2-Phenyl-2-propanol

2-Phenylpropan-2-ol

617-94-7

Dimethylphenylcarbinol

1-Hydroxycumene

Dimethylphenylmethanol

2-PHENYLISOPROPANOL

alpha-Cumyl alcohol

alpha,alpha-Dimethylbenzyl alcohol

Phenyldimethylcarbinol

2-Propanol, 2-phenyl-

2-phenyl-propan-2-ol

Dimethyl phenyl carbinol

alpha,alpha-Dimethylbenzenemethanol

a,a-dimethylbenzyl alcohol

NSC 1261

Benzyl alcohol, alpha,alpha-dimethyl-

Benzenemethanol, alpha,alpha-dimethyl-

NSC 212537

.alpha.-Cumyl alcohol

Benzenemethanol, .alpha.,.alpha.-dimethyl-

MFCD00004456

.alpha.,.alpha.-Dimethylbenzyl alcohol

Benzyl alcohol, .alpha.,.alpha.-dimethyl-

JE030BGE05

DTXSID3027247

NSC-1261

NSC-212537

Benzyl alcohol,.alpha.-dimethyl-

Benzenemethanol,.alpha.-dimethyl-

2-phenylpropanol-2

HSDB 5718

EINECS 210-539-5

BRN 1905012

UNII-JE030BGE05

AI3-05532

dimethylphenyl carbinol

2-Phenylisopropyl alcohol

1-Methyl-1-phenylethanol

2-Hydroxy-2-phenylpropane

EC 210-539-5

4-06-00-03219 (Beilstein Handbook Reference)

SCHEMBL164244

2-Phenyl-2-propanol, 97%

DTXCID107247

CHEMBL3185495

alpha,alpha-dimethylbenzyl aldohol

NSC1261

(1-hydroxy-1-methylethyl)benzene

CHEBI:131607

2-PHENYLISOPROPANOL [HSDB]

AMY25731

STR08958

Tox21_200449

NSC212537

AKOS009158102

CS-W016526

HY-W015810

MCULE-1685813708

PB47644

PS-4036

.alpha.,.alpha.-Dimethylbenzenemethanol

NCGC00248623-01

NCGC00258003-01

CAS-617-94-7

SY021550

NS00010783

P0213

BENZENEMETHANOL, ALPHA, ALPHA, DIMETHYL

EN300-120905

P15346

A868634

W-105093

Q15726116

InChI=1/C9H12O/c1-9(2,10)8-6-4-3-5-7-8/h3-7,10H,1-2H

The Henry's Law constant for 2-phenylisopropanol is estimated as 3.8X10-7 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This value indicates that 2-phenylisopropanol will be essentially nonvolatile from water surfaces(2,SRC). 2-Phenylisopropanol's vapor pressure, 0.047 mm Hg(3,SRC) indicates that volatilization from dry soil surfaces may occur. However, 2-phenylisopropanol's Henry's Law constant(1,SRC) indicates that volatilization from moist soil may not occur(SRC).
Literature: (1) Meylan WM, Howard PH; Environ Toxicol Chem 10: 1283-93 (1991) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Lyman WJ; p 31 in Environmental Exposure From Chemicals Vol I, Neely WB, Blau GE(eds), Boca Raton, FL: CRC Press (1985)

INSOL IN WATER; SOL IN ETHANOL, ETHER, BENZENE
Literature: Lide, D.R. (ed.). CRC Handbook of Chemistry and Physics. 75th ed. Boca Raton, Fl: CRC Press Inc., 1994-1995., p. 3-52

Using a structure estimation method based on molecular connectivity indexes(1), the Koc for 2-phenylisopropanol can be estimated to be about 36(SRC). The Koc of 2-phenylisopropanol can also be estimated to be approximately 274(SRC), using an estimated log Kow of 1.95(2,SRC) and a regression-derived equation(3,SRC). According to a recommended classification scheme(4), these estimated Koc values suggest that 2-phenylisopropanol has very high to medium mobility in soil(SRC).
Literature: (1) Meylan WM et al; Environ Sci Technol 28: 459-65 (1992) (2) Meylan WM, Howard PH; J Pharm Sci 84: 83-92 (1995) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington DC: Amer Chem Soc pp. 4-9 (1990) (4) Swann RL et al; Res Rev 85: 23 (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)-

3-METHYLFURAN

930-27-8

Furan, 3-methyl-

3-methylfurane

3-Methylfuran-methyl-D3

MFCD00060134

5R72A0440N

NSC-346905

3-Methylfuran 100 microg/mL in Methanol

NSC 346905

BRN 0104217

4-methylfuran

UNII-5R72A0440N

3-methyl-furan

3-methylfuran (stabilized with hq)

3-Methylfuran, AldrichCPR

5-17-01-00330 (Beilstein Handbook Reference)

DTXSID10239228

CHEBI:172946

BBL103814

GEO-01834

NSC346905

STL557624

>98.0%(GC) (stabilized with HQ)

