240125
对苯二酚
≥99%
别名:
1,4-二羟基苯, 1,4-苯二酚, HQ
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关于此项目
线性分子式:
C6H4-1,4-(OH)2
化学文摘社编号:
分子量:
110.11
EC Number:
204-617-8
UNSPSC Code:
12352103
MDL number:
Beilstein/REAXYS Number:
605970
InChI
1S/C6H6O2/c7-5-1-2-6(8)4-3-5/h1-4,7-8H
InChI key
QIGBRXMKCJKVMJ-UHFFFAOYSA-N
SMILES string
Oc1ccc(O)cc1
vapor density
3.81 (vs air)
vapor pressure
1 mmHg ( 132 °C)
assay
≥99%
autoignition temp.
930 °F
bp
285 °C (lit.)
mp
172-175 °C (lit.)
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signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 1 - Carc. 2 - Eye Dam. 1 - Muta. 2
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
329.0 °F - closed cup
flash_point_c
165 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Quan Cheng Chen et al.
Journal of natural products, 71(6), 995-999 (2008-05-29)
Five new pyronane-type monocyclic monoterpenoids, jasminodiol (1), jasminoside H (6), 6'-O-sinapoyljasminoside A (7), 6'-O-sinapoyljasminoside C (8), and jasminoside I (9), together with four known analogues, were isolated from the fruit of Gardenia jasminoides. The structures of the new metabolites were
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.
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
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
Maya Mori-Hongo et al.
Journal of natural products, 72(2), 194-203 (2009-01-10)
In the course of our search for new melanin synthesis inhibitors from plants, 40 new flavonoids and 11 known flavonoids were isolated from the roots of Lespedeza floribunda Bunge. The structures of the new compounds were determined by MS and
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