2,6-Di-tert-butyl-4-methylphenol

128-37-0

Butylhydroxytoluene

2,6-Di-tert-butyl-p-cresol

2,6-Di-t-butyl-4-methylphenol

Ionol

DBPC

Stavox

BHT

Impruvol

Ionol CP

Dalpac

Deenax

Dibunol

Ionole

Kerabit

Topanol

Vianol

Antioxidant KB

Antioxidant 4K

Sumilizer BHT

Topanol O

Topanol OC

Vanlube PC

Antioxidant 29

Antioxidant 30

Antioxidant DBPC

Sustane BHT

Tenamene 3

Vanlube PCX

Nonox TBC

Tenox BHT

Phenol, 2,6-bis(1,1-dimethylethyl)-4-methyl-

Chemanox 11

Agidol

Catalin CAO-3

Ionol 1

Advastab 401

3,5-Di-tert-butyl-4-hydroxytoluene

BUKS

Parabar 441

2,6-ditert-butyl-4-methylphenol

Antrancine 8

Vulkanox KB

Catalin antioxydant 1

2,6-Di-tert-butyl-4-cresol

Ionol (antioxidant)

Paranox 441

2,6-Bis(1,1-dimethylethyl)-4-methylphenol

Antioxidant MPJ

Antioxidant 4

Alkofen BP

AO 4K

CAO 1

CAO 3

Di-tert-butyl-p-cresol

Di-tert-butyl-p-methylphenol

Swanox BHT

Antox QT

Tenamen 3

Agidol 1

Antioxidant 264

Bht (food grade)

o-Di-tert-butyl-p-methylphenol

Antioxidant T 501

Ional

Nocrac 200

AO 29

NCI-C03598

2,6-Di-tert-butyl-1-hydroxy-4-methylbenzene

2,6-Di-tert-butyl-p-methylphenol

2,6-Di-terc.butyl-p-kresol

Dbpc (technical grade)

4-Hydroxy-3,5-di-tert-butyltoluene

FEMA No. 2184

4-Methyl-2,6-tert-butylphenol

Butylhydroxytoluenum

Di-tert-butylcresol

AOX 4K

Dibutylhydroxytoluene

2,6-ditert-butyl-4-methyl-phenol

Ionol CP-antioxidant

P 21

2,6-DI-T-BUTYL-P-CRESOL

4-Methyl-2,6-di-tert-butylphenol

AOX 4

Butyl hydroxy toluene

CCRIS 103

Popol

HSDB 1147

BHT 264

Bht(food grade)

NSC 6347

NSC-6347

4-Methyl-2,6-di-terc. butylfenol

EINECS 204-881-4

Ionol BHT

Ralox BHT

2,6-Di-tert-butyl-4-hydroxytoluene

2,6-Di-tert-butyl-4-methyl-phenol

1-Hydroxy-4-methyl-2,6-di-tert-butylbenzene

MFCD00011644

2,6-ditertiary-butyl-p-cresol

Dbpc(technical grade)

DTXSID2020216

E321

CHEBI:34247

2,6-Di-tert-butyl-4-methylhydroxybenzene

AI3-19683

p-Cresol, 2,6-di-tert-butyl-

INS-321

1P9D0Z171K

2,6-bis(tert-butyl)-4-methylphenol

2,6-Di-tert-butylcresol

CHEMBL146

Di-tert-Butyl-4-methylphenol

DTXCID20216

INS NO.321

E-321

FEMA 2184

NSC6347

2,6-di-tert-butyl-4-methyl phenol

NCGC00091761-03

Tonarol

Toxolan P

Caswell No. 291A

2,6-DI(TERT-BUTYL-D9)-4-METHYLPHENOL-3,5,O-D3

Annulex BHT

BUTYLHYDROXYTOLUENE (EP MONOGRAPH)

BUTYLHYDROXYTOLUENE [EP MONOGRAPH]

CAS-128-37-0

Butylohydroksytoluenu

Butylohydroksytoluenu [Polish]

Di-tert-butyl-p-cresol (VAN)

di-tert-butyl-methylphenol

Di tert butyl methylphenol

2,6-Di-terc.butyl-p-kresol [Czech]

EPA Pesticide Chemical Code 022105

2,6 Di tert butyl p cresol

UNII-1P9D0Z171K

4-Methyl-2,6-di-terc. butylfenol [Czech]

