phenylacetaldehyde

2-phenylacetaldehyde

122-78-1

Benzeneacetaldehyde

Hyacinthin

Phenylethanal

alpha-Tolualdehyde

2-Phenylethanal

Phenylacetic aldehyde

Oxophenylethane

alpha-Toluic aldehyde

Acetaldehyde, phenyl-

Benzylcarboxaldehyde

1-Oxo-2-phenylethane

Phenacetaldehyde

phenyl acetaldehyde

phenyl-Acetaldehyde

.alpha.-Tolualdehyde

Benzacetaldehyde

Phenylacetaldehyde (natural)

alpha-Phenylacetaldehyde

Benzenacetaldehyde

.alpha.-Toluic aldehyde

FEMA No. 2974

UNII-U8J5PLW9MR

NSC 406309

U8J5PLW9MR

EINECS 204-574-5

alpha-Tolyaldehyde

Acetaldehyde, phenyl- (8CI)

DTXSID3021483

CHEBI:16424

AI3-02175

NSC-406309

a-Tolyaldehyde

DTXCID501483

FEMA NO. 2874

CAS-122-78-1

benzeneethanal

a-Tolualdehyde

2-phenylethanone

a-toluic aldehyde

Phenylacetoaldehyde

benzene acetaldehyde

a-Phenylacetaldehyde

2-phenyl-acetaldehyde

bmse000427

NCIOpen2_003602

Phenylacetaldehyde, >=90%

SCHEMBL18972

PHENYLACETALDEHYDE [MI]

PHENYLACETALDEHYDE [FCC]

CHEMBL1233464

PHENYLACETALDEHYDE [FHFI]

STR00412

Tox21_201582

Tox21_302945

MFCD00006993

NSC406309

s9357

AKOS000119316

CCG-266073

CS-W011205

DB02178

HY-W010489

MCULE-3725701027

Phenylacetaldehyde, >=95%, FCC, FG

NCGC00249076-01

NCGC00256522-01

NCGC00259131-01

DB-041686

NS00013128

P0119

EN300-18996

C00601

D78329

10.14272/DTUQWGWMVIHBKE-UHFFFAOYSA-N.1

A804962

Q424998

doi:10.14272/DTUQWGWMVIHBKE-UHFFFAOYSA-N.1

Q-201558

F2190-0653

Z104472146

D60A2590-0A65-4BA8-A05B-D8423408535C

InChI=1/C8H8O/c9-7-6-8-4-2-1-3-5-8/h1-5,7H,6H

indole

1H-Indole

120-72-9

2,3-Benzopyrrole

Indol

1-Benzazole

Ketole

1-Azaindene

Benzopyrrole

2,3-Benzopyrole

Indole (natural)

Caswell No. 498B

1-Benzo(b)pyrrole

Indol [German]

FEMA No. 2593

CCRIS 4421

HSDB 599

EPA Pesticide Chemical Code 025000

1H-Benzo[b]pyrrole

Benzo[b]pyrrole

AI3-01540

NSC 1964

EINECS 204-420-7

MFCD00005607

UNII-8724FJW4M5

INDOLUM

DTXSID0020737

CHEBI:16881

8724FJW4M5

NSC-1964

CHEMBL15844

DTXCID40737

Indole 100 microg/mL in Acetonitrile

NCGC00167539-01

INDOLE (USP-RS)

INDOLE [USP-RS]

IND

CAS-120-72-9

benzazole

mono-indole

1-H-indole

Indole, 7

Indole (8CI)

Indole (white flake)

Indole, 98%

1H-Indole (9CI)

INDOLUM [HPUS]

INDOLE [FHFI]

INDOLE [HSDB]

INDOLE [FCC]

INDOLE [MI]

