hydroquinone
composé chimique
penn: échantillon
Resous ekstèn
| CSD Refcode | |
| numéro ZVG | |
| HCIS ID | |
| identifiant DSSTOX d'un composé chimique | |
| identifiant Encyclopædia Britannica | science/hydroquinone sous le nom: hydroquinone |
| identifiant Grande Encyclopédie de Cyrille et Méthode | |
| identifiant ChEMBL | |
| identifiant Grande Encyclopédie catalane | |
| identifiant Nikkaji | |
| identifiant Human Metabolome Database | |
| identifiant Unique Ingredient Identifier | |
| identifiant NMRShiftDB | |
| identifiant JSTOR d'un sujet | |
| identifiant de la Grande Encyclopédie russe en ligne | 2359489 sous le nom: ГИДРОХИНОН |
| RxNorm CUI | |
| numéro RTECS | MX3500000 |
| identifiant d'InfoCard ECHA | |
| identifiant UM-BBD d'un composé chimique | |
| identifiant Protein Data Bank | |
| DrugCentral ID | |
| identifiant KEGG | |
| identifiant CCDC | |
| identifiant NALT | |
| identifiant Encyclopédie de Chine (troisième édition) | |
| identifiant Probes And Drugs | |
| identifiant J9U de la Bibliothèque nationale d'Israël | |
| identifiant National Drug File | |
| idantifyan sou Freebase | |
| numéro Beilstein | 605970[15] |
| identifiant Bibliothèque du Congrès | |
| CAMEO Chemicals ID | |
| identifiant PubChem (CID) | |
| UniChem compound ID | |
| identifiant Quora d'un sujet | |
| identifiant Fiches internationales de sécurité chimique | |
| identifiant ChemSpider | |
| identifiant Protein Data Bank d'un ligand | |
| SPLASH | |
| PesticideInfo chemical ID | |
| identifiant DSSTOX | |
| identifiant Microsoft Academic | |
| identifiant ChEBI | |
| identifiant OpenAlex | |
| InChI | |
| code UNSPSC | |
| identifiant KBpedia | |
| identifiant CAB Thesaurus | |
| InChIKey | |
| Cannabis Database ID | |
| identifiant DrugBank | |
| identifiant Gran Enciclopèdia Catalana (ancien) | |
| identifiant WikiProjectMed | |
| numéro CosIng | |
| identifiant Medical Subject Headings | |
| identifiant SureChEMBL | |
| identifiant Store norske leksikon | |
| identifiant IEDB d'épitope | |
| numéro NSC | |
| identifiant KNApSAcK | |
| UMLS CUI | |
| numéro CAS | |
| OSHA Occupational Chemical Database ID | |
| identifiant Encyclopædia Universalis d'un article | |
| numéro CE | |
| identifiant Bibliothèque nationale tchèque | ph114736 sous le nom: hydrochinon |
| numéro Gmelin | 2742 |
| identifiant MassBank | |
| identifiant AHECC 2017 | 29072200 |
| identifiant Classification anatomique, thérapeutique et chimique | |
| identifiant Hazardous Substances Data Bank |
se yon
type d'entité chimique
sou-klas
benzènediol
pati nan
p-benzoquinone reductase (NADPH) activity[34]
gentisate decarboxylase activity[34]
hydroquinone glucosyltransferase activity[34]
hydroquinone:oxygen oxidoreductase activity[35]
structure chimique
modèle moléculaire
penn: modèle moléculaire boules-bâtonnets
masse
110,037 unité de masse atomique unifiée[36]
