fumes.
Melting Point · 2 Einträge

-57.8 °C

-57.8 °C

Vapor Density4.62 (Air= 1)

Physikochemische Eigenschaften

Schmelzpunkt
-58 °C · -58 °C
Siedepunkt
169 °C · 169 °C(lit.)
Dichte
0.867 g/mL · 0.867 g/mL at 25 °C(lit.)
Dampfdichte
3.16 · 3.16 (169 °C, vs air)
Dampfdruck
4.79 mm · 4.79 mm Hg ( 37.7 °C)
Brechungsindex
20 · n20/D 1.492(lit.)
Flammpunkt
94 °F · 94 °F
storage temp.
Flammables area
Löslichkeit
29.5 mg/l · 29.5mg/l
Aggregatzustand
Liquid
pka
14 · >14 (Schwarzenbach et al., 1993)
Farbe
Clear colorless to yellow
Explosionsgrenze
0.8 · 0.8-5.6%(V)
Wasserlöslichkeit
0.03 g/L · 0.03 g/L (20 ºC)
Merck
14 · 14,1551
BRN
1421537 · 1421537
Henry's Law Constant
(x 10-2 atmm3/mol): 1.17 at 25 °C (Hine and Mookerjee, 1975)
Dielectric constant
2.4 · 2.4(20℃)
Stabilität
Stable. Flammable. Incompatible with oxidizing agents, combustible material.
InChI
1S/C10H14/c1-10(2,3)9-7-5-4-6-8-9/h4-8H,1-3H3
InChIKey
YTZKOQUCBOVLHL-UHFFFAOYSA-N
SMILES
CC(C)(C)c1ccccc1
CAS Datenbank
98 · 98-06-6(CAS DataBase Reference)
NIST chemische Informationen
Benzene, tert-butyl-(98-06-6)
EPA chemische Informationen
tert-Butylbenzene (98-06-6)

Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. t-Butylbenzene is included on this list.

Flammable LimitsLower flammable limit: 0.7% at 212 °F (100 °C) by volume; Upper flammable limit: 5.7% at 212 °F (100 °C) by volume
DOT Hazard Classification · 2 Einträge

2-Methyl-2-phenylpropane

Marine pollutant

NFPA Hazard Classification · 3 Einträge

2 - Materials that, under emergency conditions, can cause temporary incapacitation or residual injury.

2 - Materials that must be moderately heated or exposed to relatively high ambient temperatures before ignition can occur. Materials would not under normal conditions form hazardous atmospheres with air, but under high ambient temperatures or under moderate heating could release vapor in sufficient quantities to produce hazardous atmospheres with air.

0 - Materials that in themselves are normally stable, even under fire conditions.

Other Hazardous ReactionsTHE TEMP RANGE FOR SMOOTH INTERACTION OF BROMOBENZENE, 1-BROMOBUTANE AND SODIUM IN ETHER TO GIVE BUTYLBENZENE IS CRITICAL. BELOW 15 °C REACTION IS DELAYED BUT LATER BECOMES VIGOROUS, AND ABOVE 30 °C THE REACTION BECOMES VIOLENT.
Hazard Classes and Categories · 3 Einträge

Flam. Liq. 3 (91.8%)

Flammable liquids - Category 3

Flammable agents - 3rd degree

State Drinking Water Guidelines · 3 Einträge

(CA) CALIFORNIA 260 ug/l

(FL) FLORIDA 280 ug/l

(NH) NEW HAMPSHIRE 260 ug/L

Shipment Methods and Regulations · 3 Einträge

No person may /transport,/ offer or accept a hazardous material for transportation in commerce unless that person is registered in conformance ... and the hazardous material is properly classed, described, packaged, marked, labeled, and in condition for shipment as required or authorized by ... /the hazardous materials regulations (49 CFR 171-177)./

The International Air Transport Association (IATA) Dangerous Goods Regulations are published by the IATA Dangerous Goods Board pursuant to IATA Resolutions 618 and 619 and constitute a manual of industry carrier regulations to be followed by all IATA Member airlines when transporting hazardous materials.

The International Maritime Dangerous Goods Code lays down basic principles for transporting hazardous chemicals. Detailed recommendations for individual substances and a number of recommendations for good practice are included in the classes dealing with such substances. A general index of technical names has also been compiled. This index should always be consulted when attempting to locate the appropriate procedures to be used when shipping any substance or article.

