Isopropylideneacetone

Isopropylidene acetone

Mesityloxyde

Mesityloxid

SHOJXDKTYKFBRD-UHFFFAOYSA-N

Isobutenyl methyl ketone

Methyl isobutenyl ketone

MESITYL OXIDE

Mesityl Oxide, pharmaceutical secondary standard

Ossido di mesitile

Oxyde de mesityle

Acetone, isopropylidene-

ACMC-1BOEP

AC1L1RU7

AC1Q1JB3

Mesityloxid [German]

Mesityloxyde [Dutch]

KSC494O1D

7471AF

UN1229

2,2-Dimethylvinyl methyl ketone

CTK3J4711

M0069

M1340

Methyl 2,2-dimethylvinyl ketone

NSC38717

Ossido di mesitile [Italian]

RP18648

HSDB 1195

Mesityl oxide, European Pharmacopoeia (EP) Reference Standard

Oxyde de mesityle [French]

3-Isohexen-2-one

BBL027732

CHEMBL3185916

DTXSID1029170

FEMA Number 3368

Jsp002461

LS-2950

Methyl 2-methyl-1-propenyl ketone

OR034477

OR219303

SBB040870

STL146350

UN 1229

A807813

CHEBI:89993

DSSTox_CID_9170

77LAC84669

AN-43889

ANW-41508

CJ-07569

CJ-32144

DSSTox_GSID_29170

KB-78313

NSC 38717

NSC-38717

SC-47106

TRA0020647

BB_NC-2260

Caswell No. 547

DSSTox_RID_78697

LMFA12000030

MFCD00008900

ZINC02038441

2-Methyl-2-pentenone-4

AI3-07702

Mesityl oxide, technical grade, 90%

RTR-005373

TR-005373

UNII-77LAC84669

AKOS000118892

EPA Pesticide Chemical Code 052401

Mesityl oxide, mixture of alpha- and beta-isomers

Q-201356

S14-1428

ZINC100019800

(CH3)2C=CHC(=O)CH3

BRN 1361550

FEMA No. 3368

FT-0628235

2-Methyl-4-oxo-2-pentene

4-Methyl-3-pentene-2-one

2-Methyl-2-penten-4-one

2-methylpent-2-en-4-one

4-Methyl-3-penten-2-on

4-Methyl-3-penten-2-one

4-Methylpent-3-en-2-one

4-Metil-3-penten-2-one

Tox21_202080

Tox21_303606

141-79-7

4-Methyl-3-penten-2-one, analytical reference material

WLN: 1Y1 & U1V1

MCULE-4922478422

NCGC00249161-01

NCGC00257514-01

NCGC00259629-01

3-Penten-2-one,4-methyl-

4-methyl-pent-3-en-2-one

CAS-141-79-7

EINECS 205-502-5

3-PENTEN,2-ONE,4-METHYL MESITYLOXIDE

Mesityl oxide [UN1229] [Flammable liquid]

3-Penten-2-one, 4-methyl-

MolPort-000-872-030

4-Methyl-3-penten-2-one, 9CI

4-Metil-3-penten-2-one [Italian]

Mesityl oxide, suitable for neutral marker for measuring electroosmotic flow (EOF), ~98%

4-Methyl-3-penten-2-on(DUTCH, GERMAN)

4-Methyl-3-penten-2-one, 90%

Mesityl oxide [UN1229] [Flammable liquid]

4-Methyl-3-penten-2-on [Dutch, German]

Mesityl oxide, technical, 90%, remainder 4-methyl-4-penten-2-one 100ml

InChI=1/C6H10O/c1-5(2)4-6(3)7/h4H,1-3H

The Henry's Law constant for mesityl oxide is estimated as 3.67X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 8.21 mm Hg(1), and water solubility, 28,900 mg/L(2). This Henry's Law constant indicates that mesityl oxide 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 11 days(SRC). Mesityl oxide's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of mesityl oxide from dry soil surfaces may exist(SRC) based upon its vapor pressure(1).
Literature: (1) Daubert TE, Danner DP; Physical & Thermodynamic Properties of Pure Chemicals Vol. 3 NY: Hemisphere Pub Corp (1989) (2) Yalkowsky SH, He Y; Handbook of Aqueous Solubility Data. CRC Press LLC, Boca Raton, FL. p. 285 (2003) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

The Koc of mesityl oxide is estimated as 15(SRC), using a water solubility of 28,900 mg/L(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that mesityl oxide is expected to have very high mobility in soil.
Literature: (1) Yalkowsky SH, He Y; Handbook of Aqueous Solubility Data. CRC Press LLC, Boca Raton, FL. p. 285 (2003) (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)

ZXNBBWHRUSXUFZ-UHFFFAOYSA-N

ZXNBBWHRUSXUFZ-UHFFFAOYSA-

sec-BUTYL METHYLCARBINOL

ACMC-1AOZB

AC1L1WZ5

2-hydroxy-3-methylpentane

SCHEMBL26336

M0850

CTK1H0243

3-Methyl-4-pentanol

NSC92741

ACMC-20m2p7

3-METHYL-2-PENTANOL

3-Methylpentan-2-ol

OR012201

OR129661

Threo-3-methylpentan-2-ol

CHEBI:77520

3-Methyl-pentan-2-ol

NSC-92741

NSC 92741

KB-32719

MFCD00004528

TC-169508

AKOS009156539

FT-0694658

2-Pentanol, 3-methyl-

3-Methyl-2-pentanol (mixture of diastereoisomers)