AKOS005255084

GS-0656

DB-016017

3-Methylfuran (stabilised with Hydroquinone)

M0939

NS00039517

EN300-88698

W18310

A844425

Q21099678

InChI=1/C5H6O/c1-5-2-3-6-4-5/h2-4H,1H

Butyl phenylacetate

butyl 2-phenylacetate

122-43-0

Benzeneacetic acid, butyl ester

n-Butyl phenylacetate

Butyl benzene acetate

Butyl alpha-toluate

Butyl benzeneacetate

Butyl phenylethanoate

ACETIC ACID, PHENYL-, BUTYL ESTER

Phenylethanoic acid butyl ester

Phenylacetic acid butyl ester

FEMA No. 2209

2-phenylacetic acid butyl ester

TR6RZ109SI

BUTYL PHENYL ACETATE

EINECS 204-543-6

UNII-TR6RZ109SI

BRN 2046682

AI3-02942

Butylphenylacetat

butylphenylacetate

n-Butyl phenyl acetate

4-09-00-01619 (Beilstein Handbook Reference)

BUTYL .ALPHA.-TOLUATE

SCHEMBL456516

DTXSID9059541

FEMA 2209

BUTYL PHENYLACETATE [FCC]

CHEBI:179903

BUTYL PHENYLACETATE [FHFI]

AKOS015890782

MCULE-5426662821

Butyl phenylacetate, >=98%, FCC, FG

AS-77100

CS-0456232

NS00012061

A804889

Q27290201

BENZYL ACETATE

140-11-4

Benzyl ethanoate

Phenylmethyl acetate

Acetic acid benzyl ester

Acetic acid, phenylmethyl ester

Acetic acid, benzyl ester

Phenylmethyl ethanoate

alpha-Acetoxytoluene

(Acetoxymethyl)benzene

NCI-C06508

Benzylester kyseliny octove

Caswell No. 081EA

FEMA No. 2135

Benzyl acetate (natural)

NSC 4550

Acetic acid phenylmethyl ester

CCRIS 1423

HSDB 2851

Plastolin I

UNII-0ECG3V79ZJ

EINECS 205-399-7

0ECG3V79ZJ

DTXSID0020151

CHEBI:52051

.alpha.-Acetoxytoluene

AI3-01996

NSC-4550

Benzyl ester of acetic acid

Benzyl-23456-d5 Acetate

DTXCID40151

EC 205-399-7

Benzyl acetate + glycine combination

MFCD00008712

BENZYL ACETATE (IARC)

BENZYL ACETATE [IARC]

CAS-140-11-4

Acetic acid-benzyl ester

Benzylester kyseliny octove [Czech]

ACETATO DE BENCILO

Benzyl acetate, primary pharmaceutical reference standard

?Benzyl acetate

FEMA 2135

J0Z

nchem.167-comp5

Benzyl acetate, >=99%

BENZYL ACETATE [MI]

WLN: 1VO1R

SCHEMBL43745

BENZYL ACETATE [FCC]

BENZYL ACETATE [FHFI]

BENZYL ACETATE [HSDB]

BENZYL ACETATE [INCI]

BENZYL ACETATE [VANDF]

CHEMBL1233714

AMY3828

NSC4550

Benzyl acetate, analytical standard

HY-N7124

Tox21_201826

Tox21_302841

s5576

STL283809

Benzyl acetate, >=99%, FCC, FG

AKOS015841099

CCG-266204

CS-W018145

MCULE-7952998506

NCGC00090779-01

NCGC00090779-02

NCGC00090779-03

NCGC00256379-01

NCGC00259375-01

LS-13613

A0022

Benzyl acetate, natural, >=99%, FCC, FG

E1501

NS00002107

Benzyl acetate, Selectophore(TM), >=99.5%

G75933

EN300-1267317

Q424223

J-007357

W-200649

Z19628364

InChI=1/C9H10O2/c1-8(10)11-7-9-5-3-2-4-6-9/h2-6H,7H2,1H

The Henry's Law constant for benzyl acetate is estimated as 1.1X10-5 atm-cu m/mole(SRC) from its experimental values for vapor pressure, 0.18 mm Hg(1), and water solubility, 3.1X10+3 mg/l(2). This value indicates that benzyl acetate is expected to volatilize from water surfaces(3,SRC). Based on this Henry's Law constant, the estimated volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec) is estimated as approximately 4.1 days(3,SRC). The estimated volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec) is estimated as approximately 34 days(3,SRC). Benzyl acetate's Henry's Law constant(1,2,SRC) indicates that volatilization from moist soil surfaces may be important(SRC).
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) 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. 3-84 (1992) (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 benzyl acetate is estimated as approximately 180(SRC), using a log Kow of 1.96(1) and a regression-derived equation(2,SRC). According to a classification scheme(3), this estimated Koc value suggests that benzyl acetate is expected to have moderate mobility in soil(SRC).
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. 57 (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: 23 (1983)

