跳转至内容
Merck
CN

C1251

Sigma-Aldrich

(+)-儿茶素 水合物

≥98% (HPLC), antioxidant, powder

别名:

(+)-儿茶精-3, (2R,3S)-2-(3,4-二羟基苯基)-3,4-二氢-1(2H)-苯并吡喃-3,5,7-三醇

登录查看公司和协议定价

选择尺寸


关于此项目

经验公式(希尔记法):
C15H14O6 · xH2O
化学文摘社编号:
分子量:
290.27 (anhydrous basis)
Beilstein:
3595244
EC 号:
MDL编号:
UNSPSC代码:
12352200
PubChem化学物质编号:
NACRES:
NA.77
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助

产品名称

(+)-儿茶素 水合物, ≥98% (HPLC), powder

质量水平

方案

≥98% (HPLC)

表单

powder

颜色

yellow to yellow with tan cast

mp

175-177 °C (anhydrous) (lit.)

溶解性

ethanol: 50 mg/mL

储存温度

2-8°C

SMILES字符串

[H]O[H].O[C@H]1Cc2c(O)cc(O)cc2O[C@@H]1c3ccc(O)c(O)c3

InChI

1S/C15H14O6.H2O/c16-8-4-11(18)9-6-13(20)15(21-14(9)5-8)7-1-2-10(17)12(19)3-7;/h1-5,13,15-20H,6H2;1H2/t13-,15+;/m0./s1

InChI key

OFUMQWOJBVNKLR-NQQJLSKUSA-N

正在寻找类似产品? 访问 产品对比指南

一般描述

儿茶素是植物化学物质,在黑葡萄、桃子、草莓和蚕豆中含量丰富。儿茶素有各种形式,如儿茶素、表儿茶素、表儿茶素没食子酸酯、表焙儿茶素和表没食子儿茶素没食子酸酯。

应用

(+)-水合儿茶素已用于以下情形:
  • 作为多酚标准品,测定红葡萄酒副产物中的多酚总量
  • 作为添加剂,通过三重进料批量方法研究对体外甲烷生产和底物降解的效果
  • 作为底物,测定L. plantarum CECT 748T 14重组鞣酸酶对儿茶素的活性

生化/生理作用

一种植物来源的抗氧化性黄酮类化合物;自由基清除剂,可在各种生物系统中防止自由基介导的损伤。例如,在生理pH条件下,儿茶素可抑制羟基自由基介导的DNA链断裂。它还可以防止人体血浆氧化。它延迟了内源性脂溶性抗氧化剂的消耗并抑制脂质氧化。儿茶素还可以作为脂肪酸合酶的抑制剂。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库

Christine Ziegler et al.
Molecular microbiology, 78(1), 13-34 (2010-10-07)
Increases in the environmental osmolarity are key determinants for the growth of microorganisms. To ensure a physiologically acceptable level of cellular hydration and turgor at high osmolarity, many bacteria accumulate compatible solutes. Osmotically controlled uptake systems allow the scavenging of
S B Lotito et al.
Free radical biology & medicine, 24(3), 435-441 (1998-01-23)
Based on the recognized capacity of (+)-catechin (CTCH) to prevent free radical-mediated damage in different biological systems, its role in the protection of human plasma from oxidation was investigated. Samples of human blood plasma were incubated with 50 mM AAPH
Nutrition and Health Info Sheet: Catechins (2008)
J Ueda et al.
Archives of biochemistry and biophysics, 333(2), 377-384 (1996-09-15)
The reactivities of various antioxidative compounds including catechol derivatives and endogenous radical scavengers toward hydroxyl radical (.OH) were investigated by an electron spin resonance-spin trapping method, thiobarbituric acid method, and DNA strand scission assay. Hydroxyl radical was generated by both
Dietary fibre content and antioxidant activity of Manto Negro red grape (Vitis vinifera): pomace and stem
Llobera A and Canellas J
Food Chemistry, 101(2), 659-666 (2007)

商品

Fatty acid synthesis supports cancer cell proliferation, essential for membrane generation, protein modification, and bioenergetics.

DISCOVER Bioactive Small Molecules for Nitric Oxide & Cell Stress Research

抗氧化剂可保护生物系统免受含氧自由基和氧化还原过渡金属离子(如铁、铜和镉)引起的氧化损伤。

Antioxidants protect biological systems from oxidative damage produced by oxygen-containing free radicals and from redoxactive transition metal ions such as iron, copper, and cadmium.

实验方案

Protocol for HPLC Analysis of Flavonoids on Ascentis® RP-Amide

我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.

联系客户支持