Results for:
Species: Antrodia cinnamomea

Compound Details

Synonymous names
methylbenzene
methylbenzol
Phenylmethane
Benzylidyne radical
paratoluene
methacide
monomethyl benzene
YXFVVABEGXRONW-UHFFFAOYSA-N
Anisen
Cresyl
Dracyl
Otoline
Tolueen
Toluen
toluene
Toluene, Spectrophotometric Grade
Tolueno
toluol
Toluolo
methyl-Benzene
phenyl methane
para-toluene
1-Methylbenzene
2-methylbenzene
4-methylbenzene
p-toluene
Toluene HPLC grade
Toluene, analytical standard
Toluene, anhydrous
Toluene, Environmental Grade
Toluene, Semiconductor Grade
AC1L1ATE
tolu-sol
Toluene ACS Grade
Toluene Reagent Grade ACS
toluene-
antisal 1a
Benzene, methyl
4i7k
Toluene disproportionation catalyst ZA-90
2-methyl benzene
AC1L4W1C
ACMC-20egwh
Toluene (Technical)
Toluene, ACS reagent
Toluene, HPLC Grade
Toluene, suitable for determination of dioxins
CHEMBL9113
Residual Solvent - Toluene
Toluene, for HPLC
Tolueno [Spanish]
Toluolo [Italian]
Benzene, methyl-
GTPL5481
Methane, phenyl-
PHENYL, METHYL-
Tolueen [Dutch]
TOLUENE- D8
Toluene, pharmaceutical secondary standard; traceable to USP
CP 25
LS-26
Toluen [Czech]
Toluene GC, for residue analysis
UN1294
3FPU23BG52
HSDB 131
S0638
WLN: 1R
BIDD:ER0288
RL00380
C01455
CCRIS 2366
LTBB002867
OTOLINE (9CI)
RCRA waste number U220
UNII-3FPU23BG52
ZINC967534
NSC406333
OR034283
OR079732
OR199992
OR242367
OR252118
OR256430
OR274999
OR328992
UN 1294
ZB015462
300204X
A801937
CHEBI:17578
DSSTox_CID_1360
NCI-C07272
AN-42912
ANW-44012
DSSTox_GSID_21360
KB-54750
SC-19104
BDBM50008558
Caswell No. 859
DSSTox_RID_76107
MFCD00008512
Toluene, 99.5%
Toluene, LR, >=99%
AI3-02261
NSC 406333
NSC-406333
RTR-002003
TR-002003
AKOS015840411
EPA Pesticide Chemical Code 080601
I01-4407
RCRA waste no. U220
Toluene, ACS spectrophotometric grade, >=99.5%
ZINC100116646
FT-0626841
FT-0654077
FT-0659221
Toluene, Laboratory Reagent, >=99.3%
Toluene, suitable for scintillation, >=99.7%
Poly(1,4-phenylenemethylene)(9CI)
Toluene, 99% 1L
Toluene, anhydrous, 99.8%
Toluene, purification grade, 99.8%
Toluene, LR, rectified, 99%
Toluene, technical grade, 95.0%
Tox21_111042
Tox21_201224
108-88-3
Toluene, ACS reagent, >=99.5%
Toluene, AR, >=99.5%
Toluene, ASTM, 99.5%
Toluene, PRA grade, >=99.8%
Toluene, UV HPLC spectroscopic, 99.5%
MCULE-4817136027
NCGC00090939-01
NCGC00090939-02
NCGC00090939-03
NCGC00258776-01
Toluene, for HPLC, >=99.8%
Toluene, for HPLC, >=99.9%
Toluene, HPLC grade, 99.8%
Toluene, JIS special grade, >=99.5%
Toluene, LR, sulfur free, 99%
CAS-108-88-3
EINECS 203-625-9
Toluene, for HPLC, 99.9%
Toluene, SAJ first grade, >=99.0%
50643-04-4
Toluene [UN1294] [Flammable liquid]
941-EP0930075A1
941-EP2269975A2
941-EP2269977A2
941-EP2269978A2
941-EP2269979A1
941-EP2269985A2
941-EP2269986A1
941-EP2269987A1
941-EP2269988A2
941-EP2269989A1
941-EP2269990A1
941-EP2269991A2
941-EP2269992A1
941-EP2269993A1
941-EP2269995A1
941-EP2269997A2
941-EP2270000A1
941-EP2270001A1
941-EP2270002A1
941-EP2270003A1
941-EP2270004A1
941-EP2270006A1
941-EP2270008A1
941-EP2270009A1
941-EP2270010A1
941-EP2270011A1
941-EP2270014A1
941-EP2270101A1
941-EP2270113A1
941-EP2270114A1
941-EP2270505A1
941-EP2272509A1
941-EP2272516A2
941-EP2272517A1
941-EP2272537A2
941-EP2272813A2
941-EP2272817A1
941-EP2272822A1
941-EP2272825A2
941-EP2272827A1
941-EP2272828A1
941-EP2272829A2
941-EP2272830A1
941-EP2272831A1
941-EP2272832A1
941-EP2272834A1
941-EP2272835A1
941-EP2272837A1
941-EP2272838A1
941-EP2272839A1
941-EP2272840A1
941-EP2272841A1
941-EP2272842A1
941-EP2272843A1
941-EP2272844A1
941-EP2272847A1
941-EP2272848A1
941-EP2272849A1
941-EP2272935A1
941-EP2274983A1
941-EP2275102A1
941-EP2275395A2
941-EP2275401A1
941-EP2275403A1
941-EP2275404A1
941-EP2275407A1
941-EP2275409A1
941-EP2275410A1
941-EP2275411A2
941-EP2275413A1
941-EP2275414A1
941-EP2275415A2
941-EP2275416A1
941-EP2275418A1
941-EP2275427A1
941-EP2275469A1
941-EP2277848A1
941-EP2277858A1
941-EP2277861A1
941-EP2277865A1
941-EP2277867A2
941-EP2277871A1
941-EP2277875A2
941-EP2277877A1
941-EP2277878A1
941-EP2277880A1
941-EP2277881A1
941-EP2279750A1
941-EP2280000A1
941-EP2280001A1
941-EP2280003A2
941-EP2280004A1
941-EP2280005A1
941-EP2280006A1
941-EP2280007A1
941-EP2280008A2
941-EP2280009A1
941-EP2280010A2
941-EP2280011A1
941-EP2280012A2
941-EP2280014A2
941-EP2280020A1
941-EP2280021A1
941-EP2281563A1
941-EP2281810A1
941-EP2281812A1
941-EP2281813A1
941-EP2281815A1
941-EP2281817A1
941-EP2281818A1
941-EP2281819A1
941-EP2281820A2
941-EP2281821A1
941-EP2281822A1
941-EP2281899A2
941-EP2284148A1
941-EP2284149A1
941-EP2284150A2
941-EP2284151A2
941-EP2284152A2
941-EP2284153A2
941-EP2284155A2
941-EP2284156A2
941-EP2284157A1
941-EP2284158A1
941-EP2284159A1
941-EP2284160A1
941-EP2284164A2
941-EP2284165A1
941-EP2284167A2
941-EP2284168A2
941-EP2284169A1
941-EP2284170A1
941-EP2284172A1
941-EP2284174A1
941-EP2284920A1
941-EP2286811A1
941-EP2286915A2
941-EP2287140A2
941-EP2287141A1
941-EP2287147A2
941-EP2287148A2
941-EP2287150A2
941-EP2287152A2
941-EP2287153A1
941-EP2287154A1
941-EP2287155A1
941-EP2287156A1
941-EP2287157A1
941-EP2287159A1
941-EP2287161A1
941-EP2287162A1
941-EP2287165A2
941-EP2287166A2
941-EP2287167A1
941-EP2287168A2
941-EP2287940A1
941-EP2289509A2
941-EP2289510A1
941-EP2289868A1
941-EP2289876A1
941-EP2289877A1
941-EP2289879A1
941-EP2289883A1
941-EP2289884A1
941-EP2289885A1
941-EP2289887A2
941-EP2289888A2
941-EP2289890A1
941-EP2289892A1
941-EP2289893A1
941-EP2289894A2
941-EP2289896A1
941-EP2289897A1
941-EP2289965A1
941-EP2292227A2
941-EP2292228A1
941-EP2292233A2
941-EP2292586A2
941-EP2292589A1
941-EP2292592A1
941-EP2292593A2
941-EP2292595A1
941-EP2292596A2
941-EP2292597A1
941-EP2292599A1
941-EP2292601A1
941-EP2292602A1
941-EP2292603A1
941-EP2292604A2
941-EP2292606A1
941-EP2292607A2
941-EP2292609A1
941-EP2292610A1
941-EP2292612A2
941-EP2292615A1
941-EP2292617A1
941-EP2292618A1
941-EP2292619A1
941-EP2292620A2
941-EP2292621A1
941-EP2292622A1
941-EP2292624A1
941-EP2292628A2
941-EP2292629A1
941-EP2293650A1
941-EP2295053A1
941-EP2295399A2
941-EP2295401A2
941-EP2295406A1
941-EP2295407A1
941-EP2295409A1
941-EP2295410A1
941-EP2295411A1
941-EP2295412A1
941-EP2295413A1
941-EP2295414A1
941-EP2295415A1
941-EP2295416A2
941-EP2295417A1
941-EP2295418A1
941-EP2295419A2
941-EP2295420A1
941-EP2295421A1
941-EP2295423A1
941-EP2295425A1
941-EP2295426A1
941-EP2295427A1
941-EP2295429A1
941-EP2295432A1
941-EP2295433A2
941-EP2295437A1
941-EP2295438A1
941-EP2295439A1
941-EP2295503A1
941-EP2298312A1
941-EP2298313A1
941-EP2298729A1
941-EP2298731A1
941-EP2298734A2
941-EP2298735A1
941-EP2298736A1
941-EP2298737A1
941-EP2298739A1
941-EP2298740A1
941-EP2298741A1
941-EP2298742A1
941-EP2298743A1
941-EP2298744A2
941-EP2298745A1
941-EP2298746A1
941-EP2298747A1
941-EP2298748A2
941-EP2298749A1
941-EP2298750A1
941-EP2298751A2
941-EP2298752A1
941-EP2298753A1
941-EP2298754A1
941-EP2298755A1
941-EP2298756A1
941-EP2298757A2
941-EP2298758A1
941-EP2298759A1
941-EP2298761A1
941-EP2298763A1
941-EP2298764A1
941-EP2298765A1
941-EP2298767A1
941-EP2298768A1
941-EP2298770A1
941-EP2298771A2
941-EP2298772A1
941-EP2298774A1
941-EP2298775A1
941-EP2298776A1
941-EP2298777A2
941-EP2298778A1
941-EP2298779A1
941-EP2298780A1
941-EP2298783A1
941-EP2298828A1
941-EP2299326A1
941-EP2299509A1
941-EP2299510A1
941-EP2299785A1
941-EP2301536A1
941-EP2301538A1
941-EP2301627A1
941-EP2301911A1
941-EP2301918A1
941-EP2301919A1
941-EP2301920A1
941-EP2301921A1
941-EP2301922A1
941-EP2301923A1
941-EP2301924A1
941-EP2301925A1
941-EP2301926A1
941-EP2301927A1
941-EP2301928A1
941-EP2301929A1
941-EP2301930A1
941-EP2301931A1
941-EP2301932A1
941-EP2301933A1
941-EP2301934A1
941-EP2301935A1
941-EP2301936A1
941-EP2301937A1
941-EP2301939A1
941-EP2301940A1
941-EP2301983A1
941-EP2302003A1
941-EP2302015A1
941-EP2305219A1
941-EP2305250A1
941-EP2305254A1
941-EP2305257A1
941-EP2305625A1
941-EP2305627A1
941-EP2305633A1
941-EP2305636A1
941-EP2305637A2
941-EP2305640A2
941-EP2305641A1
941-EP2305642A2
941-EP2305643A1
941-EP2305646A1
941-EP2305647A1
941-EP2305648A1
941-EP2305649A1
941-EP2305650A1
941-EP2305651A1
941-EP2305652A2
941-EP2305655A2
941-EP2305656A1
941-EP2305658A1
941-EP2305659A1
941-EP2305660A1
941-EP2305662A1
941-EP2305664A1
941-EP2305666A1
941-EP2305667A2
941-EP2305668A1
941-EP2305669A1
941-EP2305671A1
941-EP2305672A1
941-EP2305674A1
941-EP2305675A1
941-EP2305676A1
941-EP2305677A1
941-EP2305679A1
941-EP2305680A2
941-EP2305682A1
941-EP2305684A1
941-EP2305685A1
941-EP2305686A1
941-EP2305687A1
941-EP2305688A1
941-EP2305695A2
941-EP2305696A2
941-EP2305697A2
941-EP2305698A2
941-EP2305769A2
941-EP2305808A1
941-EP2305825A1
941-EP2306788A1
941-EP2306789A1
941-EP2308471A1
941-EP2308479A2
941-EP2308492A1
941-EP2308510A1
941-EP2308562A2
941-EP2308812A2
941-EP2308828A2
941-EP2308831A1
941-EP2308833A2
941-EP2308838A1
941-EP2308839A1
941-EP2308840A1
941-EP2308841A2
941-EP2308843A1
941-EP2308844A2
941-EP2308845A2
941-EP2308846A2
941-EP2308848A1
941-EP2308849A1
941-EP2308850A1
941-EP2308851A1
941-EP2308853A1
941-EP2308854A1
941-EP2308857A1
941-EP2308858A1
941-EP2308861A1
941-EP2308862A1
941-EP2308864A1
941-EP2308865A1
941-EP2308867A2
941-EP2308868A1
941-EP2308869A1
941-EP2308870A2
941-EP2308871A1
941-EP2308872A1
941-EP2308873A1
941-EP2308874A1
941-EP2308875A1
941-EP2308876A1
941-EP2308877A1
941-EP2308879A1
941-EP2308880A1
941-EP2308882A1
941-EP2308926A1
941-EP2308960A1
941-EP2309564A1
941-EP2309584A1
941-EP2311455A1
941-EP2311464A1
941-EP2311801A1
941-EP2311802A1
941-EP2311803A1
941-EP2311804A2
941-EP2311805A1
941-EP2311806A2
941-EP2311807A1
941-EP2311808A1
941-EP2311811A1
941-EP2311813A1
941-EP2311814A1
941-EP2311815A1
941-EP2311816A1
941-EP2311817A1
941-EP2311818A1
941-EP2311820A1
941-EP2311822A1
941-EP2311823A1
941-EP2311824A1
941-EP2311826A2
941-EP2311827A1
941-EP2311829A1
941-EP2311830A1
941-EP2311831A1
941-EP2311835A1
941-EP2311836A1
941-EP2314295A1
941-EP2314558A1
941-EP2314571A2
941-EP2314574A1
941-EP2314575A1
941-EP2314576A1
941-EP2314577A1
941-EP2314578A1
941-EP2314579A1
941-EP2314581A1
941-EP2314582A1
941-EP2314583A1
941-EP2314585A1
941-EP2314586A1
941-EP2314587A1
941-EP2314588A1
941-EP2314590A1
941-EP2314591A1
941-EP2314593A1
941-EP2315303A1
941-EP2315502A1
941-EP2316452A1
941-EP2316457A1
941-EP2316824A1
941-EP2316825A1
941-EP2316826A1
941-EP2316827A1
941-EP2316829A1
941-EP2316831A1
941-EP2316832A1
941-EP2316833A1
941-EP2316835A1
941-EP2316836A1
941-EP2370383A2
941-EP2371795A1
941-EP2371797A1
941-EP2371798A1
941-EP2371800A1
941-EP2371804A1
941-EP2371805A1
941-EP2371810A1
941-EP2371811A2
941-EP2371812A1
941-EP2371813A1
941-EP2371814A1
941-EP2371831A1
941-EP2372804A1
941-EP2374454A1
941-EP2374783A1
941-EP2374787A1
941-EP2374788A1
941-EP2374790A1
941-EP2374895A1
941-EP2377841A1
941-EP2377845A1
941-EP2377847A1
941-EP2378585A1
941-EP2380568A1
941-EP2380867A1
941-EP2380873A1
941-EP2380874A2
EC 203-625-9
SR-01000944565
Toluene, AR, rectified, 99.5%
4489-EP2272846A1
Toluene, suitable for 5000 per JIS, for residue analysis
1053657-77-4
1202864-97-8
Toluene [UN1294] [Flammable liquid]
28403-EP2269977A2
28403-EP2311830A1
28403-EP2314581A1
28443-EP2269995A1
28443-EP2275403A1
28443-EP2284178A2
28443-EP2284179A2
28443-EP2292615A1
28443-EP2298738A1
28443-EP2298776A1
28443-EP2301627A1
28443-EP2301937A1
28443-EP2305685A1
28443-EP2305686A1
28443-EP2311464A1
28443-EP2314581A1
28443-EP2371805A1
28443-EP2377847A1
48782-EP2272834A1
48782-EP2275398A1
48782-EP2284165A1
48782-EP2298745A1
48782-EP2301929A1
48782-EP2301935A1
48782-EP2305674A1
48782-EP2311812A1
56745-EP2272846A1
56745-EP2275408A1
56745-EP2275422A1
56745-EP2277862A2
56745-EP2277868A1
56745-EP2277869A1
56745-EP2277870A1
56745-EP2281861A2
56745-EP2284166A1
56745-EP2287164A1
56745-EP2289483A1
56745-EP2289881A1
56745-EP2292608A1
56745-EP2292616A1
56745-EP2292625A1
56745-EP2295422A2
56745-EP2295436A1
56745-EP2298076A1
56745-EP2298077A1
56745-EP2298305A1
56745-EP2298749A1
56745-EP2298762A2
56745-EP2298769A1
56745-EP2298773A1
56745-EP2301353A1
56745-EP2305031A1
56745-EP2305033A1
56745-EP2305034A1
56745-EP2305035A1
56745-EP2308866A1
56745-EP2308878A2
56745-EP2371806A1
56745-EP2371807A1
56745-EP2371823A1
56745-EP2374791A1
56745-EP2380874A2
Toluene, p.a., 99.5%
133890-EP2275410A1
133890-EP2295420A1
SR-01000944565-1
Toluene liquid density, NIST(R) SRM(R) 211d
Toluene, for residue analysis, >=99.8% (GC)
Toluene, anhydrous, ZerO2(TM), 99.8%
Toluene, for HPLC, >=99.7% (GC)
Toluene, puriss., >=99.5% (GC)
TOLUENE (TECHNICAL) (SEE ALSOTOLUENE (NITRATION GRADE) NTP10009-V)
TOLUENE (SEE ALSO TOLUENE (TECHNICAL), NTP 11617-L)
Toluene, suitable for 300 per JIS, for residue analysis, >=99.8%
Toluene, HPLC Plus, for HPLC, GC, and residue analysis, >=99.9%
Toluene, suitable for 1000 per JIS, for residue analysis, >=99.8%
Toluene, p.a., ACS reagent, reag. ISO, 99.5%
Toluene, absolute, over molecular sieve (H2O <=0.005%), >=99.7% (GC)
InChI=1/C7H8/c1-7-5-3-2-4-6-7/h2-6H,1H
Toluene, p.a., ACS reagent, reag. ISO, reag. Ph. Eur., 99.5%
Toluene, puriss. p.a., ACS reagent, reag. ISO, reag. Ph. Eur., >=99.7% (GC)
IUPAC nametoluene
SMILESCC1=CC=CC=C1
InchiInChI=1S/C7H8/c1-7-5-3-2-4-6-7/h2-6H,1H3
FormulaC6H5CH3
PubChem ID1140
Molweight92.141
LogP2.49
Atoms15
Bonds15
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationBenzenoids alkylbenzenes

