benzaldehyde

100-52-7

Benzoic aldehyde

Phenylmethanal

Benzenecarboxaldehyde

Benzenecarbonal

Benzenemethylal

Benzaldehyde FFC

Benzene carbaldehyde

Benzene carboxaldehyde

benzanoaldehyde

Benzylaldehyde

Benzoyl hydride

NCI-C56133

Benzoic acid aldehyde

FEMA No. 2127

Caswell No. 076

Phenylformaldehyde

Benzaldehyde (natural)

NSC 7917

Benzadehyde

Benzyaldehyde

CCRIS 2376

HSDB 388

NSC-7917

EINECS 202-860-4

UNII-TA269SD04T

Benzaldehyde-carbonyl-13C

Benzaldehyde [NF]

EPA Pesticide Chemical Code 008601

Benzaldehyde-formyl-d

TA269SD04T

Benzaldehyde-alpha-d1

DTXSID8039241

CHEBI:17169

AI3-09931

MFCD00003299

8013-76-1

Benzaldehyde, methyl-

CHEMBL15972

DTXCID90134

NSC7917

EC 202-860-4

Phenylmethanal benzenecarboxaldehyde

Benzaldehyde (NF)

NCGC00091819-01

NCGC00091819-02

BENZALDEHYDE (II)

BENZALDEHYDE [II]

BENZALDEHYDE (MART.)

BENZALDEHYDE [MART.]

benzaldehyd

Benzaldhyde

BENZALDEHYDE (USP IMPURITY)

BENZALDEHYDE [USP IMPURITY]

BDBM50139371

CAS-100-52-7

FENTANYL IMPURITY E (EP IMPURITY)

FENTANYL IMPURITY E [EP IMPURITY]

TRIBENOSIDE IMPURITY C (EP IMPURITY)

TRIBENOSIDE IMPURITY C [EP IMPURITY]

BENZYL ALCOHOL IMPURITY A (EP IMPURITY)

BENZYL ALCOHOL IMPURITY A [EP IMPURITY]

FENTANYL CITRATE IMPURITY E (EP IMPURITY)

FENTANYL CITRATE IMPURITY E [EP IMPURITY]

AMFETAMINE SULFATE IMPURITY D (EP IMPURITY)

AMFETAMINE SULFATE IMPURITY D [EP IMPURITY]

UN1990

BENZALKONIUM CHLORIDE IMPURITY B (EP IMPURITY)

BENZALKONIUM CHLORIDE IMPURITY B [EP IMPURITY]

GLYCOPYRRONIUM BROMIDE IMPURITY F (EP IMPURITY)

GLYCOPYRRONIUM BROMIDE IMPURITY F [EP IMPURITY]

HYDROUS BENZOYL PEROXIDE IMPURITY A (EP IMPURITY)

HYDROUS BENZOYL PEROXIDE IMPURITY A [EP IMPURITY]

benzaidehyde

benzaldehvde

benzaldehye

benzaldeyde

BENZOYLL PEROXIDE HYDROUS IMPURITY A (EP IMPURITY)

BENZOYLL PEROXIDE HYDROUS IMPURITY A [EP IMPURITY]

C7H6O

phenyl-methanone

Benzene methylal

Aromatic aldehyde

Benzoylwasserstoff

(phenyl)methanone

benzenecarbaldehyde

Benzaldehyde,(S)

PhCHO

Benzene carcaboxaldehyde

2vj1

WLN: VHR

BENZALDEHYDE [MI]

SCHEMBL573

BENZALDEHYDE [FCC]

BENZALDEHYDE [FHFI]

BENZALDEHYDE [HSDB]

BENZALDEHYDE [INCI]

BENZALDEHYDE [VANDF]

ghl.PD_Mitscher_leg0.170

BENZALDEHYDE [USP-RS]

Benzaldehyde, AR, >=99%

Benzaldehyde, LR, >=99%

BIDD:ER0249

BDBM60953

Benzaldehyde, analytical standard

Ald3-H_000012

Benzaldehyde, >=98%, FG, FCC

Ald3.1-H_000160

Ald3.1-H_000479

Ald3.1-H_000798

Tox21_113069

Tox21_113244

Tox21_200634

s5574

STL194067

Benzaldehyde, for synthesis, 95.0%

AKOS000119172

Benzaldehyde [UN1990] [Class 9]

CCG-266041

MCULE-7744113682

NA 1989

Benzaldehyde, purum, >=98.0% (GC)