565-60-6

3-Methyl-2-pentanol, 99%

1502-93-8

EINECS 209-281-6

99212-18-7

2-Pentanol, 3-methyl- (8CI)(9CI)

InChI=1/C6H14O/c1-4-5(2)6(3)7/h5-7H,4H2,1-3H3

1.74e+01 g/l
Literature: ALOGPS

Methylisopropylcarbinol

Isopropylmethylcarbinol

MXLMTQWGSQIYOW-UHFFFAOYSA-N

sec-Isoamyl alcohol

ACMC-1AOXT

ACMC-20apgh

ACMC-20apkz

AC1Q76MQ

1,2-Dimethylpropanol

AC1Q1O29

AC1L1Y06

CTK1H1103

M0171

CHEMBL443470

NE10328

OR10026

NSC71162

2-Methyl-3-butanol

3-Methylbutan-2-ol

3-METHYL-2-BUTANOL

OR035256

CHEBI:77517

NSC-71162

KB-32703

ANW-33382

DL-3-Methyl-2-butanol

NSC 71162

MFCD00004527

3-Methyl-butan-2-ol

1,2-dimethylpropan-1-ol

1,2-Dimethyl-1-propanol

TR-020739

AKOS000249588

FEMA No. 3703

FT-0604375

FT-0604412

FT-0604463

(CH3)2CHCH(OH)CH3

I14-49339

2-Butanol, 3-methyl-

598-75-4

(?)-3-Methyl-2-butanol

3-Methyl-2-butanol, 98%

Butan-2-ol, 3-methyl-

EINECS 209-950-2

70116-68-6

MolPort-001-759-244

DL-3-Methyl-2-butanol, >=98%, FG

207703-EP2380568A1

(+/-)-3-Methyl-2-butanol

2-Butanol, 3-methyl-, (S)-

(.+/-.)-3-Methyl-2-butanol

3-Methyl-2-butanol, purum, >=98.0% (GC)

Acetylfuran

IEMMBWWQXVXBEU-UHFFFAOYSA-N

2-acetylfurane

2-Furylethanone

Furyl methyl ketone

2-Acetylfuran

AC1Q1JXY

AC1L23YX

ACMC-1BPS0

PubChem6939

2-Acetyl furan

I896

KSC175C9R

Methyl 2-furyl ketone

2-Furyl methyl ketone

SCHEMBL43960

NSC4665

CTK0H5198

A0091

2-Aminomethyl-azetidine-1-carboxylic acid tert-butylester

1-Furan-2-ylmethanone

Q5ZRP80K02

NSC49133

2-Furyl methyl ketone, analytical standard

STR05504

AM91073

RP18952

ZINC157401

CCRIS 3161

Ketone, 2-furyl methyl

UNII-Q5ZRP80K02

NSC 4665

NSC-4665

PS-4586

SBB040248

HE110254

HE017372

STK400329

ZB006673

DTXSID0051601

BBL027427

CHEBI:59983

A804234

AJ-15008

NSC-49133

NSC 49133

1-Furan-2-yl-ethanone

LS-87211

KB-12200

SC-00529

AB1001236

AC-11853

ST2415091

AK-53418

Furan, 2-acetyl-

ANW-17304

AN-20640

TRA0078485

CJ-01650

1-(2-FURANYL)ETHANONE

1-(2-Furyl)ethanone

BB_SC-6820

2-Furyl methyl ketone (natural)

MFCD00003242

ZINC00157401

DB-003253

RTR-003241

AI3-23586

TR-003241

ST50213408

AKOS000119584

Epitope ID:136039

I14-0303

Q-100089

1-(2-Furyl)ethanone #

1-(furan-2-yl)ethanone

1-(2-Furanyl)-ethanone

2-Furyl methyl ketone, 99%

BRN 0107909

(2-furanyl)-1-ethanone

FEMA No. 3163

FT-0610977

I14-22249

Ethanone, 1-(furanyl)-

F0001-0316

1-(furan-2-yl)-ethanone

MCULE-6389695813

1192-62-7

EINECS 214-757-1

2-Furyl methyl ketone, >=99%, FG

80145-44-4

Ethanone, 1-(2-furanyl)-

1-(2-Furanyl)ethanone; 2-Furyl methyl ketone

1-(Furan-2-yl)ethan-1-one

MolPort-000-871-221

2-Furyl methyl ketone, natural (US), >=97%, FG

5-17-09-00381 (Beilstein Handbook Reference)

2-Furyl methyl ketone, purum, >=99.0% (GC)

