Recommended Products
grade
technical grade
Assay
90%
refractive index
n20/D 1.435 (lit.)
bp
74-75 °C/34 mmHg (lit.)
functional group
amine
storage temp.
2-8°C
SMILES string
CC(C)(C)N([O])C(C)(C)C
InChI
1S/C8H18NO/c1-7(2,3)9(10)8(4,5)6/h1-6H3
InChI key
CKJMHSMEPSUICM-UHFFFAOYSA-N
Application
Di-tert-butyl nitroxide (DTBN) can be used as:
- An additive for the synthesis of N-sulfenylimines by oxidative coupling of amines and disulfides or thiols using a copper-based metal-organic framework (MOF) as a catalyst.
- An initiator in the controlled radical polymerization reactions.
- A reagent in the preparation of N-aroyl-o-aroyl-N-tert-butylhdroxylamines by reacting with aromatic acid chlorides.
Reagent for the room-temperature oxidation of primary and secondary benzylamines to imines and for the ESR study of Lewis acid centers in Zeolite X.
Spin label. Has been used in localization of lipid microdomains and thermal phenomena in murine stratum corneum.
accessory
Product No.
Description
Pricing
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
114.8 °F - closed cup
Flash Point(C)
46 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Direct synthesis of N-sulfenylimines through oxidative coupling of amines with disulfides/thiols over copper based metal-organic frameworks
Royal Society of Chemistry Advances, 6(47), 40945-40952 (2016)
The Journal of Organic Chemistry, 50, 5382-5382 (1985)
Lipids, 45(5), 419-427 (2010-04-03)
In this work, we have used electron paramagnetic resonance (EPR) spectroscopy of the small spin label di-tert-butyl nitroxide (DTBN), which partitions the aqueous and hydrocarbon phases, to study the interaction of the terpenes alpha-terpineol, 1,8-cineole, L(-)-carvone and (+)-limonene with the
Z. Chem., 25, 253-253 (1985)
Chemical research in toxicology, 9(4), 737-744 (1996-06-01)
Oxidation of human LDL is implicated as an initiator of atherosclerosis. Isolated low density lipoprotein (LDL) and high density lipoprotein (HDL2) were exposed to aqueous radicals generated from the thermolabile azo compound 2,2'-azobis(2-amidinopropane) dihydrochloride. The primary nonpolar lipid products formed
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