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  • α-生育酚醋酸酯

    alpha-Tocopherol acetate

    α-生育酚醋酸酯
    产品编号 CFN98999
    CAS编号 58-95-7
    分子式 = 分子量 C31H52O3 = 472.8
    产品纯度 >=98%
    物理属性 Oil
    化合物类型 Phenols
    植物来源 The herbs of Isodon adenantha
    ChemFaces的产品在影响因子大于5的优秀和顶级科学期刊中被引用
    提供自定义包装
    产品名称 产品编号 CAS编号 包装 QQ客服
    α-生育酚醋酸酯 CFN98999 58-95-7 10mg QQ客服:3257982914
    α-生育酚醋酸酯 CFN98999 58-95-7 20mg QQ客服:3257982914
    α-生育酚醋酸酯 CFN98999 58-95-7 50mg QQ客服:3257982914
    α-生育酚醋酸酯 CFN98999 58-95-7 100mg QQ客服:3257982914
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    ChemFaces的产品在许多优秀和顶级科学期刊中被引用

    Cell. 2018 Jan 11;172(1-2):249-261.e12.
    doi: 10.1016/j.cell.2017.12.019.
    IF=36.216(2019)

    PMID: 29328914

    Cell Metab. 2020 Mar 3;31(3):534-548.e5.
    doi: 10.1016/j.cmet.2020.01.002.
    IF=22.415(2019)

    PMID: 32004475

    Mol Cell. 2017 Nov 16;68(4):673-685.e6.
    doi: 10.1016/j.molcel.2017.10.022.
    IF=14.548(2019)

    PMID: 29149595

    ACS Nano. 2018 Apr 24;12(4): 3385-3396.
    doi: 10.1021/acsnano.7b08969.
    IF=13.903(2019)

    PMID: 29553709

    Nature Plants. 2016 Dec 22;3: 16206.
    doi: 10.1038/nplants.2016.205.
    IF=13.297(2019)

    PMID: 28005066

    Sci Adv. 2018 Oct 24;4(10): eaat6994.
    doi: 10.1126/sciadv.aat6994.
    IF=12.804(2019)