2,6 Di t butyl 4 methylphenol

Lowinox BHT

Nipanox BHT

BHT Swanox

BHT, food grade

4-Methyl-2,6-di-t-butyl-phenol

2, food grade

2,6 Di tert butyl 4 methylphenol

3IM

Dibutyl-para-cresol

NAUGARD BHT

PERMANAX BHT

TOPANOL BHT

YOSHINOX BHT

ANTAGE BHT

TOPANOL OL

VANOX PC

IONOL K

Spectrum_001790

BHT FCC/NF

SpecPlus_000768

CATALIN CAO 3

Methyldi-tert-butylphenol

Spectrum3_001849

Spectrum5_001612

BHT [INCI]

Hydagen DEO (Salt/Mix)

BHT [FCC]

LUBRIZOL 817

ULTRANOX 226

EC 204-881-4

2,6-di-Butyl-para-cresol

2.6-di-t-butyl-p-cresol

SCHEMBL3950

2,6-ditert-butyl-p-cresol

p-Cresol,6-di-tert-butyl-

Di-tert-Butylparamethylphenol

BSPBio_003238

KBioSS_002281

2,6-di-tert.butyl-p-cresol

IONOL 330

MLS000069425

BIDD:ER0031

DivK1c_006864

P 21 (PHENOL)

SPECTRUM1600716

2,6-bis-tert-butyl-p-cresol

2,6-di-tert-butyl-paracresol

2,6-di-tert-butylmethylphenol

2,6-di-tert. butyl-p-cresol

2,6-di-tert.-butyl-p-cresol

T 501 (PHENOL)

2,6-di-tert-butyl-para-cresol

2,6-di-tert-Butyl-methylphenol

2,6-ditertbutyl-4-methylphenol

2,6-di-t butyl-4-methylphenol

2.6-di-t-butyl-4-methylphenol

KBio1_001808

KBio2_002280

KBio2_004848

KBio2_007416

KBio3_002738

2,6-di-tert-butyl-4-methylenol

2,6-di-tert-butyl-4methylphenol

2,6-di-tert-butyl4-methylphenol

2,6-di-tertbutyl-4-methylphenol

2,6-ditert.butyl-4-methylphenol

BHT1506

2,6-Di(tert-butyl)hydroxytoluene

18 - Anti-oxidants in copra oil

2,6-di(t-butyl)-4-methylphenol

2,6-di-t- butyl-4-methylphenol

2,6-di-t-butyl 4-methyl phenol

2,6-di-t-butyl-4-methyl phenol

2,6-di-t-butyl-4-methyl-phenol

3,5-di-t-butyl-4-hydroxytoluene

HMS2091E21

HMS2231M22

HMS3369G17

HMS3750M21

Pharmakon1600-01600716

2,1-dimethylethyl)-4-methylphenol

2,6-di-tert-butyl 4-methylphenol

2,6-di-tert-butyl-4 methylphenol

2,6-di-tert-butyl4-methyl phenol

2,6-di-tert.butyl-4-methylphenol

2,6-ditert.-butyl-4-methylphenol

2.6-di-tert-butyl-4-methylphenol

4-methyl-2,6-di-tert.butylphenol

2,6-di-ter-butyl-4-methyl-phenol

2,6-Di-tert.-Butyl4-methylphenol

2,6-ditertiarybutyl-4-methylphenol

2.6-di- t-butyl- 4-methylphenol

AMY40200

HY-Y0172

STR04334

2,6 -di-tert-butyl-4-methylphenol

2,6-di(tert-butyl)-4-methylphenol

2,6-Di-tert-butyl-p-cresol, 8CI

2,6-di-tert.-butyl-4-methylphenol

Tox21_113537

Tox21_201093

Tox21_303408

2,6-di-tert-butyl-p-cresol (BHT)

2,6-Di-tert-butyl-para-methylphenol

BDBM50079507

NSC759563

s6202

STL277184

2,6-di-tert. butyl-4-methyl phenol

2,6-Di-(tert-butyl)-4-methylphenol

AKOS000269037

Tox21_113537_1

CCG-207937

CS-W020053

MCULE-4627478482

NSC-759563

2,6-TERT-BUTYL-4-METHYLPHENOL

Phenol, 2,6-di-tert-butyl-4-methyl-

NCGC00091761-01

NCGC00091761-02

NCGC00091761-04

NCGC00091761-05

NCGC00091761-06

NCGC00091761-07

NCGC00257275-01

NCGC00258645-01

AC-10553

SMR000059076

2,6-Di-tert-butyl-4-methylphenol (BHT)

