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Chemical compound
2-Hexanol (hexan-2-ol) is a six-carbon alcohol in which the hydroxy group (OH) is located on the second carbon atom. Its chemical formula is C6H14O or
2-Hexanol
Chemical compound
ether and ethanol. Two additional straight chain isomers of 1-hexanol, 2-hexanol and 3-hexanol, exist, both of which differing by the location of the hydroxyl
1-Hexanol
Chemical compound
review on 2-ethyl-1-hexanol". Food and Chemical Toxicology. 48: S115–S129. doi:10.1016/j.fct.2010.05.042. PMID 20659633. "Product Spotlight: 2-Ethylhexanol"
2-Ethylhexanol
Index of chemical compounds with the same name
Hexanol may refer to any of the following isomeric organic compounds with the formula C6H13OH: Cyclohexanol Amyl alcohol This set index article lists
Hexanol
Simplest secondary alcohol
Isopropyl alcohol (IUPAC name propan-2-ol and also called isopropanol or 2-propanol, commonly abbreviated as IPA) is a colorless, flammable, organic compound
Isopropyl_alcohol
Chemical compound
3-Hexanol (IUPAC name: hexan-3-ol; also called ethyl propyl carbinol) is an organic chemical compound. It occurs naturally in the flavor and aroma of
3-Hexanol
Isoamyl alcohol 2-Methyl-1-butanol Neopentyl alcohol 2-Pentanol 3-Methyl-2-butanol 3-Pentanol tert-Amyl alcohol 1-Hexanol 2-Hexanol 3-Hexanol 2-Methyl-1-pentanol
List_of_alkanols
Chemical compound
2-Nonanol is a simple alcohol. It has the odor of cucumber, and has been identified in oysters. It is used by several insects as pheromones. It is commercially
2-Nonanol
Natural sweetener
Xylitol is an organic compound with the formula HOCH(CH(OH)CH2OH)2. Two other isomeric sugar alcohols exist. It is a colorless or white crystalline solid
Xylitol
Index of chemical compounds with the same molecular formula
3-Dimethyl-1-butanol Dipropyl ether 2-Ethyl-1-butanol Ethyl tert-butyl ether Hexanols 1-Hexanol 2-Hexanol 3-Hexanol Methylpentanols 2-Methyl-1-pentanol 3-Methyl-1-pentanol
C6H14O
Dissociative anesthetic and anti-depressant
antagonists ketamine and PCP have direct effects on the dopamine D(2) and serotonin 5-HT(2)receptors-implications for models of schizophrenia". Molecular
Ketamine
Organic compound
feedstock. As of 2024, world production of ethanol fuel was 120 gigaliters (3.2×1010 U.S. gallons), coming mostly from the U.S. (51%) and Brazil (30%). The
Ethanol
Organic compound ethane-1,2-diol
(IUPAC name: ethane-1,2-diol) is an organic compound with the formula (CH2OH)2. It is the simplest vicinal diol. It is mainly used for two purposes: as a
Ethylene_glycol
Sugar alcohol that is used as a sweetener
using enzymes and fermentation. Its formula is C 4H 10O 4, or HO(CH2)(CHOH)2(CH2)OH. Erythritol is 60–70% as sweet as table sugar. However, erythritol
Erythritol
Chemical compound
(sometimes represented as t-BuOH). Its isomers are 1-butanol, isobutanol, and 2-butanol. tert-Butyl alcohol is a colorless solid, which melts near room temperature
Tert-Butyl_alcohol
Chemical compound (C6H14)
reported to have suffered hexane poisoning. n-Hexane is biotransformed to 2-hexanol and further to 2,5-hexanediol in the body. The conversion is catalyzed
Hexane
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
1-Dotriacontanol
Chemical compound
Sandal hexanol at thegoodscentscompany.com 3-(5,5,6-Trimethylbicyclo(2.2.1)hept-2-yl)cyclohexan-1-ol at Sigma-Aldrich GHS: PubChem 103005 "sandal hexanol".