Lower Explosive Limit (LEL)7000 [ppm]

Sicherheit und Schutzausrüstung

Fire Fighting ProceduresTo fight fire, use foam, carbon dioxide, dry chemical, water spray, fog, mist.
Disposal Methods · 1 Eintrag

SRP: At the time of review, criteria for land treatment or burial (sanitary landfill) disposal practices are subject to significant revision. Prior to implementing land disposal of waste residue (including waste sludge), consult with environmental regulatory agencies for guidance on acceptable disposal practices.

Protective Action Criteria (PAC) · 3 Einträge

7.5 [mg/m3]

83 [mg/m3]

500 [mg/m3]

Toxikologische Informationen

Toxicological InformationRanking: 409 (total points: 528.34)
Environmental Fate · 3 Einträge

TERRESTRIAL FATE: Based on a classification scheme(1), an estimated Koc value of 1181(SRC), determined from a structure estimation method(2), indicates that t-butylbenzene is expected to have low mobility in soil(SRC). Volatilization of t-butylbenzene from moist soil surfaces is expected to be an important fate process(SRC) given an Henry's Law constant of 1.32X10-2 atm-cu m/mole(3), derived from its vapor pressure, 2.20 mm Hg(4), and water solubility, 29.5 mg/l(5). The potential for volatilization of t-butylbenzene from dry soil surfaces may exist(SRC) based upon its vapor pressure(4). However, adsorption to soil is expected to attenuate volatilization(SRC). Biodegradation from soil may occur based on activated sludge study results(6-9).

AQUATIC FATE: Based on a classification scheme(1), an estimated Koc value of 1181(SRC), determined from a structure estimation method(11), indicates that t-butylbenzene is expected to adsorb to suspended solids and sediment(SRC). Volatilization from water surfaces is expected(3) based upon an estimated Henry's Law constant of 1.32X10-2 atm-cu m/mole(4), derived from it's vapor pressure of 2.20 mm Hg(7) and water solubility of 29.5 mg/l(8). Using this Henry's Law constant and an estimation method(3), volatilization half-lives for a model river and model lake are 1 hr and 4 days, respectively(SRC). The volatilization half-life from a model pond is 30 days if adsorption is considered(9). According to a classification scheme(5), an estimated BCF of 291(SRC), from its log Kow of 4.11(2) and a regression-derived equation(6), suggests the potential for bioconcentration in aquatic organisms is high. Biodegradation from water may occur(10).

ATMOSPHERIC FATE: According to a model of gas/particle partitioning of semivolatile organic compounds in the atmosphere(1), t-butylbenzene, which has a vapor pressure of 2.20 mm Hg at 25 °C(2), is expected to exist solely as a vapor in the ambient atmosphere. Vapor-phase t-butylbenzene is degraded in the atmosphere by reaction with photochemically-produced hydroxyl radicals(SRC); the half-life for this reaction in air is estimated to be 3 days(SRC), calculated from its rate constant of 4.60X10-12 cu cm/molecule-sec at 25 °C(3).

Food Survey Valuest-Butylbenzene was identified as one of the 420 volatile flavor components of Idaho Russet Burbank baked potatoes, at a relative concn of 0.16, the most abundant being "1"(1).
Adverse EffectsNeurotoxin - Acute solvent syndrome
Effluent Concentrations · 1 Eintrag

t-Butylbenzene was detected, not quantified in the raw influent to a waste treatment system at a polyester finishing plant effluent(1). The compound was identified as a volatile from pre-aeration wastewater samples taken from a sewage treatment plant in Singapore(4). It was also identified as one of the 400 gas-phase hydrocarbon compounds in emissions from gasoline-powered motor vehicles in highway operation in the Allegheny Mountain Tunnel of the Pennsylvania Turnpike in 1979(2). t-Butylbenzene has been identified in effluent resulting from coal/refuse combustion(3).