Benzaldehyde, ReagentPlus(R), >=99%

NCGC00091819-03

NCGC00258188-01

PS-11959

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

DB-023673

B2379

Benzaldehyde, SAJ special grade, >=98.0%

NS00008510

Benzaldehyde, Vetec(TM) reagent grade, 98%

Benzaldehyde 1000 microg/mL in Dichloromethane

Benzaldehyde 2000 microg/mL in Dichloromethane

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

C00193

C00261

D02314

A800226

Q372524

SR-01000944375

Benzaldehyde, purified by redistillation, >=99.5%

SR-01000944375-1

F1294-0144

Flavor and Extract Manufacturers' Association No. 2127

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

Benzaldehyde, European Pharmacopoeia (EP) Reference Standard

Benzaldehyde, United States Pharmacopeia (USP) Reference Standard

Benzaldehyde, Pharmaceutical Secondary Standard; Certified Reference Material

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)

m-cresol

3-methylphenol

108-39-4

Metacresol

Phenol, 3-methyl-

meta-cresol

3-cresol

3-hydroxytoluene

m-methylphenol

m-kresol

m-cresylic acid

1-hydroxy-3-methylbenzene

m-oxytoluene

m-toluol

m-Hydroxytoluene

meta-cresylic acid

1-Methyl-3-hydroxybenzene

Cresol, m-

FEMA No. 3530

hydroxy-3-methylbenzene

CRESOL, META

m-cresylic

m-Cresole

3-methyl-1-hydroxybenzene

NSC 8768

GGO4Y809LO

CHEMBL298312

DTXSID6024200

CHEBI:17231

NSC-8768

m-Cresol, 99%

TOLUENE,3-HYDROXY (META-CRESOL)

Franklin Cresolis

Metacresol (3-Methylphenol)

CRS

m-Kresol [German]

DTXCID804200

Rover's Dog Shampoo

Caswell No. 261A

meta cresol

3-methyl phenol

Cresol, m-isomer

CAS-108-39-4

CCRIS 645

HSDB 1815

Metacresol [USP:BAN]

EINECS 203-577-9

Metacresol; 3-Methylphenol; Amylmetacresol Impurity B

UNII-GGO4Y809LO

EPA Pesticide Chemical Code 022102

3methylphenol

AI3-00136

3-methyl-phenol

Cresol,m-

m-Cresol;

Celcure Dry Mix (chemicals for wood preserving)

Metacresol (USP)

METACRESOL [II]

M-CRESOL [INCI]

METACRESOL [HSDB]

bmse000350

EC 203-577-9

M-CRESOL [WHO-DD]

METACRESOL [USP-RS]

WLN: QR C1

SCHEMBL10736

m-Cresol, analytical standard

m-Cresol, >=98%, FG

SCHEMBL7410931

m-Cresol, for synthesis, 99%

m-Cresol, reagent grade, 97%

METACRESOL [EP IMPURITY]

DTXSID00165845

DTXSID10194060

METACRESOL [EP MONOGRAPH]

METACRESOL [USP IMPURITY]

NSC8768

METACRESOL [USP MONOGRAPH]

3-Methylphenol, analytical standard

Tox21_201941

Tox21_302645

2-TERT-BUTYL-5-METHYL PHENO

BDBM50008548

MFCD00002302

STL185666

AKOS000119006

AM62795

CCG-230271

DB01776

MCULE-6836106503

NCGC00159366-02

NCGC00159366-03

NCGC00159366-04

NCGC00159366-05

NCGC00159366-06

NCGC00256824-01

NCGC00259490-01

AC-14350

BS-23591

m-Cresol, SAJ first grade, >=97.0%

3-Methylphenol 100 microg/mL in Methanol

m-Cresol [UN2076] [Poison, Corrosive]

NS00010658

EN300-19428

AMYLMETACRESOL IMPURITY B [EP IMPURITY]

C01467

D04951

A801870

Q312240

J-002137

J-521679

F0001-0167

Z104473820

Metacresol, United States Pharmacopeia (USP) Reference Standard

InChI=1/C7H8O/c1-6-3-2-4-7(8)5-6/h2-5,8H,1H

The Henry's Law constant for propionaldehyde is 7.34X10-5 atm-cu m/mole(1). This Henry's Law constant indicates that propionaldehyde 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 11 hrs(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 5.8 days(SRC). Propionaldehyde is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 317 mm Hg(3).
Literature: (1) Buttery RG et al; J Agric Food Chem 17: 385-9 (1969) (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. Design Inst Phys Prop Data, Amer Inst Chem Eng NY, NY: Hemisphere Pub Corp (1989)

The Koc of propionaldehyde is estimated as 50(SRC), using a log Kow of 0.59(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that propionaldehyde is expected to have very high mobility in soil.
Literature: (1) Hansch C et al; Exploring QSAR. Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Heller SR, consult. ed., Washington, DC: Amer Chem Soc p. 6 (1995) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 4-9 (1990) (3) Swann RL et al; Res Rev 85: 17-28 (1983)

