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1071421-86-7

1(3)-Feruloyl monobutyryl-glycerol (FMB) is a feruloylated lipid synthesized via enzymatic transesterification of ferulic acid and tributyrin. It exhibits strong antioxidant properties, outperforming ferulic acid in lipophilic systems due to improved solubility in hydrophobic media. FMB demonstrates notable radical scavenging activity, including against hydroxyl, superoxide anion, and DPPH radicals, as well as inhibition of lipid peroxidation. Its antioxidant efficacy is comparable to or exceeds that of synthetic antioxidants like BHT, making it a promising natural alternative for applications in lipid-based products.

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  • 1071421-86-7 Structure

  • Basic information

    1. Product Name: 1(3)-feruloyl monobutyryl-glycerol
    2. Synonyms:
    3. CAS NO:1071421-86-7
    4. Molecular Formula:
    5. Molecular Weight: 338.357
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1071421-86-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1(3)-feruloyl monobutyryl-glycerol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1(3)-feruloyl monobutyryl-glycerol(1071421-86-7)
    11. EPA Substance Registry System: 1(3)-feruloyl monobutyryl-glycerol(1071421-86-7)

  • 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: 1071421-86-7(Hazardous Substances Data)

1071421-86-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1071421-86-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,1,4,2 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1071421-86:
(9*1)+(8*0)+(7*7)+(6*1)+(5*4)+(4*2)+(3*1)+(2*8)+(1*6)=117
117 % 10 = 7
So 1071421-86-7 is a valid CAS Registry Number.

1071421-86-7Downstream Products

1071421-86-7Relevant articles and documents

Enzymatic synthesis of novel feruloylated lipids and their evaluation as antioxidants

Zheng, Yan,Branford-White, Christopher,Wu, Xiao-Mei,Wu, Cheng-Yao,Xie, Jian-Gang,Quan, Jing,Zhu, Li-Min

, p. 305 - 311 (2010)

Concerns about the use of chemical synthetic antioxidants that promote carcinogenesis has led to the development of natural antioxidants. Ferulic acid (4-hydroxy-3-methoxy cinnamic acid, FA) is a monophenolic phenylpropanoid present in the plant kingdom. It has shown a high antioxidant capacity and biological activities, including antiviral, anticarcinogenic and antimicrobial ones. However, due to poor solubility in hydrophobic media, FA can only be used in aqueous environments and this is a key factor that to a certain extent limits its application and bioavailability. In the present study, novel feruloylated lipids 1(3)-feruloyl-mono- butyryl-glycerol (FMB) and 1(3)-feruloyl-dibutyryl- glycerol (FDB) were prepared by lipase-catalysed transesterification between FA and tributyrin. The structure of FMB and FDB was confirmed by NMR and ESI-MS, respectively. The radical scavenging and antioxidant properties of FA, FMB and FDB were evaluated using several different antioxidant assays, including hydroxyl radical scavenging, superoxide anion radical scavenging, 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging, inhibition of peroxidation of linoleic acid and reducing power. The antioxidant activities decreased in the following order: BHT ≥ FMB > FDB > FA. The results suggested that FMB and FDB exhibited a strong effect against oxidation in lipophilic systems making them promising antioxidants.

Enhancement in the synthesis of novel feruloyl lipids (feruloyl butyryl glycerides) by enzymatic biotransformation using response surface methodology

Zheng, Yan,Quan, Jing,Ning, Xin,Zhu, Li-Min

, p. 11493 - 11498 (2008)

Response surface methodology was successfully employed to optimize lipase-catalyzed synthesis of feruloyl butyryl glycerides (FBGs). The effects of the reaction parameters, including the reaction time, reaction temperature, enzyme concentration, substrate

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