METHYL BENZOATE

93-58-3

Methylbenzoate

Benzoic acid, methyl ester

benzoic acid methyl ester

Clorius

Methyl benzenecarboxylate

Essence of niobe

Oxidate le

FEMA No. 2683

Methyl benzoate (natural)

Methylester kyseliny benzoove

NSC 9394

CCRIS 5851

HSDB 5283

EINECS 202-259-7

UNII-6618K1VJ9T

DTXSID5025572

CHEBI:72775

AI3-00525

CLORIUS-

6618K1VJ9T

NSC-9394

MFCD00008421

Methyl ester of benzoic acid

DTXCID405572

EC 202-259-7

CAS-93-58-3

UN2938

Methylester kyseliny benzoove [Czech]

Benzoato de metilo

methyloxycarbonylbenzene

benzoic acid methylester

Methyl benzoate, 99%

Methyl-benzenecarboxylate

Benzoic acid-methyl ester

WLN: 1OVR

SCHEMBL7200

METHYL BENZOATE [MI]

MLS001050185

CHEMBL16435

METHYL BENZOATE [FCC]

METHYL BENZOATE [FHFI]

METHYL BENZOATE [HSDB]

METHYL BENZOATE [INCI]

SCHEMBL4790973

SCHEMBL10330498

NSC9394

Methyl benzoate, >=99% (GC)

Methyl benzoate, analytical standard

Tox21_201832

Tox21_303198

BBL010502

STK021498

AKOS000120640

Methyl benzoate, >=98%, FCC, FG

AT34734

MCULE-3681534655

UN 2938

Methyl benzoate, for synthesis, 98.0%

NCGC00091665-01

NCGC00091665-02

NCGC00256939-01

NCGC00259381-01

BP-31073

SMR001216584

VS-02533

B0074

NS00012849

EN300-15500

Methyl benzoate, natural, >=98%, FCC, FG

C20645

A844641

Q417328

J-522592

Methyl benzoate [UN2938] [Keep away from food]

Z19825577

F0001-2239

InChI=1/C8H8O2/c1-10-8(9)7-5-3-2-4-6-7/h2-6H,1H

The Henry's Law constant for methyl benzoate is estimated as 3.24X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 0.38 mm Hg(1), and water solubility, 2.1X10+3 mg/L(2). This Henry's Law constant indicates that methyl benzoate 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 22 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 14 days(SRC). Methyl benzoate's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Methyl benzoate is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 0.38 mm Hg(1).
Literature: (1) Daubert TE, Danner RP; Data Compilation Tables of Properties of Pure Compounds New York, NY: Amer Inst for Phys Prop Data (1989) (2) Riddick JA et al; Organic Solvents 4th ed. New York, NY: Wiley (1986) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

The adsorption of methyl benzoate was determined by a modified version of the OECD guideline 106, a batch equilibrium method, in three soils with different characteristics: an acid forest soil (Podzol), an agricultural soil (Alfisol), and a sediment. The respective Freundlich constants, Kf (1/n), for the three soils were 8.64 (0.81), 1.29 (0.85), and 1.51 (0.84)(1). Koc values for the Podzol, Alfisol and sediment were 178, 103, and 95, respectively(1). Methyl benzoate also has a reported log Koc value of 2.10 (Koc = 126)(2). Using a structure estimation method based on molecular connectivity indices(3), the Koc of methyl benzoate can be estimated to be 70(SRC). According to a classification scheme(3), methyl benzoate is expected to have moderate to high mobility in soil.
Literature: (1) Von Oepen B et al; Chemosphere 22: 285-304 (1991) (2) Schuurmann G et al; Environ Sci Technol 40: 7005-11 (2006) (3) Swann RL et al; Res Rev 85: 17-28 (1983)

Phenylacetone

1-phenylpropan-2-one

1-Phenyl-2-propanone

103-79-7

Benzyl methyl ketone

Methyl benzyl ketone

Phenyl-2-propanone

1-Phenylacetone

2-Propanone, 1-phenyl-

3-Phenyl-2-propanone

Phenylmethyl methyl ketone

phenyl acetone

1-phenyl-propan-2-one

136675-26-8

phenylaceton

O7IZH10V9Y

CHEMBL3800510

NSC-9827

NSC 9827

Phenylacetone, 99%

EINECS 203-144-4

UNII-O7IZH10V9Y

(phenyl)acetone

AI3-02938

DEA No. 8501

methylbenzyl ketone

phenyl 2-propanone

1-phenyl propanedione

1-Phenylpropane-2-one

PHENYLACETONE [MI]

SCHEMBL43943

ghl.PD_Mitscher_leg0.660

DTXSID1059280

SCHEMBL13341529

CHEBI:52052

HSDB 8385

NSC9827

Phenylacetone, analytical standard

BCP22277

BDBM50167968

STL373560

AKOS004905656

MCULE-2102027204

NS00017966

A800807

Q418831

AMFETAMINE SULFATE IMPURITY B [EP IMPURITY]

InChI=1/C9H10O/c1-8(10)7-9-5-3-2-4-6-9/h2-6H,7H2,1H

The Henry's Law constant for phenyl 2-propanone is estimated as 4.0X10-6 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that phenyl 2-propanone 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 7 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 80 days(SRC). Phenyl 2-propanone's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Phenyl 2-propanone has an estimated vapor pressure of 0.16 mm Hg(SRC), determined from a fragment constant method(3) and exists as a liquid under environmental conditions; therefore, phenyl 2-propanone may volatilize from dry soil.

