Stearoylbenzoylmethane Chemical Properties

Melting point:

56°C

Boiling point:

493.4±18.0 °C(Predicted)

Density 

0.931±0.06 g/cm3(Predicted)

storage temp. 

Sealed in dry,Room Temperature

pka

8.87±0.23(Predicted)

CAS DataBase Reference

58446-52-9(CAS DataBase Reference)

EPA Substance Registry System

1,3-Eicosanedione, 1-phenyl- (58446-52-9)

Stearoylbenzoylmethane Usage And Synthesis

Description

Stearyl Benzoylmethane has high transmittance, non-toxic and tasteless; and solid or liquid calcium / zinc, barium / zinc and other heat stabilizer and can greatlyimprove the initial coloring of PVC, transparency, long-term stability, and processing In the precipitation and “zinc burning” and so on; it ischaracterized by zinc soap has a good synergistic effect, the formula added to the product can effectively inhibit the “zinc burn”, suitable for hard, non-toxic, odorless areas of implementation, promote calcium / Zinc composite stabilizer replacement, widely used in medical, food packaging and other non-toxic transparent PVC products (such as PVC bottles, sheet, transparent film, etc.).

Uses

Stearoyl benzoyl methane can greatly improve initial coloring performance of PVC, transparency, and long-term stability if it is used with solid or liquid calcium/zinc, barium/zinc and other heat stabilizers. It is widely used in non-toxic and transparent PVC products such as pharmaceutical and food packages.

Definition

ChEBI: 1-Phenyl-1,3-eicosanedione is an aromatic ketone.

Synthesis

The general procedure for the synthesis of 1-phenylene eicosane-1,3-dione from methyl stearate and acetophenone is as follows: the experimental setup is a 1 liter volume classical glass double jacketed chemical engineering reactor equipped with an efficient mixing system. A separation column with variable reflux condenser was mounted on top of the reactor and a recirculation loop equipped with a gear pump and a 600 W microwave generator. First, 440 ml of xylene, 178.76 g of methyl sulfate and 42.87 g of powdered sodium methanol were added to the reactor. After the reagents were added, a continuous stream of nitrogen was used to inert the reactor's internal environment. The reaction mixture was circulated at a rate of 15 kg/h through an external loop. The mixture was allowed to boil and maintained at full reflux followed by activation of the microwave source. 68.45 g of acetophenone was slowly added over a period of 1 hour. After the addition of acetophenone was completed, the reaction was continued for 15 min, during which the generated methanol and ethanol were removed from the reaction mixture.After 15 min, the microwave source was switched off and the reaction mixture was heated to acidify the reaction mixture, followed by washing. Gas chromatographic analysis showed that acetophenone was almost completely consumed and the titer of 1-phenyloctane-1,3-dione was 98.3%. The production rate of 1-phenyleicosane-1,3-dione in the reaction stage was 173.2 kg-h?1-m?3.

storage

Stearoylbenzoylmethane can store in a cool dry place, to prevent moisture, heat. Do not damage the packaging when handling.

References

[1] Patent: US2014/88325, 2014, A1. Location in patent: Paragraph 0125; 0126; 0127; 0128; 0129
[2] Patent: US6410795, 2002, B1
[3] Patent: US5015777, 1991, A
[4] Patent: EP507013, 1992, A1

Stearoylbenzoylmethane(58446-52-9)Related Product Information

• Cupric stearate
• STEARYLDIETHANOLAMINE
• Benzoylacetone
• Ethyl benzoylformate
• Sodium stearyl lactate
• Stearic acid
• Benzoyl peroxide
• P-AMINOBENZAMIDE GLUTAMIC ACID
• 1-Bromooctadecane
• Barium stearate
• Butyl stearate
• Lithium stearate
• Octadecanamide
• Sodium stearate
• Dibenzoylmethane
• 1-Octadecanol
• STEARAMIDOPROPYL DIMETHYLAMINE
• Magnesium stearate
• Stearoyl Benzoyl Methane