acétophénone
composé chimique
Resous ekstèn
| CSD Refcode | |
| numéro ZVG | |
| HCIS ID | |
| identifiant DSSTOX d'un composé chimique | |
| identifiant ChEMBL | |
| identifiant Grande Encyclopédie catalane | |
| identifiant Fiches internationales de sécurité chimique | |
| identifiant RÖMPP-Online | |
| identifiant de la Grande Encyclopédie russe en ligne | |
| identifiant d'InfoCard ECHA | |
| identifiant UM-BBD d'un composé chimique | |
| identifiant Protein Data Bank | |
| CAMEO Chemicals ID | |
| identifiant CCDC | |
| identifiant Encyclopédie de Chine (troisième édition) | |
| identifiant J9U de la Bibliothèque nationale d'Israël | |
| idantifyan sou Freebase | |
| identifiant Microsoft Academic | |
| identifiant Bibliothèque du Congrès | |
| identifiant PubChem (CID) | |
| UniChem compound ID | |
| identifiant Unique Ingredient Identifier | |
| identifiant ChEBI | |
| identifiant Protein Data Bank d'un ligand | |
| SPLASH | |
| PesticideInfo chemical ID | |
| identifiant DSSTOX | |
| identifiant KEGG | |
| identifiant OpenAlex | |
| identifiant Gran Enciclopèdia Catalana (ancien) | |
| identifiant Bibliothèque nationale centrale de Florence | |
| InChIKey | |
| Cannabis Database ID | |
| identifiant DrugBank | |
| identifiant ZTH Elhuyar | |
| numéro CosIng | |
| identifiant Human Metabolome Database | |
| identifiant SureChEMBL | |
| InChI | |
| identifiant Store norske leksikon | |
| identifiant Lex | |
| numéro CAS | |
| numéro FL | 07.004[22] |
| identifiant Medical Subject Headings | |
| identifiant KNApSAcK | |
| numéro JECFA | 806[25] |
| OSHA Occupational Chemical Database ID | |
| identifiant ChemSpider | |
| numéro CE | |
| identifiant Probes And Drugs | |
| identifiant ScienceDirect d'un sujet | |
| identifiant GND (DNB) | |
| identifiant MassBank | |
| identifiant Grande Encyclopédie russe d'un article | |
| numéro NSC | |
| identifiant NMRShiftDB | |
| identifiant Hazardous Substances Data Bank |
se yon
type d'entité chimique
structure chimique
masse
120,058 unité de masse atomique unifiée[28]
formule chimique
C₈H₈O[9]
SMILES canonique
CC(=O)C1=CC=CC=C1[9]
énergie d'ionisation
moment dipolaire électrique
masse volumique
point de fusion
point d'ébullition
202,1±0,2 Degre Sèlsiyis[31]
pression: 101,325 kilopascal
incertitude correspond à: incertitude élargie
point de phase
point critique[32]
pression: 4,01±0,05 mégapascal
volume molaire: 373±40 centimètre cube par mole
température: 709,5±0,7 Kelven
viscosité dynamique
tension de surface
pression de vapeur
solubilité
indice de réfraction
système cristallin
système cristallin monoclinique[31]
point d'éclair
limite inférieure d’explosivité
55 gramme par mètre cube[35]
classification et étiquetage de sécurité
NFPA 704: Standard System for the Identification of the Hazards of Materials for Emergency Response[39]
code NFPA spécial: aucune valeur
code NFPA santé: 2
code NFPA feu: 2
code NFPA réactivité: 0
règlement relatif à la classification, à l'étiquetage et à l'emballage des substances et des mélanges[40]
pictogramme de danger du SGH: SGH07: point d'exclamation
mention de danger du SGH: H302, H319
conseil de prudence du SGH: P305+P351+P338
terme d'avertissement du SGH: danger
trouvé dans le taxon
figuier de Barbarie[43]
rooibos[44]
Pivoine de Chine[45]
Daphne odora[46]
Hypericum hyssopifolium[48]
Nepeta racemosa[51]
Amorphophallus cicatricifer[52]
Aronia melanocarpa[53]
Artemisia xanthochroa[54]
pâquerette[56]
Castanopsis cuspidata[57]
Chamaecrista greggii[58]
Euphorbe petit-cyprès[60]
Evernia Prunastri[61]
Gossypium hirsutum[62]
Helichrysum ambiguum[63]
Malpighia punicifolia[64]
Nepeta nepetella[65]
Ophrys araignée[66]
Polygala senega[67]
Sauromatum venosum[68]
Scutellaria baicalensis[69]
Strobilanthes auriculatus[70]
Tamarix aphylla[72]
Trèfle des prés[74]
Medicago sativa[75]
canneberge à gros fruits[76]