    PMID: 30417089
    我们的产品现已经出口到下面的研究机构与大学,并且还在增涨
  • University of Stirling (United Kingdom)
  • National Chung Hsing University (Taiwan)
  • Indian Institute of Science (India)
  • Uniwersytet Gdański (Poland)
  • Weizmann Institute of Science (Israel)
  • Subang Jaya Medical Centre (Malaysia)
  • Rio de Janeiro State University (Brazil)
  • Istanbul University (Turkey)
  • Chiang Mai University (Thailand)
  • Mendel University in Brno (Czech Republic)
  • Seoul National University (Korea)
  • Worcester Polytechnic Institute (USA)
  • Shanghai Institute of Biochemistry and Cell Biology (China)
  • Institute of Bioorganic Chemistry Polish Academy of Sciences (Poland)
  • More...
  • 国外学术期刊发表的引用ChemFaces产品的部分文献
  • Nutraceutical Research . 2021, 19(1),p90-105.
  • Ajou University2024, 4688116
  • Biomed Chromatogr.2022, 36(11):e5462.
  • Kangwon National University2022, 37(1):29-37
  • Molecules.2019, 24(4):E744
  • Sci Rep.2018, 8(1):12970
  • Korean J of Medicinal Crop Science2018, 220-226
  • Int J Mol Sci.2018, 19(9):E2681
  • Asian J Beauty Cosmetol2020, 18(3): 265-272.
  • Mol Med Rep.2022, 25(1):8.
  • Journal of Mushroom2023, 21(4):215-221.
  • In Vitro Cellular & Developmental Biology - Plant2022, 58:972-988.
  • Plant J.2017, 90(3):535-546
  • bioRxiv-Pharm.&Toxi.2022, 2022.481203.
  • Biochem Biophys Res Commun.2019, 518(4):732-738
  • Anticancer Agents Med Chem.2023, 23(10):1204-1210.
  • Front Immunol.2018, 9:2091
  • Nutrients.2023, 15(12):2644.
  • Food Science and Human Wellness2022, 11(4):965-974
  • Anal Chim Acta.2018, 1039:162-171
  • Ind Crops Prod.2015, 67:185-191
  • Foods.2023, 12(2):318.
  • J of Physics Conference Series2019, 1349(1)
  • ...
  • 生物活性
    Description: The alpha-Tocopherol acetate form is often used in foods and other products due to its high biological activity and chemical stability.Alpha-Tocopherol acetate reduces substantially lipid peroxidation, especially at lower level (200 mg kg(-1) flesh).Alpha-Tocopherol acetate during treatment and dry period resulted in reduced oxidative stress, heat shock protein Hsp70 levels, improved antioxidant, and improved immunity status.
    Targets: HSP (e.g. HSP90)
    In vitro:
    Food Chem. 2013 Nov 1;141(1):473-81.
    Vitamin E bioaccessibility: influence of carrier oil type on digestion and release of emulsified α-tocopherol acetate.[Pubmed: 23768382]
    Vitamin E is an essential micronutrient for humans and animals due to its antioxidant and non-antioxidant biological activities. The α-tocopherol acetate form is often used in foods and other products due to its high biological activity and chemical stability.
    METHODS AND RESULTS:
    In this study, we examined the influence of carrier oil type on the bioaccessibility and molecular form of emulsified vitamin E using a simulated gastrointestinal model. Oil-in-water emulsions containing α-tocopherol acetate were prepared using quillaja saponin as a natural surfactant, and either long chain triacylglycerols (LCT) or medium chain triacylglycerols (MCT) as carrier oils. The rate and extent of lipid digestion was higher for MCT- than LCT-emulsions, which was attributed to differences in the water dispersibility of the free fatty acids formed during lipolysis. Conversely, the total bioaccessibility of vitamin E after digestion was higher for LCT- than MCT-emulsions, which was attributed to the greater solubilisation capacity of mixed micelles formed from long chain fatty acids. The conversion of α-tocopherol acetate to α-tocopherol after in vitro digestion was also considerably higher for LCT- than MCT-emulsions, which may impact the subsequent absorption of vitamin E.
    CONCLUSIONS:
    Overall, this research has important implications for the design and fabrication of effective emulsion-based delivery systems for increasing the bioavailability of vitamin E.
    Food Funct. 2015 Jan;6(1):84-97.
    Enhancing vitamin E bioaccessibility: factors impacting solubilization and hydrolysis of α-tocopherol acetate encapsulated in emulsion-based delivery systems.[Pubmed: 25312787]
    Vitamin E is an essential micronutrient for humans and animals due to its antioxidant and non-antioxidant biological activities. The α-tocopherol acetate form is often used in foods and other products due to its high biological activity and chemical stability.
    METHODS AND RESULTS:
    In this study, we examined the influence of carrier oil type on the bioaccessibility and molecular form of emulsified vitamin E using a simulated gastrointestinal model. Oil-in-water emulsions containing α-tocopherol acetate were prepared using quillaja saponin as a natural surfactant, and either long chain triacylglycerols (LCT) or medium chain triacylglycerols (MCT) as carrier oils. The rate and extent of lipid digestion was higher for MCT- than LCT-emulsions, which was attributed to differences in the water dispersibility of the free fatty acids formed during lipolysis. Conversely, the total bioaccessibility of vitamin E after digestion was higher for LCT- than MCT-emulsions, which was attributed to the greater solubilisation capacity of mixed micelles formed from long chain fatty acids. The conversion of α-tocopherol acetate to α-tocopherol after in vitro digestion was also considerably higher for LCT- than MCT-emulsions, which may impact the subsequent absorption of vitamin E.
    CONCLUSIONS:
    Overall, this research has important implications for the design and fabrication of effective emulsion-based delivery systems for increasing the bioavailability of vitamin E.
    In vivo:
    Food Chem Toxicol. 2013 Nov;61:227-32.
    Investigation of in vivo toxicity of hydroxylamine sulfate and the efficiency of intoxication treatment by α-tocopherol acetate and methylene blue.[Pubmed: 23872126]
    Investigation of hydroxylamine sulfate toxicity mechanism in vivo and estimation of α-tocopherol acetate and methylene blue efficiency in poisoning treatments.
    METHODS AND RESULTS:
    In vivo experiments were conducted on 102 Wistar Han rats. The experiments investigated the hematotoxic and oxidative stress effects of hydroxylamine sulfate in acute and subacute toxicity treatment of animals. Electron Spin Resonance was used for quantitative determination of blood and liver tissue parameters alterations after intoxication. The osmotic fragility of erythrocytes, lipid peroxidation intensity and level of SH-groups in liver of rats were determined by established biochemical assays. Hydroxylamine sulfate cause an acute hematotoxicity and oxidative stress in vivo as demonstrated by the appearance of free oxidized iron in blood, reduced glutathione content and increased lipid peroxidation in liver. The experimental studies showed the formation of Hb-NO, MetHb in erythrocytes and as well of stable complex of reduced iron (Fe(2+)) with hydroxylamine sulfate. Methylene blue treatment does not reduce the Hb-NO or MetHb levels in intoxicated animals while administration of α-tocopherol acetate reduces substantially lipid peroxidation.
    CONCLUSIONS:
    Oxidative stress is a key mechanism of acute hematotoxicity caused by hydroxylamine sulfate. Methylene blue is not suitable antidote in case of hydroxylamine intoxication.
    制备储备液(仅供参考)
    1 mg 5 mg 10 mg 20 mg 25 mg
    1 mM 2.1151 mL 10.5753 mL 21.1506 mL 42.3012 mL 52.8765 mL
    5 mM 0.423 mL 2.1151 mL 4.2301 mL 8.4602 mL 10.5753 mL
    10 mM 0.2115 mL 1.0575 mL 2.1151 mL 4.2301 mL 5.2876 mL
    50 mM 0.0423 mL 0.2115 mL 0.423 mL 0.846 mL 1.0575 mL
    100 mM 0.0212 mL 0.1058 mL 0.2115 mL 0.423 mL 0.5288 mL
    * Note: If you are in the process of experiment, it's need to make the dilution ratios of the samples. The dilution data of the sheet for your reference. Normally, it's can get a better solubility within lower of Concentrations.
    部分图片展示
    产品名称 产品编号 CAS编号 分子式 = 分子量 位单 联系QQ
    去羟基-Delta-生育酚,2,8-二甲基-2-(4,8,12-三甲基十三烷基)-2H-1-苯并吡喃-6-醇; Dehydro-Delta-tocopherol CFN97674 802909-72-4 C27H44O2 = 400.65 5mg QQ客服:1457312923
    (+)-Delta-生育酚; (+)-Delta-Tocopherol CFN91145 119-13-1 C27H46O2 = 402.7 5mg QQ客服:3257982914
    Confluentin; Confluentin CFN98991 585534-03-8 C22H30O2 = 326.5 5mg QQ客服:1457312923
    Daurichromenic acid; Daurichromenic acid CFN97302 82003-90-5 C23H30O4 = 370.5 5mg QQ客服:2159513211
    Beta-生育三烯酚; Beta-Tocotrienol CFN92822 490-23-3 C28H42O2 = 410.6 5mg QQ客服:2056216494
    5,8-二甲基母育酚/维生素E; Beta-Tocopherol CFN96393 148-03-8 C28H48O2 = 416.7 5mg QQ客服:2159513211
    (+)-gamma-生育酚; (+)-gamma-Tocopherol CFN91685 54-28-4 C28H48O2 = 416.7 5mg QQ客服:2056216494
    Gamma-生育三烯酚; Gamma-Tocotrienol CFN92817 14101-61-2 C28H42O2 = 410.6 5mg QQ客服:1413575084
    Alpha-生育三烯酚; Alpha-Tocotrienol CFN92821 1721-51-3 C29H44O2 = 424.7 5mg QQ客服:1457312923
    天然维生素E; DL-alpha-Tocopherol CFN90041 59-02-9 C29H50O2 = 430.7 20mg QQ客服:2056216494

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