4-Vinylbenzyl chloride
ALDRICH/436887 - 90%
Synonym: 4-
CAS Number: 1592-20-7
Empirical Formula (Hill Notation): C9H9Cl
Molecular Weight: 152.62
EC Number: 216-471-2
MDL Number: MFCD00051362
Linear Formula: H2C=CHC6H4CH2Cl
Product Type: Chemical
This picture is provided solely for illustration purposes. Optical properties of the actual product may deviate. Relevant product information is printed on labeled products and other accompanying or available information material. This image depicts SKU: 436887-100ML.
| assay | 90% |
| bp | 229 °C (lit.) |
| contains | 500 ppm tert-butylcatechol as inhibitor |
| density | 1.083 g/mL at 25 °C (lit.) |
| form | liquid |
| InChI | 1S/C9H9Cl/c1-2-8-3-5-9(7- |
| InChI key | ZRZHXNCATOYMJH-UHFFFAOYSA |
| Quality Level | 200  |
| refractive index | n |
| SMILES string | ClCc1ccc(C=C)cc1 |
| storage temp. | 2-8°C |
| viscosity | 1,830 cP(25 °C)(lit.) |
| Application: | 4-Vinylbenzyl chloride can be used as a monomer to synthesize: • The hypercross-linked polymer for supercapacitor applications. Incorporation of 4-vinyl benzyl chloride contributes to the formation of a porous structure and specific surface area which facilitate efficient electrolyte ion diffusion and provide ample sites for charge storage, leading to enhanced electrochemical performance. • The polymeric thin films by the matrix-assisted pulsed laser evaporation (MAPLE) technique. The resulting polymeric thin films can exhibit non-linear optical effects such as optical second harmonic generation, electro-optic modulation, or optical frequency conversion. These properties make them suitable for various applications in non-linear optic devices. |
| General description: | 4-Vinylbenzyl chloride (VBC) is commonly used as a monomer that belongs to the class of aryl chlorides and contains both a vinyl group (CH2=CH-) and a benzyl chloride group (C6H4CH2Cl) in its structure. It is used as a reactive building block in various polymerization reactions to synthesize different types of polymers with excellent thermal stability, chemical resistance and good film-forming properties. It is commonly utilized in the production of resins, coatings, adhesives, and ion-exchange resins. It offers versatility in polymer synthesis, allowing for the introduction of desired functionalities into polymers. It is also: • A component of ion exchange resins, photo-resist polymers, cross-linkable fibers, coupling agents and electroconducting polymers. • Starter for various copolymer preparations. • Dual functional monomer. Readily derivatized by chloride displacement. |
| Packaging: | 25, 100 mL in glass bottle |
| Symbol |   GHS05,GHS06 |
| Signal word | Danger |
| Hazard statements | H302 - H311 - H314 - H317 |
| Precautionary statements | P261 - P270 - P280 - P301 + P312 - P303 + P361 + P353 - P305 + P351 + P338 |
| Hazard Codes | C |
| Risk Statements | 21/22-34-43 |
| Safety Statements | 26-36/37/39-45 |
| RIDADR | UN 3265 8 / PGII |
| WGK Germany | WGK 3 |
| Flash Point(F) | 219.2 °F - closed cup |
| Flash Point(C) | 104 °C - closed cup |
| Purity | 90% |
| bp | 229 °C (lit.) |
| Density | 1.083 g/mL at 25 °C (lit.) |
| Refractive Index | n |
| Storage Temp. | 2-8°C |
| UNSPSC | 12162002 |