Baccharis[77]
Acca sellowiana[78]
Strobilanthes auriculata[70]
Elsholtzia eriostachya[79]
Mangifera indica[80]
Cymbopogon citratus[81]
Malpighia glabra[64]
Malpighia emarginata[64]
Chrysocephalum ambiguum[63]
Tricholoma matsutake[85]
décrit par
Grande Encyclopédie soviétique
affirmation détaillée dans: Q43447952
XIe édition de l'Encyclopædia Britannica
affirmation détaillée dans: 1911 Encyclopædia Britannica/Acetophenone
Meyers Konversations-Lexikon, 4e édition (1885–1890)
affirmation détaillée dans: Q112753740
Grande Encyclopédie soviétique
affirmation détaillée dans: Q110375593
caractérisé par
amertume[86]
code MCN
2914.39.10
à ne pas confondre avec
Benzophénone
catégorie Commons
Acetophenone
Referans
- ↑ 1,0 et 1,1 Cambridge Structural Database, 10 janvye 2023, InChIKey match
- ↑ 2,0 et 2,1 ChEMBL, 20 novanm 2016, angle, ACETOPHENONE, CHEMBL274467
- ↑ base de données InfoCard de l'ECHA, 27 desanm 2018, 100.002.462, Acetophenone, CAS no.: 98-86-2
- ↑ Protein Data Bank, 19 oktòb 2016, angle, 1ZK4, 1ZK4
- ↑ Protein Data Bank, 19 oktòb 2016, angle, 1ZK1, 1ZK1
- ↑ National Library of Israel Names and Subjects Authority File
- ↑ sauvegarde de la base de données Freebase, 28 oktòb 2013
- ↑ Gemeinsame Normdatei
- ↑ 9,0 9,1 9,2 9,3 et 9,4 PubChem, 20 novanm 2016, angle, 7410, ACETOPHENONE
- ↑ 10,0 10,1 10,2 10,3 10,4 10,5 10,6 et 10,7 KWOLFJPFCHCOCG-UHFFFAOYSA-N, InChIKey
- ↑ UniChem
- ↑ 12,0 12,1 et 12,2 Global Substance Registration System, 20 novanm 2016, angle, acetophenone, RK493WHV10
- ↑ InChI=1S/C8H8O/c1-7(9)8-5-3-2-4-6-8/h2-6H,1H3, International Chemical Identifier
- ↑ Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
- ↑ OpenAlex, 26 janvye 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
- ↑ Nuovo soggettario
- ↑ ChEBI release 2020-09-01
- ↑ Cannabis Database
- ↑ base de données CosIng, 28 desanm 2019, 74153, ACETOPHENONE, CAS no.: 98-86-2
- ↑ 20,0 20,1 et 20,2 inferred from InChIKey
- ↑ CAS Common Chemistry, 8 avril 2021, https://commonchemistry.cas.org/detail?cas_rn=98-86-2, KWOLFJPFCHCOCG-UHFFFAOYSA-N
- ↑ EFSA database, 23 janvye 2021, CAS no.: 98-86-2, 07.004
- ↑ Medical Subject Headings, 14 mas 2018, C038699
- ↑ ChEBI, 19 oktòb 2016, angle, acetophenone, 27632
- ↑ Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 13 me 2021
- ↑ ChemSpider, 20 novanm 2016, angle, 7132, Acetophenone
- ↑ Hazardous Substances Data Bank, 10 me 2021, 28 oktòb 2019, Acetophenone, 969
- ↑ PubChem, 19 oktòb 2016, angle, 7410, ACETOPHENONE
- ↑ Basic laboratory and industrial chemicals: A CRC quick reference handbook
- ↑ CRC Handbook of Chemistry and Physics (97th edition), 9-60
- ↑ 31,0 31,1 31,2 31,3 et 31,4 CRC Handbook of Chemistry and Physics (97th edition), 3-6
- ↑ CRC Handbook of Chemistry and Physics (97th edition), 6-67
- ↑ 33,0 et 33,1 CRC Handbook of Chemistry and Physics (97th edition), 6-243
- ↑ 34,0 34,1 et 34,2 CRC Handbook of Chemistry and Physics (97th edition), 6-190
- ↑ 35,0 35,1 35,2 35,3 35,4 35,5 35,6 et 35,7 base de données Gestis, 30 jiyè 2018, angle, 22380, Acetophenone
- ↑ 36,0 36,1 et 36,2 CRC Handbook of Chemistry and Physics (97th edition), 15-13, 16-17
- ↑ 37,0 37,1 et 37,2 CRC Handbook of Chemistry and Physics (97th edition), 5-139
- ↑ CRC Handbook of Chemistry and Physics (97th edition), 5-173
- ↑ https://fscimage.fishersci.com/msds/00002.htm, Fisher Scientific, angle, 30 jiyè 2018, Acetophenone, 99%, 10 desanm 2007
- ↑ base de données Gestis, 30 jiyè 2018, angle, 22380, Acetophenone, 2016
- ↑ Studies on the Volatile Compounds of Camellia Flowers
- ↑ Volatile Compounds from Flowers
- ↑ Volatile constituents of prickly pear (Opuntia ficus indica Mill., de Castilla variety)
- ↑ Volatile components of Rooibos tea (Aspalathus linearis)
- ↑ "Essential oil constituents of \"PAEONIAE RADIX\" Peaonia lactiflora Pall. (P. albilora Pall.)."