CALAMENENE

cis-Calamenene

483-77-2

72937-55-4

(+/-)-Cadina-1,3,5-triene

Calamenene, cis-(+/-)-

5C6W67N6XM

Naphthalene, 1,2,3,4-tetrahydro-1,6-dimethyl-4-(1-methylethyl)-, (1S-cis)-

R8O22WBF8L

UNII-5C6W67N6XM

(1S,4S)-1,6-dimethyl-4-propan-2-yl-1,2,3,4-tetrahydronaphthalene

(-)-Calamenene

Naphthalene, 1,2,3,4-tetrahydro-1,6-dimethyl-4-(1-methylethyl)-, (1R,4R)-rel-

(Z)-calamenene

1-S-cis-Calamenene

Cadina-1,3,5-triene

1S-CIS-CALAMENENE

UNII-R8O22WBF8L

CALAMENENE, (-)-

(1S,4S)-4-Isopropyl-1,6-dimethyl-1,2,3,4-tetrahydronaphthalene

(1S,4S)-1,6-dimethyl-4-(propan-2-yl)-1,2,3,4-tetrahydronaphthalene

CALAMENENE, CIS-(-)-

IT SHOULD BE NOTED THAT cis-calamenene is eluted late vs trans-calamenene

DTXSID40880702

CHEBI:218611

PGTJIOWQJWHTJJ-STQMWFEESA-N

DTXSID501042907

(-)-CADINA-1,3,5-TRIENE

NS00095902

Q63398612

(1S-cis)-1,6-Dimethyl-4-(1-methylethyl)-1,2,3,4-tetrahydronaphthalene

1,2,3,4-tetrahydro-1,6-dimethyl-4(1-methylethyl)-(1s-cis)-naphthalene

Rel-(1S,4S)-4-isopropyl-1,6-dimethyl-1,2,3,4-tetrahydronaphthalene

(1S,4S)-1,2,3,4-TETRAHYDRO-1,6-DIMETHYL-4-(1-METHYLETHYL)NAPHTHALENE

naphthalene, 1,2,3,4-tetrahydro-1,6-dimethyl-4- (1-methylethyl)-, (1S-cis)-

NAPHTHALENE, 1,6-DIMETHYL-4-(1-METHYLETHYL)-1,2,3,4-TETRAHYDRO-, (1S-Z)-

2-HEPTYLFURAN

2-n-Heptylfuran

3777-71-7

Furan, 2-heptyl-

FEMA No. 3401

7W55A39QXM

Furan, heptyl-

CCRIS 6901

UNII-7W55A39QXM

2-heptyluran

EINECS 223-236-8

HEPTYLFURAN, 2-N-

2-HEPTYLFURAN [FHFI]

SCHEMBL1868812

DTXSID2063187

FEMA 3401

CHEBI:167091

MFCD00051820

AKOS005266535

MCULE-4055197722

PS-11660

DB-021419

NS00012524

A823864

Q27268935

2-PENTYLFURAN

3777-69-3

2-Amylfuran

2-n-Pentylfuran

Furan, 2-pentyl-

Furan, pentyl-

PENTYLFURAN

FEMA No. 3317

6I0QAJ1JZQ

DTXSID9047679

CHEBI:89197

64079-01-2

2-Pentylfuran (natural)

2-(N-Pentyl)furan

EINECS 223-234-7

UNII-6I0QAJ1JZQ

BRN 0107854

2-pentylfurane

CCRIS 8807

2-pentyl-furan

2-Pentylfuran; 2-Amylfuran; 2-n-Pentylfuran; Dihydro-5-pentyl-2(hydro)-furan

Furane, 2-pentyl

MFCD00036497

AMYLFURAN

5-17-01-00390 (Beilstein Handbook Reference)

2-Amylfuran; 2-Pentyl furan

2-PENTYLFURAN [FHFI]

Amyl furan (2-Pentyl furan)

SCHEMBL221257

CHEMBL3182720

DTXCID7027679

2-Pentylfuran, >=98%, FG

FEMA 3317

2-Pentylfuran, analytical standard

HY-N7398

Tox21_303542

s9334

AKOS015913798

SB61015

NCGC00257337-01

BS-22948

PD144438

CAS-3777-69-3

DB-003325

CS-0119428

NS00011970

P1209

2-Pentylfuran 100 microg/mL in Acetonitrile

2-Pentylfuran, natural (US), >=97%, FG

H11330

EN300-7399562

A823863

W-106514

Q27161382

Z1255423587

phenol

108-95-2

carbolic acid

Hydroxybenzene

Phenic acid

Oxybenzene

Benzenol

Phenylic acid

Phenylic alcohol

Monophenol

Phenyl hydrate

Phenyl hydroxide

PhOH

Monohydroxybenzene

Paoscle

Phenole

Izal

Phenyl alcohol

Phenol alcohol

Acide carbolique

Phenol, liquefied

Fenolo

Carbolsaure

Phenosmolin

Fenol

Liquid phenol

Phenol, pure

Benzene, hydroxy-

Rcra waste number U188

Liquefied phenol

Liquified Phenol

Carbolicum acidum

Fenolo [Italian]