Indole, >=99%

SCHEMBL698

bmse000097

Indole, analytical standard

Indole, >=99%, FG

WLN: T56 BMJ

BIDD:GT0304

SCHEMBL940818

INDOLE BENZO-PYRROLE

SCHEMBL1921769

SCHEMBL9559244

AMY3411

NSC1964

185l

BCP27232

STR01201

Tox21_112536

Tox21_201677

Tox21_302937

BBL011739

BDBM50094702

s6358

STL163380

Indole, 3-Benzopyrrole, 1-benzazole

AKOS000119629

Tox21_112536_1

AT36838

CG-0501

CS-W001132

DB04532

HY-W001132

Indole, puriss., >=98.5% (GC)

MCULE-9442796928

NCGC00167539-02

NCGC00167539-03

NCGC00256348-01

NCGC00259226-01

BP-10563

DS-011308

I0021

NS00010849

EN300-18285

C00463

I-0800

I-0810

Q319541

SR-01000944736

SR-01000944736-1

Z57833933

F2190-0647

InChI=1/C8H7N/c1-2-4-8-7(3-1)5-6-9-8/h1-6,9

82451-55-6

The Henry's Law constant for indole is estimated as 5.3X10-7 atm-cu m/mole(SRC) from its experimental values for vapor pressure, 0.0122 mm Hg(1), and water solubility, 3560 mg/l(2). This value indicates that indole will be essentially nonvolatile from water surfaces(3,SRC). Indole's Henry's Law constant(1,2,SRC) indicates that volatilization from moist soil surfaces should not occur(SRC).
Literature: (1) Yaws CL; Handbook of Vapor Pressure. Volume 3. C8 to C28 Compounds. HOuston,TX: Gulf Publ Co (1994) (2) Yalkowsky SH, Dannenfelser RM; Aquasol Database of Aqueous Solubility. Ver 5. College of Pharmacy, University of Arizona - Tucson, AZ. PC Ver (1992) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

A Koc of 187 was measured for indole on a synthetic soil consisting of 88-90% sand, 10% clay and 0-2% humic acid(1). The Koc of indole is estimated as approximately 350(SRC), using a measured log Kow of 2.14(2) and a regression-derived equation(3,SRC). According to a recommended classification scheme(4), these Koc values suggest that indole has moderate mobility in soil(SRC).
Literature: (1) Rebhun M et al; Water Res 26: 79-84 (1992) (2) Hansch C et al; Exploring QSAR. Hydrophobic, Electronic, and Steric Constants. ACS Prof Ref Book. Amer Chem Soc, Washington, DC. p. 6 (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)

2,4-Di-tert-butylphenol

96-76-4

2,4-DI-T-BUTYLPHENOL

Antioxidant No. 33

1-Hydroxy-2,4-di-tert-butylbenzene

Prodox 146

Phenol, 2,4-bis(1,1-dimethylethyl)-

Phenol, 2,4-di-tert-butyl-

2,4-bis(tert-butyl)phenol

2,4-ditert-butylphenol

Prodox 146A-85X

2,4-Bis(1,1-dimethylethyl)phenol

2,4-tert-butylphenol

MFCD00008828

NSC 174502

2,4-Di-tert-butylphenol-d18

FOB94G6HZT

2,4-di-tert-butyl phenol

2,4-Di-tert-butyl-phenol

2,4-di~{tert}-butylphenol

CHEMBL29873

DTXSID2026602

2,4-Di-tert-butylhydroxybenzene

2,4-Bis(1,1'-dimethylethyl)phenol

2,4-bis(1,1-dimethylethyl)-phenol

NSC-174502

DTXCID606602

1246816-88-5

CAS-96-76-4

2,4-ditert-butyl-phenol

EINECS 202-532-0

UNII-FOB94G6HZT

Phenol, 2,4-di(1,1-dimethylethyl)-

BRN 1910383

2,4-DTBP

2,4-ditertbutylphenol

2,4-di-tertbutylphenol

2,4di-tert-butylphenol

,4-Di-tert-butylphenol

2,4-di-t-butyl-phenol

2,4-di-tert.butylphenol

2,4-di-tertbutyl phenol

2,4-ditert-butyl phenol

2,4-ditertiarybutylphenol

Phenol,4-di-tert-butyl-

AGIDOL 10

EC 202-532-0

?2,4-Di-tert-butylphenol

2,4-Di-tert.-butylphenol

2,4-ditertiary-butyl phenol

SCHEMBL109921

CHEBI:89188

HSDB 8453

2,4-Di-tert-butylphenol, 99%

BCP24012

Phenol,4-bis(1,1-dimethylethyl)-

Tox21_202320

Tox21_300114

BDBM50409544

NSC174502

Phenol,2,4-Bis(1,1-dimethylethyl)

