acide hexanoïque

composé chimique

Resous ekstèn

numéro ZVG
identifiant DSSTOX d'un composé chimique
identifiant Encyclopædia Britannica
science/caproic-acid

sous le nom: caproic acid

numéro NSC
identifiant ChEMBL
identifiant Grande Encyclopédie catalane
identifiant Nikkaji
identifiant Fiches internationales de sécurité chimique
identifiant JSTOR d'un sujet
identifiant d'InfoCard ECHA
identifiant Protein Data Bank
identifiant NMRShiftDB
CAMEO Chemicals ID
identifiant Encyclopédie de Chine (troisième édition)
identifiant Probes And Drugs
identifiant LIPID MAPS
idantifyan sou Freebase
numéro Beilstein
773837[14]
identifiant PubChem (CID)
UniChem compound ID
identifiant Protein Data Bank d'un ligand
SPLASH
PesticideInfo chemical ID
identifiant OpenAlex
identifiant Vietherb d'un métabolite
InChIKey
Cannabis Database ID
identifiant Unique Ingredient Identifier
numéro Gmelin
185066
identifiant Brockhaus Enzyklopädie
identifiant DSSTOX
identifiant MassBank
numéro CosIng
identifiant J-GLOBAL
numéro FL
08.009[23]
identifiant SureChEMBL
identifiant Foundational Model of Anatomy
82769[25]

sous le nom: Caproic acid

identifiant Microsoft Academic
identifiant Nationalencyklopedin
InChI
numéro CE
code d'entité du langage de programmation Wolfram
identifiant KNApSAcK
UMLS CUI
numéro JECFA
identifiant KEGG
identifiant ChemSpider
JECFA database ID
identifiant Gran Enciclopèdia Catalana (ancien)
identifiant GND (DNB)
identifiant Human Metabolome Database
identifiant ChEBI
30776[1][29]

lien de concordance: équivalence exacte

numéro CAS
identifiant Hazardous Substances Data Bank

se yon

type d'entité chimique

sou-klas

straight chain fatty acids

structure chimique

masse

116,084 unité de masse atomique unifiée[32]

formule chimique

C₆H₁₂O₂[15]

SMILES canonique

CCCCCC(=O)O[15]

énergie d'ionisation

10,12 électronvolt[33]

rang dans la série: 1

point de fusion

−4 Degre Sèlsiyis[34]
−3 Degre Sèlsiyis[33]

point d'ébullition

205,25 Degre Sèlsiyis[33]

pression: 101,325 kilopascal

classification et étiquetage de sécurité

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

code NFPA santé: 3

code NFPA feu: 1

code NFPA réactivité: 0

trouvé dans le taxon

Artemisia xerophytica[35]
Tussilage[36]
Rhododendron mucronulatum[37]
Deschampsia antarctica[38]
Serenoa repens[39][40][41]
Syagrus romanzoffiana[39]
Sabal minor[39]
Haricot d'Espagne[42]
Erigeron philadelphicus[43]
Quercus agrifolia[44]
Daphne odora[45]
Actaea simplex[47]
Cimicifuga simplex[47]
Saussurea involucrata[48]
Truncocolumella citrina[49]
Plumeria rubra[50]
Freesia hybrida[51]
Festuca arundinacea[52]
Geum heterocarpum[53]
Polygala senega[54]
réglisse[55]
Capsicum annuum var. annuum[58]
Mélisse[59]
Ganoderme luisant[60]
Canarium album[61]
Evernia Prunastri[62]
Haploclathra leiantha[65]
Haploclathra paniculata[66]
Lactuca saligna[67]
Medicago sativa[68]
Pélargonium à forte odeur[69]
Trèfle d'Alexandrie[68]
Morinda citrifolia[72]
Oecophylla smaragdina[73][74]
Onagre bisannuelle[75]
Euphorbia tithymaloides[76]
Hypericum gentianoides[77]
Viburnum prunifolium[78]
Yanm[79]
iris[80]
Grenad[81]
Datura alba[82]
Womaren[83]
Staphisaigre[84]
Caenorhabditis elegans[85]
Rhodiola rosea[86]
Mangifera indica[87][88][89][90]
merisier[91][92]
houblon[94]
Garcinia dulcis[95]
Crocus sativus[98]
Magnolia obovata[99]
Chrozophora verbascifolia[100]
Staphisagria macrosperma[84]
Chrozophora tinctoria[100]
Chrozophora obliqua[100]
Cyperus erectus[101]
Datura metel[82]
Hypericum japonicum[77]
Arabidopsis thaliana[103]
Datura leichhardtii[82]
Rhododendron sichotense[37]
Festuca rubra[52]
Eucalyptus globulus[104]
Chrozophora plicata[100]
Streptomyces[105]

décrit par

encyclopédie Otto[106]

affirmation détaillée dans: Ottův slovník naučný/Hexoylové kyseliny

catégorie Commons

Caproic acid

Referans

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  4. Protein Data Bank, 19 oktòb 2016, angle, 4I4C, 4I4C
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