NCI-C50124

Phenole [German]

Campho-Phenique Gel

phenylalcohol

UN 2312 (molten)

Phenol [JAN]

UN 1671 (solid)

Phenic

Carbolsaure [German]

Caswell No. 649

Campho-Phenique Liquid

Phenol, molten

2-allphenol

Baker's P & S liquid & Ointment

Fenol [Dutch, Polish]

NSC 36808

Phenol, liquified

Baker's P and S Liquid and Ointment

Monohydroxy benzene

Acide carbolique [French]

CCRIS 504

Campho-Phenique Cold Sore Gel

Carbolsaeure

FEMA No. 3223

Karbolsaeure

HSDB 113

Phenoxy

acide phenique

DTXSID5021124

Phenic alcohol

Phenol,liquified

Synthetic phenol

Phenol, dimer

AI3-01814

RCRA waste no. U188

EINECS 203-632-7

UNII-339NCG44TV

MFCD00002143

NSC-36808

UN1671

UN2312

UN2821

EPA Pesticide Chemical Code 064001

339NCG44TV

CHEBI:15882

Phenol [USP:JAN]

ENT-1814

27073-41-2

CHEMBL14060

DTXCID501124

EC 203-632-7

NSC36808

Phenol, Glass Distilled Under Argon

65996-83-0

Phenol, solid [UN1671] [Poison]

Phenol (USP:JAN)

Phenol, molten [UN2312] [Poison]

NCGC00091454-04

Fenosmoline

Fenosmolin

PHENOL (IARC)

PHENOL [IARC]

PHENOL (USP-RS)

PHENOL [USP-RS]

PHENOL (II)

PHENOL [II]

PHENOL (MART.)

PHENOL [MART.]

Phenol, >=99.0%

17442-59-0

PHENOL (EP MONOGRAPH)

PHENOL [EP MONOGRAPH]

PHENOL (USP MONOGRAPH)

PHENOL [USP MONOGRAPH]

Phen-2,4,6-d3-ol-d

Carbol

hydroxy benzene

Phenol 100 microg/mL in Methanol

Phenol, liquid

Phenol, solid

Baker's p and s

Phenol, sulfurated

CAS-108-95-2

METACRESOL IMPURITY A (EP IMPURITY)

METACRESOL IMPURITY A [EP IMPURITY]

(14C)Phenol

HEXYLRESORCINOL IMPURITY A (EP IMPURITY)

HEXYLRESORCINOL IMPURITY A [EP IMPURITY]

PHENOL (2,3,4,5,6-D5)

arenols

Benzophenol

Karbolsaure

Phylorinol

Ulcerease

Hydroxy-benzene

Phenol liquid

Phenol molten

Fungus Fighte

Phenol synthetic

Pandy's reagent

Cepastat lozenges

Fortinia ID

Phenol, labeled with carbon-14

Acidum Carbolicum

Phenol (liquid)

2-phenyl alcohol

Sore ThroatCherry

Phenol, synthetic

Phenol, ultrapure

ABC Sore Throat

HEB Sore Throat

Phenol ACS grade

RugbyCherry Flavor

Sore ThroatMenthol

Sore Throat Spray

Meijer Sore Throat

Sore Throat Cherry

Sore Throat Relief

Liquefied phenol BP

Paoscle (TN)

Topcare Sore Throat

Carbolic acid liquid

Phenol (TN)

Phenol,(S)

TopCareCherry Flavor

Phenol, ACS reagent

PUBLIX Sore Throat

Carbolic acid, liquid

CepastatExtra Strength

Walgreens Sore Throat

63496-48-0

Sore ThroatReadyInCase

Vortex Moisturizer Oral

1ai7

1li2

4i7l

Liquefied phenol (TN)

DRx Choice Sore Throat

PHENOL [VANDF]

Wild Horse 777 Oral

PHENOL [FHFI]

PHENOL [HSDB]

PHENOL [INCI]

Sore Throat ReliefCherry

Castellani Paint 1.5%

Phenol (JP17/USP)

PHENOL [WHO-DD]

Phenol, detached crystals

Pain RelievingPetro Carbo

PHENOL [MI]

Phenol, >=99%

Sore Throat ReliefMenthol

WLN: QR

Good Neighbor Sore Throat

Liquefied phenol (JP17)

bmse000290

bmse010026

C6H5OH

Fenol(DUTCH, POLISH)

