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)

hydroxymethylbenzene

Alcoolbenzylique

Hydroxymethyl polystyrene

PENTADEOTEROBENZYL ALCOHOL

Phenylcarbinolum

Polystyrene crosslinked with divinylbenzene, hydroxymethylated

Benzencarbinol

Benzenecarbinol

benzenemethanol

benzenmethanol

Hydroxytoluene

Phenolcarbinol

phenylcarbinol

phenylmethanol

Benzalalcohol

benzylalcohol

Benzylalkohol

enzylalcohol

alcoholum benzylicum

alpha-hydroxytoluene

aplha-Hydroxytoluene

Benzalcohol

Benzylicum

Phenylmethyl alcohol

(Hydroxymethyl)polystyrene

Alcohol bencilico

Alcool benzylique

Averteax

Bentalol

Bentanol

Polystyrene cross-linked with divinylbenzene, hydroxymethylated

WVDDGKGOMKODPV-UHFFFAOYSA-N

a-Hydroxytoluene

Alcool benzilico

Aromatic alcohol

Aromatic primary alcohol

Benzene Carbinol

benzene-methanol

Benzoyl alcohol

Benzyl Alcohole

benzylic alcohol

Methanol benzene

Phenyl Methanol

Phenyl-Methanol

Ulesfia

(Hydroxymethyl)benzene

alpha-Toluenol

Benzal alcohol

benzyl alcohol

Benzyl alcohol Natural

Benzyl alkohol

BENZYL-ALCOHOL

OBZ

TOLUENE,ALPHA-HYDROXY

a-Toluenol

Benzyl alcohol polymer-bound

Benzyl alcohol, analytical standard

ACMC-1BQPG

Benzyl Alcohol Reagent ACS Grade

Itch-X

.alpha.-Hydroxytoluene

Babys Own Teething Gel

CHEMBL720

METHYL, HYDROXYPHENYL-

phenylmethan-1-ol

SCHEMBL147

Zilactin Early Relief Cold Sore

AC1L18SY

BENZYL ALCOHOL, ACS

Benzyl alcohol, polymer-bound

Nat. Benzyl Alcohol

StratoSpheres™ PL-HMS (Hydroxymethylstyrene) resin

Babys Own Gora Teething Lot

LKG8494WBH

Methanol, phenyl-

.alpha.-Toluenol

AC1Q7C20

Benzyl alcohol (natural)

HSDB 46

I765

KSC176G5N

Alcohol bencilico [INN-Spanish]

Alcoholum benzylicum [INN-Latin]

Alcool benzilico [DCIT]

NSC8044

TB 13G

UNII-LKG8494WBH

Alcool benzylique [INN-French]

B2378

BDBM16418

CTK0H6356

E1519

HMDB03119

Sunmorl BK 20

Ulesfia (TN)

WLN: Q1R

AS04466

BIDD:ER0248

DB06770

LS-307

LS41488

RP18893

Benzyl alcohol, European Pharmacopoeia (EP) Reference Standard

bmse000407

C00556

C03485

CCRIS 2081

D00077

DSSTox_CID_152

HMS3264B16

PINAPUR™ 9 BA-R

ZINC895302

AK146334

BBL011938

BC222892

Benzyl alcohol, pharmaceutical secondary standard; traceable to USP and PhEur

DTXSID5020152

Euxyl K 100

HY-B0892

Jsp000133

NSC 8044

NSC-8044

NSC760098

OR034579

OR214344

OR246346

SBB058558

STL163453

ZB015017

A800221

Benzyl alcohol, certified reference material, TraceCERT(R)

Benzyl alcohol, United States Pharmacopeia (USP) Reference Standard

CHEBI:17987

NCI-C06111

AJ-24171

Benzyl alcohol [USAN:INN:JAN]

Caswell No. 081F

DSSTox_GSID_20152

SC-47293

Baby's Own Teething Gel 2.5%

BB_SC-7027

DSSTox_RID_75404

MFCD00004599

MFCD03792087

ZINC00895302

AI3-01680

Benzyl alcohol, LR, >=99%

Benzyl alcohol, tested according to Ph.Eur.

CCG-213843

KB-200532

NSC-760098

RTR-033774

ST24048908

ST51028320

TR-033774

AKOS000119907

Benzyl alcohol (JP15/NF)

EPA Pesticide Chemical Code 009502

I01-4406

J-000153

BRN 0878307

FEMA No. 2137

FT-0622812

FT-0673838

Benzyl alcohol (JP17/NF/INN)