mVOC Specific Details

Volatilization
The Henry's Law constant for toluene is 6.64X10-3 atm-cu m/mole(1). This Henry's Law constant indicates that toluene 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 2.9 hours(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 3.8 days(SRC). Toluene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Toluene is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 28.4 mm Hg(3). The air-water interface equilibrium partitioning coefficient for toluene, at a concentration of 0.47 mg/L, has been reported to be 0.223, 0.226, 0.273, and 0.336 at 26.9, 31.9, 36.9, and 41.9 deg C, respectively(4). A first-order volatilization rate calculated for toluene from water using an inverse reactive simulation was reported as 6.62X10-6/sec(5). The volatilization half-life of toluene from a water column of one meter depth was estimated to be 5.18 hours(6). Toluene was reported to have a disappearance half-life of <2 days due to volatilization in two different soil types, a Captina silt loam and a McLaurin sandy loam(7).
Literature: (1) Mackay D et al; Environ Sci Technol 13: 333-6 (1979) (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 (1989) (4) Cheng W-H et al; Atmos Environ 37: 4807-4815 (2003) (5) Keefe SH et al; Environ Sci Technol 38: 2209-2216 (2004) (6) Mackay D, Leinonen PJ; Environ Sci Technol 9: 1178-80 (1975) (7) Anderson TA et al; J Environ Qual 20:420-4 (1991)
Soil Adsorption
The Koc of toluene was reported as 178 in a sandy soil(1) and as 37 (Wendover silty loam), 160 (Grimsby silt loam), 160 (Vaudreil sandy loam) and 46 (sandy soil)(2). The Koc of toluene in lake sediment was measured as 166(3). According to a classification scheme(4), these measured Koc values suggest that toluene is expected to have high to moderate mobility in soil.
Literature: (1) Wilson JT et al; J Environ Qual 10: 501-6 (1981) (2) Nathwani JS, Phillips CR; Chemosphere 6: 157-62 (1977) (3) Kan AT et al; Environ Sci Technol 32: 892-902 (1998) (4) Swann RL et al; Res Rev 85: 17-28 (1983)
Literature: #In association with clay minerals, toluene's adsorption is inversely proportional to the pH of the soil. Approximately 40-70% of toluene applied to the surface of sandy soils is volatilized.
Literature: IARC. Monographs on the Evaluation of the Carcinogenic Risk of Chemicals to Humans. Geneva: World Health Organization, International Agency for Research on Cancer, 1972-PRESENT. (Multivolume work). Available at: http://monographs.iarc.fr/ENG/Classification/index.php, p. V47: 90 (1989)
Vapor Pressure
PressureReference
28.4 mm Hg at 25 deg CDaubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
MS-Links
1D-NMR-Links

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiTuber Aestivumn/aAgricultural Centre of Castilla and León Community (Monasterio de la Santa Espina, Valladolid, Spain) and Navaleno (Soria, Spain).Diaz et al., 2003
BacteriaBurkholderia Sp. AD24bacterial interationsrhizosphere and bulk soil of Carex arenariaTyc et al. 2017
BacteriaBurkholderia Tropica MTo431n/aTenorio-Salgado et al., 2013
BacteriaCarnobacterium Divergens 9Pn/aErcolini et al., 2009
BacteriaPaenibacillus Sp. AD87bacterial interationsrhizosphere and bulk soil of Carex arenariaTyc et al. 2017
BacteriaPseudomonas Fragi 25Pn/aErcolini et al., 2009
BacteriaSerratia Proteamaculans 42Mn/aErcolini et al., 2009
FungiTuber Aestivumn/aFortywoodland of the Basilicata regionMauriello et al., 2004
FungiTuber Borchiin/aFortywoodland of the Basilicata regionMauriello et al., 2004
FungiTuber Brumalen/aFortywoodland of the Basilicata regionMauriello et al., 2004
FungiTuber Excavatumn/aFortywoodland of the Basilicata regionMauriello et al., 2004
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiTuber Aestivumn/aHeadspace solid-phase microextraction (HS-SPME) combined with GC-MS
BacteriaBurkholderia Sp. AD24TSBAGC-Q-TOFno
BacteriaBurkholderia Tropica MTo431Potato dextrose agarHeadspace trapping/ GC-MS
BacteriaCarnobacterium Divergens 9Pn/an/a
BacteriaPaenibacillus Sp. AD87TSBAGC-Q-TOFno
BacteriaPseudomonas Fragi 25Pn/an/a
BacteriaSerratia Proteamaculans 42Mn/an/a
FungiTuber Aestivumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)
FungiTuber Borchiin/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)
FungiTuber Brumalen/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)
FungiTuber Excavatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)


4,7,7-trimethylbicyclo[2.2.1]heptan-3-one

Mass-Spectra

Compound Details

Synonymous names
Alcanfor
Alphanon
Camphora
DSSYKIVIOFKYAU-UHFFFAOYSA-N
Matricaria camphor
camphor
Formosa
Formosa camphor
Japanese camphor
Kampfer
Japan camphor
Laurel camphor
Camphor oil
Camphor USP
dextro,laevo-camphor
Gum camphor
Camphor, synthetic
DL-Camphor
l-Camphor
2-Camphanone
2-Camphonone
AC1L1DWH
Huile de camphre
Root bark spirit
Spirit of camphor
2-Bornanone
2-Kamfanon
Root bark oil
AC1Q2CF0
camphor (natural)
Camphor Powder - Synthetic
d-2-Bornanone
d-2-Camphanone
Bornan-2-one
GTPL2422
HSDB 37
Kampfer [German]
KSC378C7P
Q964
Camphor (USP)
CHEMBL15768
SCHEMBL16068
UN2717
C1251
camphor, (synthetic)
Camphor, D-
CTK2H8177
HMS502E06
1,7,7-Trimethylnorcamphor
DL-Bornan-2-one
JFD03998
LS-126
(1R)-Camphor
C00809
C18369
D00098
HMS2268A06
Huile de camphre [French]
Sarna (Salt/Mix)
AC-5284
BBL012963
BT000174
DTXSID5030955
Heet (Salt/Mix)
LS-1691
OR001346
OR116929
OR327727
STK803534
UN 2717
(-)-Alcanfor
2-Kamfanon [Czech]
A838646
ACMC-209k77
CHEBI:36773
D(+)-Camphor
(-)-Camphor
(+)-Camphor
AC-15523
AN-11174
AN-17868
AN-23465
AN-23893
ANW-30449
Bornane, 2-oxo-
DSSTox_GSID_30955
KB-00097
KB-50285
LS-48718
TRA0077646
BB_NC-0198
CAMPHOR POWDER D.A.B.8
Caswell No. 155
DSSTox_CID_10955
DSSTox_RID_78860
MFCD00064149
NINDS_000724
AI3-01698
AI3-18783
Camphor, (1R)-Isomer
DB-070734
dl-Camphor (JP17)
KB-270826
RTR-037701
TR-037701
2-Keto-1,7,7-trimethylnorcamphane
AKOS000118728
AKOS022060577
D-(+)-Camphor
DivK1c_000724
EPA Pesticide Chemical Code 015602
I06-1217
KBio1_000724
l-(-)-Camphor
Q-200784
W-109539
W-110530
(+-)-Camphor
BRN 1907611
BRN 3196099
FEMA No. 2230
FT-0607017
IDI1_000724
MLS001055495
SMR000386909
(+)-2-Bornanone
1,7,7-trimethylnorbornan-2-one
76-22-2
I14-16513
LMPR0102120001
Z940713494
Tox21_200237
464-48-2
F0001-0763
(+/-)-Camphor
Camphor, (+)-
CAS-76-22-2
Norcamphor, 1,7,7-trimethyl-
Camphor, (+-)-Isomer
MCULE-2476865084
NCGC00090681-05
NCGC00090730-01
NCGC00090730-02
NCGC00257791-01
EINECS 200-945-0
EINECS 207-355-2
EINECS 244-350-4
21368-68-3
CAMPHOR, (+-)-
(1R)-(+) Camphor
(1R)-(+)-amphor
MolPort-002-506-944
Camphor, synthetic [UN2717] [Flammable solid]
(.+/-.)-Camphor
Camphor, (+/-)-
(1R, 4R)-(+) Camphor
(1R,4R)-1,7,7-trimethylnorbornan-2-one
Camphor, (.+/-.)-
1,7,7-Trimethylbicyclo(2.2.1)-2-heptanone
1,7,7-Trimethylbicyclo(2.2.1)heptan-2-one
1,7,7-Trimethylbicyclo[2.2.1]-2-heptanone
1,7,7-Trimethylbicyclo[2.2.1]heptan-2-one
4,7,7-trimethyl-3-bicyclo[2.2.1]heptanone
4,7,7-trimethylbicyclo[2.2.1]heptan-3-one
Camphor, (1R,4R)-(+)-
1,7,7-Trimethyl-bicyclo(2,2,1)Heptan-2-one
1,7,7-Trimethyl-bicyclo[2.2.1]heptan-2-one
1,7,7-trimethyl-bicyclo[2.2.1]heptan-6-one
(+/-)-Camphor, 96% 100g
Bicyclo(2.2.1)heptane-2-one, 1,7,7-trimethyl-
Bicyclo[2.2.1]heptane-2-one, 1,7,7-trimethyl-
Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-
(+/-)-1,7,7-trimethyl-bicyclo[2,2,1]heptane-2-one
Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1theta)-
Bicyclo(2.2.1)heptan-2-one, 1,7,7-trimethyl-, (1R)-
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1R)-
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1S)-
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (1S,4S)-
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (+/-)-
CAMPHOR (SEE ALSO DL-CAMPHOR (21368-68-3) AND D-CAMPHOR (464-49-3))
Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-, (.+/-.)-
DL-CAMPHOR (SEE ALSO D-CAMPHOR (464-49-3) AND DL-CAMPHOR (21368-68-3))
IUPAC name4,7,7-trimethylbicyclo[2.2.1]heptan-3-one
SMILESCC1(C2CCC1(C(=O)C2)C)C
InchiInChI=1S/C10H16O/c1-9(2)7-4-5-10(9,3)8(11)6-7/h7H,4-6H2,1-3H3
FormulaC10H16O
PubChem ID2537
Molweight152.237
LogP2.55
Atoms27
Bonds28
H-bond Acceptor1
H-bond Donor0
Chemical ClassificationTerpenes Ketones Bicyclo

mVOC Specific Details

Volatilization
The Henry's Law constant for camphor is estimated as 8.3X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 0.65 mm Hg(1), and water solubility, 1.570X10+3 mg/L(2). This Henry's Law constant indicates that camphor 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 17 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 9 days(SRC). Camphor's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Camphor is expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).
Literature: (1) Jones AH; J Chem Eng Data 5: 196-200 (1960) (2) Yalkowky SH et al; Handbook of Aqueous Solubility Data. 2nd ed., Boca Raton, FL: CRC Press, p. 721 (2010) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of camphor can be estimated to be 117(SRC). According to a classification scheme(2), this estimated Koc value suggests that camphor 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 May 21, 2014: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
0.65 mm Hg at 25 deg CJones AH; J Chem Eng Data 5: 196-200 (1960)

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10063n/aDickschat et al., 2005_3
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10267n/aDickschat et al., 2005_3
BacteriaStreptomyces Albusn/aSchulz and Dickschat, 2007
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
FungiGanoderma Lucidumnasaprophytic on deciduous treesZiegenbein et al., 2006
FungiTuber Magnatumn/aItalian geographical areas (Emilia Romagna, Border region area between Emilia Romagna and Marche)Gioacchini et al., 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10063n/an/a
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10267n/an/a
BacteriaStreptomyces Albusn/an/a
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiFomitopsis PinicolanaGC/MSNo
FungiGanoderma LucidumnaGC/MSNo
FungiTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)


