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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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Properties

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

Description

Application

Antioxidant

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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

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