(Q419164)

Statements

instance of

type of chemical entity

0 references

subclass of

dihydroxybenzene

0 references

part of

hydroquinone binding

subject has role

reactant

1 reference

stated in

Gene Ontology release 2019-11-16

p-benzoquinone reductase (NADPH) activity

1 reference

stated in

Gene Ontology release 2020-05-02

Rhea release 113

gentisate decarboxylase activity

1 reference

stated in

Gene Ontology release 2020-05-02

Rhea release 113

hydroquinone glucosyltransferase activity

1 reference

stated in

Gene Ontology release 2020-05-02

Rhea release 113

hydroquinone:oxygen oxidoreductase activity

1 reference

reference URL

http://geneontology.org/external2go/rhea2go

retrieved

1 February 2021

has use

reducing agent

0 references

polymerization inhibitor

0 references

medication

0 references

chemical structure

Hydrochinon.svg
70 × 178; 5 KB

1 reference

imported from Wikimedia project

German Wikipedia

image

Hydroquinone crystal.jpg
500 × 667; 79 KB

depicts

sample

0 references

image of molecular model or crystal lattice model

Trans-hydroquinone-from-xtal-3D-balls.png
1,100 × 789; 129 KB

depicts

ball-and-stick model

0 references

mass

110.037 dalton

1 reference

stated in

PubChem

PubChem CID

785

language of work or name

English

title

hydroquinone (English)

retrieved

19 October 2016

has effect

hydroquinone exposure

1 reference

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

chemical formula

C₆H₆O₂

1 reference

stated in

PubChem

PubChem CID

785

language of work or name

English

title

hydroquinone (English)

retrieved

19 November 2016

canonical SMILES

C1=CC(=CC=C1O)O

1 reference

stated in

PubChem

PubChem CID

785

language of work or name

English

title

hydroquinone (English)

retrieved

19 November 2016

ionization energy

7.95±0.01 electronvolt

series ordinal

1

2 references

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

stated in

Basic laboratory and industrial chemicals: A CRC quick reference handbook

density

1.33±0.01 gram per cubic centimetre

temperature

20±1 degree Celsius

1 reference

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

melting point

338±1 degree Fahrenheit

1 reference

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

172 degree Celsius

1 reference

stated in

International Chemical Safety Card

ICSC ID

0166

title

HYDROQUINONE (English)

retrieved

13 June 2013

171 degree Celsius

1 reference

stated in

Jean-Claude Bradley Open Melting Point Dataset

172.3 degree Celsius

1 reference

stated in

Basic laboratory and industrial chemicals: A CRC quick reference handbook

boiling point

545±1 degree Fahrenheit

under pressure

760±1 torr

1 reference

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

287 degree Celsius

1 reference

stated in

International Chemical Safety Card

ICSC ID

0166

title

HYDROQUINONE (English)

retrieved

13 June 2016

286 degree Celsius

under pressure

101.325 kilopascal

1 reference

stated in

Basic laboratory and industrial chemicals: A CRC quick reference handbook

vapor pressure

0.00001±0.00001 millimetre of mercury

temperature

68±1 degree Fahrenheit

1 reference

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

solubility

7±1 gram per 100 gram of solvent

temperature

68±1 degree Fahrenheit

solvent

water

1 reference

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

flash point

329±1 degree Fahrenheit

determination method

Pensky–Martens closed-cup test

1 reference

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

safety classification and labelling

NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response

NFPA Health

2

NFPA Fire

1

NFPA Instability

0

NFPA Special

no value

1 reference

reference URL

https://www.sigmaaldrich.com/MSDS/MSDS/DisplayMSDSPage.do?country=US&language=en&productNumber=H9003&brand=SIAL&PageToGoToURL=https%3A%2F%2Fwww.sigmaaldrich.com%2Fcatalog%2Fproduct%2Fsial%2Fh9003%3Flang%3Dpl

publisher

Sigma-Aldrich

title

Hydroquinone (English)

language of work or name

English

point in time

11 June 2018

retrieved

18 July 2018

NIOSH Pocket Guide ID

0338

0 references

time-weighted average exposure limit

2±1 milligram per cubic metre

applies to jurisdiction

United States of America

duration

8±1 hour

1 reference

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

ceiling exposure limit

2±1 milligram per cubic metre

applies to jurisdiction

no value

duration

15±1 minute

1 reference

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

immediately dangerous to life or health

50±10 milligram per cubic metre

1 reference

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

found in taxon

Xanthium strumarium

1 reference

stated in

Isolation and redefinition of the toxic agent from cocklebur (Xanthium strumarium)

