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Merck

756377

Sigma-Aldrich

3-(2-乙酰氧基-4,6-二甲基苯基)-3-甲基丁酸

97%

别名:

2-(Acetyloxy)-β,β,4,6-tetramethylbenzenepropanoic acid, 3-(2-Acetoxy-4,6-dimethylphenyl)-3-methylbutanoic acid

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About This Item

经验公式(希尔记法):
C15H20O4
分子量:
264.32
MDL编号:
UNSPSC代码:
12352108
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

表单

solid

mp

113-118 °C

官能团

carboxylic acid
ester

储存温度

2-8°C

SMILES字符串

CC(=O)Oc1cc(C)cc(C)c1C(C)(C)CC(O)=O

InChI

1S/C15H20O4/c1-9-6-10(2)14(12(7-9)19-11(3)16)15(4,5)8-13(17)18/h6-7H,8H2,1-5H3,(H,17,18)

InChI key

IRUYOPOSEOEWIN-UHFFFAOYSA-N

应用

Used as a trimethyl lock in stable chromogenic substrates for esterases

象形图

Skull and crossbones

警示用语:

Danger

危险声明

危险分类

Acute Tox. 3 Oral - Eye Irrit. 2

储存分类代码

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Michael N Levine et al.
Molecules (Basel, Switzerland), 13(2), 204-211 (2008-02-29)
p-Nitrophenyl acetate is the most commonly used substrate for detecting the catalytic activity of esterases, including those that activate prodrugs in human cells. This substrate is unstable in aqueous solution, limiting its utility. Here, a stable chromogenic substrate for esterases

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