Phenylmethanal benzenecarboxaldehyde

Benzenecarboxaldehyde

Phenylformaldehyde

PENTADEOTERO BENZALDEHYDE

benzanoaldehyde

Benzenecarbonal

Benzenemethylal

Benzylaldehyde

Phenylmethanal

Phenylmethanone

benzaidehyde

benzaldehvde

benzaldehyde

Benzene carboxaldehyde

Benzyaldehyde

Benzadehyde

benzaldehyd

Benzaldehyde Natural

Benzene carbaldehyde

Natural Benzaldehyde

Aromatic aldehyde

HUMNYLRZRPPJDN-UHFFFAOYSA-N

Benzaldehyde FFC

Benzaldehyde, analytical standard

Benzene methylal

Benzoic aldehyde

Benzoyl hydride

Almond artificial essential oil

Bitter almond

Artificial almond oil

Benzoic acid aldehyde

HBX

Artificial bitter almond oil

bitter almond oil synthetic

(phenyl)methanone

Artificial essential oil of almond

Ben zoyl hydride

Artifical essential oil of almond

2vj1

Benzaldehyde (natural)

Ethereal oil of bitter almonds

SCHEMBL573

Synthetic oil of bitter almond

AC1L18SM

AC1Q6PV7

Benzaldehyde [USAN]

Benzaldehyde, pharmaceutical secondary standard; traceable to USP

Bitter almond oil, synthetic

Oil Of bitter almond

Benzaldehyde (NF)

