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D47404

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

Name: 2,6-Di-<I>tert</I>-butyl-4-methylphenol
Brand: ALDRICH

99%

Synonym(s):

2,6-Di-tert-butyl-p-cresol, BHT, Butylated hydroxytoluene, Butylhydroxytoluene, DBPC

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About This Item

Linear Formula:

[(CH₃)₃C]₂C₆H₂(CH₃)OH

CAS Number:

128-37-0

Molecular Weight:

220.35

EC Number:

204-881-4

UNSPSC Code:

12162002

PubChem Substance ID:

329798801

Beilstein/REAXYS Number:

1911640

MDL number:

MFCD00011644

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vapor density

7.6 (vs air)

vapor pressure

<0.01 mmHg ( 20 °C)

assay

99%

autoignition temp.

878 °F

bp

265 °C (lit.)

mp

69-73 °C (lit.)

SMILES string

Cc1cc(c(O)c(c1)C(C)(C)C)C(C)(C)C

InChI

1S/C15H24O/c1-10-8-11(14(2,3)4)13(16)12(9-10)15(5,6)7/h8-9,16H,1-7H3

InChI key

NLZUEZXRPGMBCV-UHFFFAOYSA-N

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Application

Antioxidant

pictograms

GHS09

signalword

Warning

hcodes

H410

pcodes

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

260.6 °F - open cup

flash_point_c

127 °C - open cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Hantzsch reaction: synthesis and characterization of some new 1,4-dihydropyridine derivatives as potent antimicrobial and antioxidant agents.

A M Vijesh et al.

European journal of medicinal chemistry, 46(11), 5591-5597 (2011-10-05)

In the present study two new series of Hantzsch 1,4-dihydropyridine derivatives (1,4-DHPs) containing substituted pyrazole moiety (4a-f and 5a-f) were synthesized by the reaction of 3-aryl-1H-pyrazole-4-carbaldehydes with 1,3-dicarbonylcompounds (ethylacetoacetate and methylacetoacetate) and ammonium acetate. The newly synthesized compounds were characterized

Butylated hydroxytoluene (BHT): a review.

H Babich

Environmental research, 29(1), 1-29 (1982-10-01)

Effects of feeding Spodoptera littoralis on lima bean leaves: IV. Diurnal and nocturnal damage differentially initiate plant volatile emission.

Gen-ichiro Arimura et al.

Plant physiology, 146(3), 965-973 (2008-01-01)

Continuous mechanical damage initiates the rhythmic emission of volatiles in lima bean (Phaseolus lunatus) leaves; the emission resembles that induced by herbivore damage. The effect of diurnal versus nocturnal damage on the initiation of plant defense responses was investigated using

Metabolism and pulmonary toxicity of butylated hydroxytoluene (BHT).

H Witschi et al.

Pharmacology & therapeutics, 42(1), 89-113 (1989-01-01)

Review: putative mutagens and carcinogens in foods. III. Butylated hydroxytoluene (BHT).

A M Malkinson

Environmental mutagenesis, 5(3), 353-362 (1983-01-01)

Although the average American's daily consumption of BHT can be measured in milligrams, there are numerous reports that BHT causes organ damage in laboratory animals. Only a few genotoxic effects of BHT have been reported, however, including mutagenicity in the

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