NICE SORE THROAT Cherry

PHENOL, 80% in ethanol

Phenol, LR, >=99%

HEB Sore ThroatCherry Flavor

MLS001065591

Phenol (CGA 73330)

Phenol, for molecular biology

BIDD:ER0293

Phenol for disinfection (TN)

ABC Sore ThroatMenthol Flavor

HEB Sore ThroatMenthol Flavor

NICE SORE THROAT Spearmint

Phenol, natural, 97%, FG

CHLORASEPTIC SORE THROAT

Chloraseptic Sore Throat Cherry

Chloraseptic Sore Throat Citrus

Cuticura pain relieving ointment

Sore Throat ReliefCherry Flavor

CARBOLICUM ACIDUM [HPUS]

DTXSID9075294

Phenol, AR, >=99.5%

PHENOL,LIQUIFIED [VANDF]

BDBM26187

CHEBI:33853

Phenol for disinfection (JP17)

Topcare Sore ThroatMenthol Flavor

3f39

Phenol 10 microg/mL in Methanol

PUBLIX Sore ThroatMenthol Flavor

Walgreens Sore ThroatCherry Flavor

phenol 0.6% anesthetic oral rinse

Tox21_113463

Tox21_201639

Tox21_300042

DRx Choice Sore ThroatMenthol Flavor

Phenol 5000 microg/mL in Methanol

STL194294

AKOS000119025

Eos Medicated Pain Relieving Lip Balm

Tox21_113463_1

DB03255

Good Neighbor Sore ThroatCherry Flavor

MCULE-9943948107

NA 2821

Phenol, BioXtra, >=99.5% (GC)

Phenol, SAJ first grade, >=98.0%

UN 1671

UN 2312

UN 2821

USEPA/OPP Pesticide Code: 064001

NCGC00091454-01

NCGC00091454-02

NCGC00091454-03

NCGC00091454-05

NCGC00091454-06

NCGC00091454-07

NCGC00254019-01

NCGC00259188-01

Phenol, JIS special grade, >=99.0%

61788-41-8

73607-76-8

AM802906

BP-30160

METHYL SALICYLATE IMPURITY B [EP]

SMR000568492

Phenol 1000 microg/mL in Dichloromethane

Phenol, PESTANAL(R), analytical standard

Liquified Phenol (contains 7-10 % water)

NS00010045

P1610

P2771

EN300-19432

C00146

D00033

Phenol, unstabilized, ReagentPlus(R), >=99%

SALICYLIC ACID IMPURITY C [EP IMPURITY]

Phenol, p.a., ACS reagent, 99.5-100.5%

PUBLIX Sore Throat Fast Relief Oral Anesthetic

Q130336

CVS Health Sore Throat Fast Relief Oral Anesthetic

J-610001

Phenol, for molecular biology, ~90% (T), liquid

A13-01814

F1908-0106

Phenol, unstabilized, purified by redistillation, >=99%

Z104473830

InChI=1/C6H6O/c7-6-4-2-1-3-5-6/h1-5,7

Phenol, BioUltra, for molecular biology, >=99.5% (GC)

Phenol, United States Pharmacopeia (USP) Reference Standard

Liquified Phenol, meets USP testing specifications, >=89.0%

Phenol, BioUltra, for molecular biology, TE-saturated, ~73% (T)

phenol;phenol [jan];phenol, pure;phenol phenol [jan] phenol, pure

Phenol, puriss. p.a., ACS reagent, reag. Ph. Eur., 99.0-100.5%

Phenol, contains hypophosphorous as stabilizer, loose crystals, ACS reagent, >=99.0%

Phenol, puriss., meets analytical specification of Ph. Eur., BP, USP, 99.5-100.5% (GC)

Phenol, puriss., meets analytical specification of Ph. Eur., BP, USP, >=99.5% (GC), crystalline (detached)

The Henry's Law constant for phenol is 3.33X10-7 atm-cu m/mol at 25 deg C(1). This Henry's Law constant indicates that phenol is expected to be essentially nonvolatile from water surfaces(2). Phenols's Henry's Law constant indicates that volatilization from moist soil surfaces in not expected to occur(SRC). Phenol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.35 mm Hg(3).
Literature: (1) Gaffney JS et al; Environ Sci Technol 21: 519-23 (1987))(2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Bingham E et al, eds; Patty's Toxicology. 5th ed. NY, NY: John Wiley & Sons Inc. 4: 383 (2001)