danger associé
intoxication à l'hydroquinone
a pour effet
intoxication à l'hydroquinone[37]
formule chimique
C₆H₆O₂[18]
SMILES canonique
C1=CC(=CC=C1O)O[18]
masse volumique
point de fusion
338±1 Degre Farennayt[37]
172 Degre Sèlsiyis[39]
171 Degre Sèlsiyis[40]
172,3 Degre Sèlsiyis[38]
point d'ébullition
287 Degre Sèlsiyis[41]
pression de vapeur
point d'éclair
classification et étiquetage de sécurité
NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response[42]
code NFPA spécial: aucune valeur
code NFPA santé: 2
code NFPA feu: 1
code NFPA réactivité: 0
identifiant NPG
0338
valeur (limite) moyenne d’exposition
valeur plafond d'exposition
IDLH
50±10 milligramme par mètre cube[37]
trouvé dans le taxon
Lampourde glouteron[43]
Brassica olearacea[44]
Coffea arabica[44]
Triticum aestivum[44]
Achillée millefeuille[45]
Ipomopsis aggregata[46]
Glycosmis citrifolia[47]
Glycosmis parviflora[47]
Gastrodia elata[48]
Pavier de Californie[49]
Agaricus hondensis[50]
Antennaria microphylla[51]
Arctostaphylos columbiana[52]
Citrus nobilis[55]
Citrus reticulata[55]
Crotalaria sessiliflora[56]
Nageia wallichiana[57]
Eriosema tuberosum[58]
Hernandia ovigera[59]
Onobrychis kachetica[63]
Onobrychis meschetica[63]
Onobrychis radiata[63]
Origanum majorana[64]
Phagnalon rupestre[65]
Pyrus bourgaeana[66]
Salvia rhyacophila[70]
Salvia yosgadensis[71]
Spiranthes sinensis[72]
Cullen corylifolia[77]
Cullen corylifolium[77]
Afraegle paniculata[78]
Euphorbia tithymaloides[79]
Protea repens[80]
Pyrus pashia[81]
Onobrychis michauxii[63]
Podocarpus salignus[82]
Dysidea[83]
Adina trichotoma[88]
Citrus deliciosa[55]
Dactylorhiza hatagirea[89]
Plante caméléon[90]
Lespedeza cyrtobotrya[91]
Spiranthes vernalis[72]
Hernandia guianensis[59]
poirier commun[92]
décrit par
Petit Dictionnaire encyclopédique Brockhaus-Efron
affirmation détaillée dans: Q24756197
Dictionnaire encyclopédique Brockhaus et Efron
affirmation détaillée dans: Q24403924
Grande Encyclopédie soviétique
affirmation détaillée dans: Q99708927
Encyclopédie soviétique arménienne, tome 6
page(s): 402
caractérisé par
poudre combustible[37]
comprend
élément doublon permanent
Q5846523
catégorie Commons
Hydroquinone
kategori
Catégorie:Hydroquinone
Referans
- ↑ 1,0 1,1 1,2 et 1,3 Cambridge Structural Database, 10 janvye 2023, InChIKey match
- ↑ 2,0 et 2,1 ChEMBL, 19 novanm 2016, angle, HYDROQUINONE, CHEMBL537
- ↑ 3,0 3,1 et 3,2 inferred from InChIKey
- ↑ 4,0 4,1 4,2 4,3 4,4 4,5 4,6 et 4,7 QIGBRXMKCJKVMJ-UHFFFAOYSA-N, InChIKey
- ↑ 5,0 5,1 5,2 5,3 5,4 et 5,5 Global Substance Registration System, 19 novanm 2016, angle, hydroquinone, XV74C1N1AE
- ↑ base de données InfoCard de l'ECHA, 27 desanm 2018, 100.004.199, Hydroquinone, CAS no.: 123-31-9
- ↑ Protein Data Bank, 19 oktòb 2016, angle, 5I3B, 5I3B
- ↑ Protein Data Bank, 19 oktòb 2016, angle, 4QOP, 4QOP
