Results for:
PubChem ID: 8842

3,7-dimethyloct-6-en-1-ol

Mass-Spectra

Compound Details

Synonymous names
Citronellol
106-22-9
3,7-Dimethyloct-6-en-1-ol
beta-Citronellol
DL-Citronellol
Cephrol
6-Octen-1-ol, 3,7-dimethyl-
3,7-DIMETHYL-6-OCTEN-1-OL
Elenol
2,3-Dihydrogeraniol
Dihydrogeraniol
Rodinol
(+/-)-beta-Citronellol
2,6-Dimethyl-2-octen-8-ol
Citronellol, dl-
.beta.-Citronellol
Citronellol (natural)
(+-)-beta-citronellol
26489-01-0
68916-43-8
CHEBI:50462
C10H20O
(+-)-CITRONELLOL
NSC 8779
UNII-565OK72VNF
565OK72VNF
CCRIS 7452
DTXSID3026726
NSC-8779
EINECS 203-375-0
EINECS 247-737-6
(+/-)-3,7-dimethyloct-6-en-1-ol
BRN 1721507
AI3-25080
DTXCID006726
3,7-dimethyl-oct-6-en-1-ol
CITRONELLOL, (+/-)-
HSDB 6805
NSC8779
EC 203-375-0
4-01-00-02188 (Beilstein Handbook Reference)
MFCD00002935
(+/-)-3,7-dimethyl-6-octen-1-ol
6-Octen-1-ol, 3,7-dimethyl-, (+/-)-
Insect Repellent
CAS-106-22-9
D-Citronellol;(R)-(+)-beta-Citronellol
(+/-)-beta-Citronellol analytical standard
(+/-)-Citronellol;(+/-)-beta-Citronellol
(S)-(-)-|A-Citronellol
(R)-(+)-.beta.-Citronellol
nardus
mite attractant
rac-Citronellol
(+/-)-beta-Citronellol, primary pharmaceutical reference standard
Levo-citronellol
MFCD00063215
|A-Citronellol
Citronellol Natural
acyclic monoterpenoid
pelargonium geraniums
geranium oil saponified
ST069325
beta-Citronellol, 95%
(+-)-beta;-Citronellol
SCHEMBL21320
6-Octen-1-ol,7-dimethyl-
MLS002415719
3,7-dimethyl-oct-6-en1-ol
CHEMBL395827
()-Citronellol;()--Citronellol
.BETA.-CITRONELLOL [MI]
WLN: Q2Y1&3UY1&1
beta-CITRONELLOL, (+/-)-
HMS2267B17
Citronellol, >=95%, FCC, FG
Tox21_202119
Tox21_300003
(+/-)-.BETA.-CITRONELLOL
BBL009826
BDBM50037035
s5584
STK085542
AKOS005393175
CCG-266265
CS-W010917
HY-W010201
MCULE-4204888723
.BETA.-CITRONELLOL, (+/-)-
NCGC00091348-01
NCGC00091348-02
NCGC00091348-03
NCGC00091348-04
NCGC00254145-01
NCGC00259668-01
AS-14688
BP-21491
SMR000112138
SY066737
SY114862
( inverted exclamation markA)-b-Citronellol
DB-060123
DB-074976
DB-307766
(+/-)-beta-Citronellol, analytical standard
NS00093536
EN300-1270486
W-108771
W-109198
W-110227
Q27122080
Z87001681
Microorganism:

Yes

IUPAC name3,7-dimethyloct-6-en-1-ol
SMILESCC(CCC=C(C)C)CCO
InchiInChI=1S/C10H20O/c1-9(2)5-4-6-10(3)7-8-11/h5,10-11H,4,6-8H2,1-3H3
FormulaC10H20O
PubChem ID8842
Molweight156.26
LogP3.2
Atoms11
Bonds5
H-bond Acceptor1
H-bond Donor1
Chemical Classificationalcohols terpenes
CHEBI-ID50462
Supernatural-IDSN0309689

