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1,3-dioxan-5-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15180-69-5

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15180-69-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15180-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,8 and 0 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 15180-69:
(7*1)+(6*5)+(5*1)+(4*8)+(3*0)+(2*6)+(1*9)=95
95 % 10 = 5
So 15180-69-5 is a valid CAS Registry Number.

15180-69-5Downstream Products

15180-69-5Relevant academic research and scientific papers

Green Acetylation of Solketal and Glycerol Formal by Heterogeneous Acid Catalysts to Form a Biodiesel Fuel Additive

Dodson, Jennifer R.,Leite, Thays d C. M.,S. Pontes, Nathália,Peres Pinto, Bianca,Mota, Claudio J. A.

, p. 2728 - 2734 (2014)

A glut of glycerol has formed from the increased production of biodiesel, with the potential to integrate the supply chain by using glycerol additives to improve biodiesel properties. Acetylated acetals show interesting cold flow and viscosity effects. Herein, a solventless heterogeneously catalyzed process for the acetylation of both solketal and glycerol formal to new products is demonstrated. The process is optimized by studying the effect of acetylating reagent (acetic acid and acetic anhydride), reagent molar ratios, and a variety of commercial solid acid catalysts (Amberlyst-15, zeolite Beta, K-10 Montmorillonite, and niobium phosphate) on the conversion and selectivities. High conversions (72–95 %) and selectivities (86–99 %) to the desired products results from using acetic anhydride as the acetylation reagent and a 1:1 molar ratio with all catalysts. Overall, there is a complex interplay between the solid catalyst, reagent ratio, and acetylating agent on the conversion, selectivities, and byproducts formed. The variations are discussed and explained in terms of reactivity, thermodynamics, and reaction mechanisms. An alternative and efficient approach to the formation of 100 % triacetin involves the ring-opening, acid-catalyzed acetylation from solketal or glycerol formal with excesses of acetic anhydride.

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