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)