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Chemical compound
1-Octen-3-ol, octenol for short and also known as mushroom alcohol, is an organic compound with the formula CH2=CHCH(OH)(CH2)4CH3. It is a chiral secondary
1-Octen-3-ol
Chemical compound
1-Octen-3-ol, the alcohol analog that is used by mosquitoes as an odor cue[citation needed] "Human Metabolome Database: Showing metabocard for 1-Octen-3-one
Oct-1-en-3-one
Chemical compound
1-Octen-3-yl acetate is a chemical compound with molecular formula C10H18O2. It is an ester of acetic acid and oct-1-en-3-ol. It exists as two enantiomers
1-Octen-3-yl_acetate
Species of fungus
University of Iowa Press. p. 75. ISBN 978-1-58729-627-7. Wood WF, Archer CL, Largent DL (2001). "1-Octen-3-ol, a banana slug antifeedant from mushrooms"
Clitopilus_prunulus
French soft cheese
(buttery flavoring for popcorn), 3-methylbutanal, methional (degradation product of methionine), 1-octen-3-ol and 1-octen-3-one (degradation products of fats)
Camembert
delta-Octalactone gamma-Octalactone Octanal Octanoic acid 1-Octanol 2-Octanone 3-Octen-2-one 1-Octen-3-ol 1-Octen-3-yl acetate 2-Octenal Octyl isobutyrate Oleic acid
List of additives in cigarettes
List_of_additives_in_cigarettes
Species of fungus
amounts of 1-octen-3-ol, a compound found in many mushrooms that has a typical mushroom-like odour. Both methyl cinnamate and 1-octen-3-ol have been shown
Tricholoma_magnivelare
Fruiting body of a subterranean ascomycete fungus
(C8-alcohols and aldehydes with a characteristic fungal odor, such as 1-octen-3-ol and 2-octenal). The former is derived from linoleic acid and produced
Truffle
Species of fungus
Penicillium which can spoil cereal grains. Penicillium paneum produces 1-Octen-3-ol and penipanoid A, penipanoid B, penipanoid C, patulin and roquefortine
Penicillium_paneum
Unpleasant characteristic of a wine
mushroom, earthy odors and include geosmin, 2-methylisoborneol, 1-octen-3-ol, 2-octen-1-ol, fenchol and fenchone. Wine portal Oenology Acids in wine Browning
Wine_fault
Species of fungus
ISBN 978-0-7627-3109-1. Wood W. F.; Largent D. L.; Henkel T. W. (2004). "Headspace analysis identifies indole and 1-octen-3-ol as the "coal tar" odor
Tricholoma_inamoenum
Chemical compound
"Monitoring of aglycons of yew glycosides (3,5-dimethoxyphenol, myrtenol and 1-octen-3-ol) as first indicator of yew presence". Drug Testing and Analysis. 5 (6):
Myrtenol
Family of flies
hunt for hosts by smelling substances such as carbon dioxide (CO2) and 1-octen-3-ol (mushroom alcohol, found in exhaled breath) produced from the host, and
Mosquito
Flowering plant species in the carrot family
estragole (resembling licorice), fenchone (mint and camphor), limonene, 1-octen-3-ol (mushroom). Other phytochemicals found in fennel fruits include polyphenols
Fennel
Genus of herbs
the main bio-active and toxic constituents. additional compounds: 1-octen-3-ol, 3-octanone, β-myrcene, and β-caryophyllene. Catnip (Nepeta cataria) Kang
Schizonepeta
Air quality within and around buildings and structures
characterized including 1-octen-3-ol (mushroom alcohol), 3-Methylfuran, 2-pentanol, 2-hexanone, 2-heptanone, 3-octanone, 3-octanol, 2-octen-1-ol, 1-octene, 2-pentanone
Indoor_air_quality
Cheese with blue veins of mold
components in creamy Gorgonzola cheese contribute to odor with 2-nonanone, 1-octen-3-ol, 2-heptanol, ethyl hexanoate, methylanisole and 2-heptanone being the
Blue_cheese
Spores produced in an ascus
species wait for chemical or mechanical signals: the volatile substance 1-octen-3-ol released by packed spores inhibits germination until air flow disperses
Ascospore
Species of puffball fungus in the family Agaricaceae with a cosmopolitan distribution
and (23E)-lanosta-8,23-dien-3β,25-diol. The compounds 3-octanone, 1-octen-3-ol, and (Z)-3-octen-1-ol are the predominant components of the volatile chemicals
Lycoperdon_perlatum
Genus of fungi
that three odoriferous compounds; 1-octen-3-ol, indole and 3-chloroindole are emitted from sporocarps. Indole and 3-chloroindole have fecal-like odors
Hygrophorus
Index of chemical compounds with the same molecular formula
4-Methylcyclohexanemethanol Octanal Octanones 2-Octanone 3-Octanone 4-Octanone 1-Octen-3-ol Tetramethyltetrahydrofurans 2,2,5,5-Tetramethyltetrahydrofuran
C8H16O
Cosmopolitan species of fungus
abundance of volatile eight-carbon compounds (including 1-octanol, 1-octen-3-ol, and 1-octen-3-one) that imparted a "mushroom-like, earthy, and pungent
Astraeus_hygrometricus