Brassica oleracea

1 reference

stated in

Human exposure to naturally occurring hydroquinone

Coffea arabica

1 reference

stated in

Human exposure to naturally occurring hydroquinone

Triticum aestivum

1 reference

stated in

Human exposure to naturally occurring hydroquinone

Achillea millefolium

1 reference

stated in

Mosquito repelling activity of compounds occurring inAchillea millefolium L. (asteraceae)

Ipomopsis aggregata

1 reference

stated in

Potential anticancer agents XXXII. Hydroquinone from Ipomopsis aggregata

Glycosmis citrifolia

1 reference

stated in

Acridone alkaloids. Part 9. Chemical constituents of Glycosmis citrifolia(Willd.) Lindl. Structures of novel linear pyranoacridones, furoacridones, and other new acridone alkaloids

Glycosmis parviflora

1 reference

stated in

Acridone alkaloids. Part 9. Chemical constituents of Glycosmis citrifolia(Willd.) Lindl. Structures of novel linear pyranoacridones, furoacridones, and other new acridone alkaloids

Gastrodia elata

1 reference

stated in

Neuroprotective Principles fromGastrodiaelata

Aesculus californica

1 reference

stated in

Combined effect on plant growth of (-)-epicatechin and hydroquinone, compounds from Aesculus californica NUTT. (Hippocastanaceae).

Agaricus hondensis

1 reference

stated in

Hydroquinone: the toxic compound of Agaricus hondensis

Antennaria microphylla

1 reference

stated in

Allelopathy of Small Everlasting (Antennaria microphylla): Identification of Constituents Phytotoxic to Leafy Spurge (Euphorbia esula)

Arctostaphylos columbiana

1 reference

stated in

Phytochemical Investigation of Arctostaphylos columbiana Piper and Arctostaphylos patula Greene (Ericaceae)

Citrus grandis

2 references

stated in

Alkaloids and coumarins of Citrus grandis

stated in

Acridone alkaloids and a coumarin from Citrus grandis

Citrus nobilis

1 reference

stated in

A 2,2-dimethylpyranoflavonol from citrus nobilis

mandarin orange

1 reference

stated in

A 2,2-dimethylpyranoflavonol from citrus nobilis

Crotalaria sessiliflora

1 reference

stated in

Antioxidative Compounds fromCrotalaria sessiliflora

Nageia wallichiana

1 reference

stated in

Extractives of Decussocarpus wallichianus

Eriosema tuberosum

1 reference

stated in

Phenolic glycosides from Eriosema tuberosum

Hernandia ovigera

1 reference

stated in

Isolation of 6,7-Demethylenedesoxypodophyllotoxin from Hernandia ovigera.

Murraya euchrestifolia

4 references

stated in

Murrayamine-A,-B,-C and (+)-mahanine, carbazole alkaloids from Murraya euchrestifolia

stated in

Murrayamine-C from murraya euchrestifolia

stated in

Chemical constituents of Murraya euchrestifolia Hayata. Structures of novel carbazolequinones and other new carbazole alkaloids.

stated in

Murrayamine-C from murraya euchrestifolia

Onobrychis kachetica

1 reference

stated in

Arbutin fromOnobrychis kachetica

Onobrychis meschetica

1 reference

stated in

Arbutin fromOnobrychis kachetica

Onobrychis radiata

1 reference

stated in

Arbutin fromOnobrychis kachetica

marjoram

1 reference

stated in

Preliminary study of phenolic glycosides from Origanum majorana; quantitative estimation of arbutin; cytotoxic activity of hydroquinone

Phagnalon rupestre

1 reference

stated in

Phagnalon rupestre as a source of compounds active on contact hypersensitivity

Pyrus bourgaeana

1 reference

stated in

New benzyl alcohol glycosides from Pyrus bourgaeana

Rhodiola sacra

3 references

stated in

Active-oxygen scavenging activity of traditional nourishing-tonic herbal medicines and active constituents of Rhodiola sacra.

stated in

Prolyl endopeptidase inhibitors from the underground part of Rhodiola sacra S. H. Fu.

stated in

Neuroprotective effects of constituents of the oriental crude drugs, Rhodiola sacra, R. sachalinensis and Tokaku-joki-to, against beta-amyloid toxicity, oxidative stress and apoptosis.