mVOC Specific Details

Boiling Point
DegreeReference
224 deg CHaynes, W.M. (ed.). CRC Handbook of Chemistry and Physics. 95th Edition. CRC Press LLC, Boca Raton: FL 2014-2015, p. 3-216
Volatilization
The Henry's Law constant for citronellol is estimated as 2.1X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 0.02 mm Hg(1), and water solubility, 200 mg/L(2). This Henry's Law constant indicates that citronellol is expected to volatilize from water surfaces(3). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 2.4 days(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 21 days(SRC). Citronellol's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Even though the vapor pressure is low environmentally at standard temperature and pressure, there is a detectable odor; therefore, citronellol may volatilize from dry soil(SRC). Patch testing to determine the evaporation rate of fragrance chemicals from skin found that citronellol evaporation was not sensitive to pH changes from 4.0 to 7.0 and that 26-27% of applied citronellol was lost within 40 minutes to 24 hours(4).
Literature: (1) Sell CS; Terpenoids. Kirk-Othmer Encyclopedia of Chemical Technology. (1999-2015). New York, NY: John Wiley & Sons. Online Posting Date: Sep 15, 2006. (2) Yalkowsky SH et al; Handbook of Aqueous Solubility Data. 2nd ed. Boca Raton, FL: CRC Press, p. 739 (2010) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (4) Gilpin SJ et al; Dermatitis 20(4): 200-7 (2009)
Solubility
In water, 200 mg/L at 25 deg C
Literature: Yalkowsky, S.H., He, Yan, Jain, P. Handbook of Aqueous Solubility Data Second Edition. CRC Press, Boca Raton, FL 2010, p. 739
Literature: #In water, 307 mg/L at 25 deg C; 300 mg/L at 20 deg C
Literature: ECHA; Search for Chemicals. Citronellol (CAS 106-22-9) Registered Substances Dossier. European Chemical Agency. Available from, as of July 16, 2015: http://echa.europa.eu/
Literature: #Soluble in fixed oils, propylene glycol; insoluble in glycerin
Literature: Lewis, R.J. Sr. (ed) Sax's Dangerous Properties of Industrial Materials. 12th Edition. Wiley-Interscience, Wiley & Sons, Inc. Hoboken, NJ. 2012., p. 1166
Literature: #Miscible in ethanol and ether /(+)-citronellol/; very soluble in ethanol and ether /(-)-citronellol/
Literature: Haynes, W.M. (ed.). CRC Handbook of Chemistry and Physics. 95th Edition. CRC Press LLC, Boca Raton: FL 2014-2015, p. 3-216
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of citronellol can be estimated to be 94(SRC). According to a classification scheme(2), this estimated Koc value suggests that citronellol is expected to have high mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.11. Nov, 2012. Available from, as of July 17, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
0.02 mm Hg at 25 deg CSell CS; Terpenoids. Kirk-Othmer Encyclopedia of Chemical Technology. (1999-2015). New York, NY: John Wiley & Sons. Online Posting Date: Sep 15, 2006.
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaBacillus Sp.antifungal activity against Fusarium solaniRhizosphere soil of avocadoGuevara-Avendaño et al. 2019
EukaryotaCandida SakeKing George Island, South Shetland Islands, AntarcticaArrarte et al. 2017
EukaryotaAspergillus Fumigatuscompost Fischer et al. 1999
EukaryotaAspergillus Versicolorcompost Fischer et al. 1999
EukaryotaZygosaccharomyces RouxiiNANAPei et al. 2022
EukaryotaSaccharomyces CerevisiaeNANAGe et al. 2021
EukaryotaMeyerozyma GuilliermondiiNANAZhao et al. 2022
EukaryotaSaccharomyces CerevisiaeNANAZhao et al. 2022
EukaryotaSaccharomycopsis ViniNANAZhao et al. 2022
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaBacillus Sp.LB agarSPME-GC-MSno
EukaryotaCandida SakeYeast Nitrogen base with 1% pectinSPME / GCMSno
EukaryotaAspergillus Fumigatusyest extract sucroseTenax/GC-MSno
EukaryotaAspergillus Versicoloryest extract sucroseTenax/GC-MSno
EukaryotaZygosaccharomyces RouxiiYPD mediumGC-MSno
EukaryotaSaccharomyces Cerevisiaegrape juiceLC-15C HPLCno
EukaryotaMeyerozyma Guilliermondiisynthetic grape juiceHS-SPMEno
EukaryotaSaccharomyces Cerevisiaesynthetic grape juiceHS-SPMEno
EukaryotaSaccharomycopsis Vinisynthetic grape juiceHS-SPMEno