Species of fungus
(PDF). Acta Chemica Scandinavica B. 30 (3): 235–44. doi:10.3891/acta.chem.scand.30b-0235. Cotton S. "1-Octen-3-ol". Molecule of the Month. University of
Lactarius_torminosus
Pine bolete mushroom
component of the aroma of porcini mushrooms; 1-Octen-3-ol, 2-octen-1-ol, 3-Octanone, (E)-2-octenal, oct-1-en-3-one and 1,7,7-trimethyl-heptan-2-one, 2-propenoic
Boletus_pinophilus
Species of edible fungus of the family Hydnaceae distributed in Europe
fruity aroma of the mushroom include eight-carbon derivatives, such as 1-octen-3-ol, (E)-2-octenol, and (E)-1,3-octadiene. European studies conducted after
Hydnum_repandum
Species of fungus in the family Boletaceae
in vitro. The compounds 3-Octanone (47.0% of total volatile compounds), 3-Octanol (27.0%), 1-octen-3-ol (15.0%), and limonene (3.6%) are the predominant
Caloboletus_calopus
Species of fly
determine where to lay their eggs. They detect chemicals, such as 1-octen-3-ol and 3-octatone which trigger oviposition. These chemicals are oftentimes
Delia_platura
Species of herbaceous plant
ethyl ester, 2-ethyl-1-hexanol, 1-phenyl-1,2-propanediol, 1-octen-3-ol, 1-nonanol, 1-dodecanol, 1,7,7-trimethyl-bicyclo(2.2.1)hept-2-ene, and (Z)-butanoic
Strobilanthes_tonkinensis
Species of fungus
1-octen-3-ol on infected hosts of L. fungicola. While more research is needed to contribute its effects on management, it has been shown that 1-octen-3-ol
Verticillium_dry_bubble
Species of flowering plant
distillation. The major components are oleic acid, hexadecanoic acid, 1-octen-3-ol, and caryophyllene.[citation needed] It has the ability to inhibit of
Leucas_zeylanica
Class of chemical compounds
the products of the enzymatic cleavage reaction of linoleic acid to 1-octen-3-ol and 10-oxo-trans-8-decenoic acid in mushrooms (Psalliota bispora)". Biochimica
Decenoic_acid
American fungal geneticist and advocate for women in science
investigate the biological effects of VOCs, demonstrating, for instance, that 1-octen-3-ol ("mushroom alcohol") is the neurotoxic in Drosophila melanogaster and
Joan_W._Bennett
Species of fungus
2-phenylethanal, 2-phenylethanol, phenylacetic acid, N-formylaniline, and 1-octen-3-ol. H. radicosum produces a rusty brown to cinnamon-brown spore print. Spores
Hebeloma_radicosum
Chemical compound
chemical compound 3,7-dimethyloct-7-en-1-ol. As the (3S) isomer it is CAS 6812-78-8, and as the racemate it is CAS 141-25-3. In the field of perfumery materials
Rhodinol
Species group of the subgenus Drosophila
odourants that are common in rotting mushrooms, such as 1-pentanol, 1-octen-3-ol, and 3-methyl-1-butanol. Compared to Drosophila melanogaster, D. falleni
Drosophila quinaria species group
Drosophila_quinaria_species_group
Brand of toilet cleaner
Pine: Acid Blue #9, FD&C Yellow #5, 2,4-dimethyl-3-cyclohexene carboxaldehyde, 2,6-dimethyl-7-octen-2-ol, 2-methylundecanal, borneol, coumarin, dipropylene
Toilet_Duck
Chemical compound
Collected Volumes, vol. 3, p. 185. Jarowicki, K.; Kocienski, P. J.; Qun, L. "1,2-Metallate Rearrangement: (Z)-4-(2-Propenyl)-3-Octen-1-ol". Organic Syntheses
Copper(I)_bromide
Chemical compound
; Qun, Liu (2002). "1,2-Metallate Rearrangement: (Z)-4-(2-Propenyl)-3-Octen-1-Ol". Organic Syntheses. 79: 11. doi:10.15227/orgsyn.079.0011. ISSN 2333-3553
Tert-Butyllithium
Chemical compound
Kocienski; Liu Qun (2002). "1,2-Metallate Rearrangement: (Z)-4-(2-Propenyl)-3-octen-1-ol". Org. Synth. 79: 11. doi:10.15227/orgsyn.079.0011. Tschantz, M. A.;
2,3-Dihydrofuran
Glands found near the anus in many mammals
indicated that some of the volatile compounds, specifically 2-octenal, 2-octen-1-ol and indole, were produced by microbes. The anal gland of the Indian mongoose
Anal_gland
Family of insects
Retrieved 9 September 2015. French, Frank E.; Kline, Daniel L. (1989). "l-Octen-3-ol, an effective attractant for Tabanidae (Diptera)". Journal of Medical
Tabanidae
Chemical compound
Structural Relationship of (Z)-6-Nonenal and (Z)-5-Octen-l-ol to Fruit Fly Attractants". J. Agric. Food Chem. 29 (3): 647–649. doi:10.1021/jf00105a053.
6-Nonenal
Species of fungus
between 21 °C and 23 °C. Metabolic products of this fungi include 2-octen-1-ol and 1-octanol and ochratoxin A, brevianamide A, citrinin, penicillic acid
Penicillium_verrucosum
Chemical compound
Vol. 74, p.205 (1997). Conjugate Addition Of A Vinylzirconium Reagent: 3-(1-Octen-1-Yl)Cyclopentanone, Organic Syntheses, Coll. Vol. 9, p.640 (1998); Vol
Schwartz's_reagent
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