Linalool

78-70-6

3,7-Dimethylocta-1,6-dien-3-ol

Linalol

LINALYL ALCOHOL

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

allo-Ocimenol

beta-Linalool

(+-)-Linalool

Phantol

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

p-Linalool

Linanool

Linolool

(+/-)-linalool

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

2,6-Dimethylocta-2,7-dien-6-ol

.beta.-Linalool

2,6-Dimethyl-2,7-octadiene-6-ol

FEMA No. 2635

NSC 3789

(RS)-Linalool

DIABEXALL

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

CHEBI:17580

LINALOOL, DL-

NSC-3789

3,7-dimethyl-octa-1,6-dien-3-ol

D81QY6I88E

DTXSID7025502

LINALOOL, (+/-)-

NSC3789

L 260-2

MFCD00008906

Linalool 1000 microg/mL in Isopropanol

LINALOOL (USP-RS)

LINALOOL [USP-RS]

(+/-)-3,7-Dimethyl-3-hydroxy-1,6-octadiene

Licareol

22564-99-4

Linalool (natural)

DTXCID305502

Caswell No. 526A

(S)-Linalol

dl-Linalool

FEMA Number 2635

CAS-78-70-6

CCRIS 6557

HSDB 645

EINECS 201-134-4

EINECS 245-083-6

EPA Pesticide Chemical Code 128838

BRN 1721488

UNII-D81QY6I88E

AI3-00942

Linalool b

|A-Linalool

Linalool, .beta.

Linalool,(S)

( )-linalool

Linalool, 97%

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

LINALOOL OIL

3,6-octadien-3-ol

2,7-octadiene-6-ol

LINALOOL [FHFI]

LINALOOL [HSDB]

LINALOOL [INCI]

LINALOOL [FCC]

2,7-dien-6-ol

3,6-dien-3-ol

dl-3,7-Dimethyl-3-hydroxy-1,6-octadiene

LINALOOL [MI]

LINOLOOL (D)

(.+/-.)-Linalool

LINALOOL [WHO-DD]

EC 201-134-4

SCHEMBL20316

Linalool, analytical standard

0-01-00-00462 (Beilstein Handbook Reference)

MLS002152908

CHEMBL25306

LINALOOL, (+-)-

GTPL2469

NDI 595 [FDMS]

FEMA 2635

NDI 595

HMS2268E18

HMS3886G07

Linalool, >=97%, FCC, FG

1, 3,7-dimethyl-, (-)-

HY-N0368

WLN: 1U1XQ1&3UY1&1

Tox21_201658

Tox21_303037

AC-551

BBL027734

BDBM50459894

MFCD09025547

s4957

STL373777

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

AKOS015901617

( inverted exclamation markA)-Linalool

CCG-266253

MCULE-2407576698

NCGC00091688-01

NCGC00091688-02

NCGC00091688-03

NCGC00091688-04

NCGC00257060-01

NCGC00259207-01

AS-56047

SMR000112394

SY264412

WLN: 1Y1&U3XQ1&1U1 -,-

DB-062552

(+/-)-3,7-Dimethyl-1,6-octadien-3-ol

CS-0008916

L0048

NS00005142

C03985

EN300-174564

F17676

Linalool, primary pharmaceutical reference standard

Q410932

CU-01000013132-2

Q-201306

Linalool, certified reference material, TraceCERT(R)

Z1255402668

The Henry's Law constant for linalool is 2.15X10-5 atm-cu m/mole at 25 deg C(1). This Henry's Law constant indicates that linalool 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 54 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 20 days(SRC). Linalool's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Linalool exists as a liquid environmentally at standard temperature and pressure, therefore, it is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.159 mm Hg(3).
Literature: (1) Altschuh J et al; Chemosphere 39: 1871-87 (1999) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Li J et al; Environ International 24: 353-58 (1998)

Using a structure estimation method based on molecular connectivity indices(1), the Koc of linalool can be estimated to be 75(SRC). According to a classification scheme(2), this estimated Koc value suggests that linalool 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 Nov 20, 2015: http://www2.epa.gov/tsca-screening-tools (2) Swann RL et al; Res Rev 85: 17-28 (1983)

CAMPHENE

79-92-5

Comphene

2,2-Dimethyl-3-methylenenorbornane

(+/-)-Camphene

DL-Camphene

3,3-Dimethyl-2-methylenenorbornane

3,3-Dimethyl-2-methylenenorcamphane

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

FEMA No. 2229

2,2-Dimethyl-3-methylenebicyclo[2.2.1]heptane

565-00-4

Bicyclo[2.2.1]heptane, 2,2-dimethyl-3-methylene-

CCRIS 3783

HSDB 900

NSC 4165

3,3-Dimethyl-2-methylenenorcamphene

EINECS 201-234-8

EINECS 209-275-3

UNII-G3VG94Z26E

CHEBI:3830

G3VG94Z26E

DTXSID8026488

AI3-01775

CAMPHENE, DL-

NSC-4165

2,2-Dimethyl-3-methylenebicyclo(2.2.1)heptane

Camphene (2,2-dimethyl-3-methylene-norbornane)

Bicyclo(2.2.1)heptane, 2,2-dimethyl-3-methylene-

DTXCID006488

CAMPHENE, (+/-)-

Camphene, (1R,4S)-(+)-

EC 201-234-8

(1)-2,2-Dimethyl-3-methylenebicyclo(2.2.1)heptane

CAMPHENE (MART.)

CAMPHENE [MART.]