The Koc of phenyl 2-propanone is estimated as 80(SRC), using a log Kow of 1.44(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that phenyl 2-propanone is expected to have high mobility in soil.

METHYL ANTHRANILATE

Methyl 2-aminobenzoate

134-20-3

2-Aminobenzoic acid methyl ester

Methyl o-aminobenzoate

o-Carbomethoxyaniline

Anthranilic acid methyl ester

2-Carbomethoxyaniline

2-(Methoxycarbonyl)aniline

Benzoic acid, 2-amino-, methyl ester

Anthranilic acid, methyl ester

O-methyl anthranilate

FEMA No. 2682

o-Aminobenzoic acid methyl ester

methyl antranilate

NSC 3109

Methylester kyseliny anthranilove

CHEBI:73244

o-Amino methyl benzoate

MFCD00007710

DTXSID6025567

2-Aminobenzoic acid-methyl ester

o-Aminobenzoic acid, methyl ester

2-amino-benzoic acid methyl ester

981I0C1E5W

Methyl ester of o-Aminobenzoic acid

NSC-3109

Methyl 2-Aminobenzoate (Methyl Anthranilate)

DTXCID105567

Amino methyl benzoate, o-

Benzoic acid, amino-, methyl ester

CAS-134-20-3

Methyl anthranilate (natural)

CCRIS 1349

HSDB 1008

EINECS 205-132-4

Epa Pesticide Chemical Code 128725

BRN 0606965

Methylester kyseliny anthranilove [Czech]

METHYL-2-AMINOBENZOATE

UNII-981I0C1E5W

AI3-01022

Methylanthranilate; Methyl 2-aminobenzoate; 2-Aminobenzoic acid methyl ester

FEMA 2682

Carbomethoxyaniline

2-Aminobenzoic acid, methyl ester

methyl aminobenzoate

o-methoxycarbonylaniline

methyl 2-amino-benzoate

WLN: ZR BVO1

SCHEMBL57713

Methyl 2-aminobenzoate, 99%

CHEMBL1493986

METHYL ANTHRANILATE [MI]

METHYL ANTHRANILATE [FCC]

NSC3109

2-amino benzoic acid methyl ester

METHYL ANTHRANILATE [FHFI]

METHYL ANTHRANILATE [HSDB]

METHYL ANTHRANILATE [INCI]

METHYL ANTHRANILATE [VANDF]

METHYL ANTHRANILATE [MART.]

STR00871

Tox21_201657

Tox21_300347

BDBM50581836

METHYL ANTHRANILATE [WHO-DD]

methyl ester of o-amino benzoic acid

STK045541

AKOS000119222

AM10669

CS-W019645

MCULE-3500477192

Methyl anthranilate, >=98%, FCC, FG

NCGC00091409-01

NCGC00091409-02

NCGC00091409-03

NCGC00254347-01

NCGC00259206-01

AC-11600

BENZOIC ACID METHYL ESTER,2-AMINO

HY-77342

Methyl-2-aminobenzoate Methyl anthranilate

5-NITRO-PYRIDINE-2-SULFONYLCHLORIDE

DB-042220

Methyl anthranilate, natural, >=99%, FG

A0500

NS00002018

C20634

D77860

Methyl 2-aminobenzoate, ReagentPlus(R), >=99%

Methyl anthranilate, natural (US), >=99%, FG

Q420894

W-108288

F2141-0131

Methyl 2-aminobenzoate, Vetec(TM) reagent grade, 98%

InChI=1/C8H9NO2/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5H,9H2,1H

The Henry's Law constant for methyl anthranilate is estimated as 1.9X10-6 atm-cu m/mole(SRC) derived from its vapor pressure, 0.027 mm Hg(1), and water solubility, 2,850 mg/liter(2). This Henry's Law constant indicates that methyl anthranilate 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 16 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 178 days(SRC). Methyl anthranilate's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Methyl anthranilate 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. NY, NY: McGraw-Hill 6th ed (1984) (2) Beilstein Handbook of Organic Chemistry; 4th ed, EIV, 14: 1008 (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 methyl anthranilate is estimated as 250(SRC), using a log Kow of 1.88(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that methyl anthranilate is expected to have moderate mobility in soil(SRC).
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. 42 (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)