2,6-Di-tert-butyl-4-methylphenol, 99%

BUTYLHYDROXYTOLUENUM [WHO-IP LATIN]

SBI-0052890.P002

4-HYDROXY-3,5-DI-T-BUTYL-TOLUENE

2,6-Di-tert-butyl-4-methylphenol, >=99%

D0228

NS00010740

Phenol,6-bis(1,1-dimethylethyl)-4-methyl-

T 501

2,6-bis-(1,1-dimethylethyl)-4-methylphenol

4-Methyl-2,6- di(1,1-dimethylethyl)phenol

4-METHYL-2,6-DITERTIARY-BUTYL-PHENOL

EN300-52982

PK04_181024

2,6-Di-tert-butyl-1-hydroxy-4-methyl benzene

D02413

D77866

MLS-0146297.0001

AB00053233_09

Phenol, 3,5-bis(1,1-dimethylethyl)-4-methyl-

2,6-Bis(1,1-dimethylethyl)-4-methylphenol, 9CI

2,6-Di-tert-butyl-4-methylphenol, puriss., 99%

A937188

AC-907/25014329

Q221945

SR-01000735918

SR-01000735918-2

W-108376

9FC4DFC8-480D-487C-A74A-2EC9EECE92C4

BENZENE,1,3-DITERT.BUTYL,2-HYDROXY,5-METHYL

BRD-K53153417-001-01-3

BRD-K53153417-001-06-2

F0001-0395

Z764922868

2,6-Di-tert-butyl-4-methylphenol, purum, >=99.0% (GC)

WLN: 1X1 & 1 & R BQ E1 CX1 & 1 & 1

2,6-Di-tert-butyl-4-methylphenol, >=99.0% (GC), powder

2,6-Di-tert-butyl-4-methylphenol, SAJ first grade, >=99.0%

2,6-Di-tert-butyl-4-methylphenol, tested according to Ph.Eur.

3,5-Di-tert-4-butylhydroxytoluene (BHT), analytical standard

2,6-Di-tert-butyl-4-methylphenol 1000 microg/mL in Acetonitrile

Butylhydroxytoluene, European Pharmacopoeia (EP) Reference Standard

2,6-Di-tert-butyl-4-methylphenol, certified reference material, TraceCERT(R)

2,6-DI-TERT-BUTYL-P-CRESOL2,6-BIS(1,1-DIMETHYLETHYL)-4-METHYL-PHENOL

InChI=1/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H

The Henry's Law constant for 2,6-di-t-butyl-p-cresol is estimated as 2.5X10-3 atm-cu m/mole(SRC) using a fragment constant estimation method(1). 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 5 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 6 days(SRC). However, volatilization from water surfaces is expected to be attenuated by adsorption to suspended solids and sediment in the water column. The volatilization half-life from a model pond is about 120 days when adsorption is considered(3). 2,6-Di-t-butyl-p-cresol's Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). 2,6-Di-t-butyl-p-cresol is not expected to volatilize from dry soil surfaces(SRC) based upon a vapor pressure of 5.16X10-3 mm Hg(4).
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) Perry RH, Green D; Perry's Chemical Handbook. Physical and Chemical Data. 6th ed., New York, NY: McGraw-Hill (1984) (3) US EPA; EXAMS II Computer Simulation (1987) (4) Meylan WM, Howard PH; Chemosphere 26: 2293-99 (1993)

Using a structure estimation method based on molecular connectivity indices(1), the Koc of 2,6-di-t-butyl-p-cresol can be estimated to be 1.5X10+4(SRC). According to a classification scheme(2), this estimated Koc value suggests that 2,6-di-t-butyl-p-cresol is expected to be immobile in soil.
Literature: (1) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of Nov 3, 2016: http://www2.epa.gov/tsca-screening-tools (2) Swann RL et al; Res Rev 85: 17-28 (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).