NATURAL RSTD CASSIA OIL DIST FLAVOR

WLN: VHR

Benzaldehyde, European Pharmacopoeia (EP) Reference Standard

KSC176K2J

ACMC-1C91Y

CHEMBL15972

LS-27

NSC7917

UN1990

B2379

BDBM60953

Benzaldehyde, United States Pharmacopeia (USP) Reference Standard

CTK0H6524

HMDB06115

HSDB 388

nchembio814-comp15

TA269SD04T

BIDD:ER0249

LS41490

RP18863

C00193

C00261

CCRIS 2376

D02314

DSSTox_CID_134

UNII-TA269SD04T

ZINC895145

AK109012

BENZALDEHYDE REACTION PRODUCTS WITH HEPTANAL DISTN. LIGHTS

DTXSID8039241

NA 1989

NSC 7917

NSC-7917

OR035988

OR192667

PL039416

A800226

Benzaldehyde, AR, >=99%

Benzaldehyde, LR, >=99%

CHEBI:17169

NCI-C56133

AJ-24149

ANW-14310

DSSTox_GSID_39241

SC-19173

BDBM50139371

Caswell No. 076

DSSTox_RID_79432

MFCD00003299

MFCD00801585

ZINC00895145

AI3-09931

Benzaldehyde, purified by redistillation, >=99.5%

Benzaldehyde, ReagentPlus(R), >=99%

DB-023673

KB-250682

LT00939687

ST24030100

TC-103055

AKOS000119172

EPA Pesticide Chemical Code 008601

ghl.PD_Mitscher_leg0.170

I01-1667

I14-7330

FEMA No. 2127

FT-0622622

Benzaldehyde, >=98%, FG, FCC

Benzaldehyde, for synthesis, 95.0%

I14-90980

Benzaldehyde, 98% 250g

Benzaldehyde, SAJ special grade, >=98.0%

Tox21_113069

Tox21_113244

Tox21_200634

100-52-7

Ald3-H_000012

Benzaldehyde, Vetec(TM) reagent grade, 98%

F1294-0144

MCULE-7744113682

NCGC00091819-01

NCGC00091819-02

NCGC00091819-03

NCGC00258188-01

Benzaldehyde, natural, >=98%, FCC, FG

CAS-100-52-7

EINECS 202-860-4

55279-75-9

SR-01000944375

Ald3.1-H_000160

Ald3.1-H_000479

Ald3.1-H_000798

5044-EP2269979A1

5044-EP2269990A1

5044-EP2272491A1

5044-EP2272827A1

5044-EP2275404A1

5044-EP2275411A2

5044-EP2275412A1

5044-EP2277858A1

5044-EP2277865A1

5044-EP2277878A1

5044-EP2281818A1

5044-EP2284157A1

5044-EP2286915A2

5044-EP2287152A2

5044-EP2287159A1

5044-EP2289868A1

5044-EP2292593A2

5044-EP2295402A2

5044-EP2295410A1

5044-EP2295441A2

5044-EP2298767A1

5044-EP2298776A1

5044-EP2301534A1

5044-EP2301536A1

5044-EP2301538A1

5044-EP2305625A1

5044-EP2305629A1

5044-EP2305662A1

5044-EP2305679A1

5044-EP2305687A1

5044-EP2305769A2

5044-EP2305808A1

5044-EP2308562A2

5044-EP2311451A1

5044-EP2311455A1

5044-EP2311806A2

5044-EP2311840A1

5044-EP2314295A1

5044-EP2314586A1

5044-EP2314587A1

5044-EP2314593A1

5044-EP2316450A1

5044-EP2316832A1

5044-EP2316833A1

5044-EP2371831A1

5044-EP2374454A1

5044-EP2374783A1

5044-EP2377841A1

5044-EP2380871A1

Benzaldehyde, purum, >=98.0% (GC)

53585-EP2305651A1

53585-EP2308854A1

Benzaldehyde [UN1990] [Class 9]

Benzaldehyde on polystyrene, 0.8-1.5 mmol/g

125826-EP2287158A1

125826-EP2295422A2

SR-01000944375-1

Benzaldehyde [UN1990] [Class 9]

Benzaldehyde, puriss. p.a., >=99.0% (GC)

InChI=1/C7H6O/c8-6-7-4-2-1-3-5-7/h1-6

The Henry's Law constant for benzaldehyde is 2.67X10-5 atm-cu m/mole(1). This Henry's Law constant indicates that benzaldehyde 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 1.5 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 14 days(SRC). Benzaldehyde's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Benzaldehyde is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.27 mm Hg at 25 deg C(3).
Literature: (1) Betterton EA, Hoffmann MR; Environ Sci Technol 22: 1415-8 (1988) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Ambrose D et al; J Chem Therm 7: 1143-57 (1975)

Using a structure estimation method based on molecular connectivity indices(1), the Koc of benzaldehyde can be estimated to be 11(SRC). According to a classification scheme(2), this estimated Koc value suggests that benzaldehyde is expected to have very high mobility in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of May 30, 2016: http://www2.epa.gov/tsca-screening-tools/ (2) Swann RL et al; Res Rev 85: 17-28 (1983)

octylalcohol

KBPLFHHGFOOTCA-UHFFFAOYSA-N

caprylic alcohol

Heptyl carbinol

octanol

Octilin

Capryl alcohol

Octyl alcohol

octyl-alcohol

Primary octyl alcohol

1-Hydroxyoctane

1-hydroxyoctyl

n-Caprylic alcohol

N-octanol

Octyl alcohol normal-primary

AC1L1AEQ

n-Capryl alcohol

n-Heptyl carbinol

OC9

Alcohol C8

C8 alcohol

n-Octyl alcohol

N-octyl-alcohol

1-octanol

1-Oktanol

Lorol C8

Octyl alcohol, primary

Sipol L8

1-Octyl alcohol

2-Capryl alcohol

AC1Q2WB6

Alfol 8

EPAL 8

Octyl alcohol, normal-primary

Off-Shoot T

Off-shoot-T

Prim-n-octyl alcohol

SCHEMBL8822

1-Octanol, analytical standard

Alcohol C-8

Alcohol, C8

Fair 85

GTPL4278

KSC176Q9D

Lorol 20

CHEMBL26215

NSC9823

Octan-1-ol

Octyl alcohol (natural)

BDBM22606

c0045

CTK0H6891

Fatty alcohol(C8)

HMDB01183

HSDB 700

O0036

O0212

Octanol (all isomers)

WLN: Q8

Dytol M-83

RL00475

2-Octanol ~99%

bmse000970

bmse000980

C00756

C6-12 Alcohols

CCRIS 9099

Emery 3322

Emery 3324

HMS3039O07

n-Octan-1-ol

C6-C12 Alkyl alcohol

DTXSID7021940

FEMA Number 2800

LP064439

LP069551

LS-2996

NSC 9823

NSC-9823

octan-1-ol;

Octanol-(1)

