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535583

Sigma-Aldrich

p-Divinylbenzene

85%

Synonym(s):

1,4-Diethenylbenzene, 1,4-Divinylbenzene

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About This Item

Empirical Formula (Hill Notation):
C10H10
CAS Number:
105-06-6
Molecular Weight:
130.19
MDL number:
MFCD00008622
UNSPSC Code:
12162002
PubChem Substance ID:
24878089
NACRES:
NA.23

Quality Level

200

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.

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H302,H315,H319,H411

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Applied Catalysis. B, Environmental, 100(3-4), 472-480 (2010)
I Linhart et al.
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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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