Phenol is reported to have low adsorptivity to clay soils and silt loam(1) and no adsorption to aquifer material(3) and montmorillonite and kaolinite clays(8). The Koc for phenol to a Batcombe silt loam soil (pH 6.7, organic carbon 2.51%) was 30(6). It was 16 for a Brookstone clay loam (pH 5.7, organic matter 5.1%) and varied with pH and iron content of the soil(7). The Freundlich K and (1/N) for phenol in Captina (pH 5.7, 1.1 % organic matter) and Palouse silt loam (pH 5.7, 3.6% organic matter) soils were 0.58 (1.15) and 0.81 (1.00)(2); the Koc values for these soils are 91 and 39(SRC). Based on the reported Koc values, phenol would be expected to generally exhibit very high mobility in soil, based on a classification scheme(4). In a study of the adsorption of phenol onto siltstone associated with a Wyoming coal deposit suitable for in situ gasification, the pH of the solution was the major controlling factor with adsorption occurring at pH's below the pKa of phenol and no adsorption occurring at pH's above the pKa(5). The log of the Freundlich K value was approximately -4(5). Therefore, phenol may be transported by groundwater near in situ coal gasification sites due to the elevated pH's at these sites after gasification(5). The pKa of phenol is 9.99(9), indicating that it will be partially dissociated at the upper end of environmental pH range and its mobility may be pH dependent(SRC). In general, anions generally do not adsorb to organic carbon and clay as strongly as their neutral counterparts(10).
Literature: (1) Artiola-Fortuny J, Fuller WH; Soil Sci 133: 18-26 (1982) (2) Scott HD et al; J Environ Qual 12: 91-5 (1983) (3) Ehrlich GG et al; Groundwater 20: 703-10 (1982) (4) Swann RL et al; Res Rev 85: 17-28 (1983) (5) Laquer FC, Manahan SE; Chemosphere 16: 1431-45 (1987) (6) Briggs GG; J Agric Food Chem 29: 1050-9 (1981) (7) Boyd SA et al; Appl Environ Microbiol 46: 50-4 (1983) (8) Luh MD, Baker RA; pp. 534-42 in Proc 25th Ind Waste Conf Purdue Univ (1970) (9) Lide DR, ed; CRC Handbook of Chemistry and Physics. 81st Ed. Boca Raton, FL: CRC Press LLC, p. 5-89 (2000) (10) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)

Cyclohexyl isothiocyanate

1122-82-3

ISOTHIOCYANATOCYCLOHEXANE

Cyclohexane, isothiocyanato-

Isothiocyanocyclohexane

Cyclohexyl-isothiocyanat

Isothiocyanic acid, cyclohexyl ester

Cyclohexylisothiocyanate

Cyclohexyl isothiocyanate, isothiocyanato-

isothiocyanato-cyclohexane

NSC-60129

Cyclohexyl-isothiocyanat [German]

EINECS 214-361-9

NSC 60129

Cyclohexyl-isothiocyanat [German]

cylcohexyl isothiocyanate

cyclohexane isothiocyanate

WLN: L6TJ ANCS

2UF76U4DED

SCHEMBL330620

Cyclohexyl isothiocyanate, 98%

DTXSID5061532

CHEBI:229386

CYCLOHEXANE,ISOTHIOCYANATO-

Isothiocyanic Acid Cyclohexyl Ester

NSC60129

BBL011352

GEO-00873

MFCD00003841

STL146442

AKOS000120219

MCULE-5106041105

BP-12923

VS-02927

DB-041071

I0187

NS00010669

EN300-20282

D91097

J-670005

J-801004

J-802179

F0001-0272

InChI=1/C7H11NS/c9-6-8-7-4-2-1-3-5-7/h7H,1-5H

2,4,6-Trimethyl-1-nonene

144043-16-3

2,4,6-trimethylnon-1-ene

2,4,6,-trimethyl-1-nonene

DTXSID10336761

NS00010710

octane

n-octane

111-65-9

Oktan

Oktanen

Ottani

n-Oktan

Oktanen [Dutch]

Oktan [Polish]

Ottani [Italian]

HSDB 108

UNII-X1RV0B2FJV

X1RV0B2FJV

NSC 9822

EINECS 203-892-1

DTXSID0026882

CHEBI:17590

AI3-28789

NSC-9822

MFCD00009556

DTXCID406882

CH3-[CH2]6-CH3

EC 203-892-1

Heptane, methyl-

Octane, all isomers

CH3-(CH2)6-CH3

octano

Normal octane

normal-Octane

octan

Octanes

Octil

MG8

OTTANE

OCTANE [INCI]

N-OCTANE [HSDB]