OR000625

SBB059902

STL264193

UNII-6X61I5U3A4 component KBPLFHHGFOOTCA-UHFFFAOYSA-N

ACMC-2099b5

CHEBI:16188

DSSTox_CID_1940

ZINC1532735

AN-43095

ANW-16335

BP-21329

Caswell No. 456E

Caswell No. 611A

DSSTox_GSID_21940

EBD2203381

NV1779205D

TRA0009495

Alcohols, C6-12

DSSTox_RID_76416

LMFA05000130

MFCD00002988

AI3-02169

Lorol C 8-98

RTR-002327

ST51046170

TR-002327

UNII-NV1779205D

1-Octanol, ACS spectrophotometric grade, >=99%

AKOS000120100

EPA Pesticide Chemical Code 079029

EPA Pesticide Chemical Code 079037

J-002650

1-Octanol, anhydrous, >=99%

FEMA No. 2800

FT-0608179

MLS001055318

SMR000673567

I14-17870

(C6-C12) Alkyl alcohol

Tox21_201373

Tox21_300096

1-Octanol, ACS reagent, >=99%

111-87-5

F0001-0248

Mixed fatty alcohols (C6-C12)

Z1262253001

1-Octanol, for HPLC, >=99%

MCULE-2656577895

NCGC00091003-01

NCGC00091003-02

NCGC00091003-03

NCGC00091003-04

NCGC00091003-05

NCGC00254099-01

NCGC00258924-01

Octan-2-ol 98+ %

CAS-111-87-5

EINECS 203-917-6

EINECS 266-920-1

EINECS 271-642-9

1-Octanol, natural, >=98%, FCC

1-Octanol, ReagentPlus(R), 99%

12676-73-2

67700-96-3

68603-15-6

SDA 13-060-00

220713-26-8

1-Octanol, >=98%, FCC, FG

1-Octanol, 99% 500ml

MolPort-001-787-163

1-Octanol, JIS special grade, >=98.0%

1-Octanol, SAJ first grade, >=75.0%

1-Octanol, Vetec(TM) reagent grade, 98%

81301-EP2270018A1

81301-EP2272817A1

81301-EP2289891A2

81301-EP2305687A1

81301-EP2305825A1

81301-EP2380568A1

Alcohols, C8-18 and C18-unsatd.

103517-EP2270018A1

103517-EP2275416A1

103517-EP2287158A1

103517-EP2298313A1

103517-EP2301924A1

(C8-C18) and (C18) Unsaturatedalkyl alcohol

1-Octanol, puriss., >=99.5% (GC)

958E4752-AAC3-4F72-A0BF-02D95F9E8071

InChI=1/C8H18O/c1-2-3-4-5-6-7-8-9/h9H,2-8H2,1H

The Henry's Law constant for 1-octanol is reported as 2.5X10-5 atm-cu m/mole(1). This Henry's Law constant indicates that 1-octanol 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 43 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 17 days(SRC). 1-Octanol's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 1-Octanol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.0794 mm Hg(3).
Literature: (1) Yaws CL et al; Waste Manag 17: 541-7 (1997) (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; Data Compilation, Tables of Properties of Pure Cmpds, Design Inst for Phys Prop Data, Am Inst for Phys Prop Data, New York, NY (1989)

The Koc of 1-octanol is reported as 38(1). According to a classification scheme(2), this Koc value suggests that 1-octanol is expected to have very high mobility in soil(SRC).
Literature: (1) Schuumann G et al; Environ Sci Technol 40 :7005-11 (2006) (2) Swann RL et al; Res Rev 85: 17-28 (1983)

CDOSHBSSFJOMGT-UHFFFAOYSA-N

Linalool

Linanool

Linolool

Linalol

Linalool, primary pharmaceutical reference standard

LINALYL ALCOHOL

Natural Linalool

Phantol

allo-Ocimenol

beta-Linalool

Linalool, analytical standard

Howood Oil

p-Linalool

AC1L1MRY

AC1Q1NVD

AC1Q1NVE

Linalool ex orange oil

AC1Q2BP3

Linalool (natural)

Linalool ex ho oil

.beta.-Linalool

GTPL2469

KSC377K8J

LINALOOL EX BOIS DE ROSE

CHEMBL25306

NSC3789

SCHEMBL20316

(S)-Linalol

CTK2H7584

HSDB 645

L0048

Linalool, 97%

LINOLOOL (D)

AC-551

ACMC-209pf1

Linalool ex bois de rose oil

RP21877

C03985

CCRIS 3726

CCRIS 6557

HMS2268E18

Linalool, .beta.