- ↑ Protein Data Bank, 19 oktòb 2016, angle, 3ZOF, 3ZOF
- ↑ Protein Data Bank, 19 oktòb 2016, angle, 3ZOD, 3ZOD
- ↑ Protein Data Bank, 19 oktòb 2016, angle, 5FSE, 5FSE
- ↑ Protein Data Bank, 19 oktòb 2016, angle, 5I3A, 5I3A
- ↑ Protein Data Bank, 19 oktòb 2016, angle, 4E3H, 4E3H
- ↑ 14,0 et 14,1 UniChem
- ↑ 15,0 15,1 15,2 et 15,3 ChEBI, 19 oktòb 2016, angle, hydroquinone, 17594
- ↑ National Library of Israel Names and Subjects Authority File
- ↑ sauvegarde de la base de données Freebase, 28 oktòb 2013
- ↑ 18,0 18,1 18,2 18,3 et 18,4 PubChem, 19 novanm 2016, angle, 785, hydroquinone
- ↑ Quora
- ↑ ChemSpider, 19 novanm 2016, angle, 764, Hydroquinone
- ↑ Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
- ↑ InChI=1S/C6H6O2/c7-5-1-2-6(8)4-3-5/h1-4,7-8H, International Chemical Identifier
- ↑ OpenAlex, 26 janvye 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ KBpedia, 9 jiyè 2020
- ↑ CAB Thesaurus, 6 avril 2020
- ↑ ChEBI release 2020-09-01
- ↑ Cannabis Database
- ↑ base de données CosIng, 28 desanm 2019, 76687, HYDROQUINONE, CAS no.: 123-31-9
- ↑ Medical Subject Headings, 14 mas 2018, C031927
- ↑ Immune Epitope Database and Analysis Resource, 1 mas 2022, 116206
- ↑ CAS Common Chemistry, 9 avril 2021, https://commonchemistry.cas.org/detail?cas_rn=123-31-9, QIGBRXMKCJKVMJ-UHFFFAOYSA-N
- ↑ Hazardous Substances Data Bank, 10 me 2021, 28 oktòb 2019, HYDROQUINONE, 577
- ↑ Gene Ontology release 2019-11-16
- ↑ 34,0 34,1 et 34,2 Gene Ontology release 2020-05-02, Rhea release 113
- ↑ 1 fevriye 2021, http://geneontology.org/external2go/rhea2go
- ↑ PubChem, 19 oktòb 2016, angle, 785, hydroquinone
- ↑ 37,00 37,01 37,02 37,03 37,04 37,05 37,06 37,07 37,08 37,09 37,10 et 37,11 http://www.cdc.gov/niosh/npg/npgd0338.html
- ↑ 38,0 38,1 et 38,2 Basic laboratory and industrial chemicals: A CRC quick reference handbook
- ↑ Fiches internationales de sécurité chimique, 13 jen 2013, 0166, HYDROQUINONE
- ↑ Jean-Claude Bradley Open Melting Point Dataset
- ↑ Fiches internationales de sécurité chimique, 13 jen 2016, 0166, HYDROQUINONE
- ↑ 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, Sigma-Aldrich, angle, 18 jiyè 2018, Hydroquinone, 11 jen 2018
- ↑ Isolation and redefinition of the toxic agent from cocklebur (Xanthium strumarium)
- ↑ 44,0 44,1 et 44,2 Human exposure to naturally occurring hydroquinone
- ↑ Mosquito repelling activity of compounds occurring inAchillea millefolium L. (asteraceae)
- ↑ Potential anticancer agents XXXII. Hydroquinone from Ipomopsis aggregata
- ↑ 47,0 et 47,1 Acridone alkaloids. Part 9. Chemical constituents of Glycosmis citrifolia(Willd.) Lindl. Structures of novel linear pyranoacridones, furoacridones, and other new acridone alkaloids
- ↑ Neuroprotective Principles from Gastrodia elata
- ↑ Combined effect on plant growth of (-)-epicatechin and hydroquinone, compounds from Aesculus californica NUTT. (Hippocastanaceae).
