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)

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)

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)

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))

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)

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)

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-, (.+/-.)-

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)

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)

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)

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

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)

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

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)

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

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)

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

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.

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)-

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)

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)

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)

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

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)-

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)-(-)-

Eremophilene

QEBNYNLSCGVZOH-GZBFAFLISA-N

OPI7MD81JT

UNII-OPI7MD81JT

DTXSID30144729

ZINC49538670

AKOS015903138

I14-18983

10219-75-7

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

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)-

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)

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)

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)-