InChI=1/C6H6O2/c1-5(7)6-3-2-4-8-6/h2-4H,1H

Monocyclic terpene hydrocarbons

Polydipentene

Polylimonene

Polymerized dipentene

Absolute petitgrain

Cajeputene

Terpodiene

Achilles dipentene

Cajeputen

Dipenten

Dipentene

Dipentene polymer

Inactive limonene

Kautschin

LIMONENE

Methyl-4-isopropenylcyclohexene

XMGQYMWWDOXHJM-UHFFFAOYSA-N

Cinene

Dipanol

Eulimen

Limonen

Limonene polymer

Petitgrain citronnier oil

Unitene

Absolue orange flower decoloree

Absolute orange flowers

alpha-Limonene

beta-Limonene

Ciene

Cinen

Cyclil decene

Flavor orange

Lemon extract

Lemon tincture

Nesol

Orange flavor

Orange flower absolute

Orange oil concentrate

Petitgrain bigarade sur fleurs d'oranger

Absolue orange flower

Acintene DP

Acintene DP dipentene

Citrus limon extract

DL-Limonene

Goldflush II

Lemon oil concentrate

Lemon petitgrain oil

a-limonene

Cedro oil

Citrus sinensis oil

LEMON OIL

Lemon petigrain oil

Neroli oil

Orange flower water absolute

Orange oil

AC1Q2ODZ

Citrus limon oil

Dipentene, crude

Extract of lemon

Oil sweet orange

Orange flower oil

Sweet orange oil

1-Methyl-4-isopropenylcyclohexene

4-Isopropenyl-1-methylcyclohexene

Absolue orange flower from water

Citrus sinensis peel oil

Orange leaf oil

Terpenes and Terpenoids, limonene fraction

d,l-Limonene

Oil of lemon

OIL OF ORANGE

Oils, orange

Orange oil, distilled

AC1L2K5B

AC1Q1J4Q

AC1Q1J4R

Dipentene, mixture of isomers

Lemon oil, distilled

Neroli oil, pommade

Oil of sweet orange

Oils, citrus limonia

Oils, lemon

Sweet orange oil, terpeneless

DL-4-Isopropenyl-1-methylcyclohexene

ESSENCE DE PIN PF

Lemon oil, Guinea

Lemon oil, Italian

NSC844

Orange oil, sweet

Orange sweet oil, expressed

.alpha.-Limonene

4-isopropenyl-1-methyl-cyclohexene

Dipentene 200

Dipentene, tech.

Methyl-4-isopropenyl-1-cyclohexene

Neat oil of sweet orange

C10H16

CHEMBL15799

DIPENTENE 38 PF

Limonene, dl-

Orange peel oil, sweet

Racemic: DL-limonene; dipentene

UN2052

(?)-Limonene

c0626

CCRIS 683

Citrus medica var. limonum oil

CTK5C8417

d-Limonene (Limonene)

L0046

Limonene, L-

Zitronen oel [German]

delta-1,8-Terpodiene

Methyl-4-(1-methylethenyl)cyclohexene

NSC 844

NSC-844

NSC21446

Oils, orange, sweet

Orange oil, distilled, sweet

Orange oil, sweet, expressed

PC 560

RP20299

Zonarez 7085

Zonarez 7115

1-Methyl-p-isopropenyl-1-cyclohexene

1,8-p-Menthadiene

C06078

d-Limonene (JAN)

D00194

HMS3264E05

HSDB 1809

HSDB 1931

HSDB 1934

HSDB 1944

AK176153

BT000140

DTXSID2029612

LS-2278

LS-2880

Mentha-1,8-diene

NSC757069

OR012480

OR111377

OR111378

OR217376

OR339605

OR369142

STK801934

UN 2052

( inverted exclamation markA)-limonene(dipentene)

1-Methyl-4-isopropenyl-1-cyclohexene

1-methyl-4-isopropenylcyclohex-1-ene

4-Isopropenyl-1-methyl-1-cyclohexene

CHEBI:15384

DSSTox_CID_9612

AN-19448

AN-21149

AN-21151

AN-21831

AN-23147

Caswell No. 425A

d(R)-4-Isopropenyl-1-methylcyclohexene

DSSTox_GSID_29612

limonene, (S)-isomer

LS-89490

LS-89491

LS-98217

NSC 21446

NSC-21446

SC-80005

Caswell No. 526

Cyclohexene, 4-Isopropenyl-1-methyl-

DSSTox_RID_78787

MFCD00062992

p-Mentha-1,8-diene

1-Methyl-4-(1-methylethenyl)cyclohexene

AI3-00739

AI3-25390

CCG-214016

LS-180589

LS-181342

NSC-757069

ST51046654

(+-)-Dipentene

(+-)-Linonene

AKOS009031280

DIPENTENE (+-)

EPA Pesticide Chemical Code 040501

EPA Pesticide Chemical Code 040517

EPA Pesticide Chemical Code 079701

J-007186

J-520048

.delta.-1,8-Terpodiene

4-mentha-1,8-diene

Di-p-mentha-1,8-diene

DL-p-mentha-1,8-diene

FEMA No. 2822

FEMA No. 2853

FT-0600409

FT-0605227

(+-)-alpha-Limonene

I14-18195

I14-53978

Mentha-1,8-diene, DL

p-Mentha-1, dl-

p-Mentha-1,8-diene, polymers

4-(1-methylethenyl)-1-methyl-cyclohexene

EN300-21627

NCI60_041856

Tox21_112068

Tox21_201818

Tox21_303409

(+/-)-Limonene

1-methyl-4-(1-methylethenyl)-cyclohexen

1,8(9)-p-Menthadiene

138-86-3

555-08-8

Limonene, (+)-

limonene, (+-)-isomer

7705-14-8

8022-90-0

8050-32-6

9003-73-0

Dipentene, p.a., 95%

MCULE-2462317444

MENTHA-1,8-DIENE (DL)

NCGC00163742-01

NCGC00163742-02

NCGC00163742-03

NCGC00163742-04

NCGC00257291-01

NCGC00259367-01

AB01563249_01

CAS-138-86-3

Cyclohexene, 1-methyl-4-(1-methylethynyl)

Cyclohexene,1-methyl-4-(1-methylethenyl)-

Dipentene [UN2052] [Flammable liquid]