N-METHYLANILINE

100-61-8

Methylaniline

Monomethylaniline

Benzenamine, N-methyl-

N-Methyl aniline

Methylphenylamine

N-Methylbenzenamine

N-Monomethylaniline

N-Phenylmethylamine

N-Methylaminobenzene

(Methylamino)benzene

Aniline, N-methyl-

Anilinomethane

N-Methylphenylamine

Benzeneamine, N-methyl-

methyl-phenyl-amine

NSC 3502

N-Methyl-N-phenylamine

TH45GK410O

DTXSID9021841

CHEBI:15733

NSC-3502

CCRIS 2870

HSDB 1654

EINECS 202-870-9

UN2294

UNII-TH45GK410O

N-metylaniline

N-Methlaniline

AI3-19498

N-Methylanlne

N-methyl-aniline

methyl(phenyl)amine

methyl-phenyl amine

n-methylphenyl amine

N-methyl phenylamine

N-methyl-benzenamine

MFCD00008283

N-Methylanilinium ion

N-methyl-phenyl-amine

ANILINE,N-METHYL

N-Methylaniline, 98%

METHYLANILINE [MI]

N-Methyl-N-phenylamine #

EC 202-870-9

N-Methylaniline, >=99%

SCHEMBL4454

WLN: 1MR

MLS002415757

BIDD:ER0250

BIDD:GT0230

CHEMBL170781

DTXCID301841

SCHEMBL1415355

NSC3502

HMS3039I05

N-Methylaniline, analytical standard

Tox21_200298

STL183283

AKOS000119086

AM10675

MCULE-6046773954

RP10006

UN 2294

N-Methylaniline [UN2294] [Poison]

NCGC00091265-01

NCGC00091265-02

NCGC00257852-01

AS-12865

BP-31133

CAS-100-61-8

SMR001370917

N-Methylaniline, purum, >=98.0% (GC)

M0147

NS00010869

EN300-19055

C02299

J-000182

J-523671

Q1959597

F2190-0405

Z104472478

InChI=1/C7H9N/c1-8-7-5-3-2-4-6-7/h2-6,8H,1H

1MR

The Henry's Law constant for N-methylaniline estimated from its vapor pressure, 0.453 mm Hg(1), and water solubility, 5624 mg/L(2), is 1.14X10-5 atm-cu-m/mol(SRC). Using this value for the Henry's Law constant, one can estimate a volatilization half-life of 3.5 days for N-methylaniline in a model river 1 m deep flowing at 1 m/s with a wind speed of 3 m/s(3). Similarly, the volatilization half-life for N-methylaniline from a model lake 1 m deep, with a 0.05 m/s current and a 0.5 m/s wind is estimated to be 28 days(3).
Literature: (1) Riddick JA et al; Organic Solvents 4th ed; NY, NY: Wiley (1986) (2) Yalkowsky SH, Dannenfelser RM; Aquasol Data Base of Water Solubility Ver 5, Tuscon,. AZ: Univ Arizona, College of Pharmacy (1992) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods, NY: McGraw-Hill Chapt 15 (1982)

Since the pKa of N-methylaniline is 4.848(2), N-methylaniline will be partially ionized at acidic environmental pHs and its adsorption to soil would be expected to be pH-dependent(SRC). The Koc for N-methylaniline predicted from molecular structure is 65(3). According to a suggested classification scheme(5), this estimated Koc suggests that N- methylaniline will be highly mobile in soil(SRC). Batch equilibrium studies used to determine the adsorption isotherms for N-methylaniline to a Podzol (4.85% OC pH 2.8), an Alfisol (1.25% OC, pH 6.7) and a sediment (1.58% OC, pH 7.1) yielded the results (soil, Freundlich adsorption constants (Kf), Freundlich exponent (1/n), Koc): Podzol, 22.29, 0.89, 460; Alfisol, 0.59, 0.78, 47; Sediment, 1.12, 0.77, 71(1). N-Methylaniline will be almost completely ionized at the pH of the Podzol and therefore ionic interactions may be dominant(1,SRC). N-Methylaniline reacts slowly with humates possibly by adding to quinoidal structures in the humic substances(4). Covalent bond formation is inferred by the lack of extractability of the aniline from the humic material as well as reactions with model compounds(4).
Literature: (1) Von Oepen B et al; Chemosphere 22: 285-304 (1991) (2) Riddick JA et al; Organic Solvents 4th ed; NY, NY: Wiley (1986) (3) Meylan WM et al; Environ Sci Technol 26:1560-7 (1992) (4) Parris GE; Environ Sci Technol 14: 1099-105 (1980) (5) Swann RL et al; Res Rev 85:17-28 (1983)

benzyl alcohol

phenylmethanol

benzenemethanol

100-51-6

phenylcarbinol

benzylalcohol

Benzoyl alcohol

Benzenecarbinol

alpha-Toluenol

Phenylmethyl alcohol

Hydroxytoluene

(Hydroxymethyl)benzene

Phenolcarbinol

Benzal alcohol

benzylic alcohol

Alcool benzylique

Benzylicum

Methanol, phenyl-

Phenylcarbinolum

alpha-hydroxytoluene

Euxyl K 100

hydroxymethylbenzene

Bentalol

Ulesfia

Phenyl Methanol

Phenyl-Methanol

66072-40-0

BENZYL-ALCOHOL

Caswell No. 081F

alcoholum benzylicum

Benzyl alcohol (natural)