OCTANE [MI]

bmse000480

Octane, analytical standard

WLN: 8H

Octane, anhydrous, >=99%

Octane, reagent grade, 98%

n-C8H18

Octane, p.a., 99.0%

CHEMBL134886

NSC9822

Octane; NSC 9822; n-Octane

Tox21_202452

c0044

LMFA11000002

AKOS015904009

MCULE-3248084959

NCGC00249228-01

NCGC00260001-01

CAS-111-65-9

LS-13532

NS00006444

O0022

O0118

O0151

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

C01387

Q150681

J-002613

F0001-0244

EEE64B73-0375-4303-AFD5-0795361807FF

InChI=1/C8H18/c1-3-5-7-8-6-4-2/h3-8H2,1-2H

Octane, electronic grade, >=99.999% metals basis, >=99% (CP)

31372-91-5

9065-92-3

The Henry's Law constant for n-octane is estimated as 3.2 atm-cu m/mole(SRC) derived from its vapor pressure, 14.1 mm Hg(1), and water solubility, 0.66 mg/L(2). This Henry's Law constant indicates that n-octane 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 4.2 days(SRC). Volatilization from water surfaces may be attenuated by adsorption to suspended solids and sediment in the water column(SRC). The estimated volatilization half-life from a model pond is 11 months if adsorption is considered(4). However, in a study using a jet fuel mixture and sterile freshwater controls from the Escambia River (Florida), a 99% loss of n-octane was attributed to evaporation at 25 deg C(5). n-Octane's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The disappearance of n-octane was rapid in soil/water mixture (concentration of soil, 25 g/150 mL)(6); an initial concentration of 0.177 ug/mL n-octane disappeared completely in 5 days using a sterile sandy loam soil with an organic matter content of 5.1%(6). The potential for volatilization of n-octane from dry soil surfaces may exist(SRC) based upon its vapor pressure(1).
Literature: (1) Yaws CL; Handbook of Vapor Pressure. Houston, TX: Gulf Pub Co. 3: 78 (1994) (2) Yalkowsky SH, He Y, eds; Handbook of aqueous solubility data. Boca Raton, FL: CRC Press p. 536 (2003) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (4) US EPA; EXAMS II Computer Simulation (1987) (5) Spain JC et al; Degrad of Jet Fuel Hydrocarbons by Aquatic Microbial Communities. Tyndall AFB, FL: Air Force Eng Serv Ctr. AFESC/ESL-TR-83-26 (NTIS AD-A139791/8) p 226 (1983) (6) Dean-Ross D; Bull Environ Contam Toxicol 51: 596-99 (1993)

The Koc of n-octane is estimated as 3.1X10+4(SRC), using a log Kow of 5.18(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that n-octane is expected to be immobile in soil. Freundlich absorption coefficients of log 4.04 and log 3.49 were measured in Oberlausitz lignite (11.1% moisture content; 53.5 wt% carbon content; 0.6 wt % nitrogen content) and Pahokee peat soil (10.2% moisture content; 46.1 wt% carbon content; 3.3 wt % nitrogen content), respectively(4). Gaseous transport of volatile n-octane in unsaturated porous media was shown to be influenced by air-water interfacial adsorption and water-partitioning(5). Sorption of n-octane from air to snow was measured, resulting in a sorption coefficient of log -4.41 cu m/sq m at -6.8 deg C(6).
Literature: (1) Miller MM et al; Environ Sci Technol 19:522-9 (1985) (2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of Oct 30, 2013: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (3) Swann RL et al; Res Rev 85: 17-28 (1983) (4) Endo S et al; Environ Sci Technol 42): 5897-5903 (2008) (5) Kim H et al; Environ Sci Technol 35: 4457-62 (2001) (6) Roth CM et al; Environ Sci Technol 38: 4078-84 (2004)

Caryophyllene oxide

(-)-Caryophyllene oxide

1139-30-6

beta-Caryophyllene oxide

beta-Caryophyllene epoxide

(-)-Epoxycaryophyllene

Epoxycaryophyllene

trans-caryophyllene oxide

(-)Carophyllene oxide

UNII-S2XU9K448U

(-)-Epoxydihydrocaryophyllene

S2XU9K448U

Caryophylene oxide

HSDB 5466

EINECS 214-519-7

MFCD00134216

(-)-BETA-CARYOPHYLLENE EPOXIDE

CARYOPHYLLENE, EPOXIDE

CHEMBL508894

DTXSID4051586

FEMA NO. 4085

CHEBI:67818

4,11,11-Trimethyl-8-methylene-5-oxatricyclo(8.2.0.0(4,6))dodecane

.beta.-Caryophyllene oxide

(1R,4R,6R,10S)-4,12,12-trimethyl-9-methylidene-5-oxatricyclo[8.2.0.04,6]dodecane

4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane, (1R,4R,6R,10S)-

5-Oxatricyclo(8.2.0.0(4,6))dodecane, 4,12,12-trimethyl-9-methylene-, (1R,4R,6R,10S)-