Soil Adsorption/Mobility · 2 Einträge

Soil (Mediterranean red sandy clay) samples with different moisture contents (0.0, 0.8, 4.0, and 12%, wt/wt) were contaminated by vapors and/or liquid from a mixture containing 5 kerosene components (m-xylene, pseudo-cumene, t-butylbenzene (6.67% by vol), n-decane and n-dodecane). Vapor adsorption was found to be dependent on the vapor concn of each component and on the soil moisture content. Adsorption of t-butylbenzene on soil was 50 and 15 ug/g at 7 °C, 120 and 47 at 17 °C, 210 and 60 at 27 °C, and 330 and 100 ug/g at 34 °C for oven dried and air dried soil, respectively. The sorption coefficients of t-butylbenzene decr with incr temp but showed only a very slight variability between 20 and 34 °C, in air-dried soil. Volatilization from soil was high: 92.5% of t-butylbenzene was desorbed in less than 2 hr, and 99.7% in 16 hr.

Using a structure estimation method based on molecular connectivity indices(1), the Koc for t-butylbenzene can be estimated to be 1181(SRC). According to a classification scheme(2), this estimated Koc value suggests that t-butylbenzene is expected to have low mobility in soil.

TSCA Test Submissions · 5 Einträge

Acute oral toxicity was evaluated in groups of 10 ChR-CD male rats administered a single dose of tert-butyl-benzene by oral gavage at dose levels of 3000, 3400 and 3800 mg/kg body weight. Mortality was observed in one rat at 3000 mg/kg, 2 rats at 3400 mg/kg and 9 rats at 3800 mg/kg body weight; the LD50 value was calculated to be 3503 mg/kg body weight. Clinical observations after dosing included rapid and labored respiration, salivation, prostration, lacrimation, stained nose and mouth, diarrhea, chromodacryorrhea, a stained and wet perineal area, weakness, alopecia on the abdomen, stained eyes, stained abdominal area, and lethargy. Animals at all dose levels exhibited weight loss after dosing. Gross necropsy was not reported.

Acute dermal toxicity was evaluated in 4 male and 4 female rats receiving single occluded, percutaneous doses of undiluted tertiary butyl benzene at a dose level of 2000 mg/kg of body weight. The test article was held in contact with the intact skin for a 24 hour period. Mortality was not observed witihn 14 days of treatment and the LD50 was estimated to be greater than 2000 mg/kg of body weight. Clinical observation revealed no signs of intoxiciation. Gross necropsy was not reported.

Acute inhalation toxicity was evaluated in groups of 5 male and 5 female Wistar strain rats exposed to tertiary butyl benzene at measured concentrations of 4.0, 4.4 and 4.6 mg/lof air. The test armosphere was generated by using a thermostated wick-type saturator. Mortality was observed within 14 days of treatment in 3 of the female rats at the 4.6 mg/l dose; the LC50 was estimated to be approximately 4.6 mg/l. Clinical observations included salivation, lachrymation, a high stepping gait, dyspnoea, fasiculations, tremors, endophthalamus, and convulsions. Gross necropsy evaluation revealed no pathological changes in the survivors but was not reported for those animals that died.

The frequency of chromosomal aberrations was evaluated in vitro by exposing rats liver (RL1) cells to 10, 20 and 40 ug/ml of tertiary butyl benzene. No increases in the frequency of chromatid gaps, chromatid breaks or total chromosome aberrations was observed at any dose level. Tertiary butyl benzene did not induce chromosome damage in this assay.

For more TSCA Test Submissions (Complete) data for T-BUTYLBENZENE (6 total), please visit the HSDB record page.

Atmospheric Concentrations · 2 Einträge

URBAN/SUBURBAN: t-Butylbenzene was detected using gas chromatographic analysis of Paris air during the fall of 1972(1). The ambient air of the Los Angeles, CA basin contained t-butylbenzene at concns ranging from 0.019 to 0.045 ppm v/v(2). t-Butylbenzene was detected in the ambient air of the Kanawha Valley, WV, Houston, TX and vicinity, and the Los Angeles, CA basin(3). It was detected in ambient air of Los Angeles, CA during 1966-1968 and in Azusa, CA in 1967(4).

SOURCE DOMINATED: t-Butylbenzene was identified not quantified in the air of six industrial cities of the USSR(1). t-Butylbenzene was detected at concns ranging from 0 to 39 ug/cu m in ambient air samples from six sites around Gatwick Airport, London, collected during August to November 1979(2).

Artificial Pollution Sources · 1 Eintrag

t-Butylbenzene's production and use as a chemical intermediate and solvent(1) may result in its release to the environment through various waste streams(SRC). A composite gasoline sample obtained in Los Angeles, CA contained 0.12% t-butylbenzene by weight(2).