4,6,6-trimethylbicyclo[3.1.1]hept-3-ene

Mass-Spectra

Compound Details

Synonymous names
Phosphosulfurized alpha-pinene
ALPHA-PINENEPOLYMER
alphapinene
GRWFGVWFFZKLTI-UHFFFAOYSA-N
Cyclic dexadiene
alpha-Pinene, phosphosulfurized
Pinene isomer
alpha pinene
ALPHA-PINENE
Sylvapine A
Acintene A
Acitene A
Wilt Pruf
Alpha Pinene PF
DL-ALPHA-PINENE
2-Pinene
PINENE, ALPHA
1R-alpha-Pinene
AC1L1N0D
alpha-pinene, pinene
alpha-Pinene(dextro)
1R-a-Pinene
.alpha.-Pinene
alpha-Pinene (natural)
NSC7727
pin-2-ene
UN2368
CCRIS 697
CTK5E7908
HMDB06525
HSDB 720
CHEMBL442565
NSC94522
NSC94523
PC 500
alpha [D] Pinene
alpha [L] Pinene
C09880
BT000143
DTXSID4026501
FEMA Number 2902
LS-2348
NSC 7727
NSC-7727
OR038360
OR246844
OR249294
Pinene, .alpha.
SBB060477
UN 2368
1R-.alpha.-Pinene
1S-.alpha.-Pinene
CHEBI:36740
DSSTox_CID_6501
AN-19420
AN-19426
AN-42193
DSSTox_GSID_26501
NSC-94522
NSC-94523
SC-18193
DSSTox_RID_78126
PINENE, ALPHA (D)
PINENE, ALPHA (L)
AI3-24594
ST51046656
AKOS000121239
Q-201582
(+)-a-Pinene
BRN 3194807
FEMA No. 2902
FT-0604379
FT-0604414
FT-0622197
FT-0698080
pin-2(3)-ene
(R)-.alpha.-Pinene
80-56-8
(+-)-alpha-pinene
Tox21_110996
Tox21_200108
Tox21_303385
1R-(+)-alpha-pinene
alpha-Pinene, phosphorus pentasulfide reaction product (4:1)
DL-Pin-2(3)-ene
CAS-80-56-8
1R-(+)-a-pinene
MCULE-3589656574
NCGC00090682-01
NCGC00090682-02
NCGC00257379-01
NCGC00257662-01
(+-)-2-pinene
(+/-)-alpha-Pinene
EINECS 201-291-9
EINECS 219-445-9
EINECS 267-032-7
25766-18-1
39388-04-0
39423-40-0
50815-61-7
53569-35-0
56833-58-0
57762-87-5
67762-73-6
68411-25-6
72510-05-5
102640-64-2
103657-08-5
459844-87-2
alpha-Pinene [UN2368] [Flammable liquid]
(+/-)-2-Pinene
MolPort-003-926-536
(1R)-(+)-a-Pinene
(+)-Pin-2(3)-ene
2,6-Trimethylbicyclo[3.1.1]-2-heptene
(.+/-.)-.alpha.-Pinene
2,6,6-Trimethylbicyclo(3.1.1)hept-2-ene
2,6,6-Trimethylbicyclo[3.1.1]-2-heptene
2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene
4,6,6-trimethylbicyclo[3.1.1]hept-3-ene
4,6,6-Trimethylbicyklo(3,1,1)hept-3-en
Bicyclo[3.1.1]hept-2-ene,6,6-trimethyl-
2,6-Trimethylbicyclo[3.1.1]-2-hept-2-ene
2,6,6-trimethyl-Bicyclo(3.1.1)hept-2-ene
2,6,6-trimethyl-bicyclo[3.1.1]hept-2-ene
2-Pinene, (1S,5S)-(-)-
2,6,6-Trimethyl bicyclo-(3,1,1)-2 heptene
Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl
Bicyclo[3.1.1]hept-2-ene,2,6,6-trimethyl-
2,6,6-Trimethylbicyclo(3.1.1)-2-hept-2-ene
4,6,6-Trimethylbicyklo(3,1,1)hept-3-en [Czech]
Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl-, phosphosulfurized
Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl-
Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-
(1R)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene
(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene
Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl-, homopolymer
Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-, (1R)-
Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-, (1S)-
Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-, (.+/-.)-
IUPAC name4,6,6-trimethylbicyclo[3.1.1]hept-3-ene
SMILESCC1=CCC2CC1C2(C)C
InchiInChI=1S/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h4,8-9H,5-6H2,1-3H3
FormulaC10H16
PubChem ID6654
Molweight136.238
LogP2.8
Atoms26
Bonds27
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes Alkenes Bicyclo

mVOC Specific Details

Volatilization
The Henry's Law constant for alpha-pinene is estimated as 0.29 atm-cu m/mole(SRC) derived from its vapor pressure, 4.75 mm Hg(1), and water solubility, 2.49 mg/L(2). This Henry's Law constant indicates that alpha-pinene is expected to volatilize rapidly 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 3 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 5 days(SRC). alpha-Pinene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of alpha-pinene from dry soil surfaces may exist based upon a vapor pressure of 4.75 mm Hg(1).
Literature: (1) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals: Data Compilation. Design Inst Phys Prop Data, Amer Inst Chem Eng NY, NY: Hemisphere Pub Corp (1989) (2) Li J, Perdue EM; Physicochemical properties of selected monoterpenes. Pre-print extended abstract, Presented before the Division of Environmental Chemistry, Amer. Chem. Soc., Anaheim, CA, April 2-7, 1995 (1995) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)
Solubility
ALMOST INSOLUBLE IN PROPYLENE GLYCOL & GLYCERINE
Literature: Fenaroli's Handbook of Flavor Ingredients. Volume 2. Edited, translated, and revised by T.E. Furia and N. Bellanca. 2nd ed. Cleveland: The Chemical Rubber Co., 1975., p. 486
Literature: #Sol in alcohol, chloroform, ether, glacial acetic acid, fixed oils
Literature: Lewis, R.J. Sax's Dangerous Properties of Industrial Materials. 10th ed. Volumes 1-3 New York, NY: John Wiley & Sons Inc., 1999., p. 2970
Literature: #In water, 2.49 mg/L at 25 deg C
Literature: Li J, Perdue EM; Physicochemical Properties of Selected Monoterpenes. Pre-print Extended Abstract, Presented Before The Division of Environmental Chemistry, Amer Chem Soc, Anaheim, Ca: April 2-7 (1995)
Soil Adsorption
The Koc of alpha-pinene is estimated as 2,600(SRC), using a water solubility of 2.49 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that alpha-pinene is expected to have slight mobility in soil.
Literature: (1) Li J, Perdue EM; Physicochemical properties of selected monoterpenes. Pre-print extended abstract, Presented before the Division of Environmental Chemistry, Amer. Chem. Soc., Anaheim, CA, April 2-7, 1995 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-5 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
4.75 mm Hg at 25 deg CDaubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
MS-Links

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaBacillus Amyloliquefaciens FZB42Agriculture University of Nanjing, ChinaTahir et al. 2018
BacteriaBacillus Artrophaeus LSSC22Agriculture University of Nanjing, ChinaTahir et al. 2031
BacteriaBurkholderia Sp. AD24bacterial interationsrhizosphere and bulk soil of Carex arenariaTyc et al. 2017
BacteriaPaenibacillus Sp. AD87bacterial interationsrhizosphere and bulk soil of Carex arenariaTyc et al. 2017
BacteriaStreptomyces Griseus Subsp. Griseus DSM 40236nasoilWilkins, 1996
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiAspergillus Fumigatuscompost Fischer et al. 2045
FungiCladosporium CladosporiodesHedlund et al 1995
FungiCladosporium HerbarumHedlund et al 1995
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
FungiGanoderma Lucidumnasaprophytic on deciduous treesZiegenbein et al., 2006
FungiMortierella Isabellinamor horizon of a spruce forest soil southeastern SwedenBengtsson et al 1991
FungiPenicillium Commune Pittnain dry-cured meat products, cheeseSunesson et al., 1995
FungiPenicillium SpinulosumHedlund et al 1995
FungiPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al., 2000
FungiSpongiporus Leucomallellusnasaprophytic mostly on wet, old pinesZiegenbein et al., 2006
BacteriaCalothrix Parietina PCC 6303n/aHoeckelmann et al., 2004
BacteriaCarnobacterium Divergens 9Pn/aErcolini et al., 2009
BacteriaMix Of Bacteria(Serratia Proteamaculans 42Mn/aErcolini et al., 2009
BacteriaPhormidium Sp.n/aHoeckelmann et al., 2004
BacteriaPseudomonas Fragi 25Pn/aErcolini et al., 2009
BacteriaRivularia Sp.n/aHoeckelmann et al., 2004
BacteriaStreptomyces Griseusn/aSchulz and Dickschat, 2007
FungiAgrocybe AegeritaFranceBreheret et al. 1997
FungiAmanita OvoideaFranceBreheret et al. 1997
FungiAspergillus Fumigatus Strain FGSC A1163Heddergott et al. 2014
FungiBoletus AestivalisFranceBreheret et al. 1997
FungiCantharellus CibariusFranceBreheret et al. 1997
FungiCortinarius CinnamomeusFranceBreheret et al. 1997
FungiCystoderma AmianthinumFranceBreheret et al. 1997
FungiCystoderma CarchariasFranceBreheret et al. 1997
FungiFusarium Graminearum 15AcDONn/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON 1001tan/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON ZFR 29n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_4n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_5n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_6n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_7n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_8n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_9n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 1002tn/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 11791n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 1509n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 8046n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON NRRL38369n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON NRRL6394n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON ZFR 15n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON ZFR 37n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON ZFR 51n/aBusko et al., 2014
FungiFusarium Graminearum NIVn/aBusko et al., 2014
FungiFusarium Graminearum NIV ZFR 119n/aBusko et al., 2014
FungiFusarium Graminearum NIV ZFR 23n/aBusko et al., 2014
FungiFusarium Graminearum NIV ZFR 48n/aBusko et al., 2014
FungiFusarium Graminearum NIV_5n/aBusko et al., 2014
FungiFusarium Graminearum NIV_6n/aBusko et al., 2014
FungiFusarium Graminearum NIV_7n/aBusko et al., 2014
FungiFusarium Graminearum NIV_8n/aBusko et al., 2014
FungiFusarium Graminearum NIV_9n/aBusko et al., 2014
FungiGomphidius GlutinosusFranceBreheret et al. 1997
FungiHydnum RepandumFranceBreheret et al. 1997
FungiHygrophorus AgathosmusFranceBreheret et al. 1997
FungiMycena PuraFranceBreheret et al. 1997
FungiMycena RoseaFranceBreheret et al. 1997
FungiSuillus LuteusFranceBreheret et al. 1997
FungiTricholoma CaligatumFranceBreheret et al. 1997
FungiTricholoma PortentosumFranceBreheret et al. 1997
FungiTricholoma SulfureumFranceBreheret et al. 1997
BacteriaBurkholderia Tropica MTo431n/aTenorio-Salgado et al., 2013
BacteriaEscherichia Coli MG1655Bokinsky et al., 2011
FungiTuber Magnatumn/aItalian geographical areas ( Marche, Border region area between Emilia Romagna and Marche)Gioacchini et al., 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaBacillus Amyloliquefaciens FZB42LBSPME-GC-MSno
BacteriaBacillus Artrophaeus LSSC22LBSPME-GC-MSno
BacteriaBurkholderia Sp. AD24TSBAGC-Q-TOFno
BacteriaPaenibacillus Sp. AD87TSBAGC-Q-TOFno
BacteriaStreptomyces Griseus Subsp. Griseus DSM 40236Nutrient agar CM3GC/MS
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiAspergillus Fumigatusyest extract sucroseTenax/GC-MSno
FungiCladosporium CladosporiodesGC-MSno
FungiCladosporium HerbarumGC-MSno
FungiFomitopsis PinicolanaGC/MSNo
FungiGanoderma LucidumnaGC/MSNo
FungiMortierella Isabellinadiethyl extraction, GC-MSno
FungiPenicillium Commune PittDG18GC/MS
FungiPenicillium SpinulosumGC-MSno
FungiPiptoporus BetulinusnaGC/MSNo
FungiSpongiporus LeucomallellusnaGC/MSNo
BacteriaCalothrix Parietina PCC 6303n/an/a
BacteriaCarnobacterium Divergens 9Pn/an/a
BacteriaMix Of Bacteria(Serratia Proteamaculans 42Mn/an/a
BacteriaPhormidium Sp.n/an/a
BacteriaPseudomonas Fragi 25Pn/an/a
BacteriaRivularia Sp.n/an/a
BacteriaStreptomyces Griseusn/an/a
FungiAgrocybe Aegeritaforest soilsolvent extraction, headspace, GCMSno
FungiAmanita Ovoideaforest soilsolvent extraction, headspace, GCMSno
FungiAspergillus Fumigatus Strain FGSC A1163Brian`s broth, AMM, RPMI 1642SPME / GC-MS
FungiBoletus Aestivalisforest soilsolvent extraction, headspace, GCMSno
FungiCantharellus Cibariusforest soilsolvent extraction, headspace, GCMSno
FungiCortinarius Cinnamomeusforest soilsolvent extraction, headspace, GCMSno
FungiCystoderma Amianthinumforest soilsolvent extraction, headspace, GCMSno
FungiCystoderma Carchariasforest soilsolvent extraction, headspace, GCMSno
FungiFusarium Graminearum 15AcDONyeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON 1001tayeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON ZFR 29yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_4yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_5yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_6yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_7yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_8yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_9yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 1002tyeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 11791yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 1509yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 8046yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON NRRL38369yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON NRRL6394yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON ZFR 15yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON ZFR 37yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON ZFR 51yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIVyeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV ZFR 119yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV ZFR 23yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV ZFR 48yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_5yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_6yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_7yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_8yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_9yeast extract sucrose agarSPME/GC-MS
FungiGomphidius Glutinosusforest soilsolvent extraction, headspace, GCMSno
FungiHydnum Repandumforest soilsolvent extraction, headspace, GCMSno
FungiHygrophorus Agathosmusforest soilsolvent extraction, headspace, GCMSno
FungiMycena Puraforest soilsolvent extraction, headspace, GCMSno
FungiMycena Roseaforest soilsolvent extraction, headspace, GCMSno
FungiSuillus Luteusforest soilsolvent extraction, headspace, GCMSno
FungiTricholoma Caligatumforest soilsolvent extraction, headspace, GCMSno
FungiTricholoma Portentosumforest soilsolvent extraction, headspace, GCMSno
FungiTricholoma Sulfureumforest soilsolvent extraction, headspace, GCMSno
BacteriaBurkholderia Tropica MTo431Potato dextrose agarHeadspace trapping/ GC-MS
BacteriaEscherichia Coli MG1655Luria-Bertani (LB)
FungiTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)


