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240125

Sigma-Aldrich

Hydroquinone

≥99%

Synonym(s):

1,4-Benzenediol, 1,4-Dihydroxybenzene, HQ

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About This Item

Linear Formula:
C6H4-1,4-(OH)2
CAS Number:
123-31-9
Molecular Weight:
110.11
Beilstein:
605970
EC Number:
204-617-8
MDL number:
MFCD00002339
UNSPSC Code:
12352103

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.)

SMILES string

Oc1ccc(O)cc1

InChI

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

InChI key

QIGBRXMKCJKVMJ-UHFFFAOYSA-N

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Description
Pricing

Signal Word

Danger

Hazard Statements

H302,H318,H341,H351,H410

Hazard Classifications

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

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

329.0 °F - closed cup

Flash Point(C)

165 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
Suhee Song et al.
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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