33433-82-8

Basic information

• Product Name: CALCIUM DIPROPYLACETATE HYDRATE
• Synonyms: 2-propyl-pentanoicacicalciumsalt;2-propylpentanoicacidcalciumsalt;2-propyl-valericacicalciumsalt(2:1);2-propylvalericacidcalciumsalt(2:1);calciumalpha,alpha-dipropylacetate;calciumdipropylacetate;calciumvalproate;dipropylacetatedecalcium
• CAS NO: 33433-82-8
• Molecular Formula: 2C₈H₁₅O₂*Ca
• Molecular Weight: 326.49
• EINECS: 251-521-7
• Mol File: 33433-82-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 220 °C at 760 mmHg
• Flash Point: 116.6 °C
• Appearance: /
• Density: g/cm³
• Vapor Pressure: 0.0435mmHg at 25°C
• CAS DataBase Reference: CALCIUM DIPROPYLACETATE HYDRATE(CAS DataBase Reference)
• NIST Chemistry Reference: CALCIUM DIPROPYLACETATE HYDRATE(33433-82-8)
• EPA Substance Registry System: CALCIUM DIPROPYLACETATE HYDRATE(33433-82-8)

Safety Data

• Hazardous Substances Data: 33433-82-8(Hazardous Substances Data)

Usage

General Description

Calcium Dipropylacetate Hydrate (also known as Calcium Propionate Hydrate) is a chemical compound commonly used as a preservative in food due to its anti-fungal properties. Its molecular formula is C6H10CaO4. This white powdered substance is found in a variety of foods like bread, processed meat, and dairy products. It prevents the growth of mold and some bacteria, thereby increasing the shelf life of food products. It is safe for consumption in regulated amounts, although some people may experience allergic reactions or other side effects. It is also used in tobacco products and pharmaceuticals, indicating its versatile applications.

InChI:InChI=1/2C8H16O2.Ca/c2*1-3-5-7(6-4-2)8(9)10;/h2*7H,3-6H2,1-2H3,(H,9,10);/q;;+2/p-2

Downstream Products

• 99-66-1 valproic acid 

Relevant articles and documents

Divalproex sodium method for the recovery and use of the crystallization mother liquor

The invention provides a recycling method of divalproex sodium crystallization mother liquor. The method comprises the following steps: 1) concentrating the divalproex sodium crystallization mother liquor to obtain a solid-state mixture containing divalproex sodium; 2) mixing the solid-state mixture obtained in the step 1) with an alkaline solution to dissolve the solid-state mixture to further obtain a mixed solution; 3) mixing the mixed solution obtained in the step 2) with an inorganic salt to produce a valproate precipitate, and separating to obtain the valproate precipitate; 4) mixing the valproate precipitate obtained in the step 3) with an acid solution to obtain an organic layer, and performing fractionation on the organic layer to obtain valproic acid. Through the method provided by the invention, the yield of obtained valproic acid can be as high as 93%, the purity is not lower than 99.6%, and valproic acid can meet medicinal requirements; the method provided by the invention has the advantages of simplicity, easiness in operation, easiness in control of reaction process and effect of reducing actual production cost, and is in line with requirements of industrial mass production.