Linalool, certified reference material, TraceCERT(R)

BBL027734

BC207603

BT000180

DTXSID7025502

FEMA Number 2635

LP067292

LS-1752

NSC 3789

NSC-3789

OR341488

SBB012353

ST069326

STL373777

( )-linalool

CHEBI:17580

DSSTox_CID_5502

AK-50127

AN-15757

AN-22986

ANW-37211

Caswell No. 526A

DSSTox_GSID_25502

FCH1115719

LS-97796

SC-74998

BB_NC-0123

DSSTox_RID_77812

MFCD00008906

AI3-00942

DB-062552

KB-179981

RTR-030706

TR-030706

WLN: 1U1XQ1&3UY1&1

( -)-Linalool

(+-)-Linalool

AKOS015901617

BB_NC-00123

EPA Pesticide Chemical Code 128838

Q-201306

2,7-octadiene-6-ol

3,6-octadien-3-ol

BRN 1721488

FEMA No. 2635

FT-0614785

MLS002152908

SMR000112394

78-70-6

I14-13929

2,7-dien-6-ol

3,6-dien-3-ol

Tox21_201658

Tox21_303037

(+/-) LINALOOL

Linalool, >=97%, FCC, FG

CAS-78-70-6

MCULE-2407576698

NCGC00091688-01

NCGC00091688-02

NCGC00091688-03

NCGC00091688-04

NCGC00257060-01

NCGC00259207-01

EINECS 201-134-4

EINECS 204-811-2

EINECS 245-083-6

11024-20-7

22564-99-4

LINALOOL, (+-)-

EC 201-134-4

MolPort-001-783-101

(.+/-.)-Linalool

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

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

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

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

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

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

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

CU-01000013132-2

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

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

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

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

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

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

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

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

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

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

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

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

1,6-Octadien-3-ol, 3,7-dimethyl-, (R)-

1,6-Octadien-3-ol, 3,7-dimethyl-, (3R)-

1,6-Octadien-3-ol, 3,7-dimethyl-, (3S)-

1,6-OCTADIEN-3-OL, 3,7-DIMETHYL-, (-)-

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)

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)

DDIZAANNODHTRB-UHFFFAOYSA-N

methyl4-methoxybenzoate

Methyl p-methoxybenzoate

Methyl anisate

METHYL 4-METHOXYBENZOATE

4-methoxy methylbenzoate

METHYL PARA-ANISATE

Methyl p-anisate

methyl P-methoxy benzoate

Methyl-p-anisate

Methyl-p-Methoxy Benzoate

p-Methoxybenzoic acid methyl ester

ANISIC ACID METHYL ESTER

4-Methoxybenzoic acid methyl

4-(Methoxycarbonyl)anisole

Methyl 4-Anisate

AC1L1R4M

Methyl ester of p-Methoxybenzoic acid

4-Methoxybenzoic acid methyl ester

p-Anisic acid methyl ester

KSC119E6R

NSC7324

ACMC-209ajc

ZINC87933

4-methoxy-benzoic acid methyl ester

SCHEMBL231243

AS02499

ARONIS011593

RP22885

p-Anisic acid, methyl ester

2MFL7873W9

FEMA 2679

bmse010016

AN-9346

NSC 7324

ZB003141

DTXSID7047645

NSC-7324

OR011231

OR209324

SY003911

STK041805

AC-7084

CHEMBL1762668

SBB058204

LS-2900

M-5922

CHEBI:86903

UNII-2MFL7873W9

WLN: 1OVR DO1

SC-24120

KB-54413

AJ-10791

BR-46595

ST2413419

AK-46595

CJ-00703

Methyl p-anisate, 99%

DSSTox_GSID_47645

ANW-17926

DSSTox_CID_27645

RARECHEM AL BF 0083

MFCD00008437

ZINC00087933

BDBM50340087

DSSTox_RID_82472

TR-003554

DB-012814

AM20050128

RTR-003554

ST45048310

AI3-00229

AKOS000501135

I01-8152

W-108443

BRN 2208571

Benzoic acid, p-methoxy-, methyl ester

FT-0628647

FEMA No. 2679

LABOTEST-BB LT00782008

Tox21_302682

Methyl p-anisate, >=99%, FG

F1335-0002

Benzoic acid, 4-methoxy-, methyl ester

121-98-2

MCULE-7764530900

Methyl p-anisate, >=99% (capillary GC)