Fluoren-9-ol, 3,6-dimethoxy-9-(2-phenylethynyl)-

NBXSDRNTJOXRMZ-UHFFFAOYSA-N

3,6-dimethoxy-9-(2-phenylethynyl)-fluoren-9-ol

3,6-Dimethoxy-9-(phenylethynyl)-9H-fluoren-9-ol #

2-Aminoanthracene

anthracen-2-amine

613-13-8

2-Anthramine

2-Anthrylamine

2-ANTHRACENAMINE

2-Anthracylamine

beta-Aminoanthracene

.beta.-Aminoanthracene

DTXSID2024458

CHEBI:34260

MFCD00003582

8240818JGU

NSC-400535

2-Anthracenamide

DTXCID904458

CCRIS 22

CAS-613-13-8

HSDB 4041

EINECS 210-330-9

NSC 400535

BRN 2209414

AI3-52501

2-aminoanthracen

UNII-8240818JGU

Anthracene, 2-amino

2-Aminoanthracene, 96%

AMINOANTHRACENE, 2-

MLS002302986

BIDD:ER0574

BIDD:GT0166

CHEMBL83154

SCHEMBL103680

WLN: L C666J EZ

2-ANTHRACENAMINE [HSDB]

YCSBALJAGZKWFF-UHFFFAOYSA-

HMS3039P14

STR04539

Tox21_201567

Tox21_303299

NSC400535

AKOS004904683

MCULE-3149525306

NCGC00091622-01

NCGC00091622-02

NCGC00091622-03

NCGC00257001-01

NCGC00259116-01

SMR001307303

SY011614

DB-053837

NS00010865

2-Aminoanthracene 10 microg/mL in Cyclohexane

2-Aminoanthracene, technical, >=90% (HPLC)

T71122

A833154

Q26841182

InChI=1/C14H11N/c15-14-6-5-12-7-10-3-1-2-4-11(10)8-13(12)9-14/h1-9H,15H2

The Henry's Law constant for 2-anthracenamine has been estimated to be 3.0X10-7 atm-cu m/mol at 25 deg C by combining a measured Henry's Law Constant for anthracene of 7.2X10-4 atm-cu m/mole at 25 deg C(1) with an estimation method based on structural bond contributions to intrinsic hydrophilic character(2,SRC). Given this value of Henry's Law constant and the relatively high Koc (15904 to 94276(4)) of 2-anthracenamine, it appears as though volatilization would not be a significant removal process from soil or water(3,SRC). This is apparent from the result of an EXAMS run for a model pond in which the effects of adsorption were considered. In this case, the volatilization half-life was determined to be 98 years(5,SRC).
Literature: (1) Mackay D et al; Environ Sci Tech 13: 333-7 (1982) (2) Hine J, Mookerjee PK J Org Chem 40: 292-8 (1975) (3) Lyman WJ et al; Handbook of Chemical Property Estimation Methods NY: McGraw-Hill pp. 15-1 to 15-32 (1982) (4) Means JC et al; Environ Sci Tech 16: 93-8 (1982) (5) USEPA; EXAMS II computer simulation (1987)

Koc ranging between 94276 and 15904 were measured for 2-anthracenamine in fourteen different soils and sediments(1). These Koc are indicative of extremely strong adsorption to soil and suspended solids and sediments in water(2,SRC).
Literature: (1) Means JC et al; Environ Sci Tech 16: 93-8 (1982) (2) Swann RL et al; Res Rev 85: 117-28 (1983)

2,4,4,6,6,8,8-Heptamethyl-2-nonene

Sulfurous acid, decyl 2-propyl ester

FJBUSDYACCIUEW-UHFFFAOYSA-N

Dimethyl trisulfide

3658-80-8

Trisulfide, dimethyl

Methyl trisulfide

DIMETHYLTRISULFIDE

2,3,4-Trithiapentane

Dimethyl trisulphide

(methyltrisulfanyl)methane

dimethyltrisulfane

DMTS

FEMA No. 3275

CH3SSSCH3

3E691T3NL1

NSC-97324

UNII-3E691T3NL1

Dimethyl trisufide

EINECS 222-910-9

2,4-Trithiapentane

NSC 97324

trisulfane, dimethyl-

1,3-Dimethyltrisulfane

AI3-26172

1,3-Dimethyltrisulfane #

SCHEMBL446658

methylsulfanyldisulfanyl-methane

CHEBI:4614

DTXSID9063118

DIMETHYL TRISULFIDE [FHFI]

Dimethyl trisulfide, >=98%, FG

NSC97324

MFCD00039808

NSC801680

s6311

AKOS015897465

NSC-801680

2,3,4-Trithiapentane; NSC 97324

Dimethyl trisulfide, analytical standard

BS-43830

1,3-Dimethyltrisulfane (ACD/Name 4.0)