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

Z955123784

Benzyl alcohol, anhydrous, 99.8%

Tox21_111172

Tox21_202447

Tox21_300044

100-51-6

Benzyl alcohol, natural, >=98%, FG

F0001-0019

Benzyl alcohol on polystyrene, 3.5 mmol/g

Benzyl alcohol, ACS reagent, >=99.0%

Benzyl alcohol, AR, >=99.5%

1336-27-2

Baby's Own Teething Gel - 2.5%

Benzyl alcohol, >=99%, FCC, FG

MCULE-6011707909

NCGC00091865-01

NCGC00091865-02

NCGC00091865-03

NCGC00091865-04

NCGC00254154-01

NCGC00259996-01

AB01563201_01

Benzyl alcohol, 99% 250g

Benzyl alcohol, SAJ special grade, >=99.0%

CAS-100-51-6

EINECS 202-859-9

66072-40-0

Benzyl alcohol, SAJ first grade, >=98.5%

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

Pharmakon1600-01502555

SR-01000872610

185532-71-2

3983-EP2269992A1

3983-EP2270004A1

3983-EP2270005A1

3983-EP2270011A1

3983-EP2270505A1

3983-EP2272516A2

3983-EP2272813A2

3983-EP2272817A1

3983-EP2272822A1

3983-EP2272825A2

3983-EP2272841A1

3983-EP2274983A1

3983-EP2275102A1

3983-EP2275401A1

3983-EP2275411A2

3983-EP2275414A1

3983-EP2275425A1

3983-EP2277565A2

3983-EP2277566A2

3983-EP2277567A1

3983-EP2277568A2

3983-EP2277569A2

3983-EP2277570A2

3983-EP2277848A1

3983-EP2277867A2

3983-EP2277876A1

3983-EP2277879A1

3983-EP2279750A1

3983-EP2280001A1

3983-EP2280003A2

3983-EP2280005A1

3983-EP2280008A2

3983-EP2280010A2

3983-EP2280012A2

3983-EP2281823A2

3983-EP2284149A1

3983-EP2284160A1

3983-EP2287155A1

3983-EP2287160A1

3983-EP2287165A2

3983-EP2287166A2

3983-EP2289884A1

3983-EP2289887A2

3983-EP2289888A2

3983-EP2289892A1

3983-EP2289894A2

3983-EP2292227A2

3983-EP2292280A1

3983-EP2292596A2

3983-EP2292611A1

3983-EP2292612A2

3983-EP2292614A1

3983-EP2292615A1

3983-EP2292620A2

3983-EP2295402A2

3983-EP2295406A1

3983-EP2295411A1

3983-EP2295412A1

3983-EP2295413A1

3983-EP2295426A1

3983-EP2295427A1

3983-EP2295437A1

3983-EP2295550A2

3983-EP2298731A1

3983-EP2298734A2

3983-EP2298735A1

3983-EP2298743A1

3983-EP2298744A2

3983-EP2298750A1

3983-EP2298755A1

3983-EP2298768A1

3983-EP2298772A1

3983-EP2298775A1

3983-EP2298783A1

3983-EP2301918A1

3983-EP2301931A1

3983-EP2301936A1

3983-EP2305243A1

3983-EP2305636A1

3983-EP2305640A2

3983-EP2305651A1

3983-EP2305673A1

3983-EP2305676A1

3983-EP2305695A2

3983-EP2305696A2

3983-EP2305697A2

3983-EP2305698A2

3983-EP2305808A1

3983-EP2308812A2

3983-EP2308828A2

3983-EP2308833A2

3983-EP2308839A1

3983-EP2308844A2

3983-EP2308845A2

3983-EP2308846A2

3983-EP2308854A1

3983-EP2308857A1

3983-EP2308858A1

3983-EP2308861A1

3983-EP2308867A2

3983-EP2308870A2

3983-EP2308872A1

3983-EP2308873A1

3983-EP2308875A1

3983-EP2308877A1

3983-EP2311806A2

3983-EP2311815A1

3983-EP2311816A1

3983-EP2311817A1

3983-EP2311823A1

3983-EP2311824A1

3983-EP2311829A1

3983-EP2311831A1

3983-EP2311834A1

3983-EP2311837A1

3983-EP2311842A2

3983-EP2314575A1

3983-EP2314584A1

3983-EP2314585A1

3983-EP2316470A2

3983-EP2316829A1

3983-EP2316831A1

3983-EP2316834A1

3983-EP2316835A1

3983-EP2316836A1

3983-EP2372017A1

3983-EP2374454A1

3983-EP2374783A1

3983-EP2374790A1

3983-EP2374792A1

3983-EP2380568A1

BENZYL ALCOHOL, U.S.P./N.F.

MolPort-001-783-216

Benzyl alcohol, PharmaGrade, USP/NF, Ph Eur, Manufactured under appropriate GMP controls for pharma or biopharmaceutical production.

SR-01000872610-3

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

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

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

(Hydroxymethyl)polystyrene, 200-400 mesh, extent of labeling: ~1.7 mmol/g loading

(Hydroxymethyl)polystyrene, 200-500 mesh, extent of labeling: ~1.1 mmol/g loading

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

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

Benzyl alcohol, polymer-bound, 70-90 mesh, extent of labeling: 2.0-3.0 mmol loading, 1 % cross-linked

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

Benzyl alcohol, polymer-bound, 70-90 mesh, extent of labeling: 0.5-1.0 mmol/g loading, 1 % cross-linked with divinylbenzene

Benzyl alcohol, polymer-bound, 70-90 mesh, extent of labeling: 1.0-1.5 mmol/g loading, 1 % cross-linked

Benzyl alcohol, polymer-bound, 100-200 mesh, extent of labeling: 1.0-2.0 mmol/g loading, 1 % cross-linked with divinylbenzene

Benzyl alcohol, polymer-bound, 100-200 mesh, extent of labeling: 0.5-1.0 mmol/g 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)

