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Merck
CN

169978

2-甲氧基苯甲酸

ReagentPlus®, 99%

别名:

O-甲基水杨酸, 邻茴香酸

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线性分子式:
CH3OC6H4CO2H
化学文摘社编号:
分子量:
152.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-447-8
Beilstein/REAXYS Number:
509929
MDL number:
Assay:
99%
Form:
powder
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InChI key

ILUJQPXNXACGAN-UHFFFAOYSA-N

InChI

1S/C8H8O3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3,(H,9,10)

SMILES string

COc1ccccc1C(O)=O

product line

ReagentPlus®

assay

99%

form

powder

mp

98-100 °C (lit.)

functional group

carboxylic acid

Quality Level

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General description

2-甲氧基苯甲酸在奥斯陆莫拉菌培养基中可作为碳补充剂进行添加 。使用时间相关的单光子计数和荧光上转换技术已对2-甲氧基苯甲酸的光物理学进行了研究

Application

在通过HPLC对番茄(Lycopersicon esculentum)细胞中游离和共轭水杨酸进行定量的过程中,使用2-甲氧基苯甲酸作为内标进行测定。它也可用于合成苯酞

Legal Information

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

291.2 °F - closed cup

flash_point_c

144 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Involvement of endogenous salicylic acid content, lipoxygenase and antioxidant enzyme activities in the response of tomato cell suspension cultures to NaCl.
Molina A, et al.
The New phytologist, 156(3), 409-415 (2002)
Heterocycles, 39, 47-47 (1994)
The photophysics of salicylic acid derivatives in aqueous solution.
Pozdnyakov IP, et al.
Journal of the Physical Society of Japan, 22(5), 449-454 (2009)
R L Crawford et al.
Journal of bacteriology, 121(3), 794-799 (1975-03-01)
Gentisate:oxygen 1,2-oxidoreductase (decyclizing) (EC 1.13.11.4; gentisate 1,2-dioxygenase) from Moraxella osloensis was purified to homogeneity as shown by polyacrylamide gel electrophoresis. The enzyme has a molecular weight of about 154,000 and gives rise to subunits of molecular weight 40,000 in the
T Sasaki et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 50(5), 905-909 (1999-04-24)
For in vivo measurement of the hydroxyl radical (.OH), we synthesized [11C]salicylic acid, [11C]O-acetylsalicylic acid and [11C]2-methoxybenzoic acid by carboxylation of 2-bromomagnesiumanisol using [11C]CO2. The radiochemical yield of [11C]salicylic acid, [11C]O-acetylsalicylic acid and [11C]2-methoxybenzoic acid calculated from trapped [11C]CO2 in

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