EINECS 205-341-0

EINECS 227-815-6

EINECS 231-732-0

(.+-.)-Dipentene

(.+-.)-Limonene

1-methyl-4-prop-1-en-2-ylcyclohexene

26123-39-7

65996-98-7

68246-90-2

p-Mentha-1,8(9)-diene

Pharmakon1600-00307080

p-Mentha-1,8-diene, dl-

SR-01000872759

1-methyl-4-(1-methylvinyl)cyclohex-1-ene

WLN: L6UTJ A1 DY1 & U1

(+-)-(RS)-limonene

Cyclohexene, 1-methyl-4-(1-methylethenyl)-

Dipentene [UN2052] [Flammable liquid]

MolPort-001-782-985

(.+/-.)-Dipentene

(.+/-.)-Limonene

1-METHYL-4-PROP-1-EN-2-YL-CYCLOHEXENE

Limonene, (+/-)-

Orange oil, terpeneless (Citrus sinensis (L.) Osbeck)

(1)-1-Methyl-4-(1-methylvinyl)cyclohexene

Cyclohexene, 1-methyl-4-(1-methylethenyl)-, homopolymer

Cyclohexene, (.+-.)-

SR-01000872759-1

1-methyl-4-(prop-1-en-2-yl)cyclohexene

ORANGE, OIL, DISTILLED (CITRUS SINENSIS (L.) OSBECK)

( inverted exclamation markA)-1,8-p-menthadiene,( inverted exclamation markA)-limonene

Dipentene, technical, for use as solvent (for the paint industry), mixture of various terpenes

1-Methyl-4-(1-methylethenyl)cyclohexene, (S)-

ORANGE PEEL, SWEET, OIL (CITRUS SINENSIS (L.) OSBECK)

(.+/-.)-.alpha.-Limonene

(+/-)-p-Mentha-1,8-diene

Petitgrain lemon oil (Citrus limon (L.) Burm. f.)

(s)-(-)-4-isopropenyl-1-methyl-1-cyclohexene

1-methyl-4-(prop-1-en-2-yl)cyclohex-1-ene

p-Mentha-1,8-diene, (+-)-

p-Mentha-1, (.+-.)-

lemon, oil (citrus limon (l.) burm. f.)

Cyclohexene, 1-methyl-4-(1-methylethenyl)-, (R)-

Cyclohexene, 1-methyl-4-(1-methylethenyl)-, (S)-

4B4F06FC-8293-455D-8FD5-C970CDB001EE

Cyclohexene,3-methyl-6-(1-methylethenyl)-, (3R,6R)-rel-

Dipentene, mixt. of limonene, 56-64%, and terpinolene, 20-25%

p-Mentha-1,8-diene, (.+/-.)-

Cyclohexene, 1-methyl-4-(1-methylethenyl)-, (+/-)-

Cyclohexene, 1-methyl-4-(1-methylethenyl)-, (.+/-.)-

Turpentine typically contains alpha-pinene (59%), beta-pinene (24%) and other isomeric terpenes(1). The Henry's Law constant for alpha- and beta-pinene have been measured as 0.134 and 0.0679 atm-cu m/mole respectively at 25 deg C(2). These Henry's Law constants indicate that alpha- and beta-pinene are expected to volatilize rapidly from water surfaces(3). Based on these Henry's Law constants, 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 3.4 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 4.6 days(SRC). alpha- and beta-Pinene's Henry's Law constants indicate that volatilization from moist soil surfaces may occur(SRC). alpha- and beta-Pinene are expected to volatilize from dry soil surfaces(SRC) based upon respective vapor pressures of 4.75 and 2.93 mm Hg at 25 deg C(1).
Literature: (1) USEPA; Screening-Level Hazard Characterization, Bicyclic Terpene Hydrocarbons Category, September 2010; Available from, as of Dec 26, 2014: http://www.epa.gov/chemrtk/hpvis/hazchar/Category_Bicyclic%20Terpene%20Hydrocarbons_%20September_2010.pdf (2) Copolovici LO, Niinemets U; Chemosphere 61: 1390-400 (2005) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)
Literature: #The Henry's Law constant for limonene is estimated as 0.032 atm-cu m/mole(SRC) derived from its vapor pressure, 1.55 mm Hg(1), and water solubility, 7.57 mg/L(2). This Henry's Law constant indicates that limonene 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). Limonene's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of limonene from dry soil surfaces may exist(SRC) based upon its vapor pressure(1).
Literature: (1) Boublik T et al; The vapor pressures of pure substances. Vol. 17. Amsterdam, Netherlands: Elsevier Sci Publ (1984) (2) Miller DJ, Hawthorne SB; J Chem Eng Data 44: 315-8 (2000) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)
Literature: #The Henry's Law constant for d-limonene is reported as 0.0281 atm-cu m/mole(1). This Henry's Law constant indicates that d-limonene 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 3.5 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 4.6 days(SRC). d-Limonene's reported Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of d-limonene from dry soil surfaces may exist based upon a vapor pressure of 1.98 mm Hg(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) Yaws CL; Handbook of Vapor Pressure. Vol 3: C8-C28 Compounds. Houston, TX: Gulf Pub Co (1994)