Neomenthol

Racementhol

Fisherman's friend lozenges

Mentholum

NOOLISFMXDJSKH-UHFFFAOYSA-N

MENTHOL

Menthyl alcohol

Robitussin Cough Drops

Therapeutic mineral ice

d-Neomenthol

Mineral ice

dl-Menthol

AC1Q2QQM

2-Isopropyl-5-methylcyclohexanol

DL-Menthol, analytical standard

AC1L1B2E

ACMC-1BQW4

L7T10EIP3A

SCHEMBL4612

2-Isopropyl-5-methylcyclohexanol #

3-p-Menthol

K601

2-Isopropyl-5-methyl-cyclohexanol

Fisherman's friend lozenges (TN)

Menthol (USP)

Menthol [USP]

UNII-L7T10EIP3A

(?)-Menthol

dl-3-p-Menthanol

H2461

M0321

Menthol, 99%

AM81446

CHEMBL256087

LS-886

Menthol(-)

p-Menthan-3-ol

RL02685

RP22054

1-methyl-4-isopropyl-3-hydroxycyclohexane

19863P

CCRIS 9231

D04849

D04918

DSSTox_CID_805

AK111256

BBL009325

BT000185

DL-MENTHOL, CRYSTAL, USP

DR000160

DTXSID8029650

OR223322

OR240888

OR273366

STK802468

A808833

CHEBI:25187

L(-)-Menthol

RACEMIC MENTHOL U.S.P.

(-) menthol

(+) Menthol

(+)-Menthol

2-Isopropyl-5-methylcyclohexan-1-ol

4-Isopropyl-1-methylcyclohexan-3-ol

AN-19301

AN-19302

AN-19706

AN-20764

AN-24175

ANW-21459

D-p-Menthan-3-ol

DSSTox_GSID_29650

KB-78308

LS-57201

LS-89531

SC-01321

SC-54016

SC-84251

Caswell No. 540

DSSTox_RID_78794

MFCD00001484

(+)-Neo-menthol

AI3-08161

DB-063989

dl-Menthol (JP17)

KB-231063

ST24028056

TC-030785

TC-110204

5-Methyl-2-(1-methylethyl)cyclohexanol

AKOS000119740

AKOS016843634

EPA Pesticide Chemical Code 051601

I14-7371

J-500418

FT-0620596

FT-0625488

FT-0693479

FT-0695077

FT-0695078

FT-0695079

89-78-1

Tox21_200010

Tox21_303464

491-01-0

5-Methyl-2-(1-methylethyl)-cyclohexanol

Z1258992394

(+/-) menthol

(+/-)-Menthol

5-methyl-2-(propan-2-yl)cyclohexanol

1490-04-6

MCULE-3070949324

Menthol, SAJ special grade, >=98.0%

NCGC00159382-03

NCGC00159382-04

NCGC00159382-05

NCGC00159382-06

NCGC00257403-01

NCGC00257564-01

5-methyl-2-propan-2-yl-1-cyclohexanol

5-methyl-2-propan-2-ylcyclohexan-1-ol

EINECS 216-074-4

MENTHOL, (+)-neo-

Menthol, puriss., 99.0%

15356-70-4

20747-49-3

Cyclohexanol 5-methyl-2-(1-methylethyl)-

DL-Menthol, >=95%, FCC, FG

(+)-p-Menthan-3-ol

CAS-1490-04-6

EC 216-074-4

(DL)-5-methyl-2-(1-methylethyl)cyclohexanol

5-methyl-2-propan-2-yl-cyclohexan-1-ol

MolPort-000-849-729

Cyclohexanol, 5-methyl-2-(1-methylethyl)-

(1S,2R,5R)-2-isopropyl-5-methyl-cyclohexanol

5-methyl-2-(propan-2-yl)cyclohexan-1-ol

Menthol, trans-1,3,trans-1,4-

(+/-)-p-Menthan-3-ol

(1S,2R,5R)-(+)-Isomenthol

Menthol, (.+/-.)-

5-methyl-2-(1-methylethyl)cyclohexanol (1alpha, 2beta, 5alpha)

(1S, 2S, 5R)-(+)-Neomenthol

cis-1,3-trans-1,4-(+-)-menthol

cis-1 ,3-trans-1,4-(+-)-menthol

(+/-)-Menthol, racemic, >=98.0% (GC)

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1R,2S,5S)-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1S,2R,5R)-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1S,2S,5R)-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1R,2R,5S)-rel-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1R,2S,5R)-rel-

Cyclohexanol, 5-methyl-2-propyl-, (1S-(1-alpha,2-alpha,5-beta))-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, [1S-(1?,2?,5ss)]-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, [1S-(1?,2ss,5?)]-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1alpha,2beta,5alpha)-(+-)-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1.alpha.,2.alpha.,5.beta.)-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1.alpha.,2.beta.,5.alpha.)-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1?,2ss,5?)-(+/-)-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, [1R-(1.alpha.,2.alpha.,5.beta.)]-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, [1S-(1.alpha.,2.alpha.,5.beta.)]-

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, [1S-(1.alpha.,2.beta.,5.beta.)]-

Menthol solution, NMR reference standard, 30 wt. % in chloroform-d (99.8 atom % D), NMR tube size 5 mm x 8 in.