4-methyl-1-propan-2-ylcyclohex-3-en-1-ol

Mass-Spectra

Compound Details

Synonymous names
Melaleucol
WRYLYDPHFGVWKC-UHFFFAOYSA-N
4-Carvomenthenol
Terpinenolu-4
Terpinenol-4
AC1Q2ODY
AC1L1WWJ
4-Terpinenol
Terpineol-4
4-Terpineol
L-4-terpineneol
dl-4-Terpineol
TERPINENE-4-OL
Terpinen-4-ol
L-4-terpineol
S145
Terpinen 4-ol, primary pharmaceutical reference standard
Terpin-4-ol
Terpene-4-ol
alpha-terpinen-4-ol
SCHEMBL22344
rac Terpinen-4-ol
CTK3J7764
M0319
4-Carvomenthenol (natural)
CHEMBL507795
L-terpinen-4-ol
HSDB 8264
CCRIS 9067
Terpinenolu-4 [Czech]
C17073
NSC147749
1-Terpinen-4-ol
OR040948
OR114584
1-Menthene-4-ol
DTXSID4044824
SBB071495
LS-2615
ST096089
CHEBI:78884
DSSTox_GSID_44824
AN-23698
SC-46918
DSSTox_RID_80505
1-para-Menthen-4-ol
DSSTox_CID_24824
MFCD00001562
NSC 147749
NSC-147749
RTR-019770
Terpin-4-en-1-ol
TR-019770
1-p-Menthen-4-ol
AKOS015903412
FT-0619472
FEMA No. 2248
BRN 1906603
I14-19182
para-Menth-1-en-4-ol
p-Menth-1-en-4-ol
Tox21_301785
562-74-3
4-Carvomenthenol, natural, >=95%, FG
MCULE-6511194668
1336-05-6
NCGC00256250-01
EINECS 209-235-5
4-Carvomenthenol, >=95%, FCC, FG
4-Methyl-1-isopropyl-3-cyclohexen-1-ol
1-isopropyl-4-methylcyclohex-3-en-1-ol
1-Methyl-4-isopropyl-1-cyclohexen-4-ol
CAS-562-74-3
EINECS 248-910-9
28219-82-1
(+/-)-4-Terpineol
1-isopropyl-4-methyl-cyclohex-3-en-1-ol
MolPort-003-959-981
4-methyl-1-(methylethyl)cyclohex-3-en-1-ol
4-methyl-1-propan-2-ylcyclohex-3-en-1-ol
(-)-p-Menth-1-en-4-ol
4-Methyl-1-(1-methylethyl)-3-cyclohexen-1-ol
1-(1-Methylethyl)-4-methyl-3-cyclohexen-1-ol
(-)-4-Hydroxy-4-isopropyl-1-methyl-1-cyclohexene
4-06-00-00250 (Beilstein Handbook Reference)
(+-)-p-Menth-1-en-4-ol
(-)-1-Isopropyl-4-methyl-3-cyclohexen-1-ol
4-Methyl-1-(propan-2-yl)cyclohex-3-en-1-ol
1-Isopropyl-4-methyl-3-cyclohexen-1-ol, (R)-
(+/-)-p-Menth-1-en-4-ol
3-CYCLOHEXEN-1-OL; 4-METHYL-1-(1-METHYLETHYL)-
3-Cyclohexen-1-ol, 4-methyl-1-(1-methylethyl)-
(+/-)-4-Hydroxy-4-isopropyl-1-methyl-1-cyclohexene
(1)-1-(Isopropyl)-4-methylcyclohex-3-en-1-ol
(+/-)-1-Isopropyl-4-methyl-3-cyclohexen-1-ol
IUPAC name4-methyl-1-propan-2-ylcyclohex-3-en-1-ol
SMILESCC1=CCC(CC1)(C(C)C)O
InchiInChI=1S/C10H18O/c1-8(2)10(11)6-4-9(3)5-7-10/h4,8,11H,5-7H2,1-3H3
FormulaC10H18O
PubChem ID11230
Molweight154.253
LogP2.33
Atoms29
Bonds29
H-bond Acceptor1
H-bond Donor1
Chemical ClassificationTerpenes Alcohols Alkenes

mVOC Specific Details

Boiling Point
DegreeReference
209 deg CLide, D.R., G.W.A. Milne (eds.). Handbook of Data on Organic Compounds. Volume I. 3rd ed. CRC Press, Inc. Boca Raton ,FL. 1994., p. V3: 2311
Volatilization
The Henry's Law constant for 4-terpineol is estimated as 3.2X10-6 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that 4-terpineol 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 15 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 110 days(SRC). 4-Terpineol's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 4-Terpineol is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 0.04 mm Hg(SRC), determined from a fragment constant method(1).
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of July 22, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)
Solubility
In water, 3.87X10+2 mg/L at 25 deg C (est)
Literature: US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of July 22, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of 4-terpineol can be estimated to be 80(SRC). According to a classification scheme(2), this estimated Koc value suggests that 4-terpineol is expected to have high mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of July 22, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
0.04 mm Hg at 25 deg C (est)US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of July 22, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
MS-Links
1D-NMR-Links

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
BacteriaStigmatella Aurantiaca DW4/3-1n/aDickschat et al., 2005_5
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10063n/aDickschat et al., 2005_3
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10267n/aDickschat et al., 2005_3
FungiGanoderma Lucidumnasaprophytic on deciduous treesZiegenbein et al., 2006
Method


6,6-dimethyl-4-methylidenebicyclo[3.1.1]heptane

Mass-Spectra

Compound Details

Synonymous names
Pseudopinene
Terebenthene
Pseudopinen
Terbenthene
Nopinene
Rosemarel
WTARULDDTDQWMU-UHFFFAOYSA-N
Nopinen
beta-Pinene homopolymer
beta pinene
BETA-PINENE
ss-Pinene
AC1Q2AIT
B-pinene
beta-Pinene resin
PINENE, BETA
AC1L24RF
I943
Piccolyte 115
.beta.-Pinene
beta-Pinene (natural)
P0441
6,6-Dimethyl-2-methylenenorpinane
CHEMBL501351
laevo-.beta.-Pinene
NSC21447
NSC59190
Beta Pinene 95 PF
Beta Pinene PF 85%
Beta Pinene PF 95%
Beta Pinene T 85%
Beta Pinene T 95%
C09882
HSDB 5615
AK113983
BT000141
DTXSID7027049
Jsp001748
L-.beta.-Pinene
LS-3052
NSC406265
OR025387
OR211823
OR213994
SBB061306
CHEBI:50025
DSSTox_CID_7049
( inverted exclamation markA)-b-pinene
6,6-dimethyl-2-methylene-norpinane
AB1006761
AN-18767
AN-23009
DSSTox_GSID_27049
EBD2156726
NSC 21447
NSC-21447
NSC-59190
SC-48739
D-alpha-PINENE, 95%
DSSTox_RID_78293
2(10)-Pinene
AI3-24483
NSC-406265
ST50330587
AKOS004119987
(-)-b-Pinene
4CH-024531
FEMA No. 2903
FT-0604382
FT-0622936
I14-45220
Pin-2(10)-ene
Tox21_200029
127-91-3
9081-94-1
NCGC00248498-01
NCGC00257583-01
(-)-.beta.-Pinene
CAS-127-91-3
EINECS 204-872-5
EINECS 245-424-9
25719-60-2
37203-45-5
39475-62-2
50922-56-0
51273-99-5
55963-81-0
55963-82-1
59828-47-6
59828-48-7
60976-31-0
211108-08-6
(+)-I(2)-Pinene
MolPort-004-956-468
6,6-dimethyl-2-methylidenebicyclo[3.1.1]heptane
6,6-dimethyl-4-methylidenebicyclo[3.1.1]heptane
6,6-Dimethyl-2-methylenebicyclo(3.1.1)heptane
6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptane
(1S)-(-)-b-Pinene
(-)-2(10)-Pinene
Bicyclo[3.1.1]heptane,6-dimethyl-2-methylene-
2,6-Trimethylbicyclo[3.1.1]hept-2-ene
6,6-Dimethyl-2-methylene-bicyclo(3.1.1)heptane
(-)-Pin-2(10)-ene
.beta.-Pinene-(1S)-(-)
(1S)-(-)-.beta.-Pinene
(1S,5S)-2-(10)-Pinene
2,2,6-Trimethylbicyclo(3.1.1)hept-2-ene
Bicyclo(3.1.1)heptane, 6,6-dimethyl-2-methylene-
Bicyclo[3.1.1]heptane, 6,6-dimethyl-2-methylene-
(1)-6,6-Dimethyl-2-methylenebicyclo(3.1.1)heptane
BICYCLO(3.1.1)HEPTANE, 6,6-DIMETHYL-2-METHYLENE-, HOMOPOLYMER
(1S,5S)-6,6-Dimethyl-2-methylenebicyclo[3.1.1] heptane
6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptane-, (S)-
2(10)-Pinene, (1S,5S)-(-)-
Bicyclo[3.1.1]heptane, 6,6-dimethyl-2-methylene-, (1S)-
Bicyclo(3.1.1)heptane, 6,6-dimethyl-2-methylene-, (1S,5S)-
Bicyclo[3.1.1]heptane, 6,6-dimethyl-2-methylene-, (1S,5S)-
2(10)-Pinene; 6,6-Dimethyl-2-methylenebicyclo[3.1.1]heptane; Pin-2(10)-ene
IUPAC name6,6-dimethyl-4-methylidenebicyclo[3.1.1]heptane
SMILESCC1(C2CCC(=C)C1C2)C
InchiInChI=1S/C10H16/c1-7-4-5-8-6-9(7)10(8,2)3/h8-9H,1,4-6H2,2-3H3
FormulaC10H16
PubChem ID14896
Molweight136.238
LogP2.86
Atoms26
Bonds27
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes Ketones Bicyclo Alkane

mVOC Specific Details

Boiling Point
DegreeReference
166 deg CLide, D.R. CRC Handbook of Chemistry and Physics 86TH Edition 2005-2006. CRC Press, Taylor & Francis, Boca Raton, FL 2005, p. 3-436
Volatilization
The Henry's Law constant for beta-pinene is estimated as 0.16 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that beta-pinene is expected to volatilize rapidly 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 3 hours(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 5 days(SRC). beta-Pinene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The volatilization half-life from a model pond is about 340 days when adsorption is considered(3). beta-Pinene is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 2.93 mm Hg(4).
Literature: (1) Meylan WM, Howard PH; Environ Toxicol Chem 10: 1283-93 (1991) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) US EPA; EXAMS II Computer Simulation (1987) (4) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1989)
Solubility
ALMOST INSOL IN PROPYLENE GLYCOL
Literature: Fenaroli's Handbook of Flavor Ingredients. Volume 2. Edited, translated, and revised by T.E. Furia and N. Bellanca. 2nd ed. Cleveland: The Chemical Rubber Co., 1975., p. 486
Literature: #Soluble in benzene, ethanol and ethyl ether
Literature: Lide, D.R. CRC Handbook of Chemistry and Physics 86TH Edition 2005-2006. CRC Press, Taylor & Francis, Boca Raton, FL 2005, p. 3-436
Literature: #Soluble in alcohol and chloroform
Literature: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Whitehouse Station, NJ: Merck and Co., Inc., 2006., p. 1283
Literature: #In water, 4.89 mg/L at 25 deg C (est)
Literature: US EPA; Estimation Program Interface (EPI) Suite. Ver.3.12. Nov 30, 2004. Available from, as of Sept 24, 2008: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
Soil Adsorption
The Koc of beta-pinene is estimated as 4,400(SRC), using a log Kow of 4.16(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that beta-pinene is expected to have slight mobility in soil.
Literature: The Koc of beta-pinene is estimated as 4,400(SRC), using a log Kow of 4.16(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that beta-pinene is expected to have slight mobility in soil.
Vapor Pressure
PressureReference
2.93 mm Hg at 25 deg CDaubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
MS-Links

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
BacteriaCollimonas Fungivorans Ter331n/aGarbeva et al., 2013
BacteriaCollimonas Pratensis Ter91n/aGarbeva et al., 2013
BacteriaStreptomyces Griseus Subsp. Griseus DSM 40236nasoilWilkins, 1996
FungiPenicillium Commune Pittnain dry-cured meat products, cheeseSunesson et al., 1995
BacteriaCollimonas Pratensis TER91narhizosphere of Marram grass in sandy dune soils, NetherlandsGarbeva et al., 2014
BacteriaPaenibacillus Sp. P4narhizosphere of Marram grass in sandy dune soils, NetherlandsGarbeva et al., 2014
BacteriaPedobacter Sp. V48narhizosphere of Marram grass in sandy dune soils, NetherlandsGarbeva et al., 2014
BacteriaSerratia Plymuthica PRI-2Cnamaize rhizosphere, NetherlandsGarbeva et al., 2014
BacteriaStreptococcus Mutans DSM 20523 as a biomarker for a breath test for detection of cariesHertel et al., 2015
BacteriaStreptomyces Griseusn/aSchulz and Dickschat, 2007
FungiAmanita OvoideaFranceBreheret et al. 1997
FungiGomphidius GlutinosusFranceBreheret et al. 1997
FungiMycena PuraFranceBreheret et al. 1997
FungiSuillus LuteusFranceBreheret et al. 1997
FungiTricholoma CaligatumFranceBreheret et al. 1997
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
BacteriaCollimonas Fungivorans Ter331sand supplemented with artificial root exudatesHeadspace trapping/GC-MS
BacteriaCollimonas Pratensis Ter91sand supplemented with artificial root exudatesHeadspace trapping/GC-MS
BacteriaStreptomyces Griseus Subsp. Griseus DSM 40236Nutrient agar CM3GC/MS
FungiPenicillium Commune PittDG18GC/MS
BacteriaCollimonas Pratensis TER91sand containing artificial root exudatesGC/MSNo
BacteriaPaenibacillus Sp. P4sand containing artificial root exudatesGC/MSNo
BacteriaPedobacter Sp. V48sand containing artificial root exudatesGC/MSNo
BacteriaSerratia Plymuthica PRI-2Csand containing artificial root exudatesGC/MSNo
BacteriaStreptococcus Mutans DSM 20523Brain-Heart-Infusion agarTenaxâ„¢-trap/GC-MS
BacteriaStreptomyces Griseusn/an/a
FungiAmanita Ovoideaforest soilsolvent extraction, headspace, GCMSno
FungiGomphidius Glutinosusforest soilsolvent extraction, headspace, GCMSno
FungiMycena Puraforest soilsolvent extraction, headspace, GCMSno
FungiSuillus Luteusforest soilsolvent extraction, headspace, GCMSno
FungiTricholoma Caligatumforest soilsolvent extraction, headspace, GCMSno


2-(4-methylcyclohex-3-en-1-yl)propan-2-ol

Mass-Spectra

Compound Details

Synonymous names
Monocyclic terpenealcohols
CARVOMENTHENOL
Terpineol schlechthin
TERPINEOLS
Terpenol
Terpineol
WUOACPNHFRMFPN-UHFFFAOYSA-N
alpha-Terpinenol
alpha-TERPINEOL
Terpene alcohol
Terpineol Normal
alpha-Terpineol, primary pharmaceutical reference standard
TERPINEOL OR
alpha-Terpineol, AldrichCPR
alpha-Terpineol, analytical standard
dl-alpha-Terpineol
TERPINEOL, ALPHA
DL a-terpineol
Terpineol, mixed isomers
1-alpha-terpineol
Mixture of p-methenols
Terpineol (natural)
.alpha.-Terpineol
Alpha-Terpineol, Mixture of Isomers
Terpilenol, alpha-
AC1L29B5
alpha-Terpineol (natural)
KSC486Q4B
Terpineol 350
SCHEMBL28466
CTK3I6840
V0385
CHEMBL449810
NSC21449
PC 593
C16772
CCRIS 3204
HSDB 5316
1-.alpha.-Terpineol
1-Menthene-8-ol
AK122298
DTXSID5026625
FEMA Number 3045
LS-3106
NSC403665
OR034447
OR126371
OR342936
OR343294
SBB061191
4-Trimethyl-3-cyclohexene-1-methanol
CHEBI:22469
DSSTox_CID_6625
AN-18294
AN-19422
AN-24486
DSSTox_GSID_26625
DSSTox_GSID_40775
NSC 21449
NSC-21449
SC-46794
alpha-Terpineol, 90%, technical grade
Caswell No. 823
DSSTox_RID_78167
DSSTox_RID_79596
MFCD00001557
MFCD00166983
1-p-Menthen-8-ol
AI3-00275
alpha,alpha,4-Trimethyl-3-cyclohexene-1-methanol
KB-223071
LS-148797
NSC-403665
ST24039469
ST50824481
TR-030336
AKOS015840815
EPA Pesticide Chemical Code 067005
J-500272
Menth-1-en-8-ol
W-100076
BRN 1906604
FEMA No. 3045
FT-0622202
FT-0698995
98-55-5
I14-51686
d-1-p-Menthen-8-ol
p-Menth-1-en-8-ol
Tox21_112118
Tox21_200112
Tox21_302298
(+)-.alpha.-Terpineol
CAS-98-55-5
1-Methyl-4-isopropyl-1-cyclohexene-8-ol
2438-12-2
3-Cyclohexene-1-methanol,.alpha.4-trimethyl-
8000-41-7
8031-32-1
MCULE-9798755896
NCGC00164431-01
NCGC00248528-01
NCGC00255464-01
NCGC00257666-01
1-Methyl-4-isopropyl-1-cyclohexen-8-ol
3-Cyclohexene-1-methanol, alpha,alpha,4-trimethyl-
EINECS 202-680-6
EINECS 219-448-5
EINECS 232-268-1
p-Menth- 1-en-8-ol
11103-96-1
22347-88-2
37195-01-0
CAS-8000-41-7
SR-01000944873
2-(4-Methyl-3-cyclohexenyl)-2-propanol
2-(4-methylcyclohex-3-enyl)propan-2-ol
3-Cyclohexene-1-methanol, ?,?,4-trimethyl-
MolPort-002-042-108
(1)-alpha,alpha,4-Trimethylcyclohex-3-ene-1-methanol
SR-01000944873-1
68540-43-2 (hydrochloride salt)
(1R)-a,a,4-trimethyl-3-cyclohexene-1-methanol
3-Cyclohexene-1-methanol, .alpha.,.alpha.4-trimethyl-
2-(4-methylcyclohex-3-en-1-yl)propan-2-ol
3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-
2-(4-methyl-1-cyclohex-3-enyl)-propan-2-ol
3-Cyclohexene-1-methanol, ?,?,4-trimethyl-, (R)-
3-Cyclohexene-1-methanol, ?,?,4-trimethyl-, (S)-
3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-, (S)-
3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-, (1R)-
3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-, (1S)-
3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-, sodium salt, (1S)-
3-Cyclohexene-1-methanol, .alpha.,.alpha.,4-trimethyl-, sodium salt (1:1), (1S)-
IUPAC name2-(4-methylcyclohex-3-en-1-yl)propan-2-ol
SMILESCC1=CCC(CC1)C(C)(C)O
InchiInChI=1S/C10H18O/c1-8-4-6-9(7-5-8)10(2,3)11/h4,9,11H,5-7H2,1-3H3
FormulaC10H18O
PubChem ID17100
Molweight154.253
LogP2.17
Atoms29
Bonds29
H-bond Acceptor1
H-bond Donor1
Chemical ClassificationAlcohols terpenes