In water, 0.65 to 2.1 mg/L at 25 deg C /primary pinene constituents of turpentine oil/
Literature: USEPA; Screening-Level Hazard Characterization, Bicyclic Terpene Hydrocarbons Category, September 2010. Available from, as of Dec 26, 2014: http://www.epa.gov/chemrtk/hpvis/hazchar/Category_Bicyclic%20Terpene%20Hydrocarbons_%20September_2010.pdf
Literature: #Insol in water
Literature: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1822
Literature: #Soluble in 5 volumes alcohol; miscible with benzene, chloroform, ether, carbon disulfide, petroleum ether and oils.
Literature: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1822
Literature: #SLIGHTLY SOL IN WATER; SOL IN 3 VOL ALCOHOL; MISCIBLE WITH CARBON DISULFIDE, GLACIAL ACETIC ACID
Literature: The Merck Index. 9th ed. Rahway, New Jersey: Merck & Co., Inc., 1976., p. 883
Literature: #In water, 7.57 mg/L at 25 deg C
Literature: Miller DJ, Hawthorne SB; J Chem Eng Data 44: 315-8 (2000)
Literature: #Miscible with alcohol
Literature: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1021
Literature: #Miscible with 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. V4: 2827
Literature: #Slightly soluble in water
Literature: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1262
Literature: #Soluble in 2 vol 90% alcohol, 1 volume glacial acetic acid; miscible with absolute alcohol, carbon disulfide
Literature: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. Cambridge, UK: Royal Society of Chemistry, 2013., p. 1262
Literature: #In water, 13.8 mg/L at 25 deg C
Literature: Massaldi HA, King CJ; J Chem Eng Data 18: 393-7 (1973)
Literature: #Miscible with ethanol and ether; soluble in carbon tetrachloride
Literature: Haynes, W.M. (ed.). CRC Handbook of Chemistry and Physics. 95th Edition. CRC Press LLC, Boca Raton: FL 2014-2015, p. 3-338
Literature: #Miscible with fixed oils; slightly soluble in glycerin; insoluble in propylene glycol
Literature: Lewis, R.J. Sr. (ed) Sax's Dangerous Properties of Industrial Materials. 12th Edition. Wiley-Interscience, Wiley & Sons, Inc. Hoboken, NJ. 2012., p. V4: 2741

Turpentine typically contains alpha-pinene (59%), beta-pinene (24%) and other isomeric terpenes(1). Using a structure estimation method based on molecular connectivity indices(2), the Koc of alpha- and beta-pinene can be estimated to be 1000(SRC). According to a classification scheme(3), this estimated Koc value suggests that alpha- and beta-pinene are expected to have low mobility in soil.
Literature: (1) USEPA; Screening-Level Hazard Characterization, Bicyclic Terpene Hydrocarbons Category, September 2010. Available from, as of Dec 26, 2014: http://www.epa.gov/chemrtk/hpvis/hazchar/Category_Bicyclic%20Terpene%20Hydrocarbons_%20September_2010.pdf (2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.11. Nov, 2012. Available from, as of Dec 27, 2014: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm
Literature: #Using a structure estimation method based on molecular connectivity indices(1), the Koc for limonene can be estimated to be 1,100(SRC). According to a classification scheme(2), this estimated Koc value suggests that limonene is expected to have low mobility in soil(SRC).
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of Apr 24, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)
Literature: #Using a structure estimation method based on molecular connectivity indices(1), the Koc of d-limonene can be estimated to be 1120(SRC). According to a classification scheme(2), this estimated Koc value suggests that d-limonene 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 Apr 24, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)

UAHWPYUMFXYFJY-UHFFFAOYSA-N

beta-geraniolene

MYRCENE

Myrcene, primary pharmaceutical reference standard

beta-Myrcene

b-Myrcene

Myrcene, analytical standard

AC1Q1NVC

Myrcene, technical grade

MYRCENE, TECH

AC1Q1J8N

AC1L1L8S

.beta.-Geraniolene

MYRCENE 90

Myrcene (natural)

.beta.-Myrcene

3M39CZS25B

M0235

Myrcene (stabilized with BHT)

V0542

RP20298

LS-678

CHEMBL455491

C06074

CCRIS 3725

UNII-3M39CZS25B

HSDB 1258

STL477735

Jsp001569

DTXSID6025692

LP070397

OR028249

NSC406264

AK116901

ZINC1530331

A805060

CHEBI:17221

DSSTox_CID_5692

CC-31053

AJ-26651

FCH1116940

AN-22914

DSSTox_GSID_25692

CJ-23958

DSSTox_RID_77883

MFCD00008908

C-34801

TR-003681

NSC-406264

NSC 406264

ST24029965

Myrcene, .beta.-

WLN: 1Y1&U3YU1&1U1

AI3-00738

Q-201417

AKOS015904015

BRN 1719990

FEMA No. 2762

FT-0629050

LMPR0102010005

I14-17984

7-?Methyl-?3-?methylene-?1,6-?octadiene

7-methyl-3-methylideneocta-1,6-diene

Tox21_300351

2-Methyl-6-methylene-2,7-octadiene

3-Methylene-7-methyl-1,6-octadiene

7-Methyl-3-methylene-1,6-octadiene

123-35-3

7-Methyl-3-methyleneocta-1,6-diene

NCGC00091420-01

NCGC00091420-02

NCGC00254252-01

2153-31-3

EINECS 204-622-5

1, 7-methyl-3-methylene-

CAS-123-35-3

7-methyl-3-methylidene-octa-1,6-diene

7-Methyl-3-methylene-octa-1,6-diene

Myrcene, >=95%, stabilized, FCC, FG

7-Methyl-3-methyleneoctadiene-(1,6)

MolPort-001-792-515

1,6-OCTADIENE; 7-METHYL-3-METHYLENE-

1,6-Octadiene, 7-methyl-3-methylene-

4-01-00-01108 (Beilstein Handbook Reference)