Cyclohexanol, 5-methyl-2-(1-methylethyl)-, (1.alpha.,2.beta.,5.alpha.)-(.+/-.)-

Menthol solution, NMR reference standard, 50% in chloroform-d (99.8 atom % D), chromium(III) acetylacetonate 0.5 %, NMR tube size 5 mm x 8 in.

The Henry's Law constant for menthol is estimated as 2.6X10-5 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that menthol 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 2 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 18 days(SRC). Menthol's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). Menthol is not expected to volatilize from dry soil surfaces(SRC) based upon an estimated vapor pressure of 7.7X10-3 mm Hg(SRC), determined from a fragment constant method(1).
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of May 13, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington, DC: Amer Chem Soc pp. 15-1 to 15-29 (1990)

Using a structure estimation method based on molecular connectivity indices(1), the Koc of menthol can be estimated to be 88(SRC). According to a classification scheme(2), this estimated Koc value suggests that menthol 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 May 13, 2015: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm

hexadecylalcohol

Isohexadecanol

cetylalcohol

Cetylalkohol

HEXADECANOL

Isohexadecyl alcohol

BXWNKGSJHAJOGX-UHFFFAOYSA-N

Cetaffine

Hexadecyl alcohol

Cetanol

Cetylic alcohol

Cetylol

Hyfatol

Isocetyl alcohol

palmitic alcohol

Palmityl alcohol

1-Hydroxyhexadecane

Cetal

cetyl alcohol

Ethal

Ethol

Hexadecanol NF

Loxanwachs SK

N-Hexadecanol

Normal primary hexadecyl alcohol

Ceraphyl ICA

Crodacol-CAS

Crodacol-CAT

Cyclal cetyl alcohol

1-Hexanedecanol

Cetalol CA

Crodacol C

Elfacos C

Fancol CA

Lipocol C

Loxanol K

n-Hexadecyl alcohol

Siponol CC

1-Hexadecanol

Atalco C

Cetyl alcohol NF

Cetyl alcohol, analytical standard

Hexadecyl alcohol, normal

Lanol C

Rita CA

1-Hexadecyl alcohol

ACMC-1AJXA

Loxanol K extra

n-Cetyl alcohol

SSD RP

1-Cetanol

16-Hexadecanol

CHEMBL706

Crodacol C95NF

Siponol wax-A

1-Hexadecyl alc

C16 alcohol

Crodacol C70

Eutanol G16

n-1-Hexadecanol

936JST6JCN

Adol 52NF

Alfol 16RD

Cetyl alcohol (hexadecanol)

Epal 16NF

Hexadecan-1-ol

Hexadecanol (VAN)

Hyfatol 16

Lanette 16

Laurex 16

Lorol C16

LorolL 24

SCHEMBL3381

AC1L1E85

Adol 52

Adol 54

Aldol 54

Alfol 16

Epal 16

KSC206A8T

Lorol 24

ARONIS25150

Crodacol C95 NF

Dehydag wax 16

NSC4194

Product 308

UNII-936JST6JCN

Adol 520

Alcohol C-16

Cachalot C-50

Cachalot C-51

Cachalot C-52

Cetanol (TN)

CTK1A6089

HMDB03424

n-Hexadecan-1-ol

Philcohol 1600

Adol 52 NF

Cetyl alcohol (NF)

Cetyl alcohol [NF]

Dytol F-11

Kalcol 6098

NE10353

UNII-2DMT128M1S component BXWNKGSJHAJOGX-UHFFFAOYSA-N

UNII-S4827SZE3L component BXWNKGSJHAJOGX-UHFFFAOYSA-N

bmse000487

C00823

Cetyl alcohol, European Pharmacopoeia (EP) Reference Standard

D00099

Fatty alcohol(C16)

HMS3652H05

HSDB 2643

1-Hexadecanol, >=99%

Cachalot C-50 NF

CO-1670

CO-1695

CS-D1348

DTXSID4027991

FEMA Number 2554

LP003429

LS-2793

NSC 4194

NSC-4194

SBB060167

SSD (Salt/Mix)

ST075158

STL283943

UNII-B1K89384RJ component BXWNKGSJHAJOGX-UHFFFAOYSA-N

1-Hexadecanol, 95%

Cetanol (JP17)

Cetyl Alcohol, pharmaceutical secondary standard; traceable to USP and PhEur

Cetyl alcohol, United States Pharmacopeia (USP) Reference Standard

CHEBI:16125

DSSTox_CID_7991

Loxiol VPG 1743

ZINC8214519

AK-48193

ANW-28459

Caswell No. 165D

DSSTox_GSID_27991

Hyfatol 16-95

SC-18656

ST2415347

TRA0159983

DSSTox_RID_78633

LMFA05000061

MFCD00004760

SSD RP (Salt/Mix)

AI3-00755

KB-218917

RTR-036616

TR-036616

AKOS005287456

Alcohols, C14-18

EPA Pesticide Chemical Code 001508

xOemicro (1/4)

