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Merck
CN

752525

2-羟基对苯二甲酸

greener alternative

97%

别名:

2-羟基-1,4-苯二甲酸, H2BDC-OH

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关于此项目

经验公式(希尔记法):
C8H6O5
化学文摘社编号:
分子量:
182.13
NACRES:
NA.23
PubChem Substance ID:
UNSPSC Code:
26111700
MDL number:
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产品名称

2-羟基对苯二甲酸, 97%

InChI

1S/C8H6O5/c9-6-3-4(7(10)11)1-2-5(6)8(12)13/h1-3,9H,(H,10,11)(H,12,13)

SMILES string

OC(=O)c1ccc(C(O)=O)c(O)c1

InChI key

CDOWNLMZVKJRSC-UHFFFAOYSA-N

assay

97%

form

solid

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

mp

312-317 °C

greener alternative category

Quality Level

General description

我们致力于为您提供更环保的替代产品,以符合“绿色化学的12项原则”的一项或多项原则要求。该产品为增强型,提高了能源效率。点击此处,查看更多详情。

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Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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分析证书(COA)

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Physical chemistry chemical physics : PCCP, 10(20), 2986-2992 (2008-05-14)
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X Qu et al.
Photochemistry and photobiology, 71(3), 307-313 (2000-03-25)
The known photoreactions of melanin include production of melanin free radicals and oxygen consumption. While qualitative descriptions of the intermediates and products of these processes have been published, no quantitative procedures have been reported that allow the convenient measurement of
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Journal of the American Chemical Society, 133(7), 2064-2067 (2011-02-01)
Covalent functionalization of 1,4-benzenedicarboxylate (bdc) with methoxyethoxy groups induces conformational freedom in this molecule. Applying these 2,5-disubstituted bdc derivatives in metal-organic framework synthesis together with 4,4'-bipyridine as coligand yields novel honeycomb-like structures. The cylindrical channels of these materials are populated
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The functionalisation of well-known rigid metal-organic frameworks (namely, [Zn(4)O(bdc)(3)](n), MOF-5, IRMOF-1 and [Zn(2)(bdc)(2)(dabco)](n); bdc = 1,4-benzene dicarboxylate, dabco = diazabicyclo[2.2.2]octane) with additional alkyl ether groups of the type -O-(CH(2))(n)-O-CH(3) (n = 2-4) initiates unexpected structural flexibility, as well as high

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