DB-003633

HY-128454

CS-0099182

D3418

NS00022106

C08372

D90187

InChI=1/C2H6S3/c1-3-5-4-2/h1-2H

A823301

Q-100435

Q5277321

FLAMMABLE LIQUID, N.O.S. (DIMETHYL TRISULPHIDE)

2,2,4,4,5,5,7,7-Octamethyloctane

5171-85-7

Octane, 2,2,4,4,5,5,7,7-octamethyl-

DTXSID20199662

2,2,4,4,5,5,7,7-octamethyl-octane

NS00096349

Oxime-, methoxy-phenyl-_

67160-14-9

Methyl N-hydroxybenzimidate

SCHEMBL8530447

HUYDCTLGGLCUTE-HJWRWDBZSA-N

Methyl N-hydroxybenzenecarboximidoate #

methyl (z)-N-hydroxybenzenecarboximidate

Benzenecarboximidic acid, N-hydroxy-, methyl ester

2,4-Dimethyloxazole

7208-05-1

2,4-Dimethyl-1,3-oxazole

Oxazole, 2,4-dimethyl-

dimethyl oxazole

2,4-DIMETHYL-OXAZOLE

G0W5QQT2LD

UNII-G0W5QQT2LD

2,4-Dimethyl-1,3-oxazole #

DTXSID60222408

CHEBI:195692

MFCD00234124

AKOS006280508

CS-W011337

DB-074523

DB-243437

D3766

EN300-102560

T71266

A837415

InChI=1/C5H7NO/c1-4-3-7-5(2)6-4/h3H,1-2H

NONANE

n-Nonane

111-84-2

Shellsol 140

Nonyl hydride

nonan

Iotrochotin

CCRIS 6081

HSDB 107

Lodyne S

EINECS 203-913-4

UNII-T9W3VH6G10

NSC 72430

T9W3VH6G10

DTXSID9025796

CHEBI:32892

Lodyne S 100

NSC-72430

NONANE-5-C12

DTXCID005796

66039-00-7

EC 203-913-4

MFCD00009574

Heptane, ethyl-

Nonane, analytical standard

144637-82-1

CH3-(CH2)7-CH3

CH3-[CH2]7-CH3

CAS-111-84-2

Nonanes

Nonane; NSC 72430; Nonane-5-C12; Shellsol 140; n-Nonane

n-C9H20

DD9

n-Nonane 10 microg/mL in Cyclohexane

n-Nonane 1000 microg/mL in Methanol

Nonane, 99%

NONANE [HSDB]

