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Merck

240125

Sigma-Aldrich

对苯二酚

≥99%

别名:

1,4-二羟基苯, 1,4-苯二酚, HQ

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About This Item

线性分子式:
C6H4-1,4-(OH)2
CAS号:
分子量:
110.11
Beilstein:
605970
EC號碼:
MDL號碼:
分類程式碼代碼:
12352103

蒸汽密度

3.81 (vs air)

蒸汽壓力

1 mmHg ( 132 °C)

化驗

≥99%

自燃溫度

930 °F

bp

285 °C (lit.)

mp

172-175 °C (lit.)

SMILES 字串

Oc1ccc(O)cc1

InChI

1S/C6H6O2/c7-5-1-2-6(8)4-3-5/h1-4,7-8H

InChI 密鑰

QIGBRXMKCJKVMJ-UHFFFAOYSA-N

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说明
价格

訊號詞

Danger

危險分類

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Muta. 2

儲存類別代碼

13 - Non Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

329.0 °F - closed cup

閃點(°C)

165 °C - closed cup

個人防護裝備

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


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Maya Mori-Hongo et al.
Journal of natural products, 72(1), 63-71 (2008-12-24)
From the roots of Lespedeza cyrtobotrya, 45 flavonoids were isolated along with 20 new and 25 known compounds. Lipophilic flavonoids 2, 3, 7, 9, 11, 28, 30, and 39 exhibited strong inhibitory activities on melanin synthesis in normal human epidermal
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Bioorganic & medicinal chemistry letters, 17(2), 461-464 (2006-10-27)
Oxyresveratrol and resveratrol, with hydroxy substituted trans-stilbene structure, exert potent inhibitory effects on cyclooxygenase, rat liver mitochondrial ATPase activity, and tyrosinase. As the isosteres of oxyresveratrol, a new family of hydroxyl substituted phenyl-naphthalenes were synthesized to show excellent inhibition of
Charles Bodet et al.
European journal of medicinal chemistry, 43(8), 1612-1620 (2007-12-21)
The aim of this study was to investigate the effect of 3-(4'-geranyloxy-3'-methoxyphenyl)-2-trans propenoic acid, active principle isolated from Acronychia baueri Schott, and its ester derivatives on biofilm formation by two important oral pathogens, Porphyromonas gingivalis and Streptococcus mutans. The parent
Woo Duck Seo et al.
European journal of medicinal chemistry, 45(5), 2010-2017 (2010-02-13)
The 4'-(p-toluenesulfonylamino)-4-hydroxychalcone (TSAHC), which bears inhibitory chemotypes for both alpha-glucosidase and tyrosinase, was evaluated for tyrosinase activity and depigmenting ability relative to compounds designed to only target tyrosianse activity. TSAHC emerged to be a competitive reversible inhibitor of mushroom tyrosinase.

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