FEMA No. 2137

Benzylalkohol

Alcohol,benzyl

NCI-C06111

.alpha.-Hydroxytoluene

Alcool benzilico

Aromatic alcohol

Alcohol, Benzyl

Alcohol bencilico

.alpha.-Toluenol

Alcool benzilico [DCIT]

Itch-X

NSC 8044

HSDB 46

benzenmethanol

Benzalalcohol

Benzalcohol

CCRIS 2081

Aromatic primary alcohol

Alcoolbenzylique

Alcool benzylique [INN-French]

Benzyl alkohol

Alcohol bencilico [INN-Spanish]

Methanol benzene

Alcoholum benzylicum [INN-Latin]

UNII-LKG8494WBH

Alcohol benzylicus

NSC-8044

EINECS 202-859-9

BnOH

LKG8494WBH

EPA Pesticide Chemical Code 009502

BRN 0878307

Sunmorl BK 20

DTXSID5020152

CHEBI:17987

INS NO.1519

AI3-01680

INS-1519

MFCD00004599

Hydroxymethyl resin (100-200 mesh)

TOLUENE,ALPHA-HYDROXY

DTXCID70152

Benzyl alcohol (Benzenemethanol)

benzyl alcohol (ring-13c6)

E-1519

EC 202-859-9

4-06-00-02222 (Beilstein Handbook Reference)

185532-71-2

NCGC00091865-01

BENZYL-ALPHA,ALPHA-D2 ALCOHOL

BENZYL ALCOHOL (II)

BENZYL ALCOHOL [II]

MBN

BENZYL ALCOHOL (MART.)

BENZYL ALCOHOL [MART.]

Alcool benzylique (INN-French)

BENZYL ALCOHOL (USP-RS)

BENZYL ALCOHOL [USP-RS]

Alcohol bencilico (INN-Spanish)

Alcoholum benzylicum (INN-Latin)

BENZYL ALCOHOL (EP MONOGRAPH)

BENZYL ALCOHOL [EP MONOGRAPH]

phenylmethan-1-ol

CAS-100-51-6

Ulesfia (TN)

201740-95-6

Benzyl alcohol [USAN:INN:JAN]

enzylalcohol

Protocoxil

phenyl carbinol

benzene-methanol

Benzyl Alcohole

a-Hydroxytoluene

a-Toluenol

Alcohol benzilico

Benzyl alcohol [INN:JAN:NF]

Hydroxymethyl resin (200-400 mesh)

PhCH2OH

Bn-OH

SCHEMBL147

Benzyl alcohol, ACS grade

bmse000407

C6H5CH2OH

CHEMBL720

WLN: Q1R

BENZYL ALCOHOL [MI]

Benzyl alcohol (JP15/NF)

BENZYL ALCOHOL [FCC]

BENZYL ALCOHOL [INN]

BENZYL ALCOHOL [JAN]

BENZYL ALCOHOL [FHFI]

BENZYL ALCOHOL [HSDB]

BENZYL ALCOHOL [INCI]

BIDD:ER0248

ALCOHOL,BENZYL [VANDF]

BENZYL ALCOHOL [VANDF]

ZilactinEarly Relief Cold Sore

TB 13G

Benzyl alcohol, LR, >=99%

BENZYL ALCOHOL [WHO-DD]

BENZYL ALCOHOL [WHO-IP]

BDBM16418

NSC8044

Benzyl alcohol (JP17/NF/INN)

HMS3264B16

HMS3885F10

Pharmakon1600-01502555

Benzyl alcohol, analytical standard

Benzyl alcohol, AR, >=99.5%

HY-B0892

Benzyl alcohol, anhydrous, 99.8%

Tox21_111172

Tox21_202447

Tox21_300044

BBL011938

BENZYL ALCOHOL [ORANGE BOOK]

NSC760098

s4600

STL163453

Benzyl alcohol, >=99%, FCC, FG

AKOS000119907

Benzyl alcohol, natural, >=98%, FG

CCG-213843

DB06770

MCULE-6011707909

NSC-760098

USEPA/OPP Pesticide Code: 009502

NCGC00091865-02

NCGC00091865-03

NCGC00091865-04

NCGC00254154-01

NCGC00259996-01

ALCOHOL BENZYLICUS [WHO-IP LATIN]

Benzyl alcohol, ACS reagent, >=99.0%

Benzyl alcohol, ReagentPlus(R), >=99%

Benzyl alcohol, USP, 98.0-100.5%

B2378

Benzyl alcohol, tested according to Ph.Eur.