InChI=1/C10H16/c1-5-10(4)8-6-7-9(2)3/h5,7H,1,4,6,8H2,2-3H

The Henry's Law constant for myrcene is estimated as 0.0916 atm-cu m/mole(SRC) derived from its vapor pressure, 2.09 mm Hg(1), and water solubility, 4.09 mg/L(2). This Henry's Law constant indicates that myrcene 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 3.4 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 4.6 days(SRC). Myrcene's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of myrcene from dry soil surfaces may exist based upon a vapor pressure of 2.09 mm Hg(1).
Literature: (1) Haynes, W.M. (ed.); CRC Handbook of Chemistry and Physics. 91th ed. Boca Raton, FL: CRC Press Inc., p. 6-112 (2010-2011) (2) Yalkowsky SH et al eds; Handbook of aqueous solubility data. Second edition. Boca Raton, FL: CRC Press p. 714 (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 myrcene can be estimated to be 1074(SRC). According to a classification scheme(2), this estimated Koc value suggests that myrcene is expected to have low mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Jan, 2011. Available from, as of Oct 19, 2011: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Swann RL et al; Res Rev 85: 17-28 (1983)

MXDMETWAEGIFOE-UHFFFAOYSA-N

AC1L3HLS

.delta.-EIemene

CTK1B5923

OR239872

OR200828

OR050744

AKOS030591339

370572-92-2

4-ethenyl-4-methyl-1-propan-2-yl-3-prop-1-en-2-ylcyclohexene

3-Isopropenyl-1-isopropyl-4-methyl-4-vinyl-1-cyclohexene-, (3R-trans)-

Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-

(3R-trans)-4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)cyclohexene

3-Isopropenyl-1-isopropyl-4-methyl-4-vinyl-1-cyclohexene-, (3R,4R)-

p-Menth-3-ene, 2-isopropenyl-1-vinyl-, (1S,2R)-(-)-

Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R-trans)-

Cyclohexene, 4-ethenyl-4-methyl-3-(1-methylethenyl)-1-(1-methylethyl)-, (3R,4R)-

D-ELEMENE,(3R-TRANS)-4-ETHENYL-4-METHYL-3-(1-METHYLETHENYL)-1-(1-METHYLETHYL)-CYCLOHEXENE,(1S,2R)-(-)-2-ISOPROPENYL-1-VINYL-P-MENTH-3-ENE

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

GERANIOL

GLZPCOQZEFWAFX-JXMROGBWSA-N

GLZPCOQZEFWAFX-UHFFFAOYSA-N

Neraniol

Geraniol alcohol

Geranyl alcohol

Guaniol

Lemonol

Meranol

racemic Geraniol

beta-Geraniol

Geraniol Extra

trans-Geraniol

AC1LCUHT

Geraniol, analytical standard

t-geraniol

AC1Q7BUA

2E-geraniol

Geraniol 98

Geraniol (natural)

.beta.-Geraniol

GTPL2467

CHEMBL25719

NCI9279

NSC9279

SCHEMBL19824

SCHEMBL19826

(E)-Geraniol

G0027

Geraniol (E)

Geraniol, 98%

HMS500J15

HSDB 484

(E)-Nerol

NSC46105

RP21876

C01500

CCRIS 7243

HMS1921H17

L837108USY

SPECTRUM1501132

AK109284

DTXSID8026727

Jsp000567

LP066354

LS-2765

LS-2977

NSC 9279

NSC-9279

SBB007719

A834344

CHEBI:17447

CHEBI:24221

DSSTox_CID_6727

UNII-L837108USY

ZINC1529210

AJ-26579

AN-22418

BSPBio_002919

CCG-37618

CJ-05167

DSSTox_GSID_26727

EBD2761143

FCH2256423

FCH3409296

FCH4510642

KB-52242

NSC-46105

SC-22671

SC-79539

BDBM50037023

DSSTox_RID_78202

MFCD00002917

NCGC00013095

Spectrum5_001513

ZINC01529210

AI3-00206

AI3-28202

RTR-001237

ST24026345

ST50824486

TR-001237

3,7-Dimethyloctan-1-ol, tetradehydro derivative

AKOS009031393

EPA Pesticide Chemical Code 597501

Epitope ID:181525

I14-6948

Q-201154

2,6-octadien-8-ol

3,6-octadien-1-ol

BRN 1722456

FEMA No. 2507

FEMA No. 2770

IDI1_000193

Geraniol, natural, >=97%, FG

I14-17819

LMPR0102010016

3,7-Dimethyl-2,6-octadienol

BBV-34551455

Tox21_110010

Tox21_202386

Tox21_300136

trans-3,6-octadien-1-ol

106-24-1

624-15-7

cis-3,6-octadien-1-ol

Geraniol, >=97%, FCC, FG

WLN: Q2UY1&3UY1&1 -T

8007-13-4

Geraniol, Vetec(TM) reagent grade, 97%

NCGC00013095-01

NCGC00013095-02

NCGC00013095-03

NCGC00013095-04

NCGC00013095-05

NCGC00013095-06

NCGC00013095-07

NCGC00013095-08

NCGC00013095-10

NCGC00094905-01

NCGC00094905-02

NCGC00094905-03

NCGC00094905-04

NCGC00094905-05

NCGC00253926-01

NCGC00259935-01

CAS-106-24-1

EINECS 203-377-1

EINECS 203-378-7

EINECS 210-831-2

EINECS 269-750-6

68311-14-8

SR-05000002389

Tox21_110010_1

MolPort-001-769-751

2,6-Dimethyl-2,6-octadien-8-ol

3,7-Dimethyl-2,6-octadien-1-ol

3,7-dimethylocta-2,6-dien-1-ol

1-Octanol, 3,7-dimethyl-, tetradehydro deriv.