1-Hydroxy-2, 4-di-tert-butylbenzene

AKOS003669719

CS-W015305

HY-W014589

MCULE-6010467095

NCGC00164059-01

NCGC00164059-02

NCGC00164059-03

NCGC00254167-01

NCGC00259869-01

AS-13983

PD158314

2,4-Ditert-butylphenol (ACD/Name 4.0)

WLN: 1X1&1&R BQ CX1&1&1

D0229

NS00010683

EN300-20927

E76999

A845633

Q-200191

Q26840829

2,4-Di-tert-butylphenol 100 microg/mL in Acetonitrile

F0001-2302

(2S)-N-[(1S)-2-[[(1S)-2-[[(1S)-2-[[(1S)-2-[[2-[[(1S)-1-[[(1S)-4-amino-1-[(2S)-2-[(2-amino-2-oxo-ethyl)carbamoyl]pyrrolidine-1-carbonyl]-4-oxo-butyl]carbamoyl]-3

InChI=1/C14H22O/c1-13(2,3)10-7-8-12(15)11(9-10)14(4,5)6/h7-9,15H,1-6H

UGW

The Henry's Law constant for 2,4-di-tert-butylphenol is estimated as 3.7X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 4.77X10-3(1) and water solubilty, 35 mg/L(2). This Henry's Law constant indicates that 2,4-di-tert-butylphenol 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)(3) is estimated as 1.6 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 16 days(SRC). 2,4-Di-tert-butylphenol's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The estimated volatilization half-life from a model pond is 120 months if adsorption is considered(4). 2,4-Di-tert-butylphenol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure(1).

Using a structure estimation method based on molecular connectivity indices(1), the Koc of 2,4-di-tert-butylphenol can be estimated to be 9000(SRC). According to a classification scheme(2), this estimated Koc value suggests that 2,4-di-tert-butylphenol is expected to be immobile in soil(SRC).

1,2,3-TRIMETHYLBENZENE

526-73-8

Hemimellitene

Trimethylbenzene

Hemellitol

Hemimellitol

Benzene, 1,2,3-trimethyl-

25551-13-7

ZK4R7UPH6R

1,2,3-trimethyl-benzene

DTXSID8047769

CHEBI:34037

NSC-5167

1,3-Trimethylbenzene

Hemimellitene, 90.5%

Benzene,2,3-trimethyl-

Trimethyl benzene

1,2,3-Trimethylbenzene 100 microg/mL in Methanol

WLN: 1R B1 C1

1,3-Trimethylbenzene, 90.5%

TRIMETHYLBENZENES

HSDB 6830

NSC 5167

1,2,3-Trimethylbenzene, 90.5%

EINECS 208-394-8

EINECS 247-099-9

UNII-ZK4R7UPH6R

BRN 1903410

Trimethylbenzene, 1,2,3-

CCRIS 8145

UNII-A3F3279Q14

HSDB 7551

Benzene, 1,2,3-trimethyl-; 1,2,3-Trimethylbenzene; Hemimellitene; Hemimellitol; NSC 5167; NSC 65599

1,2,3-TrimethyIbenzene

HEMIMELLITENE [HSDB]

4-05-00-01007 (Beilstein Handbook Reference)

BIDD:ER0517

CHEMBL1797279

DTXCID7027750

DTXSID6049808

CHEBI:38641

NSC5167

1,2,3-TRIMETHYL BENZENE

AMY25707

NSC65599

1,2,3-Trimethylbenzene (>90%)

