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4'-Isopropylacetophenone, 97%, Thermo Scientific Chemicals
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Catalog number B20581.14
also known as B20581-14
Price (USD)/ Each
145.00
-
Quantity:
25 g
Price (USD)/ Each
145.00
4'-Isopropylacetophenone, 97%, Thermo Scientific Chemicals
Catalog numberB20581.14
Price (USD)/ Each
145.00
-
Chemical Identifiers
CAS645-13-6
Specifications
Specification Sheet
Specification SheetAssay (GC)≥96.0%
Refractive Index1.5205-1.5255 @ 20?C
Appearance (Color)Clear colorless to pale yellow
FormLiquid
Identification (FTIR)Conforms
4'-Isopropylacetophenone is used as perfuming agents. It is also used as flavoring and fragrance agent. Indenes are yielded from the derivatives if this compound in one step synthesis using a heterogeneous catalyst.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
4′-Isopropylacetophenone is used as perfuming agents. It is also used as flavoring and fragrance agent. Indenes are yielded from the derivatives if this compound in one step synthesis using a heterogeneous catalyst.
Solubility
Soluble in alcohol. Insoluble in water.
Notes
Store at room temperature. Incompatible with strong oxidizing agents.
4′-Isopropylacetophenone is used as perfuming agents. It is also used as flavoring and fragrance agent. Indenes are yielded from the derivatives if this compound in one step synthesis using a heterogeneous catalyst.
Solubility
Soluble in alcohol. Insoluble in water.
Notes
Store at room temperature. Incompatible with strong oxidizing agents.
RUO – Research Use Only
General References:
- R Roesky.; J Weiguny.; H Bestgen.; U Dingerdissen. An improved synthesis method for indenes and styrenes by use of a ZnO/Al2O3 spinel catalyst. Appl. Catal., A. 1999, 176 (2),213-220 .
- Jacek Kijeński.; Marek Gliński.; C.W. Aquilar Quiroz. The direct synthesis of alkenylaromatics during catalytic transfer reduction (CTR) of aralkyl ketones with isopropyl alcohol over MgO of enhanced acidity. Appl. Catal., A. 1997, 150 (1), 77-84 .