mVOC Specific Details

Volatilization
The Henry's Law constant for alpha-terpineol is reported as 2.23X10-6 atm-cu m/mole(1). This Henry's Law constant indicates that alpha-terpineol 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 20 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 150 days(SRC). alpha-Terpineol's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). alpha-Terpineol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.0423 mm Hg at 24 deg C(3).
Literature: (1) Copolovici LO, Niinemets U; Chemosphere 61: 1390-400 (2005) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Li J, Perdue, EM; Preprints of Papers Presented at the 209th ACS National Meeting, Anaheim, CA, April 2-7, 1995, 35: 134-7 (1995)
Solubility
1:8 OR MORE IN 50% ALCOHOL; SOL IN PROPYLENE GLYCOL
Literature: Fenaroli's Handbook of Flavor Ingredients. Volume 2. Edited, translated, and revised by T.E. Furia and N. Bellanca. 2nd ed. Cleveland: The Chemical Rubber Co., 1975., p. 522
Literature: #Very soluble in benzene, acetone
Literature: Lide, D.R. CRC Handbook of Chemistry and Physics 88TH Edition 2007-2008. CRC Press, Taylor & Francis, Boca Raton, FL 2007, p. 3-468
Literature: #Very soluble in alcohol, ether
Literature: Lewis, R.J. Sr. (ed) Sax's Dangerous Properties of Industrial Materials. 12th Edition. Wiley-Interscience, Wiley & Sons, Inc. Hoboken, NJ. 2012., p. 4151
Literature: #In water, 7100 mg/L at 25 deg C
Literature: Li J, Perdue EM; Preprints of Papers Presented at the 209th ACS National Meeting, Anaheim, CA, April 2-7, 1995, 35: 134-7 (1995)
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of alpha-terpineol can be estimated to be 80(SRC). According to a classification scheme(2), this estimated Koc value suggests that alpha-terpineol is expected to have high mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of June 29, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
0.0423 mm Hg at 24 deg CLi J, Perdue EM; Preprints of Papers Presented at the 209th ACS National Meeting, Anaheim, CA, April 2-7, 1995, 35: 134-7 (1995)

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiHypoxylon Antochroum Blacinaendophytic in Bursera lancifoliaUlloa-Benítez et al., 2016
FungiPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al., 2000
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10063n/aDickschat et al., 2005_3
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10267n/aDickschat et al., 2005_3
BacteriaPseudomonas Fragi 25Pn/aErcolini et al., 2009
BacteriaSerratia Proteamaculans 42Mn/aErcolini et al., 2009
BacteriaStigmatella Aurantiaca DW4/3-1n/aDickschat et al., 2005_5
BacteriaStigmatella Aurantiaca Sg A15n/aDickschat et al., 2005_5
BacteriaBacillus Pumilus ES4promotion of performance of Chlorella sorokiniana ShihAmavizca et al. 2017
BacteriaEscherichia Coli DH5apromotion of performance of Chlorella sorokiniana ShihAmavizca et al. 2017
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiGanoderma Lucidumnasaprophytic on deciduous treesZiegenbein et al., 2006
FungiSpongiporus Leucomallellusnasaprophytic mostly on wet, old pinesZiegenbein et al., 2006
BacteriaBacillus SimplexReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.Gu et al., 2007
BacteriaBacillus SubtilisReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.Gu et al., 2007
BacteriaBacillus WeihenstephanensisReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.Gu et al., 2007
BacteriaMicrobacterium OxydansReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.Gu et al., 2007
BacteriaSerratia MarcescensReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.Gu et al., 2007
BacteriaStenotrophomonas MaltophiliaReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.Gu et al., 2007
BacteriaStreptomyces LateritiusReduction of movement or death of Panagrelleus redivivus and Bursaphelenchus xylophilus.Gu et al., 2007
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiHypoxylon Antochroum BlaciPDA/WA + 500 mg l^-1 ChloramphenicolSPME-GC/MSNo
FungiPiptoporus BetulinusnaGC/MSNo
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10063n/an/a
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10267n/an/a
BacteriaPseudomonas Fragi 25Pn/an/a
BacteriaSerratia Proteamaculans 42Mn/an/a
BacteriaStigmatella Aurantiaca DW4/3-1n/an/a
BacteriaStigmatella Aurantiaca Sg A15n/an/a
BacteriaBacillus Pumilus ES4TSASPME-GCno
BacteriaEscherichia Coli DH5aTSASPME-GCno
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiGanoderma LucidumnaGC/MSNo
FungiSpongiporus LeucomallellusnaGC/MSNo
BacteriaBacillus Simplexn/an/a
BacteriaBacillus Subtilisn/an/a
BacteriaBacillus Weihenstephanensisn/an/a
BacteriaMicrobacterium Oxydansn/an/a
BacteriaSerratia Marcescensn/an/a
BacteriaStenotrophomonas Maltophilian/an/a
BacteriaStreptomyces Lateritiusn/an/a


(1S,8aR)-4,7-dimethyl-1-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene

Compound Details

Synonymous names
delta-Amorphene
DELTA-CADINENE
AC1L9ADP
C6H8P2
6614AB
X3450
CHEMBL445759
7848KI47OS
C06394
AK110299
ZINC8220462
UNII-7848KI47OS
CHEBI:15385
DTXSID70858792
AJ-57371
(+)-delta-Cadinene
AKOS016008860
(1S,8aR)-delta-cadinene
(+)-D-Cadinene
LMPR0103330001
483-76-1
Cadina-1(10),4-diene
(1S,8aR)-1-Isopropyl-4,7-dimethyl-1,2,3,5,6,8a-hexahydronaphthalene
(1S,8aR)-1-isopropyl-4,7-di-methyl-1,2,3,5,6,8a-hexahydronaphthalene
(1S,8aR)-4,7-dimethyl-1-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene
(1S,8aR)-4,7-dimethyl-1-(propan-2-yl)-1,2,3,5,6,8a-hexahydronaphthalene
IUPAC name(1S,8aR)-4,7-dimethyl-1-propan-2-yl-1,2,3,5,6,8a-hexahydronaphthalene
SMILESCC1=CC2C(CCC(=C2CC1)C)C(C)C
InchiInChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h9-10,13,15H,5-8H2,1-4H3/t13-,15-/m0/s1
FormulaC15H24
PubChem ID441005
Molweight204.357
LogP4.4
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes Alkenes Bicyclo

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiArmillaria Mellean/aMueller et al., 2013
FungiLaccaria Bicolorn/aMueller et al., 2013
FungiPaxillus Involutus MAJn/aMueller et al., 2013
FungiPaxillus Involutus NAUn/aMueller et al., 2013
FungiPholiota Squarrosan/aMueller et al., 2013
FungiStropharia Rugosoannulatan/aMueller et al., 2013
FungiTrichoderma Viriden/aMueller et al., 2013
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiAspergillus Ustusnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
FungiGanoderma Lucidumnasaprophytic on deciduous treesZiegenbein et al., 2006
FungiLaccaria Bicolor S238NnanaDitengou et al., 2015
FungiPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al., 2000
BacteriaStreptomyces Caviscabiesn/aSchulz and Dickschat, 2007
BacteriaStreptomyces Citreusn/aSchulz and Dickschat, 2007
BacteriaStreptomyces Sp. GWS-BW-H5.n/aDickschat et al., 2005_2
FungiAspergillus UstusPolizzi et al., 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiLaccaria BicolorMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus MAJMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus NAUMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiStropharia RugosoannulataMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiAspergillus Ustusmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiFomitopsis PinicolanaGC/MSNo
FungiGanoderma LucidumnaGC/MSNo
FungiLaccaria Bicolor S238Nmodified Pachlewski mediumcapillary gas chromatography, GC/MSYes
FungiPiptoporus BetulinusnaGC/MSNo
BacteriaStreptomyces Caviscabiesn/an/a
BacteriaStreptomyces Citreusn/an/a
BacteriaStreptomyces Sp. GWS-BW-H5.n/an/a
FungiAspergillus Ustusmalt extract agar (MEA), wallpaper, plasterboardSPME/GC-MS


1,6-dimethyl-4-propan-2-yl-1,2,3,4,4a,7-hexahydronaphthalene

Mass-Spectra

Compound Details

Synonymous names
JUQGWBAOQUBVFP-UHFFFAOYSA-N
AC1LAS2N
1,4-Cadinadiene
OR105991
16728-99-7
4-Isopropyl-1,6-dimethyl-1,2,3,4,4a,7-hexahydronaphthalene
1,2,3,4,6,8a-Hexahydro-1-isopropyl-4,7-dimethyl-naphthalene
4,10-Dimethyl-7-isopropyl[4,4,0]-bicyclo-1,4-decadiene
1,6-dimethyl-4-propan-2-yl-1,2,3,4,4a,7-hexahydronaphthalene
Naphthalene, 1,2,3,4,6,8a-hexahydro-1-isopropyl-4,7-dimethyl-
1,2,3,4,4A,7-hexahydro-1,6-dimethyl-4-(1-methylethyl)-naphthalene
Naphthalene, 1,2,3,4,4a,7-hexahydro-1,6-dimethyl-4-(1-methylethyl)-
IUPAC name1,6-dimethyl-4-propan-2-yl-1,2,3,4,4a,7-hexahydronaphthalene
SMILESCC1CCC(C2C1=CCC(=C2)C)C(C)C
InchiInChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h7,9-10,12-13,15H,5-6,8H2,1-4H3
FormulaC15H24
PubChem ID519298
Molweight204.357
LogP4.45
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes Alkenes benzenoids

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
BacteriaChondromyces Crocatusn/aSchulz et al., 2004
FungiPhoma Sp.n/aStrobel et al., 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
BacteriaChondromyces Crocatusn/an/a
FungiPhoma Sp.n/aSolid phase microextraction (SPME)


(4E)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene

Compound Details

Synonymous names
Caryophyllene
trans-Caryophyllene
NPNUFJAVOOONJE-IZZDOVSWSA-N
L-Caryophyllene
AC1NS5Q9
E-.beta.-caryophyllene
NSC11906
(-)-Caryophyllene
NSC-11906
CARYOPHYLLENE ,ALPHA + BETA MIXT.
(E)-.beta.-Caryophylene
(+)(E)-Caryophyllene
87-44-5
.beta.-Caryophyllene, (-)
MolPort-028-929-265
8-Methylene-4,11-(trimethyl)bicyclo[7.2.0]undec-4-ene
(4E)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene
Bicyclo[7.2.0]undec-4-ene,11,11-trimethyl-8-methylene-, [1R-(1R*,4E,9S*)]-
Bicyclo[7.2.0]undec-4-ene,11,11-trimethyl-, (E)-(1R,9S)-(-)-
Bicyclo[7.2.0]undec-4-ene,11,11-trimethyl-8-methylene-, (E)-(1R,9S)-(-)-
IUPAC name(4E)-4,11,11-trimethyl-8-methylidenebicyclo[7.2.0]undec-4-ene
SMILESCC1=CCCC(=C)C2CC(C2CC1)(C)C
InchiInChI=1S/C15H24/c1-11-6-5-7-12(2)13-10-15(3,4)14(13)9-8-11/h6,13-14H,2,5,7-10H2,1,3-4H3/b11-6+
FormulaC15H24
PubChem ID5354499
Molweight204.357
LogP4.52
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes Alkenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10063n/aDickschat et al., 2005_3
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10267n/aDickschat et al., 2005_3
FungiTrichoderma AtrovirideCrutcher et al., 2013
FungiTrichoderma ReeseiCrutcher et al., 2013
FungiTrichoderma VirensCrutcher et al., 2013
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10063n/an/a
BacteriaCytophaga-Flavobacterium-Bacteroides Group Strain ARK 10267n/an/a
FungiTrichoderma AtroviridePotato dextrose agarHS-SPME/GC-MS no
FungiTrichoderma ReeseiPotato dextrose agarHS-SPME/GC-MS no
FungiTrichoderma VirensPotato dextrose agarHS-SPME/GC-MS no
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes


(3R,4aR,5S)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene

Compound Details

Synonymous names
Eremophilene
QEBNYNLSCGVZOH-GZBFAFLISA-N
OPI7MD81JT
UNII-OPI7MD81JT
DTXSID30144729
ZINC49538670
AKOS015903138
I14-18983
10219-75-7
IUPAC name(3R,4aR,5S)-4a,5-dimethyl-3-prop-1-en-2-yl-2,3,4,5,6,7-hexahydro-1H-naphthalene
SMILESCC1CCC=C2C1(CC(CC2)C(=C)C)C
InchiInChI=1S/C15H24/c1-11(2)13-8-9-14-7-5-6-12(3)15(14,4)10-13/h7,12-13H,1,5-6,8-10H2,2-4H3/t12-,13+,15+/m0/s1
FormulaC15H24
PubChem ID12309744
Molweight204.357
LogP4.52
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes Alkenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaChondromyces Crocatusn/aSchulz and Dickschat, 2007
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaChondromyces Crocatusn/an/a
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes


(1S,4aS,8aR)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene

Compound Details

Synonymous names
gamma-Muurolene
(?)-gamma-Muurolene
C20273
CHEBI:64798
(+)-gamma-muurolene
24268-39-1
(1S,4aS,8aR)-1-isopropyl-7-methyl-4-methylene-1,2,3,4,4a,5,6,8a-octahydronaphthalene
(1S,4aS,8aR)-7-methyl-4-methylene-1-(propan-2-yl)-1,2,3,4,4a,5,6,8a-octahydronaphthalene
IUPAC name(1S,4aS,8aR)-7-methyl-4-methylidene-1-propan-2-yl-2,3,4a,5,6,8a-hexahydro-1H-naphthalene
SMILESCC1=CC2C(CC1)C(=C)CCC2C(C)C
InchiInChI=1S/C15H24/c1-10(2)13-8-6-12(4)14-7-5-11(3)9-15(13)14/h9-10,13-15H,4-8H2,1-3H3/t13-,14+,15-/m0/s1
FormulaC15H24
PubChem ID12313020
Molweight204.357
LogP4.51
Atoms39
Bonds40
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes Alkenes Bicyclo

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiArmillaria Mellean/aMueller et al., 2013
FungiFusarium Culmorum PVnasandy dune soil, NetherlandsSchmidt et al., 2016
BacteriaStreptomyces Caviscabiesn/aSchulz and Dickschat, 2007
BacteriaStreptomyces Sp. GWS-BW-H5.n/aDickschat et al., 2005_2
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiFusarium Culmorum PVpotato dextrose agarGC/MS-Q-TOFNo
BacteriaStreptomyces Caviscabiesn/an/a
BacteriaStreptomyces Sp. GWS-BW-H5.n/an/a
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiFomitopsis PinicolanaGC/MSNo


Methyl 2-phenylacetate

Mass-Spectra

Compound Details

Synonymous names
Methyl benzeneethanoate
Methyl benzeneacetate
Methyl phenylethanoate
METHYL PHENYLACETATE
CRZQGDNQQAALAY-UHFFFAOYSA-N
Phenylacetic acid methyl
Methyl benzene acetate
Methyl phenylacetate, analytical standard
Methyl alpha-toluate
methyl phenyl acetate
Phenylacetic Acid Methyl Ester
alpha-phenylacetic acid methyl ester
AC1Q5ZUJ
Methyl 2-phenylacetate
benzene acetic acid methyl ester
Benzeneacetic acid, methyl ester
phenyl acetic acid methyl ester
Phenyl-acetic acid methyl ester
Phenylacetic acid, methyl ester
AC1L1P1D
Methyl 2-phenyl acetate
2-Phenylacetic acid methyl ester
SCHEMBL4675
Methyl alpha-toluate; Phenylacetic acid methyl ester
KSC175C1T
NSC9405
Methyl .alpha.-toluate
CTK0H5119
D4PDC41X96
P0125
EBD50083
WLN: 1OV1R
RP17360
ZINC388061
UNII-D4PDC41X96
BBL010506
DTXSID1044352
NSC-9405
NSC401667
OR034300
AK163377
SBB058223
STL146152
ZB011258
LS-2954
CHEMBL3189123
ACMC-2097v7
CJ-03094
SC-26761
ANW-14465
DSSTox_GSID_44352
AN-24576
AB1011175
KB-54814
MFCD00008453
DSSTox_CID_24352
ZINC00388061
BB_SC-7169
DSSTox_RID_80161
AI3-01971
RTR-000377
Acetic acid, phenyl-, methyl ester
NSC-401667
NSC 401667
ST24047740
ST50824226
TR-000377
Methyl phenylacetate, ReagentPlus(R), >=99%
I14-7331
AKOS000119976
FT-0653159
TRA-0184135
FEMA No. 2733
Tox21_300792
Methyl phenylacetate, >=98%, FCC, FG
101-41-7
Methyl phenylacetate, Vetec(TM) reagent grade, 98%
MCULE-9593207528
NCGC00254696-01
NCGC00248170-01
EINECS 202-940-9
CAS-101-41-7
EC 202-940-9
MolPort-001-788-281
InChI=1/C9H10O2/c1-11-9(10)7-8-5-3-2-4-6-8/h2-6H,7H2,1H
IUPAC namemethyl 2-phenylacetate
SMILESCOC(=O)CC1=CC=CC=C1
InchiInChI=1S/C9H10O2/c1-11-9(10)7-8-5-3-2-4-6-8/h2-6H,7H2,1H3
FormulaC9H10O2
PubChem ID7559
Molweight150.177
LogP1.76
Atoms21
Bonds21
H-bond Acceptor1
H-bond Donor0
Chemical Classificationbenzenoids esters

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaMycobacterium Tuberculosisn/aRespiratory clinical isolates (Canterbury Health Laboratories, Christchurch, New Zealand)Syhre et al., 2008
Fungi Antrodia CamphorataChiang et al. 2013
Fungi Antrodia CinnamomeaChen et al. 2007
FungiGleophyllum OdoratumnaSachsenwald near HamburgRösecke et al., 2000
Fungi Gloeophyllum OdoratumKahlos et al. 1994
BacteriaSalinispora Tropica CNB-440namarine sedimentGroenhagen et al., 2016
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaMycobacterium TuberculosisLoewenstein-Jensen/Glycerol, sheep blood agar and BacT/Alerts MPSolid phase micro-extraction (SPME), GC/MS-MS
Fungi Antrodia Camphoratano
Fungi Antrodia Cinnamomeano
FungiGleophyllum OdoratumnaGC/MSNo
Fungi Gloeophyllum Odoratumno
BacteriaSalinispora Tropica CNB-440seawater-based A1GC/MS


3,3-dimethyl-2-methylidenebicyclo[2.2.1]heptane

Mass-Spectra

Compound Details

Synonymous names
CAMPHENE
CRPUJAZIXJMDBK-UHFFFAOYSA-N
Comphene
DL-Camphene
ACMC-1ARGM
AC1L1MX7
DL-CAMPHENE, TECH
KSC378G0P
NSC4165
HSDB 900
CTK2H8307
3,3-Dimethyl-2-methylenenorcamphene
3,3-Dimethyl-2-methylenenorcamphane
3,3-Dimethyl-2-methylenenorbornane
2,2-Dimethyl-3-methylenenorbornane
C06076
CHEBI:3830
CCRIS 3783
AK175981
DTXSID8026488
STK801857
SBB060158
LS-2612
CHEMBL2268550
NSC 4165
NSC-4165
BBL033861
OR342768
OR285856
OR021726
DSSTox_CID_6488
ANW-41333
AN-24008
AN-23709
AN-19994
KB-67126
KB-00127
2,2-dimethyl-3-methylene-norbornane
DSSTox_GSID_26488
DSSTox_RID_78121
MFCD00066603
BB_NC-0785
AI3-01775
DB-053130
DB-056393
DB-057848
RTR-025333
ST50330642
TR-025333
AKOS004119935
FT-0635856
FT-0609260
FEMA No. 2229
TRA-0205299
I14-10696
I14-52149
Z955123744
79-92-5
Tox21_303152
Tox21_202014
(+/-)-Camphene
565-00-4
CAS-79-92-5
Camphene (2,2-dimethyl-3-methylene-norbornane)
5794-04-7
MCULE-1011863584
NCGC00259563-01
NCGC00257126-01
NCGC00249149-01
EINECS 201-234-8
EINECS 209-275-3
SR-01000944833
MolPort-001-785-795
3,3-dimethyl-2-methylidenebicyclo[2.2.1]heptane
2,2-dimethyl-3-methylidenebicyclo[2.2.1]heptane
2,2-Dimethyl-3-methylenebicyclo(2.2.1)heptane
3,3-dimethyl-2-methylenebicyclo[2.2.1]heptane
2,2-Dimethyl-3-methylenebicyclo[2.2.1]heptane
Bicyclo[2.2.1]heptane,2-dimethyl-3-methylene-
SR-01000944833-1
WLN: L55 A CYTJ CU1 D1 D1
2,2-Dimethyl-3-methylenebicyclo[2.2.1]heptane #
Camphene, (1R,4S)-(+)-
Bicyclo(2.2.1)heptane, 2,2-dimethyl-3-methylene-
Bicyclo[2.2.1]heptane, 2,2-dimethyl-3-methylene-
(1)-2,2-Dimethyl-3-methylenebicyclo(2.2.1)heptane
Bicyclo[2.2.1]heptane, 2,2-dimethyl-3-methylene-, (1S)-
Bicyclo[2.2.1]heptane, 2,2-dimethyl-3-methylene-, (1R)-
Bicyclo[2.2.1]heptane, 2,2-dimethyl-3-methylene-, (1S,4R)-
Bicyclo[2.2.1]heptane, 2,2-dimethyl-3-methylene-, (1R,4S)-
IUPAC name3,3-dimethyl-2-methylidenebicyclo[2.2.1]heptane
SMILESCC1(C2CCC(C2)C1=C)C
InchiInChI=1S/C10H16/c1-7-8-4-5-9(6-8)10(7,2)3/h8-9H,1,4-6H2,2-3H3
FormulaC10H16
PubChem ID6616
Molweight136.238
LogP2.86
Atoms26
Bonds27
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details

Volatilization
The Henry's Law constant for camphene is estimated as 0.098 atm-cu m/mole(SRC) derived from its vapor pressure, 2.5 mm Hg(1), and water solubility, 4.6 mg/L(2). This Henry's Law constant indicates that camphene is expected to volatilize rapidly 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 1 hour(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 5 days(SRC). Camphene's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of camphene from dry soil surfaces may exist(SRC) based upon a vapor pressure of 2.5 mm Hg(1).
Literature: (1) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1989) (2) Chemicals Inspection and Testing Institute; Biodegradation and Bioaccumulation Data of Existing Chemicals Based on the CSCL Japan. Japan Chemical Industry Ecology - Toxicology and Information Center. ISBN 4-89074-101-1 p.4-40 (1992) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)
Soil Adsorption
Using a structure estimation method based on molecular connectivity indices(1), the Koc of camphene can be estimated to be 1000(SRC). According to a classification scheme(2), this estimated Koc value suggests that camphene is expected to have low mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of May 29, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Vapor Pressure
PressureReference
2.5 mm Hg at 25 deg CDaubert, T.E., R.P. Danner. Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, D.C.: Taylor and Francis, 1989.
MS-Links
1D-NMR-Links

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaPedobacter Sp. V48narhizosphere of Marram grass in sandy dune soils, NetherlandsGarbeva et al., 2014
FungiAmanita OvoideaFranceBreheret et al. 1997
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiAspergillus Fumigatuscompost Fischer et al. 2025
FungiAspergillus Fumigatus Strain FGSC A1163Heddergott et al. 2014
FungiBoletus AestivalisFranceBreheret et al. 1997
FungiCantharellus CibariusFranceBreheret et al. 1997
FungiCystoderma CarchariasFranceBreheret et al. 1997
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
FungiFusarium Culmorum PVaffects swarming and swimming motility of Serratia plymuthica PRI-2C; affects swarming ability of Collimonas pratensis Ter291sandy dune soil, NetherlandsSchmidt et al., 2016
FungiGomphidius GlutinosusFranceBreheret et al. 1997
FungiHydnum RepandumFranceBreheret et al. 1997
FungiMycena PuraFranceBreheret et al. 1997
FungiMycena RoseaFranceBreheret et al. 1997
FungiPenicillium Commune Pittnain dry-cured meat products, cheeseSunesson et al., 1995
FungiSpongiporus Leucomallellusnasaprophytic mostly on wet, old pinesZiegenbein et al., 2006
FungiSuillus LuteusFranceBreheret et al. 1997
FungiTricholoma SulfureumFranceBreheret et al. 1997
FungiTuber Magnatumn/aItalian geographical areas (Emilia Romagna, Border region area between Emilia Romagna and Marche)Gioacchini et al., 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaPedobacter Sp. V48sand containing artificial root exudatesGC/MSNo
FungiAmanita Ovoideaforest soilsolvent extraction, headspace, GCMSno
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiAspergillus Fumigatusyest extract sucroseTenax/GC-MSno
FungiAspergillus Fumigatus Strain FGSC A1163Brian`s broth, AMM, RPMI 1643SPME / GC-MS
FungiBoletus Aestivalisforest soilsolvent extraction, headspace, GCMSno
FungiCantharellus Cibariusforest soilsolvent extraction, headspace, GCMSno
FungiCystoderma Carchariasforest soilsolvent extraction, headspace, GCMSno
FungiFomitopsis PinicolanaGC/MSNo
FungiFusarium Culmorum PVpotato dextrose agarGC/MS-Q-TOFNo
FungiGomphidius Glutinosusforest soilsolvent extraction, headspace, GCMSno
FungiHydnum Repandumforest soilsolvent extraction, headspace, GCMSno
FungiMycena Puraforest soilsolvent extraction, headspace, GCMSno
FungiMycena Roseaforest soilsolvent extraction, headspace, GCMSno
FungiPenicillium Commune PittDG18GC/MS
FungiSpongiporus LeucomallellusnaGC/MSNo
FungiSuillus Luteusforest soilsolvent extraction, headspace, GCMSno
FungiTricholoma Sulfureumforest soilsolvent extraction, headspace, GCMSno
FungiTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)


