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Safety Information

34800

Sigma-Aldrich

2,6-Di-tert-butylphenol

purum, ≥98.0% (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:
12352100

vapor pressure

<0.01 mmHg ( 20 °C)

grade

purum

Assay

≥98.0% (GC)

bp

253 °C (lit.)

mp

34-37 °C (lit.)
34-37 °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 Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

34800-50G-F:
34800-250G-F:
34800-BULK-F:
34800-1KG-F:

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Certificates of Analysis (COA)

Lot/Batch Number
SZBG3300H
SZBG2940H
SZBG2870H
SZBG2670H
SZBG2570H

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Jörg Ahrens et al.
Anesthesia and analgesia, 99(1), 91-96 (2004-07-30)
The anesthetic propofol (2,6 diisopropylphenol) mediates some of its effects by activating inhibitory chloride currents in the lower brainstem and spinal cord. The effects comprise direct activation of gamma-aminobutyric acid-A and glycine receptors in the absence of the natural agonist
Synthesis and biological evaluation of 2,6-di-tert-butylphenol hydrazones as 5-lipoxygenase inhibitors.
A M Cuadro et al.
Bioorganic & medicinal chemistry, 6(2), 173-180 (1998-04-21)
Juan Ruiz et al.
Bioorganic & medicinal chemistry, 11(19), 4207-4216 (2003-09-03)
The dual or selective ability of 24 derived mono- and 2,6-di-tert-butylphenols (DTBP) to act as inhibitors of cyclooxygenase (COX) and/or 5-lipoxygenase (LOX) enzymes is investigated. Firstly, we explored the conformational variability of the compounds. It is found that dual inhibitors
Zhen-wei Fang et al.
Huan jing ke xue= Huanjing kexue, 25(3), 98-101 (2004-08-26)
A degrading bacterial strain F-3-4 for 2,6-Di-tert-butylphenol (2,6-DTBP) was isolated from biofilm in acrylic fiber wastewater treatment structures. By acclimation, its capacity for degradation of 2,6-DTBP was enhanced by 26%. It was identified as Alcaligenes sp. according to morphological, physiological
Jörg Ahrens et al.
Pharmacology, 83(2), 95-98 (2008-12-10)
Modulation of inhibitory synaptic transmission within the central nervous system contributes considerably to the anaesthetic effects of propofol and its analogues in vivo. We have studied the effects of the non-anaesthetic propofol analogue 2,6-di-tert-butylphenol on rat alpha(1)beta(2)gamma(2) GABA(A) receptors expressed
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