Bicyclo[2.2.1]heptane, 2,2-dimethyl-3-methylene-, (1R)-

CAS-79-92-5

2,2-dimethyl-3-methylidenebicyclo(2.2.1)heptane

MFCD00066603

2,2-dimethyl-3-methylene-norbornane

CAMPHENE [FHFI]

CAMPHENE [HSDB]

CAMPHENE [INCI]

CAMPHENE [FCC]

CAMPHENE [MI]

2,2-Dimethyl-3-methylenebicyclo[2.2.1]heptane #

CAMPHENE, D,L-

3,3-Dimethylenenorcamphene

CAMPHENE [WHO-DD]

Bicyclo-(2.2.1)heptane

2,2-Dimethyl-3-methylene-

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

CHEMBL2268550

2,2-Dimethyl-3-methylenebicyclo

NSC4165

2,2-Dimethyl-3-methylene-norborane

Tox21_202014

Tox21_303152

BBL033861

STK801857

AKOS004119935

CCG-266137

MCULE-1011863584

NCGC00249149-01

NCGC00257126-01

NCGC00259563-01

WLN: L55 A CYTJ CU1 D1 D1

VS-12317

2,2-DIMETHYL-3-METHYLENE NORBORANE

DB-053130

DB-056393

DB-057848

NS00006622

3,3-DIMETHYL-2-METHYLENE NORCAMPHANE

EN300-20391

(1R,4S)-2,2-dimethyl-3-methylene-norbornane

C06076

E87135

Bicyclo[2.2.1]heptane,2-dimethyl-3-methylene-

Q416775

SR-01000944833

Bicyclo(2.2.1)heptane, 2,2-dimethyl-3-methylene

SR-01000944833-1

CAMPHENE(2,2-DIMETHYL-3-METHYLENE-NORBORNANE)

Z104478010

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)

ALPHA-PINENE

80-56-8

2-Pinene

Acintene A

.alpha.-Pinene

2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene

pin-2(3)-ene

Pinene isomer

alfa-Pinene

Sylvapine A

PINENE, ALPHA

(+/-)-alpha-Pinene

(+/-)-2-Pinene

NSC 7727

pin-2-ene

Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-

Leavo-95

DTXSID4026501

CHEBI:36740

(+-)-2-pinene

NSC-7727

2,6,6-Trimethylbicyclo(3.1.1)-2-hept-2-ene

PC-500(TERPENE)

FEMA No. 2902

alpha-Pinene (natural)

2437-95-8

FEMA Number 2902

DTXCID006501

4,6,6-Trimethylbicyklo(3,1,1)hept-3-en

2,6,6-Trimethylbicyclo(3.1.1)hept-2-ene

(1R)-(+)-alpha-Pinene

NSC94522

NSC94523

CCRIS 697

PC-500

HSDB 720

NCGC00090682-01

(-)-?-Pinene

DL-Pin-2(3)-ene

EINECS 201-291-9

EINECS 219-445-9

UNII-JPF3YI7O34

BRN 3194807

(1R)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene

25766-18-1

AI3-24594

Bicyclo(3.1.1)hept-2-ene, 2,6,6-trimethyl

1S-.alpha.-Pinene

CAS-80-56-8

2,6,6-Trimethylbicyclo(3.1.1)-2-heptene

2,6,6-Trimethylbicyclo[3.1.1]-2-heptene

EC 201-291-9

4-05-00-00456 (Beilstein Handbook Reference)

alphapinene

alpha pinene

an alpha-pinene

Cyclic dexadiene

alpha -pinene

alpha.-pinene

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

Acitene A

(-)alpha-pinene

Pinene, .alpha.

alpha [D] Pinene

alpha [L] Pinene

AUSTRALENE

(+-)-alpha-pinene

1R-.alpha.-Pinene

2,6,6-trimethyl-bicyclo[3.1.1]hept-2-ene

(R)-.alpha.-Pinene

PINENE (ALPHA)

? PINENE

(1S)-2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene

PINENE, ALPHA (D)

PINENE, ALPHA (L)

Pesticide Code: 067004.

(.+/-.)-.alpha.-Pinene

alpha-PINENE, (+/-)-

CHEMBL442565

NSC7727

alpha-Pinene (+/-)-alpha-Pinene

AMY22338

Tox21_110996

Tox21_200108

Tox21_303385

NSC-94522

NSC-94523

PC 500

AKOS000121239

AB86235

AB86464

AB93066

DB15573

MCULE-3589656574

UN 2368

NCGC00090682-02

NCGC00257379-01

NCGC00257662-01

LS-13835

Trimethyl Bicyclo (3.1.1) hept-2-ene

2,6-Trimethylbicyclo[3.1.1]-2-heptene

DB-017892

Bicyclo[3.1.1]hept-2-ene,6,6-trimethyl-

NS00067073

2,6-Trimethylbicyclo[3.1.1]-2-hept-2-ene

EN300-21685

C09880

A839247

Q-201582

(3Z)-5-METHYL-1H-INDOLE-2,3-DIONE3-OXIME

Q27104380

2,6,6-TRIMETHYLBICYCLO (3.1.1)HEPT-2-ENE, 9CL

BICYCLO(3.1.1)HEPT-2-ENE,2,6,6-TRIMETHYL-2-PINENE

Bicyclo[3.1.1]hept-2-ene, 2,6,6-trimethyl-, (.+/-.)-

(+/-)-2-Pinene, 2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene, alpha-Pinene

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)