Compound Details

Synonymous names
Ethenylbenzene
Phenylethylene
Styrene-divinylbenzene Copolymer
Ethylbenzene alkylate
Phenethylene
Phenylethene
Vinylbenzene
Cinnamenol
Cinnaminol
Ethylenated benzene
POLYSTYRENE
Vinylbenzen
Vinylbenzol
Annamene
Cinnamene
Cinnamol
Polysorb
PPBRXRYQALVLMV-UHFFFAOYSA-N
Styrolene
Styropol
Styropor
Vinyl-polystyrene
CARINE
phenyl ethylene
Phenylethylene, inhibited
Polystyrene, hydrogenated
Stirolo
Styreen
Styren
STYRENE
Styrene monomer
Styrene polymer
Styrol
Styrole
Styron
Vinyl benzene
Vinyl-benzene
Vinylbenzene, inhibited
Polystyrene, atactic
Polystyrene,flame retarding and impact resistant
Styrene polymer-bound
Styropol SO
viny lbenzol
Styrene, analytical standard
AC1L1OWJ
AC1Q2AAB
Styrene monomer, inhibited
p-vinyl benzene
TRANS-STYRENE-BETA-D
Vinylbenzen [Czech]
Vinylbenzen [Dutch]
Benzene, ethenyl-
BETA-CIS-STYRENE-D
Ethylene, phenyl-
Stirolo [Italian]
Styrene (monomer)
Benzene, vinyl-
KSC176E4F
Styreen [Dutch]
Styrol (German)
Styrol [German]
8053AF
Styren [Czech]
Styrene, >=99%
UN2055
Benzene, ethenyl-, homopolymer
CCRIS 564
CTK0H6242
Diarex hf 77
HSDB 171
S0095
S0651
BIDD:ER0247
CHEMBL285235
LS-304
NSC62785
RP18837
Styropol (Salt/Mix)
Styropor (Salt/Mix)
44LJ2U959V
Benzene, ethenyl-, homopolymer, hydrogenated
C07083
C19506
Polystyrene high Mol. Wt.
Styron (Salt/Mix)
WLN: 1U1R
ZINC968269
DTXSID2021284
FEMA Number 3234
OR034234
OR192559
OR211724
OR242081
OR245032
OR247888
OR328508
Polystyrene med Mol. Wt.
STL283958
ZB015538
A800199
CHEBI:27452
DSSTox_CID_1284
ETHENYL, 2-PHENYL-
NCI-C02200
UNII-44LJ2U959V
AN-24550
ANW-14280
BP-13451
CJ-04646
DSSTox_GSID_21284
KB-60631
NSC 62785
NSC-62785
SC-75569
TRA0031624
DSSTox_RID_76057
MFCD00008612
MFCD00084450
Polystyrene latex microsphere, 1 micron, dry form
AI3-24374
RT-000109
AKOS000119972
Benzene-d5, ethenyl-d3-
I01-4405
ZINC112958499
FEMA No. 3233
FT-0659991
FT-0689054
Bulstren K-525-19
Z966690906
Styrene Resin (Med.M.Wt.)
Tox21_113245
Tox21_200808
100-42-5
F1908-0130
Diarex hf 77 (Salt/Mix)
9003-53-6
9044-64-8
9055-91-8
MCULE-4715354738
NCGC00091056-01
NCGC00091056-02
NCGC00091056-03
NCGC00091056-04
NCGC00091056-05
NCGC00258362-01
Styrene solution, certified reference material, 200 mug/mL in methanol
CAS-100-42-5
EINECS 202-851-5
EINECS 273-493-5
Styrene, SAJ first grade, >=99.0%
11120-46-0
12627-11-1
12770-88-6
25038-60-2
25086-18-4
39470-87-6
40494-15-3
51609-83-7
51609-87-1
52932-49-7
53112-49-5
53986-84-8
54578-24-4
54596-41-7
55128-06-8
55465-00-4
56451-72-0
56748-62-0
57657-06-4
58033-91-3
60120-16-3
60328-46-3
60880-98-0
61584-89-2
61584-90-5
63849-49-0
68441-35-0
78354-47-9
79637-11-9
81834-12-0
86090-91-7
98444-30-5
POLY(1-PHENYL-2,2-ETHANEDIYL))
Polystyrene latex microsphere, 1 micron, 10 wt% dispersion in water
Polystyrene latex microsphere, 2 micron, 10 wt% dispersion in water
Styrene, 99%, stabilized 100ml
Styrene, ReagentPlus(R), 99.9%
UN 2055 (Salt/Mix)
EC 202-851-5
105270-05-1
110866-50-7
120037-99-2
120534-26-1
124229-31-8
124229-48-7
131495-39-1
137262-45-4
144637-93-4
149212-19-1
155197-45-8
157243-21-5
157929-02-7
161776-45-0
171022-02-9
171022-09-6
172641-48-4
172867-64-0
219782-52-2
260975-79-9
359762-95-1
360046-70-4
373601-20-8
441772-62-9
471865-10-8
487021-46-5
644984-36-1
726192-11-6
730985-59-8
851588-70-0
852837-17-3
5487-EP2269995A1
5487-EP2270101A1
5487-EP2270113A1
5487-EP2272832A1
5487-EP2272849A1
5487-EP2272935A1
5487-EP2275418A1
5487-EP2277945A1
5487-EP2280014A2
5487-EP2284165A1
5487-EP2287168A2
5487-EP2289883A1
5487-EP2289896A1
5487-EP2292593A2
5487-EP2295415A1
5487-EP2295420A1
5487-EP2295426A1
5487-EP2295427A1
5487-EP2295438A1
5487-EP2298313A1
5487-EP2298743A1
5487-EP2298753A1
5487-EP2301924A1
5487-EP2305668A1
5487-EP2305685A1
5487-EP2305686A1
5487-EP2308832A1
5487-EP2308857A1
5487-EP2308865A1
5487-EP2309584A1
5487-EP2311796A1
5487-EP2311797A1
5487-EP2311798A1
5487-EP2311799A1
5487-EP2311804A2
5487-EP2314577A1
5487-EP2314579A1
5487-EP2380568A1
5487-EP2380867A1
MolPort-001-779-766
1083095-63-9
1160710-79-1
1161074-30-1
1187742-34-2
1191987-17-3
1198090-46-8
1227265-55-5
1263545-74-9
Polystyrene latex microsphere, 1 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 2 micron, 2.5 wt% dispersion in water
Styrene monomer, inhibited [UN2055] [Flammable liquid]
Styrene, 99.5% stab. with 4-tert-Butylcatechol
37291-EP2311802A1
37291-EP2311803A1
Styrene, ReagentPlus(R), contains 4-tert-butylcatechol as stabilizer, >=99%
Polystyrene (100-200 mesh, PEG crosslinked)
117294-EP2275408A1
117294-EP2287158A1
117294-EP2298762A2
143365-EP2287165A2
143365-EP2287166A2
143365-EP2292620A2
Styrene monomer, inhibited [UN2055] [Flammable liquid]
Polystyrene latex microsphere, 4.5 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 6.0 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 0.05 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 0.10 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 0.20 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 0.50 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 0.75 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 10.0 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 15.0 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 20.0 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 25.0 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 45.0 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 75.0 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, 90.0 micron, 2.5 wt% dispersion in water
Polystyrene latex microsphere, fluorescent, 6.0 micron, 2.5 wt% dispersion in water
Polystyrene, minimum number average molecular weight (in amu), 50,000
Polystyrene standard, M.W. 1,300, Mw/Mn 1.06
Polystyrene standard, M.W. 2,000, Mw/Mn 1.10
Polystyrene standard, M.W. 2,200, Mw/Mn 1.06
Polystyrene standard, M.W. 3,350, Mw/Mn 1.10
Polystyrene standard, M.W. 4,000, Mw/Mn 1.06
Polystyrene standard, M.W. 5,200, Mw/Mn 1.06
Polystyrene standard, M.W. 13,000, Mw/Mn 1.06
Polystyrene standard, M.W. 25,000, Mw/Mn 1.06
Polystyrene standard, M.W. 30,000, Mw/Mn 1.06
Polystyrene standard, M.W. 50,000, Mw/Mn 1.06
Polystyrene standard, M.W. 65,000, Mw/Mn 1.06
Polystyrene standard, M.W. 123,000, Mw/Mn 1.08
Polystyrene standard, M.W. 170,000, Mw/Mn 1.06
Polystyrene standard, M.W. 290,000, Mw/Mn 1.06
Polystyrene standard, M.W. 400,000, Mw/Mn 1.06
Polystyrene standard, M.W. 650,000, Mw/Mn 1.06
Polystyrene standard, M.W. 900,000, Mw/Mn 1.10
Polystyrene standard, MW ~ 1,300, MW/MN = 1.06 1g
Polystyrene standard, M.W. 2,000,000, Mw/Mn 1.30
InChI=1/C8H8/c1-2-8-6-4-3-5-7-8/h2-7H,1H
Benzene-1,2,3,4,5-d5, 6-(ethenyl-1,2,2-d3)-
IUPAC namestyrene
SMILESC=CC1=CC=CC=C1
InchiInChI=1S/C8H8/c1-2-8-6-4-3-5-7-8/h2-7H,1H2
FormulaC8H8
PubChem ID7501
Molweight104.152
LogP2.71
Atoms16
Bonds16
H-bond Acceptor0
H-bond Donor0
Chemical Classificationalkenes benzenoids

mVOC Specific Details

Volatilization
The Henry's Law constant for styrene is reported as 2.75X10-3 atm-cu m/mole(1). This Henry's Law constant indicates that styrene is expected to volatilize from water surfaces(2). Under laboratory conditions, 50% of 2 to 10 mg styrene per liter (depth not specified) was lost by volatilization in 1 to 3 hrs in lake water samples and in 6 to 7 hrs in distilled water, respectively(3). In other studies, the level of styrene in water samples fell from 23 to 3.3 and 0.4 mg/L in 2 hrs and 7 days, respectively, and from 46 to 12.5 and 1.5 mg/L in 2 hrs and 10 days, respectively(4). These findings are relevant to surface waters but not to deeper waters(4). The volatilization half-life of styrene in Rhine River water was 14 days(5). Volatilization of styrene from moist soil surfaces would be slower than in water(4). Samples at 1.5 cm deep of a loamy soil, 26% of 2 mg/kg styrene added volatilized in 31 days(3). The transfer to the air was even slower and less extensive from deep soil(4). The potential for volatilization of styrene from dry soil surfaces may exist(SRC) based upon a vapor pressure of 6.4 mm Hg(6).
Literature: (1) Bocek K; Experimetia, Suppl 23: 231-40 (1976) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Fu MH, Alexander M; Environ Sci Technol 26: 1540-4 (1992) (4) Alexander M; Crit Rev Env Sci Technol 27: 383-410 (1997) (5) Zoeteman BCJ et al; Chemosphere 9: 231-49 (1980) (6) Chao J et al; J Phys Chem Ref Data 12: 1033-63 (1983)
Soil Adsorption
The log Koc of styrene is reported to be 2.96(1). According to a classification scheme(2), this Koc value suggests that styrene is expected to have low mobility in soil. More than 85% of styrene is sorbed in 78 hrs on samples from a sandy aquifer(3). Styrene is retained by particulates particularly in organic matter-rich soils(3). Of styrene that had been allowed to sorb for 3 days, 61.0 and 66.7% was desorbed in 16 days from soil and aquifer soils, respectively(4).
Literature: (1) Schuurmann G et al; Environ Sci Technol 40: 7005-11 (2006) (2) Swann RL et al; Res Rev 85: 17-28 (1983) (3) Fu MH, Alexander M; Environ Sci Technol 26: 1540-4 (1992) (4) Fu MH et al; Environ Toxicol Chem 13: 749-53 (1994)
Vapor Pressure
PressureReference
6.40 mm Hg at 25 deg CChao J et al; J Phys Chem Ref Data 12: 1033-63 (1983)
MS-Links
1D-NMR-Links

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
BacteriaPseudomonas Aeruginosacan be used as biomarker for detection of this bacteriaYusuf et al., 2015
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiFusarium Graminearum 15AcDONn/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON 1001tan/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON ZFR 29n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_4n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_5n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_6n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_7n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_8n/aBusko et al., 2014
FungiFusarium Graminearum 15AcDON_9n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 1002tn/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 11791n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 1509n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON 8046n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON NRRL38369n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON NRRL6394n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON ZFR 15n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON ZFR 37n/aBusko et al., 2014
FungiFusarium Graminearum 3AcDON ZFR 51n/aBusko et al., 2014
FungiFusarium Graminearum NIVn/aBusko et al., 2014
FungiFusarium Graminearum NIV ZFR 119n/aBusko et al., 2014
FungiFusarium Graminearum NIV ZFR 23n/aBusko et al., 2014
FungiFusarium Graminearum NIV ZFR 48n/aBusko et al., 2014
FungiFusarium Graminearum NIV_5n/aBusko et al., 2014
FungiFusarium Graminearum NIV_6n/aBusko et al., 2014
FungiFusarium Graminearum NIV_7n/aBusko et al., 2014
FungiFusarium Graminearum NIV_8n/aBusko et al., 2014
FungiFusarium Graminearum NIV_9n/aBusko et al., 2014
FungiPaecilomyces Variotiicompost Fischer et al. 2066
FungiPenicillium Brevicompactumcompost Fischer et al. 2066
FungiPenicillium Clavigerumcompost Fischer et al. 2066
FungiPenicillium Crustosumcompost Fischer et al. 2066
FungiPenicillium Expansumcompost Fischer et al. 2066
FungiPenicillium Glabrumcompost Fischer et al. 2066
FungiPenicillium Polonicumnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiTuber Borchiin/aFortywoodland of the Basilicata regionMauriello et al., 2004
FungiTuber Brumalen/aFortywoodland of the Basilicata regionMauriello et al., 2004
FungiTuber Excavatumn/aFortywoodland of the Basilicata regionMauriello et al., 2004
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
BacteriaPseudomonas Aeruginosablood agar base (TSBA)SPME/GC-MS
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiFusarium Graminearum 15AcDONyeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON 1001tayeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON ZFR 29yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_4yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_5yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_6yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_7yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_8yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 15AcDON_9yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 1002tyeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 11791yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 1509yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON 8046yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON NRRL38369yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON NRRL6394yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON ZFR 15yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON ZFR 37yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum 3AcDON ZFR 51yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIVyeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV ZFR 119yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV ZFR 23yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV ZFR 48yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_5yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_6yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_7yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_8yeast extract sucrose agarSPME/GC-MS
FungiFusarium Graminearum NIV_9yeast extract sucrose agarSPME/GC-MS
FungiPaecilomyces Variotiiyest extract sucroseTenax/GC-MSno
FungiPenicillium Brevicompactumyest extract sucroseTenax/GC-MSno
FungiPenicillium Clavigerumyest extract sucroseTenax/GC-MSno
FungiPenicillium Crustosumyest extract sucroseTenax/GC-MSno
FungiPenicillium Expansumyest extract sucroseTenax/GC-MSno
FungiPenicillium Glabrumyest extract sucroseTenax/GC-MSno
FungiPenicillium Polonicummalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiTuber Borchiin/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)
FungiTuber Brumalen/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)
FungiTuber Excavatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)


4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane

Mass-Spectra

Compound Details

Synonymous names
Sabenene
NDVASEGYNIMXJL-UHFFFAOYSA-N
SABINENE
Sabinen
AC1L2CV6
AC1Q2A93
CHEMBL452687
C16777
OR259717
OR196226
OR014753
NSC407278
Sabinene, natural, 75%
CHEBI:50027
SC-21181
CC-34338
FCH1122054
C-25396
MFCD00064917
4(10)-Thujene
NSC-407278
NSC 407278
J-019353
AKOS024318970
FT-0634821
Thuj-4(10)-ene
EN300-250199
3387-41-5
MCULE-3593242171
THUJENE, 4(10)-
1-Isopropyl-4-methylenebicyclo[3.1.0]hexane
MolPort-006-115-296
2-methylidene-5-propan-2-ylbicyclo[3.1.0]hexane
4-methylene-1-(1-methylethyl)bicyclo[3.1.0]hexane
4-methylidene-1-(propan-2-yl)bicyclo[3.1.0]hexane
4-Methylene-1-(1-methylethyl)-bicyclo[3.1.0]hexane
Bicyclo[3.1.0]hexane, 4-methylene-1-(1-methylethyl)-
IUPAC name4-methylidene-1-propan-2-ylbicyclo[3.1.0]hexane
SMILESCC(C)C12CCC(=C)C1C2
InchiInChI=1S/C10H16/c1-7(2)10-5-4-8(3)9(10)6-10/h7,9H,3-6H2,1-2H3
FormulaC10H16
PubChem ID18818
Molweight136.238
LogP2.86
Atoms26
Bonds27
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAmanita OvoideaFranceBreheret et al. 1997
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiGomphidius GlutinosusFranceBreheret et al. 1997
FungiMycena PuraFranceBreheret et al. 1997
FungiPhomopsis Sp.naendophyte of Odontoglossum sp.Singh et al., 2011
FungiSuillus LuteusFranceBreheret et al. 1997
FungiTricholoma CaligatumFranceBreheret et al. 1997
FungiTricholoma SulfureumFranceBreheret et al. 1997
FungiTuber Magnatumn/aItalian geographical areas ( Marche, Border region area between Emilia Romagna and Marche)Gioacchini et al., 2008
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiAmanita Ovoideaforest soilsolvent extraction, headspace, GCMSno
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiGomphidius Glutinosusforest soilsolvent extraction, headspace, GCMSno
FungiMycena Puraforest soilsolvent extraction, headspace, GCMSno
FungiPhomopsis Sp.PDA mediumSPME-GC/MSYes
FungiSuillus Luteusforest soilsolvent extraction, headspace, GCMSno
FungiTricholoma Caligatumforest soilsolvent extraction, headspace, GCMSno
FungiTricholoma Sulfureumforest soilsolvent extraction, headspace, GCMSno
FungiTuber Magnatumn/amicroextraction-gas chromatography-mass spectrometry analysis (SPME-GC-MS)


1,2-dimethoxy-4-[(E)-prop-1-enyl]benzene

Mass-Spectra

Compound Details

Synonymous names
Isomethyleugenol
Methylisoeugenol
Isohomogenol
trans-isomethyleugenol
trans-Methylisoeugenol
Methyl isoeugenol
NNWHUJCUHAELCL-SNAWJCMRSA-N
NNWHUJCUHAELCL-UHFFFAOYSA-N
O-Methylisoeugenol
Isoeugenenyl methyl ether
Methyl IsoEugenol Natural
Isoeugenyl methyl ether
Isoeugenol methyl ether
4-Propenylveratrole
trans-4-Propenylveratrole
4-trans-Propenylveratrole
AC1LCUXZ
O-Methyl Isoeugenol
3,4-Dimethoxypropenylbenzene
J6M6C71VVR
AC1Q575S
M582
UNII-J6M6C71VVR
(E)-Methyl isoeugenol
P1103
NSC46111
UNII-46RN7Q97DE component NNWHUJCUHAELCL-SNAWJCMRSA-N
1-Veratryl-1-propene
CHEMBL465829
Veratrole, 4-propenyl-
ZINC404370
CHEBI:6877
C10478
1,4-Isoeugenol methyl ether
4-Propenyl-1,2-dimethoxybenzene
1,2-Dimethoxy-4-propenylbenzene
BBL009809
AK142028
OR025190
OR377427
OR377428
ZB013511
STK801268
Benzene,2-dimethoxy-4-propenyl-
CHEBI:14469
4-(1-Propenyl)pyrocatechol Dimethyl Ether
FCH3507890
4CN-3022
NSC-46111
LS-29884
AJ-22358
4CN-1393
FCH4094399
1-Propene,4-dimethoxyphenyl)-
AX8053336
Methyl isoeugenol, >=98%, FG
ZINC00404370
BB_NC-0656
MFCD00009282
TR-030873
RTR-030873
ST24035011
I01-7257
1,3,4-Isoeugenol methyl ether
W-100250
ghl.PD_Mitscher_leg0.366
AKOS005608367
FT-0627412
BRN 1911285
93-16-3
Benzene, 1,2-dimethoxy-4-propenyl
BBV-47013885
WLN: 2U1R CO1 DO1
1,2-Dimethoxy-4-propenylbenzene, 99%
6379-72-2
Benzene, 1,2-dimethoxy-4-propenyl-
EINECS 228-958-7
4-(1-Propenyl)-1,2-dimethoxybenzene
54349-79-0
BENZENE,1,2-DIMETHOXY,4-PROPENYL ISOEUGENOL,METHYL ETHER
1-(3,4-Dimethoxyphenyl)-1-propene
Benzene,2-dimethoxy-4-(1-propenyl)-
MolPort-000-698-027
1,2-Dimethoxy-4-[1-propenyl]benzene #
1,2-Dimethoxy-4-(1-propenyl)-benzene
1,2-dimethoxy-4-prop-1-en-1-ylbenzene
Benzene, 4-(1-propenyl)-1,2-dimethoxy
Benzene, 1,2-dimethoxy-4-(1-propenyl)-
1,2-dimethoxy-4-(prop-1-en-1-yl)benzene
1,2-dimethoxy-4-[(E)-prop-1-enyl]benzene
Benzene, 1,2-dimethoxy-4-propenyl-, (E)-
Benzene, 1,2-dimethoxy-4-(1E)-1-propenyl-
Benzene, 1,2-dimethoxy-4-(1-propen-1-yl)-
Benzene,1,2-dimethoxy-4-(1E)-1-propen-1-yl-
(E)-1,2-Dimethoxy-4-(prop-1-en-1-yl)benzene
1,2-dimethoxy-4-[(1E)-prop-1-en-1-yl]benzene
InChI=1/C11H14O2/c1-4-5-9-6-7-10(12-2)11(8-9)13-3/h4-8H,1-3H3/b5-4
IUPAC name1,2-dimethoxy-4-[(E)-prop-1-enyl]benzene
SMILESCC=CC1=CC(=C(C=C1)OC)OC
InchiInChI=1S/C11H14O2/c1-4-5-9-6-7-10(12-2)11(8-9)13-3/h4-8H,1-3H3/b5-4+
FormulaC11H14O2
PubChem ID637776
Molweight178.231
LogP2.78
Atoms27
Bonds27
H-bond Acceptor2
H-bond Donor0
Chemical Classificationbenzenoids alkenes ethers phenylpropanoids

