Results for:
PubChem ID: 8663

Naphthalen-2-ol

Mass-Spectra

Compound Details

Synonymous names
2-NAPHTHOL
naphthalen-2-ol
135-19-3
beta-naphthol
2-Naphthalenol
Betanaphthol
2-Hydroxynaphthalene
Isonaphthol
Developer A
Developer BN
Naphthol B
2-Naphtol
Azogen developer A
beta-Naphtol
beta-Napthol
Developer AMS
beta-Hydroxynaphthalene
2-Naftolo
2-Naftol
Developer sodium
C.I. Developer 5
.beta.-Naphthol
beta-Naphthyl alcohol
beta-Monoxynaphthalene
beta-Naftol
beta-Naftolo
beta-Naphthyl hydroxide
NAPHTHOL, BETA
C.I. Azoic Coupling Component 1
.beta.-Hydroxynaphthalene
Antioxygene BN
.beta.-Naftolo
.beta.-Naphtol
.beta.-Napthol
.beta.-Naftol
NSC 2044
C.I. 37500
MFCD00004067
.beta.-Naphthyl alcohol
.beta.-Monoxynaphthalene
.beta.-Naphthyl hydroxide
P2Z71CIK5H
CHEMBL14126
2-Naphthol(Flakes or Chunks)
DTXSID5027061
CHEBI:10432
Naphthalen-2-ol (beta-Naphthol)
NSC-2044
DTXCID907061
2-Naftol [Dutch]
beta-Naftol [Dutch]
2-Naphtol [French]
Caswell No. 590
2-Naftolo [Italian]
beta-Naphtol [German]
beta-Naftolo [Italian]
2-Napththol
CAS-135-19-3
Betanaphthol [NF]
HSDB 6812
EINECS 205-182-7
UNII-P2Z71CIK5H
EPA Pesticide Chemical Code 010301
Hydronaphthol
Naphthols
AI3-00081
2-napthol
napthalen-2-ol
2-naphthylalcohol
naphth-2-ol
Naphthol, .beta.
03V
EINECS 215-322-9
2-hydroxy naphthalene
2-Naphthol, Reagent
2-Naphthol, Purified
BRN 1817321
2-Naphthol, 98%
2-Naphthol, 99%
Naphth-2-ol, 10
beta.-hydroxynaphthalene
Microcidin (Salt/Mix)
BETANAPHTHOL [II]
2-NAPHTHOL [MI]
2-Naphthol, 98.5%
BETANAPHTHOL [HSDB]
EC 205-182-7
2-NAPHTHOL [INCI]
SCHEMBL28781
WLN: L66J CQ
BETANAPHTHOL [MART.]
BETANAPHTHOL [WHO-DD]
SGCUT00131
2-Naphthol, LR, >=98%
NSC2044
4b32
Sodium 2-naphthoxide (Salt/Mix)
HMS3264N15
Pharmakon1600-01504501
HY-Y0110
to_000010
Tox21_201884
Tox21_303038
BDBM50159250
NSC758883
s6035
STL281866
AKOS000119842
AM86551
CCG-213932
HR-0304
MCULE-2675031485
NSC-758883
2-Naphthol, purum, >=98.0% (GC)
NCGC00249132-01
NCGC00257077-01
NCGC00259433-01
AC-10464
2-Naphthol, BioXtra, >=99.0% (GC)
SBI-0207084.P001
2-Naphthol, SAJ first grade, >=98.0%
TOLNAFTATE IMPURITY A [EP IMPURITY]
CS-0008403
N0027
NS00003415
EN300-18025
2-Naphthol, fluorescence indicator, >=99.0%
D86186
AB01314260_03
4-06-00-04208 (Beilstein Handbook Reference)
A806896
AB-131/40299865
Q949232
SR-01000872753
Q-200736
SR-01000872753-1
BRD-K21164796-001-01-0
Z57127515
F0001-0455
InChI=1/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11
26716-78-9
Microorganism:

Yes

IUPAC namenaphthalen-2-ol
SMILESC1=CC=C2C=C(C=CC2=C1)O
InchiInChI=1S/C10H8O/c11-10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H
FormulaC10H8O
PubChem ID8663
Molweight144.17
LogP2.7
Atoms11
Bonds0
H-bond Acceptor1
H-bond Donor1
Chemical Classificationaromatic compounds phenols benzenoids
CHEBI-ID10432
Supernatural-IDSN0176833

mVOC Specific Details

Boiling Point
DegreeReference
285 °C peer reviewed
Volatilization
The Henry's Law constant for 2-naphthol is as 2.74X10-8 atm-cu m/mole(1). This Henry's Law constant indicates that 2-naphthol is expected to be essentially nonvolatile from water surfaces(2). 2-Naphthol's Henry's Law constant indicates that volatilization from moist soil surfaces for the neutral species may not occur(SRC). 2-Naphthol is not expected to volatilize from dry soil surfaces(SRC) based upon an extrapolated vapor pressure of 3.2X10-4 mm Hg(3).
Literature: (1) Abraham MH et al; J. Pharm. Sci. 83: 1085-100 (1994) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Boublik T et al; The Vapor Pressure of Pure Substances: Selected Values of the Temperature Dependence of the Vapor Pressures of some Pure Substances in the Normal and Low Pressure Region Vol 17. Amsterdam, Netherlands: Elsevier Sci Publ p 768 (1984)
Soil Adsorption
The Koc of 2-naphtol is estimated as 390(SRC), using a log Kow of 2.7(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that 2-naphthol is expected to have moderate mobility in soil. The pKa of 2-naphthol is 9.51(4), indicating that this compound will exist partially in the anion form in the environment and anions generally do not adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts(5).
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. 66 (1995) (2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of Oct 14, 2014: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (3) Swann RL et al; Res Rev 85: 17-28 (1983) (4) Bhattacharyya D et al; Haz. Waste Haz. Mater 3: 405-29 (1986) (5) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)
Vapor Pressure
PressureReference
3.2X10-4 mm Hg at 25 deg C (solid) (Extrapolated using value obtained from Boublik T et al (1984))Bidleman TF; Environ Sci Technol 22: 361-367 (1988)
MS-Links
1D-NMR-Links
Massbank-Links

Species emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
ProkaryotaPseudomonas Putidanablack pepper rootSheoran et al. 2015
ProkaryotaPseudomonas Putidapositive influence of the plant root growth and protection against soil-borne pathogensNASheoran et al. 2015
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
ProkaryotaPseudomonas PutidaLuria Bertani AgarHeadspace GC/MSno
ProkaryotaPseudomonas PutidaTSBPropak Q adsorbent trap/GC-MSno