Results for:
PubChem ID: 7966

Cyclohexanol

Mass-Spectra

Compound Details

Synonymous names
Hydroxycyclohexane
Cyanomethylthioacetic acid
Cyclohexanone cyclohexanol mixture
Hexahydrophenol
Cicloesanolo
CYCLOHEXANOL
Cyclohexanols
Cykloheksanol
Hydrophenol
Cyclohexyl alcohol
cyclohexyl-alcohol
HPXRVTGHNJAIIH-UHFFFAOYSA-N
Hydralin
Adronal
Adronol
Cyclohexanol, analytical standard
Hexalin
Anol
Naxol
CXL
cykloheksanol(polish)
1-Cyclohexanol
BDBM5
AC1L1PYO
Cicloesanolo [Italian]
Cyclohexane, hydroxy-
Cykloheksanol [Polish]
AC1Q7AM2
Cyclohexan-1-ol
ACMC-1BU4Y
Phenol, hexahydro-
SCHEMBL5545
HSDB 61
KSC175M7H
CHEMBL32010
BIDD:ER0291
DB03703
LS-474
RP18714
8E7S519M3P
bmse000431
C00854
CCRIS 5896
CYCLOHEXYL, 1-HYDROXY-
HMS3039K08
WLN: L6TJ AQ
AK113065
BBL013186
DTXSID4021894
NSC403656
OR025413
OR188686
OR242167
SBB060483
STL163965
CHEBI:18099
DSSTox_CID_1894
UNII-8E7S519M3P
ZINC1532765
AJ-26810
AN-42916
CJ-05270
CJ-24252
DSSTox_GSID_21894
SC-47179
TRA0058880
TRA0078627
BB_SC-7055
DSSTox_RID_76390
MFCD00003855
ZINC01532765
AI3-00040
DB-040851
KB-251250
NSC 403656
NSC-403656
ST51046660
TC-167349
TR-002010
AKOS000119038
Cyclohexanol, ReagentPlus(R), 99%
Q-200903
ZINC100502981
BRN 0906744
FT-0624192
MLS001055343
SMR000677941
I14-16591
I14-20888
Cyclohexanol, 99% 100ml
Cyclohexanol, JIS special grade, >=98.0%
Tox21_201481
Tox21_302803
108-93-0
Cyclohexanol, SAJ first grade, >=95.0%
Cyclohexanol, Vetec(TM) reagent grade, 98%
F0001-0184
MCULE-8217921343
NCGC00090982-01
NCGC00090982-02
NCGC00256434-01
NCGC00259032-01
CAS-108-93-0
EINECS 203-630-6
603-EP2270113A1
603-EP2272817A1
603-EP2272849A1
603-EP2272935A1
603-EP2275411A2
603-EP2275469A1
603-EP2277861A1
603-EP2280005A1
603-EP2281810A1
603-EP2284154A1
603-EP2284157A1
603-EP2286811A1
603-EP2287158A1
603-EP2287165A2
603-EP2287166A2
603-EP2287940A1
603-EP2289884A1
603-EP2289965A1
603-EP2292620A2
603-EP2298746A1
603-EP2298828A1
603-EP2301918A1
603-EP2301983A1
603-EP2305033A1
603-EP2308471A1
603-EP2308812A2
603-EP2308857A1
603-EP2308926A1
603-EP2309564A1
603-EP2311815A1
603-EP2311820A1
603-EP2314558A1
603-EP2374783A1
603-EP2380568A1
Cyclohexanol, p.a., 99.0%
MolPort-001-783-729
Cyclohexanol, puriss., >=99.0% (GC)
4-06-00-00020 (Beilstein Handbook Reference)
Microorganism:

Yes

IUPAC namecyclohexanol
SMILESC1CCC(CC1)O
InchiInChI=1S/C6H12O/c7-6-4-2-1-3-5-6/h6-7H,1-5H2
FormulaC6H12O
PubChem ID7966
Molweight100.161
LogP1.28
Atoms19
Bonds19
H-bond Acceptor1
H-bond Donor1
Chemical ClassificationAlcohols

mVOC Specific Details

Volatilization
The Henry's Law constant for cyclohexanol is 4.40X10-6 atm-cu m/mole(1). This Henry's Law constant indicates that cyclohexanol is expected to volatilize from water surfaces(2). 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)(2) is estimated as 8.4 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 64 days(SRC). Cyclohexanol's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Cyclohexanol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.657 mm Hg(3).
Literature: (1) Altschuh JR et al; Chemosphere 39: 1871-87 (1999) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1998)
Soil Adsorption
The Koc of cyclohexanol is estimated as 11(SRC), using a log Kow of 1.23(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that cyclohexanol is expected to have very high mobility in soil.
Literature: (1) Hansch C et al; Exploring QSAR. Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Heller SR, consult. ed., Washington, DC: Amer Chem Soc p. 24 (1995) (2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.0. Jan, 2009. Available from, as of March 29, 2010: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm. (3) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
0.657 mm Hg at 25 deg CDaubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1998.

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaPseudomonas AurantiacaInhibition of mycelium growth and spore germinationFernando et al., 2005
BacteriaPseudomonas ChlororaphisInhibition of mycelium growth and spore germinationFernando et al., 2005
BacteriaPseudomonas CorrugateInhibition of mycelium growth and spore germinationFernando et al., 2005
BacteriaPseudomonas FluorescensInhibition of mycelium growth and spore germinationFernando et al., 2005
FungiTuber Indicumn/aSplivallo et al., 2007
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaPseudomonas Aurantiacan/an/a
BacteriaPseudomonas Chlororaphisn/an/a
BacteriaPseudomonas Corrugaten/an/a
BacteriaPseudomonas Fluorescensn/an/a
FungiTuber Indicumn/an/a