Benzylalcohol 100 microg/mL in Acetonitrile

E1519

NS00009775

Benzyl alcohol, p.a., ACS reagent, 99.0%

Benzyl alcohol, SAJ first grade, >=98.5%

EN300-20016

Benzyl alcohol, SAJ special grade, >=99.0%

Benzyl alcohol, Vetec(TM) reagent grade, 98%

C00556

C03485

D00077

D70182

Q52353

AB01563201_01

A800221

SR-01000872610

J-000153

SR-01000872610-3

BENZALKONIUM CHLORIDE IMPURITY A [EP IMPURITY]

F0001-0019

Z104476418

3762963D-6C2A-4BFF-AD94-3180E51BCA68

Benzyl alcohol, certified reference material, TraceCERT(R)

Benzyl alcohol, European Pharmacopoeia (EP) Reference Standard

Benzyl alcohol, puriss. p.a., ACS reagent, >=99.0% (GC)

Benzyl alcohol, United States Pharmacopeia (USP) Reference Standard

InChI=1/C7H8O/c8-6-7-4-2-1-3-5-7/h1-5,8H,6H

Benzyl alcohol, Pharmaceutical Secondary Standard; Certified Reference Material

Benzyl alcohol, puriss., meets analytical specification of Ph.??Eur., BP, NF, 99-100.5% (GC)

StratoSpheres(TM) PL-HMS (Hydroxymethylstyrene) resin, 50-100 mesh, extent of labeling: 2.0 mmol loading, 1 % cross-linked

The Henry's Law constant for benzyl alcohol is 3.37X10-7 atm cu m/mole(1). This Henry's Law constant indicates that benzyl alcohol is expected to be essentially nonvolatile from water and moist soil 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 113 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 825 days(SRC). Benzyl alcohol's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Benzyl alcohol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 9.4X10-2 mm Hg(3).
Literature: (1) Abraham MH et al; J Pharm Sci 83: 1085-100 (1994) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1989)

Experimental Koc values for benzyl alcohol were <5 for three different soils; Apison (0.11% organic carbon), Fullerton (0.06% organic carbon), and Dormont (1.2% organic carbon)(1). An experimental Koc of 15 was determined for benzyl alcohol on a red-brown Australian soil (1.09% organic carbon)(2,3). A log Koc of 1.43 has also been reported(4). According to a classification scheme(5), these Koc values suggest that benzyl alcohol is expected to have very high mobility in soil.
Literature: (1) Southworth GR, Keller JL; Water Air Soil Poll 28: 239-48 (1986) (2) Briggs GG; Aust J Soil Res 19: 61-8 (1981) (3) Briggs GG; J Agric Food Chem 29: 1050-9 (1981) (4) Xu F et al; J Environ Qual 30: 1618-23 (2001) (5) Swann RL et al; Res Rev 85: 17-28 (1983)

2-PHENYLETHANOL

Phenethyl alcohol

Phenylethyl alcohol

60-12-8

Benzeneethanol

Phenylethanol

Benzyl carbinol

Phenethanol

2-Phenylethyl alcohol

2-PHENYL-ETHANOL

beta-Phenylethanol

2-Phenethyl alcohol

Benzylmethanol

2-Phenylethan-1-Ol

Benzylcarbinol

Methanol, benzyl-

2-Hydroxyethylbenzene

1-Phenyl-2-ethanol

Ethanol, 2-phenyl-

FEMA No. 2858

2-PEA

Benzenethanol

Phenethylalcohol

Phenyl ethyl alcohol

beta-PEA

beta-Phenylethyl alcohol

beta-Hydroxyethylbenzene

Caswell No. 655C

beta-Fenylethanol

FEMA Number 2858

1321-27-3

beta-Fenethylalkohol

Phenethyl alcohol (natural)

beta-Phenethyl alcohol

HSDB 5002

2-Phenethanol

.beta.-Hydroxyethylbenzene

.beta.-Phenylethyl alcohol

Hydroxyethylbenzene

EINECS 200-456-2

UNII-ML9LGA7468

MFCD00002886

PhenethylAlcohol-d5

EPA Pesticide Chemical Code 001503

NSC 406252

NSC-406252

BRN 1905732

.beta.-Phenylethanol

ML9LGA7468

.beta.-PEA

DTXSID9026342

CHEBI:49000

AI3-00744

(2-Hydroxyethyl)benzene

.beta.-Phenethyl alcohol

Phenylethyl alcohol [USP]

.beta.-(hydroxyethyl)benzene

DTXCID206342

EC 200-456-2

4-06-00-03067 (Beilstein Handbook Reference)

NSC406252

NCGC00166215-02

Phenylethyl alcohol (USP)

Ethanol, phenyl-

PHENYLETHYL ALCOHOL (II)

PHENYLETHYL ALCOHOL [II]

PHENETHYL ALCOHOL (MART.)

PHENETHYL ALCOHOL [MART.]

