4-Tert-Butylstyrene

Product Information

Molecular Formula:
C12H16
Molecular Weight:
160.25
Description
Applications: 4-TERT-BUTYLSTYRENE is a useful research chemical.
Synonyms
1-(1,1-dimethylethyl)-4-ethenyl-benzen; 1-(1,1-Dimethylethyl)-4-ethenylbenzene; 1-tert-Butyl-4-vinylbenzene; Benzene, 1-(1,1-dimethylethyl)-4-ethenyl-; p-t-Butylstyrene; p-tert-Butylstyrene
IUPAC Name
1-tert-butyl-4-ethenylbenzene
Canonical SMILES
CC(C)(C)C1=CC=C(C=C1)C=C
InChI
InChI=1S/C12H16/c1-5-10-6-8-11(9-7-10)12(2,3)4/h5-9H,1H2,2-4H3
InChI Key
QEDJMOONZLUIMC-UHFFFAOYSA-N
Boiling Point
212.6±10.0 °C at 760 mmHg
Melting Point
-38ºC
Flash Point
177.8 ℃F - closed cup
Purity
>90% by GC
Density
0.9±0.1 g/cm3
Appearance
Colorless Liquid
Application
Used to make unsaturated polyester resin and rubber and plastic products.
Storage
Freezer
Refractive Index
n20/D 1.526 (lit.)

Safety Information

Hazards
H315:
Causes skin irritation.
H319:
Causes serious eye irritation.
Precautionary Statement
P264:
Wash thoroughly after handling.
P280:
Wear protective gloves/protective clothing/eye protection/face protection.
P302+P352:
IF ON SKIN:
Wash with plenty of soap and water.
P332+P313:
If skin irritation occurs:
Get medical advice/attention.
P337+P313:
If eye irritation persists:
Get medical advice/attention.
P362+P364:
Take off contaminated clothing. [As modified by IV ATP].
And wash it before reuse. [Added by IV ATP].
Signal Word
Warning

Computed Properties

XLogP3
4.4
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
0
Rotatable Bond Count
2
Exact Mass
160.125200510 g/mol
Monoisotopic Mass
160.125200510 g/mol
Topological Polar Surface Area
0Ų
Heavy Atom Count
12
Formal Charge
0
Complexity
142
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-114057934-A Dispersing agent for drilling fluid and preparation method thereof 2021-12-02
CN-113881114-A Modified rubber and preparation method thereof 2021-11-10
CN-113754601-A Synthesis method of N2-beta-sulfanyl triazole derivative 2021-10-25
CN-113880873-A Hydroboration reaction method for catalyzing olefin by calcium halide 2021-10-25
CN-113717209-A Synthesis method of alkyl silicon compound 2021-10-12
CN-113912795-A Polyisomonoolefin copolymer, preparation method thereof, initiator and application 2021-09-30
CN-113897049-A Damping material containing pore embedded particles and preparation method thereof 2021-09-10
CN-113801551-A Two-component coating composition and articles made therefrom 2021-08-26
CN-113621099-A Fluorescent microsphere and preparation method and application thereof 2021-08-25
CN-113736207-A Multi-component surface organic-inorganic composite nano particle and preparation method and application thereof 2021-08-17

Literatures

PMID Publication Date Title Journal
22763487 2012-08-18 A ligand exchange strategy for one-pot sequential synthesis of (hyperbranched polyethylene)-b-(linear polyketone) block polymers Chemical communications (Cambridge, England)
21241147 2011-01-14 Temperature-ramping measurement of dye reorientation to probe molecular motion in polymer glasses The Journal of chemical physics
19826731 2009-11-07 Palladium(II)-catalyzed copolymerization of styrenes with carbon monoxide: mechanism of chain propagation and chain transfer Dalton transactions (Cambridge, England : 2003)
18455384 2009-01-01 Recycling of waste tyre rubber into oil absorbent Waste management (New York, N.Y.)
15914079 2005-12-01 Vibrational spectroscopic encoding of polystyrene-based resin beads: converting the encoding peaks into barcodes Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
16171341 2005-09-27 Preparation and spectroscopic properties of multiluminophore luminescent oxygen and temperature sensor films Langmuir : the ACS journal of surfaces and colloids
12940737 2003-09-03 Preparation, physical properties, on-bead binding assay and spectroscopic reliability of 25 barcoded polystyrene-poly(ethylene glycol) graft copolymers Journal of the American Chemical Society
12841751 2003-07-10 Poly(4-tert-butylstyrene) as a soluble polymer support in homogeneous catalysis Organic letters
12822939 2003-07-02 Photodecomposition of an acaricide, fenazaquin, in aqueous alcoholic solution Journal of agricultural and food chemistry
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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