furfural

Siidosisdoallu ii dorjo eará gielaide.

kjemisk forbindelse

Eksterne ressurser

Art & Architecture Thesaurus-ID
ZVG-nummer
HCIS ID
DSSTOX compound identifier
Encyclopædia Britannica Online-ID
science/furfural

namain: furfural

NSC-numero
ChEMBL-ID
Gran Enciclopèdia Catalana -tunniste
HMDB-ID
Römpp online -tunniste
MeSH-kode
AICS Chemical ID (BEING DELETED)
RTECS-nummer
LT7000000
ECHA InfoCard -tunniste
UM-BBD compound ID
PDB ID
FEMA number
CAMEO Chemicals ID
NALT-gilkor
Encyclopedia of China (Third Edition) ID
Probes And Drugs ID
De Agostini ID
furfurale

namain: furfurale

Freebase-gilkor
CA PROP 65 ID
Microsoft Academic-ID
UniChem compound ID
Quora-fáddágilkor
YSO-gilkor
UNII
PDB ligand ID
SPLASH
PesticideInfo chemical ID
National Library of Israel J9U ID
DSSTox substance ID
MassBank accession ID
KEGG-ID
OpenAlex-ID
WordNet 3.1 Synset ID
14900624-n
InChI
EU-nummer
202-627-7[13]
InChIKey
Cannabis Database ID
LCAuth-gilkor
ChEBI-ID
34768[16]

SKOS-relasjonstype: eksakt samsvar

CosIng-tunnistenumero
Gran Enciclopèdia Catalana-ID
CAS-nummer
Reaxys registry number
105755[16]
SNL-gilkor
MeSH-ID
D005662

namain: Furaldehyde

ICSC ID
NDL-nummer
PubChem-id (CID)
KNApSAcK-tunniste
UMLS CUI
JECFA number
450[24]
OSHA Occupational Chemical Database ID
ChemSpider-ID
JECFA database ID
FL number
13.018[26]
NKC-gilkor
ph314893

namain: furfural

GND-gilkor
HSDB-tunniste

lea

type kjemisk entitet

gullá čuovvovaš kategoriijai

heterosyklisk forbindelse
aldehyd

del av

response to furfural[28]

subjekt har rollen: reaktant

furaldehyde metabolic process[29]

subjekt har rollen: participant

kjemisk struktur

masse

96,021 atommasseenhet[18]

čuovvumušat

furfural exposure[30]

kjemisk formel

C₅H₄O₂[18]

SMILES

C1=COC(=C1)C=O[18]

ioniseringsenergi

9,21±0,01 elektronvolt[30][31]

sadji ráiddus: 1

tetthet

1,16±0,01 grammaa per kuutiosenttimetri[30]

temperatuvra: 20±1 grader celsius

smeltepunkt

−34±1 grader fahrenheit[30]
−38 grader celsius[32]
−36,5 grader celsius[31]

kokepunkt

323±1 grader fahrenheit[30]

trykk: 760±1 torr

161,75 grader celsius[31]

trykk: 101,325 kilopascal

damptrykk

2±1 millimeter kvikksølv[30]

temperatuvra: 68±1 grader fahrenheit

løselighet

8±1 gram per 100 gram of solvent[30]

temperatuvra: 68±1 grader fahrenheit

løsemiddel: čáhci

flammepunkt

140±1 grader fahrenheit[30]

bestemmelsesmetode: Pensky–Martens closed-cup test

nedre eksplosjonsgrense

2,1±0,1 volumprosent[30]

øvre eksplosjonsgrense

19,3±0,1 volumprosent[30]

NIOSH Pocket Guide ID

0297

time-weighted average exposure limit

20±1 milligrammaa kuutiometrissä[30]

administrasjonsvei: hudkontakt

doaibmaváldi, masa gullá: Amerihká ovttastuvvan stáhtat

bistu: 8±1 diibmu

immediately dangerous to life or health

393±1 milligrammaa kuutiometrissä[30]

finnes i takson

mandel[33]
vandreblomst[34]
Coffea arabica[35]
Paeonia lactiflora[36]
Edelråte[37]
Sapodilletre[38]
Swertia japonica[39]
ingefær[40]
jordskokk[41]
Pueraria montana var. lobata[42]
lakrisplante[43][44]
Sitronmelisse[45]
Ruutubukko[46]
Asarum canadense[47]
havre[48]
Malabarinpinaatti[49]
Campsis grandiflora[50]
Castanopsis cuspidata[51]
Rohtosammakonputki[52]
endivie[53]
Cinnamomum zeylanicum[54]
Daphne genkwa[55]
mangostantre[56]
Geum heterocarpum[62]
Hagebønne[63]
Polygala senega[64]
Saussurea involucrata[65]
Kryddernellik[66]
Tamarind[67][68]
Kakaotre[69]
Vitis rotundifolia[70]
Kapers[71]
Streptomyces cavourensis[72]
Angelica gigas[73]
Manankukka[74]
blodkløver[75]
løkurt[76]
Streptomyces bacillaris[72]
seller[77]
papaya[78]
Garcinia dulcis[79]
gran[80]
Viherkameleonttilehti[81]
Tobakksplante[82][83]
asparges[84]
Ligusticum chuanxiong[85]
Palsamiköynnös[86]
Viburnum orientale[87]
Magnolia obovata[88]
Vetiveriaheinä[89]
Conioselinum anthriscoides[85]
Ligusticum striatum[85]
Ceyloninkaneli[54]
morell[33]
Scleromitrion diffusum[90]
febertre[91]
Eucalyptus polyanthemos[91]
Eucalyptus perriniana[91]
Ekte vinranke[92]

