ChemicalBook Product Catalog Chemical Reagents Organic reagents Aromatics 1,4-Di-tert-butylbenzene

1,4-Di-tert-butylbenzene

1,4-Di-tert-butylbenzene Basic information
Product Name:1,4-Di-tert-butylbenzene
Synonyms:P-DI-TERT-BUTYL BENZENE;1,4-bis(1,1-dimethylethyl)-benzen;1,4-tert-dibutylbenzene;Benzene, p-di-tert-butyl-;benzene,1,4-di-tert-butyl-;bis(1,1-dimethylethyl)-benzen;bis(1,1-dimethylethyl)benzene;p-di-tert-butyl-benzen
CAS:1012-72-2
MF:C14H22
MW:190.32
EINECS:213-790-9
Product Categories:Aromatic Hydrocarbons (substituted) & Derivatives;Benzene derivates;Arenes;Building Blocks;Organic Building Blocks
Mol File:1012-72-2.mol
1,4-Di-tert-butylbenzene Structure
1,4-Di-tert-butylbenzene Chemical Properties
Melting point 76-78 °C(lit.)
Boiling point 236 °C(lit.)
density 0.985
refractive index 1.4955 (estimate)
Fp 236°C
storage temp. Sealed in dry,Room Temperature
form crystalline
color white
Water Solubility Insoluble in water. Soluble in ethanol, benzene, carbon tetrachloride.
BRN 1617000
CAS DataBase Reference1012-72-2(CAS DataBase Reference)
NIST Chemistry ReferenceBenzene, 1,4-bis(1,1-dimethylethyl)-(1012-72-2)
EPA Substance Registry Systemp-Di-tert-butylbenzene (1012-72-2)
Safety Information
Hazard Codes N
Risk Statements 50/53
Safety Statements 22-24/25-60-61
RIDADR UN 3077 9/PG 3
WGK Germany 3
RTECS CY8444000
TSCA Yes
HazardClass 9
PackingGroup III
HS Code 29029090
MSDS Information
ProviderLanguage
1,4-Bis(1,1-dimethylethyl)-benzene English
SigmaAldrich English
ACROS English
ALFA English
1,4-Di-tert-butylbenzene Usage And Synthesis
Chemical Propertieswhite crystals or crystalline powder
Uses1,4-di-tert-butylbenzene (DTBB) is crystallized from several organic solvents to study the effect of solvents and crystallization conditions on its habit.
Uses1,4-di-tert-butylbenzene (DTBB) is used as a crystallized form from several organic solvents to study the effect of solvents and crystallization conditions on its habit. It is also used as a solvent and an intermediate in the manufacture of other organic compounds for the finished products of such as curing agents, engineering plastics and cross-linking agents.
Purification MethodsCrystallise it from Et2O or EtOH and dry it under vacuum over P2O5 at 55o. [Tanner et al. J Org Chem 52 2142 1987, Beilstein 5 II 344.]
2,5-BIS(1,1-DIMETHYLBUTYL)-4-METHOXYPHENOL 2,5-DI-TERT-BUTYLANILINE C21 RING-C MONOAROMATIC STERANE (5ALPHA(H),10BETA(CH3)/5BETA(H),10BETA(CH3)) 4-t-Butylbenzamide 2-Acetoxy-5-acetoxymethyl-1,3-di-tert-butylbenzene 1,4-DI-TERT-BUTYL-2,5-DIMETHOXYBENZENE Recombinant Human Telomerase ALPHA,ALPHA'-BIS(4-HYDROXYPHENYL)-1,4-DIISOPROPYLBENZENE N N'-BIS(2 5-DI-T-BU-PHENYL)-3 4 9 10- ALPHA,ALPHA,ALPHA'-TRIS(4-HYDROXYPHENYL)-1-ETHYL-4-ISOPROPYLBENZENE P-DI-TERT-HEXYL BENZENE 2,5-Bis(1,1,3,3-tetramethylbutyl)hydroquinone 1,4-DI-TERT-PENTYLBENZENE ALPHA,ALPHA'-BIS(4-AMINOPHENYL)-1,4-DIISOPROPYLBENZENE ALPHA,ALPHA'-DI-TERT-BUTYL-ALPHA,ALPHA'-DICYANO-2,3,5,6-TETRAFLUORO-1,4-BENZENEDIACETONITRILE C27 RING-C MONOAROMATIC STERANE (5BETA(H),10BETA(CH3)/5A(H),10BETA(CH3)) 1,1,4,4,5,5,8,8-OCTAMETHYL-1,2,3,4,5,6,7,8-OCTAHYDROANTHRACENE C28/C29 RING-C MONOAROMATIC STERANE
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