Environmental Biodegradation · 1 Eintrag

AEROBIC: t-Butylbenzene reached 0.3% of its theoretical BOD using an acclimated activated sludge inoculum and the 5-day BOD test at 20 °C(1). Theoretical BODs ranging from 0.6% to 39.8% were measured using the Warburg test(1,3-5). Alkylbenzenes are known to be oxidized by microorganisms(2). t-Butylbenzene was degraded using Moustorod Refinery wastewater inoculum, exhibiting 14, 100, and 100 % degradation in 7, 15, and 23 days, respectively; similar results were observed in non-aerated tests(6). t-Butylbenzene at a concn of 19-25 ppm was 10 and 30% removed after 20 and 80 days, respectively, in a grab sample study using water from the Ohio River, although volatilization could not be ruled out(7). Biological loss of t-butylbenzene was noted using artificial seawater acclimated with 100 ml gas oil at 20 °C for 3 days and then inoculated with North Sea coast water although the sample compound could not be resolved from 1,2,4-trimethylbenzene(8). t-Butylbenzene at a concn of 100 mg/l in an automated continuous respirometer study resulted in a growth rate of 1.21 1/day using an activated sludge inoculum following a lag of 4.40 days(9).

Sediment/Soil ConcentrationsSOIL: t-Butylbenzene was detected at a maximum concn of 141 mg/kg in soil under a building which was recently demolished. Contamination was caused by leakages of solvents and paint raw materials over many years(1).
Environmental Bioconcentration · 1 Eintrag

An estimated BCF of 291 was calculated for t-butylbenzene(SRC), using a log Kow of 4.11(1) and a regression-derived equation(2). According to a classification scheme(3), this BCF suggests the potential for bioconcentration in aquatic organisms is high.

Regulatorische Informationen

TSCA Requirements · 1 Eintrag

Pursuant to section 8(d) of TSCA, EPA promulgated a model Health and Safety Data Reporting Rule. The section 8(d) model rule requires manufacturers, importers, and processors of listed chemical substances and mixtures to submit to EPA copies and lists of unpublished health and safety studies. t-Butylbenzene is included on this list.

State Drinking Water Guidelines · 3 Einträge

(CA) CALIFORNIA 260 ug/l

(FL) FLORIDA 280 ug/l

(NH) NEW HAMPSHIRE 260 ug/L

Sicherheitsdaten

wgk
1
tsca
TSCA listed
ridadr
UN 2709 3/PG 3
hs_code
29029080
RTECS-Nr.
CY9120000
risk_code
10-20-38-51/53-36
hazard_code
Xn,F,Xi,N
hazard_note
Irritant/Flammable
safety_code
23-24/25-61-26
hazard_class
3
packing_group
III
Speicherklasse
3 - Flammable liquids
Giftige Stoffe Daten
98-06-6(Hazardous Substances Data)
Hazard Classifications
Flam. Liq. 3Skin Irrit. 2
Selbstentzündungstemperatur
842 °F
Formulations/Preparations
Technical, pure, research
Household ProductsInformation on 3 consumer products that contain tert-butylbenzene in the following categories is provided:
General Manufacturing Information · 2 Einträge

Paint and Coating Manufacturing

Benzene, (1,1-dimethylethyl)-: ACTIVE

Anwendungen

Verwendentert-Butylbenzene is an useful intermediate for manufacturing agrochemicals and pharmaceuticals. tert-Butyl Toluene is used as a solvent for resins.

Vor- und nachgelagerte Produkte

Vorgelagerte Rohstoffe

2-Chlor-2-methylpropanIsobutylene2-Methylpropanol-21-ChlorbutanDodecylbenzolAluminiumchloridBenzolHydrogenchloridAluminium chloride hexahydrate

Nachgelagerte Produkte

2-(1,1-Dimethylethyl)-1,4-benzoldiol4-t-Butyl propiophone1-Brom-4-(1,1-dimethylethyl)benzol2-(4-tert-Butylbenzyl)propionaldehyd5-tert-Butyl-2,4,6-trinitro-m-xylol4-[3-[4-(1,1-Dimethylethyl)phenyl]-2-methylpropyl]-2,6-dimethylmorpholin2-(4-tert-Butylphenoxy)cyclohexyl-prop-2-ynyl-sulfitp-(tert-Butyl)-α-chlortoluol4-tert-ButylbenzylaminBuclizin3-p-Cumenyl-2-methylpropionaldehyd