BRN 1748475

FEMA No. 2554

I14-18880

Michel XO-150-16

EN300-19351

Tox21_111609

Tox21_300325

124-29-8

F0001-1047

1-Hexadecanol, ReagentPlus(R), 99%

8014-51-5

8023-37-8

8032-16-4

8032-17-5

8032-89-1

MCULE-9457426256

NCGC00159368-02

NCGC00159368-03

NCGC00159368-04

NCGC00159368-05

NCGC00159368-06

NCGC00254286-01

AB01566915_01

Cetyl alcohol, SAJ special grade, >=98.0%

EINECS 252-964-9

EINECS 253-149-0

29354-98-1

36653-82-4

51260-59-4

55069-45-9

Cetyl alcohol, Selectophore(TM), >=99.0%

Cetyl alcohol, puriss., 95.0%

SR-01000944409

Tox21_111609_1

1-Hexadecanol, Vetec(TM) reagent grade, 94%

CAS-36653-82-4

MolPort-001-783-290

1173838-87-3

1-E(R)AuIe (1/4)

SR-01000944409-1

19141-82-3 (aluminum salt)

Cetyl alcohol, puriss., >=99.0% (GC)

S4173,36653-82-4

4-01-00-01876 (Beilstein Handbook Reference)

810F139F-C57E-4DF1-916A-A320AD0DAF4D

InChI=1/C16H34O/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17/h17H,2-16H2,1H

The Henry's Law constant for 1-hexadecanol is estimated as 4.6X10-5 atm-cu m/mole(SRC) derived from its vapor pressure, 6.0X10-6 mm Hg(1), and water solubility, 4.1X10-2 mg/L(2). This Henry's Law constant indicates that 1-hexadecanol 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 23 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 12 days(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 1.8 years if adsorption is considered (4). 1-Hexadecanol's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 1-Hexadecanol is not expected to volatilize from dry soil surfaces(SRC) based upon its vapor pressure(1).
Literature: (1) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation Washington, DC: Taylor and Francis supplement 5 (1995) (2) Yalkowsky SH, He Y; Handbook of Aqueous Solubility Data. CRC Press LLC, Boca Raton, FL. p. 1063 (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)

The Koc of 1-hexadecanol is estimated as 25,000(SRC), using a water solubility of 4.122X10-2(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that 1-hexadecanol is expected to be immobile in soil.
Literature: (1) Yalkowsky SH, He Y; Handbook of Aqueous Solubility Data. CRC Press LLC, Boca Raton, FL. p. 1063 (2003) (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)

Wintergruenoel

Gaultheriaoel

methyl hydroxybenzoate

Methylester kyseliny salicylove

Metylester kyseliny salicylove

Panalgesic

Theragesic

Flucarmit

methyl salicylate

Methyl2-Hydroxybenzoate

Methylis salicylas

OSWPMRLSEDHDFF-UHFFFAOYSA-N

PredaLure

2-Carbomethoxyphenol

Analgit

Betula

Exagien

Methyl o-hydroxybenzoate

Synthetic Wintergreen Oil

Wintergreen oil

Anthrapole ND

Gaultheria oil

Natural Wintergreen Oil

paragraph sign notAIUO

paragraph sign notCaOI

salicylate methyl ester

Spicewood Oil

Betula Lenta

Methyl salicylate, analytical standard

salicylic acid methyl

Teaberry oil

Betula oil

Birch oil

Methyl 2-hydroxybenzoate

methyl-2-hydroxybenzoate

OIL OF WINTERGREEN

Salicylic Acid Methyl Ester

AC1L1HHJ

Ben Gay

Betula lenta oil

BIRCH-ME

Gaultheria oil, artificial

Methyl salicylate, BioXtra

WINTER GREEN OIL

Wintergreen Oil, synthetic

1-O-methylsalicylate

ACMC-1BSKR

Birch Bark oil

Black birch oil

Sweet birch oil

Methylester kyseliny salicylove [Czech]

2-(Methoxycarbonyl)phenol

2-Hydroxybenzoic acid methyl ester

AC1Q42RT

Metylester kyseliny salicylove [Czech]

Salicylic acid, methyl ester

Wintergreen oil, China origin

ZINC490

Betula oil, Wintergreen oil

Methyl salicylate (natural)

o-Hydroxybenzoic acid, methyl ester

Oils, sweet birch

SCHEMBL5312

Birch oil, sweet

GTPL2431

H364

KSC175K7B

Methyl salicylate, pharmaceutical secondary standard; traceable to USP

Methyl salicylate (TN)

Methyl salicylate [JAN]

NSC8204

2-Hydroxy-benzoic acid methyl ester

2-Hydroxybenzoic acid, methyl ester

CTK0H5570

LAV5U5022Y

methyl ester 2-hydroxy benzoic acid

Methyl salicylate, 98%

S0015

Theragesic (Salt/Mix)

BIDD:ER0323

CHEMBL108545

LS-616

NE10156

RP21593

Salonpas (Salt/Mix)

C12305

CCRIS 6259

D01087

HMS1398J05

HMS2089H12

HSDB 1935

Methyl salicylate [JAN:NF]

Methyl salicylate, United States Pharmacopeia (USP) Reference Standard

UNII-LAV5U5022Y

WLN: QR BVO1

AK105942

BBL010504

BT000168

DTXSID5025659

FEMA Number 2745

Methyl ester of 2-hydroxy-benzoic acid

NSC 8204

NSC-8204

OR001314

OR207884

OR207885

SBB053705

STK397388

CHEBI:31832

DSSTox_CID_5659

AC-11584

AJ-07901

AN-22802

AN-37948

ANW-17321

CJ-00014

DSSTox_GSID_25659

Enamine_001611

KB-53924

KB-54838

LS-98262

Methyl salicylate, tested according to Ph.Eur.