3,7-dimethyl-trans-2,6-octadiene-1-ol

2,6-Dimethyl-trans-2,6-octadien-8-ol

3,7-Dimethyl-trans-2,6-octadien-1-ol

SR-05000002389-1

trans-2,6-Dimethyl-2,6-octadien-8-ol

trans-3,7-Dimethyl-2,6-octadien-1-ol

2, 3,7-dimethyl-, trans-

WLN: Q2UY1 & 3UY1 & 1-C

WLN: Q2UY1 & 3YU1 & 1-Z

trans-3,7-Dimethyl octa-2,6-dien-1-ol

2-trans-3,7-dimethyl-2,6-octadiene-1-ol

(E)-3,7-dimethyl-2,6octadien-1-ol

2-trans-3,7-Dimethyl-2,6-octadien-1-ol

2,6-Octadien-1-ol, 3,7-dimethyl-

2, 3,7-dimethyl-,(Z)-

4-01-00-02277 (Beilstein Handbook Reference)

(E)-3,7-Dimethyl-2,6-octadien-1-ol

(E)-3,7-Dimethylocta-2,6-dien-1-ol

2, 3,7-dimethyl-, (E)-

2, 3,7-dimethyl-, (Z)-

BRD-K03568070-001-01-1

(2E)-3,7-dimethyl-1-octa-2,6-dienol

(2E)-3,7-Dimethyl-2,6-octadien-1-ol

(2E)-3,7-dimethylocta-2,6-dien-1-ol

(E)-3,7-dimethyl-octa-2,6-dien-1-ol

Octadien-1-ol, 3,7-dimethyl-, (E)-

(2E)-3,7-Dimethyl-2,6-octadien-1-ol #

2,6-Octadien-1-ol, 3,7-dimethyl-, trans-

2,6-Octadien-1-ol,3,7-Dimethyl-,(E)-

3,7-Dimethyl-2,6-octadien-1-ol, (E)-

3,7-Dimethyl-2,6-octadien-1-ol, (Z)-

A884F9B1-42B7-4350-ACC7-8E71E86A9943

2,6-Octadien-1-ol, 3,7-dimethyl-, (E)-

2,6-OCTADIEN-1-OL; 3,7-DIMETHYL-; (E)-

2,6-Octadien-1-ol, 3,7-dimethyl-, (2E)-

InChI=1/C10H18O/c1-9(2)5-4-6-10(3)7-8-11/h5,7,11H,4,6,8H2,1-3H3/b10-7

The Henry's Law constant for geraniol is estimated as 1.15X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 3.0X10-2 mm Hg(1), and water solubility, 100 mg/L(2). This Henry's Law constant indicates that geraniol 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 3 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)(3) is estimated as 34 days(SRC). Geraniol's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Geraniol is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).
Literature: (1) Perry RH, Green D; Perry's Chemical Handbook. Physical and Chemical data. 6th ed., New York, NY: McGraw-Hill (1984) (2) Chem Inspect Test Inst; Biodegradation and Bioaccumulation Data of Existing Chemicals Based on the CSCL Japan; Published by Japan Chemical Industry Ecology-Toxicology & Information Center. ISBN 4-89074-101-1 (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 geraniol can be estimated to be 90(SRC). According to a classification scheme(2), this estimated Koc value suggests that geraniol 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 2, 2016: http://www2.epa.gov/tsca-screening-tools (2) Swann RL et al; Res Rev 85: 17-28 (1983)