Isobornyl_cyclohexanol
Chemical compound
2-Methyl-2-pentanol (IUPAC name: 2-methylpentan-2-ol) is an organic chemical compound. It can be added to a gas chromatograph to help distinguish between
2-Methyl-2-pentanol
Chemical compound
Dictionary. National Cancer Institute. 2 February 2011. Archived from the original on 2 May 2019. Retrieved 2 May 2019. E. Bertani; A. Chiappa; R. Biffi;
Glycerol
Chemical compound
2-Heptanol is a chemical compound which is an isomer of heptanol. It is a secondary alcohol with the hydroxyl on the second carbon of the straight seven-carbon
2-Heptanol
Chemical compound
name: 3-methylpentan-3-ol) is an organic chemical compound and a tertiary hexanol. It is used in the synthesis of the tranquilizer emylcamate, and has similar
3-Methyl-3-pentanol
Chemical compound
2-dehydrogenase. Sorbitol is an isomer of mannitol, another sugar alcohol; the two differ only in the orientation of the hydroxyl group on carbon 2.
Sorbitol
Secondary alcohol CH3CH(OH)CH2CH3
Butan-2-ol, or sec-butanol, is an organic compound with formula CH3CH(OH)CH2CH3. Its structural isomers are 1-butanol, isobutanol, and tert-butanol. 2-Butanol
2-Butanol
Organic compounds
is obtained by the fermentation of glucose and sucrose. Ethylene glycol (2-carbon) Glycerol (3-carbon) Erythritol (4-carbon) Threitol (4-carbon) Arabitol
Sugar_alcohol
Mixture of sugar alcohols
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
Hydrogenated starch hydrolysates
Hydrogenated_starch_hydrolysates
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
1-Pentanol
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
1-Heptacosanol
Set of reactions to attach substituents to an aromatic ring
aluminium chloride is replaced by graphite in an alkylation of p-xylene with 2-bromobutane. This variation will not work with primary halides from which
Friedel–Crafts_reaction
Chemical reaction
Christoph Elschenbroich: Organometallics, Third, Completely Revised and Extended Edition 2006, Wiley-VCH Weinheim, Germany. ISBN 978-3-527-29390-2.
Ether_cleavage
Chemical compound
alcohol; the two differ only in the orientation of the hydroxyl group on carbon 2. While similar, the two sugar alcohols have very different sources in nature
Mannitol
Chemical compound
2-Fluoroethanol is the organic compound with the formula CH2FCH2OH. This colorless liquid is one of the simplest stable fluorinated alcohols. It was once
2-Fluoroethanol
CH3OH; simplest possible alcohol
areas, especially polymers. The conversion entails oxidation: 2 CH3OH + O2 → 2 CH2O + 2 H2O Acetic acid can be produced from methanol. Methanol and isobutene
Methanol
Chemical reaction which exchanges the R groups of an alcohol and ester
transesterification, giving access to vinyl ethers: ROH + AcOCH=CH 2 ⟶ ROCH=CH 2 + AcOH The reaction can be effected with high enantioselectivity when
Transesterification
Carbocyclic sugar
Cellular and Medical Aspects. Academic Press. p. 348. ISBN 978-0-08-047207-2. Goel, Meenakshi; Azev, Viatcheslav N; d‘Alarcao, Marc (April 2009). "The
Inositol
Chemical compound (C4H9OH)
CH3(CH2)3OH and a linear structure. Isomers of 1-butanol are isobutanol, butan-2-ol and tert-butanol. The unmodified term butanol usually refers to the straight
1-Butanol
Chemical compound
2-Methyl-1-butanol (IUPAC name, also called active amyl alcohol) is an organic compound with the formula CH3CH2CH(CH3)CH2OH. It is one of several isomers
2-Methyl-1-butanol
Class of chemical compounds
relatively benign materials, with LD50 (oral, rat) ranging from 3.1–4 g/kg for hexanol to 6–8 g/kg for octadecanol. For a 50 kg person, these values translate
Fatty_alcohol
Chemical compound
tert-Amyl alcohol (TAA) or 2-methylbutan-2-ol (2M2B), is a branched pentanol. Historically, TAA has been used as an anesthetic and more recently as a
Tert-Amyl_alcohol
Chemical compound
Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C8H10O or C6H5(CH2)2OH. It is a colourless liquid with a pleasant
Phenethyl_alcohol
Chemical compound