Tox21_303868

MFCD00008520

NSC-65599

AKOS009031505

MCULE-1130443786

1,2,3-Trimethylbenzene (>90per cent)

NCGC00357131-01

CAS-526-73-8

DB-246429

1,2,3-Trimethylbenzene, analytical standard

NS00010824

T0468

EN300-19373

1,2,3-Trimethylbenzene, technical grade, 90%

A829196

Q4352416

W-105806

F0001-1357

Z104473658

InChI=1/C9H12/c1-7-5-4-6-8(2)9(7)3/h4-6H,1-3H

The Henry's Law constant for 1,2,3-trimethylbenzene is 4.36X10-3 atm-cu m/mole(1). This Henry's Law constant indicates that 1,2,3-trimethylbenzene 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 3.4 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 4.4 days(SRC). 1,2,3-Trimethylbenzene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 1,2,3-Trimethylbenzene is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 1.69 mm Hg(3).
Literature: (1) Sanemasa I et al; Bull Chem Soc Jpn 55:1054-62 (1982) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Yaws CL; IN: Handbook of Vapor Pressure V3 C8-C28 Compounds p. 124 (1994)

1,2,3-Trimethylbenzene has measured log Koc values of 3.04(1) and 2.80(2-5). These values correspond to Koc values of 1,096 and 630. 1,2,3-Trimethylbenzene also has a reported log Kom value of 2.80(6-7). According to a classification scheme(8), these Koc values suggest that 1,2,3-trimethylbenzene is expected to have low mobility in soil(SRC).
Literature: (1) Borisover MD, Graber ER; Chemosphere 34: 1761-76 (1997) (2) Gao C et al; Environ Toxicol Chem 15: 1089-96 (1996) (3) Park JH, Lee HJ; Chemosphere 26: 1905-16 (1993) (4) Sabljic A et al; Chemosphere 31: 4489-514 (1995) (5) Xu F et al; J Environ Qual 30: 1618-23 (2001) (6) Okouchi S, Saegusa H; Bull Chem Soc Jpn 62: 922-4 (1989) (7) Sabljic A; Environ Sci Technol 21: 358-66 (1987) (8) Swann RL et al; Res Rev 85: 17-28 (1983)

MESITYLENE

1,3,5-Trimethylbenzene

108-67-8

sym-Trimethylbenzene

3,5-Dimethyltoluene

Fleet-X

Trimethylbenzol

Benzene, 1,3,5-trimethyl-

s-Trimethylbenzene

2,4,6-trimethylbenzene

NSC 9273

Trimethylbenzene, 1,3,5-

HSDB 92

1,3,5-trimethyl-benzene

EINECS 203-604-4

UNII-887L18KQ6X

CCRIS 8147

DTXSID6026797

CHEBI:34833

AI3-23973

887L18KQ6X

NSC-9273

DTXCID506797

EC 203-604-4

CAS-108-67-8

UN2325

Symmetrical trimethylbenzene

Mesitylene, 98%

MESITELENE

MESITYLENE [MI]

MESITYLENE [HSDB]

MESITYLENE [INCI]

1,3, 5-Trimethylbenzene

(3,5-dimethylphenyl)methyl

BIDD:ER0286

Mesitylene (ACD/Name 4.0)

Mesitylene, analytical standard

CHEMBL1797281

WLN: 1R C1 E1

Mesitylene, reagent grade, 97%

NSC9273

BENZENE,1,3,5-TRIMETHYL

DTXSID601311725

STR03436

Tox21_201452

Tox21_300341

MFCD00008538

STL268905

1,3,5-Trimethylbenzene (Mesitylene)

AKOS000120144

MCULE-4050779572

Mesitylene, purum, >=98.0% (GC)

UN 2325

NCGC00247999-01

NCGC00247999-02

NCGC00254430-01

NCGC00259003-01

NS00004224

S0658

T0470

EN300-19371

A801911

Q425161

J-002179

J-521685

1,3,5-Trimethylbenzene [UN2325] [Flammable liquid]

F0001-0175

Mesitylene, certified reference material, TraceCERT(R)