NONANE MFC9 H20

Nonane, anhydrous, >=99%

CHEMBL335900

Nonane, ReagentPlus(R), 99%

NSC72430

Tox21_201479

Tox21_303148

LMFA11000579

AKOS015904046

MCULE-1865327912

UN 1920

NCGC00091787-01

NCGC00091787-02

NCGC00257029-01

NCGC00259030-01

LS-13716

DB-041010

DB-063623

N0286

NS00007716

S0281

2-ISOPROPYL-4-METHYL-6-HYDROPYRIMIDINE

A802420

Q150694

W-108667

C8F3CAB9-DAF5-4085-84EB-07C0AB04D3A1

InChI=1/C9H20/c1-3-5-7-9-8-6-4-2/h3-9H2,1-2H

61193-19-9

The Henry's Law constant for n-nonane is estimated as 3.4 atm-cu m/mole(SRC) derived from its vapor pressure, 4.45 mm Hg(1), and water solubility, 22 mg/L)(2). This Henry's Law constant indicates that n-nonane is expected to volatilize rapidly from water surfaces(3). Based on this Henry's Law constant, the volatilization half-life from a model river (1 m deep, flowing 1 m/sec, wind velocity of 3 m/sec)(3) is estimated as 3.3 hours(SRC). The volatilization half-life from a model lake (1 m deep, flowing 0.05 m/sec, wind velocity of 0.5 m/sec)(3) is estimated as 4.5 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 155 days if adsorption is considered(4). n-Nonane's estimated Henry's Law constant indicates that volatilization from moist soil surfaces may occur(SRC). The potential for volatilization of n-nonane from dry soil surfaces may exist(SRC) based upon the vapor pressure(1).
Literature: (1) Daubert TE, Danner RP; Physical and Thermodynamic Properties of Pure Chemicals Data Compilation. Washington, DC: Taylor and Francis (1989) (2) Riddick JA et al; Techniques of Chemistry. 4th ed. Volume II. Organic Solvents. New York, NY: John Wiley and Sons (1985) (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 n-nonane is estimated as 8.0X10+4(SRC), using a log Kow of 5.65(1) and a regression-derived equation(2). According to a classification scheme(3), this estimated Koc value suggests that n-nonane is expected to be immobile in soil. Freundlich absorption coefficients of log 4.50 and log 4.01 were measured in Oberlausitz lignite (11.1% moisture content; 53.5 wt% carbon content; 0.6 wt % nitrogen content) and Pahokee peat soil (10.2% moisture content; 46.1 wt% carbon content; 3.3 wt % nitrogen content), respectively(4).
Literature: (1) Sangster J; LOGKOW Database. A databank of evaluated octanol-water partition coefficients (Log P). Available from, as of Oct 30, 2013: http://logkow.cisti.nrc.ca/logkow/search.html (2) US EPA; Estimation Program Interface (EPI) Suite. Ver. 4.1. Nov, 2012. Available from, as of Oct 30, 2013: http://www.epa.gov/oppt/exposure/pubs/episuitedl.htm (3) Swann RL et al; Res Rev 85: 17-28 (1983) (4) Endo S et al; Environ Sci Technol 42): 5897-5903 (2008)

2-DODECANOL

Dodecan-2-ol

10203-28-8

(S)-dodecan-2-ol

Dodecanol-2

Decyl methyl carbinol

91681-57-1

dodecanol 2

2-hydroxydodecane

2-lauryl alcohol

decylmethylcarbinol

secondary dodecanol

NSC86142

EINECS 233-500-4

2-Dodecanol, 99%

AI3-35259

SCHEMBL120359

CHEMBL446067

DTXSID70864232

CHEBI:195616

CCG-40548

MFCD00004551

NSC 86142

NSC-86142

4-(4-NITROPHENYL)-3-BUTEN

AKOS009156867

HY-W142410

MCULE-9407036721

AS-56322

CS-0204457

D2960

NS00045094

D90139

J-000549

(RS)-2-Dodecanol; (+/-)-2-Dodecanol; 2-Lauryl alcohol; NSC 86142

2,4,4-Trimethylpentan-1-ol

2,4,4-Trimethyl-1-pentanol

16325-63-6

1-Pentanol, 2,4,4-trimethyl-

NSC24283

EINECS 240-403-0

1-Pentanol,4,4-trimethyl-

SCHEMBL195061

ZNRVRWHPZZOTIE-UHFFFAOYSA-

DTXSID301311590

MFCD00004741

NSC 24283

NSC-24283

2,4,4-Trimethyl-1-pentanol, 98%

AKOS009156948

SB84344

LS-08700

CS-0275754

NS00053618

EN300-1251153

J-010025

InChI=1/C8H18O/c1-7(6-9)5-8(2,3)4/h7,9H,5-6H2,1-4H3

5-METHYL-3-HEXEN-2-ONE

5166-53-0

(E)-5-methylhex-3-en-2-one

3-Hexen-2-one, 5-methyl-

2-Oxo-5-methylhex-3-ene

5-Methyl-3E-hexen-2-one

FEMA No. 3409

1821-29-0

(3E)-5-methylhex-3-en-2-one

8L0NZD2EIQ

(E)-5-Methyl-3-hexen-2-one

3-Hexen-2-one, 5-methyl-, (E)-

(3E)-5-Methyl-3-hexen-2-one

filbert hexenone

BRN 1720101

3-Hexen-2-one, 5-Me

5-methyl-hex-3-en-2-one

EINECS 225-950-5

AI3-22171

MFCD00012166

isobutylidene acetone

UNII-8L0NZD2EIQ

3-01-00-03005 (Beilstein Handbook Reference)

SCHEMBL320739

CHEBI:195655

5-Methyl-3-hexen-2-one (contains 5-Methyl-4-hexen-2-one)

DTXSID601310541

3-Hexen-2-one, 5-methyl-, trans

BBL027791

LMFA12000010

STL372951

METHYL-3-HEXEN-2-ONE, 5-

AKOS009158783

3-Hexen-2-one, 5-methyl-, (3E)-

5-METHYL-3-HEXEN-2-ONE [FHFI]

VS-08592

CS-0199438

D91593

5-Methyl-3-hexen-2-one, technical grade, 75%

5-METHYL-3-HEXEN-2-ONE (ISOMERS MIXTURE)

Q27270690