3-dimethylbutan-2-ol and as pine alcohol) is one of the isomeric hexanols and a secondary alcohol. Pinacolyl alcohol appears on the List of Schedule 2 substances
Pinacolyl_alcohol
Chemical compound
3,5,5-Trimethyl-1-hexanol is a nine carbon primary alcohol, and it makes up the mixture isononanol along with isononyl alcohol. It is used for fragrance
3,5,5-Trimethyl-hexan-1-ol
Chemical compound (CH3)2CHCH2OH
Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH3)2CHCH2OH (sometimes represented as i-BuOH). This colorless
Isobutanol
Method for preparing ethers
Development. 9 (2): 206–211. doi:10.1021/op050001h. Tanabe, Masato; Peters, Richard H. (1981). "(R,S)-Mevalonolactone-2-13C (2H-Pyran-2-one-13C,
Williamson_ether_synthesis
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
1-Octen-3-ol
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
Arachidyl_alcohol
Class of organic compounds
several milliliters are tolerated. For pentanols, hexanols, octanols, and longer alcohols, LD50 range from 2–5 g/kg (rats, oral). Ethanol is less acutely toxic
Alcohol_(chemistry)
Chemical compound
behavior modifying activity". Comparative Biochemistry and Physiology C. 60 (2): 175–185. doi:10.1016/0306-4492(78)90091-6. PMID 28889. Gil C, Gómez-Cordovés
Tryptophol
Chemical compound
2-Pentanol (IUPAC name: pentan-2-ol; also called sec-amyl alcohol) is an organic chemical compound. It is used as a solvent and an intermediate in the
2-Pentanol
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
1-Tridecanol
Chemical compound
2-Methyl-1-pentanol (IUPAC name: 2-methylpentan-1-ol) is an organic chemical compound. It is used as a solvent and an intermediate in the manufacture of
2-Methyl-1-pentanol
Aromatic alcohol
reproductive effects. Benzyl alcohol has low acute toxicity with an LD50 of 1.2 g/kg in rats. It oxidizes rapidly in healthy individuals to benzoic acid,
Benzyl_alcohol
Trade name for hydrogenated glucose syrup
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
Lycasin
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
Isoamyl_alcohol
Chemical compound
flour hydrolysates have also been evaluated. Merck Index, 11th Edition, 789 "2-Carb-19". Arabitol at the Human Metabolome Database "Candida and Yeast Overgrowth"
Arabitol
Primary alcohol with formula C26H54O
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
1-Hexacosanol
29-carbon primary fatty alcohol
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
1-Nonacosanol
Primary alcohol compound (CH3CH2CH2OH)
represented as PrOH or n-PrOH. It is a colourless liquid and an isomer of 2-propanol. 1-Propanol is used as a solvent in the pharmaceutical industry,
1-Propanol
Sugar alcohol used as a sweetener
capsules, as an emollient, and as a humectant. Maltitol provides between 2 and 3 kilocalories per gram [kcal/g] (8–10 kJ/g). Maltitol is largely unaffected
Maltitol
Type of chemical reaction
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
Fischer–Speier_esterification
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
Volemitol
Chemical compound family ( C4H9OH)
carbon is sec-butyl alcohol or 2-butanol. The branched isomer with the alcohol at a terminal carbon is isobutanol or 2-methyl-1-propanol, and the branched
Butanol
Sedative-hypnotic drug
structure is considerably simpler. The systematic name is usually given as ethyl 2-chlorovinyl ethynyl carbinol or 1-chloro-3-ethylpent-1-en-4-yn-3-ol. Its empirical
Ethchlorvynol
Chemical compound
Borocillina. A low-pH throat lozenge containing dichlorobenzyl alcohol (1.2 mg) and amylmetacresol (0.6 mg) has been found to deactivate respiratory syncytial
2,4-Dichlorobenzyl_alcohol
Chemical compound
ISBN 978-3-527-30673-2. Schwarzenbach RP, Gschwend PM, Imboden DM (2003). Environmental organic chemistry. John Wiley. ISBN 0-471-35053-2. McCarley KD, Bunge
1-Octanol
Chemical compound
amyl alcohol. It is found naturally and has a role as an insect pheromone. 2-Pentanol Lide, David R. (1998), Handbook of Chemistry and Physics (87 ed.)