Salvia rhyacophila

1 reference

stated in

7-epi-rhyacophiline, a 5,6-secoclerodane diterpene from Salvia rhyacophila

Salvia yosgadensis

1 reference

stated in

Sesterterpenes and other constituents of Salvia yosgadensis

Spiranthes sinensis

1 reference

stated in

Homocyclotirucallane and two dihydrophenanthrenes from Spiranthes sinensis

Vernonanthura montevidensis

3 references

stated in

Guaianolides and other constituents from Vernonia nitidula

stated in

Piptocarphol esters and other constituents from Vernonia cognata

stated in

Diterpenes from Vernonanthura amplexicaulis

Escherichia coli

1 reference

stated in

A comprehensive genome-scale reconstruction of Escherichia coli metabolism--2011.

Cullen corylifolia

1 reference

stated in

Bioactive Metabolites from the Fruits of Psoralea corylifolia

Cullen corylifolium

1 reference

stated in

Bioactive Metabolites from the Fruits of Psoralea corylifolia

Afraegle paniculata

1 reference

stated in

Coumarins and other components of Afraegle paniculata

Euphorbia tithymaloides

1 reference

stated in

Antimicrobial and phytochemical studies on Pedilanthus tithymaloides

Protea repens

1 reference

stated in

Zur Geschichte des Proteacins

Pyrus pashia

1 reference

stated in

Chemical constituents of Diospyros buxifolia, D. tomentosa, D. ferra, D. lotus, Rhus parviflora, Polygonum recumbens, Balanites aegyptiaca and Pyrus pashia

Onobrychis michauxii

1 reference

stated in

Arbutin fromOnobrychis kachetica

Podocarpus salignus

1 reference

stated in

Norditerpene dilactones from Podocarpus saligna

Dysidea

1 reference

stated in

Anti-inflammatory sesquiterpene-quinones from the New Zealand sponge Dysidea cf. cristagalli

Arctostaphylos uva-ursi

4 references

stated in

HPLC Analysis of Phenolics and Flavonoids inArctostaphylos uvae-ursi

stated in

[Anti-tyrosinase activity constituents of Arctostaphylos uva-ursi]

stated in

Determination of arbutin in uvae-ursi folium (bearberry leaves) by capillary zone electrophoresis

stated in

High-performance liquid chromatographic separation and quantitative determination of arbutin, methylarbutin, hydroquinone and hydroquinone-monomethylether in Arctostaphylos, Bergenia, Calluna and Vaccinium species (author's transl)

Adina trichotoma

1 reference

stated in

Glycosides from the bark of Adina polycephala

Citrus × deliciosa

1 reference

stated in

A 2,2-dimethylpyranoflavonol from citrus nobilis

Dactylorhiza hatagirea

1 reference

stated in

Studies on Nepalese Crude Drugs. XXVI. Chemical Constituents of Panch Aunle, the Roots of Dactylorhiza hatagirea D. DON.

Houttuynia cordata

1 reference

stated in

Anti-complementary constituents of Houttuynia cordata and their targets in complement activation cascade

Lespedeza cyrtobotrya

1 reference

stated in

Melanin synthesis inhibitors from Lespedeza cyrtobotrya

Spiranthes vernalis

1 reference

stated in

Homocyclotirucallane and two dihydrophenanthrenes from Spiranthes sinensis

pomelo

2 references

stated in

Alkaloids and coumarins of Citrus grandis

stated in

Acridone alkaloids and a coumarin from Citrus grandis

Hernandia guianensis

1 reference

stated in

Isolation of 6,7-Demethylenedesoxypodophyllotoxin from Hernandia ovigera.

Pyrus communis

1 reference

stated in

Chemical constituents from Commelina communis

described by source

Small Brockhaus and Efron Encyclopedic Dictionary

statement is subject of

Q24756197

0 references

Brockhaus and Efron Encyclopedic Dictionary

statement is subject of

Q24403924

0 references

Great Soviet Encyclopedia (1926–1947)

statement is subject of

Q99708927

0 references

Armenian Soviet Encyclopedia, vol. 6

page(s)

402

0 references

has characteristic

combustible powder

1 reference

reference URL

http://www.cdc.gov/niosh/npg/npgd0338.html

subject has role

enzyme inhibitor

1 reference

stated in

NDF-RT

NDF-RT ID

N0000147180

retrieved

5 March 2018

mutagen

1 reference

stated in

Medical Subject Headings

MeSH descriptor ID

C031927

retrieved

15 March 2018

antioxidant

1 reference

stated in

Medical Subject Headings

MeSH descriptor ID

C031927

retrieved

15 March 2018

radiation protection agent

1 reference

stated in

Medical Subject Headings

MeSH descriptor ID

C031927

retrieved

15 March 2018

has part(s)

carbon

0 references

permanent duplicated item

Q5846523

0 references

Commons category

Hydroquinone

0 references

topic's main category

Category:Hydroquinones

0 references

Identifiers