GAIBLDCXCZKKJE-QRYCCKSOSA-N

Germacrene D

AC1NSVTC

V2I9ATG34E

UNII-V2I9ATG34E

C16142

CHEBI:49044

ZINC30730221

(-)-Germacrene D

23986-74-5

(-)-(S)-germacrene D

(-)-(7S)-germacrene-D

1(10),4(14),5-Germacratriene

(1E,6E,8S)-8-isopropyl-1-methyl-5-methylenecyclodeca-1,6-diene

(1E,6E,8S)-1-methyl-5-methylidene-8-propan-2-ylcyclodeca-1,6-diene

(1E,5E)-germacra-1(10),4(15),5-triene

(1E,6E,8S)-1-methyl-8-(1-methylethyl)-5-methylidenecyclodeca-1,6-diene

(1E,6E,8S)-1-methyl-5-methylidene-8-(propan-2-yl)cyclodeca-1,6-diene

1,6-Cyclodecadiene, 1-methyl-5-methylene-8-(1-methylethyl)-, (S-(E,E))-

OPFTUNCRGUEPRZ-QLFBSQMISA-N

AC1OCFDE

beta-Elemen

BETA-ELEMENE

Levo-beta-elemene

2QG8CX6LXD

UNII-2QG8CX6LXD

8064AH

SDP-111

CHEMBL448502

C17094

CHEBI:62855

ZINC14096289

E- .beta.-Elemene

2,4-Diisopropenyl-1-methyl-1-vinylcyclohexane

(-)-beta-Elemene

Epitope ID:153551

AKOS028108977

(-)-beta-Elemene, analytical standard

515-13-9

beta-Elemene, (-)-

33880-83-0

20296-36-0

11033-44-6

154028-29-2

1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-cyclohexane

(1S,2S,4R)-2,4-diisopropenyl-1-methyl-1-vinylcyclohexane

(1S,2S,4R)-(-)-1-methyl-1-vinyl-2,4-diisopropenylcyclohexane

Cyclohexane, 2,4-diisopropenyl-1-methyl-1-vinyl-, (1S,2S,4R)-

(1S,2S,4R)-1-ethenyl-1-methyl-2,4-bis(prop-1-en-2-yl)cyclohexane

(1S,2S,4R)-1-ethenyl-1-methyl-2,4-di(prop-1-en-2-yl)cyclohexane

(1S,2S,4R)-1-methyl-2,4-di(prop-1-en-2-yl)-1-vinylcyclohexane

Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1S,2S,4R)-

Cyclohexane, 1-ethenyl-1-methyl-2,4-bis(1-methylethenyl)-, (1S-(1-alpha,2-beta,4-beta))-

isodihydroagarofuran

Deoxyisobaimuxinol

Dihydroagarofuran

alpha-Dihydroagarofuran

Dihydro-alpha-agarofuran

20053-66-1

2H-3,9a-Methano-1-benzoxepin, octahydro-2,2,5a,9-tetramethyl-, (3R-(3alpha,5aalpha,9beta,9aalpha))-

Bicyclogermacrene

trans-Bicyclogermacradiene

VPDZRSSKICPUEY-IBYSFASBSA-N

(?)-Isolepidozene

(+)-bicyclogermacrene

OR325726

BICYCLO[8.1.0]UNDECA-2,6-DIENE, 3,7,11,11-TETRAMETHYL-,(1R,2E,6E,10S)-

JLPUXFOGCDVKGO-TUAOUCFPSA-N

GEOSMIN

AC1L1I2Q

MYW912WXJ4

UNII-MYW912WXJ4

SCHEMBL50009

C16286

OR238484

4,8a-Dimethyl-decahydronaphthalen-4a-ol

OR031361

4,8alpha-dimethyl-octahydro-naphthalen-4alpha-ol

CHEMBL2374043

CHEBI:46702

ZINC3870304

(-)-geosmin

LS-95000

trans-1,10-dimethyl-trans-decalol

Octahydro-4alpha,8abeta-dimethyl-4aalpha(2H)-naphthol

AKOS006282977

trans-1,10-Dimethyl-trans-9-decalol

4,8a-Dimethyloctahydro-4a(2H)-naphthalenol #

Octahydro-4,8a-dimethyl-4a(2H)-naphthalenol

NCGC00165950-01

EINECS 243-239-8

19700-21-1

4a-alpha-(2H)-Naphthol, octahydro-4-alpha,8a-beta-dimethyl-

(4S,4aS,8aR)-4,8a-dimethyloctahydronaphthalen-4a(2H)-ol

4a-alpha-(2H)-Naphthol, octahydro-4-alpha,8a-beta-dimethyl- (8CI)

(4S-(4alpha,4aalpha,8abeta))-Octahydro-4,8a-dimethyl-4a(2H)-naphthol

4a-.alpha.-(2H)-Naphthol, octahydro-4-.alpha.,8a-.beta.-dimethyl-

4a(2H)-Naphthalenol, octahydro-4,8a-dimethyl-,(4.alpha.,4a.alpha.,8a.beta.)-

4a(2H)-Naphthalenol, octahydro-4,8a-dimethyl-, (4S-(4-alpha,4a-alpha,8a-beta))-

(4S,4aS,8aR)-4,8a-dimethyl-1,2,3,4,5,6,7,8-octahydronaphthalen-4a-ol

4a(2H)-Naphthalenol, octahydro-4,8a-dimethyl-, [4S-(4.alpha.,4a.alpha.,8a.beta.)]-

CALARENE

MBIPADCEHSKJDQ-PBOSXPJTSA-N

17334-55-3

1H-Cyclopropa[a]naphthalene, 1a,2,3,5,6,7a,7b-octahydro-1,1,7,7a-tetramethyl-, 1aR-1a.alpha.,7.alpha.,7a.alpha.,7b.beta.

Germacradienol

ZVZPKUXZGROCDB-BRNABIDRSA-N

C16143

CHEBI:46734

CHEBI:80351

ZINC30730225

LMPR0103090009

(1E,5E)-Germacra-1(10),5-diene-11-ol

(1E,4S,5E,7R)-Germacra-1(10),5-dien-11-ol

2-[(1R,2E,4S,7E)-4,8-dimethylcyclodeca-2,7-dien-1-yl]propan-2-ol

Bicyclogermacren

Bicyclogermacrene

VPDZRSSKICPUEY-BFPRWLMKSA-N

VPDZRSSKICPUEY-QVIJUPDLSA-N

AC1NSSYM

.beta.-Cyclogermacrane

(+)-bicyclogermacrene

3,7,11,11-Tetramethylbicyclo[8.1.0]undeca-2,6-diene

3,7,11,11-Tetramethylbicyclo[8.1.0]undeca-2,6-diene #

(4E,8E)-4,8,11,11-tetramethylbicyclo[8.1.0]undeca-4,8-diene

(1S,2E,6E,10R)-3,7,11,11-tetramethylbicyclo[8.1.0]undeca-2,6-diene

Bicyclo[8.1.0]undeca-2,6-diene, 3,7,11,11-tetramethyl-, (1S,2E,6E,10R)-

Bicyclo[8.1.0]undeca-2,6-diene, 3,7,11,11-tetramethyl-, (E,E)-(1S,10R)-(+)-