beskrevet i kilde

Armenske sovjetiske encyklopedi
Entsiklopeditsjeskij slovar Granat

tema for: Q87337566

har egenskap

Class IIIA combustible liquid[30]

subjekt har rollen

metabolitt

finnes i takson: Homo sapiens

dasa gullet

oksygena
čitna

Commons-kategoriija

Furfural

fáttá váldokategoriija

Luokka:Furfuraalit

Gáldu

  1. ChEMBL, 19 golggotmánnu 2016, eaŋgalsgiella, FURFURAL, CHEMBL189362
  2. a á b inferred from InChIKey
  3. ECHA Substance Infocard database, 27 juovlamánnu 2018, 100.002.389, 2-furaldehyde, CAS no.: 98-01-1
  4. Protein Data Bank, 19 golggotmánnu 2016, eaŋgalsgiella, 1QXD, 1QXD
  5. Protein Data Bank, 19 golggotmánnu 2016, eaŋgalsgiella, 3S2F, 3S2F
  6. Protein Data Bank, 19 golggotmánnu 2016, eaŋgalsgiella, 3S2G, 3S2G
  7. Protein Data Bank, 19 golggotmánnu 2016, eaŋgalsgiella, 3S2I, 3S2I
  8. Freebase-data fra Google, 28 golggotmánnu 2013
  9. California Proposition 65 list of chemicals, 6 ođđajagimánnu 2020, https://oehha.ca.gov/chemicals/furfural
  10. UniChem
  11. Quora
  12. YSOn ja Wikidatan linkitys
  13. a á Global Substance Registration System, 19 golggotmánnu 2016, eaŋgalsgiella, furfural, DJ1HGI319P
  14. National Library of Israel Names and Subjects Authority File
  15. Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard
  16. a á b c č ChEBI, 19 golggotmánnu 2016, eaŋgalsgiella, furfural, 34768
  17. OpenAlex, 26 ođđajagimánnu 2022, https://docs.openalex.org/download-snapshot/snapshot-data-format
  18. a á b c č d PubChem, 19 golggotmánnu 2016, eaŋgalsgiella, 7362, FURFURAL
  19. ChEBI release 2020-09-01
  20. Cannabis Database
  21. CosIng database, 28 juovlamánnu 2019, 33965, FURFURAL, CAS no.: 98-01-1
  22. CAS Common Chemistry, 9 cuoŋománnu 2021, HYBBIBNJHNGZAN-UHFFFAOYSA-N, https://commonchemistry.cas.org/detail?cas_rn=98-01-1
  23. UMLS 2023, 24 miessemánnu 2023, inferred by common MeSH mappings on source and on Wikidata
  24. Evaluations of the Joint FAO/WHO Expert Committee on Food Additives (JECFA), 30 skábmamánnu 2021
  25. ChemSpider, 19 golggotmánnu 2016, eaŋgalsgiella, 13863629, Furfural
  26. EFSA database, 23 ođđajagimánnu 2021, CAS no.: 98-01-1, 13.018
  27. Hazardous Substances Data Bank, 10 miessemánnu 2021, 28 golggotmánnu 2019, FURFURAL, 542
  28. Gene Ontology release 2019-11-16
  29. Gene Ontology release 2020-05-02
  30. a á b c č d đ e f g h i j http://www.cdc.gov/niosh/npg/npgd0297.html
  31. a á b Basic laboratory and industrial chemicals: A CRC quick reference handbook
  32. Jean-Claude Bradley Open Melting Point Dataset
  33. a á Components of almond hulls: possible navel orangeworm attractants and growth inhibitors
  34. PHYTOCHEMICAL STUDY OF LANTANA CAMARA I
  35. New volatile components of roasted coffee
  36. "Essential oil constituents of \"PAEONIAE RADIX\" Peaonia lactiflora Pall. (P. albilora Pall.)."
  37. Odorous metabolites of fungi, Chaetomium globosum Kinze ex Fr. and Botrytis cinerea Pers. ex Fr., and a blue-green alga, Phormidium tenue (Meneghini) Gomont.
  38. Volatile flavor components of sapodilla fruit (Achras sapota L)
  39. Semburins and Swertiols, Novel 2,8-Dioxabicyclo[3.3.1]nonanes and Their Precursory Alcohols, fromSwertia japonicaMakino
  40. Investigation of the essential oil of Vietnamese ginger
  41. Aroma volatiles of Cynara scolymus and Helianthus tuberosus
  42. Volatile flavor components of Puerariae radix (Pueraria lobata Ohwi).
  43. Components of essential oil from the root of Glycyrrhiza glabra.
  44. Volatile flavor components of licorice
  45. The Constituents ofMelissa officinalisL. Cultures
  46. Analysis of Buchu leaf oil
  47. Composition of the essential oil from Asarum canadense
  48. Volatile food attractants forOryzaephilus surinamensis (L.) from oats
  49. Volatile flavor components of malabar-nightshade (Basella rubra L.)
  50. The essential oil from the flowers ofCampsis grandiflora (Thumb.) K. Schum. from China
