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Merck
CN

48660

Sigma-Aldrich

没食子酸月桂酯

antioxidant, ≥99.0% (HPLC)

别名:

十二烷基没食子酸酯

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关于此项目

经验公式(希尔记法):
C19H30O5
化学文摘社编号:
分子量:
338.44
Beilstein:
2701981
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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方案

≥99.0% (HPLC)

表单

solid

mp

94-97 °C (lit.)

官能团

ester

SMILES字符串

CCCCCCCCCCCCOC(=O)c1cc(O)c(O)c(O)c1

InChI

1S/C19H30O5/c1-2-3-4-5-6-7-8-9-10-11-12-24-19(23)15-13-16(20)18(22)17(21)14-15/h13-14,20-22H,2-12H2,1H3

InChI key

RPWFJAMTCNSJKK-UHFFFAOYSA-N

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应用

  • Properties of artificial phospholipid membranes containing lauryl gallate or cholesterol(含没食子酸月桂酯或胆固醇的人工磷脂膜特性):研究没食子酸月桂酯如何影响膜结构及其生物功能(Jurak et al., 2018)。
  • Potential of Lauryl Gallate as Stability and Recyclability Improver of Poly (Butylene succinate-co-adipate):没食子酸月桂酯增强聚酯的稳定性和可回收性,对于可持续材料具有重要意义(Rossi et al., 2024)。
  • Lauryl Gallate Activity and Streptococcus mutans(没食子酸月桂酯活性和变形链球菌):研究评估没食子酸月桂酯对于变形链球菌的抗菌性,发现可极大地减少生物膜并影响基因表达(Gabe et al., 2020)。
  • Dodecyl gallate as a pro-ecological antioxidant for food packing materials:研究采用没食子酸月桂酯作为绿色抗氧化剂,增强食品包装的耐老化性(Masek et al., 2014)。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Skin Sens. 1

储存分类代码

11 - Combustible Solids

WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Isao Kubo et al.
Bioorganic & medicinal chemistry, 11(19), 4255-4262 (2003-09-03)
Antibacterial activity of a series of alkyl gallates (3,4,5-trihydroxybenzoates) against Gram-positive bacteria, especially methicillin resistant Staphylococcus aureus (MRSA) strains was evaluated. Gram-positive bacteria are all susceptible to alkyl gallates. Dodecyl gallate was the most effective against MRSA ATCC 33591 strain
K Fujita et al.
Journal of applied microbiology, 92(6), 1035-1042 (2002-05-16)
The aim was to investigate the antifungal actions of nonyl gallate against Saccharomyces cerevisiae ATCC 7754. The maximum potency of both the growth inhibitory and the fungicidal effect against the yeast strain was found in nonyl gallate among n-alkyl gallates
Jordi Garcia-Ubasart et al.
Bioresource technology, 112, 341-344 (2012-03-24)
A new biotechnological procedure using laccase in combination with a hydrophobic phenolic compound (lauryl gallate) for the hydrophobization of cellulose fibres and internal sizing of paper was developed. Cellulose fibres from hardwood kraft pulp were incubated with laccase (Lac), in
Carolina Hurtado et al.
Antiviral therapy, 13(7), 909-917 (2008-12-03)
Antiviral compounds are needed in the control of many animal and human diseases. We analysed the effect of the antitumoural drug lauryl gallate on the infectivity of the African swine fever virus among other DNA (herpes simplex and vaccinia) and
Isao Kubo et al.
Bioorganic & medicinal chemistry, 11(4), 573-580 (2003-01-23)
Dodecyl (C(12)) gallate (3,4,5-trihydroxybenzoate) (1) was found to possess antibacterial activity specifically against Gram-positive bacteria, in addition to its potent antioxidant activity. The time-kill curve study indicates that this amphipathic gallate exhibits bactericidal activity against methicillin resistant Staphylococcus aureus (MRSA)

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