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Safety Information

D3292

Sigma-Aldrich

2,6-Di-tert-butylphenol

~99% (GC)

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About This Item

Linear Formula:
[(CH3)3C]2C6H3OH
CAS Number:
128-39-2
Molecular Weight:
206.32
Beilstein:
1841887
EC Number:
204-884-0
MDL number:
MFCD00008820
UNSPSC Code:
12000000

vapor pressure

<0.01 mmHg ( 20 °C)

Assay

~99% (GC)

bp

253 °C (lit.)

mp

34-37 °C (lit.)

storage temp.

2-8°C

SMILES string

CC(C)(C)c1cccc(c1O)C(C)(C)C

InChI

1S/C14H22O/c1-13(2,3)10-8-7-9-11(12(10)15)14(4,5)6/h7-9,15H,1-6H3

InChI key

DKCPKDPYUFEZCP-UHFFFAOYSA-N

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Description
Pricing

Pictograms

Exclamation markEnvironment
GHS07,GHS09

Signal Word

Warning

Hazard Statements

H315,H410

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1 - Skin Irrit. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Flash Point(F)

227.3 °F - closed cup

Flash Point(C)

108.5 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
071H3467
024H3557

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Stanley J Stachelek et al.
Journal of biomedical materials research. Part A, 82(4), 1004-1011 (2007-03-21)
Polyurethane cardiovascular implants are subject to oxidation initiated surface degradation, which is mediated by monocyte-derived macrophages (MDM); this often leads to surface cracking and device failure. The present studies examined the hypothesis that covalently attaching antioxidant, di-tert-butylphenol (DBP), to the
Mehmet Tümer et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 70(3), 477-481 (2007-09-07)
Crystals of the 3,3'-5,5'-tetra-tert-butyl-4,4'-diphenoquinone (TTBDQ) in the reaction mixture DCM/MeOH (1:1, v/v) were obtained as a result of CC coupling reaction of the sterically hindered phenol (2,6-di-tert-butylphenol, DTBP) using the binuclear Co(II) complexes. The oxidation product (TTBDQ), C(28)H(40)O(2), crystallizes in
G Haeseler et al.
European journal of anaesthesiology, 20(3), 220-224 (2003-03-26)
Propofol is a phenol derivative (2,6 di-isopropylphenol) with a unique effect profile including activating effects on GABA(A) and blocking effects on voltage-operated sodium channels. If the substituents in the 2- and the 6-positions are replaced by tert-butyl groups, the resulting
Shinsuke Ishihara et al.
Journal of the American Chemical Society, 133(40), 16119-16126 (2011-08-31)
Porphyrin derivatives bearing 2,6-di-tert-butylphenol substituents at their 5,15-positions undergo reversible photoredox switching between porphyrin and porphodimethene states as revealed by UV-vis spectroscopy, fluorescence spectroscopy, and X-ray single-crystal analyses. Photoredox interconversion is accompanied by substantial variations in electronic absorption and fluorescence
Y Fujimoto et al.
The Journal of pharmacy and pharmacology, 36(3), 195-197 (1984-03-01)
The inhibitory effects of NN'-diphenyl-p-phenylenediamine (DPPD), sodium diethyldithiocarbamate (SDDC) and 2,6-di-t-butylphenol (DTBP) on the generation of medullary prostaglandin E have been compared. DPPD (1 microM) and SDDC (1 mM) failed to inhibit arachidonic acid-induced stimulation of prostaglandin E synthesis, while
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