- ↑ Volatile components of zinchoge flower (Daphne odora Thunb.).
- ↑ Volatile constituents of carambola (Averrhoa carambola L.)
- ↑ Composition and antifungal activity of essential oils isolated fromHypericum hyssopifolium andHypericum heterophyllum
- ↑ Terpenoids from Elsholtzia Species; II1. Constituents of Essential Oil from a New Chemotype of Elsholtzia cristata
- ↑ Composition of the Essential Oils from the Aerial Parts ofElsholtzia ciliata(Thunb.) Hyland. from Vietnam
- ↑ Composition of the Essential Oil of Nepeta racemosa Lam.
- ↑ Inflorescence odours of Amorphophallus and Pseudodracontium (Araceae)
- ↑ Analysis of the volatile constituents of black chokeberry (Aronia melanocarpa Ell.)
- ↑ Prenylated coumarates from Artemisia xanthochroa
- ↑ Volatile flavor components of malabar-nightshade (Basella rubra L.)
- ↑ Acetylenes and terpenoids of Bellis perennis
- ↑ Volatile constituents of Castanopsis flower
- ↑ Cassanes and anthraquinones from Chamaecrista greggii
- ↑ Volatile flavor components of watermelon (Citrullus vulgaris).
- ↑ Biologically Active Compounds from the Euphorbiaceae; 2. Two Triterpenoids ofEuphorbia cyparissias
- ↑ Qualitative analysis of the odoriferous fraction of oakmoss (Evernia prunastri)
- ↑ Survey of the volatile constituents of cotton lint and waste with regard to byssinosis
- ↑ 63,0 et 63,1 Composition and antibacterial activity of the essential oils of Helichrysum rupestre and H. ambiguum growing in the Balearic Islands (Part III)
- ↑ 64,0 64,1 et 64,2 Chemical composition of acerola fruit (Malpighia punicifolia L.) at three stages of maturity
- ↑ Constituents of Essential Oil of Nepeta nepetella
- ↑ Volatiles from the flowers of four species in the sections arachnitiformes and araneiferae of the genus Ophrys as insect mimetic attractants
- ↑ Volatile compounds ofPolygala senega L. var.latifolia Torrey et Gray roots
- ↑ Dimethyl oligosulphides, major volatiles released from Sauromatum guttatum and Phallus impudicus
- ↑ Essential oil of Scutellaria baicalensis G.
- ↑ 70,0 et 70,1 Constituents of the Essential Oil of Strobilanthes auriculatus
- ↑ Volatile components of clove essential oil (Eugenia caryophyllus SPRENG): Neutral fraction.
- ↑ Antimicrobial Activity and Phytochemical Constituents of Leaf Extracts of Cassia auriculata
- ↑ Steam volatile aroma constituents of roasted cocoa beans
- ↑ Volatile components of red clover leaves, flowers, and seed pods: possible insect attractants
- ↑ Volatiles from Medicago sativa complex flowers
- ↑ The Aroma of Cranberries. II. Vaccinium macrocarpon Ait.
- ↑ Plant growth inhibitory activity of p-hydroxyacetophenones and tremetones from Chilean endemic Baccharis species and some analogous: a comparative study
- ↑ Compositional Analysis and Aroma Evaluation of Feijoa Essential Oils from New Zealand Grown Cultivars
- ↑ The Essential Oil fromElsholtzia eriostachyavar.pusilla
- ↑ Volatile components from mango (Mangifera indica L.) cultivars
- ↑ GC-MS evaluation of Cymbopogon citratus (DC) Stapf oil obtained using modified hydrodistillation and microwave extraction methods
- ↑ Comparison of different extraction methods: steam distillation, simultaneous distillation and extraction and headspace co-distillation, used for the analysis of the volatile components in aged flue-cured tobacco leaves
- ↑ Extraction of essential oil from discarded tobacco leaves by solvent extraction and steam distillation, and identification of its chemical composition
- ↑ Volatile Flavor Components of Corn Tortillas and Related Products
- ↑ Volatile flavor compounds of Matsutake-Tricholomam atsutake (Ito et Imai) Sing.
- ↑ BitterDB
- ↑ Medical Subject Headings, 15 mas 2018, C038699