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiTuber Melanosporumn/aAgricultural Centre of Castilla and León Community (Monasterio de la Santa Espina, Valladolid, Spain) and Navaleno (Soria, Spain).Diaz et al., 2003
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiTuber Melanosporumn/an/a
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes


(1E,4E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene

Mass-Spectra

Compound Details

Synonymous names
ALPHA-CARYOPHYLLENE
Humulene
FAMPSKZZVDUYOS-HRGUGZIWSA-N
alpha-Humulene
alpha-Humalene
AC1NQYKM
alpha-Humulene, analytical standard
.alpha.-Caryophyllene
.alpha.-Humulene
6292AF
54W56MD2WD
CHEMBL251280
UNII-54W56MD2WD
CHEBI:5768
C09684
OR325391
OR031368
LS-58866
DTXSID30858793
ZINC30726967
3,7,10-Humulatriene
MFCD00042689
AKOS015965488
BRN 3240075
FT-0622161
LMPR0103110001
(1E,4E,8E)-alpha-humulene
6753-98-6
EINECS 229-816-7
65907-25-7
19132-75-3
alpha-Humulene, >=96.0% (GC)
2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene
2,6,6,9-tetramethyl-cycloundeca-1,4,8-triene
trans,trans,trans-2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene
4-05-00-01171 (Beilstein Handbook Reference)
(E,E,E)-2,6,6,9-tetramethyl-1,4,8-cycloundecatriene
(1E,4E,8E)-humula-1(11),4,8-triene
2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene (E,E,E)-
(1E,4E,8E)-2,6,6,9-tetramethyl-1,4,8-cycloundecatriene
(1E,4E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (E,E,E)-
Cycloundeca-1,4,8-triene,2,6,6,9-tetramethyl-, (E,E,E)-
2,6,6,9-Tetramethyl-1,4,8-cycloundecatriene-, (1E,4E,8E)-
1,4,8-Cycloundecatriene, 2,6,6,9-tetramethyl-, (1E,4E,8E)-
IUPAC name(1E,4E,8E)-2,6,6,9-tetramethylcycloundeca-1,4,8-triene
SMILESCC1=CCC(C=CCC(=CCC1)C)(C)C
InchiInChI=1S/C15H24/c1-13-7-5-8-14(2)10-12-15(3,4)11-6-9-13/h6-7,10-11H,5,8-9,12H2,1-4H3/b11-6+,13-7+,14-10+
FormulaC15H24
PubChem ID5281520
Molweight204.357
LogP4.88
Atoms39
Bonds39
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes sesquiterpene

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiHypoxylon Antochroum Blacinaendophytic in Bursera lancifoliaUlloa-Benítez et al., 2016
FungiFusarium Oxysporum MSA 35the results led us to propose a possible new direct long-distance mechanism of action for WT antagonistic F. oxysporum that is mediated by vocsMinerdi et al., 2009
FungiPhoma Sp.n/aStrobel et al., 2014
FungiArmillaria Mellean/aMueller et al., 2013
FungiLaccaria Bicolorn/aMueller et al., 2013
FungiPaxillus Involutus MAJn/aMueller et al., 2013
FungiPaxillus Involutus NAUn/aMueller et al., 2013
FungiPholiota Squarrosan/aMueller et al., 2013
FungiFusarium Oxysporum MSA 35long-distance antagonistic actionMinerdi et al. 2009
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiHypoxylon Antochroum BlaciPDA/WA + 500 mg l^-1 ChloramphenicolSPME-GC/MSNo
FungiFusarium Oxysporum MSA 35complete medium (CM)SPME/GC-MS
FungiPhoma Sp.n/aSolid phase microextraction (SPME)
FungiArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiLaccaria BicolorMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus MAJMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPaxillus Involutus NAUMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiFusarium Oxysporum MSA 35PDA/CMCAR/PDMS GCMSyes
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes


1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene

Mass-Spectra

Compound Details

Synonymous names
Aromandendrene
Aromadendrene
ITYNGVSTWVVPIC-UHFFFAOYSA-N
AC1Q2AIY
AC1L3LWG
ACMC-20cy6a
(-)-Alloaromadendrene
CTK0G2521
(-)-Aromadendrene
PL041172
OR031367
Aromadendr-7(15)-ene
FT-0694285
Aromadendrene, (+)-
1,1,7-Trimethyl-4-methylenedecahydro-1H-cyclopropa[e]azulene
25246-27-9
1,1,2-trimethyl-5-methylidene-decahydro-1H-cyclopropa[e]azulene
1,1,2-TRIMETHYL-5-METHYLIDENE-OCTAHYDRO-1AH-CYCLOPROPA[E]AZULENE
109119-91-7
1H-Cycloprop[e]azulene, decahydro-1,1,7-trimethyl-4-methylene-
(1aR,4aR,7R,7aR,7bS)-1,1,7-Trimethyl-4-methylenedecahydro-1H-cyclopropa[e]azulene
1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene
1,1,7-trimethyl-4-methylene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene
1H-Cycloprop(e)azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR-(1aalpha,4abeta,7alpha,7abeta,7balpha))-
1H-Cycloprop[e]azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR,4aS,7R,7aR,7bS)-(-)-
1H-Cycloprop[e]azulene, decahydro-1,1,7-trimethyl-4-methylene-, (1aR,4aR,7R,7aR,7bS)-(+)-
1,1,7-Trimethyl-4-methylenedecahydro-1H-cyclopropa[e]azulene-, [1aR-(1a.alpha.,4a.alpha.,7.alpha.,7a.beta.,7b.alpha.)]-
1H-Cycloprop[e]azulene, decahydro-1,1,7-trimethyl-4-methylene-, [1aR-(1a.alpha.,4a.beta.,7.alpha.,7a.beta.,7b.alpha.)]-
1H-Cycloprop[e]azulene, decahydro-1,1,7-trimethyl-4-methylene-, [1aR-(1a.alpha.,4a.alpha.,7.alpha.,7a.beta.,7b.alpha.)]-
IUPAC name1,1,7-trimethyl-4-methylidene-2,3,4a,5,6,7,7a,7b-octahydro-1aH-cyclopropa[e]azulene
SMILESCC1CCC2C1C3C(C3(C)C)CCC2=C
InchiInChI=1S/C15H24/c1-9-6-8-12-14(15(12,3)4)13-10(2)5-7-11(9)13/h10-14H,1,5-8H2,2-4H3
FormulaC15H24
PubChem ID91354
Molweight204.357
LogP4.15
Atoms39
Bonds41
H-bond Acceptor0
H-bond Donor0
Chemical Classificationterpenes

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiPenicillium Expansumcompost Fischer et al. 2021
FungiTrichoderma VirideHung et al., 2013
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiPenicillium Expansumyest extract sucroseTenax/GC-MSno
FungiTrichoderma VirideMalt extract agar Headspace volatiles collected with colomn/TD-GC-MSYes


Compound Details

Synonymous names
alpha-Cubebene
AC1L9CO8
438H9S5RG9
C09647
PL001071
DTXSID3058325
ZINC8234284
UNII-438H9S5RG9
CHEBI:10224
Caswell No. 264AB
(-)-alpha-Cubebene
AKOS015913737
EPA Pesticide Chemical Code 117901
I14-45219
alpha-Cubebene, (-)-
17699-14-8
1H-Cyclopenta(1,3)cyclopropa(1,2)benzene, 3a,3b,4,5,6,7-hexahydro-3,7-dimethyl-4-(1-methylethyl)-, (3aS,3bR,4S,7R,7aR)-
1H-Cyclopenta(1,3)cyclopropa(1,2)benzene, 3a,3b,4,5,6,7-hexahydro-3,7-dimethyl-4-(1-methyl-ethyl)-, (3aS-(3aalpha,3bbeta,4beta,7alpha,7aS*))-
(1R,5S,6R,7S,10R)-4,10-DIMETHYL-7-(PROPAN-2-YL)TRICYCLO[4.4.0.0(1),?]DEC-3-ENE
IUPAC name
SMILESCC1CCC(C2C13C2C(=CC3)C)C(C)C
InchiInChI=1S/C15H24/c1-9(2)12-6-5-11(4)15-8-7-10(3)13(15)14(12)15/h7,9,11-14H,5-6,8H2,1-4H3/t11-,12+,13-,14-,15+/m1/s1
FormulaC15H24
PubChem ID442359
Molweight204.357
LogP4.09
Atoms39
Bonds41
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

mVOC Specific Details


Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiPiptoporus BetulinusnaSachsenwald near HamburgRösecke et al., 2000
FungiAspergillus Ustusnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiTrichoderma Harzianum T-E5 CCTCC AF2012011n/aZhang et al., 2014
FungiArmillaria Mellean/aMueller et al., 2013
FungiPholiota Squarrosan/aMueller et al., 2013
FungiStropharia Rugosoannulatan/aMueller et al., 2013
FungiTrichoderma Viriden/aMueller et al., 2013
FungiFomitopsis PinicolanaGermanyRösecke et al., 2000
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiPiptoporus BetulinusnaGC/MSNo
FungiAspergillus Ustusmalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiTrichoderma Harzianum T-E5 CCTCC AF2012011Minimal mediaSPME/GC-MS
FungiArmillaria MelleaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiPholiota SquarrosaMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiStropharia RugosoannulataMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiTrichoderma VirideMelin-Nor krans synthetic medium (modified)Headspace trapping ( using stir bar sorptive extraction )/ GC-MS
FungiFomitopsis PinicolanaGC/MSNo


1-methyl-4-propan-2-ylcyclohexa-1,3-diene

Mass-Spectra

Compound Details

Synonymous names
YHQGMYUVUMAZJR-UHFFFAOYSA-N
Terpilene
ALPHA-TERPINENE
alpha-Terpinen
alpha-Terpinene, analytical standard
AC1L1OTD
.alpha.-Terpinene
alpha - Terpinene
.alpha.-Terpinen
.alpha.-Terpine
M0317
alpha-Terpinene, 85%
ZINC967593
I24X278AP1
CCRIS 9058
C09898
LS-3104
DTXSID9041237
CHEMBL2251642
OR382959
OR382958
OR038359
UNII-I24X278AP1
CHEBI:10334
DSSTox_GSID_41237
BB0295842
AN-24527
SC-20197
1-Methyl-4-isopropylcyclohexadiene-1,3
DSSTox_RID_79657
MFCD00001534
p-Mentha-1,3-diene
DSSTox_CID_21237
AI3-26467
Ambap99-86-5
W-100014
Epitope ID:123897
AKOS015841730
FEMA No. 3558
FT-0622940
I14-51685
1-Isopropyl-4-methyl-1,3-cyclohexadiene
99-86-5
1-isopropyl-4-methylcyclohexa-1,3-diene
1-Methyl-4-isopropyl-1,3-cyclohexadiene
LMPR0102090026
Tox21_301126
CAS-99-86-5
alpha-Terpinene, >=89%, FCC, FG
NCGC00248299-01
NCGC00255025-01
1-isopropyl-4-methyl-cyclohexa-1,3-diene
EINECS 202-795-1
alpha-Terpinene, >=95.0% (GC)
1,3-Cyclohexadiene, 1-methyl-4-isopropyl-
MolPort-003-928-066
1-methyl-4-propan-2-ylcyclohexa-1,3-diene
1-Methyl-4-(1-methylethyl)-1,3-cyclohexadiene
1-methyl-4-(propan-2-yl)cyclohexa-1,3-diene
1,3-Cyclohexadiene, 1-methyl-4-(1-methylethyl)-
InChI=1/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,6,8H,5,7H2,1-3H
IUPAC name1-methyl-4-propan-2-ylcyclohexa-1,3-diene
SMILESCC1=CC=C(CC1)C(C)C
InchiInChI=1S/C10H16/c1-8(2)10-6-4-9(3)5-7-10/h4,6,8H,5,7H2,1-3H3
FormulaC10H16
PubChem ID7462
Molweight136.238
LogP3.16
Atoms26
Bonds26
H-bond Acceptor0
H-bond Donor0
Chemical ClassificationTerpenes

Microorganisms emitting the compound
KingdomSpeciesBiological FunctionOrigin/HabitatReference
FungiHypoxylon Antochroum Blacinaendophytic in Bursera lancifoliaUlloa-Benítez et al., 2016
FungiPaecilomyces Variotiicompost Fischer et al. 2047
FungiPenicillium Clavigerumcompost Fischer et al. 2047
FungiAmanita OvoideaFranceBreheret et al. 1997
FungiPenicillium PolonicumPolizzi et al., 2012
FungiTrichoderma Atroviride ATCC 74058n/aStoppacher et al., 2010
FungiAntrodia Cinnamomea ATCC 200183nanaLu et al., 2014
FungiFusarium Culmorum PVaffects swarming and swimming motility of Serratia plymuthica PRI-2C; affects swarming ability of Collimonas pratensis Ter291sandy dune soil, NetherlandsSchmidt et al., 2016
FungiPenicillium Polonicumnawater damaged buildings, BelgiumPolizzi et al., 2012
FungiTrichoderma Atroviridenawater damaged buildings, BelgiumPolizzi et al., 2012
Method
KingdomSpeciesGrowth MediumApplied MethodVerification
FungiHypoxylon Antochroum BlaciPDA/WA + 500 mg l^-1 ChloramphenicolSPME-GC/MSYes
FungiPaecilomyces Variotiiyest extract sucroseTenax/GC-MSno
FungiPenicillium Clavigerumyest extract sucroseTenax/GC-MSno
FungiAmanita Ovoideaforest soilsolvent extraction, headspace, GCMSno
FungiPenicillium Polonicummalt extract agar (MEA), wallpaper, plasterboardSPME/GC-MS
FungiTrichoderma Atroviride ATCC 74058Potato dextrose agarHS-SPME/GC-MS
FungiAntrodia Cinnamomea ATCC 200183PDAGC/MSYes
FungiFusarium Culmorum PVpotato dextrose agarGC/MS-Q-TOFNo
FungiPenicillium Polonicummalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo
FungiTrichoderma Atroviridemalt extract agar; potato dextrose agar; water agar; yeast extract agar; Czapek agarSPME-GC/MSNo