Caryophyllene Oxide 1000 microg/mL in Isopropanol

epoxide

(-)-.beta.-Caryophyllene epoxide

4-12,12-TRIMETHYL-9-METHYLENE-5-OXATRICYLO (8.2.0.04,6) DODECANE

(1R,4R,6R,10S)-4,12,12-TRIMETHYL-9-METHYLIDENE-5-OXATRICYCLO[8.2.0.0?,?]DODECANE

5-Oxatricyclo(8.2.0.04,6)dodecane, 4,12,12-trimethyl-9-methylene-, (1R,4R,6R,10S)-

[1R-(1R*,4R*,6R*,10S*)]-4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane

5-Oxatricyclo(8.2.0.0(sup 4,6))dodecane, 4,12,12-trimethyl-9-methylene-, (1R,4R,6R,10S)-

5-OXATRICYCLO(8.2.0.04,6)DODECANE, 4,12,12-TRIMETHYL-9-METHYLENE-, (1R-(1R*,4R*,6R*,10S*))-

ambar crystal

bcp oxide

(1R-(1R*,4R*,6R*,10S*))-4,12,12-Trimethyl-9-methylene-5-oxatricyclo(8.2.0.04,6)dodecane

?-caryophyllene oxide

b-Caryophyllene Epoxide

trimethyl(methylene)[?]

Caryophyllene Oxide 90001

SCHEMBL127077

DTXCID8030138

(-)-Caryophyllene oxide, 95%

NVEQFIOZRFFVFW-RGCMKSIDSA-N

4,12,12-trimethyl-9-methylene-

4beta,5alpha-EPOXYCARYOPHYLLENE

HY-N3544

Tox21_303807

BDBM50241720

CARYOPHYLLENE 4beta,5alpha-OXIDE

s3983

AKOS030241571

CARYOPHYLLENE 4beta,5alpha-EPOXIDE

CCG-208462

(1R,4R,6R,10S)-9-Methylene-4,12,12-trimethyl-5-oxatricyclo[8.2.0.04,6]dodecane

NCGC00357089-01

AS-58060

BETA-CARYOPHYLLENE EPOXIDE, (-)-

.BETA.-CARYOPHYLLENE OXIDE [FHFI]

CAS-1139-30-6

4.BETA.,5.ALPHA.-EPOXYCARYOPHYLLENE

CS-0023810

CARYOPHYLLENE 4.BETA.,5.ALPHA.-OXIDE

(-)-BETA-CARYOPHYLLENE EPOXIDE [HSDB]

C16908

CARYOPHYLLENE 4.BETA.,5.ALPHA.-EPOXIDE

E80731

SR-05000002236

SR-05000002236-2

W-108611

(-)-Caryophyllene oxide, analytical reference material

(1R,4R,5R,9S)-4,5-epoxycaryophyllan-8(13)-ene

Q27136294

inverted exclamation markY99.0% (sum of enantiomers, GC)

(-)-Caryophyllene oxide, >=99.0% (sum of enantiomers, GC)

(1R,4R,6R,10S)- 5-Oxatricyclo[8.2.0.0(4,6)-]dodecane

4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.0~4,6~]dodecane

(-)-5-Oxatricyclo[8.2.0.0(4,6)]dodecane,4,12,12-trimethyl-9-methylene-

(1R,4R,6R,10S)-4,12,12-Trimethyl-9-methylene-5-oxatricyclo[8.2.0.04,6]dodecane

(1R,4R,6R,10S)-9-Methylene-4,12,12-trimethyl-5-oxatricyclo[8.2.0.0(4,6])dodecane

(1R,4R,6R,10S)- 4,12,12-trimethyl-9-methylene-5-oxatricyclo[8.2.0.]dodecane (caryophyllene oxide) 5-Oxatricyclo(8.2.0.0(4,6))dodecane

[1R-(1R*,4R*,6R*,10S*)]- (-)-Epoxydihydrocaryophyllene (-)-<>-Caryophyllene epoxide (-)-<>-Caryophyllene oxide 4,11,11-Trimethyl-8-methylene-5-oxatr

[1R-(1R*,4R*,6R*,10S*)]- Caryophylene oxide Caryophyllene epoxide Caryophyllene oxyde Epoxycaryophyllene [1R-(1R*,4R*,6R*,10S*)]-4,12,12-trimethyl-9-methylene-5

5-OXATRICYCLO(8.2.0.0(4,6))DODECANE, 4,12,12-TRIMETHYL-9-METHYLENE-, (1R-(1R*,4R*,6R*,10S*))-

5-OXATRICYCLO(8.20.0(4,6))DODECANE, 4,12,12-TRIMETHYL-9-METHYLENE-, (1R,4R,6R,10S)-