Skip to Content
MilliporeSigma
All Photos(1)

Key Documents

View All Documentation

523062

Sigma-Aldrich

3-Vinylbenzaldehyde

97%

Synonym(s):

3-Ethenylbenzaldehyde, 3-Formylstyrene, m-Formylstyrene, m-Vinylbenzaldehyde

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
H2C=CHC6H4CHO
CAS Number:
19955-99-8
Molecular Weight:
132.16
MDL number:
MFCD02093761
UNSPSC Code:
12352100
PubChem Substance ID:
24874294
NACRES:
NA.22

Assay

97%

refractive index

n20/D 1.58 (lit.)

density

1.04 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

[H]C(=O)c1cccc(C=C)c1

InChI

1S/C9H8O/c1-2-8-4-3-5-9(6-8)7-10/h2-7H,1H2

InChI key

CATOVPRCMWIZLR-UHFFFAOYSA-N

General description

3-Vinylbenzaldehyde (3-VBAL) contains a vinyl group bonded to the aromatic ring of benzaldehyde. Pulsed plasma polymerization of 3-VBAL has been described.

Application

3-Vinylbenzaldehyde may be used in the preparation of:
  • 2-(3-vinylphenyl)-1,3-dioxolane
  • various substituted imines
  • monomer bearing a 2,4,5-triphenylimidazole moiety
  • poly(3-vinylbenzaldehyde-co-dimethylacrylamide) (PVBA-co-PDMA) copolymers

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

210.0 °F - closed cup

Flash Point(C)

98.9 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

R P Garrod et al.
Langmuir : the ACS journal of surfaces and colloids, 23(2), 689-693 (2007-01-11)
A simple two-step plasmachemical methodology is outlined for the fabrication of microcondensor surfaces. This comprises the creation of a superhydrophobic background followed by pulsed plasma deposition of a hydrophilic polymer array. Microcondensation efficiency has been explored in terms of the
New benzylidene oxazolone derived polymeric photoswitches for light-induced tunable thermoresponsive behaviors.
Balamurugan A and Lee H.
Polym. Chem., 5(22), 6426-6430 (2014)
Laura L Santos et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 15(33), 8196-8203 (2009-07-18)
Substituted imines, alpha,beta-unsaturated imines, substituted secondary amines, and beta-amino carbonyl compounds have been synthesized by means of new cascade reactions with mono- or bifunctional gold-based solid catalysts under mild reaction conditions. The related synthetic route involves the hydrogenation of a
A novel de-cross-linking system from cross-linked polymer to linear polymer utilizing pressure or visible light irradiation.
Iwamura T and Sakaguchi M.
Macromolecules, 41(23), 8995-8999 (2008)
Protection and polymerization of functional monomers. 15. Anionic living polymerizations of 2-(3-vinylphenyl)-1, 3-dioxolane and related monomers.
Ishizone T, et al.
Macromolecules, 24(7), 1449-1454 (1991)
View All Related Papers

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service