522864
Methylstyrene
60% meta, 40% para and 1% ortho, 99%, contains ~50 ppm 4-tert-butylcatechol as inhibitor
Synonym(s):
Vinyltoluene
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About This Item
Linear Formula:
CH3C6H4CH=CH2
CAS Number:
Molecular Weight:
118.18
Beilstein/REAXYS Number:
1209317
EC Number:
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
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Quality Level
assay
99%
contains
~50 ppm 4-tert-butylcatechol as inhibitor
refractive index
n20/D 1.5425 (lit.)
bp
168 °C (lit.)
density
0.893 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
Cc1ccc(C=C)cc1.Cc2cccc(C=C)c2
InChI
1S/2C9H10/c1-3-9-6-4-8(2)5-7-9;1-3-9-6-4-5-8(2)7-9/h2*3-7H,1H2,2H3
InChI key
VAPKHDZBJXRVNG-UHFFFAOYSA-N
Related Categories
General description
Methylstyrene can be used as a monomer in the synthesis of block copolymers for resins and adhesives. It is widely used as a starting material to prepare latexes for paper coating applications.
Application
- Applications in cancer therapy: Investigation into (−)-Epicatechin incorporated in phytopharmaceuticals for cancer treatment discusses its bioactive properties and synergistic effects when combined with other therapeutic agents, providing new avenues for integrative cancer therapies (Idoudi et al., 2024).
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Danger
Hazard Classifications
Acute Tox. 4 Inhalation - Asp. Tox. 1 - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
3 - Flammable liquids
wgk_germany
WGK 3
flash_point_f
125.6 °F - closed cup
flash_point_c
52 °C - closed cup
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A comprehensive structural and electrical characterization of solution-processed blend films of 6,13-bis(triisopropylsilylethynyl) pentacene (TIPS-pentacene) semiconductor and poly(alpha-methylstyrene) (PalphaMS) insulator was performed to understand and optimize the blend semiconductor films, which are very attractive as the active layer in solution-processed organic
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The interaction of the nitroxide radical traps (Tempo and Dmpo) and radicals produced in the electrophilic fluorination of olefins (styrene and alpha-methylstyrene) and Selectfluor (1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octanebis(tetrafluoroborate) (F-TEDA-BF(4)) (1)) was investigated by electrospray ionization mass spectrometry (ESI-MS). Tempo succeeded in intercepting the
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