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58446-52-9

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58446-52-9 Usage

Description

Stearoylbenzoylmethane is a high transmittance, non-toxic, and tasteless compound that, when combined with solid or liquid calcium/zinc, barium/zinc, and other heat stabilizers, can significantly enhance the initial coloring, transparency, and long-term stability of PVC. It is characterized by its synergistic effect with zinc soap, effectively inhibiting "zinc burn" and promoting the use of calcium/zinc composite stabilizers in hard, non-toxic, and odorless applications.

Uses

Used in Non-toxic Transparent PVC Products:
Stearoylbenzoylmethane is used as a heat stabilizer and synergist for improving the initial coloring performance, transparency, and long-term stability of PVC in non-toxic and transparent applications.
Used in Medical Industry:
Stearoylbenzoylmethane is used as a stabilizer in the production of non-toxic transparent PVC products for medical applications, such as PVC bottles, sheets, and transparent films.
Used in Food Packaging Industry:
Stearoylbenzoylmethane is used as a stabilizer in the production of non-toxic transparent PVC products for food packaging, ensuring the safety and quality of the packaging materials.

storage

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

Check Digit Verification of cas no

The CAS Registry Mumber 58446-52-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,4,4 and 6 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 58446-52:
(7*5)+(6*8)+(5*4)+(4*4)+(3*6)+(2*5)+(1*2)=149
149 % 10 = 9
So 58446-52-9 is a valid CAS Registry Number.
InChI:InChI=1/C26H42O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-19-22-25(27)23-26(28)24-20-17-16-18-21-24/h16-18,20-21H,2-15,19,22-23H2,1H3

58446-52-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name Stearoylbenzoylmethane

1.2 Other means of identification

Product number -
Other names 1-phenylicosane-1,3-dione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:58446-52-9 SDS

58446-52-9Downstream Products

58446-52-9Relevant articles and documents

METHOD FOR SYNTHESIZING BETA-DICARBONYL COMPOUNDS

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Paragraph 0125; 0126; 0127; 0128; 0129, (2014/04/03)

A method for synthesizing beta-dicarbonyl compounds, particularly beta-diketones, from at least two carbonyl compounds, such as esters and ketones, in the presence of a strong base or a mixture of strong bases by Claisen condensation with a titer of greater than 95%. The method includes providing a synthesis reactor on which a separation column, provided with a condenser and with at least one microwave generator, is mounted; feeding a first carbonyl compound and the strong base into the synthesis reactor; heating the reactor and starting up the condenser; starting up the microwave generator(s); when the mixture is brought to a boil at total flux, feeding the second carbonyl compound into the reactor; and after a waiting time, stopping the reactor and acidifying and washing the reaction mixture.)

Process for the preparation of aromatic beta-diketones

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, (2008/06/13)

A process is disclosed for the preparation of aromatic beta-diketones by the reaction of an acetophenone and a molar excess of an aliphatic ester or an ester of benzoic acid in the presence of sodium alkoxide condensation agent in an aromatic hydrocarbon solvent at a temperature in the range 120-170oC. The solvent and excess ester reactant may be recycled after separation of the aromatic beta-diketone product.

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