TS-02010

BB_SC-7170

Benzoic acid, hydroxy-, methyl ester

Caswell No. 577

DSSTox_RID_77872

Methyl salicylate (JP17/NF)

MFCD00002214

ZINC00000490

AI3-00090

DB-012808

RTR-003257

ST24030969

ST50715363

TR-003257

AKOS000118977

EPA Pesticide Chemical Code 076601

I01-4358

I01-8932

Q-100939

Z19703590

BRN 0971516

FEMA No. 2154

FEMA No. 2745

FT-0612582

FT-0622968

FT-0698844

Tox21_111081

Tox21_201543

Tox21_300137

119-36-8

Benzoic acid, 2-hydroxy-, methyl ester

Birch sweet oil (Betula lenta L.)

F0001-0306

Methyl salicylate, >=98%, FCC, FG

Methyl salicylate, 98% 500g

8022-86-4

8024-54-2

MCULE-5398249325

Methyl salicylate, SAJ first grade, >=98.0%

Methyl salicylate, Vetec(TM) reagent grade, 99%

NCGC00091106-01

NCGC00091106-02

NCGC00091106-03

NCGC00091106-04

NCGC00091106-05

NCGC00254104-01

NCGC00259093-01

AB01275470-01

CAS-119-36-8

EINECS 204-317-7

68917-75-9

90045-28-6

EC 204-317-7

SR-05000001473

648434-07-5

Methyl salicylate, natural, 98%, FCC, FG

1929-EP2272835A1

1929-EP2272844A1

MolPort-001-783-865

2-[Hydroxy(methoxy)methylene]-3,5-cyclohexadiene-1-one

Methyl salicylate, ReagentPlus(R), >=99% (GC)

23256-EP2277848A1

23256-EP2289892A1

23256-EP2298735A1

23256-EP2305250A1

23256-EP2305688A1

23256-EP2308867A2

23256-EP2308870A2

23256-EP2311824A1

23256-EP2311842A2

23256-EP2314584A1

7631-93-8 (hydrochloride salt)

SR-05000001473-1

6-[(E)-Methoxyhydroxymethylene]-2,4-cyclohexadiene-1-one

4-10-00-00143 (Beilstein Handbook Reference)

Methyl salicylate, puriss., 99.0-100.5%

AUoC>>u+/-(1/2)(1/4)xEa(1/4)xo yen

2-oC>>u+/-(1/2)(1/4)xEa(1/4)xo yen

InChI=1/C8H8O3/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5,9H,1H

The Henry's Law constant for methyl salicylate is 9.3X10-7 atm-cu-m/mol(SRC) calculated from its vapor pressure, 0.0343 mm Hg(1), and water solubility, 7400 mg/L(2). Using this value for the Henry's Law constant, one can estimate a volatilization half-life of 49 days 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 of methyl salicylate 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 359 days. Methyl salicylate sprayed onto air-dried soil volatilizes rapidly(4). The amount of chemical that is adsorbed to the soil, evaporates more slowly by a diffusion-controlled mechanism(4).
Literature: (1) Daubert TE, Danner RP; Data Compilation Tables of Properties of Pure Compounds NY, NY: Amer Inst for Phys Prop Data (1989) (2) Riddick JA et al; Organic Solvents 4th ed; NY, NY: Wiley (1986) (3) Lyman WJ et al (eds); Handbook of Chemical Property Estimation Methods, NY: McGraw-Hill Chapt 15 (1982) (4) Reichman R et al; Soil Sci 148: 191-8 (1989)

The Koc for methyl salicylate estimated from molecular structure is 128(1) and is 33(3,SRC) estimated from its water solubility, 7400 mg/L(2), using a regression equation. According to a suggested classification scheme(4), these low Koc values suggest that methyl salicylate would be highly or very highly mobile in soil(SRC).
Literature: (1) Meylan WM et al; Environ Sci Technol 26: 1560-7 (1992) (2) Riddick JA et al; Organic Solvents 4th ed; NY, NY: Wiley (1986) (3) Lyman WJ et al ; Handbook of Chemical Property Estimation Methods, NY: McGraw-Hill Chapt 4 (1982) (4) Swann RL et al; Res Rev 85: 17-28 (1983)

Cincholepidine

gamma-Methylquinoline

Lepidine

MUDSDYNRBDKLGK-UHFFFAOYSA-N

p-Methylquinoline

Lepidene

Lepidin

4-METHYLQUINOLINE

p-methyl quinoline

AC1L1UVN

AC1Q2RAJ

4-Lepidine

ACMC-1AHYH

.gamma.-Methylquinoline

4-methyl quinoline

4-methyl-quinoline

quinol-4-ylmethane

CHEMBL9734

L758

KSC235Q6N

NSC3412

Lepidine (4-Methylquinoline)