Phenyl Ethanol(Natural)

2 Phenylethanol

PHENYLETHYL ALCOHOL (USP-RS)

PHENYLETHYL ALCOHOL [USP-RS]

beta-Fenylethanol [Czech]

2-phenyl ethanol

Carbinol, Benzyl

beta Phenylethanol

CAS-60-12-8

Alcohol, Phenethyl

beta-Fenethylalkohol [Czech]

PEL

SMR000059156

PHENYLETHYL ALCOHOL (USP MONOGRAPH)

PHENYLETHYL ALCOHOL [USP MONOGRAPH]

Alcohol, Phenylethyl

benzene-ethanol

Mellol

phenyl-ethanol

Benzyl-Methanol

2-PhenyIethanol

phenylethyl-alcohol

.beta.-Phenethanol

HY1

.beta.-Fenylethanol

b-Hydroxyethylbenzene

Benzyl ethyl alcohol

2-phenyl-1-ethanol

Benzeneethanol, 9CI

2-phenylethane-1-ol

betaphenylethyl alcohol

.beta.-Fenethylalkohol

2-Phenylethanol, USP

METHANOL, BENZYL

A-PEA

beta -hydroxyethylbenzene

2-Phenylethanol, 99%

.beta.-P.E.A.

(BETA-PEA)

Phenylethyl alcohol, USAN

bmse000659

Phenylethyl, beta- alcohol

2-(2-Hydroxyethyl)benzene

SCHEMBL1838

WLN: Q2R

MLS001066349

MLS001336026

FEMA NUMBER 2858.

PHENETHYL ALCOHOL [MI]

Phenethyl alcohol, 8CI, BAN

CHEMBL448500

beta-(HYDROXYETHYL)BENZENE

PHENETHYL ALCOHOL [FCC]

PHENYLETHYL, B- ALCOHOL

PHENETHYL ALCOHOL [INCI]

BDBM85807

FEMA 2858

HMS2093H05

HMS2233H06

HMS3374P04

Pharmakon1600-01505398

PHENYLETHYL ALCOHOL [FHFI]

PHENYLETHYL ALCOHOL [HSDB]

PHENETHYL ALCOHOL [WHO-DD]

BCP32115

CS-B1821

HY-B1290

NSC_6054

Tox21_113544

Tox21_201322

Tox21_303383

BBL036905

NSC759116

s3703

STL281950

2-Phenylethanol, >=99.0% (GC)

AKOS000249688

Tox21_113544_1

CCG-213419

DB02192

MCULE-8439044075

NSC-759116

CAS_60-12-8

Phenethyl alcohol, >=99%, FCC, FG

NCGC00166215-01

NCGC00166215-03

NCGC00166215-05

NCGC00257347-01

NCGC00258874-01

AC-18484

SBI-0206858.P001

NS00004212

P0084

EN300-19347

C05853

D00192

D70868

Phenethyl alcohol, natural, >=99%, FCC, FG

AB00698274_05

A832606

Q209463

SR-01000763553

Phenylethyl alcohol;Phenethyl alcohol;Benzeneethanol

Q-200318

SR-01000763553-2

0DE4CADC-AB8A-4038-BD6F-EBD009885652

F0001-1575

Z104473586

2-phenylethanol;2-Phenylethyl alcohol;Benzeneethanol;Phenylethanol

InChI=1/C8H10O/c9-7-6-8-4-2-1-3-5-8/h1-5,9H,6-7H

Phenylethyl alcohol, United States Pharmacopeia (USP) Reference Standard

Phenylethyl Alcohol, Pharmaceutical Secondary Standard; Certified Reference Material

19601-20-8

The Henry's Law constant for 2-phenylethanol estimated from its vapor pressure, 0.0868 mm Hg at 25 deg C(1), and water solubility, 16,000 mg/L(2), is 1.5X10-7 atm-cu m/mol(SRC). Using this value for the Henry's Law constant, one can estimate a volatilization half-life of 2-phenylethanol in a model river 1 m deep flowing at 1 m/s with a wind speed of 3 m/s is 46.5 days(3,SRC). 2-Phenylethanol's relatively low Henry's Law constant and vapor pressure suggest that volatilization from moist and dry soil surfaces will be minimal(SRC).
Literature: (1) Daubert TE, Danner RP; Data Compilation Tables of Properties of Pure Compounds NY, NY: Amer Inst for Phys Prop Data (1989) (2) Valvani SC et al; J Pharm Sci 70: 502-7 (1981) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods, NY: McGraw-Hill Chapt 15 (1982)

Using an estimation method based on molecular connectivity indices(1), the Koc for 2-phenylethanol is estimated to be 29(SRC). According to a suggested classification scheme(2), this Koc value suggests that 2-phenylethanol will have very high mobility in soil(SRC).
Literature: (1) Meylan WM et al; Environ Sci Technol 28: 459-65 (1992) (2) Swann RL et al; Res Rev 85: 23 (1983)