Z104473654

InChI=1/C9H12/c1-7-4-8(2)6-9(3)5-7/h4-6H,1-3H

19121-63-2

The Henry's Law constant for 1,3,5-trimethylbenzene was measured as 8.77X10-3 atm-cu m/mole(1). This Henry's Law constant indicates that 1,3,5-trimethylbenzene is expected to volatilize rapidly from water surfaces(2). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(2) is estimated as 1.2 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(2) is estimated as 4.4 days(SRC). 1,3,5-Trimethylbenzene's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 1,3,5-Trimethylbenzene is expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 2.48 mm Hg(3). Residence times (with respect to volatilization) for 1,3,5-trimethylbenzene were calculated as 220 hours for both winter and summer conditions in Narragansett Bay(4). Complete removal of 1,3,5-trimethylbenzene (at 0.035 ug/ml soil extract) from sandy loam soil samples contaminated with jet fuel was reported within 5 days; sterile samples with 1,3,5-trimethylbenzene at 0.035 ug/ml soil extract also showed complete removal of this compound within 5 days, probably by evaporation(5).
Literature: (1) Sanemasa,I et al; Bull Chem Soc Jpn 55: 1054-62 (1982) (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) (4) Wakeham SG et al; Canad J Fish Aquat Sci 40: 304-21 (1983) (5) Dean-Ross D; Bull Environ Contam Toxicol 51: 596-99 (1993)

The Koc of 1,3,5-trimethylbenzene has been measured at a range of 501-1,445(1-4). According to a classification scheme(5), this Koc range suggests that 1,3,5-trimethylbenzene is expected to have low mobility in soil. 1,3,5-Trimethylbenzene was detected in soil leachate samples following the addition of crude oil to the surface of a soil trough filled with sand(6).
Literature: (1) Schwarzenbach RP, Westall J; Environ Sci Technol 15: 1360-67 (1981) (2) Borisover MD et al; Chemosphere 34: 1761-1776 (1997) (3) Wiedemeier TH et al; Ground Water Monit Remed 16: 186-194 (1996) (4) XU F et al; J Environ Qual 30: 1618-1623 (2001) (5) Swann RL et al; Res Rev 85: 17-28 (1983) (6) Duffy JJ et al; Environ Internat 3: 107-120 (1980)

1-Ethyl-2-methylbenzene

2-Ethyltoluene

611-14-3

O-ETHYLTOLUENE

o-Methylethylbenzene

1-Methyl-2-ethylbenzene

Toluene, o-ethyl-

ortho-Ethyltoluene

Benzene, 1-ethyl-2-methyl-

1,2-methylethylbenzene

o-Ethyl methyl benzene

o-Ethylmethylbenzene

Ethyltoluene

25550-14-5

2-Methylethylbenzene

NSC 405731

2-Methyl-1-ethylbenzene

CHEMBL364233

DBX00873SV

DTXSID2050403

CHEBI:34276

NSC-405731

o-Ethyl methylbenzene

Ethyltoluene, o-

2-ethyl-1-methylbenzene

EINECS 210-255-1

1-ethyl-2-methyl-benzene

BRN 1851237

UNII-DBX00873SV

AI3-28773

2-ethyl toluene

2-ethylmethylbenzene

Toluene, 2-ethyl-

2-Ethyltoluene, 99%

2-Ethyltoluene 100 microg/mL in Methanol

4-05-00-00999 (Beilstein Handbook Reference)

BIDD:ER0573

WLN: 2R B1

DTXCID5029477

Tox21_303797

BDBM50167949

MFCD00009257

NSC405731

AKOS015842902

AC-6953

CS-W009542

DS-2369

MCULE-7161910991

NCGC00356979-01

CAS-611-14-3

DB-024735

A8492

AM20040851

E0184

NS00002055

J-504600

Q27115961

2-Ethyltoluene, certified reference material, TraceCERT(R)

InChI=1/C9H12/c1-3-9-7-5-4-6-8(9)2/h4-7H,3H2,1-2H

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)