SCHEMBL31559

Lepidine, 99%

CTK1D5866

L0024

STR06140

RP20851

4-Methylquinoline, >=99%

CCRIS 2894

HSDB 7153

A22510

A15593

Quinoline, 4-methyl-

HE000809

HE345242

DTXSID7047067

SBB058784

NSC-3412

PS-3771

NSC 3412

M-5284

ZINC1666750

CHEBI:48983

CJ-26989

SC-12713

SC-15612

ST2413199

LS-87752

AJ-29036

DSSTox_GSID_47067

AK-49826

AN-21392

KB-39726

ANW-30727

BR-49826

DSSTox_RID_82083

DSSTox_CID_27067

Lepidine (6CI,8CI)

3S211042

MFCD00006784

3S110963

ZINC01666750

TC-020151

AI3-24277

ST50823863

DB-013319

TX-017072

116169T3O8

AKOS000119150

J-515822

FT-0627792

UNII-116169T3O8

FT-0659357

FT-0083296

BRN 0110926

Z966690984

Tox21_301829

491-35-0

NCGC00184238-02

MCULE-8999201921

NCGC00184238-01

NCGC00256086-01

NCGC00184238-03

NCGC00184238-04

NCGC00184238-05

NCGC00184238-06

NCGC00184238-07

NCGC00184238-08

NCGC00184238-09

NCGC00184238-10

CAS-491-35-0

EINECS 207-734-2

Quinoline, 4-methyl- (9CI)

MolPort-001-781-554

3007-43-0 (hydrochloride)

5-20-07-00389 (Beilstein Handbook Reference)

InChI=1/C10H9N/c1-8-6-7-11-10-5-3-2-4-9(8)10/h2-7H,1H

The Henry's Law constant for 4-methylquinoline is estimated as 7.6X10-7 atm-cu m/mole(SRC) using a fragment constant estimation method(1). This Henry's Law constant indicates that 4-methylquinoline is expected to be essentially nonvolatile from water surfaces(2). 4-Methylquinoline is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 6.4X10-3 mm Hg(3).
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) Walton J; Eng Sci Data Item 77019, p. 29 (1977)

Slightly soluble in water
Literature: Lide, DR (ed.). CRC Handbook of Chemistry and Physics. 81st Edition. CRC Press LLC, Boca Raton: FL 2000, p. 3-308
Literature: #Soluble in ethanol, ether, and acetone.
Literature: Lide, DR (ed.). CRC Handbook of Chemistry and Physics. 81st Edition. CRC Press LLC, Boca Raton: FL 2000, p. 3-308
Literature: #Miscible with alcohol and benzene
Literature: O'Neil, M.J. (ed.). The Merck Index - An Encyclopedia of Chemicals, Drugs, and Biologicals. 13th Edition, Whitehouse Station, NJ: Merck and Co., Inc., 2001., p. 973
Literature: #Soluble in mineral acid; insoluble in alkali
Literature: Lide, D.R., G.W.A. Milne (eds.). Handbook of Data on Organic Compounds. Volume I. 3rd ed. CRC Press, Inc. Boca Raton ,FL. 1994., p. V5 4875
Literature: #In water, 783 mg/liter @ 25 deg C
Literature: Meylan WM et al; Environ Toxicol Chem 15: 100-106 (1996)

The Koc of 4-methylquinoline is estimated as 630(SRC), using a log Kow of 2.61(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that 4-methylquinoline is expected to have low mobility in soil(SRC). The pKa of 4-methylquinoline is 5.67(4), indicating that this compound will partially exist in cation form in the environment and cations generally adsorb to organic carbon and clay more strongly than their neutral counterparts(5).
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. 68 (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) (4) Perrin DD; Dissociation constants of organic bases in aqueous solution. IUPAC Chem Data Ser, Buttersworth, London (1965) (5) Doucette WJ; pp. 141-188 in Handbook of Property Estimation Methods for Chemicals. Boethling RS, Mackay D, eds. Boca Raton, FL: Lewis Publ (2000)

