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10588-88-2

Stearic acid 2β-phenyl-1,3-dioxan-5β-yl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 10588-88-2 Structure

  • Basic information

    1. Product Name: Stearic acid 2β-phenyl-1,3-dioxan-5β-yl ester
    2. Synonyms:
    3. CAS NO:10588-88-2
    4. Molecular Formula: C28H46O4
    5. Molecular Weight: 446.66244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 10588-88-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Stearic acid 2β-phenyl-1,3-dioxan-5β-yl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Stearic acid 2β-phenyl-1,3-dioxan-5β-yl ester(10588-88-2)
    11. EPA Substance Registry System: Stearic acid 2β-phenyl-1,3-dioxan-5β-yl ester(10588-88-2)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 10588-88-2(Hazardous Substances Data)

10588-88-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10588-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,8 and 8 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 10588-88:
(7*1)+(6*0)+(5*5)+(4*8)+(3*8)+(2*8)+(1*8)=112
112 % 10 = 2
So 10588-88-2 is a valid CAS Registry Number.

10588-88-2Relevant articles and documents

Rapid access to structured triacylglycerols acylated with n-3 polyunsaturated fatty acids for nutritional applications

Vaique, Emilie,Guy, Alexandre,Couedelo, Leslie,Gosse, Isabelle,Durand, Thierry,Cansell, Maud,Pinet, Sandra

supporting information; scheme or table, p. 8872 - 8879 (2011/01/04)

In order to better understand the metabolic fate of n-3 polyunsaturated fatty acids (PUFAs), an efficient access to symmetrical and unsymmetrical triacylglycerols (TGs), esterified with PUFAs, with known high purity, is required. In this context, we optimized the esterification of a mixture of glycerols protected as dioxane and dioxolane with PUFAs. The kinetics of this reaction depends on various factors, such as the fatty acid chain length and the stereochemistry of the dioxane. Then, one-pot acetal hydrolysis and esterification of hydroxyl groups led to the desired structured TGs without either double bond isomerization or acyl migration (except when symmetrical TGs are acylated with long-chain saturated fatty acids in external positions). PUFAs location on the glycerol backbone was assayed by NMR, HPLC and pancreatic lipase hydrolysis.

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