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About This Item
Empirical Formula (Hill Notation):
C10H10
CAS Number:
Molecular Weight:
130.19
MDL number:
UNSPSC Code:
12162002
PubChem Substance ID:
NACRES:
NA.23
Quality Level
Assay
85%
contains
3000 ppm hydroquinone as stabilizer
composition
meta isomer, ~10 wt. %
refractive index
n20/D 1.5470 (lit.)
density
0.914 g/mL at 25 °C (lit.)
shipped in
dry ice
storage temp.
−70°C
SMILES string
C=Cc1ccc(C=C)cc1
InChI
1S/C10H10/c1-3-9-5-7-10(4-2)8-6-9/h3-8H,1-2H2
InChI key
WEERVPDNCOGWJF-UHFFFAOYSA-N
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General description
p-Divinylbenzene(DVB) is a cross-linking agent, which is used in a variety of polymeric processes such as copolymerization of styrene to improve the thermo-mechanical properties of the composite.
Application
DVB can be cross-linked with styrene/vinylbenzene chloride and incorporated with multi-walled carbon nanotubes (MWCNTs) to form new microporous nanocomposites for water remediation. It can also be used in combination with polyethylene glycol diacrylate to form linkages with polyethylene oxide (PEO), which can be used as an electrolytic material for lithium batteries.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
156.2 °F - closed cup
Flash Point(C)
69 °C - closed cup
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Cross-linked solid polymer electrolyte for all-solid-state rechargeable lithium batteries.
Garcia-Calvo O, et al.
Electrochimica Acta, 220(12), 587-594 (2016)
Novel CeO2 promoted TiO2-ZrO2 nano-oxide catalysts for oxidative dehydrogenation of p-diethylbenzene utilizing CO2 as soft oxidant.
Rao KN, et al.
Applied Catalysis. B, Environmental, 100(3-4), 472-480 (2010)
I Linhart et al.
Xenobiotica; the fate of foreign compounds in biological systems, 19(6), 645-653 (1989-06-01)
1. Biotransformation of 1,4-diethenylbenzene (1) in rat was studied. Six urinary metabolites, namely, N-acetyl-S-[2-(4-ethenylphenyl)-2-hydroxyethyl]-L-cysteine (3), N-acetyl-S-[1-(4-ethenylphenyl)-2-hydroxyethyl]-L-cysteine (4), N-acetyl-S-[1-(4-formylphenyl)-2-hydroxyethyl]-L-cysteine (5), 1-(4-ethenylphenyl)ethane-1,2-diol (6), 4-ethenylbenzoic acid (9) and 4-ethenylbenzoyl-glycine (12) were isolated and identified by n.m.r. and mass spectrometry. 2. G.l.c.-mass spectral analysis
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