Hexahydrofarnesylacetone

Hexahydrofarnezylacetone

Hexahydrofarnesyl acetone

Perhydrofarnesyl acetone

WHWDWIHXSPCOKZ-UHFFFAOYSA-N

Fitone

AC1L1V4Z

AC1Q5H6P

CTK4J2356

OR13502

SCHEMBL716506

36116P

SBB012620

ST049442

LP023176

STK761211

KB-85744

AN-21434

CC-29299

MFCD00065420

C-25231

ZERO/001268

ZX-AT021772

AKOS016347358

AKOS001727037

W-109084

502-69-2

6,10,14-Trimethylpentadecan-2-one

6,10,14-TRIMETHYL-2-PENTADECANONE

6,10,14-Trimethylpentadeca-2-one

MCULE-5164481361

EINECS 207-950-7

13955-74-3

16825-16-4

6,10,14-trimethyl-pentadecane-2-one

2-Pentadecanone,6,10,14-trimethyl-

2-pentadecanone, 6,10,14-trimethyl

MolPort-001-758-493

2-Pentadecanone, 6,10,14-trimethyl-

Isovaleriansaeure

Isovalericacid

Isovalerianic

Isobutylformic acid

Isopropylacetic acid

isovalerate

Kyselina isovalerova

METHYLBUTANOIC ACID

GWYFCOCPABKNJV-UHFFFAOYSA-N

Isopentanoic acid

Isovalerianic acid

3-Methylbuttersaeure

b-Methylbutyrate

ISOVALERIC ACID

beta-Methylbutyric acid

Delphinic acid

NATURAL ISOVALERIC ACID

3-Methylbutyrate

b-Methylbutyric acid

Isobutyl formic acid

IVA

methyl butanoic acid

3-Methylbutyric

Isovaleric acid, analytical standard

3-Methylbutanoic acid

3-Methylbutyric acid|

iso-valeric acid

3-Methylbutyric acid

ACMC-1BMPI

Isopropyl Acetic Acid, natural

AC1L1V6N

iso-C4H9COOH

Kyselina isovalerova [Czech]

Methylbutanoic acid (Related)

3-methyl-butanoic acid

3,4-Diisovaleryl adrenaline

.beta.-Methylbutyric acid

3-methyl butyric acid

3-methyl-butyric acid

3-Methylbutyric acid: isopropyl-Acetate

AC1Q1P73

Isovaleric acid (natural)

KSC489M7P

S153

Acetic acid, isopropyl-

SCHEMBL43436

3-Methylbutyric acid: isopropyl-Acetic acid

CTK3I9677

HMDB00718

HSDB 629

3-methyl-n-butyric acid

CHEMBL568737

DB03750

Isovaleric acid, 99%

NSC62783

RP18769

STR08356

1BR7X184L5

bmse000373

C08262

ZINC388188

AK116943

BBL027399

BC677309

DTXSID5029182

LS-2386

OR025022

OR111348

OR376668

OR376669

STL146358

WLN: QV1Y1&1

CHEBI:28484

DSSTox_CID_9182

UNII-1BR7X184L5

AJ-20479

AN-21437

ANW-30978

Butanoic acid, 3-methyl-

DSSTox_GSID_29182

Isovaleric acid sodium salt (Salt/Mix)

KB-52997

NSC 62783

NSC-62783

SC-27287

TRA0072843

BB_NC-2309

Butyric acid, 3-methyl-

DSSTox_RID_78698

LMFA01020181

MFCD00002726

AI3-24132

FEMA Number: 3102

RTR-018005

ST24028594

TR-018005

AKOS000119861

J-522594

BRN 1098522

FEMA No. 3102

FT-0627533

I14-10601

Z955123492

Isovaleric acid, natural, >=98%, FG

Tox21_201604

503-74-2

F2191-0067

NA 1760 (Related)

Isovaleric acid, >=99%, FCC, FG

MCULE-5805071360

NCGC00249082-01

NCGC00259153-01

CAS-503-74-2

EINECS 207-975-3

35915-22-1

7050-EP2286915A2

7050-EP2287153A1

7050-EP2289892A1

7050-EP2292590A2

7050-EP2295417A1

7050-EP2301934A1

7050-EP2305656A1

7050-EP2305675A1

7050-EP2308509A1

7050-EP2308828A2

7050-EP2308848A1

7050-EP2308872A1

7050-EP2314585A1

7050-EP2316829A1

7050-EP2374791A1

MolPort-000-871-620

31567-EP2275401A1

31567-EP2277861A1

31567-EP2298763A1

31567-EP2308858A1

31567-EP2311816A1

31567-EP2311817A1

31567-EP2374790A1

66994-EP2298772A1

66994-EP2308839A1

Butanoic acid, 3-methyl-, (R)-

4-02-00-00895 (Beilstein Handbook Reference)

InChI=1/C5H10O2/c1-4(2)3-5(6)7/h4H,3H2,1-2H3,(H,6,7

The Henry's Law constant for isovaleric acid was measured as 8.33X10-7 atm-cu m/mole(1). This value indicates that isovaleric acid will volatilize slowly from water surfaces(2,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 45 days(2,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 330 days(2,SRC). In addition, a pKa of 4.78 for isovaleric acid(3) indicates that isovaleric acid will not significantly volatilize from water as it will exist predominately in the ionic form under environmental pHs(SRC). Isovaleric acid's Henry's Law constant(1) indicates that volatilization from moist soil surfaces may occur(SRC). Isovaleric acid is not expected to volatilize from dry soil surfaces(SRC) based on a measured vapor pressure of 0.44 mm Hg(4).
Literature: (1) Khan I, Brimblecombe P; J Aerosol Sci 23: S897-S900 (1992) (2) Lyman WJ et al; Handbook of Chemical Property Estimation Methods. Washington,DC: Amer Chem Soc pp. 15-1 to 15-29 (1990) (3) Leung HW, Paustenbach DJ; Am J Ind Med 18: 714-23 (1990) (4) Yaws CL; Handbook of Vapor Pressure, Vol 2 C5 to C7 Compounds, Houston,TX: Gulf Publ Co. p. 387 (1994)

The Koc of isovaleric acid is estimated as approximately 100(SRC), using a measured log Kow of 1.16(1) and a regression-derived equation(2,SRC). According to a recommended classification scheme(3), this estimated Koc value suggests that isovaleric acid is expected to have high 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. 14 (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)