- ↑ Hydroquinone: the toxic compound of Agaricus hondensis
- ↑ Allelopathy of Small Everlasting (Antennaria microphylla): Identification of Constituents Phytotoxic to Leafy Spurge (Euphorbia esula)
- ↑ Phytochemical Investigation of Arctostaphylos columbiana Piper and Arctostaphylos patula Greene (Ericaceae)
- ↑ 53,0 et 53,1 Alkaloids and coumarins of Citrus grandis
- ↑ 54,0 et 54,1 Acridone alkaloids and a coumarin from Citrus grandis
- ↑ 55,0 55,1 et 55,2 A 2,2-dimethylpyranoflavonol from citrus nobilis
- ↑ Antioxidative Compounds fromCrotalaria sessiliflora
- ↑ Extractives of Decussocarpus wallichianus
- ↑ Phenolic glycosides from Eriosema tuberosum
- ↑ 59,0 et 59,1 Isolation of 6,7-Demethylenedesoxypodophyllotoxin from Hernandia ovigera.
- ↑ Murrayamine-A,-B,-C and (+)-mahanine, carbazole alkaloids from Murraya euchrestifolia
- ↑ 61,0 et 61,1 Murrayamine-C from murraya euchrestifolia
- ↑ Chemical constituents of Murraya euchrestifolia Hayata. Structures of novel carbazolequinones and other new carbazole alkaloids.
- ↑ 63,0 63,1 63,2 et 63,3 Arbutin fromOnobrychis kachetica
- ↑ Preliminary study of phenolic glycosides from Origanum majorana; quantitative estimation of arbutin; cytotoxic activity of hydroquinone
- ↑ Phagnalon rupestre as a source of compounds active on contact hypersensitivity
- ↑ New benzyl alcohol glycosides from Pyrus bourgaeana
- ↑ Active-oxygen scavenging activity of traditional nourishing-tonic herbal medicines and active constituents of Rhodiola sacra
- ↑ Prolyl endopeptidase inhibitors from the underground part of Rhodiola sacra S. H. Fu.
- ↑ 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
- ↑ 7-epi-rhyacophiline, a 5,6-secoclerodane diterpene from Salvia rhyacophila
- ↑ Sesterterpenes and other constituents of Salvia yosgadensis
- ↑ 72,0 et 72,1 Homocyclotirucallane and two dihydrophenanthrenes from Spiranthes sinensis
- ↑ Guaianolides and other constituents from Vernonia nitidula
- ↑ Piptocarphol esters and other constituents from Vernonia cognata
- ↑ Diterpenes from Vernonanthura amplexicaulis
- ↑ A comprehensive genome-scale reconstruction of Escherichia coli metabolism--2011.
- ↑ 77,0 et 77,1 Bioactive Metabolites from the Fruits of Psoralea corylifolia
- ↑ Coumarins and other components of Afraegle paniculata
- ↑ Antimicrobial and phytochemical studies on Pedilanthus tithymaloides
- ↑ Zur Geschichte des Proteacins
- ↑ Chemical constituents of Diospyros buxifolia, D. tomentosa, D. ferra, D. lotus, Rhus parviflora, Polygonum recumbens, Balanites aegyptiaca and Pyrus pashia
- ↑ Norditerpene dilactones from Podocarpus saligna
- ↑ Anti-inflammatory sesquiterpene-quinones from the New Zealand sponge Dysidea cf. cristagalli
- ↑ HPLC Analysis of Phenolics and Flavonoids inArctostaphylos uvae-ursi
- ↑ [Anti-tyrosinase activity constituents of Arctostaphylos uva-ursi]
- ↑ Determination of arbutin in uvae-ursi folium (bearberry leaves) by capillary zone electrophoresis
- ↑ 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)
- ↑ Glycosides from the bark of Adina polycephala
- ↑ Studies on Nepalese Crude Drugs. XXVI. Chemical Constituents of Panch Aunle, the Roots of Dactylorhiza hatagirea D. DON.
- ↑ Anti-complementary constituents of Houttuynia cordata and their targets in complement activation cascade
- ↑ Melanin synthesis inhibitors from Lespedeza cyrtobotrya
- ↑ Chemical constituents from Commelina communis
- ↑ N0000147180, 5 mas 2018, NDF-RT
- ↑ 94,0 94,1 et 94,2 Medical Subject Headings, 15 mas 2018, C031927