NCGC00256751-01

CAS-121-98-2

EINECS 204-513-2

MolPort-000-690-489

AQ-917/40232598

InChI=1/C9H10O3/c1-11-8-5-3-7(4-6-8)9(10)12-2/h3-6H,1-2H

Amylethylcarbinol

Ethylamylcarbinol

Ethylhexyl alcohol

NMRPBPVERJPACX-UHFFFAOYSA-N

Ethyl-n-amylcarbinol

1-Ethylhexanol

Ethyl amyl carbinol

Amyl ethyl carbinol

AC1L1XJY

3-OCTANOL

Octanol, mixed isomers

Octanol-3

D-n-Octanol

ACMC-20apgg

3-Octyl Alcohol

Octyl alcohol, mixed isomers

ACMC-1BL6Z

3-Octanol, analytical standard

dl-3-Octanol

8768AB

Octan-3-ol

CTK1H2870

O0121

CHEMBL487998

SCHEMBL112339

n-Octan-3-ol

C17144

AK116654

LS-2998

LP084019

3-Octanol (natural)

OR019894

SBB059904

CHEBI:80945

A814407

ANW-33110

AN-25289

AN-21522

LS-98139

MFCD00004590

(S)-3-Octanol

LMFA05000568

3-Octanol, 99%

TR-037191

ST51046171

ST24048830

KB-183851

AI3-37213

AKOS009156959

I14-1163

I14-6310

FT-0616281

BRN 1697461

FT-0616280

FEMA No. 3581

589-98-0

(1)-Octan-3-ol

MCULE-6682377557

EINECS 209-667-4

EINECS 249-405-6

EINECS 243-713-4

29063-28-3

20296-29-1

3-Octanol, >=97%, FCC, FG

MolPort-001-759-253

3-Octanol, natural, >=97%, FCC, FG

4-01-00-01756 (Beilstein Handbook Reference)

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)

Pentylvinylcarbinol

Amylvinylcarbinol

Flowtron mosquito attractant

VSMOENVRRABVKN-UHFFFAOYSA-N

Matsutake alcohol

Morillol

Matsuica alcohol

Matsuika alcohol

Mushroom alcohol

Vinyl hexanol

Vinyl pentyl carbinol

Pentyl vinyl carbinol

Vinyl amyl carbinol

Amyl vinyl carbinol

1-Vinylhexanol

AC1L2CVX

ACMC-20apfw

Matsutake alcohol [Japanese]

ACMC-1CNY7

KSC223I9P

Octen-3-ol

SCHEMBL41968

CTK1C3497

O0159

ACT05316

NSC87563

3-Hydroxy-1-octene

C14272

CCRIS 8804

OR020369

DTXSID3035214

Jsp006175

LP030603

LS-3002

WLN: QY5&1U1

CHEMBL3183573

AK164470

1-Octene-3-ol

octene-1-ol-3

CHEBI:34118

AN-18986

1-Okten-3-ol

NSC-87563

NSC 87563

SC-18002

ANW-27735

TRA0097596

DSSTox_GSID_35214

1-OCTEN-3-OL

1 Octen 3 OL

DSSTox_CID_15214

LMFA05000090

DSSTox_RID_79250

MFCD00004589

RTC-020285

DB-003193

AI3-28627

TC-020285

I14-1194

Q-100412

1-Octen-3-ol, analytical standard

EPA Pesticide Chemical Code 069037

AKOS009157412

Oct-1-ene-3-ol

I14-1157

1 -Octen-3-ol

Oct-1-en-3-ol

FEMA No. 2805

FT-0608181

BRN 1744110

Nat. 1-Octen-3-ol

Tox21_302039

n-Oct-1-en-3-ol

1-Octen-3-ol (natural)

NCGC00255686-01

1-Okten-3-ol [Czech]

3191-86-4

3391-86-4

EINECS 222-226-0

1-Octen-3-ol, 98%

50999-79-6

CAS-3391-86-4

MolPort-001-782-881

1-Octen-3-ol, natural, >=95%, FG

1-Octen-3-ol, 98% 10g

1-Octen-3-ol, >=98%, FCC, FG