3-Pentanol
Group of isomers (C8H17OH)
unbranched chain of carbons. Other commercially important octanols are 2-octanol and 2-ethylhexanol. Some octanols occur naturally in the form of esters in
Octanol
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
3-Nitrobenzyl_alcohol
Chemical compound
pronunciation and meaning of cetacean taxonomic names" (PDF). Aquatic Mammals. 27 (2): 185. Archived from the original (PDF) on 2016-03-27. Retrieved 2020-04-26
Cetyl_alcohol
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
Fucitol
Chemical compound
2-Ethyl-1-butanol (IUPAC name: 2-ethylbutan-1-ol) is an organic chemical compound. It can be used to facilitate the separation of ethanol from water, which
2-Ethyl-1-butanol
Chemical compound
to shorten the healing by 17.5 hours on average (95% confidence interval: 2 to 22 hours) in a placebo-controlled trial. Another trial showed no effect
1-Docosanol
Alcohols used as antiseptics, disinfectants or antidotes
(69th ed.). British Medical Association. 2015. pp. 42, 838. ISBN 978-0-85711-156-2. Stuart MC, Kouimtzi M, Hill SR, eds. (2009). WHO Model Formulary 2008. World
Alcohols_(medicine)
Pharmaceutical compound
sterols and stanols versus policosanol". Pharmacotherapy. 25 (2): 171–183. doi:10.1592/phco.25.2.171.56942. PMID 15767233. S2CID 5608374. Gong J, Qin X, Yuan
Policosanol
Chemical compound
Florida: CRC Press, pp. 3–398, ISBN 0-8493-0594-2 Reineccius, Gary (1998), Source Book of Flavors (2 ed.), Boca Raton, Florida: Springer, p. 268, ISBN 978-0-8342-1307-4
3-Methyl-1-pentanol
Organic reduction of any carbonyl group by a reducing agent
lithium aluminium hydride is: 2 RCO2R' + LiAlH4 → LiAl(OCH2R)2(OR') LiAl(OCH2R)2(OR') + 4 H2O → LiAl(OH)4 + 2 HOCH2R + 2 HOR' Sodium borohydride can, under
Carbonyl_reduction
Chemical compound
promote tooth decay and is considered to be tooth-friendly. Its energy value is 2 kcal per gram, half that of sugars. It is less sweet than sugar, but can be
Isomalt
Chemical compound
Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_277.pub2. ISBN 978-3-527-30673-2. Kreutzer, Udo R. (February 1984). "Manufacture of Fatty Alcohols Based on
1-Tetradecanol
Pharmaceutical compound
Ketamir-2, or simply Ketamir, also known as oral ketamine analogue or as 1-(2-chlorophenyl)-N-methyl-2-oxocyclopentan-1-amine, is an NMDA receptor antagonist
Ketamir-2
Chemical reaction
aldehyde, which is transformed via an aldehyde hydrate (gem-diol, R-CH(OH)2) by reaction with water. Thus, the oxidation of a primary alcohol at the aldehyde
Alcohol_oxidation
Chemical compound
2-Octanol (octan-2-ol, 2-OH) is an organic compound with the chemical formula CH3CH(OH)(CH2)5CH3. It is a colorless oily liquid that is poorly soluble
2-Octanol
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
Undecanol
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
1-Tetracosanol
(2008). "Gas-phase conformational distributions for the 2-alkylalcohols 2-pentanol and 2-hexanol from microwave spectroscopy". Tubergen MJ, Conrad AR, Chavez
Brooks_Pate
Chemical compound