  51. Volatile constituents of Castanopsis flower
  52. Essential Oil ofCentella asiatica(L.) Urb.
  53. Neutral volatiles from blended endive (Cichorium endivia, L.)
  54. a á Volatile constituents of cinnamon (Cinnamomum zeylanicum) oils
  55. The Chemical Composition of the Essential Oil ofDaphne genkwaSieb. et Zucc.
  56. Volatile flavour components of mangosteen, Garcinia mangostana
  57. Volatile aroma constituents of mango (cv Kensington)
  58. Volatile components from mango (Mangifera indica L.) cultivars
  59. Aroma Volatile Constituents of Brazilian Varieties of Mango Fruit
  60. Glycosidically-bound aroma volatile compounds in the skin and pulp of ‘Kensington Pride’ mango fruit at different stages of maturity
  61. Characteristic Aroma Components of the Volatile Oil of Yellow Keaw Mango Fruits Determined by Limited Odor Unit Method.
  62. Composition of the Root Oil ofOrthurus heterocarpus(Boiss.) Juz.
  63. Characterization of some volatile constituents of dry red beans
  64. Volatile compounds ofPolygala senega L. var.latifolia Torrey et Gray roots
  65. Components of the Essential Oil of Saussurea involucrata (Kar. et Kir.) ex Maxim
  66. Volatile components of clove essential oil (Eugenia caryophyllus SPRENG): Neutral fraction.
  67. Volatile Flavor Components of Tamarind (Tamarindus indicaL.)
  68. Supercritical Fluid Extraction of the Volatile Constituents from Tamarind (Tamarindus indicaL.)
  69. Steam volatile aroma constituents of roasted cocoa beans
  70. Identification of the Volatile Constituents from Scuppernong Berries (Vitis rotundifolia)
  71. Nematicidal activity of 2-thiophenecarboxaldehyde and methylisothiocyanate from caper (Capparis spinosa) against Meloidogyne incognita
  72. a á Biocontrol of anthracnose in pepper using chitinase, beta-1,3 glucanase, and 2-furancarboxaldehyde produced by Streptomyces cavourensis SY224
  73. Analysis of the influence of sulfur-fumigation on the volatile components of Angelicae sinensis Radix by comprehensive two-dimensional gas chromatography/time-of-flight mass spectrometry
  74. Volatile constituents of Dactylanthus taylorii flower nectar in relation to flower pollination and browsing by animals
  75. LXXIX.—The constituents of the flowers of Trifolium incarnatum
  76. Free and Bound Volatiles of Garlic Mustard (Alliaria petiolata)
  77. Aromatic Volatile Composition of Celery and Celeriac Cultivars
  78. Volatile components of papaya (Carica papaya L., Maradol variety) fruit
  79. Volatile constituents of fruits of Garcinia dulcis Kurz. from Cuba
  80. Analysis of chemical changes in Picea abies wood decayed by different Streptomyces strains showing evidence for biopulping procedures
  81. Gas chromatography–mass spectrometry analysis of volatile compounds from Houttuynia cordata Thunb after extraction by solid-phase microextraction, flash evaporation and steam distillation
  82. 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
  83. Extraction of essential oil from discarded tobacco leaves by solvent extraction and steam distillation, and identification of its chemical composition
  84. EVALUATION OF ASPARAGUS OFFICINALIS L. FLAVOUR QUALITY FOR BREEDING PURPOSES
  85. a á b Analysis of the volatile compounds in Ligusticum chuanxiong Hort. using HS-SPME-GC-MS.
  86. Analysis of volatile fractions of Schisandra chinensis (Turcz.) Baill. using GC-MS and chemometric resolution
  87. Composition of the Essential Oil from Viburnum orientale Pallas Leaves
  88. Composition of the Bark Oil of Magnolia obovata Thunb.
  89. Headspace Constituents of Vetiver Oil
  90. Composition of the Essential Oil of Hedyotis diffusa Willd.
  91. a á b Antioxidant activities of volatile components isolated from Eucalyptus species
  92. Separation and Identification of Furanic Compounds in Fruit Juices and Drinks by High-Performance Liquid Chromatography Photodiode Array Detection