4-butanediol) 1,3-Propanediol 2-Methyl-2-propyl-1,3-propanediol Phenaglycodol Berger FM (June 1949). "Anticonvulsant action of 2-substituted-1,3-propanediols"
Prenderol
Amino acid and neurotransmitter
structure could be idealized as HOOC−CH(NH 2)−(CH 2)2−COOH, with two carboxyl groups −COOH and one amino group −NH 2. However, in the solid state and mildly
Glutamic_acid
Primary alcohol with 19 carbons
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
1-Nonadecanol
Alcohol in which the hydroxy group is bonded to a primary carbon atom
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
Primary_alcohol
Chemical compound
"Microwave Detection of Interstellar Vinyl Alcohol, CH 2=CHOH". The Astrophysical Journal. 561 (2): L207–L210. doi:10.1086/324762. Kleimeier, N. Fabian;
Vinyl_alcohol
Chemical compound
2-Dimethyl-1-butanol is an organic chemical compound; it is one of the isomeric hexanols. Its main use is as a solvent. Lide, David R. (1998), Handbook of Chemistry
2,2-Dimethyl-1-butanol
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
1-Heneicosanol
Chemical compound
2-Fluorodeschloroketamine (also known as 2'-Fl-2-Oxo-PCM, fluoroketamine, and 2-FDCK) is a dissociative anesthetic related to ketamine. Its sale and use
2-Fluorodeschloroketamine
Edible fruit
acetate, 2-methylbutyl acetate, 1-propyl butyrate, ethyl pentanoate, amyl acetate, 2-methyl-1-butanol, trans-2-hexenal, ethyl hexanoate, hexanol. The apple
Apple
Chemical compound
2-Methyl-2-propyl-1,3-propanediol (MPP) is a simple alkyl diol which has sedative, anticonvulsant and muscle relaxant effects. It is both a synthetic precursor
2-Methyl-2-propyl-1,3-propanediol
2-Methyl-2-propyl-1,3-propanediol
Chemical compound
oxidation of cyclohexane in air, typically using cobalt catalysts: 2 C6H12 + O2 → 2 C6H11OH This process coforms cyclohexanone, and this mixture ("KA oil"
Cyclohexanol
Chemical compound
alcohols (2°) 1-Phenylethanol 2-Butanol 2-Deoxyerythritol 2-Heptanol 3-Heptanol 2-Hexanol 3-Hexanol 3-Methyl-2-butanol 2-Nonanol 2-Octanol 2-Pentanol 3-Pentanol
Mannosulfan
Chemical compound
Weinheim: Wiley-VCH. doi:10.1002/14356007.a10_277.pub2. ISBN 978-3-527-30673-2. Bouveault, L.; Blanc, G. (1904). "Hydrogénation des éthers des acides possédant
Oleyl_alcohol
Type of organic chemistry oxidation
reagents such as periodic acid (HIO4) and (diacetoxyiodo)benzene (PhI(OAc)2) are commonly used. Another reagent is lead tetraacetate (Pb(OAc)4). These
Glycol_cleavage
Short-acting barbiturate
protocol provides for intravenous administration of two syringes each containing 2.5 grams of pentobarbital sodium followed by a saline flush. Like other barbiturates
Pentobarbital
Chemical compound family
(straight-chain) form, 1-pentanol. Three of these alcohols, 2-methyl-1-butanol, 2-pentanol, and 3-methyl-2-butanol (methyl isopropyl carbinol), contain stereocenters
Amyl_alcohol
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2 HEXANOL
2 HEXANOL
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2 HEXANOL
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